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.

Hey everyone is there anyone from the UK here I'm from Sheffield in the in UK ❤️🙏🏽

Hey everyone, From Chicago, IL here. Today marks one year since being diagnosed with MS and to this day, I feel like my life is over and I will never be able to move on, live a normal, healthy and happy life. I have also been diagnosed with OCD on top of my everyday norm since I was 9 of depression...

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

We don't blame you. When you apply for a Buddy, you're taking an active step to get support that will guide you along your MS journey. Interested? Of course you are! Click here to apply: https://app.shift.ms/buddy-network Or get in touch with me directly. Many thanks, Kelly

My husband was diagnosed last year with Relapsing Remitting MS. He is still awaiting his treatment which is frustrating. However, he is struggling with insomnia, jolting in his body, headaches and itchy skin. I’m wondering whether anyone else has these symptoms and whether the treatment helped whe...

Wondered if there's anyone from the Preston area who can recommend any good groups, doesn't have to be a specific MS group, I'd just like something where I could meet new people. I live in Lancashire but moved over from Yorkshire (scandalous!!) and haven't made many friends over here. Any recommenda...