| • |
Alzheimer's, Dementia, and Parkinson's Disease - Douglas Scharre, MD |
| • |
Asset Protection & Financial Management - John Greener |
| • |
Cancer Care - Richy Agajanian, MD |
| • |
Caregiver Challenges - Sue Salach-Cutler |
| • |
Communication Through The Generations - David Solie, MS, PA |
| • |
Diabetes - Joy K. Richardson, RD, CDE |
| • |
Elder Care at Home - Ethan Kassel, MSW, LCSW, C-ASWCM - Steve Barlam |
| • |
Elder Law - Shana Siegel, Esq., CELA - Ellen Morris, Esq. - Howard S. Krooks, JD, CELA, CAP |
| • |
End-of-Life Issues - Vincent Dopulos, MA, LPC, RDT |
| • |
Fitness - Deborah Quilter |
| • |
Geriatrics - Robert A Murden, MD |
| • |
Home Care Solutions - Emma R. Dickison |
| • |
Home Health Care & Palliative Care - Pamela Fishman, LCSW |
| • |
Home Health Modifications - Connie Hallquist |
| • |
Senior Housing Solutions - Tiffany Wise - Mike Campbell |
| • |
Incontinence Issues - Brian Christine, MD |
| • |
Integrative Medicine - Rashmi Gulati, MD |
| • |
Live In Care - Kathy N. Johnson, PhD, CMC |
| • |
Managing Medicare - Ross Blair |
| • |
Memory Care - AnnaMarie Barba - Crystal Roberts |
| • |
Mobility Issues - Nick Gutwein |
| • |
Nutrition Know-How - Dr. Gourmet, Timothy S. Harlan, M.D. |
| • |
Quality of Life - Joan Garbow, MSW, LCSW, CCM |
| • |
Safety and Hospitalization Concerns - Martine Ehrenclou, M.A. |
| • |
Senior Healthcare - Archelle Georgiou, MD |
| • |
Senior Medical Issues - Chris Iliades, MD |
| • |
Senior Transitions - Mary Kay Buysse, MS |
![]() | Douglas Scharre, MD, is the Director of the Division of Cognitive Neurology and an Associate Professor of Neurology at the Ohio State University Medical Center in Columbus, where he serves as the Medical Director of their Neurobehavior and Memory Disorders Clinics. Dr. Scharre is also the author of Long-Term Management of Dementia (Neurological Disease and Therapy). View Douglas's full Bio |
| Q: |
I take care of my 91 year old mother who has advanced Lewy Body Dementia, where she is hallucinating days and nights and is quite delusional. She does not recognize me or where she is, and is very repetitive with basic questions. At night, usually all night, she yells and calls out my deceased family members' names very loudly, as well as reliving past episodes of her life like "Frankie, shut off the stove before the food burns!!" as well as the occasional "Police help!" and two-sided conversations with imaginary people. Her nighttime drug protocol now is Trazadone 37 mg, also Seroquel 25 mg and Namenda 2.5 mg at about 8 PM when we put her to bed and later melatonin 10 mg at 10 PM. The medicine is not really effective for any decent length of peaceful, restful sleep (six hours would be wonderful). Could there by any success with Galantamine for reduction of hallucinations or sleeping issues? She does not sleep during the day and has no other medical conditions besides glaucoma. Louis |
| A: |
Is it possible she is talking in her sleep? Talk to her doctor about medication adjustments. I would consider changing only one medication at a time. Trazodone can often be used at 50 to 100 mg dose at night (even higher if helpful). Seroquel can often be increased to 50 or 75 mg at night. If that is not working, her doctor could consider very low dose 0.25 mg lorazepam. Other choices might include zolpidem or gabapentin. Galantamine is not known to cause sleep issues, but it would not typically get rid of them either. |
| Back To Top |
| Q: |
My mom is in the mid stage of dementia. She has been living with my family (husband and 2 elementary age children) for a year and a half. Her condition has deteriorated enough that I can no longer provide a safe, secure environment for her, and keep my family sane as well. Because she will have to be on Medicaid very soon, our living options are very limited. We are considering a memory care facility (up to 80 residents) and I know she will fight like mad to avoid it. She has times where she is higher functioning. What is the best way to approach this? I don't know what to say to make it less scary to her and also to make sure she will move in there asap. Sara from WA |
| A: |
Since I do not know your mother very well, this may be hard. Many times they will adapt very well after a honeymoon adjustment period. However, I would consider telling her that TEMPORARILY she will be staying at a new place where they will be providing activity therapy to help with her brain, that you will be coming to check in on her frequently and that you will be getting assessments of how the therapy is going. It may be helpful to ask her doctor if he/she would also recommend this place to your mother as a place than can help with her brain condition. |
| Back To Top |
| Q: |
My father is 67 years old and had a quadruple bypass 6 years ago. He has had diabetes for 15 years and a recent amputation, as well as 6 small strokes. He has dementia—I’m not sure at what stage it is, but is recently hallucinating and saying weird things at night. He wants to get out of bed 10 times a night, then sleeps a lot during the day. He takes ambient and nortriptyline at night and has body tremors as well. My question is how can we know if he has Parkinson's or dementia? We aren’t sure how to care for him. My mother is in denial and says he can do more for himself than he does. Elaine from TX |
| A: |
If he has cognitive changes and cannot perform his usual activities of daily living because of thinking problems, then he fits criteria for dementia. He may have vascular or stroke related dementia given his medical history. Parkinsonism, or tremors, stiffness and slowness, can be due to strokes. Parkinson’s disease and dementia with Lewy bodies are distinct neurodegenerative conditions that can also cause these same clinical features. His sleep disturbance may be related to REM sleep behavior disorder, often but not only seen in dementia with Lewy bodies. Parkinsonian conditions also often disrupt the circadian rhythm (sleep and wake cycles). Both nortriptyline and Ambien can cause confusion at times. Ramelteon (Rozerem) 8 mg nightly often helps the circadian sleep wake cycle dysfunction common in those with PDD. Over the counter melatonin is another choice. Trazodone nightly can safely be used for sleep issues. Seroquel at night might help both with sleep and hallucinations. If you wish further information regarding the best behavioral treatments for these conditions, you may wish to purchase my book, "Long-Term Management of Dementia" (Informa Press) through Amazon or click on the icon next to my picture. |
| Back To Top |
| Q: |
I help my grandmother who is 83 years old and lives in a LLC facility in Maryland, where I live as well. My 67-year-old mother lives in Florida, and both of them have the same health issues and both of them ask me for help. I think my grandmother’s memory is getting worse, but my mother calls her to drive her crazy! What can I do to prevent this, but at the same time help them both? Kim from MD |
| A: |
It is hard to answer your question without knowing more about the conditions they have. There are also possibly personality traits that are coming into play as well. Perhaps there are limits that can be placed on calls by the LLC from your mother to your grandmother. |
| Back To Top |
| Q: |
I have been living with my grandmother for 15 years. She has always been an upbeat person. She has been under a lot of stress because her son (my uncle) is in the ICU. This morning she just was not herself. Her speech was impaired a little. I knew what she was trying to say, but she just was scrambling her words and all mixed up. Do you think it could be stress or should she be tested? Angel from IL |
| A: |
Hopefully you took her to the emergency room right away. These symptoms could be a sign of a stroke. If it is a stroke, every minute you delay getting to the ER typically means more loss of brain function. If a stroke is ruled out than other causes can be evaluated including stress issues. |
| Back To Top |
| Q: |
My dad is 87 years old. He has had Parkinson's disease since he was in his early 70s. The doctor told him that if he could tolerate PD medication it would be 15 years before it got bad. My mom passed away in April 2010. They were married 63 years. At the time dad's doctors said he would probably live only 6 months (according to statistics). He continued to live in his own home. We hired someone to stay with him during the day and my sister and I took turns staying at night. He was never alone. In January 2012 he fell and broke his hip. After surgery he was sent to a nursing home for therapy. He has been there ever since. His PD and his mind have gotten worse. Recently, he has been very agitated, does not sleep at all some nights and has been somewhat aggressive to the caregivers, which it not like him at all. We can't figure out if it's his medication, progression of his disease or something else. He was this way at home before he went to the nursing home, just not as often and it didn't last as long as it does now. We go see him every day and talk to doctors almost daily. I know it is common for people with PD dementia to be aggressive, but we just can't stand to see him like this. Is there anything you might suggest to help with this? They keep changing his medication but nothing seems to help. Panda |
| A: |
Parkinson’s disease dementia (PDD) patients can develop agitation and sleep issues. It is common to give medication trials to see if he responds. Ramelteon (Rozerem) 8 mg nightly often helps the circadian sleep wake cycle dysfunction common in those with PDD. Over the counter melatonin is another choice. Trazodone nightly can safely be used for sleep issues. Seroquel at night might help both with sleep and agitation due to false beliefs. If you wish further information regarding the best behavioral treatments for these conditions, you may wish to purchase my book, "Long-Term Management of Dementia" (Informa Press) through Amazon or click on the icon next to my picture. |
| Back To Top |
| Q: |
My father-in-law has dementia. He’s 89 years old and is bedridden— he can only get out of bed with help. He has caregivers during the day and evening. When they leave at night, they lock up the house. My worry is what could happen in case of a fire since he can't get up and get out. I think he needs to be put in a home where he can get 24-hour care. He could have that at home, but refuses for anyone to be in the house at night. We can’t make him understand that he needs someone there all the time for his safety. He has money, but he says he can't afford it. When we show him that he can afford it, he agrees, then changes his mind. What can we do? Can we be held responsible for his safety? Karen from IN |
| A: |
He has physical problems, but it is unclear to me how severe his cognitive issues are. If his dementia is to the point that he is no longer able to make appropriate decisions, then if he has a Durable Power of Attorney (DPOA) for health care and finances set up, it should be put into effect and that individual(s) can decide for him and have someone stay the night or have him move to a facility. If he does not have a DPOA and is significantly demented, a guardian appointed by the court is the next step. Another way to approach his reluctance is to bargain with him and suggest that just temporarily, as a trial, for a week or two, you are having someone stay overnight. Tell him it is mostly for your own peace of mind and that it is affecting your health (if it is) because of worrying about him so much. After the trial period, you can reassess and maybe extend it temporarily if things are working out. |
| Back To Top |
| Q: |
My mom is 88 and on hospice, diagnosed with dementia. She has had muscle spasms for about a month that affect her entire body nonstop. Her spasms keep her mouth opened and cannot swallow very well. Hospice doctors have her on Ativan (lorazepam) and just started Neurontin (gabapentin). But it is not working. It mainly just puts her to sleep, but she wakes up in a spasms. Is there anything else we can try to help her? Tina from FL |
| A: |
I am not sure what type of spasm you are describing. Myoclonic jerks are quick, can be one side or whole body and may affect the jaw of mouth. They can occur frequently. These are best treated with divalproex sodium (Depakote). Muscle cramps, like a Charley horse can be related to electrolyte imbalances. Try tonic water or pedialyte like drink. Rarely, tetanus can occur from a wound infection and lead to facial and body spasms. |
| Back To Top |
| Q: |
My mom is 80 and underwent a breast cancer operation. She also has Parkinson’s disease. My brothers are not taking care of her. She is always sulking when thinking of them. How can I bring happiness in her life and a smile on her face? |
| A: |
Depression is a common disorder in those with Parkinson’s disease. It is caused from environmental situations, but is contributed by her brain dysfunction from the areas damaged in those with Parkinson’s disease. Increase pleasurable activities for her and talk to her physician to see if an antidepressant is suggested. |
| Back To Top |
| Q: |
Mom has a blockage in the back of her head and has been doing things that aren’t like her. She tried to adopt a 67-year-old woman and her son. And mom thinks I'm after her money and things. I don't want her stuff. I'm tired of people taking advantage of her. Could this be dementia? Joy from NC |
| A: |
She has issues with judgment and probably insight. If she is also having problems with memory, language, sense of direction, problem solving or performing activities of daily living, she is developing dementia. She needs to be evaluated by her physician to find the potential reasons and to get appropriate treatment to prevent further cognitive loss. The sooner, the better. Have her physician give her the SAGE test, a self-administered cognitive assessment tool. This is an excellent screening examination that can be downloaded free from the web at http://www.sagetest.osu.edu |
| Back To Top |
| Q: |
My father is 87 years old and has dementia. He is totally incontinent and is on coumadin for an irregular heartbeat. He lives in a very nice memory care facility. Lately his heart rate has been fluctuating. He wore a 24-hour monitor and his rate varied from 40 to 187. His cardiologist is recommending a pacemaker. We're leaning toward that because if he were to fall due to the low heart rate and become lightheaded, he might bleed out due to the coumadin. So Of course there's always the chance he could just fall just because of getting older. He still walks on his own. Wondered what your thoughts are on this. Pacemaker or not—I am torn and not sure what's the best thing to do. Carol from TX |
| A: |
I would follow the advice of the cardiologist who knows your father’s medical condition the best. |
| Back To Top |
| Q: |
My grandmother just turned 100 and was very active until around 8 months ago. Since then she has experienced multiple behavior changes. She is now in an assisted living facility. She has lost a great deal of weight, refuses to eat or take medication so they are not giving her anything. Just recently they started Ativan because they did not bathe her or change her clothes for two weeks because she would not let them or even me. What stage does she appear to be in and what does the assisted living have to do when a patient refuses meds, water, food, to change clothes or any real care? |
| A: |
The solutions to these questions would depend on the reason she is refusing care and nutrition. Sometimes when individuals get that old, they have decided they have lived long enough and wish to die. They may not tell loved ones their true intent for reasons of their own. Others that old may develop dementia and not understand the need for nutrition or care. In some cases, their organs are just shutting down after 100 years. In others, there may be some underlying depression or a mix of a lot of things. The goal at that stage is to provide quality of life and not force individuals to have to follow all the “rules.” |
| Back To Top |
| Q: |
My mother in law fell on the 15th of November. The house we live in is safe—the bathroom, living room, her bedroom and the kitchen-dining room are all on one level with easy access. She has a walker and a personal toilet in her room for her convenience. When she fell she got a bruise right on the side of her right eye, she lost mobility and couldn't get around by herself so we took her to the hospital. The next day we went to go get her and she did not feel ready to come home—they took it that she was scared to come home and told us they wanted to put her in a home. It would be devastating to her to take her away from the family, and we want her around as long as possible to see her grandchildren grow up. There is always someone her with her and willing to get her food and help her. Two days later, she was ready to come home and they let her have a physical therapist come over and a nurse who looked at the house and thought it was great and safe. Today we took her to her doctor who asked her some questions and she said she has dementia without giving her a proper test. The doctor was very rude and said she wants mom in a home and is not capable of making her own medical decisions. She wants to take my mom away from us when we have done everything to make sure she was safe and happy. What do we do? Leslie & Cody from CO |
| A: |
Even if your mother in law has a dementia condition, from your description, she is safe and well taken care of at your house. You have family that care of her and know her and so your home would be a great place for her to be. Anyone can fall, even if you are standing right next to them and try to prevent a fall. There is no reason you would need to place her into a nursing home unless Adult Protective Services (APS) for some reason felt she was not safe or well cared for at your home. You could ask APS to come to your home so they could verify that the home setting is appropriate. If your mother-in-law has the capacity to make decisions, she can designate a person as her Durable Power of Attorney (DPOA) for health care who would then be her surrogate to make decisions for her if she were no longer able to make decisions on her own. You can consider contacting the local chapter of the Alzheimer's Association to help you understand more about a DPOA. Other agencies or a lawyer skilled in elder law could be considered as well. Her dementia condition could be further evaluated with cognitive screening tests like the Self-Administered Gerocognitive Examination (SAGE), that is best taken at her doctor's office but that is also available on line at http://www.sagetest.osu.edu. |
| Back To Top |
| Q: |
Our 87 year old father suffers from dementia and a significant eye disease and is noticeably declining. He lives in the family home with my younger sibling who works during the day. Currently, dad continues to drive short distances to the store and back, and is quick to let you know that his driver's license is legal for 3 more years. In anticipation that his driving days are numbered, we have hired an aide, three times a week for six hours each time, to do activities with him as well as drive him to the store. During Dad's recent visit with his PCP, I spoke to her privately. She absolutely noticed his deteriorating awareness and agreed it was time to stop driving. I requested she contact the eye specialist to ask him to tell Dad he needs to stop driving due to his eye condition and must have his license revoked. We felt it would be easier for him to accept that his sight is no longer safe for driving rather than that his faculties have reached a point unacceptable to retain his driver's license. We hope to keep his dignity intact as much as possible. Next week is Dad's appointment with this doctor. I anticipate he will not accept this well at all! How should I prepare for a possible inappropriate outburst of anger? What can I do to console him during the 45-minute ride home? What can we do to minimize the depression he will experience moving forward? Kathlyn from NH |
| A: |
Driving issues are difficult for many. It is to your advantage that the eye doctor is willing to "be the bad guy" and tell him that it is now unsafe for him to drive. In this way you can say that it is not you but the doctors that are telling him not to drive. He will likely counter that he can see well enough to drive. In those cases, it may be wise for the doctor to refer him to a professional driver evaluation test or to his local motor vehicle department for paper and behind-the-wheel testing. If his cognitive issues are getting worse, it is likely he will fail those tests. Another technique may be to tell him that temporarily he needs to stop driving while x, y or z is being evaluated or because he is starting on a new therapy, if true. It is always easier to be accepting of something that is "temporary" rather than something permanent and stopping driving forever. Periodically, he could be re-evaluated and the doctor can declare that he still needs to temporarily hold off on the driving. |
| Back To Top |
| Q: |
I am so confused. My mother was diagnosed 13 years ago with Parkinson’s. The past five years have demanded constant one-on-one care, but recently my mother has been acting very strange. She started complaining about headaches in the back of her head about a month ago. She was taken to the emergency room and had extremely high blood pressure, thought to be based on food she ate that day. She has started talking like a baby and saying things like "Me see you, you see me?" over and over. She has complete knowledge that she is doing this and makes a point of making sure we notice this—she says that it is due to a stroke and that she has read that your speech is affected after a stroke. She has been acting very childish, actually pulling a tantrum if we don’t pay attention to her and getting upset when I go college, even going as far as to call me and insist that I not go to college anymore. My first day of college was when she actually claimed she had a stroke and told me I needed to miss school and take her to the emergency room—doctors didn’t find any evidence of a stroke. Is she acting out or perhaps experiencing dementia? How can I approach this without causing resentment? TJ from TN |
| A: |
High blood pressure can be a cause of headaches. High blood pressure can also cause strokes. However, if she had an MRI scan of her brain, strokes are very easily found, even if they are very small. If she had an MRI scan of her brain and no stroke was found, then she did not have a stroke. A CT of her head may not reveal small strokes. When strokes cause language deficits, they are usually very obvious to everyone and would not fluctuate with good and bad days. The person may not be able to comprehend well or may not be able to get words out well. Strokes affecting speech would cause slurred or strained speech patterns, which also would not fluctuate. Acting childish and having tantrums are not typically stroke behaviors. Perhaps she is afraid of you not being around. You can offer her ways to contact the emergency squad to take her to the hospital if you are not around (button around her neck to push, phone to call 911, etc). You can arrange for companions to come in to be with her while you are away. Senior centers or day care centers can be used to care for her during the day. Depression and anxiety symptoms, if present, can be treated with antidepressant medications. You need to sit down and tell her that you will be gong to college but that you can help arrange for her to be safe and protected while you are away. |
| Back To Top |
| Q: |
My mother, 85, is taking medication for Parkinson's and has a level 6 Alzheimer's. She as been doing very well on the medication, but the other day she fell and hit her head and was knocked unconscious for a few minutes. She has been admitted to the hospital as a small spot of blood was found in her brain after a CT scan was done. The doctors are monitoring her and watching to see if the blood spot changes. I have a concern with her behavior now as she can answer your questions but then goes off in her own little world and talks about “golfing and it’s your turn.” She also gets up and goes to the table in her room and starts folding the bedding and towels, piles them neatly and then goes on to say it’s your turn play a card. She has never been this confused. Has the fall made this happen? Is there anything I can do to stop this? Paul from NY |
| A: |
Head trauma with bleeding in the brain might cause confusion, depending on the degree and placement of the trauma and bleeding. Changes in environment such as being in a hospital can, in and by itself, cause confusion. Parkinson's medications can cause confusion and false beliefs. Any new medication could be a cause. Infections, like a urinary tract infection, are frequent causes of confusion. Her physicians can run some tests to determine if there are alternate causes for her confusion. During her confusional state, make sure she is very well supervised to prevent more falls or injuries. |
| Back To Top |
| Q: |
My mother, 80, has been diabetic for 30 years and on insulin. She has dementia, too. Now she is showing unusual leg movements. What could be the reason for this? Thomas |
| A: |
It would be hard to determine with such little information. Medications can cause unusual movements. Is she taking any new medications? Diabetes can cause renal disease in some cases. Chronic kidney disease can lead to abnormal movements. Restless leg syndrome is a condition where the person feels the need to move their legs as they feel uncomfortable. Sometimes that is due to low iron. There are treatments available. Her doctor may be able to evaluate for other potential causes. |
| Back To Top |
| Q: |
My 95 year old father is in the late stages of dementia. He is combative when either his caregivers or I wash his diaper area—he screams very loudly and curses. My brother claims we are hurting him and I try to point out to him that dad is screaming because he does not want to be touched, but that we are not hurting him. His brother says dad doesn't yell at him, but he doesn't clean dad, he just changes the diaper or doesn’t clean him thoroughly. Dad was getting hospice care in our home and the nurses often complimented me on the care we are giving him, saying that he has the best skin in the diaper area and overall that they have ever seen in a person with severe dementia. The brother gets verbally aggressive toward me because he feels he needs to protect Dad from me. This is the same brother who lived with and oversaw dad not taking a bath for over 2 years while I worked to gain guardianship of him. By the way, I was a hospice care nurse and my daughter is a registered nurse who also advises me, so I really think we know what we are doing. Do you have any advice on how to convince my brother that screaming and cursing is not indicative of pain, but rather part of Dad's severe condition? Lilian from DE |
