I’m Loubie, I’m 39 and was diagnosed with agressive RRMS in 2009. I was put on Tysabri straight away which worked well enough at first, but I started to get breakthrough relapses so my neuro put me on Campath (which 5 day course I finished last Friday).
I seem to be very lucky in that I have no rashes or bruises (in fact, it was the steroids that caused me more problems during treatment so I only had them twice). I get tired very easily at the moment (guessing my body is still in a ‘WTF!?!’ phase) and I get MS symptoms which last for a few seconds or minutes but then seem to be ‘batted’ away.
It’s vey early days and I’m really hoping this works. I am interested hearing from anyone else here who has had Campath therapy.