Hi Everyone, I am starting Tysabri in a couple of weeks and am curious if there are any "tips" or info that the doctors didn't share or things that might be helpful. I have had MS for almost 13 years and have been on Avonex and most recently Copaxone.
Thank you both for the advice. I have had infusions for Steroids before due to a couple of severe flare ups so I know that them finding a vein wont be a problem;) My doctor did warn me about the questions and explained why. However he did not say anything about the pain reliever or water. I will definitely do both of those! I have already been tested for the JC virus and tested negative and that is why my doctor thought this would be a good option. I pray that it will go well.
I will let you all know how it goes. Thanks again!