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Please let me start off by saying I'm not whining or being ungrateful...my current neurologist has been very efficient in organising scans and treatment over the years. But...I am wondering if I can change my neurologist. When I saw him about a year ago he encouraged me to get back with my ex husban...

What do we know about MS and menopause? How do symptoms change, Is there an increased risks of getting a relapse? How do the disability level change? Thanks ladies and sorry gents.

I am looking for feedback to my MS experiences the last few weeks. I am 71, secondary progressive now. I have been able to walk and even do some dancing in my living room. Until about two weeks ago. My legs started giving out, I took a big fall on my walk (just bruised and scraped). I am super ...

Hi! I am hoping to get some feedback. I am dx RRMS. Doing pretty well, on Glatopa (copaxone) about three years. Anyway, I am having serious joint pain in both hands and mainly thumbs. Maybe carpal tunnel but I have much joint pain in other areas like knees and feet. But the hands are the worst. An...

I think it’s time I just take a step back an re-evaluate everyone that I have in my life.. having ms literally makes my day to day living hard for me, an none of the ppl I have in my life can understand that. They say they do but actions speak louder than words. It’s tough living this life being ove...

Never meet a group of people that are not updated on new discoveries and cures.I posted a message here to help but it was removed because admin claimed i broke house rules..How am i suppose to help other patients in the community when i can not direct them where to get a cure???If you are still with...

come join is on Zoom at 11 am (uk time) where we don't just talk MS /Users/craigwatson/Desktop/Screenshot 2020-06-14 at 09.22.45.png

Hi everyone, I have rrms. I have been getting this excruciating shooting pain in the side of my head, it usually only last a few seconds. The pain is so bad, you just have to sit and wait till it passes. The pain isn't on my face. I have had it for years but it would only be a couple of times a ...

This may sound so needy 😂 but I was just wondering how people manage without having someone who actually has MS and understands how hard it is living with it. My partner is amazing but other than that there isn't any one else to talk to about it. I think sometimes I find having MS a very lonely exp...

Hi all, hope everyone is doing well. I just have a question...I've had MS for a few years now, rapidly evolving severe, I've had 2 courses of lemtrada but after 1 year of my last course I had new activity so my neurologist put me on copaxone injections. I wasn't eligible for ocrevus as my immune sys...