Tysabri 2.1 One week after #2 - I need a Hug - a big one :(

[@VernBeachy]

Yes, Sarah, it IS hard and the companionship of Chiro (in my case, Doug the Pug) is priceless. I found myself shaking my head in agreement with the litany of side effects and symptoms you talked about. It DOES get better and there is a light at the end of the tunnel, although it may be hard to see right now. A BIG HUG from a fellow MS'er in Iowa.

[@cliff501]

i was diagnosed in 1994, a lifetime ago. you will make out ok. no doctor cares more about you than you do. you know your body and what feels right to you. listen to your body. it is a crazy disease that is different for everybody. we are all pulling for you.

[@cliff501]

hang in there. its a long race. how can your doctors prescribe a treatment without your input? that's no good. you need to be the one deciding. put your foot down. good luck. i am pulling for you.

[@OlgaMesh]

I have a thin veins too, which hard to see and head to reach. Try oral session of steroids; some viewed as less effective but there is no pain, no need to go to the hospital,