Even after just 3 days with no Copaxone, I have noticed a rash that I have had on my chest for months is about half what it was. I woke last night, and realized I was warm, but not hot, and NOT sweating! yahoo! I am not supposed to be judging any of these things till at least day 5, but I have noticed some comforts already. it makes me wonder if I will even have the courage to go back. of course, I am putting the cart before the horse, and worrying well before its time to worry. I am going to try to just sit back and enjoy the pokeless fortnight.

Sometimes the side effects are worse than the dang disease! How am I supposed to keep taking stuff that makes me feel bad? The MD says that ALL MS meds have side effects, and its a trade off to have more disability free time now, because we take the DMDs vs skipping the side effects, and landing into the SPMS or you need a wheel chair zone. its all so risky. Darned if you do, and darned if you dont.

Thanks for all the pep talks.