Mavenclad
Hey,
I'm soon to switch DMD's from Brabbio to Mavenclad. I'd appreciate any feedback from people that either use Mavenclad, or have stopped using Brabbio.
I'm also wondering; how do you tell what is a side-effect from the DMD itself rather than a symptom of MS in general?
I've been having some very unpleasant bowel business, -which I'm receiving treatment for- but how can I know what is causing it?
I'm going to dive back in to all the listed side effects, -wish me luck!- but I tend to feel much better hearing from personal experiences, if anyone has something they're willing to share.
Thanks all,
May the Force be with you!
Mavenclad is a swish, low maintenance, pills at home, great stuff. See a specialist about the bowel issues to rule out other potential issues but you wouldn't be the only person on here delicately crossing the constipation/shite myself in public tightrope.
First of all I am Sandra Ables. I was diagnosed in 2007. Even though my symptoms were present in 2002. I have tried numerous meds but long story short Mavenclad is the one that helped but my MS IN REMISSION. I will recommend it to anyone with RRMS. I am now to the point of taking absolutely nothing for my MS. I do see my neurologist every six months, I have my MRI’s when needed and I am monitored for the JCV. How long have you been diagnosed? I am here if you wish to talk. I am on disability from the MS. No I wish I was working but it is what it is. I’m grateful for my disability that I receive.