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...
I'm feeling so let down by my body and so frustrated and exhausted still after months of fighting through rehabilitation. On top of that I feel like this disease is going to ruin my relationship because my fiance CANNOT handle talking about it all the time.. but it's always on my mind, and apparentl...
I think I may need more than just a cane at the moment. I can walk for about 15m with the cane and stand up for about 5m. That's the time before my fall risk becomes a fall certainty and it's a 1/3 chance I'll pass out briefly with that too. I wouldn't be as worried about this if I didn't have to wa...
Hello all you amazing MS fighters. I live in a town called Ayr. I was wondering if there are any others that live in or near Ayr. I moved here about a year ago from Kitchener. I feel very alone and secluted. It would be nice to have a coffee with someone that understands. There no food delivery for ...