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Many do as the disease progresses. Some of that is from eating problems, but sometimes the disease itself causing a kind of wasting. Check with the doctor if the weight loss is extreme. Take care, Carol
Normal is pretty much a thing of the past for people with dementia. It is common though, for them to lose weight. The meds can contribute, but there are other factors. They forget to eat, or forget to finish their meals. Their sense of smell diminishes a lot, so food doesn't have any smell or taste. They slowly lose their ability to manipulate eating utensils with predictable results. They also start to lose their skill with chewing too. And as they lose weight their dentures no longer fit well, making it even more difficlut. And many get depressed and merely lose interest in eating. Mr father's doctor ordered Magase fo Dad , and it worked great. For awhile. Because eventually Dad lost his ability to swallow. And it doesn't matter how much he wants to eat , it he can't swallow the food.
To continue with my previous post: We addressed each problem as it presented itself. We fixed more of his favoite foods. We stopped worrying about nutrition and let him eat all the donuts he wanted. (without smell the only tastes they sense are sweet and salty) , cut up his foods for him, and helped him eat , more and more, until he was totally being fed. We changed to softer foods, and had the dentist come in to adjust his dentures. Eventually switched to pureed foods....In the end......well you just get to the end. It's not a battle you can win in the long run.
Normal is pretty much a thing of the past for people with dementia. It is common though, for them to lose weight. The meds can contribute, but there are other factors. They forget to eat, or forget to finish their meals. Their sense of smell diminishes a lot, so food doesn't have any smell or taste. They slowly lose their ability to manipulate eating utensils with predictable results. They also start to lose their skill with chewing too. And as they lose weight their dentures no longer fit well, making it even more difficlut. And many get depressed and merely lose interest in eating. Mr father's doctor ordered Magase fo Dad , and it worked great. For awhile. Because eventually Dad lost his ability to swallow. And it doesn't matter how much he wants to eat , it he can't swallow the food.
My husband has both Alzheimer's and vascular dementia though is doing quite well in this moment. He has a diminished appetite and can be a bit defensive when I try to encourage him to eat more and better. I have taken to serving him rather than have him do it...since I noticed he tends to put much less on his plate than I would for him. This indirect approach seems to work better. I am trying hard to be sure he gets enough protein and veggies in addition to ice cream which he's seems to crave. The most challenging thing for me is to be indirect...not my current strength...yet I know it's important not to confront him. That doesn't support our relationship or actually solve the problem. So much learning...he's definitely my teacher?..in a good way.
My husband has lost about 40 lbs. since the ALZ started. He has had every test and nothing is physically wrong. Doctor says it is due to the dementia. His diet consists mostly of donuts and soda. He hates water and will only drink a small amount to take a pill. Tried ensure and boost but he hates them and refuses to drink them.It has only been three years since this all started but he has just changed completly. He stopped taking the Namenda on his own, doctor said why argue it doesn't help that much anyway. This won't help you much but at least you will know that you are not alone. Good Luck and keep coming back as these people have some good advice and are very caring.
Mom was diagnosed with dementia while in a NH for rehab for a shoulder replacement in 7/2015. By 8/3/15 she was labeled with dementia. Since then, she's been hospitalized for dehydration and a UTI [Labor Day weekend]. On Friday [10/9/15] she was back on an IV for fluids. This time, they found a vein and it took about 3 hours to insert the needle and get the machine set up [kept beeping]. She's lost 16 lbs. She was supposed to have been put on the appetite stimulant pill back in 8/3/15 - but that was Nameda and Remeron. Now she;'s on yucky pureed foods that she can't even reach, and won't eat when spoon fed. i bring her Ensure, puddings, yogurt - anything i can think of [and add a bit of whey protein to each item - it's flavorless]. But today they called and want to take her off PT - she can't even get out of bed herself - can't even pull up her covers. Diarrhea has hit so hard, she cries in pain - but they tell her to go in her briefs. Sorry - i really feel the NH is VERY contributory to her present state. It took me 10 days just to get the nursing staff and doc to look better at mom and see what was going on - i could see her lips peeling and she stopped talking. A week prior, she was her normal self - she still teased people and had them laughing. Something is happening there and i don't know what to do. She tried to unbutton her blouse - with both hands {!!!! yay !!!]j but the aid slapped her hands away because "it was taking too long". Aren't aids and PT or nursing more coordinated than that? Oftentimes the aides "slam dunk" her back in bed right on her surgical shoulder. They had mom afraid to say anything - so i rearranged the furniture so that they could only get her in from the other side of the bed, where mom would 'land' on her right shoulder. She's VERY afraid of falling - and the rough treatment is definitely not helping. Can they really discharge her from the PT program when she cannot get out of bed? She is ambulatory --- with her weight loss, yes she's weak, but she eats only what i bring in. The food truly is awful. i even tried dressing the pureed yams up with whipped cream and told her to think of it as pumpkin pie. Oh my --- what can i do? The social worker truly is "worthless" or uninterested in helping "residents" entrusted to them. If she can get out of bed on her own, i am confident i can bring her home --- should i try to find another facility for Rehab -- if so, how do i go about it, FAST? Oh thank you .... everything is happening so very very fast! Blessings.... gotta go now, i just got a call that they want to discharge her -- and yet was on an IV all weekend, and just put on the megase for appetite.... thank you so very much....
