This Is MS Multiple Sclerosis Knowledge & Support Community

I am really glad it works for you Red Sonja, that is great. I did not want to scare anyone with what I wrote, which is why I made it quite clear Copaxone is worth trying. Honestly, if I could take it again, I would, but, I can't. But, I do believe that by not stating my experiences on it is not help...

Thanks for the kind words. I hope that things work out for you with this drug. I had to have a re test done of the bloods too, because they thought it may have been a dodgy test or some kind of mistake, but, it wasn't. I am finding all this really hard to deal with because I have been sicker this ye...

I am glad the trial is going alright for you. Are you sure you are not on the placebo? I was taken off the trial because when I had my 3rd monthly routine blood test, my liver function was 1000 (normal is 50 or below). I have been very ill from this and I had to stop the trial immediately. I am havi...

I am on the phase II trial for oral drug Firategrast. http://www.controlled-trials.com/mrct/t ... /A4M105038

Cathie

Hello, I am new too. I accidentally came across this site while searching for, um, I can no longer remember what, except it was MS related. lol lol My name is Cathie, I live in Australia. I am 44 years old, divorced mum of three (gonna be a grandma in December)....... I was diagnosed with RR MS in N...

I just joined this forum and I read curiosers' post. I am so sorry you went through that, but, I am much relieved to read that what you went through is almost identical to what I went through with Copaxone. I was on it for nearly 5 years. On average, I was having the post injection reactions maybe o...

I just found your post. I know it has been a few months but I hope you or anyone else is on Firategrast trial is reading this. I have been on the trial for nearly 2 months. 4 tablets, twice a day. I had a bad attack of Optic Neuritis less than 2 weeks after I started the trial. I had IV steroids and...