| A: |
It may be difficult to convince your brother unless he experiences the same behaviors. However, you are correct that there are many causes of screaming and cursing that are not related to pain in severe dementia patients. Sometimes they just want to be left alone. They may feel threatened. They may think they will be hurt. The approach to your father will be most important in his behaviors. Distracting him with soft objects to hold, playing his favorite music, or adjusting the environment may help. If his screaming behaviors are occurring at other times than with care issues, behavioral medications may be useful. |
| Back To Top |
| Q: |
My mother is 76 and has been diagnosed with Lewy Bodies Dementia. Her doctor put her on seroquel, which she has just decided she is no longer going to take. She said it has too many side effects and she already feels like she is losing her mind. Her doctor has yelled at me because I do not have her in a nursing home and I feel like I can’t talk to him about her issues. What should I do? Amy from FL |
| A: |
Quetiapine (Seroquel) can often be helpful for the false beliefs, suspiciousness and visual hallucinations often seen with those with dementia with Lewy bodies (DLB). Very low doses (25 to 75 mg daily) are typically helpful. Seroquel can have side effects; the most common one is sleepiness. If she has clear side effects from the Seroquel, perhaps a lower dose would have less side effects. There are other medications in the same class of medication that could be tried if she has false beliefs, suspiciousness and/or visual hallucinations. Instead of Seroquel, ziprasidone (Geodon) may be tried (20 to 60 mg daily). In regards to communication issues with her doctor, you might try writing down your questions. You can ask if the doctor has a nurse practitioner or physician's assistant or nurse or social worker that you could talk to. They could summarize your questions and present to her doctor. Going to support groups like with the Alzheimer's Association or the Lewy Body Dementia Association may help provide you answers to questions and suggest improved ways to communicate with her doctor. |
| Back To Top |
| Q: |
My father 81 has Parkinsons, I’m sure. Shuffle, stoop and no arm swing. He now keeps his eyes closed most of the time. He has difficulty getting his legs to move and takes his clothes off and on all of the time. He can’t find the toilet in his own house and started seeing things. Examples are collecting imaginary apples off the carpet and seeing women in the room. When visitors are over, he walks better and can hold a relatively lucid conversation. But he won’t sit still for more than ten minutes, up and down like a yoyo. He is afraid of the dark and has been protecting his wallet and folding everything in sight. We have to wait four months for a specialist opinion. Del |
| A: |
If he has memory or cognitive issues in addition to his motor issues, then dementia with Lewy bodies is possible. They typically do not have much in the way of tremors and often can have visual hallucinations. Most of these patients typically perform better when others are around. They tend to sleep more and more or keep their eyes closed more often. Carbidopa/levodopa and other anti-Parkinson's disease medications can also cause excessive restlessness and hallucinations. His physician could consider that these be tapered down if he is on them. |
| Back To Top |
| Q: |
My dad is 93 and was doing very well for his age. About 10 months ago he was even driving, yet loved to walk. He would walk to the store one mile away and carry a package in each arm back to his home. He lived alone and maintained the place on his own, even the yard. Then he fell and cracked his pelvis and went to a nursing/rehab center for therapy. This is when dementia signs started. After 25 days he was walking pretty well. But the day before he was to come stay at my house, he got up in the middle of the night to go to the bathroom and slipped and broke his left femur in half. He went back to the hospital for two weeks and had a rod installed in the bone, then went back to the rehab center again where he broke his right femur. Back to the hospital for another two weeks then again back to the rehab center for 30 days of therapy. By this time the signs of dementia were much worse. He has since really pushed himself to walk with a cane. He has been doing pretty good, living with my wife and me. We are both retired now and enjoy taking care of my father. It is a hard, full-time job, but he is happy being around family. He came down with diarrhea on and off several months ago, but for the last several weeks he has become dehydrated from it and weak. When I took him to the ER, while waiting to be seen, he passed out. Going on the second week in the VA hospital they haven't been able to find the cause. They took him off any meds that can cause diarrhea and run every test they know of, yet no luck. I would really appreciate your input. Jerry from FL |
| A: |
His passing out spell seems to more likely than not be related to his dehydration and diarrhea, perhaps causing his blood pressure to be too low. Review of medications and checking for infections are reasonable to look for causes of his diarrhea. I am not an expert on gastrointestinal problems. However, if he is on anti-dementia agents like donepezil or rivastigmine, or glantamine, they could be cause of his diarrhea. I would hold those medications as well. The Exelon patch has the least diarrhea potential of those anti-dementia agents. Drinking too many nutritional products (Ensure, Boost, Health Shakes, others) may cause diarrhea. Sometimes I have had luck with using probiotics over-the-counter to help with diarrhea. Also fiber may be useful. |
| Back To Top |
| Q: |
My father is 80 years old. Over the last 4 years he has developed severe neurological problems. Initially his hands were continuously shaking. When talking, his tongue comes out. He is always tired and finds walking very difficult—even getting up from a chair has become difficult for him. Gradually he lost his control over urine and became irritable. Presently he continuously repeats the same thing, is very restless and talking incoherently, sometimes about suicide. My mother is almost 68 years old and feels absolutely helpless. My father has been getting treatment for Parkinson’s, but now nothing seems working for him. Is their any medical help for him? Kakoli from IN |
| A: |
It is hard to understand his condition given the limited information. It sounds like he has dementia, behavioral changes, and movement abnormalities. Some movement issues can be related to medication use. Normal pressure hydrocephalus can cause gait and urine and thinking problems. Strokes, Parkinsonism, and other dementia conditions are all possible. A good diagnosis from a work-up that would include a brain scan, lab tests and cognitive assessments may suggest treatments that could be useful. |
| Back To Top |
| Q: |
My grandmother is 84 and just moved in with my mother and me. She is now saying I've been stealing from her and that she has seen me in her room, which never happened. She said I did it for “the trip I was taking.” I asked her what trip and she couldn't think of it, just kept saying she knew of my trip, like she was remembering a conversation that never happened. She accused her healthcare provider of stealing and of trying to poison her. She also hears voices and noises like someone knocking on her window, but no one is there. Even at the hospital she said someone was under her bed and that the nurses were trying to poison her and she heard them planning it. She has the shakes and nosebleeds all the time and at times hemorrhages when she goes to the restroom. She can remember things from the past, but makes up current things. Could this be dementia? She has high blood pressure, breathing/oxygen issues and high cholesterol and has blood clots. She's been hospitalized for the blood clots and had a bypass. She says she has Parkinson's, but the doctor said she doesn't though she does have the symptoms of shaking and a shaky voice. I'm just trying to help my mom get help from the doctors. Am I pointing her in the right direction? Please help. Jean from TX |
| A: |
These false beliefs are very common in many dementia conditions. They are usually easy to treat with low doses of antipsychotics. Dementia conditions like Alzheimer's disease will present with significant memory deficits. Parkinsonism can be related to small strokes in the brain or may be due to a condition called dementia with lewy bodies. They tend to have more visual hallucinations. Voice tremors are usually caused by other conditions than Parkinson's disease and can occur with hand tremors. I would suggest your grandmother to see a neurologist who specializes in cognitive issues. Mental status testing can document if a dementia condition is present. Further work-up as required will help with diagnosis and then appropriate treatment and management can be applied. |
| Back To Top |
| Q: |
Could having a caregiver help you cause a worsening Alzheimer’s in an 89 year old woman with the disease? She is totally dependent when the aide is around (11 hours a day). I know she can do some things for herself, but she demands help. I am her daughter. The rest of the family has deserted her. We have been living together for about 2 years and for 1 year in the same apartment building. She has had outbursts, delusions, and has been physically and mentally abusive toward me and the aides. These symptoms are less since her doctor ordered Risperadone, Aricept, and Lexapro, and other medications, but she has stopped reading her New York Times, her New Yorker, and Newsweek. I am with her during the night and have lost so much sleep because she is up most of the night saying "Hello, hello, hello" loudly. I work from home and just cannot stand the hellos, the agitation, the restlessness anymore. I promised her never a nursing home. I've searched for Assisted Living facilities, but they aren’t something she can afford. I am getting weary and sometimes just want to give up. I feel guilty that I can't rub her back and make her feel better. She is now incontinent during the night because she is so tired she cannot make it to the bathroom. I just know that she isn't happy and I am totally miserable. I keep my promises and have always told her that I would take care of her. But it's just too much. Any suggestions? Ellen from NY |
| A: |
If her behavioral issues were better controlled, life for all caretakers would be easier. It sounds like her agitation and delusions are improved with Risperidone. Sleep issues can often be helped. Her dementia physician might consider trazodone, zolpidem, or others for sleep issues. Risperidone can cause weight gain. There are many other potential causes for weight gain. Quetiapine typically can help better with sleep than Risperidone and may be a replacement for risperidone for her agitation and delusions. Repetitive word speaking may suggest some obsessive compulsive symptoms. High doses of Lexapro or fluvoxamine (need to get to 200 or 300 mg daily) may be helpful for those symptoms. They may help depression issues. If patients are overly restless, we consider coming down on the Risperidone if it is at a high dose (more than 1 mg daily). Insomnia, feeling or acting hyper, eating a lot could suggest a hypomanic state, and the use of valproic acid or other mood stabilizers may be helpful. In regards to your predicament, the best way you can avoid burnout is to have some more respite. Consider daycare facilities, if available, in the day time so that you have more peace at home in the day. Have her "visit" and stay in a nursing home for a week so that you can get some respite periodically. You will be a much better caretaker if you can have time for yourself and have enough sleep. |
| Back To Top |
| Q: |
My aunt is 90 and her diabetic son, 70, who has always lived with her, was taken to Johns Hopkins because he stopped taking his insulin for almost a year and became very lethargic. He has been in a nursing home for 4 weeks. Now, my aunt is “seeing” her son almost every night in her home. She knows he isn't there, but she tells me she talks to him a while, then he leaves. She also told me some girls came to her house and she served them cokes and potato chips, then when one of them glared at her, she went into the kitchen and called the police. When she returned to the living room, they were gone. When a policeman came to her door, she said she apologized for calling them, but the girl left and all was okay. They were very nice to her and said if she had anymore problems to call them. My aunt shuffles her feet when she walks and says sometimes she gets a little dizzy. She says she must be crazy for seeing these people. I live two states away from her and I don't know what to do. I told her to tell her doctor about this and I will keep reminding her up to the day of her appointment. Do you think she is under stress? Jeanie from NC |
| A: |
Your aunt is having delusions or false beliefs. There are many potential causes. Some medications may cause them. They are seen commonly with infections, like urinary tract infections. Metabolic derangements or thyroid conditions might also cause these behaviors. Dementia is often associated with delusions. Stress is usually not a cause just by itself. She needs to be seen by her doctor who can evaluate her for potential causes. They can also evaluate her gait disturbance and for causes of dizziness. |
| Back To Top |
| Q: |
I put my wife in a memory care facility this past Monday. She is 59 and has fronto-temporal dementia. This is her third day and when I call her all she says to me is "Come and take me home". She doesn't know why she is there and I can't reason with her. It is so painful knowing she wants me to take her home. I have always been there for her over the past couple of years and it is breaking my heart not being able to help her. How long can it take for her to adjust or transition? Is it possible that this is just not the right place for her? (The facility is the best I could find and has many great features as far as a memory care facility goes.) Please help. Tom from AZ |
| A: |
You should feel good that you have your wife in a good place. Many patients require long-term care and it allows spouses to have quality time with their loved ones while getting help for their care. Some of the downsides to a change in environment is the natural reaction by the patients to want to go back to their comfort place, their previous home. Why would anyone with such impaired insight into their condition, as all frontotemporal patients have, want to leave their home and go to live somewhere else? They have no clue why they or their spouse would need any help in their care. Many times, as the patient gets use to their new home, these comments will decline. Exactly when these comments stop is different for each patient. It may help to not use terms like permanent or forever. It may be better to use terms such as temporary or trial period to get past these comments. Perhaps you can emphasize that the facility is helping to rehab or adjust medications to see how she does. Since you have done your homework in picking this place, stick with it and no regrets. |
| Back To Top |
| Q: |
My mum is 86, has dementia and doesn’t talk sense most of the time. She doesn't take medication and eats a lot, but seems to be losing weight. Marion from UK |
| A: |
I am not sure exactly what you’re asking. If she is supposed to take medications for her dementia or for other conditions and won’t, then crushing and placing them in her food would be advised. If she has a good appetite, giving her nutritional supplements would help her maintain her weight. These can be bought over the counter through Parentgiving, such as Ensure, Boost, Carnation Instant Breakfast and others. |
| Back To Top |
| Q: |
My dad has dementia and has just recently moved in with my sister, who is also caring for a special needs granddaughter. When dad first moved in with her, I came by and took him to lunch once a week. She said he would do better if he never left the house, so I brought lunch in. When I called to see when the best time to see him would be, she said she was very busy that week. The following week she made the same excuse. As I probed into this more she said the reason she didn't want me coming to see dad was because when I came over she said he would have a bad night and she didn't want that happening anymore. I told her that, from what I have read, dad shouldn't be harbored and he should be around people who he is familiar with. She insists on not letting me see him till "he is ready." Do you agree with this type of care? I am frustrated that I don't get to see my own dad. Vaughn from NM |
| A: |
Given that your sister has the duty of caring for your father, it is important to better understand his behaviors that cause her not to want you to see him at this time. What issues does he have at night after your visits? Perhaps there are treatments to make his nights better. In general, dementia patients enjoy being around familiar people. However at times, certain family members may make them more upset or irritable. Has she allowed you to talk to him on the phone? It is understandable you would be frustrated, but the focus should be on what is best for your father. |
| Back To Top |
| Q: |
My mom has lived with me for 7 months. She is 91 and has dementia. At certain times she’s fine and then she can be totally confused and not even know who I am. My question is, would she be better off in an assisted living or is she happier here? She's never left alone and every day I take her to senior day care or a friend’s house and then they go to a senior center. I'm a single mom who has 17 year old and works full time as a realtor. Some days, I just don't know if I'm doing the best thing for my mom, me or my daughter. Any advice? Patti from NY |
| A: |
Caregiving is very hard work. It sounds like you are doing a fantastic job. You are keeping her mind engaged with the day care and senior center activities. However, you also need to avoid burnout, which won't help you or your mom. You also have obligations to your daughter. If your mother has the money for assisted living and you can find one close by, you can still visit and have really quality time as often as you like with your mom and yet have more time for yourself and your daughter. If your mom often does not even know who you are, it may not be a big issue for her to move into another place. You could give it a trial run for a weekend or a week to see how she acclimates to a new place. It may be best for all. At assisted living facilities, they have many activities that should keep her mind active. They have more hands to help your mom around the clock. Other options could be to hire someone to come in to care for your mother to give you more time. |
| Back To Top |
| Q: |
My husband survived a stroke May 2011 and was hospitalized in China, treated and released with no therapy. We have just now returned to the US and are going through initial tests and, I hope, the therapies he missed. Among other things, his short term memory is very bad, he builds up anger over time about me telling him or reminding him of what to do, and he has some long term memory loss. What is your advice? Linda from NV |
| A: |
Strokes can cause cognitive impairment. His evaluation back in the US should investigate other causes of memory loss (through blood tests, cognitive tests, and neuroimaging). Frustration is normal when you are always telling him what to do. You can try to avoid telling him things and instead ask him—it will seem less like bossing him. Keep a calendar with reminders of what is planned for the day. Put up signs to remind him of certain duties so that he can do them without you reminding him. For things that you both need to do, perhaps like bathing, you can tell him that you are about to take your bath, but does he want to go first? In this way he may get less frustrated at always being told what to do. |
| Back To Top |
| Q: |
My Momma is 91. She lives in a very beautiful large retirement village. She lives alone, but has access to nursing and has neighbors and friends very close by. She told me today about these frequent bad dreams that have been troubling her. She becomes very involved in her dreams and she’s very anxious. She awakens in the middle of the night, thinking it is time to get up, dress and start her chores, which is what she did today. Her older sister died several years ago from the effects of dementia. I am concerned she may be headed that way. (She lives in North Carolina and I live in British Columbia!) Joanne from BC |
| A: |
Simple tests can determine if she has the beginning of a dementia condition. Her doctor can evaluate her for that. Let her doctor know of your concerns regarding her memory or thinking. Also let the physician know of her sleep issues. Make sure first she is not on medications that would increase bad dreams or insomnia. There are several safe medications that are not sleeping pills that can help with insomnia or bad dreams (e.g. trazodone and rozerem among others). Also, try good sleep hygiene habits may help, including keeping bedtime and rise time the same, avoiding caffeine or alcohol at night, and not drinking many fluids after dinner. |
| Back To Top |
| Q: |
My grandmother-in-law is 94 years old. She has begun to hear people talking to her, telling her they are going to kill her. She is constantly worried, hides in closets, covers her head. She says they know everything we are saying and they are coming up through the floor. She has always been a very devoted Christian and we have tried numerous things. Is this dementia and will it get worse? She is starting to not recognize some of her family members. Is there anything we can do to help her? Thank you in advance for your help. Tracy from SC |
| A: |
Your grandmother-in-law has psychosis (false beliefs). If she also has memory loss and perhaps trouble finding words, this is very likely a dementia condition. Be sure to check if she is on any new medications or increase in medications that can cause these symptoms. Urinary tract infection or other infections often cause similar symptoms. These can be treated. If no other cause is found, there are many medications that may help her psychotic symptoms, such as Seroquel at night or daily Geodon. Talk to her doctor to see if any treatment is right for her. She would likely only need a very small dose, given her age. Also if dementia is considered, treatment with cholinesterase inhibitors (donepezil, galantamine, or rivastigmine) may be in order to help her thinking and slow decline in her dementia symptoms. |
| Back To Top |
| Q: |
I am a live-in caregiver for an 88 year old woman with Alzheimer’s (now at the mid-severe stage), mild cardiac arrythmia problems for years and, just recently, CHF. She is having lots of peripheral edema and her furosimide was increased. I also must say that this lady is the mom of my best friend from junior high school. I have been close to the family for years. I am also a practical nurse with many years of experience in geriatrics and dementia. I accompanied mom and daughter to her physician about 3 weeks ago to address the problem with the edema. She’d also been having increased incontinence and diarrhea for close to a month. The doctor increased the diuretics, came up with something to help with diarrhea and then requested the daughter to call in a week to report whether there had been any improvement in both areas. The increased diuretics have had no effect on the amount of fluid she is retaining. Yesterday I requested the daughter to call the doctor and report on the lack of improvement. She has still not called with a report. She has decided that her mom's whole problem is due to an extra 20 lb she’s carrying and told me I am to give her mom absolutely no sweets, bread, cookies, or candy of any kind and she will lose the weight, be able to exercise and ambulate around the block without difficulty. The poor woman is so fatigued due to her real health problems that she is totally unable tolerate the kind of activity her daughter is demanding that I force her to do. She becomes out of breath with just minimal activity. She is unable to walk even to the mail box. She prefers to sleep more than anything these days. She is failing, but I cannot convince the daughter that this is probably the way things will stay with her mom and that she should follow the doctor's instructions regarding what should be done in regard to cutting out foods she enjoys. I don't know what to do about these conflicts that clearly could be serious if not addressed yet I am told that I am overstepping my bounds whenever I question her or make suggestions regarding her mom's care. I don't know what to do. I am the caregiver after all. Karen from OR |
| A: |
Increased edema is water weight and will definitely cause a lot of weight gain. It may also suggest increased problems with her congestive heart failure. Unless that issue can be addressed she would not be able to exercise or do any type of activities. Her quality of life depends on this. You sound like you are doing your best to convince the daughter. I would agree that it is best to let the doctor know the results of the intervention they suggested. You can let the daughter know that there may be other treatments to help her mother's edema and weight gain that the doctor can suggest. I suppose that it puts you in a difficult position, but keep in mind that anyone can call the doctor to give information without incurring any HIPPA violation. |
| Back To Top |
| Q: |
My father has the first signs of dementia. He has become very addicted to his pain meds to the point that’s what his life revolves around. But it has come to the point where he doesn’t remember if he has taken his pills or not and won’t let any of us to control them for him. It’s not just with prescribed medications—even over-the-counter ones. Plus he’s our dad so when he tells us he’s hurting, we give in. We need professional help with this situation. Please let us know what we can do. Georgia from MO |
