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For those of you well established on Ocrevus, has it ever exasperated your symptoms in any way or presented anything new? I recently had an infusion following a 7 month delay and am now experiencing bladder incontinence (new), leg tremors (not new, but much worse), a funky eye brow tremor and a ge...

For those of you well established on Ocrevus, has it exasperated your symptoms in any way or present anything new? I recently had an infusion following a 7 month delay and am now experiencing bladder incontinence (new), leg tremors (not new, but much worse), a funky eye brow tremor and a general ...

I first posted here in 2020 when I was having intense symptoms. Wasn't taken seriously and told it was either related to my epilepsy or anxiety. Many of my symptoms stayed but weren't as intense but recently ones that pretty much went away have come back and some other things I've noticed as well....

I tell you, trying to get hold of my doctors is proving extremely difficult. My Primary Doctor and my Neurologist. It's like they've disappeared off the face of the earth. I did let them know that I was going through some rough symptoms earlier in the week and I have heard nothing. #Disconcerting.

I tell you, trying to get hold of my doctors is proving extremely difficult. My Primary Doctor and my Neurologist. It's like they've disappeared off the face of the earth. I did let them know that I was going through some rough symptoms earlier in the week and I have heard nothing. #Disconcerting.

Life & Times of an MS Sufferer….. By Roger Deuxmont · March 31, 2019 Life & Times of an MS Sufferer….. These pages are dedicated to the following people, my father Leslie 1911-1980, my father was an indirect casualty of the smoking lobby, succumbing to the effects of lung cancer at the ag...

Apologies for the influx of posts. I have been experiencing pins and needles in my back, similar to that of when I had my lumbar puncture. I'm putting it down to the treatment and fatigue etc but it's a very disconcerting feeling. Has anyone else experienced this? And if so, do you have any way to h...

Hello, this is my first post. I'm currently somewhere between a CIS diagnosis and MS (having been told I meet the revised McDonald criteria for MS based on my MRI and current (very mild) sensory CIS). I don't (think) I know anyone with MS and just want to reach out and share my story and feelings ...

Hi all, I was wondering if anyone would know, I've recently started having problems with one of my eyes - it comes and goes but I've noticed it shortly after lunch my right eye seems to get blurry and it seems like I've got retina burn where I've just looked at a bright light, that is the basic k...

I've had a week of making life decisions based on my MS. It's been a bit disconcerting, I know it's necessary but it makes me feel sad, just more reminders of something I'd rather ignore. I'm a scientist but quit my job and career in 2012 because I felt the stress was affecting my health. Of course...

I'm sure there's been a similar post to this recently, but I can't find it just now, so I'll just put this out there. I used to be a decent speller and I've never had problems with writing English (my second-language), but since this MS lark started, I'm shocked by how many spelling mistakes I am...

Anybody else get "itchy eyes"? The muscles around my eyes seem to be tingly in a way that seems more itchy than really tingling but it's still pretty disconcerting