Last reply 22 hours ago
Mavenclad (Cladribine)

Hi guys, just looking for some advice, insight…Was on Copaxone for 1 year 1/2 but unfortunately not working… my neuro wants me to start Mavenclad. Just wondering if anyone on this medication can tell me their experience, side effects etc…very worried about low immune system

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1 week ago

Hi and welcome to the club.
Under your post above you’ll see a box markedly Mavenclad .
Click on that and it’ll take you to other posts made about it.
Along with a few other things that you might be interested in.
Feel free to ask anything you like we’ll try and find an answer one way or another.
Welcome again 😀

1 week ago

Hi @laura_pizzolitto
I’ve just finished my second year of Mavenclad and other than the feeling of nausea and feeling tired for a few weeks I’ve been fine. I was going cold, like my body temp wouldn’t regulate properly for a while but I’m OK. I don’t know if it’s worked yet, guess I need a year or so to find out but generally I’m ok 😊. My levels went up pretty quickly afterwards, they will monitor your blood to make sure your lymphocytes go back up. 😊

22 hours ago

Hi Laura,

I am in the same position right now. I took Copaxone since May this year and got 3 new spots at my last MRI. So we decided on Thursday if I change my medication to Mavenclad. I am really unsure, at this moment…

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