| A: |
You say he is addicted and so I assume he is taking narcotic pain medications. Narcotics often increase cognitive issues, especially in someone who may have other causes of dementia. It is important to get his doctor involved in this situation. The physician needs to tell the patient that it is not safe for him to take his own medications due to their potential effects if he takes them incorrectly or in the wrong dose. The doctor could make it clear that, unless he allows a trusted family member to supervise the narcotics, it may be unsafe to prescribe them to him. |
| Back To Top |
| Q: |
My dad is 82. He was first diagnosed with Parkinson's disease about 5-6 years ago. He is on syndopa plus, amanterel, and urotone (he developed urinary incontinence quite quickly). He also has the other symptoms like falling, drooling, freezing, tremors, and mask-like face etc. He was in the hospital for aspiration pneumonia in May 2010. About a year ago, he developed fecal incontinence as well. So now he wears an adult diaper all the time. He can walk, though slowly, with a walker and has physiotherapy thrice a week. He is quite alert and has only mild memory loss. A neurologist to whom we took him last month to explore deep brain stimulation said he has Parkinson’s Plus and not Parkinson’s so it cannot be used. However now there are two problems: One, he cannot drink water because even a little starts off a severe coughing fit. Two, he puts his hand inside the diaper and removes the feces when he is in bed. Can anything be done to prevent aspiration of water and other thin liquids? I am afraid that he will again develop pneumonia. Please help. Jayanthi |
| A: |
There are many thickening agent products that are designed to help individuals with swallowing difficulties. These can be bought over the counter or internet. Parkinson's disease often causes dysphagia, leading to possible aspiration. Common signs of dysphagia include drooling, coughing and choking on liquids more than solids, and more difficulty talking after swallowing. The thinner the liquid (water, apple juice), the faster it can get to the back of the throat and the less likely the individual with Parkinson's disease with slow motor skills can close their wind pipe in time. If the liquid gets into the wind pipe, choking and coughing start and it may lead to aspiration of liquid or food into their lungs. That can cause a lung infection or pneumonia (aspiration pneumonia). |
| Back To Top |
| Q: |
My father who is 74 years old is losing a great deal of weight. I recently took him to the emergency room and they took every test possible and everything came back normal. He is not bathing on a regular and he refuses to keep himself or his room clean. He will not let me clean his room and the smell is not good. I am waiting for his Medicaid card to come in the mail so that I can get him a family doctor, but in the meantime can you give me a brief summary of what you think is going on. Linda from NC |
| A: |
Well, what you tell me is that your father is losing weight, refusing bathing, and not keeping his room clean. It sounds like he is not thinking as well and not making good judgments and this suggests a brain condition. Evaluation should include a good history, family history, social history, examination, lab tests, scan of his brain, and cognitive (pen and paper) tests of his thinking and memory. That information should help with making a diagnosis. In regards to his behaviors, close supervision, if not already present, may help. People tend to eat more and more regularly if they are eating with someone else. Nutritional supplements (Boost, Ensure, Health Shakes, Carnation Instant Breakfast, ice cream…) given regularly on a daily basis may help. Having a friend, family member, or health aide come in to bathe him may be needed. Perhaps bribing him with something he likes only if he takes a good long bath may work. At times it is easier to clean up if he is not around. Have someone take him out and then clean his room when he is away. If he is developing cognitive (memory or thinking) issues, having him appoint a Durable Power of Attorney for Health Care and Finances is critical prior to his losing the capacity to make decisions on his own. |
| Back To Top |
| Q: |
Scenario: Father with dementia, Mother without dementia (but in denial, refusing to care for herself for fear of leaving her husband alone and refusing outside assistance). Considering this scenario, how should children approach the situation? The mother, in her 80's, has many health issues as well and needs knee surgery. She refuses to talk about her situation and just seems so angry when she speaks about her husband. The children are at a loss as to what they should do to help their parents. Can you offer any advice? Michelle from WA |
| A: |
These situations are always difficult. Your mother needs some respite—time for herself. If children are close by, they can volunteer to take their Father for an outing to provide supervision for 4 hours or so to give her some time. Your mother can go with her husband to a Day Care Center if there is one close by so that he gets used to the staff and guests. After a few times he (and your mother) may be very comfortable to leave him under their supervision while she gets some things done for herself. If your mother needs surgery for her knee, one of the children or a respite care facility can watch and care for her husband. Your mother may also be helped by an antidepressant if indicated to help with mood and irritability issues. |
| Back To Top |
| Q: |
My mother is 94 years old. She needs someone to come in and stay with her at least to cook two meals for her. She still doing some things for herself and lives with my sister who has to work. She trusts no one and thinks that people are coming into the house and stealing things. She does misplace things, forgetting where she put them, but it worries me that she thinks all these people are taking from her. Now she also does not want to eat. Is this dementia? Lilly from TX |
| A: |
Your mother has false beliefs (delusions) and memory loss. This is probably a dementia condition, given her age. There are many causes for dementia including Alzheimer’s disease, medications, small strokes, B12 deficiency, low thyroid and many others. Her primary care physician should look for potential causes and treat accordingly. Sometimes treating the underlying cause (like replacing B12 in B12 deficient individuals) will also clear up the false beliefs. Sometimes the false beliefs require an additional medication specifically to help those symptoms, like quetiapine (Seroquel). |
| Back To Top |
| Q: |
My mom is 93 years old and has been very healthy. Two weeks ago she developed a lot of anxiety over a huge family event and became very anxious and totally had a loss of appetite and weakness. She was diagnosed at the ER with a low sodium count and given 2 bags of IV fluids and discharged after being told that she needs to eat and drink more to bring her sodium level up! At her next blood draw her level was at 133. She is still very sick and weak and feels as though she is dying. Her memory is good. They did also put her on Ativan for her anxiety, but she has gotten worse, not better. I feel we are missing something here! Any thoughts of what is going on with my mom? Deborah from OH |
| A: |
Sometimes using Ativan, especially at age 93, could cause more problems than it helps. For some individuals it can increase confusion, it can cause a lot of sleepiness, and is addictive. Often a trial of an antidepressant, such as escitalopram (Lexapro) or sertraline (Zoloft), can work very well for anxiety and has many less side effects. Low sodium issues can be responsible for confusion, anxiety, appetite issues and weakness. Her doctors, if they have not already, should identify the cause of the low sodium and try to correct the underlying cause. |
| Back To Top |
| Q: |
My dad has Alzheimer's going on 5 years. It has got to where he takes his penis out of his diaper to urinate and doesn't put it back. Then he leaks urine in his pants, on the floor at night after he gets out of bed for some reason and in the bed. I have considered a catheter but fear he would just pull it out. Any idea to help with this? Michael from FL |
| A: |
There is not a lot that can be done except increased supervision and reminders so he is correctly positioned in the diaper. Sometimes placing notes in the bathroom or bedroom to put pants on correctly may be helpful for some patients. Some men have an enlarged prostate or prostate cancer, which may cause dribbling. His primary care physician can diagnose this and there may be medications that could be helpful. If he is up a lot at night, then maybe a medication to help with sleep (like trazodone, which is very safe at low doses of 50 or 100 mg nightly) might be prescribed by his primary care physician. This may reduce his nighttime awakenings for random reasons, but would not keep him asleep if he really needed to use the toilet. Reducing or eliminating liquids after dinner and avoiding alcohol (which causes increased urination) may reduce nighttime urination needs. Use of a catheter, I agree, would cause more problems than it would solve. |
| Back To Top |
| Q: |
Please let me know if there are any trial medicines for beginning stages of Alzheimer’s. Sue from CA |
| A: |
There are many clinical trials for mild Alzheimer's disease and the precursor condition, Mild Cognitive Impairment. Many of these are testing experimental medications. The best place to look for trials in your area is to go to the website clinicaltrials.gov |
| Back To Top |
| Q: |
My mum is 81 years old and has dementia. I moved her in and she has lived with my family and me since 2008. She is hard of hearing, forgets to eat, won't drink water (only soda) and makes up some bizarre stories. She has been more dizzy of late, and actually fell this morning in the bathroom. She hit her head. Quite a bit of blood. She managed to clean up most of the blood and crawl back into her bed. She initially didn't remember why she was bleeding and had slurred speech. An hour later, she was better with her speech. I am taking her to the doctor today. She won't take medicine due to her religion. The dizziness keeps getting worse, her appetite is down to very little (she’s 5’2", 115 pounds), and bleeds vaginally off and on. Not sure what to do to help ease her dizziness and help her eat more. Jul from CA |
| A: |
Many medications can cause dizziness. However, since she is not on any medications, some blood and urine tests may be in order to rule out infection, electrolyte issues, low thyroid, B12 deficiency, or liver or kidney problems. For weight loss, nutritional supplements (Ensure, Boost, Carnation Instant Breakfast, among others) can help to provide a lot of calories with a small amount of liquid. There is a liquid medication, megestrol, that is often helpful as an appetite enhancer. |
| Back To Top |
| Q: |
My husband has Parkinson’s/Alzheimer’s. He has become so restless, fidgeting constantly, tearing things up and breaking things. I give him things to occupy his hands, but it is getting worse. He is on Namenda, Carbidopa, Effexor, Exelon patch and Seroquel evening as well as a PRN. Any suggestions to help the constant fidgiting? The disease is worsening as just direction does not help much—he must be SHOWN how to do something, and he’s having more anger issues. Patti from MT |
| A: |
With Alzheimer's or Parkinson's disease, restless behaviors and fidgeting are not uncommon. The medications he’s on that can cause increased restlessness are Carbidopa/levodopa (typical), Effexor at times and, if giving higher doses, Seroquel. Citalopram or Depakote may be more helpful than Seroquel and Effexor for these types of behaviors. If you wish further information regarding the best behavioral treatments for these conditions, you may purchase my book, "Long-Term Management of Dementia" (Informa Press) through Amazon or click on the icon next to my picture. |
| Back To Top |
| Q: |
I have an 82 year old father who was diagnosed with dementia/possible Alzheimer's last year. Just prior to his diagnoses, he had gotten into a car accident, one for which he was responsible for causing. He was cited for not allowing enough distance between his and the other vehicle. His doctor adamantly opposed the idea of his driving and he told my dad so. I agreed with his decision, but my dad never totally accepted it. My dad lives on his own with some assistance. I pick him up and take him to my house after work to eat supper and to be with family. His neighbor also helps. I also pay his bills. Here is my issue. He rides his bike in places that are dangerous. I don't have a problem with him riding his bike in the small village where he lives. The problem I have is he tries to ride to my house, which takes him on a state route with busy traffic. I have warned him before. He doesn't listen. Do you have any thoughts? Thomas from OH |
| A: |
Safety is obviously your main concern here. Independence is his wish. At some point he may not be using good judgment to ride a bicycle at all. However currently it seems that he is still capable with restrictions for safety to ride one. Our typical recommendations are to avoid riding at night, in inclement weather, or in unfamiliar areas. I would tell him that state routes are off limits at this time as you have. You could bribe him to not ride on the state route. You could suggest you take him to ride in places that are safe or ride with him on weekends. If all that fails and his actions are dangerous, you could have a police officer notified while he is riding on the state route to pick him up if he is showing dangerous riding techniques. This may reduce his desire to do those unsafe practices. If all else fails and he is in danger with his riding, removing his bike would be the last resort. Another idea is to follow him (perhaps ride a bike with him) and to observe if he is using good judgment or not with his riding. If he is not, watch once a month. Once he is noted to be using poor judgment, it is time to restrict his riding. |
| Back To Top |
| Q: |
My 89 year old mother has been experiencing transient attacks of feeling like she is dying when she wakes in the morning. These spells pass and she is fine a few hours later. She has had extensive workups, which have all been negative. Today she called rescue and was taken to the ER and worked up again...all tests were again negative. She is "with it " and lives alone and still drives...Just do not know what to do next. Donna from NY |
| A: |
It sounds like she has severe anxiety, maybe panic, attacks. Make sure she is not taking sleeping medications (especially over-the-counter ones) or hypnotics. Have her physician evaluate all her medications and remove all that are not needed. If blood pressure, oxygenation, low blood sugar, sleep apnea, thyroid problems, vitamin B12 levels are all normal, she could try something for anxiety. Benzodiazepines are not typically recommended for individuals her age. Antidepressants (escitalopram or sertraline) or buspirone may be the first ones tried due to low side effects. |
| Back To Top |
| Q: |
I have an 81 year old mother who was diagnosed with Alzheimer’s two years ago. She has been in a care home for one year as she was no longer able to care for herself—wandering and not recognizing her own home. She was not able to tolerate carergivers in her own home, thinking they were intruders. She would not stay in my home and refused to wash. She was not eating properly to caring for herself. She is now in an excellent home where her health has improved, though her fixed delusions remain. She has some incontinence. She has no short-term memory and her ability to recognize familiar people is fading. I believe she is in the late middle stage of the disease. I am having to make complicated financial arrangements to pay for this very expensive home and would like to know what the chances are that she will live past 88. Her own mother had Alzheimer’s at the same age and lived to 88. Most of her siblings did not have Alzheimer’s and lived to around 87 years old. I realize there is no certainty, but is there any “rule of thumb” that could help in a difficult decision making process? Lorraine |
| A: |
It is hard to predict without more information about her other medical conditions and her current functional abilities. As you suggest, genetics can play a large part. If she is in the late middle stage as you suggest, 4-5 years more would be typical if she did not die of something else first. |
| Back To Top |
| Q: |
In my search for answers to what happened to my 69 year old husband during routine gall bladder surgery I came across a question and your response. The doctors caring for my husband did indeed describe what happened as "rapid onset Alzheimer's.” This "diagnosis" came after several weeks of waiting for the anesthesia to "wear-off". I’ve always believed he may have had a serious adverse reaction to the anesthesia that accelerated a latent tendency toward dementia. Thoughts? Shari from VT |
| A: |
As I mentioned in the prior question, I don't believe there is any such thing as rapid onset Alzheimer's. Dementia conditions occurring right after a surgery are almost always related to medications, infections, metabolic derangements, perhaps impaired blood flow to the brain or perhaps low oxygen to the brain during the surgery. However, other coincident causes of dementia need to be ruled out. If he had the start of a condition like Alzheimer's disease prior to the surgery then he will continue to decline very gradually with his memory, language and visuospatial problems after the surgery. However, this process is gradual (months to years) and not rapid (days to weeks). |
| Back To Top |
| Q: |
I have a father with dementia that has advanced after a pretty serious illness. He is in a wheelchair much of the time, but can use a walker for short periods of time. He has severe back pain and needs help with daily living activities. He is currently at home with 24-hour care, but is starting to not trust the people caring for him. Would he be a candidate for memory care, or do his health issues create a problem for that? Kelly from CA |
| A: |
Many people with dementia can develop false beliefs or suspiciousness. Sometimes it is caused by other medications like narcotics, carbidopa/levodopa or many others. First have his doctor review what he is taking. The caregivers might be able to reduce some of these suspicions by changing the way they approach him. They can try to empathize with his concerns and redirect to another topic if these false beliefs come up. There are some very effective medications (antipsychotics), if used in low doses, that often greatly help these types of symptoms. Whether his behavioral issues correct or not, it is likely that most nursing homes with memory care would be able to take care of all his health issues. However, the best way to find out is to visit them and explain his situation. |
| Back To Top |
| Q: |
Does mild dementia indicate that a parent has to be put away and can not reside with a daughter? She is such a joy to have and she attends an adult day care. She knits, plays cards, etc. Allison from PA |
| A: |
Absolutely not! As long as the parent is safe and needs met, they can live where it works best for them. The only reason to consider assisted living or nursing home is usually because the person is no longer safe at home or the caregiver(s) can no longer adequately care for them. Another advantage of senior living, assisted living or a nursing home is the activities and socialization provided, which help keep the person's brain stimulated, which is thought to help brain functioning. However, your parent goes to adult day care and it sounds like she is getting a lot of good brain stimulation. |
| Back To Top |
| Q: |
My almost 87 year old aunt has been recently diagnosed with mild dementia. She has only recently in the last three weeks been given Aricept. After her knee replacement surgery, we decided to move her to an independent living facility and provide additional caregiver assistance. This was over her objection, but there was no longer any way for her to live at home by herself. She has been at the facility for about 3 weeks and still is not adjusting well. She refuses overtures from other residents. She insists she will not be staying there long. I am at a loss what to do to help her adjust being 1000 miles away. This is all costing a lot of money and I am worried we have made the wrong decision. Any thoughts or ideas? Judith from TX |
| A: |
There are no easy choices. If she is not safe at home or no longer able to care for her needs appropriately at home, she either needs the safety net of an independent living facility or in-home assistance for supervision, help with daily activities and safety needs. Many times there is a honeymoon period of adjustment when moving into a new place. For some this is short and for others it may be much longer. It is costly either way, but depends on the amount of in-home supervision required. She should continue the Aricept and make sure she increases the dose to 10 mg after one month. If there is some evidence of depression, irritability or anxiety, an antidepressant (such as sertraline or escitalopram) at a low dose may be helpful for the adjustment period. Ask her doctor if any of those are appropriate for her. |
| Back To Top |
| Q: |
My mom is 67. She first started saying someone was taking her things two or maybe three years ago. In the last two months she hit her head and was fine—except now she is saying the devil is after her and people are trying to have sex with her. She’s saying "Jesus" constantly, eating less, goes out and walks until she is weak and won’t go in basement. She wants lights on and won't go back to her apartment saying, "They having sex with me through the wall," that they have a detector to find her and she only feels safe under the dining room table or outside. Are these signs of Alzheimer’s/or schizophrenia? What do I do? She says “Ain’t nothing wrong with me,” “You don’t believe me” and “The devil is real.” Pat from OH |
| A: |
Your mother has symptoms of delusions, which are false beliefs where no amount of logic or persuasion will change her mind. Typically, trying to interject reality will cause anger and disbelief on her part. Empathizing with her concerns (it would be terrible that strangers are having sex with her) will allow her not to get too angry at others. Some medications can cause these symptoms. Check for any new medication she is taking. Infections like urinary tract infections can cause such symptoms. Significant liver of kidney disease, electrolyte imbalance or endocrine conditions as well as other conditions can also contribute to these types of symptoms. If the delusions are longstanding, it may be due to a dementia condition like Alzheimer's disease. If she had dementia she would also have significant short-term memory loss. It would be unlikely schizophrenia, as that condition starts much younger as a general rule. There are many choices of medications that help delusions called antipsychotics. Her doctor should be able to decide if she is a candidate for any of those treatment choices. |
| Back To Top |
| Q: |
Who decides what time a dementia client goes to bed? Doris from GA |
| A: |
Normally the individual should decide what time they wish to go to bed. Keeping good sleep hygiene (maintaing routines for sleep and wake times and turning off distracting lights or noise at bedtime) is very important to a dementia person's functioning and for good sleep habits. If the individual is attempting to go to bed very early and then is waking up in the middle of the night causing disruption to others, we would suggest increasing pleasurable activities to keep them up to a more suitable bed time. If the individual is tending to go to bed too late, avoiding naps in the day, eliminating TV or other distractors at normal bed times or if needed, giving medications to get their sleep/wake cycle under better control may be helpful. |
| Back To Top |
| Q: |
My grandfather is 85 years old and has dementia and Alzheimer's. He was put on Aricept tablets by the doctors at the memory clinic and my mum managed to look after him at home for about 3 years until things got too bad. The worst thing of all was the bowel incontinence. He is now in an EMI unit at a local nursing home. The problem that is concerning me is that he opens his bowels up to 7 times a day and doesn't know that he has done it. He is an extremely good eater and remains so. In fact he doesn't know when he has had enough, but he has lost an awful amount of weight. He has had investigations at the hospital and all his bloods have come back normal. Is this just part of the disease? Kelly |
| A: |
Aricept (donepezil) in a small proportion of patients can cause loose stools or bowels and weight loss. If no other cause is found, donepezil may be the cause. Adding fiber to the diet daily may be helpful. Rivastigmine (Exelon) patch in some individuals will produce less gastrointestinal issues since it is a patch and not a pill and circumvents the stomach. It can be given in place of donepezil. Adding nutritional supplements to his diet may also help with weight since he has a good appetite. |
| Back To Top |
| Q: |
My dad has dementia and is not eating food well anymore. What should I do? Melanie from VT |
| A: |
If his appetite is low, consider supplementing his food intake with nutritional supplements such as Ensure, Boost, Health Shakes and others. They pack a lot of calories in a small amount of liquid. There are also medications that may help with appetite (mirtazapine, megestrol) that you can talk to his doctor about. If he is having trouble with chewing or swallowing, the only solution is to make his food softer to make it easier to swallow. If he is choking on liquids or food he should see his doctor. There are also products to thicken the consistency of liquids to make them not cause choking as much. |
| Back To Top |
| Q: |
I am with my wheelchair bound hubby @ assisted living. This Community has Azheimer’s and dementia residents. They are never hungry, but given food will eat usually—not always. When should the family be made aware of this and/or depression? Krys from OR |
| A: |
Alzheimer's patients often get to a point that they do not know how to look for or seek out food. They may lose language abilities that they can not express their desires that they are hungry. Depression should always be looked for. Crying spells, “wish I were dead” comments and apathy are all signs to watch out for. |
