Is this an approved cocktail by his neurologist? I know of no one who has RRMS take something like this. I just received my MSAA Motivator magazine and the drugs that you say he is taking I can not find. Maybe these drugs is what is causing his eyesight to diminish. Do you know what the side effects would be?

Endoxan is a cancer drug

Deltacortene is considered to be Predisone

Ciclosporin (Neoral / Sandimmun) is a powerful immunosuppressive drug. It acts
by inhibiting T-helper cell functions and blocking production of the cytokine

I'm not too sure what to say about Azatioprine as what I found is mostly experimental.

Is he aware that there are other drugs that he can take for RRMS one being Copaxone. Yes it is a daily injection but the side effects are so minimal and there is no feeling like you have the flu for 2 - 3 days after each injection. When I was injecting Copaxone my main fuss was burning and itching at the site for a few seconds and those bumps so I avoided my backside...so in truth my lumps were probably mostly from not rotating the sites like I should have.

I never went the Interferon route just because of the side effects alone. I wanted something that I could inject and not worrying that it would interfere with my life (as much as possible).

Other than the Optic Neuritis and failing vision, how is your friend doing?

~Zig