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Hi everyone,

My name is Sandy and I am from Salem, Oregon.

5 years ago they told me I had M.S. I under went useing Avonex and

then Rebif, I also had chemotherapy for the treatment of M.S. My

neurologist was stumped at why I continued to get worse and sent me

to a specialist where they found out all my tests were unconclusive

of M.S and said that I have P.L.S. My right side is effected, arm,leg

ect. If possible I would like to know how other people are effected

by this disease, and be able to learn more and chat.

Thank you, Sandy

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