This Is MS Multiple Sclerosis Community: Knowledge & Support

did today. how did you people sleep? they were taking my vitals every fifteen minutes. holy cow. my bones hurt. i'm tired. i'm going to bed. little nauseous, but mostly i have a headache. i just want the dog to go outside and do her thing so i can go to sleep.

so.... i got the campath arm of this thing. which is good, because i hate rebiff with a passion. now i'm kinda scared. i start tomorrow. my husband is working nights this week, and my sister is going to watch my kids(she lives nextdoor). they said i'd probably be able to drive myself. but i have to ask people that have already done this: were you nauseous? do i need to take some sort of ...

So I needed to switch tx after 4 years on copaxone. Doc recommended I choose between tysabri and Campath, as he is involved in the study. It was a really hard decision, especially since I was dead set against taking an interferon. The research nurse said that if I was randomized onto the rebif I could drop out. So I went thru the entire process, then on randomization day - hooray!!!
I got my five ...

http://www.forbes.com/feeds/ap/2009/06/ ... 91891.html

David is a Campath recipient who set up a website to share his experience. Partly as a result of his diary I went for the Campath option. David has updated his diary - May 2009 update. Thankfully, he has nothing to report and seems to be doing very well.

http://www.davidscampathstory.org/experience.html

hello all. i'm sara, 33... i will find out on the 15 of june if i get the campath or the rebiff. i'm actually hoping for the camp. as i've been on rebiff before with nothing good of it... hence why i stopped taking it. actually i've been on everything that you can inject into yourself... but keep having these crazy relapses. so my doc suggested this trial. why not? ...

WOW, what an interesting but very stressful journey to finally get to this point! The short version of the story is that I was a Tovaxin lab rat who received Tovaxin during the 1 year of the Phase IIb trial and then 4 out of 5 vaccinations in the extension phase before Opexa ran out of money and shut the study down. At that point it seemed like the obvious thing to do was enter ...

Any updates/reports from the Campath recipients?

I am unsure what to do about the Phase 3 Alemtuzumab study. I have been approved for it, but have not yet done the Screening and Baseline visits. They made some changes to it on 3/5/09, and now I would have a 1 - 3 chance of being radomized into the Rebif group, when before it was 1 - 5.

I am almost 50 years old. Yikes, I've never seen that in print, if ...

I went into the Neuro's office today, 'cause I just can't get my legs to work right. They're super duper spastic and the dropped foot is way worse. The team was supportive, they gave me some different drugs to try for the spasticity and some oral steroids to see that if that didn't help me feel better and get walking better sooner. Tomorrow I have to go back to work so I was nervous about ...