(written by his mother, Carolyn)
Why do we ride?
Because... our seven year old son was diagnosed with MS at the young age of five;
Because... “Kids Don’t Get MS”;
Because... treatments are not FDA approved for children and the long term affects are unknown;
Because... our brave little boy endures weekly injections and side effects to try and stay healthly;
Because... he is still just a child and just wants to be;
Because... he will never remember a time when MS wasn’t a part of his life;
Because... he deserves a chance at a normal future;
Because... MS needs better treatments and a cure.