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This is my first time here in a chat room on the

computer and it will be my first time since I have

been diagnosed a year ago to know or talk to anyone

with my same disease. I am so very excited on the one

hand because I have felt so alone with this disease.

On the other hand I feel so scared because it might be

way to much reality for me. Anyways I have had

symptoms for about seven years they were subtle and I

didn't pay much attention to them until two years ago

when my left side quit working. Then it took a year to

get diagnosed with MSA. My MSA seems to have

progressed very fast in the last two years and my

doctor is so depressing because he gives me no hope to

work with. I've dealt with a lot of losses in the last

two years. I've went from a totally healthy 45 year

old women to an old 95 year old woman in just two

years. Actually some 95 year old women probably get

around better than myself. The hardest thing for me is

that I have to depend on others for so much. I feel

like a burden sometimes to my husband and kids. I am

very grateful for all the wonderful friends and the

wonderful family I have. I could not handle this

horrible cruel mean disease with out there love and

support. I hope I'm not being way to dramatic but it

does seem cruel at times to me and cruel to my family

and friends who have to live with it. greercj

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