Hello!
This is the first time I use this forum. I'm really glad to have found this site!
I come from France.
To sum up I had avonex but I had some cognitive problems and I stopped it. Then it was copaxone. I had no luck I was among the 0,01% people to have voltage drop.
I started to participate in the opera II (I'm not sure) Rebif and Ocrelizumab trial 2 years and a half ago.
The first three months it was ok no side effects. Then, when the docs decided to increase the rebif I started to have the flu symptoma and I knew I got rebif.
Yesterday I began the extended open part and I had my first infusion of ocrelizumab. I felt headeaches and dizzyness.
Today I'm feeling exhausted and a bit of headeache. I hope it will get better in a few days.
I'm the last person in the world to take part in the extension so sorry you will have 2 years to wait to finish the trials