| Back To Top |
| Q: |
My Dad just went into a Memory Card facility six days ago. The facility staff wanted no family contact for at least two days to get him "acclimated". On the third day they said he is still too anxious and did not want my mother or me to visit. I decided to go anyway and found dad to be very agitated, thinking mom had left him, thinking it had been two or three weeks rather than two or three days since anyone has seen him and he cried in front of me for the first time since his mother passed away 25 years ago. Thus, I have told my mom to go ahead and visit him daily. However, his agitation really has not got any better. He keeps wanting to leave, still thinks mom has left him, and so I don't know what to think. Do we leave him alone for several days to "adjust" or do we still keep seeing him and reassuring him, even though this makes him anxious when we leave and he can't go with us? Looking for some advice. Mike from TX |
| A: |
Many demented patients have a tough transition when moved to another environment, especially when familiar people or things are not present anymore. Often over time (and that varies with the individual) they acclimate to their new home as they get accustomed to the staff, other residents and their environment. Depending on the stage of their disease and the degree of comprehension of their environment, that can take a long time in some cases. Some patients do better if the family visits often and others seem to do better if out of sight, out of mind. It depends on how he reacts to family to determine if that is more anxiety-producing than not. Anxiety and depression can be treated very well during the adjustment period and I would talk to his doctor for consideration of starting a medication to help. |
| Back To Top |
| Q: |
My mother-in-law is 73 and is having serious issues with her memory and paranoia. Most of the time she appears to be normal, or just maybe hiding it very well. She lives in a 4-bedroom house by herself, which she manages to keep clean and maintain. She also drives and does her own shopping. Every so often she will insist that the neighbors are moving the property markers and are moving fences and driveways onto her property. Most recently she took a 2 week trip to Florida and upon returning insists that someone has broken into her house and has replaced all the furnishings with items that are not hers. She has even called the police to tell them that her car has been replaced with another car. Dorothy from NJ |
| A: |
Evaluation is needed to find the cause of her false beliefs including memory screening and assessments. Please see the answer below for more details. |
| Back To Top |
| Q: |
On December 11th 2010, my dad had a heart attack, then kidney failure along with sever COPD. Due his illness he was placed in a rehab facility to recover. Over the past year his health has gone up and down, but lately he has been making up stories that no one comes and sees him, or that he has gone somewhere (like when his friends visit he drives their car and other stuff). I will follow up and none of this is true. He will tell me that he's not getting his meds etc. Seems like a lot of stories—none of it's true but he believes it. It's almost like lying! I will ask him something and won't tell me the truth. My dad has visitors all the time, but will then say the next day no one comes by, but his memory of the majority of his is still there. I guess what I'm asking is, is making up stuff to the point he believes it part of dementia? Yvonne from CA |
| A: |
What you are describing, false beliefs can be caused by many conditions. Certainly people with dementia (Alzheimer's disease, Lewy body dementia, Parkinsonian dementia and others) can have false beliefs due to their dementia. However, certain medications in some people may also cause false beliefs (steroids, anticholinergics, antihistamines, pain medications, amiodarone, mexiletine, antiarrhythmics, many antibiotics, sleeping pills, anticonvulsants, some antihypertensives, anti-Parkinson agents, and others) in some individuals. Toxins like alcohol can cause false beliefs. Lack of oxygen to the brain (hypoxia) from sleep apnea, COPD, poor heart function can cause false beliefs in some individuals. Significant liver or kidney disease can cause this. Low B12 or thyroid abnormalities can cause this in some people. In short, just because here are false beliefs does not mean the person has dementia. A careful and complete evaluation should be done to find the specific cause. There are medications that can reduce false beliefs (antipsychotics) that may be considered by their physician. |
| Back To Top |
| Q: |
My mother died last year and since then my dad, who is 88, has moved in with my husband and me. He has dementia, can't feed himself and is given his medicine. He spends a lot of time in his bed. Also has to use a bedside commode. Any advice or ideas? Karen from LA |
| A: |
The usual goals of care would include safety and quality of life. Increasing pleasurable activities and using day care centers to increase brain stimulation may help quality of life. Look at all his medications to make sure they are not sedating him. Make sure that all caregivers get enough respite so that they can increase the amount of quality time with him. Consider a companion to get him out of the house. |
| Back To Top |
| Q: |
Do you think that "memory care" as marketed by Assisted Living facilities is in essence a scam of sorts? I am coming to this conclusion for two reasons: A) There is no regulation whatsoever of this area, or enforced standards as to what works and what doesn't and B) Needless to say, "Memory Care" costs more money. My mother has Alzheimer’s and I have been looking into a new AL facility for her. I think anyone with Alzheimer’s or Dementia benefits from one on one attention and love, but to market it as "memory care" seems false to me. What say you? Cheryl from LA |
| A: |
There is great variation of care provided in Assisted Living facilities. For some "memory care" is just having a locked unit where the dementia residents stay so that the Assisted Living facility can advertise they have a special place for dementia residents. The best places not only have secured units, but also have extensive training in the care of dementia residents. They have dementia specific activities based on the individual resident's level of functioning. They have more, rather than less, activities that are resident specific. They have environmental cues and stable nursing staff to help provide routine and stable environments for those with memory loss. They have training regarding behavioral modification techniques and ways to improve communication to those with dementia. They have training with ways to approach and care for those with fear, suspicions, anxiety, intrusiveness, and agitation other than always using chemical or physical restraints. They have expertise with their physician staff who know when and with what medication (behavioral stabilization and cognitive enhancers) using the appropriate dosing will lead to improved quality of life for a specific resident. They communicate routinely and often between each other and with their physicians to notice issues early and to take appropriate actions early. In looking for an assisted living facility you can ask about the topics I mentioned above. You can also ask how often they have to send a resident out to the hospital for behavioral or dementia issues or how often they give someone a 30 day notice to leave due to the resident's behavior or dementia issues. The best facilities rarely have to send the residents out or away as they have great staff and the training to appropriately care for the resident in place. Good luck on your search. |
| Back To Top |
| Q: |
My father is 73 years old and has a shunt from normal pressure hydrocephalus and now they are saying he is in full-blown dementia and on his death bed. Could you please tell me if this can happen like this? It all happened in a matter of a few days. He is combative, spitting and yelling. Renetta from LA |
| A: |
If the shunt that was placed malfunctions or is clogged, it can cause acute hydrocephalus leading to severe headaches and lethargy leading to unresponsiveness. If there is an infection of the shunt in the brain, that can lead to sudden and severe cognitive impairments. A bleed in the brain related or not to the shunt (subdural hematoma, cerebral hemorrhage) can cause rapid deterioration. Degenerative dementias never progress in a matter of days. A CT head of his head or a shuntogram can help with diagnosis of the problem. |
| Back To Top |
| Q: |
My Dad has had three different cognitive tests and has failed each one. The last test was in August 2011. He was told he would have to stop driving. Each time the doctor prescribed medication for Alzheimer's, but my mother would not administer the meds. She said it affected him too much in negative ways and never let him have those meds for more than 2 days. She also let him to continue to drive. I told the doctor that he was still driving and they contacted the state and had his license revoked. How do I deal with a second parent who has dementia also, but has all control? Tony from MS |
| A: |
I am sorry that you and your family have had to go through all of this turmoil. I am not sure of your question. Do both parents have dementia? Is it your mother or father that has all control? If your father continues to drive, is not using good judgment in his driving and is not safe, then disabling the car or removing it may be potential options. If your mother is overly controlling, you need to discuss with her that her husband's dementia syndrome will decline more slowly in the future by getting and staying on Alzheimer's medication if that is what his doctor is recommending. The longer the husband stays functional and able to take care of day-to-day activities, the less work it is for the wife. If it is the husband that is controlling, the family must try to do what they can to keep him safe. His doctor needs to bargain with him to just try the medication temporarily to see if he likes it or if it seems to have benefit. For a fair trial, make sure he gets up to the best dose. After a couple of months, the medication may be more routine and he will not complain about taking the medication or the doctor can suggest to keep on it a little while longer to see how it does. |
| Back To Top |
| Q: |
My 80 year old aunt who was diagnosed with dementia has suddently started hallucinating. I’m very concerned about her meds and dosages. Could these meds be contributing to problems (Namenda 5mg morning and 5mg night, Seroquel 25mg morning and 50 mg at night, Razadynde 12 mg at night, Prazosin 1mg night and Meloxican morning and night). Or maybe her meds are not strong enough? Anne from LA |
| A: |
Medications can often cause hallucinations. Of the ones you listed, meloxicam might cause issues in some individuals, but it is not common. The other medications do not typically cause these issues. If any of these medications were started just before these behavioral symptoms started, then talk to her doctor about coming off that medication if possible. It is possible that she is having false beliefs or delusions and not specifically seeing or hearing things (hallucinations) that others do not see or hear. Seroquel is a medication specifically for these false beliefs. Perhaps she was started on it for that reason. The usual does range for Seroquel is 50 mg to 150 mg total dose daily in dementia individuals. Since there are many causes of these behaviors, including infections (urinary tract infection), metabolic disturbances, environmental considerations, among others, it is best to get her back in to her physician so they can make sure she does not have an infection and to check for other causes to treat. |
| Back To Top |
| Q: |
My Mother has dementia. She has a husband, but my siblings and I feel he is not taking care of her. We thought about guardianship, but not sure where to start. The husband does not follow the doctors’ orders and most of the time does what he thinks is best (regarding medicine, etc.). She is losing weight because of not eating properly. I have medical POA, but have been told it would not work if we decide to try and place her somewhere. I guess he can override that. Diana from NC |
| A: |
If you have a Durable Power of Attorney (DPOA) for healthcare and your mother no longer had the capacity to make these decisions on her own and your father and siblings are all agreeable to place her, then there is no need for guardianship and you can make the arrangements to place her in a long-term care facility. If there is disagreement between family members, this becomes harder to do and then a guardianship may be the best option. To get a guardianship, you will need her physician to fill out paperwork obtained from the courts to provide information on her capacity. The courts then decide if a guardianship is appropriate and who the guardian will be. They may choose a non-family member. Another option is to contact Adult Protective Services to come into the home and evaluate the situation, particularly if you feel that her husband is not taking care of her properly. They can help as well in getting the process started for a guardianship if they feel that is needed. |
| Back To Top |
| Q: |
How do I get my mother-in-law Barb from acting out around my daughter when we are not home? We live with Barb and my daughter gets her off the bus from daycare before we get home and Barb treats her just horrible, yelling, cussing, throwing—it is just awful. This never happens when we are home, but we have heard this over the phone several times and the neighbors have told us. Please help. Sherry from AZ |
| A: |
There are many potential reasons for her behaviors and so it will be hard to be very specific. In general if your daughter can bribe her with something she likes to eat or do, this may help. In other words increasing pleasurable activities usually helps. Perhaps you calling Barb just after she arrives home may ease the irritability. If none of that helps, you could talk to Barb's doctor about medications, like antidepressants that may help calm her a bit more. |
| Back To Top |
| Q: |
If the research shows that UTI can cause dementia-like symptoms, is there a treatment with prophylactic antibiotics to prevent the infections from establishing themselves? Janet from AZ |
| A: |
Yes. In some individuals who have frequent urinary tract infections, physicians at times prescribe daily low toxicity antibiotics to help prevent them from occurring. |
| Back To Top |
| Q: |
My grandmother of 92 had a episode the other night where she said that she saw a man in her closet and a little girl was sitting on her bed. Could this be a result of a UTI? Kirsten from IA |
| A: |
Many things may cause false beliefs or hallucinations in elderly people. An infection such as a urinary tract infection or pneumonia could cause this. New medications or overdose on medications is another common cause. Metabolic conditions or liver problems may cause these symptoms. If they are recurrent and especially if they are associated with fevers, confusion or other new symptoms, your grandmother should be seen by her physician. |
| Back To Top |
| Q: |
I have a mother with dementia. She paces back and forth, requires frequent attention and lately has been getting quite agitated, yelling irrationally at times. She lives with my 85 year old father in their long time home. He's getting to the point of exhaustion, but is worried that she will react very negatively if she is put into a nursing home or memory care, separated from my father. What would be your advice? Second, are there ways to search for places that have nursing homes AND regular assisted living on the same premises? Memory care without Medicaid is not affordable for us. Anjon from DC |
| A: |
Behavioral issues are common in those with dementia. They are due to loss of brain cells and due to neurotransmitter changes in the brain related to the brain damage. Environmental or behavioral modification techniques can be helpful to reduce unwanted behaviors. However, they are often not enough and medication supplementation is often required to help even out the neurotransmitter impairments. Agitation, irritability, false beliefs and mood issues can often be relieved dramatically with appropriate pharmacotherapy. If your mother has fewer of these behaviors, it is much easier to care for her. Your father may also benefit from more respite. You could have your mother go to day care, have a paid caregiver come in or take her out or have family watch her while your dad gets some time to himself. Regular respite is invaluable and reduces burnout for caregivers. To evaluate how negatively she would respond to a nursing facility or assisted living facility, she could be taken there for a weekend or a trial period and see how she reacts. Many facilities have all levels of care in the same campus (independent living, assisted living and nursing home). A husband could be very close even if a wife has to move to the nursing facility when more care is required. Your local Alzheimer's Association chapter or Area Agency on Aging could give you a list of facilities that have those choices. My edited book, "Long-Term Management of Dementia" (Informa Publishers) has great information about all these management issues and much more (see the link next to my expert column at Parentgiving). |
| Back To Top |
| Q: |
What are the symptoms of Parkinson’s disease. I am a man of 60 years of age. My hands shake and I am unable to hold a cup of water without spilling it. The shaking is throughout my entire body and shaky in bed as well as in my sleep. I’ve been dealing with this for many years after Desert Storm. They called it Desert Storm Syndrome. Recently I had my gallbladder removed—my blood pressure went up and I now have anxiety attacks. I am taking meds for it, but the shaking is still there and has affected my writing. I feel like falling backwards at times. Please help. James from FL |
| A: |
Parkinson's disease usually starts with tremors/shaking on one side much more than the other. The shaking is worse when the hand is at rest and much less when the hand is moving such as when drinking from a cup. Other features are stiffness, lack of facial expression, slowness of movements and trouble with balance. When the shaking or tremors affect both sides of the body or head or jaw and are worse when trying to write or move, Parkinson's is less likely. Essential tremor, medication or toxin-induced tremors or familial tremors are more often the causes. Individuals with restless leg syndrome have a desire to move the legs or sometimes the arms and a feeling of not being comfortable. It often keeps them up at night. Medications for anxiety can also at times increase tremors as can other medications like those for asthma or breathing issues. My suggestion is to seek out a neurologist for a complete evaluation of potential causes and treatments. |
| Back To Top |
| Q: |
I just heard that music therapy can be helpful with Dementia patients. What are your thoughts on this? Would it be beneficial for us to try it? Frank from OH |
| A: |
Any activity that helps stimulate the brain is helpful for dementia patients…in moderation. Too much stimulation of anything can cause anxiety and confusion. A variety of stimulating activities at different times is better than only one activity. Music therapy can be very helpful to calm a person and stimulate certain parts of their brain. As with any activity, if the patient responds to it, it is worthwhile to continue. If their response is more anxiety or distress, then it is worthwhile to discontinue it. |
| Back To Top |
| Q: |
My divorced father is 79 and has been diagnosed with dementia. He is at the stage of being unable to pay bills, care for the house and remember recent events such as doctor appointments. He insists on living at home and has an unmarried couple and her two teenage daughters renting the basement who help me with his care. My father seems to like the boyfriend, who is of good character and looks out for him like a son. Recently, my father has begun to make up allegations that the man is molesting his girlfriend's daughters. Both my knowledge of the people involved, and the fact that my father cannot remember details such as how many daughters there are, leaves no question in my mind that he is making it up. He also shows an inappropriate interest in sex and likes to embarrass people with his talk. I have been aware of my father's accusations for a few months and refused to give him an audience, but he recently confronted the boyfriend with some “friendly advice.” The boyfriend is now rightfully scared. A close friend of my father's has also confided that my father brought the accusations up to him as well. Would a psychological exam as a demonstration of his mental incompetence help, should this ever become a legal issue? Or is a retirement home the safest way to protect others from his accusations? Kimberly from WA |
| A: |
About 70 percent of individuals with dementia, particularly with Alzheimer's disease, develop false beliefs. Only 3 percent develop hypersexuality with physical sexual aggressiveness. However, more commonly we see frequent verbal sexual comments. Typically, one can first try to use logic to dissuade the patient of their false belief or try to ignore the behaviors if they are not harmful. However, many times these techniques do not work due to the nature of the condition. When the behavior issues get to a point where they are causing significant problems for the patient or others, it is time to consider medications. Due to the potential seriousness of the accusations, use of an atypical antipsychotic (like quetiapine or ziprasidone or risperidone) to help reduce the false beliefs may be something his doctor may consider. There are also medications that may help with hypersexual behaviors, particularly antidepressants like selective serotonin reuptake inhibitors. Chapter 4 in my edited book, “Long-Term Management of Dementia” (Informa) goes into detail about dealing with problem behaviors if interested (see the link next to my expert column). It is also important that these concerns get documented by his primary care physician or dementia specialist. Evaluation and management of these problems by his physician, including a clear diagnosis of his dementia will help in case there are any legal issues that arise. If the behaviors are not treated, it may not matter where he lives as he may have the same accusations everywhere he goes. This is more typically the case than not. |
| Back To Top |
| Q: |
My 86 year old mother has just lost 15 lbs in 10 days. What is going on? (Yes, she is eating.) Marianne from PA |
| A: |
You can lose a lot of weight quickly if the weight is from water or fluid loss. Some patients are on diuretics that will cause them to urinate out excess fluids that may be building up in their legs or elsewhere. I would have her seen by her primary care doctor to look for reasons. |
| Back To Top |
| Q: |
My mom has been diagnosed with dementia for three years now. She is 80 years old. My brother took care of her for three years, then in July 2011 he felt he could no longer take care of her. Not one of her nine children offered to take Mom except me. When Mom first came to love with me, she weighed 65 lbs. She eats very well and I can see she is gaining. She was admitted to the hospital 2 days ago for a bladder infection—they weighed her and she is still at 65 lbs. How can this be? Was she not weighed right? Marie from CA |
| A: |
I suppose it is possible they weighed her incorrectly. However, in general, patients with this low a weight who have dementia have a very hard time gaining weight. Also, a person can become dehydrated and lose a lot of weight if they are not drinking or eating much for two days. It is possible after her bladder infection is corrected, she will gain weight again. Continue supplements with or between meals and eat with her to help with weight gain. There are some medications that can also improve appetite (mirtazapine and megestrol), but they also may have significant side effects to watch for. |
| Back To Top |
| Q: |
My father is 67 years old, and Alzheimer’s was diagnosed last year. Mostly he has cognitive deficit, and I am very concerned because the neurologists in our region tell me that we can do nothing. He takes Exelon 9.5 mg each day and he has had cerebrolysin infusion/30 ml for 20 days. Please tell me, what else could I do for him? What do you think about vaccination, and which one: passive or active? Thank you! Karin |
| A: |
Exelon at 9.5 mg/24hour patch is an effective dose for individuals with Alzheimer's disease. This medication is often combined with memantine titrated up to 10 mg twice a day. I have no experience with the use of cerebrolysin as it is not often used in the United States. More studies are needed for that agent in regards to how long it can remain effective for patients. Vitamin E 200 units daily can be helpful as an antioxidant in Alzheimer's disease patients. There have been encouraging signs from the monoclonal antibody "vaccine" against amyloid in human studies. More research is required to see how well it works. The same is true for the other passive and active approaches. If he is eligible and willing to participate in a clinical trial and there is a center close by doing these trials, I would be very supportive of getting involved. Altruistic patients with Alzheimer's disease wiling to participate in research will help to speed up the discovery of new therapies for them and others. |
| Back To Top |
| Q: |
My father in law has dementia and sundowners. He also just broke his hip so the trauma has made him much worse. What kind of doctor should he be seeing? Is a neurologist that specializes in management of dementia the best bet? How about a psychiatrist that specializes in dementia/Alzheimer’s? Just trying to get him the best and correct kind of doctor. Linda from OH |
| A: |
There is no question that he would be best served by a physician who specializes in dementia. It would not matter if they are a neurologist or psychiatrist as long as they specialize in dementia. |
| Back To Top |
| Q: |
My dad lives in Florida with his wife. He is 80 years old and has had Parkinson’s for about 5 years. Now they are saying he has dementia. He’s in a hospital, but has to go to a rehab center tomorrow for three weeks. I am really worried about him. Is there any surgery or other things that can be done for him? Mitch from NY |
