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She cries out when sitting with her legs up or down.
She struggles when she moves with her walker to get to her stair lift and on bad days even when she uses the commode only a couple of steps away.
The district nurses, who dress her legs daily, say they aren't that bad compared to some they see and some are sceptical about the amount of crying out she does when they change the bandages.
Some days she is gasping saying, "I can't stand it." and "It's sheer agony." literally continuously. She grimaces and clenched her hands. It's awful to watch and not to be able to help her.
Other times she is less hysterical but still constantly saying her legs are so sore and she can't stand it.
The only peace she gets is when she's asleep.
She is on a huge amount of painkillers which actually seem to make no difference:
10mc butrans morphine patch weekly
5 ml oral morphine 4 or more times a day
600mg Gabapentin 4 times a day
2 paracetamol 4 times a day.
Last week the doctor tried 1/2 Lorazepam twice a day but she fell over twice so we stopped that.
She has now increased to a 20mc morphine patch but even this has't eased her pain and distress.
Has anyone else experienced an Alzheimer's sufferer feeling such extreme pain and have you found a solution?
Thanks, Margaret Neil
Are you still out there?
I learned from that experience though, the Dr's had really no idea how to communicate with someone suffering with dementia.
I explained the Dementia issue and they still looked at her as if I were out of my mind because I was speaking/translating for her.
This is when I learned that talking to a general physical illness Dr about mental illness, is like expecting your plumber to give you answers about your hair care issues.
the nerves.
Kind of off the path but relevant here...I heard of a woman that had back pain walked hunch over and for years, prior to Alzheimer's. One day her son went to visit her, he did not recognize her because she was walking as straight as she was before the back pain. Her Alzheimer's seemed to have affected the brain in a way that the pain signals we not working as normal and signal wasn't happening as it should.
General speaking... I think we tend to forget that our brains have functions and do things that we take for granted. Our brains alert us of pain, release hormones to protect us from pain etc, when the brain is not functioning as normal due to dementia,of any type, these signals are possibly malfunctioning.
I guess what I am trying to say is, if all other tests are ruling out a cause for a change of the normal, such as a chronic complaint of pain, or change in behavior or personality, etc. occurs it could be a mental condition that is the cause.
Sorry LeaAnn, I didn't intend for my post to take the focus away from your question but needed to respond to a misunderstanding.
Regarding her wanting to see a doctor -- is her memory such that you can say, "yes, we will go this afternoon" and have her feel comforted? That wouldn't work with my husband's level of memory, but I wouldn't hesitate to use that approach if it would work.