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And what I originally meant was maybe he is taking medication like Cipro that can cause legg weakness.unfortunately doctors do not know side effects of medicines they prescribe which is ashame.
I was thinking the same as you, Scott, until I read the Alzheimer's Care Guide referenced on this site (and also on this screen for me). That's why I said PT worked for my father after his stroke but I hadn't considered that as one of the potential consequences of AZ.
Glad is right all the PT or whatever will not get someone walking again if they have dementia, they just don't know how, they have forgotten how to use thos muscles. how many totally paraysed veterans have you seen get to walk again unaided when their spinal cord has been severed. it ain't gonna happen Scott. It is being realistic not negative. If you understand what is happening you can make the best possible plans for your loved ones future. for example do you need to renovate the bathroom, build a ramp or buy a handicapped vehicle.
Scott, it is not negativity, it is the result of Alzheimer's disease and the brain slowly dying. As this process continues there is no way to predict what activity or function will go next. Alzheimer's is a wretched disease for each person a bit different while there are many aspects in common. There is not a cure for Alzheimer's disease nor is there a way to prevent it.
Everyone here just seems like they give up and so negative.There is never a positive side when negativity is looming.If you people are so sure on giving up put your parents in a nursing home otherwise stop being so negative and work little by little to get your parents up and walking again its not Dementia stopping the walking its atrophy from you not working the muscles a little every day.
Thanks everyone for your responses. My uncle was x-rayed hips to ankles and there is no physical reason he stopped walking. A visiting nurse will be coming to his home for physical therapy at least to try to preserve the range of motion in his legs. Despite the doctors reaction, my mother is satisified that she asked the question and now she is gradually coming to terms with the situation.
There appear to be two schools of thought on this issue - one is that it loss of mobility is inevitable to due progress of AZ and the other is to maintain as much of your physical body as possible for as long as possible. I think most people would agree that the more sedentary you become, the faster your downhill progress will be physically and mentally. After my father's stroke, he got PT and became physically stronger than he was before. After we finished the program, he did not maintain the exercise schedule and now his legs are bothering him again. This question reminded me that I need to do just as your mother did and ask the doctor for more PT. That therapist can get him to do things that I can't.
Sherry1anne - I was merely stating perhaps a reason why the person's legs no longer were working, and I was not diagnosing. My very best to your 103 yr. young mother and hope she has many more birthdays!
ferris, how can you give a diagnosis without ever having seen the patient? It may be the case, but I believe that where there is life, there is hope. My 103 yo mother is a prime example of that. I was told she had dementia and it was a UTI. She's back to showering and eating on her own. We are getting ready to go to PT now. She loves her "exercise classes".
The right chemical messages are not being received by his muscles due to the dementia. My husband's legs give out occasionally, and the neurologist just stated the disease is progressing. My best to both of you.
In my area, the local assisted living facilities habe seminars. You may want to check it out and see iff the public is welcome. These are very informative and u can ask questions. Check with local homecares too. Maybe even some Churches.
I'd agree that this is likely part of the dementia process, but I also agree with mar126 that every effort should be made to see if pain is the reason for inactivity rather than brain failure.
Pain is a complicated issue for elders with dementia since they often can't say what hurts and sometimes aren't even aware that pain is the issue. All we can do is our best, which in this case would mean to see if there seems to be a physical issue other than AD that is causing this change. If not, then the doctor is likely right in that this is part of the progression of the disease. Please keep us posted on how he is doing. Carol
Extragarlic, don't accept it without more evaluation. My husband started resisting sitting down about two months ago. He was fine walking but did not want to sit at the table to eat or sit on the toilet. Six months ago, the gerontologist said he was nearing the time for palliative care so I accepted the change. With warmer weather, I dressed him in shorts and noticed his knee was extremely swollen after walking. I feel really stupid that I didn't notice earlier as he probably injured it during a stumble. We are going to get it checked out and hopefully get physical therapy. I'm trying to keep him out of a nursing home as long as I can. I've found that my husband's family doctor is much more likely to prescribe physical therapy than the neurologist or gerontologist.
My husband in his mid-seventies has vascular dementia and is slowly losing his mobility. I hadn't realized so completely that this is part of the process, so to speak. We do attend a fitness center for the elderly and work with a personal trainer to keep us functioning as much as we can. Sometimes I feel guilty because my favorite "chant" is Move! Our doctor even said that if he wasn't doing the fitness he would be in a wheelchair. I surely am getting a lot out of this site!
Nick, has your mother read any of the materials on this website or elsewhere about Alzheimers ? If she hasn't someone needs to explain ( or perhaps re-explain) the progressive nature of the disease. One of the hardest things to let go of ( and one of the most important things to let go of) is the "fix-it" mentality that many of us bring to this table. Your mom needs to better understand how this is going to play out so that realistic plans can be made.
I would not think that he would be able to walk again not using the muscles will cause the muscles to become weaker. Pehaps that is where the thought of PT came in, use the muscles, everthing will get better. Unfortunately losing the ability to walk is part of the progression of dementia as is the ability to swallow, talk, breathe and the list goes on. If he is still eating at this point I would think that will be the next function to be lost.
Where is he living? If he is at home it may be time to find a skilled nursing facility. This sort of care is too difficult for most to handle in the home.
My MIL had vascular dementia and we were told once a patient stopped walking death usually followed within six months so it seems to be an expected part of the progression.
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.
I'd agree that this is likely part of the dementia process, but I also agree with mar126 that every effort should be made to see if pain is the reason for inactivity rather than brain failure.
Pain is a complicated issue for elders with dementia since they often can't say what hurts and sometimes aren't even aware that pain is the issue. All we can do is our best, which in this case would mean to see if there seems to be a physical issue other than AD that is causing this change. If not, then the doctor is likely right in that this is part of the progression of the disease. Please keep us posted on how he is doing.
Carol
Where is he living? If he is at home it may be time to find a skilled nursing facility. This sort of care is too difficult for most to handle in the home.