| A: |
There are many potential reasons for dementia and most are treatable. His physician can assess for potential treatable causes and start appropriate treatment to help the condition. Some causes of dementia are treated by surgery like those with hydrocephalus. There are also some cases of Parkinson's disease where the symptoms can best be treated with deep brain stimulation or surgery. Potential candidates must be evaluated at specialized centers that offer these treatments. His neurologist would be able to let you know if he would be a potential candidate. |
| Back To Top |
| Q: |
My mother, age 91, seems to be healthy physically (she has not seen a doctor since my brother was born 57 years ago), but mentally, has memory loss. She will only talk about her childhood and cannot carry on a conversation about anything else. She refuses to leave her home, since my dad died 6 years ago. My husband and I bring her food, clean the house and do the laundry. She refuses to have anyone come in to help her and refuses to move to an assisted living facility. I know she does not eat well, appears to be losing weight. Recently she has become agitated and is very negative toward my husband, saying that he hates her and that he has shoved her and yelled at her. This happened after we made her go have her hair washed as she is not taking care of personal hygiene. I have offered to wash her hair and trim her nails—she refuses. Since she sees no one but my husband and myself, I have no one to ask for help. She refuses to let my children or grandchildren in the house. I feel like I am neglecting her care, but don't know how to get her to agree to any help. I know she is depressed, she refuses to see a doctor and without just physically removing her from her home, yelling and screaming, I don't see another solution. I have called adult protective services and they said, "Just because she chooses to live differently from what you would like, doesn't mean she is wrong." Marge from IN |
| A: |
Sorry to hear about the situation. It sounds like she may be suffering from a progressive degenerative condition. However, there may be treatable issues if she would allow an evaluation. This may not be possible until she gets so ill or gets an infection that she has to go to the hospital. She also sounds like she is a bit suspicious and maybe paranoid. Many times medications will help her behaviors enough that she would be more amenable to increased supervision, a shower, food, and an evaluation. Since no physician will prescribe without seeing her, it may be possible to get a visiting physician to come to her house when you are coming out to see her. They may assess the situation as dangerous to her and Adult Protective Services may have to come out. They may be able to get enough of a flavor of her behaviors that they may be willing to prescribe a medication. Some medications like risperidal come in liquid formulation and can be placed in something she drinks if she refuses to take any pills. You may have to visit daily to make sure she drinks her drink with the medication in it. This may help her suspiciousness and increase her willingness to allow more supervision and evaluations. Best of luck. |
| Back To Top |
| Q: |
My father who is 81 years old just had back surgery to repair 3 herniated lumbar disks. He entered the hospital coherent and without any problem that was remarkable. After surgery he is now in full blown dementia. We have taken him to a neurologist who believes he has Alzheimer's, but this is post surgery. How can a man who showed no signs now be properly diagnosed with this? Could this be due to anesthesia, medication, post operative brain dysfunction or what? We cannot seem to get anyone to help us. Would appreciate your opinion. Susan from TX |
| A: |
Many times if there is a sudden change after surgery, it suggests that he is suffering from an acute confusional state. There may be many causes. The most common causes include medication effects, infection or strokes. Metabolic issues like impaired liver or kidney function can play a role. Not getting enough oxygen (short of breath) can be a cause. A scan of his head would rule out a stroke. Infection from the surgery or other causes (urinary tract infection) can lead to confusion. Often after surgery people are placed on pain medications and many of these can cause confusion. The faster he can get off these medications the better for his confusion. Anesthesia should wear off and would not cause long lasting impairment. Those individuals with underlying dementia would have less cognitive reserve and so will be much more sensitive to having medications, infections or other conditions cause a confusional state. They will recover most of the time completely, but it may just take a few weeks. Alzheimer's disease is a gradual progressive condition and there is no such thing as rapid onset Alzheimer's disease. If there is a sudden change in cognition there is always something else (maybe in combination with a mild dementia) as the main cause of the issues. |
| Back To Top |
| Q: |
My 81 year old mother in the late middle stages of Alzheimer’s. She is waking in the middle of the night. The physician has my dad giving her a sleeping pill. My dad contacted the physician again and was told to give her two pills. My dad says this is the sundowner’s syndrome, but I thought that was occurred late afternoon early evening. Do you have suggestions to help my mom sleep through the night? Margaret from CA |
| A: |
There are many ways to help with sleep. First, try to make sure she does not nap in the day. Avoid alcohol and caffeine. Keep on a strict sleep schedule, go to bed and wake up the same times each day. As far as sleep aides, the least toxic for Alzheimer's disease is trazodone, maybe 50 to 150 mg nightly. Avoid all over the counter sleep aids as they can make her confusion worse. Other that can be tried include mirtazapine, zolpidem, gabapentin, and others. My book, Long-Term Management of Dementia (see information to the right of my column on Parentgiving) has other choices listed. |
| Back To Top |
| Q: |
My dad is 87 and doesn't get around well, so doesn't get a lot of exercise. He doesn't have much of an appetite, so doesn't eat well. I am going to offer a supplement drink, but I am wondering. Is there something he can take, or eat or drink, that will give him more of an appetite? Kim from FL |
| A: |
Supplements are the first best choice. Ensure, health shakes, Carnation instant breakfast, Boost and others are all pretty good. Start with one can a day. However also make sure that someone eats with him as this will usually increase food intake. There are medications that can stimulate appetite like mirtazapine or megestrol. These can work very well in situations where there is severe appetite loss. However both can have side effects that are best avoided if supplements will work. |
| Back To Top |
| Q: |
My grandfather is in hospice care and recently aspirated and contracted pneumonia. No treatment of the pneumonia has been given and a steady diet of morphine and ativan with no food and limited water has been the staple for the last few days. He is in the middle stages of dementia. Is this typical treatment? Annaq from GA |
| A: |
Hospice care usually means end of life care to keep someone comfortable just prior to death. However, the amount of treatments given while in hospice care is usually left up to the doctor and family. Some families will treat infections, like pneumonia with antibiotics. Some families will not treat and just provide comfort care. Morphine is often given to help with pain issues and anxiety symptoms to make the patient comfortable. Ativan can be used for sedation or anxiety. Just prior to death, no food and limited water makes the patient more comfortable. Too much fluid may build up in their lungs giving a sense of drowning. Fairly soon the patient cannot drink anymore and death ensues quickly and comfortably. Often the patient may have made a Living Will that instructed family members that he would not wish to live if certain irreversible conditions became so unbearable that it made his life not worth living anymore. Exactly what medical issues or combination of medical issues occur that lead to that conclusion is very variable for different patients and different families. |
| Back To Top |
| Q: |
My 87 year old mother has been in an assisted living facility for a little over a year now. She cannot remember things from maybe five minutes ago. Other times, she can't remember something that happened many years ago. Is this dementia or Alzheimer's? Other than memory, she seems to be okay. My brother lives in the same city as the assisted living facility location. I live several states away. Can you give me some insight and suggestions as to how to cope from a distance. Thanks, Mom's Daughter Barbara from NE |
| A: |
Anyone age 87 with progressive memory or thinking problems is very likely to have a degenerative condition like Alzheimer's disease. Her doctor should have run some lab tests and a scan of her brain to look for reasons for her memory loss. Dementia is a non-specific symptom, meaning someone is having trouble thinking and doing day to day activities. One cause of dementia is Alzheimer's disease, which is due to an abnormal accumulation of toxic proteins that accumulate in the brain and kill some of the brain cells, particularly in the memory areas. Dementia can also be caused by head trauma, having many strokes, low thyroid, vitamin deficiencies, kidney or liver problems or drugs, to mention a few other conditions. Many causes of dementia can be treated including Alzheimer's disease. I would ask her physicians what type of dementia they think she has. Then get more information about that condition. Visit the Alzheimer's Association for information and think about going to a support group meeting where you live. Inform the assisted living facility of the types of activities your mother would enjoy so that they can direct her to those types of activities. |
| Back To Top |
| Q: |
My mother is 86 years old and was diagnosed with dementia in the past few months. I noticed all the changes that the doctor told me as far as her physical and mental state of mind. My question to you is she keeps asking to go back home (to another state hundreds of miles away) and wants to see my dad, who passed away 36 years ago, wants to have lunch with him and then go to the garden and see God which she wants to see my dad in the cemetery. Is this another wave of mental thoughts and do I tell her and remind her that dad has passed away or change the subject? I go and spend dinner time with her and have some giggle moments with her. I also get out some of the old pictures and she gets somewhat happy with that too. Maureen from GA |
| A: |
It is alright to reorient your mother to reality if it does not cause her significant grief and anxiety. If reminding her that her husband has died many years ago causes her much distress or disbelief, then it may be better to change the subject. You might agree that it would be nice to visit with him (her husband) and that it may be something to think about later. |
| Back To Top |
| Q: |
I care for my mother-in-law and my aunt who both have very different forms of dementia. My mother-in-law has diabetes, congestive heart failure and kidney failure that fluctuates between stage 3 and 4. I noticed her having trouble with her memory about 5 years ago and took her to the doctor. They evaluated her and told me to do memory games with her. Later they put her on aracept, which seems to help. Well, you can tell when she has forgotten to take it anyway. She has trouble with numbers and remembering birthdays and spelling and has quite a bit of confusion, but I have not noticed any suspicious behavior and only a few times has she had hallucinations. Could her dementia be caused by her kidney failure? And if so, does this kind of dementia cause brain damage and is it reversible? My aunt is 86 years old and has had dementia for many years. She does have suspicious behavior and hallucinations. She was never evaluated that I know of and her doctor does not seem to think it is necessary at this time. She has never been on medication. She did have a UTI, which could explain some of the hallucinations, but not all of them because she does it to a lesser extent when she does not have a UTI. It is strange because one day I can hold a normal conversation with her and the next she is out of it. She is now becoming incontinent and just recently having trouble controlling her bowels. It will be bad for a few days with constant accidents and then she will be fine for a little while and then it will start up again. What kind of progression can I expect next? It is hard not knowing what to expect next. If I had some kind of Idea maybe I could prepare myself to deal with it. Sheree from MI |
| A: |
In regards to your mother-in-law, yes, significant kidney dysfunction can cause dementia. Toxins in the blood that the kidneys normally would remove may not be removed as well and so more get into the brain and effect its functioning. However, many conditions that affect the kidney (e.g. diabetes) can also affect the brain as well. If the dementia is only from the kidney dysfunction, it can be partially reversed by correcting the kidney problem or giving dialysis. If the brain dysfunction is due to several conditions then reversibility is less likely. In regards to your aunt, given her long history of progressive decline, a degenerative brain condition is most likely. Those conditions, like Alzheimer's disease or dementia with Lewy bodies have a fairly predictable course. Patients lose more and more abilities to do day to day activities. The rate of decline is usually fairly stable and the speed that she has declined can help predict how fast she will continue to decline. Obviously UTIs, intercurrent illness, diet issues and other conditions can cause fluctuations in her bowels, incontinence, thinking and moods. Her physician can help with these intercurrent illness or conditions. Another excellent source of support and information about prognosis may be obtained at Alzheimer's disease support groups where families going through similar issues can share their experiences. |
| Back To Top |
| Q: |
My Dad has a lot of medical things going on: Parkinson’s, Alzheimer’s, copd, acute renal failure, a blood clot in his chest. He’s on dialysis, he also has high blood pressure, diabetes, and cholesterol. My question is it safe to put my dad on a medication called trazodone to make him get sleep? He doesn’t sleep at all—he’s up around the clock. He’s 74 years old and has fallen and even has a history of strokes and a bleed in the brain, which has resolved thankfully. What can be done so that my dad can get some rest?? Thank you! Lisette from NJ |
| A: |
In general, trazodone is a very safe medication and often helpful for sleep issues. It is best taken every night to promote sleep. I use it often in dementia patients. It can be titrated to effect, usually helping with dosages from 50 to 100 mg nightly. In specifics for your father, it would be important to talk to his physician so that they can review his medical issues and other medications to make sure that he would not have problems taking trazodone. None of the conditions you mention that your father has would necessarily be contradictory to taking trazodone. It would most likely work fine, but his physician would have to review his case prior to prescribing it. |
| Back To Top |
| Q: |
Lately I've noticed changes in both my 81 year old mom-in-law and her sister who’s 84 years old. My mom-in-law who was already experiencing memory difficulty at night (she called me two days in a row and had the same exact conversation with me twice), now asks the same questions over and over at night (about new info). My neighbor called it looping. I'm concerned because she still drives and lives on her own. Our aunt (her sister), who has always been sharp, was really fuzzy the last time the family was together and said "I don't know who half of these people are." They were all family that she knew this summer. She lives at an assisted living center because of back problems and mild Parkinson’s. Our mom and aunt had a sister who died last year of sudden severe dementia at 86. Please tell me what you think we should do? Bonnie from OH |
| A: |
There are many potential causes of cognitive problems including medications, thyroid issues and vitamin B12 deficiencies that are completely reversible. Other causes including degenerative conditions like Parkinson's disease dementia or Alzheimer's disease are very treatable and those medications help to slow down the cognitive decline. Both family members need to be evaluated by their primary care doctor for causes of their impairments. Also family can ride with the mother-in-law to ensure she is still using good judgment with her driving. If there are questions regarding her driving skills, driver evaluation centers can be contacted for professional evaluations. |
| Back To Top |
| Q: |
My Mother-in-law has Alzheimer's, diagnosed 4 years ago. She removes all her clothes after bedtime, including her adult diaper. When she wakens with a need to toilet she doesn't make it to the bathroom and has an accident, which causes her to slip and fall. So far only bumps and bruises, but it is only a matter of time before she really injures herself. Any suggestions on keeping her clothed? Barb from NY |
| A: |
You mention that she removes all her clothes after bedtime. Does that mean she originally goes to bed with them on? If that is the case, perhaps using a medication that promotes sleep like trazodone may help her sleep through the night and decrease the times she wakes to remove her clothes. Is any one living with her? If she has a bed alarm, or a baby monitor, the other person could be notified when she gets up and assist her to the toilet to prevent falls. Consider also the use of a commode at the bedside, which should reduce the time to reach the toilet and perhaps she will make it on time to the commode. Also be sure to enforce no fluids after dinner. Avoid caffeine or alcohol as these promote urination. Hopefully some combination of these ideas may be helpful to your situation. |
| Back To Top |
| Q: |
My Dad is 85 years old and was diagnosed with Alzheimer’s about 4 years ago. About a month ago he fell and broke two ribs. Since the accident his condition has worsen. Conditions include the following: 1. Can't walk 2. Cannot feed himself 3. Difficulty swallowing 4. No bladder control 5. No recognition of family 6. Most vocabulary is gibberish or made up words. 7. Constant flinching. Many of these conditions existed prior to the fall. After the accident, Dad was originally on drugs that made him sleep. He is now off these drugs, but remains agitated and more in a constant state of confusion. We are considering switching the meds back so that he can sleep most of the time and let nature take its course. Dad receives full time nursing and would not want to live as he does today. We think Dad would want to sleep through his final stage, which would perhaps speed up the enviable. The question is keep him awake and agitated or let him sleep through the final state of his Alzheimer’s? D.B. from NC |
| A: |
I am sure it is very disturbing to see your father like this. At the end stage we are focused most on quality of life for him. Certainly if part of his agitation is due to pain, that should be addressed. Also a review of any medications he is on that can increase confusion or agitation would be suggested. With the broken ribs, is he breathing well? Air hunger will cause agitation and confusion. Getting good sleep at night is always important. Trazodone may be of use if needed. The key, however, is to control his agitation and, do to that, one needs to figure out the cause (anxiety, air hunger, pain, fear, restless...). If his agitation is improved, then he has a better quality of life. Good luck. |
| Back To Top |
| Q: |
I am looking for a recommended dementia/Alzheimer’s specialist in the Seattle area and was hoping you might have a suggestion. My mother has recently had some health problems (back surgery and some heart problems), and I was trying to find out if her recent memory problems over the past year or two are due to medications/depression/etc. or if she truly is seeing some early onset of Alzheimer’s. George from WA |
| A: |
In Seattle, the first place I would suggest your mother be evaluated is at the Alzheimer's Disease Research Center at the University of Washington. They have expert neurologists who specialize in Alzheimer's and cognitive disorders. Dr. Murray Raskind is the Director of their center. Residents of other cities can get on the American Academy of Neurology website to "find a |
| Back To Top |
| Q: |
My mother has been diagnosed with Parkinson’s and my sister claims she is in the early stages of Alzheimer’s, but I really think it is dementia. In any case, she refuses to eat anything and will go days without eating. She claims she can't taste anything but then says all food is too salty. My sister claims she has anorexia, but I believe it is due to the Parkinson’s and dementia. Lois from WA |
| A: |
The term dementia is a symptom and not a condition. Dementia just means that someone has trouble with thinking and functioning. It does not tell anyone what the cause of those symptoms are. Some causes of dementia are multiple strokes, head trauma, Alzheimer's disease, Parkinson's disease dementia, alcohol toxicity, medication toxicity, etc. Your mother's physician should have completed an evaluation to determine the cause of her dementia symptoms (her thinking and functioning problems). You can have a diagnosis of Parkinson's disease without dementia (just called Parkinson's disease) and you can have Parkinson's disease with dementia (called Parkinson's Disease Dementia). In some cases, those with dementia and Parkinsonian symptoms (stiffness, balance issues, tremors, slow movements) have a condition called dementia with Lewy bodies. It is possible to have Alzheimer's disease and Parkinson's disease, but that would be very rare and very unlucky. In regards to the anorexia, there could be many causes. Some people with Alzheimer's disease, Parkinson's disease, Parkinson's disease dementia, dementia with Lewy bodies and other dementia producing conditions can be a cause of poor appetite and weight loss. Providing increased supervision during eating times, providing foods they like to eat, and providing nutritional supplements (Ensure, Health Shakes, Boost, Carnation Instant Breakfast, others) often help. Her doctor should look for other causes of appetite loss like the use of certain medications (cholinesterase inhibitors for example), gastrointestional conditions, renal or liver conditions, thyroid conditions, etc. |
| Back To Top |
| Q: |
My 87-year old mother fell at her assisted living facility and broke her femur (bad break nearest the hip joint—an orthopedist inserted a clamp around the splintered bone and a pin with screws.) The physician informed the family that it would be a lengthier time period than a clean break for the bone to heal. No longer able to stand, walk, go the bathroom unassisted, dress herself, she cannot return to "her home," as she refers to her room at assisted living. The doctor recommended she be moved to a skilled nursing facility for physical therapy to rehabilitate. At this point, we know she won't be returning to her "home." Every day she asks when she can go home and the and dress yourself unassisted.” I have observed her as she struggles to take even a small step without fear of falling again. Mother has always been thin and a picky eater. However, with this fall and the move to nursing care, she seems to have given up. She does not engage my brother and I in any conversation except to ask about going "home." She does have fairly severe hearing loss that she will not acknowledge and this keeps her from understanding clearly what is said. She refuses a hearing aid. I think this makes her dementia worse than it is. She now can't remember what happened a few minutes previously when asked, but has clear moments at times. The worst obstacle to her recovery is her refusal to eat. The doctor prescribed an appetite stimulant, but nothing works. She has a partial late top and bottom that interferes somewhat with her eating, but we know it is not the real problem. The speech therapist said she has no trouble swallowing. When food is served, she says she is not hungry. We have tried everything she likes, but she will not swallow anything except something smooth and maybe only a teaspoon. Nutrition-wise the hospital did test her protein levels, which are non-existent. Without protein and some food and liquids, she will not make it. She has a strange and fairly unsightly tic or OCDC habit she has had for the last two years. Any food she eats, she chews, then puts her finger in her mouth, runs her finger around her gums, and takes whatever food is in her mouth and scrapes it off into the edge of her plate or tray. It is not just the texture of the food that bothers her, it is food in general. She quits eating after one or two bites. She will not drink water, tea, only coffee, and becomes dehydrated easily. No matter how many times I explain to her that she needs to eat to live, she is ambivalent about it. My brother and I stopped saying anything after she became angry and told us to leave her alone. I don't know what to do or what is going on in her mind that is keeping her from eating. Can you make any observations or give us some suggestions as to how we could get her to eat. I even thought of a hypnotist I am so desperate. I am afraid she is very depressed. Do we have the doctor increase her Lexapro dosage? Would any of her meds decrease her appetite this much? Thank you for reading this lengthy description and for your suggestions. Monte from TX |
| A: |
