Cellcept for MS - experiences? opinions?
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Hi everyone,
I've had MS for a long time now which has become progressive after various treatments. I started taking Cellcept in 2017 and I'd love to hear from anyone else taking it because since about January my MS has been progressing pretty quickly and I've starting having some serious walking problems.
Has anyone else been on Cellcept and been through this? I'd appreciated any feedback or advice!
Beginning of the discussion - 5/28/20
Cellcept for MS - experiences? opinions? https://www.carenity.us/forum/multiple-sclerosis/your-opinion-on-multiple-sclerosis-treatments/cellcept-for-ms-experiences-opinions-1981@siemprelucha Hello siemprelucha, thank you for starting this discussion. I'm sorry you're seeing such such changes in your MS. Let me tag some members who may have taken Cellcept or may know about it.
Hello all, I hope you're doing well! Have you taken Cellcept for your MS? If so, have you had any side effects? Did you notice your MS progressing quicker than usual while on it? Feel free to share here.
@Grace4a2ndchance @cmm2514 @Jsbconsulting @VIRGODIVA59 @Nikki.blue @Nidiaicela @mdwithms @Lorilyn @stephanieb1971 @Smwwks @Sugamomma415 @lhager115 @Mlarso86 @mzclay124 @Amandan83
Take care,
Courtney
Sorry I can't be of any help here. I have not taken Cellcept.
I'm sorry I haven't been on Cellcept and neither has my husband. He has PPMS and they are going to put him on Ocrevus when the pandemic is safer to use that. Sorry I can't help more,
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