I was diagnosed in 2004 with remitting relapsing MS, in the last year it progressed to secondary progressive MS and I was put on Rebif. I am coping well with my condition and medication. My right hand is numb and I walk with a stick but when I read some of the experiences of people here and from other sources I feel like a charlatan. Like I don’t have “bad” MS so shouldn’t be part of the community.
This is probably making me sound like a weirdo but it has bugged me for a while and I had to say something.
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