Unfortunately, broken femurs lead to significant disability that the patient may never recover from. This is especially true for those individuals with dementia who are unable to learn new procedures well. Watch for symptoms of depression as that condition can be treated with antidepressants. Sometimes appetite loss is a sign of depression. I would not go higher than 20 mg of Lexapro. If her compulsive habits are contributing to her appetite loss, sometimes fluvoxamine at higher doses may be helpful (most patients may need 200-300 mg daily in divided doses slowly titrated to effect). In regards to the anorexia, there could be many causes. In some people dementia conditions by themselves can be a cause of poor appetite and weight loss. Providing increased supervision during eating times, providing foods they like to eat, and providing nutritional supplements (Ensure, Health Shakes, Boost, Carnation Instant Breakfast, others) often help. I have found megestrol acetate (400-800 mg/day in two divided doses) may help with appetite. Her doctor should look for other causes of appetite loss like use of certain medications (cholinesterase inhibitors for example), gastrointestional conditions, renal or liver conditions, thyroid conditions, etc... The term dementia is a symptom and not a condition. Dementia just means that someone has trouble with thinking and functioning. It does not tell anyone what the cause of those symptoms are. Some causes of dementia are multiple strokes, head trauma, Alzheimer's disease, Parkinson's disease dementia, alcohol toxicity, medication toxicity, etc. Finally remember you can only do so much to help her and it seems like you are trying everything you can do. Sometimes the disease conditions take over and we are left with our loving support |
| Back To Top |
| Q: |
My stepdad has Parkinson’s and my mum is his caregiver, she is showing signs of memory loss, she has osteoporosis, and they live together at the moment. What care do they need? Elaine |
| A: |
If your mother has not already been evaluated for her memory loss, she needs to be seen right away. There are many causes of memory impairment that are reversible. Some examples include certain prescription medications, some over-the-counter drugs, sleep apnea, low thyroid, vitamin deficiencies, and many others. Even if she is found to have a degenerative dementia like Alzheimer’s disease, the earlier she starts on treatments, the slower the decline of her memory and functional abilities. This allows her to be a functional caregiver for her husband for a longer period of time. It may also be a good idea to get an in-home assessment to identify potential safety issues in the house and to suggest possible home modifications to make caring easier. In addition, providing more supervision and increased respite opportunities will help to prevent early burnout. |
| Back To Top |
| Q: |
My grandfather suffers from dementia. Recently he fell down a flight of stairs and broke his neck (C7 if I remember right). Because of his age, they placed him in a cervical collar and sent him to a rehabilitation center. He can't remember why he is there and keeps removing the cervical collar. I believe he is ripping it off because whenever the family visits we find pieces of it all over and sometimes it's broken. The staff at the rehab isn't able to keep the collar on him and if he takes it off they don't put it back on him. We're at our wit’s end. Any thoughts on how to keep a c-collar on a dementia patient? Christy from UT |
| A: |
There may be limited options. It would be most important to know how severe the neck fracture was and how unstable his cervical spine is because of the fracture. If there is substantial risk to cervical spine stability and he does not wear his collar, then it may be worth the risk to have surgery to stabilize the neck. Other options may include placing a more secure neck |
| Back To Top |
| Q: |
My father has late stage Alzheimer's and is rarely continent—bladder and bowel. He wears Depends and is taken to the toilet every 2 hours, day and night. Is it standard to wake an incontinent, dementia patient every 2 hours at night to take him/her to the toilet? Would waking every 2 hours at night disturb sleep cycles and increase irritability or stress levels? Are there any studies that address this question? Jud from VA |
| A: |
A toileting schedule can be very useful to prevent incontinence and urgency issues. However, I typically do not have them toilet every 2 hours while they are sleeping. This would be especially true if it appears that waking him is disrupting his sleep cycles and making him irritated. Unfortunately, I am not aware of any studies that have looked at this. |
| Back To Top |
| Q: |
My father recently had a stroke and is physically recovering, although mentally he is struggling with evening agitation and sleeplessness. He is still in rehab, but if he has a "bad night" and wakes and yells, the nurses give him anti-psychotic medicine that hinders his ability to function normally the next day. Is there a mild medication that can help prevent the evening agitation without compromising his ability to function normally during the day and continue his rehab? Jean from OH |
| A: |
There are several things to consider that may be helpful. During the day, increasing daytime activities and reducing the chance for naps may help him fall asleep more easily at night. Also avoiding liquids before bed reduces the waking at night for toileting. Medications, pain issues and mood states may all lead to sleep disturbances that should be considered. To help with sleep issues, trazodone, an antidepressant, helpful to promote sleep, can be given at night. This may help to reduce sleeplessness without any hangover effect the next day. Zolpidem may be another choice to try to help with sleep issues if trazodone is not useful.
If he has significant false beliefs or suspiciousness or paranoia, then an anti-psychotic medication may be the correct choice to give. Perhaps lowering the dose or giving it in the late afternoon may help with the evening behaviors and not cause next day side effects. |
| Back To Top |
| Q: |
My mother has Alzheimer's and her ability to control her bowels and bladder has gotten worse. She refuses to wear any kind of protective garments and becomes very argumentative when asked to wear them. Any other suggestions would be greatly appreciated. We do monitor fluid intake and she does not have anything to drink after dinner except water to take her evening meds. Susan from MD |
| A: |
One of the best techniques is to get your mother on a toileting schedule. That is, have her sit down on the toilet every 2 to 3 hours whether she has to go or not. This will reduce the urgency and her not getting to the toilet on time in many cases. At times, patients may not like to be told what to do. They may also not like to be told to go to the toilet every 2-3 hours when they do not feel the need. Often suggesting that you are also going to use the toilet but do they want to go first, may ease their notion that they are being picked upon or bossed around. Giving them other excuses to go use the toilet may be helpful such as suggesting that they should go to the bathroom before they go out, etc. Also try to avoid prescription medications to control urinary leakage or incontinence as they often reduce the effectiveness of medications that are helpful for memory such as Aricept, Exelon or galantamine. |
| Back To Top |
| Q: |
What is the best medicine for a man who has Parkinsons and is a diabetic? Carol from IA |
| A: |
Parkinson's disease treatment will vary depending on the stage of the disease and the patient's other medical conditions. Unfortunately I cannot be more specific. Most medications for Parkinson's disease and for diabetes do not contradict each other. |
| Back To Top |
| Q: |
My mother has Parkinson's, osteoporosis and some dementia, is bed-bound, on hospice for some time and very thin. She is getting more and more contracted, so turning is difficult without her experiencing extreme pain, even through pain meds. She had a catheter briefly but was removed due to bladder spasms and UTI. What can be done to alleviate pain so she can be turned, changed, washed and disimpacted? She takes aibuprofen, morphine, ativan, vitamins, benadryl and pedialyte. Her appetite is generally very good, when the meds don't interfere. |
| A: |
It would be hard to be specific with any recommendations for medications, not knowing her condition and medical issues. However, consider anxiety or mood as a contributor to pain when turning. Use of an antidepressant (SSRI) or divalproex sodium may be considered. Also, if it has not already been addressed, the type of bed or chair that she lies in may make a big difference in her pain issues when she is turned. Specialty beds and chairs should be discussed with her therapists. |
| Back To Top |
| Q: |
Our 86 year old mother has been bed bound for 19 months. She lives in her own house with one of my sisters and has visits from her children daily. Over the winter her short-term memory started to fail. The last 6 weeks every afternoon she asks to be brought home. We tell her she is home. She feels like she is not home and is pleading with us to bring her home. By early evening after dinner she becomes quiet and in the morning she is fine. Is there anything we can do to help her with this confusion? Sarah from MA |
| A: |
If she has not had a medical evaluation for her memory issues, this would be suggested. Many conditions causing memory loss are reversible or treatable. Checking for thyroid issues, vitamin deficiencies and metabolic problems should be performed. Looking at her medication list to eliminate those medications, where possible, that can cause cognitive issues and confusion could also help. If a degenerative disorder is thought likely, starting anti-dementia medications will be very helpful. Behavioral modification techniques can be used to help reduce her anxiousness about wanting to go home in the evenings. It is always nice to be "home" especially as evening is coming. For many people trying to redirect her to the reality that she really is home does not often work. So, empathize with her concerns. Tell her that it is getting late and that she should stay here for the night and you will have her home first thing in the morning. Tell her not to worry and that you will be with her until she gets home. If she has other symptoms of false beliefs, paranoia or suspiciousness, talk to her doctor about possible medication use (antipsychotics) that may be considered. If she has other symptoms of anxiety, angst, or fretfulness, talk to her doctor about possible medication use (anti-depressants) that may be considered. |
| Back To Top |
| Q: |
My husband is in assisted living. He is having hallucinations. Would he be better in memory care rather than assisted living? He fears being on the memory care side because it's locked and asked me to promise not to allow them to move him there. He is so out of it, seeing things that don’t exist. Janet from OR |
| A: |
It sounds like you are saying that your husband is having hallucinations and false beliefs. These types of symptoms in dementia patients are common and are usually very treatable. If the symptoms are mild or infrequent, changing the subject or empathizing with the patient may be all that is needed. If the hallucinations and false beliefs are persistent and causing a lot of distress, then use of low dose antipsychotic medications can be very useful. His physician can prescribe such medications if needed. Locked units are to protect patients so that they will not wander away. I am not sure if he has these issues. If he is safe where he is currently living or after behavioral treatments, then there may be no reason that he would have to go to a locked unit at this time. |
| Back To Top |
| Q: |
My 80 year old mother has Parkinson's and dementia diagnoses. In spite of using Exelon 9.2 patch daily for over a year, she seems to be rapidly declining in her ability to speak and comprehend. She no longer seems to understand time, and after an early afternoon nap, her brain seems to reset and she thinks it's time for breakfast. Paranoia is increasing as well. In assisting her after toileting, she frequently accuses me of touching her inappropriately or of pushing her. She has also recently become markedly unsteady, swaying whenever she stands and falls very easily. The most difficult/challenging aspect of her care, however, involves her very frequent trips to the bathroom to urinate. If she happens to sleep through the night and wakes with a full bladder, she goes into a full blown panic attack. She seems to think that urine is a poison that she needs to "get rid of" as often as possible, and when she finds she cannot go because there is nothing there to pass, she also becomes quite upset. No UTI, her urine is clean. She keeps me up all night sometimes. How can we manage this aspect of her behavior? Alice |
| A: |
Hopefully you have some respite as it appears your mother requires much supervision and care. In regards to the dementia component, you are probably doing what you can with the Exelon patch. The dementia will continue to progress unfortunately. There may be some help for her behavioral issues. You mention paranoia and false beliefs. Some Parkinson medications may cause these symptoms (Sinemet, Requip, Parlodel, Amantadine, others). Perhaps her physician can taper down on some of these medications if she is on any and this may help. At times adding a vey low dose of an antipsychotic like quetiapine may be in order to help with those symptoms. The motor symptoms may be difficult to treat except for close supervision and aid when she ambulates. If she is fainting due to low blood pressure with standing there may be some medications that can help that. Sometimes frequent urination may be an obsessive-compulsive behavior and not related to bladder issues or UTIs. At times high doses of antidepressant medications (SSRIs) like fluvoxamine may be useful to reduce the repetitive behaviors. If the behaviors are worse at night and she is up constantly, trazodone may be useful to help with nighttime sleep promotion. Talk to her physician about all these issues. |
| Back To Top |
| Q: |
My mother is 81 years old and has dementia/Alzheimer's. I think she really has Alzheimer's and my sister is in denial. She has a very good appetite but continues to lose weight. She is very thin and fragile. Her frame looks emaciated? What can be done to stop the rapid weight loss? Or is this just part of the disease? Donna |
| A: |
There are many causes of weight loss and this should be addressed by her family physician. However if she has a good appetite, trying nutritional supplements such as Ensure, Boost or Health Shakes or similar products 1 to 2 cans daily may help to keep her weight up. Carnation Instant Breakfast, ice cream and other more calorie-laden foods may also work. In many of those with dementia at the end stages, weight loss is an issue. However, this is not typical in earlier stages. In more severe cases, there are appetite enhancers (medications like mirtazapine or megesterol) that may help reduce weight loss. These can be discussed with her doctor to see if they are appropriate for her. If your mother does have dementia, make sure she has an evaluation to find out the cause so that she gets started on treatments that may be available. Treatments usually work better if started earlier and not put off for months or years. |
| Back To Top |
| Q: |
What is the best method of finding support groups for children of parents with dementia? Marilyn from GA |
| A: |
Every community is much different in their availability of support groups. The first place I would contact would be the local Alzheimer's Association. They may know of such a support group or help you start one. Other organizations that may help include the Alzheimer's Foundation of America, Children of Aging Parents (http://www.caps4caregivers.org), National Family Caregivers Association (http://www.thefamilycaregiver.org) and ParentGiving. Some of these organizations have chat rooms and message boards that can be utilized as well. |
| Back To Top |
| Q: |
My husband was diagnosed with Parkinson’s disease about 10 years ago. So far he has been affected with tremors on the right side only (controlled fairly well by meds), but is now starting to notice his left side has become involved with mild signs of tremors in his left hand. Does this mean we can expect the same degree of tremors he has had on the right or is this entirely unpredictable? His right leg has also suddenly become worse with tremors in spite of medications. Are there any adult stem cell studies being done at this time? We've heard of success in this area. Thank you for any help or answers you may have. Mrs S from AL |
| A: |
Most of the time those with Parkinson's disease will have more problems (like tremors or slow movements) on one side of their body more than the other. Usually they may get symptoms on both sides, but almost always one side is worse than the other. Medication adjustments may help these new symptoms. Stem cell research is ongoing but not available outside of research. Deep brain stimulation (DBS) has been approved for some Parkinson's cases and can be done in some centers. This is usually reserved for those patients that are refractory to medications. |
| Back To Top |
| Q: |
Any suggestions on how to give medications to a person who is VERY combative when it comes to giving meds in the evening? Mom is fine in the morning (coming off of Seroquel in the p.m.), but the 5 pm meds—it's a battle every evening. Due to stroke, she has dysphagia and I mix her meds with chocolate pudding (which again she takes just fine in the a.m.) and 4 ml of Dilantin. Once I can get the 1 spoonful of pudding in her mouth, it’s usually ok (although on occasion she spits it out), but it's getting it into her mouth that’s the problem. Others suggest tieing her arms down, and she has hit the spoon out of my hands, she will move her head so much and bat at my hands that it is almost impossible to put in her mouth. What is so funny is that Mom probably only weighs 120, but her hands are lethal! I have had a nurse tell me to put a blanket over her arms and sometimes that helps, but on occasion I have bruised her arms by evidently holding her down too hard (and I only weigh 105!). I know elderly skin is tender and I want to be as careful and kind as possible. I do give her Antivan occasionally and perhaps that's the best bet prior to giving her the pudding. Any other suggestions? Debbie from CA |
| A: |
Taking medications in pudding, applesauce or yogurt does help in patients with swallowing problems. Most medications can also be safely crushed and place in food or drink if they are not coated or not special extended release formulations. It would help to know when she is refusing to let you feed her the pudding with the medication—whether it is the sight of the medication or just the food or that at the moment she is not interested in eating and wants to be left alone. If it is the sight of the medication, crushing the medication to hide it in the food may be helpful. If she is just not interested in eating at that time, try changing the timing of the medication administration to when she is hungry. Also try to front-load her medications all in the morning if possible—you need to talk to her physician about any medication timing changes—when she is more in the mood to take her medications. Also check with her doctor to see if any more of her medications can be switched to liquid formulation as sometimes they will accept something to drink more than something to eat. It sounds like the use of Seroquel at night is helpful for her behaviors. You may talk to her doctor to see if an additional dose one hour before she normally develops her "attitude" in the afternoon may be advised. Ativan typically is to be avoided in most dementia patients because if given too often it will cause confusion and sleepiness and is addictive with withdrawal symptoms. Antipsychotics, like Seroquel, may be a better choice to help with certain unwanted behaviors. It is far better to avoid physical restraining if at all possible for many reasons (i.e. safety, psychological). I have written extensively on behavior management in dementia in my book, Long-Term Management of Dementia (Informa Healthcare Publishers). Best of luck to you and your mother. |
| Back To Top |
| Q: |
How often should I send my parents above to senior center for activities? Do you have any specific activities I should be looking for? Karen from FL |
| A: |
If they like to do the activities or like the socialization, then as often as they can afford it or are able to. Encourage any of the activities that they enjoy (it doesn't matter what the activity is); otherwise they will not continue to do them. Even if they do not participate, they will get good brain stimulation just watching others. |
| Back To Top |
| Q: |
I have moved my father to an assisted living facility near to me, after his wife made it clear she could not live with him anymore. He is confused about not living with her any longer, and I have patiently explained the situation every day when we talk. Is there anything I can do to help him understand he is living here now? His wife has problems with health and depression. She will not tell him the truth about his having to stay here, which makes it more difficult for me to help him understand. Your advice is very welcome. Marilyn from GA |
| A: |
It appears your father does not recall your conversations due to memory issues. He also seems to have poor insight. I assume he needs an assisted living facility as he is having trouble with performing day-to-day activities. It sounds like he is concerned and anxious about when he will return "home." Most likely he will continue with these concerns. Sometimes it helps to not tell patients with dementia or Alzheimer's disease that something is permanent (as indeed it usually is not). I would say that "temporarily he is staying in this new place." Perhaps you can mention that temporarily he is there since his wife has been ill (health problems and depression). Sometimes making a permanent note and placing it in a place where he can see it will remind him that he is at the new place for now as his wife has had health problems. Generally over time, as people get more accustomed to the new place, they will ask less and less. They will usually have less anxiety about being away from their spouse. If the anxiety does not get better, sometimes an antidepressant (such as sertraline or citalopram) will help. |
| Back To Top |
| Q: |
My close relative is 72 and has advancing dementia. He just had a kidney stone and is dealing with recurring urinary tract infections. Are these physical ailments an indication of widening effects of the dementia? What sort of prognosis does he have? Wendy from DC |
| A: |
There is no relationship between most forms of dementia and kidney stones or urinary tract infections. However, if the kidney function is very poor, it does not filter out toxins in the blood and they can build up, leading to uremia and a dementia condition. These ailments are not an indication of widening effects of dementia. That is, dementia does not cause these types of conditions. Prognosis would be impossible for me to speculate with so little information regarding your relative's case. |
| Back To Top |
| Q: |
I am 67 and have always had a poor memory and my mum has had Alzheimer’s for last 6 years and is now 94—her sister also had it. I feel my memory is worsening and I forget words I want to use quite frequently and if someone asks me something I am aware that I am saying that I can't remember more and more often. I don't know if it is related, but recently have been feeling dizzy and find it hard to control my hands if trying to do something precise—they shake. Carole |
| A: |
Typically people that inherit Alzheimer's disease from their parents will get the disease at about the same decade in life as their parents did. However, since you have been worrying about this, it might be useful to talk to your primary care physician. They can test your thinking and memory to see if there are problems and also get a good baseline to compare to future years ahead. One simple screening test they can consider using is called SAGE (Self-Administered Georcognitive Examination). This self-administered test is best taken at your doctor's office so that they can score the test and interpret the results. Your primary care physician can download SAGE from the web (sagetest.osu.edu) and give it for you to take. |
| Back To Top |
| Q: |
My 86 year old grandmother has been diagnosed with a mild form of dementia. However, over the last few months she has been getting much much worse. She is constantly hiding her things (such as keys, jewelry, shoes) and when she can't find them she accuses various family members of stealing them but then finds the stuff the next day and still says someone took it. My aunt and mother have been the primary caregivers, but my grandmother has kicked my aunt out so now it's just my parents and I. It is getting consistently harder to help her because all she does is argue. She even had the locks changed and unplugged all her phones without telling anyone. I can see that this is taking a severe toll on my family. She is just impossible to reason with and only getting worse. Do you have any ideas of what we can do? Brianna from FL |
| A: |
Many patients with dementia develop behavioral problems, which are very treatable. These behaviors are a direct result of the damage in the brain from the dementia condition. In addition, infections like urinary tract infections, anticholinergic or other mind altering medications, and other medical conditions will exacerbate these behaviors or cause new behaviors. Treating any underlying infections, reducing specific medications or resolving medical issues may help reduce problematic behaviors. These behaviors are also treated by judicious use of psychotropic medications meant to adjust neurotransmitters (chemicals) in the brain that become imbalanced due to the dementia condition. In your grandmother's case, she is displaying a lot of suspiciousness, false beliefs and agitation. Trying to use logic or trying to re-orient to reality will usually not work very well. Medications are often necessary to help with these types of behaviors. Atypical antipsychotics may be advised for similar behaviors. Please talk to her dementia physician or primary care physician about the possible use of psychotropic medications to help with her significant behavioral problems. I have written extensively on behavior management in dementia in my book, Long-Term Management of Dementia (Informa Healthcare Publishers). Best of luck to you, your mother and your grandmother. |
| Back To Top |
| Q: |
I am 50 years old and diagnosed with Picks Disease/FTD (D=degeneration, not dementia). I cannot find a doctor that knows how to differentiate between Alzheimer's treatments/medications, etc. and FTD's. I need a doctor to treat my disease and I need to learn coping skills. Do you have any suggestions? Thank you.
