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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...

Hi all, first post. I'm 22 and slogging through the long and troublesome diagnostic process to figure out what's going on. My strong suspicion is MS, but my objective clinical indicators are either barely there or nonexistent ⁠— I have small demyelinated lesions and speckled ANA blood titer, but tha...

I was diagnosed with RRMS last week. The neuro gave me some options in regards to treatment; I'm to take a week to educate myself and hopefully come to a decision. Tomorrow will be one week. I'm leaning towards Tecfidera, but I'm absolutely terrified. I'm terrified about all of this, but in regards ...

I'm going to be on ocrevus in a few weeks, what are the best options for treatment so far?

Hi all, hope you are keeping well and safe in these unusual times. I am newly diagnosed in March, first symptoms 18 months ago and 1 minor relapse 6 months ago. Other than that I am lucky not to have any symptoms of note. I discussed with my MS nurse DMT drugs early March and my neurologist recom...