Re: shydrager syndrome -- rhanrahan

[Guest guest]

Hi there,

Glad you were able to find this group. You've come to the right place.

Symptoms can vary greatly from person to person and there is no definite

pattern of progression. If you tell us her symptoms at present we can try

to guide you in how to best manage them.

These sites give a good general overview of MSA:

http://www.parkinson.org/atrophy.htm

http://www.emedicine.com/neuro/topic671.htm

Take care,

Pam

shydrager syndrome

> My wife was diagnosed with Parkinson's disease about 13 yrs. ago and was

> changed to Shy_Drager about 2 yrs. ago. I would appreciate any

> information as to what is to be expected at this stage. She is under the

> care of a local neurolgist at present. Since I am a hemipelvectomy

> amputee with blood pressure problems (under control) we have help here

> most of the time. Thanks!

>

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