Ferrell from OH |
| A: |
To find a doctor knowledgable in your condition, there are several places you can contact. First ask your primary care physician who they might recommend. Call the Alzheimer's Association in your area; they often know which doctors in your region are specialists in FTD and Alzheimer's. Call your regional medical center; they can refer you to their Neurology (or Psychiatry) Department who will know who in their department is |
| Back To Top |
| Q: |
Is there any solution to correct Alzheimer (my wife) so she could walk with cane or not? Wallace from HI |
| A: |
Alzheimer's disease often does not cause gait or balance problems until late in the disease. Balance or walking problems may occur earlier if apraxia (difficulty in sequencing movements to result in a smooth gait) exists. I would talk to her physician to ask if there may be other causes for her walking issues. |
| Back To Top |
| Q: |
My 78 year old mother has been on Aricept and Namenda for several years. Her memory loss seemed to have leveled off, but now it seems to be progressing again. Our biggest concern, however, is her depression and anxiety, which spikes when she gets up in the morning. She had been on Paxil for about 8 years, but was recently switched to Lexapro. She seemed to do better for a while, but the past 3 weeks she has been just awful—depressed, anxious, not willing to go out of the house, not able to perform normal daily home tasks. Three weeks ago is when she returned from Florida (where she and dad spend the winter); she is always worse after either coming home from Florida or upon arrival there, but this time her symptoms seem to be worse than ever and lasting longer. Is there a drug you would recommend for an Alzheimer’s patient with both depression and anxiety? Thank you. Tonia from OH |
| A: |
There are many medications that might be useful for depression and anxiety associated with Alzheimer's disease. However, do not confuse apathy (no interest in doing things) with depression (sad, crying, feeling low). Not wanting to go out of the house or not wanted to perform tasks may represent more apathy symptoms than depression. Apathy is not helped much by antidepressants. It can be helped by Aricept. If she does have apathy, you may wish to maximize her Aricept. If she is not taking 23 mg every morning, that would be a consideration by her physician. If she has significant depression or anxiety, one could increase her Lexapro (maximum dose 20 mg daily) or switch to another antidepressant (sertraline) to see if a better response can be obtained. I have written extensively on behavior management in dementia in my book, "Long-Term Management of Dementia" (Informa healthcare publishers). |
| Back To Top |
| Q: |
My mom is 89 and has some form of dementia. She is constantly losing her dentures and finally has really lost them. What would be a good solution? Are there semi permanent dentures? We look forward to your response. Liz from NH |
| A: |
Some individuals can have dental procedures that may allow for fixed bridges or the like. Discussion with her dentist is recommended regarding those options. Dentures are often misplaced or hidden by dementia patients. If in an institutional setting, engraving of dentures may help to identify whose dentures belong to whom. Also be sure to look for missing dentures in any device that holds water. We have found dentures in toilet tanks commonly. Also it may be most important to determine if the patient wants to wear the dentures. If she has no interest in the dentures and views them as some foreign object, than I would avoid using them at all. Individuals are still able to eat softer diets without needing teeth. If the family is concerned by appearance, than they may put the dentures in only when she has company. |
| Back To Top |
| Q: |
My 87 year old grandfather was just diagnosed with dementia last year, and he is currently on aricept. I am his primary care giver and have been since June of 2010. He is having an issue with distinguishing family members, their names and who they are to him. The worse part is my mother is his oldest daughter and he cannot remember her. He thinks my mother is his deceased sister or another person with the same name but not his daughter. I have told him numerous times that she is his daughter, but he doesn't understand, I am frustrated and don't know what to do so that he understands, and doesn't treat her like a stranger. Also he is very suspicious about what people say—he will take a piece from a conversation that others are having and turn it into something totally off of the wall and make up his own scenario. Do you have any suggestions on what I should do? Kim from AZ |
| A: |
Forgetting names of relatives and their relationship is common with Alzheimer's disease patients. Confusing daughters with sisters is common as they live more in the past where his daughter was much younger and his sister was not yet passed. He may not be able to learn that this person is really his daughter and not someone else. If their relationship is pleasant, then it may not be so important to always get him back to reality which he would have a hard time believing. If he is suspicious of this daughter and wants her to leave or makes it unpleasant for him or her to be together, then treatment with medications to reduce his suspiciousness may be warranted. This may also help other significant false beliefs or suspiciousness. If medications are considered, low dose of quetiapine, ziparsidone or others may be considered by his physician. |
| Back To Top |
| Q: |
My mom, 80, was diagnosed with Alzheimer's/dementia approximately 3-1/2 years ago, and was put on Aricept. A neurologist saw her and put her on Namenda, but she could not take it—it made her feel bad, she said. He tried again starting with a smaller dose; still she could not take it. During these past years, she has broken her hip, had many falls due to a bad knee, has to use a walker and is very stubborn. A neurologist had stated after her 3rd visit that he did not need to see her. She has an internist, who sees her for pain management. He upped her Prozac from 20 mg to 40 mg 3 weeks ago for her temperament. A week ago she woke from her nap in panic, thought she was somewhere else, did not recognize me and says she was kidnapped. We keep assuring her she was not and tried to comfort her, but nothing worked. I called the doctor as I was afraid she may have had a stoke. She still does not recognize me and also gets confused. Could this decline happen that suddenly? It is becoming very difficult to comfort her. She does not want to eat much, and is agitated during the day. Any suggestion you could offer would be greatly appreciated. Shirin from CA |
| A: |
Patients with Alzheimer's disease can develop many behavior symptoms including irritability, anxiousness, depression and false beliefs. These can be part of the disease. However, if there is some other active medical condition (urinary tract infection, pneumonia, drugs or drug interactions, significant heart, liver, or kidney disease, etc) going on, then there are often more sudden changers in behavior. The false belief of not recognizing family members as family members is called Capgras delusions. These false beliefs are best treated with atypical antipsychotic medications (like quetiapine and ziprasidone). If there are other concurrent medical issues, then those of course should also be treated. Increasing Prozac may possibly be contributing and since that was a recent medication change, I would consider lowering her dose back to 20 mg daily if agreeable by her doctor. |
| Back To Top |
| Q: |
My wife and I are currently the caregivers for her aging mother. The mother is in the final stages of Alzhemer's. She was talking less and less until she was not talking at all. I starting singing songs to her, and after a week or so she is starting to respond by singing along with me, a few words of the song. Is it possible that memory will increase with additional music therapy? Ron from SC |
| A: |
If she does have Alzheimer's disease in the late stages, then music therapy will not help improve memory. However, singing with her is a great form of brain stimulation and is a pleasurable activity, both of which probably improve her quality of life. Songs known for a long time are longterm memories and are retained much longer than memory for recent events or learning new songs. Words that accompany songs are stored in a different place in the brain than regular words and are a form of automatic speech. She probably does not understand the words she is singing, but they go along with the melody. |
| Back To Top |
| Q: |
My mother was diagnosed with Alzheimer's at age 61 and will be 66 this year. She in the final stage of the disease. We are told she has "adult failure to thrive" She eats a lot of food and has a great appetite, but she has consistently lost 2 pounds per month for 2 1/2 years (she is still at home with my father taking very good care of her). She started losing weight in the fall of 2008 at 121 pounds and now weighs 77 pounds. The doctor told us that even if we put in a feeding tube (which she doesn't need because she wants to eat, does eat and eats good foods), that it wouldn't matter because the body isn't metabolizing the food properly. My questions are: 1. Is there anything we can do? 2. Is there anything to make you believe that her weight loss will "level off" or will we lose her due to the weight loss? If that is the case, at what weight can a person die due to low BMI? (She is at about 13.3 BMI, as she is 5'4" tall). B'Ann from IL |
| A: |
There may not be much to do at this stage. She apparently has a good appetite, but is losing weight. Does she pace or move constantly so that she is metabolizing and exercising off all her calories? Sometimes a trial of mirtazapine can reduce over-restless activity and increase appetite. Other antidepressants may also help with restless activity. Might she have another process going on like cancer that can cause weight loss or does she have a lot of diarrhea that can reduce weight? Her weight loss is unlikely to level off if nothing is done since it has proven to steadily get worse over 3 years. I have had fair success stemming weight loss with the use of megestrol, giving at least 300 mg twice a day. It may be worth a try if she has no contraindications. Please check with her doctor. I do not know the answer to your last question but a dietitian may be one to ask. |
| Back To Top |
| Q: |
My father will be 60 tomorrow. Three months ago, he was diagnosed with Parkinson's and Dementia. He also has a bit of PTSD and depression. He already had high blood pressure and cholesterol. He has been prescribed medication for all of it. Problem is, he refuses to eat and take his meds. Two weeks ago, I placed him in a nursing home that specializes in dementia. He has been wandering, wanting to leave all the time, lays on the ground because he is "dizzy." He has gotten to the point we can't understand a word he says. It is horrible. I don't know what to do anymore. What can we do to get him to eat and take his medication? Using "yes and no," he has told us he wants to die when questioned. I hate this more than anything. I am so upset and don't know where to turn anymore. Can I get any suggestions on where to turn? Kelly from IL |
| A: |
There are a lot of questions I have regarding his clinical course of depression, dementia and Parkinson's disease. You seem to describe a rapid course. Is he more depressed or suicidal due to his nursing home placement? Has his difficulty talking been something new or gradually worsened? In regards to your question as to what can be done to get him to eat or take his medications, since he is in a nursing home with dementia expertise, they should be looking for ways to crush his medications, camouflage his medications into ice cream or pudding that he might eat or switch his medications to liquid formulations. Megestrol liquid 600 mg to 800 mg daily is helpful for many patients to improve appetite. Antidepressants may help if depression is the cause of his refusal to eat. Also consider increasing pleasurable activities or take him out of the facility for the afternoon if possible to be with friends or family. This case is very complicated and discussion with his doctor that has expertise in dementia is needed right away. |
| Back To Top |
| Q: |
My dad is 73 and is in the last stages of Parkinson’s. He lives at home with 3 caregivers, one of whom lives in the home with him; the other comes in 3 times a week to check vitals and help with bathing. He gets a UTI every 25 days like clockwork. He is on a low dose of bactrim, but it does not prevent the infections. He has been on the bactrim for 2 months. Is there anything he can take to prevent UTIs or is it just part of the disease—the kidneys not working like they used to? The hallucinations and confusion and falling increase dramatically when he has a UTI and I would love to prevent this added stress to his body. I would refer you to an urology specialist to look for other reasons for his recurrent UTIs and to suggest other choices for UTI prevention. It is unusual for males to get recurrent UTIs unless there are unique circumstances. Becky from CO |
| A: |
I would refer you to a urologist specialist to look for other reasons for his recurrent UTIs and to suggest other choices for UTI prevention. It is unusual for males to get recurrent UTIs unless there are unique circumstances. |
| Back To Top |
| Q: |
My 93 year old mother has moderate dementia. She has severe osteoarthritis heart problems. Newly diagnosed with pancreatic and a recurrence of colon cancer. I am not certain how much to share with her in the coming months. Her short term memory is poor and whatever I tell her will soon be forgotten. What do you suggest? Priscilla from CO |
| A: |
If she is interested in knowing about her medical condition, there is no reason not to tell her. She will probably forget what you said soon enough and it is less likely to cause her significant anxiousness or depression. If she is not interested in knowning than you do not have to force it on her. You can ask her if she wants any details regarding her updated medical condition. This news is probably more uspetting to you than it would be to her. |
| Back To Top |
| Q: |
My mom is taking Reminyl for Alzhiemer's and is now having difficulty swallowing her pills and is chewing them. She has not shown any side effects by chewing the time release pill. Is this dangerous or harmful? If so, could you please advise me on what steps to take. Peter |
| A: |
Extended release galantamine (also known as Reminyl) comes in capsules that are filled with tiny pellets that are time released. When there is difficulty swallowing, it is usually easiest to open the capsule and sprinkle the pellets over food to make it simpler to consume. The gelatin capsule that contains the pellets is just a container and can be discarded if the contents are opened and sprinkled on food. It is not harmful or dangerous to chew the capsules or the pellets. However if some of the chewed pellets are crushed, they may lose their time release effect. Therefore it is best to sprinkle the contents onto pudding, yogurt, applesauce or other soft food so the contents are more easily swallowed without being chewed. |
| Back To Top |
| Q: |
I take care of an 81 year client in the severe stage of Alzheimer's. We have tried many meds to help him sleep at night. He seems to fight them off or they have the reverse affect. We went from Zyprexa to Restoril to Haldol, all with the same effects. He is either up for days or sleeps for days. Do you have any suggestions? Andrea from OH |
| A: |
Trazodone may be a good place to start. It is very safe and does not usually give any hang over effect. It does not make Alzheimer's patient's more confused. I usually start out at 50 mg nightly, but the dose can be raised up to 100 mg or even 150 mg nightly if initially not effective. If that is not helpful, zolpidem 5 mg or Ramelteon 8 mg may be useful. I would try to stay away from benzodiazepines like Restoril or antipsychotics like Haldol or Zyprexa for sleep issues as they can have other unwanted side effects. |
| Back To Top |
| Q: |
I am working on a training tool for home care providers and would like to provide some resources that could be purchased for music therapy with Alzheimer’s patients. Are there any wonderful tapes/resources that you would recommend and could share with me? Ellen from OH |
| A: |
From the Parentgiving team: Based on the research that's been done, the simplest approach is using music from the person's past. Here's an excerpt from an article we ran: How to make music therapy work The full article can be found at: This website also lists many of the published research papers on this topic: |
| Back To Top |
| Q: |
My dad is 62 and has had Parkinson’s for 10 years. He has had small bouts of confusion in the past that have lasted for no more than a day or two and have usually been triggered by massive stress or a fall. I always know the reason. He fell about a month ago and broke a hip and I have him in rehab now. He was fine until 8 days ago. They have had to call me to calm him down, take meds and simply eat because he refuses. He is convinced that they are killing people there and have beaten him. I do not know what has triggered this. Are we possibly moving on to another stage? I was told about 1-1/2 years ago that he has dementia. His oldest brother died a month ago. Could that have possibly triggered it? I just can't get him to come back to me fully. Any help would be appreciated. Tonya from AR |
| A: |
Individuals with Parkinson's disease dementia (as well as most other dementing conditions) often develop confusional states with changes in health, stress or environment. Medications can also be a cause of increased confusion, false beliefs or hallucinations. Medications for Parkinson's disease are often the cause of false beliefs (people killing people and beating him up) and hallucinations. This occurs much more often if the Parkinson's disease patient has dementia. Often these spells of confusion and agitation are transient. The first thing to determine is if any new medications have been given to him or if he has been increased on any of his medications. Lowering his Parkinson's disease medications, if possible, may be very helpful. Keeping routines, familiar environments and familiar faces often help very much. At times, low doses of antipsychotic medications, like quetiapine, maybe useful for his false beliefs. It is also critical that he maintains good nutrition to help him recover more quickly. Supplementation of his meals with high calorie liquid supplements may be helpful in maintaining his weight. |
| Back To Top |
| Q: |
My dad is 80 years old and has been diagnosed with dementia. He appears fine and knows date and time. He also has no problem recognizing people. He, however, has been saying he has another house and frequently wants me and my brothers to take him there. He will even say we moved it with our vehicles. He will call us and tell us he is at his other house and want us to pick him up. This paranoia makes him very anxious and at times agitated. Other than this he seems mostly oriented. He is on Aricept and Trazodone. How can he have these thoughts and seem so oriented? Is there any medication you would recommend to help this? Delsie from MD |
| A: |
His false belief of not believing that his home is not his home is a form of Capgras type delusion. The belief that his house has been duplicated and/or relocated to another site is called reduplicative paramnesia. Both are forms of misidentification syndromes. These type of false beliefs(delusions) can be seen in Alzheimer's disease patients. Head injury involving the right side of the brain and the frontal lobes may also cause this condition. It is nearly impossible to re-orient the individual as these thoughts are fixed. If the thoughts do not bother the person or others, then you can just empathize with their concerns. It is not typically helpful to disagree or try to correct as this often leads to agitation. If the false beliefs are bothersome, treatments with atypical antipsychotic medications often help the best. Low doses may be used. It is always a good idea to make sure he is not on other medications that may be a cause of these symptoms as well. |
| Back To Top |
| Q: |
My Mother has dementia and has spent the last year in an assisted living center. The facility has now closed—poor quality food, marginal help, staff reports that were incorrect and fabricated. My Mother has lost over 15 pounds in three months. We have been recommended to a memory care facility. When is a person ready for memory care? Lonnie |
| A: |
For any dementia patient, the best care is given at places that specialize in that kind of care, like memory care facilities. Definitely consider moving your mother to such a place. |
| Back To Top |
| Q: |
The doctor put my mother on Plavix 75 MG about three months ago. She also was taking 325 mg coated asprin. After about five days she started getting bad nosebleeds. The doctor told her to cut the aspirin back to two to three times a week. Every time I give her aspirin, within 24-36 hours she gets nosebleeds. She now does not get aspirin. I had her meds refilled five days ago and instead of giving her Aricept 10mg because of insurance they gave her Donepezil HCL 10mg GRN. Now she is getting nose bleeds. Can the Donepezil be having anything to do with it? Steve from NC |
| A: |
Donepezil is the generic form for Aricept. They are the same medication. Since the dose is also the same, Donepezil should act the same as Aricept has done for her. I have not heard of any increased or different side effects when a person is given the generic form of Aricept. If she has tolerated Aricept without nosebleeds, my guess is that the Donepezil does not have anything to do with it. |
