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Hi all,

Is there any research that shows that people with one

form of MSA live longer than those with another

(generally speaking, of course)? Most of my father's

symptoms were of the " SND variety " and he lived just

over a year after his dx, considerably less than the

3-7 years I've read is typical. I realize that he had

MSA for several years before his dx, but even looking

back, his symptoms were present for just 3-4 years

before he was dx. It seems to me that, when compared

to many on this list whose symptoms are predominantly

" non-SND " (for lack of a better term), his

progression/decline was much more rapid and the

disease seemed quite a bit more insidious...(Not to

minimize what anyone else is going through. It's

terrible regardless of where you are in the disease).

Just wondering...

__________________________________________________

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Guest guest

Hi .

I have read some research studies that tried to compare

progression rates of the various flavours of MSA. I don't

recall the exact details but I can try to dig it up for you

sometime.

You can also try hunting for it yourself. Go to:

http://www.ncbi.nlm.nih.gov/entrez

Try typing in " multiple system atrophy progression "

as your search term.

Hugs,

Pam

Prognosis

Hi all,

Is there any research that shows that people with one

form of MSA live longer than those with another

(generally speaking, of course)? Most of my father's

symptoms were of the " SND variety " and he lived just

over a year after his dx, considerably less than the

3-7 years I've read is typical. I realize that he had

MSA for several years before his dx, but even looking

back, his symptoms were present for just 3-4 years

before he was dx. It seems to me that, when compared

to many on this list whose symptoms are predominantly

" non-SND " (for lack of a better term), his

progression/decline was much more rapid and the

disease seemed quite a bit more insidious...(Not to

minimize what anyone else is going through. It's

terrible regardless of where you are in the disease).

Just wondering...

__________________________________________________

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Guest guest

Hi .

I have read some research studies that tried to compare

progression rates of the various flavours of MSA. I don't

recall the exact details but I can try to dig it up for you

sometime.

You can also try hunting for it yourself. Go to:

http://www.ncbi.nlm.nih.gov/entrez

Try typing in " multiple system atrophy progression "

as your search term.

Hugs,

Pam

Prognosis

Hi all,

Is there any research that shows that people with one

form of MSA live longer than those with another

(generally speaking, of course)? Most of my father's

symptoms were of the " SND variety " and he lived just

over a year after his dx, considerably less than the

3-7 years I've read is typical. I realize that he had

MSA for several years before his dx, but even looking

back, his symptoms were present for just 3-4 years

before he was dx. It seems to me that, when compared

to many on this list whose symptoms are predominantly

" non-SND " (for lack of a better term), his

progression/decline was much more rapid and the

disease seemed quite a bit more insidious...(Not to

minimize what anyone else is going through. It's

terrible regardless of where you are in the disease).

Just wondering...

__________________________________________________

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Share on other sites

Guest guest

Hi .

I have read some research studies that tried to compare

progression rates of the various flavours of MSA. I don't

recall the exact details but I can try to dig it up for you

sometime.

You can also try hunting for it yourself. Go to:

http://www.ncbi.nlm.nih.gov/entrez

Try typing in " multiple system atrophy progression "

as your search term.

Hugs,

Pam

Prognosis

Hi all,

Is there any research that shows that people with one

form of MSA live longer than those with another

(generally speaking, of course)? Most of my father's

symptoms were of the " SND variety " and he lived just

over a year after his dx, considerably less than the

3-7 years I've read is typical. I realize that he had

MSA for several years before his dx, but even looking

back, his symptoms were present for just 3-4 years

before he was dx. It seems to me that, when compared

to many on this list whose symptoms are predominantly

" non-SND " (for lack of a better term), his

progression/decline was much more rapid and the

disease seemed quite a bit more insidious...(Not to

minimize what anyone else is going through. It's

terrible regardless of where you are in the disease).

Just wondering...

__________________________________________________

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Guest guest

--My mother JOyce (71, died 11/5/00) had the SND form, too, and lived

less than 2 years after her MSA diagnosis and less than 4 after her PD

diagnosis. I thought I had read somewhere that one form of MSA had a better

prognosis than the others. It's hard to believe you have had MSA and be

luckier than others with it. Debbie

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--My mother JOyce (71, died 11/5/00) had the SND form, too, and lived

less than 2 years after her MSA diagnosis and less than 4 after her PD

diagnosis. I thought I had read somewhere that one form of MSA had a better

prognosis than the others. It's hard to believe you have had MSA and be

luckier than others with it. Debbie

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Guest guest

--My mother JOyce (71, died 11/5/00) had the SND form, too, and lived

less than 2 years after her MSA diagnosis and less than 4 after her PD

diagnosis. I thought I had read somewhere that one form of MSA had a better

prognosis than the others. It's hard to believe you have had MSA and be

luckier than others with it. Debbie

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