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So I had my MRI yesterday. Everything was normal except- Rare scattered foci of nonenhancing signal abnormality noted in the supratentorial white matter. Differential diagnosis ulcerations include chronic small vessel ischemic change, demyelinating plaques, and migraine related signal abnormality. I...

Hi everyone. I have RRMS but I believe I might be progressing to different type. This disease can be so frustrating at times. I can't get an appointment with my neuro until next month and my symptoms are increasing. I don't currently take a DMT - I had a bad reaction to Copaxone and haven't wanted ...

Unfortunately I am having my first relapse in 2.5 years and I am still on tysabri (going into ocrevus in a few weeks) I feel angry as I was kind of in denial as everything was going to so great. My father passed away in May and I thought since I didn’t have a relapse then I’d be safe but here it is...

I’m still waiting on neurology appointment since February for a diagnosis of MS. Ended up back in hopsital all day today due to losing control of my bladder. Worst thing is it was at work and I don’t think I’ve her been so embarrassed. I didn’t realise I had wet myself until it was too late. I’m so ...

Hi all. Been keen to meet up with similar folk with similar symptoms in my area (West Sussex). Lots of the sites and groups just look so old fashioned or staid and this one just had a bit more buzz. Bit nervous about joining a group full of very different people to me but would love to share a beer,...

Hi you lovely lot! I’m thinking of going on a cruise next June (big 60 bday!) I’ve never done 1 before & haven’t been abroad since before my diagnosis 3.5 yrs ago & before pandemic lockdowns, the last time was Sept ‘19 😳🥴. By the time we were to be going I’ll be using a motorised wheelchair. Any ...

Yes I know we are all very different in the way the MS affects us but can anyone give me any helpful advice with my very new and recent symptoms. So basically my stomach is constantly feeling like I have butterfly's and I feel like I keep getting massive amounts of adrenaline dumped in my system eve...

Hi I’m not 100% diagnosed in fact im in the dark, I have suspected I may have ms for around 3-4yrs but put off seeking help things are just getting worse to the point my mobility is now being affected, I made a list of things bother me ie painful spasums weird vibrations and many other things and we...

Hello! I'm 17 and new to this site, I've joined because I might have MS... So my first two symptoms of MS were trigeminal neuralgia and leg pain on walking, no matter the distance. I have been to my local GP a number of times, sometimes referred to my nearest hospital. Fast forward to now and I hav...

Hi everyone. My family physician believes I have MS- i have issues swallowing and speaking, bowel bladder problems, numbness/tingling to the point that I couldnt feel my legs and went to emerg, cognitive issues severe fatigue- however when my neurologist sent me for an MRI he said it came back looki...