| Back To Top |
| Q: |
Please compare Lewy Body Syndrome progression with Alzheimer’s, including life expectancy. Also, my husband seems to get much better in all ways after taking antibiotics. Is there an explanation for this? How often can he take antibiotics? Ginny from GA |
| A: |
Individuals with Lewy Body Dementia often progress faster than those with Alzheimer's disease. Average life expectancy with Lewy Body Dementia varies with age, but is typically about 6 years. Some longer, some less. Most Alzheimer's disease patients live 8 to 12 years after diagnosis, also depending on their age of onset. Infections often cause confusion, and antibiotics that clear up infections may improve thinking. You would have to ask his doctor about the frequency of antibiotics. It depends on many factors that are patient-related. |
| Back To Top |
| Q: |
My dad has Parkinson's, dementia and essential tremor. He is currently has sundowner's syndrome. He keeps wanting to go home. What do I tell him when he is home? He gets irate and tells me I'm not his daughter and won't talk to me. He is currently on Exelon 9.5mg/24 hrs and Namenda 10mg twice a day. He also takes Tylenol w/codeine 1 at bedtime for arthritis. He also has a cough. He is on inderal for his essential tremor which he takes 3 times a day. He has just started to ask to go home and I don't know how to respond. I finally got him to go to bed when I put my mom to bed then later he was fine and he talked to me and knew who I was. Patti from OH |
| A: |
He has Capgras delusions. This is where he thinks that a familiar person (daughter) or place (home) is not their real daughter or home. First I would just try to empathize with his concern and tell him that it is getting late or cold or dark and that we can get him home the next day or find his daughter soon. If he does this excessively and it is causing him angst or he is attempting to wander away to find his home or daughter, it may be necessary to try pharmacotherapy with an antipsychotic medication. For Parkinson's disease, my first choice would be quetiapine at a low dose, maybe 25 mg, every evening prior to his behaviors. This could be titrated up to good effect if needed. Discuss with his physician if this is a good choice for him. |
| Back To Top |
| Q: |
My mom has had dementia for about 4 or 5 years now and we finally put her in assisted living in August of this year. My sister is her legal guardian and I am second. She is not adjusting to this at all, will not make friends, thinks we threw her to the wolves and stole all her money. She calls sometimes 8 to 12 times a day and cries. We think some of this is just her personality coming out, but don't know how to deal with it. My husband is also 74 and has dementia and my sister’s husband has 3 kinds of cancer plus emphysema and COPD. She had a stroke 10 years ago and is not coping with this well either. Should we just not go to see her for a while and not answer the phone when she calls? Sometimes she seems so normal in her ranting and raving and other times she just acts crazy. We are at a loss. Judy from MI |
| A: |
Behavioral disturbances are common with dementia and may include paranoia, suspiciousness, depression and irritability. Many times environmental changes or medications may help. At times it may be advisable to not contact her for a while as this may bring up the unpleasantness of her situation. However, if she is the one contacting you, then she could be more upset that no one responds to her. In that case, if she is in a high degree of angst over this, it may be best to consider behavioral medications. Often a selective serotonin reuptake inhibitor (SSRI) may help and they have very few side effects. If she shows a lot of false beliefs and suspiciousness, then an antipsychotic medication may be in order. Ask her physician what they may recommend. |
| Back To Top |
| Q: |
My 81 year old mom is experiencing memory loss and argues with us when we try to prompt her to remember. Should we be prompting her? What can we do. She is on Exelon. Laurie from IN |
| A: |
If prompting causes grief and argument than I would not prompt and instead just tell her the answer she seeks. If she has a lot of irritability then talk to her doctor about the use of an antidepressant such as citalopram or sertraline may be useful. They have very few side effects for most patients. If she has a diagnosis of Alzheimer's disease, check with her doctor to see if she is on the 9.5 mg/24 hour patch Exelon and Namenda to titrate up to 10 mg twice a day. |
| Back To Top |
| Q: |
My Mom is 76 years old and has had Alzheimer’s for around 5-6 years. Two and a half years ago she had her gallbladder removed, which made it worse. I have been taking care of her since January of this year. I took her to the doctor this past Friday and she wants to take her off of Aricept (10 mg once a day). She is also taking Namenda (10 mg twice a day). My mother is getting worse on memory since she has been here. The doctor said that the Aricept is not doing her any good at the stage she is in. Is that true? Should I take her off or get a second opinion? Steve from NC |
| A: |
Aricept and similar cholinesterase inhibitors usually will be useful for many years in those with Alzheimer's disease. It works very well in combination with Namenda. When the disease becomes vey severe, there is a point that these medications are not useful. That point varies a little bit from patient to patient and family to family. These medications will work less and less well as the disease progresses as there are fewer live nerve cells for them to work on. If your mother is no longer able to bathe, feed, dress or toilet herself and has little or no meaningful language abilities, then it may be time to stop the medications. If she still has meaningful function, then I would stay the course. |
| Back To Top |
| Q: |
My father, 85, has been chewing his food and spitting it out instead of swallowing. He won’t drink many liquids either. He has had a pacemaker for 2 years. Then one day he ended up with his heart racing and fell. He was not able to get up, and he was clammy. He had not been talking the past few days either. After he went to the hospital, they said he was very dehydrated. One day there, he was talking, eating most of the meals and feeling better. How can we teach him to swallow and drink again? Is this a common thing with dementia? Beth from IL |
| A: |
There may be many factors that are paying a part in his decreased fluid and food intake. Very late stage dementia patients may "forget" how to eat or swallow. They are unable to correctly sequence the normal swallowing reflex and food does not get moved to the back of their throat to swallow. I am not sure your father is at that late stage. Other causes could include medication side effects. Is he on anything new since this problem has gotten worse? If you chronically do not take in enough fluids, you will be dehydrated, which often leads to increased confusion and poor food intake. If he has a tendency to choke on liquids he may not want to drink, and use of a thickening agent (ask his pharmacist for a recommendation) may help prevent choking. Use of softer foods or even puree may help with food intake. Food that does not need much chewing may be swallowed easier. |
| Back To Top |
| Q: |
Where can I find good, reliable info on Parkinson's. My dad was diagnosed about 15 years ago and besides the leg and hand shaking, he had been doing pretty well. Over the last 5 years, he had to stop driving completely and needed a walker to assist him with walking and getting out of the chair. Lately, he has been falling quite a bit, mostly after sitting or laying for a long period of time and he sleeps for most of the day and needs to be woken to eat lunch and goes off into these “fogs” and doesn't respond when questioned. What can we expect next? Thank you. Kare from IL |
| A: |
It is impossible to comment on any specific individual situation as I do not have the background data to make any prediction. However, since there are changes in his behaviors and possibly cognition, I would get back to his neurologist to discuss prognosis. Sometimes medications, nighttime sleep issues or the disease itself can cause alertness issues. |
| Back To Top |
| Q: |
My dad is losing muscle control in his legs, not related to his knees. He has seen a neurologist and and orthaepedic doctor. All tests have been normal. Do you have a recommendation as to the type of Donna from NJ |
| A: |
I am not sure what is causing the symptoms. However, I would follow back up with his neurologist. If they are at a loss than perhaps a second opinion by another neurologist would be advised. |
| Back To Top |
| Q: |
My wife has Alzhimers Disease and is incontinent. When traveling by car, how does one handle rest stops? She gets confused in new surroundings and needs help. Most rest stops do not have an attendant available to help. Alexander from AL |
| A: |
If she has incontinence, does she wear adult diapers? If not that may be an option for longer trips by car. Then it would be a matter of finding a restroom that you could lock the door or a unisex bathroom to change her Depends as needed. Sometimes you might try a medication to help retain urine in the bladder a bit longer. All of those medications will counter the effect of medications like Aricept or Exelon or galantamine commonly used for Alzheimer's disease. However, it may be worth it to give this medication only if traveling long distances and not at other times. |
| Back To Top |
| Q: |
Q: My dad has Alzheimer’s. He’s 87 years old, still at home, my Mom is His sole caregiver. Lately he sits in the living room, staring at the family pictures on the wall for many hours and yells out. At times he will yell “Oh my god” or “Lord no, no.”--for hours every day. When my mom tries to comfort him, he gets very irate. My dad takes namenda and aricept. He is no longer lucid, When I am with him I can see in his eyes he is trying, but recently he did not know my name. He goes to the bathroom by himself, but having a lot of accidents lately. My mom cannot get him to shower, sometimes for months. Goes to bed about 10pm, but wakes my Mom at 1am, makes her help him dress, proceeds to go downstairs, wants something to eat and just stares. Angie from NJ |
| A: |
There are many behaviors that Alzheimer's disease patients may develop. Many can be helped with relatively safe medications or environmental modification. I would make sure he is taking his Aricept in the morning as that can cause sleep disturbance in some and may help activate more in the daytime. Sleep disturbance, not staying asleep, can be a big problem and can usually be aided by trazodone at night. Avoid Tylenol PM and like agents. Irritability during the day may be helped by anti-depressants and sertraline may be good for those that are more apathetic. It is wise to figure out if the cause of his irritability is due to any false beliefs as an antipsychotic treatment may work better in those cases. It is best to talk to his physician to see if any of these choices would work for him and his medical problems. Changes in the environment may also make life easier but it is hard to suggest what given the limited information I have. |
| Back To Top |
| Q: |
During recovery from an exam, my aunt, 84 with dementia became lucid, knowing people she hasn't for years, recognizing she wasn't in the hospital she knows/knew. About 4-6 hours later, her mental state returned--not even knowing she had the test earlier. Is this something we should expect when she has anesthesia? Mary Ellen from PA |
| A: |
Typically, most dementia patients have increased sedation and increased confusion after anesthesia. I'm glad to hear of your aunt's story but do not know what to make of it without knowing more about her medical history. |
| Back To Top |
| Q: |
My father is taking concerta, namenda, reminyl and trazidone. He yells out a lot but no one can figure out why! We were told it is from his Alzheimer's, but I think there are too many medicines and he may not need all of them. Debbie from MA |
| A: |
Since I do not have any information on why he is on these medications, it is difficult to say if they are related or not. Did the yelling start just after one of these medications was added? Alzheimer's disease patients can yell out at times and there may be many causes. First changing the environment to reduce overstimulation may be useful. In some it can be a compulsive tendency (teated with high doses of antidepressants) or due to pain or suspiciousness or wanting attention and all of these may be treated in different ways. Explore with his doctor possible causes and solutions. |
| Back To Top |
| Q: |
My boyfriend's mom has had dementia for the past 6 years. She thinks he's a friend from high school. Recently she's starting to "come onto him" (i.e. asking him for a kiss in a sexy way, etc.) He's totally freaked out and isn't sure how to handle this. His father refuses to get a caregiver. My boyfriend takes care of her 2 to 3 times a week, for hours at a time. Is there anything he can do to prevent it or is there something he can say? Please help, he's beside himself that his mother unknowingly does this. Kimberly from CA |
| A: |
Not recognizing family members is not uncommon in some dementia conditions. If you can reorient her to the fact that you are her son, it may help. Giving her a piece of paper that says your name and relationship to her may be helpful. If her advances are significant, medication therapy may be in order. Sometimes selective serotonin re-uptake inhibitors help reduce these type of symptoms. In severe cases, clomipramine may be helpful. I would further discuss with her doctor to come up with a management plan. |
| Back To Top |
| Q: |
My husband's father Poppy died this past year of Alzheimer's at the age of 85. Poppy's 3 brothers also had Alzheimer's. My husband is concerned that he will get this very sad disease. He is interested in being involved in a test situation. Do you have any suggestions? Paulette from CA |
| A: |
If you have a computer, there are a number of groups that list research opportunities and clinical trials for Alzheimer's disease. You could contact those research sites near where you live to see if you may qualify in any ongoing research: ADEAR (Alzheimer’s Disease Education and Referral Center): www.nia.nih.gov/alzheimers |
| Back To Top |
| Q: |
My husband had sundowners. He cannot stand or walk without falling right, left or backwards. Why has he lost his sense of balance? Jean from OK |
| A: |
It is difficult to say why your husband may have balance issues. Many patients with a Parkinsonian dementia syndrome may get postural instability in that they are unable to maintain their center of balance for very long and will topple one way or the other. Of course, there may be issues with balance from inner ear problems, neuropathy, small strokes, brain lesions, nutritional deficiencies, endocrine problems, infections, heart problems, and diabetes, among many other causes. |
| Back To Top |
| Q: |
Our staff assists residents with brushing their teeth and removing dentures. Some of the Alzheimer residents do not want to remove dentures. They see themselves as decades younger and feel the teeth should not come out. Do you have any ideas? Jo from Florida |
| A: |
The best method I know is to place your fingers inside their mouth on the side between their dentures and their cheek and pull them out. Be very careful not to get your fingers in the way of their teeth. In the short term, you can try brushing their dentures with them in their mouth. However, you will need to approach them again later and just take the dentures out for appropriate oral hygiene. |
| Back To Top |
| Q: |
My 85 year-old mother is in stage 5 Parkinson's Disease. I can find a wealth of information in books and online regarding the nature of the disease, diagnoses, treatment and coping techniques. What I'm failing to find is what to expect next. Elizabeth from MO |
| A: |
Stage 5 Parkinson's disease usually denotes the final stage where the individual is unable to assist with basic activities like dressing, bathing, feeding and toileting. They are at risk for infections like pneumonia and urinary track infections. They may develop difficulties eating as they may have trouble figuring out how to chew and swallow. Thick-It or other thickeners for thin liquids may help prevent gagging while drinking fluids and reduce the risk of getting the liquid into the lung causing aspiration pneumonia. Soft foods or puree foods are often required. Eventually they may be overwhelmed by an infection or just stop eating and drinking. |
| Back To Top |
| Q: |
My Aunt is in her seventies and we talk frequently on the phone. Our conversations last maybe around 45 minutes or so. I am finding that early on in the conversation she will share a story or something that she maybe had experienced recently. As time starts passing during our conversation, she will all of a sudden reiterate the same story/experience again. She states, "Oh, did I tell about.." Just curious if you would consider that this may be occurring due to fatigue or overstimulation? But it has happened several times. Should I be concerned? Linda from MD |
| A: |
Yes. This could indicate early memory loss. I would encourage her to see her primary care physician as many conditions causing memory loss are treatable. I would ask her permission to share your concerns and observations with the primary care doctor or go with her to her appointment. The primary care provider can do simple testing to see if there is any concern. |
| Back To Top |
| Q: |
My mom has Alzheimer's. She took several medicines that we feel made her able to function in her home alone until she was 88. She now has a live-in helper to take care of her, is unable to walk, and does not know her family. Her mother had "hardening of the arteries", and three of four brothers died with Alzheimer's. I am 61 and would like to start the medicine for it. My doctor says that we will talk about it next year after I retire. I am OK with this because I don't think it has started yet. How does one know when it is time to start? Nancy from VA |
| A: |
Normally, if Alzheimer's is going to run in the family it will typically start about the same decade of life as the previous generation. Right now, we do not have treatments to prevent the accumulations of the toxic proteins that build up in the brains of Alzheimer's disease patients. Hopefully we will have such treatments in the future. Currently we only have symptomatic treatments which mean that these treatments are known to help only if the person has symptoms of significant memory loss or thinking problems. If you do not have such problems yet, the effectiveness of these symptomatic treatments are unproven and in studies shown not to be helpful. I would suggest a cognitive screening test to help identify the start of any memory or thinking issues that you may have. This test could be repeated periodically over time, maybe every couple of years, to watch for any declines. |
| Back To Top |
| Q: |
How do you tell the difference between normal memory loss (not remembering certain events and people from the past) from Alzheimer's cognition problems? |
| A: |
As we get older, our brain also ages and most commonly we become slower in our thinking processes. We may become forgetful momentarily, but with a reminder we are back on track. The memory and thinking problems that arise with a condition like Alzheimer’s disease is distinctly different from that seen with normal aging. Alzheimer's disease causes trouble with encoding, or getting memories into storage. These individuals will ask the same question over and over as if they never asked it before. Reminders or clues do not help as much. The memory was never stored well to begin with. People with Alzheimer's also often have trouble with finding names of less frequently used objects. In normal aging vocabulary remains intact, although momentarily forgetting names of people is very common. Getting lost in a familiar area is not normal aging and could be a sign of Alzheimer's disease. Decreased insight is also common with Alzheimer's patients, as typically significant others will notice the memory and cognitive problems more than the individual. If you notice memory issues in yourself more than those who know you best, Alzheimer's disease is less likely. |
| Back To Top |
| Q: |
I think my mother is showing signs of Alzheimer's. Where to do I turn first? |
| A: |
Any time there is a change in a person's memory, thinking, functioning or behavior it is a sign of something affecting the brain. The first step is to get them into their primary care provider for an assessment. Many conditions affecting the brain are treatable and some are reversible. The treatments are most successful when they are started as early as possible. Do not put off an evaluation to see if things get worse. Health care providers will take a history, perform an examination and assess memory and thinking with pen and paper testing. If it is necessary lab testing and scans of the brain may be done. Having the correct diagnosis is critical in planning the next steps. After a diagnosis is made, appropriate treatments, provision for increased supervision needs and referral to any needed social agencies can be arranged. |
| Back To Top |
All content on Parentgiving.com, including articles, newsletters, and news, is for information only and not intended to diagnose, treat or advise on medical, health, legal, financial or other issues. See additional information. Use of this website is subject to our terms of use and privacy policy.