Dear Diane--glad you have found this list---you will surely get
some helpful responses. You didn't say how long your mum has been
diagnosed, or if she sees a neurologist (preferably a movement disorder
specialist or one with lots of experience with PD). Your description of
her "twitchy" legs sounds like dyskinesia, an effect of the meds. Perhaps
someone can refer you to the British PD group/list whatever. Meanwhile,
you may be interested in the sublist we have here for Caregivers of PWPs.
Its a place where CGs can support and inform each other, and you can join by
sending a request to:
[log in to unmask]
in body of message just put:
SUBscribe CARE (your first and last names)
you will be notified of your "connection" and will get furthe info and
instructions. A wonderful, caring group of some 250 CGs from all over
the world awaits you!
Camilla Flintermann, CG for Peter, 78/7, Oxford,Ohio
[log in to unmask]
* * * * * * * * * * * * * *
"Ask me about the CARE list for PD caregivers!"
* * * * * * * * * * * * * *
