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Hi all New to the site. Been given 3 options for treatment and I am siding with Rebif as we are thinking of starting a family soon. What’s people’s thoughts on it? So much information to take it. I’m feeling very confused and overwhelmed. Got diagnosed about 3 weeks ago. Thanks in advance Lucy

I was supposed to have my first Ocrevus infusion today but it has been deferred in light of the coronavirus outbreak and I will be treated with Brabio for the time being instead. I had emailed some concerns to my hospital (The National Hospital for Neurology and Neurosurgery in London) as I was worr...

Morning all, I've been med free for 15+ years since diagnosis but a couple of recent relapses (including my first learning to walk again episode) have put me on a treatment plan. I'm due to start taking tecfidera soon and wondered how it may affect my exercising? I currently cycle on a static trai...

Hi, I'm Sofia and I was literally diagnosed last week after suffering very mild symptoms here and there since January 2019 which were overlooked, belittled and misdiagnosed. Unfortunately I ended up going into a massive episode (I still don't know lingo) and i woke up one morning not being able to w...

I am contemplating a move to Margate from London. Does anyone have advice on neurologist/hospital in East Kent please? Somewhere that has an outpatient program? I’m very happy with my Neurologist in London so moving hospitals makes me slightly nervous. Thank you 😊

Hey guys, it’s been a while since I’ve come here and hope you are all doing well. I have been suffering quite a lot of late due to the immobility of my legs and the constant pains below the waist. Does anyone recommend any treatment to take or maybe some advice to treat spasticity and prolonged ag...

I have spent 3 months in hospital and 6 weeks of that was in a rehab ward. I have returned home now and haven’t made much of a recovery . I am doing exercises and physio but feel very scared that I may stay like this, unable to move both legs or stand.

Hello! I’ve been told today how amazingly positive this site is and I can already see from just having a little nose it’s just what I need! I was diagnosed 3 weeks ago, shock probably was an understatement. I haven’t googled anything really, just had conversations with the Neurologist and my nurse. ...

Hi there, I just finished my 1st cycle of Mavenclad treatment...free now for 4 weeks before the next lot No real side affects...just a little exhausted...more than the usual kind I could feel burning sensation while swallowing the medication..make sure anyone taking this medication has plenty of w...