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, 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...
This a poem form a fellow volunteer/Buddy Mark Lynch. For those of you who are lucky enough to have met Mark, or any of the buddys, you will know this is what we try to achieve in supporting MS ers across the world.
Shifted Horizons
There was a time
when the world felt smaller—
rooms measured in s...
Hi everyone, I’m new here. I don’t personally have MS, but someone very important to me does, and I joined this community to learn more and better understand what people living with MS go through. I hope to listen, learn, and support where I can. Wishing strength and good days to everyone here. 🤍