pennyd

I have been diagnosed with M.S. since 1987, yet my first attack was in 1984. Started with benign m.s., then relapse/remitting, and now secondary progressive. Since I was selected for the lottery when Betaseron was released my progression has been very slow. I come from a family with 5 people who were diagnosed with this disease, yet only me and my Mom are the only ones alive. The other three include an aunt (her mom's sister) and my mom's brother and sister. I am the first one from the third generation. Originally I was inquiring for my Mom, but after speaking with someone from StemGenex I became intrigued. My only concern is paying the large sum for the treatment.

don't have time, except for traveling when I can