Looking for
something specific?

I am thinking some kinda virtual/online/face to face mtg......? Is there anything like that? We all have different stories, but with likeminded people, it should make it easier? Let me know your thoughts....we all need someone...

Does support look different for a male vs female living with M.S? My husband has recently been diagnosed (he is in his 40's) and I am struggling knowing how to support him.

Hi all, I am new to this group but not new too MS R&R which I've had since 2003, it's been a tough 2 years with separation and symptoms slowly getting worse and not being able to really speak to anyone who understands as live on my own, it's the first time in 4 years I saw my neurologist today who w...

Hello all, like yourselves I have been hit with a crippling disease that has cost me everything, my career, my home and my life really How have you managed financially to make ends meet, I am 46 this Friday and now unemployed, I can no longer do the work I was trained to do, I have many qualificatio...

Hi all love the site would love to chat to people with Ms, so interesting what I have read about so far. Looking forward to chatting to people

Mental health

Has anyone been to any ms support groups? They don't seem to have any in my area 😔 x

Why are they nearly all in places that you cannot get to unless you drive. To me, that doesn't seem very inclusive. Especially considering they are meant for people with all variants of MS and the whole range of symptoms or disabilities. Never paid much attention to this when my brother was diagno...

Hi All, Diagnosed after around 2 months of private testing, all started after what was supposed labyrinthitis [I was unable to move without vertigo, double vision, fatigue and completely hearing loss in left ear] I then developed a hemifacial spasm in my left face which varies in severity, asked ...

Hi everyone! With my MS, I have intense chronic pain and I’m finding it difficult to meet people who have significant chronic pain who are around my age. Does anybody know of support groups in my area (Calgary, Canada), informal or formal, that targets young people with MS and who have chronic pain...