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possible MSA of my father

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Hi all!

its good to see that there is a group here at yahoo that allows

people to exchange their thoughts and experiences with MSA.

I´ve been looking up a lot about this disease lately because it seems

that my 58 year old father shows symptoms of it (slurred speech was

the first sign starting nearly 2 years ago, orthostatic hypotension

and some ataxia). The first docttor he went to 6 months ago said, its

just a low blood pressure problem; now another doc says its perhaps

MSA...

He has been in the hospital for a week so they could check out

things, but found nothing, they could just confirm the symptoms and

orthostatic hypotension. But as far as I can see, no matter what

diagnosis they'll come up with, it wont be good...

Since the low bloodpressue when standing really seems to be a problem

for him already , especially in the afternoon, he probably has to

give up his job very soon.

My mother and sisters are of course very nervous and afraid of what

lies ahead; MSA or ShyDrager seems to be a devastating desease in

many cases.

Since I´m the oldest sibling I feel somehow responsible for helping

them and dealing with the things that my father cannot deal anymore

(especially in the future), but I´m not sure how... I also dont know

if I should tell my family about the stuff I read on the internet

about MSA, I dont know if they can deal with that dark glipse in the

future...

thanks for reading, I just had to " talk " to someone :)

greetings from germany!

chris

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