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@Littlerosee 

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Littlerosee

Mavenclad- Cladrabine

Just finished my second year of Mavenclad treatment and my recent MRI shows no changes which is great because I was told I had very highly active RRMS when I was diagnosed march last year and have between 23-33 lesions on my brain, I’ve been told I don’t need any more treatment for at least 4-5 years if I continue to have no changes but I just feel a bit lost about where to go next. Has anyone been on Mavenclad and how has it been for you after the two years of treatment? I guess I’m just worried about the future and not being on any treatment for the forseable
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3
@DCMashamS
@DCMashamS
 

Hi, just finished 2nd Yr earlier this year. No new sessions on last MRI, after very active MS before starting cladrebine. Hopefully stays this way for a few years.

2
@Luce6661111
@Luce6661111
 

Does anyone know if any treatment for optic neuritis in SPMS as struggling with serious headache and optician felt that could be reason for it any treatment ideas?