It s funny. My mom is 94 and has at Alzheimer's for several years. She is pretty much sedentary. But boy does she have a great appetite. She has actually out on weight and we have to make sure she certainly eats but monitor what she eats, because of the gain. My husband, who also has alzhiemers ... Has a great apetitie but I notice that his tastes have changed. Things he used to love are now distasful to him. I suppose everyone is different.
The weight loss is part of the deterioration going on in his brain with dying cells. Try to keep him hydrated and fed as much as you possibly can, and even if he says he is not hungry, put food in front of him.
By proceeding, I agree that I understand the following disclosures:
I. How We Work in Washington.
Based on your preferences, we provide you with information about one or more of our contracted senior living providers ("Participating Communities") and provide your Senior Living Care Information to Participating Communities. The Participating Communities may contact you directly regarding their services.
APFM does not endorse or recommend any provider. It is your sole responsibility to select the appropriate care for yourself or your loved one. We work with both you and the Participating Communities in your search. We do not permit our Advisors to have an ownership interest in Participating Communities.
II. How We Are Paid.
We do not charge you any fee – we are paid by the Participating Communities. Some Participating Communities pay us a percentage of the first month's standard rate for the rent and care services you select. We invoice these fees after the senior moves in.
III. When We Tour.
APFM tours certain Participating Communities in Washington (typically more in metropolitan areas than in rural areas.) During the 12 month period prior to December 31, 2017, we toured 86.2% of Participating Communities with capacity for 20 or more residents.
IV. No Obligation or Commitment.
You have no obligation to use or to continue to use our services. Because you pay no fee to us, you will never need to ask for a refund.
V. Complaints.
Please contact our Family Feedback Line at (866) 584-7340 or ConsumerFeedback@aplaceformom.com to report any complaint. Consumers have many avenues to address a dispute with any referral service company, including the right to file a complaint with the Attorney General's office at: Consumer Protection Division, 800 5th Avenue, Ste. 2000, Seattle, 98104 or 800-551-4636.
VI. No Waiver of Your Rights.
APFM does not (and may not) require or even ask consumers seeking senior housing or care services in Washington State to sign waivers of liability for losses of personal property or injury or to sign waivers of any rights established under law.
I agree that:
A.
I authorize A Place For Mom ("APFM") to collect certain personal and contact detail information, as well as relevant health care information about me or from me about the senior family member or relative I am assisting ("Senior Living Care Information").
B.
APFM may provide information to me electronically. My electronic signature on agreements and documents has the same effect as if I signed them in ink.
C.
APFM may send all communications to me electronically via e-mail or by access to an APFM web site.
D.
If I want a paper copy, I can print a copy of the Disclosures or download the Disclosures for my records.
E.
This E-Sign Acknowledgement and Authorization applies to these Disclosures and all future Disclosures related to APFM's services, unless I revoke my authorization. You may revoke this authorization in writing at any time (except where we have already disclosed information before receiving your revocation.) This authorization will expire after one year.
F.
You consent to APFM's reaching out to you using a phone system than can auto-dial numbers (we miss rotary phones, too!), but this consent is not required to use our service.
Take care,
Carol
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