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Is anyone using this medication? if you are, how have you found it, how often are you monitored whilst on it and have you had any side effects from it?

Who else is on Mavenclad or will be starting Mavenclad soon ?

Pros and cons please

Hi all 🤗 Hope you are well. After the last MRI, I had a new medication offer. Mavenclad or Kesimpta. I’m still on Tecfidera since the diagnosis in 2015, pills are easier than injections. As I’m usually travelling between two countries, going with a portable fridge is not appetizing, to be honest. ...

New here 👋🏼. I have been on Brabio for the past 3 years, but had a relapse recently. The 1st one that I had to take steroids for (that was fun…NOT) and have a few more legions on my spine and brain. With worsening symptoms, my Neurologist wants me to move over to more “affective” meds. Still going...

My neurologist wants to make the translation from me taking Ocrevus to Mavenclad She gave me a pamphlet with information, but I want to know the experience from anyone currently on it.

Hello lovely people! I’m currently taking my last week of Mavenclad and even though have tolerated the previous week’s treatments quite well, I’m finding I feel just awful this time - gut pain, back aches, exhausted, feeling week. Has anyone else experienced this?! Thankfully it seems to wear off by...

Finished my first year of taking Mavenclad.But it seems that I had more muscle spasms and walking problems .Now using a stick,and just found out from latest my MRI scan that I have another brain lesions .Which wasn't there on my MRI scan beforehand . My question ,what symptoms or problems have oth...

Hi everyone. I’ve been on Tecfidera since 2019 and I thought it was working well for me, I haven’t had any relapses or even any symptoms at all really. However my most recent MRI’s showed a new lesion in my thoracic spine. Some of my lesions have shrunk however there is the one new one. My neurologi...