Looking for
something specific?

I can’t find any groups that meet or anything close to me. I want and need friends. I am feeling super beyond frightened for my future!! It’s kinda like I’m “due” or past due for a relapse…an MS “attack” as I have not had a bad one for years. But I’ve had a ton of stress and trauma over and over ..I...

I can’t find any groups that meet or anything close to me. I want and need friends. I am feeling super beyond frightened for my future!! It’s kinda like I’m “due” or past due for a relapse…an MS “attack” as I have not had a bad one for years. But I’ve had a ton of stress and trauma over and over ..I...

Hey everyone, thanks so much for your comments and support on my last post. Really appreciated it! ❤️‍🩹🙏 where I was having a lot of symptoms and weird sensations that had me scared. Since then it all got much worse the past few days where I just had super weak achy limbs, exhaustion and strange n...

I have RRMS and its been slowish in development. Im now on ocrevus but things are happening with my cognitive behaviour - memory, focus, clarity of thought, problem solving. This has been getting gradually worse for a few years, but i knew my job inside out, so not too much of a problem. Of course i...

My legs have completely given up on me, they are unbelievably solid, like Stonehenge. I am currently on no medication, trying to see if this is a relapse or something. This has lasted 2-3 weeks already and seems to be gradually getting worse. Does anyone have any ideas on what I could be doing to im...

Just wondering if a stiff and painful neck and shoulders is likely to be a relapse? I woke up a couple of weeks ago with a really stiff neck and it was really hard to sleep and move it which I put down to camping in the garden. I spoke to my neuro a week or so ago and he thought that my aches and p...

Hi guys, Please can I ask for some direct advice, I am sick of reading government docs etc lol.. anywhere here I go. On copaxone (I have read this is not a risk), relapsed a few months ago, need to return to work so please advise on what is required in the way of a risk assessment?

Just joined and thought I’d say hi 👋 I was diagnosed with ms in April 2008 , after I had my eldest son. My relapse effected my eyes and my face and mouth where numb, I was given a course of intravenous steroids and that seemed to make a difference, but within 4 weeks I had another relapse that al...

Hello all, I'd like some thoughts from you knowledgable folk plz. I was diagnosed rrms in September 2017 and have been on tec since March 2019. I have remained stable, however my most recent MRI last month (delayed from March) has shown 4 new areas of inflammation. I have not had a noticable relap...

So I had a second relapse this year, this year has been far too much D: so I started my treatment on the 17th August, which is grand, but I have been extremely tired, to the point where I cannot function at all. I have recently finished folic acid, which I was talking for two months, but then starte...