Hi All, I am coming up on my 1 year anniversary of being diagnosed but I’d been living with what I know now was MS for the year previous to that. I take Tecfidera and apart from the hot flushes it keeps everything else at bay. I was on holiday in Canada during the summer and was introduced t…

Hi Guys, this is my first post and I am just writing this now because I really feel like I could do with some help. I don’t know if anyone else feels like they are trapped in their own head but I do. I was formally diagnosed with MS over summer but have been living with the symptoms for about…

I am new here so hello everyone . i really dont know where to begin ,sorry i will try to keep this a short as i can . beginning of July 2017 ,i woke up with a terrible backache ,so went to the doctors and was given pain killers ,but they didn’t help and the pain got worse .so i visited my GP …

Now the cold weather is setting in, how’s everyone doing? For me it’s pretty tough. I’m more tired due to it being harder n tougher moving about on pins. Heating on n laid on settee, paradise!

Hi guys, I am looking for some advice. I am having a flare up, I have a bad cold, worst I have had in years. It has flared up some old symptoms but also a new one. My arm is very achey and painful and my finger tips are so sensitive it is uncomfortable to use my hand at all. I also feel like I have…

I was diagnosed with MS in Aug following recent episode of optic neuritis, fatigue and previous lhemittes sign going back to 2016, worsening with heat and a brain MRI. Starting to get my head round it when I was seen by a specialist a couple of weeks who has said in his opinion MRI is normal and do…