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Cellcept for MS - experiences? opinions?
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Courtney_J
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Courtney_J
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Last activity on 08/08/2022 at 11:09 AM
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@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
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Courtney_J, Community Manager, Carenity US
Smwwks
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Smwwks
Last activity on 09/29/2023 at 12:27 AM
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4 comments posted | 1 in the Multiple sclerosis Forum
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Sorry I can't be of any help here. I have not taken Cellcept.
Grace4a2ndchance
Grace4a2ndchance
Last activity on 05/30/2020 at 7:21 PM
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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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Grace4a2ndChance
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siemprelucha
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siemprelucha
Last activity on 11/30/2023 at 1:55 AM
Joined in 2018
46 comments posted | 40 in the Multiple sclerosis Forum
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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!