We also found PT, OT, speech therapy and a few Parkinson's exercise classes (dance, yoga, etc) helpful in the initial phase - something to do and until he bad fall in April, it had made a real difference for both is us! We have spoken to a few social workers and hospice nurses to make sure I am clear on my moms wishes for the end and to talk about her sadness and fears.
Things to do: We also found PT, OT, speech... - PSP Association
Things to do
Written by
NHGrace
To view profiles and participate in discussions please or .
Read more about...
2 Replies
•
Good luck to the two of you your mom is going to need you and your going to need her.
Best wishes and stay strong.
My mum was diagnosed approx 7 years ago ( originally as Parkinson). She started walking and would walk almost 5 km or more at a brisk pace daily. strangely she never fell while doing this activity. all falls occured while moving slowly inside the house. Anyway I feel that the walking gave her a lease of life and delayed the onset.
regards
Som.
Not what you're looking for?
You may also like...
Do I need to see things from another perspective?
My mom has PSP, and my dad was unable to cope with caring for her, and moved her into a care home...
Don't know what to do
My mum has gone from eating last Sunday in a restaurant to having a temporary NG tube and having a...
The little things ...
We just spent a few days up at the lake house with our friend Linda. Mom loves riding around the...
Things to do for PSP – sing a PSP country song (badly!)
A bit of fun for a good cause. You have to watch the video - sorry!...
Things I like, things that help and things which don't
Someone asked what my days are like, what do I do, what helps and what not.
So I thought I would...