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Hi everyone. I love doing sports. It has always been my go to. Now with MS, when I play a sport it reminds me of my loss. 😢 I have always been sporty, because that was my thing. Now I feel that walking is becoming too hard. Any suggestions for what to do instead 🤷‍♀️. Should I worry about bone den...

would i be putting myself at risk of another relapse by going back to football or make my ms worse by doing so.

Hi all, Totally random I know, but any UK peeps with MS who used to do gymnastics or something similar? I’m part of the team putting together a full Paralympic GB cheerleading squad and we’re short on flyers, so thought I would see if anyone here would be interested. If so please let me know and ...

Doodle Baseball is a delightful game that is integrated within the homepage of the well-known search engine. It provides a fun and nostalgic way to spend a few moments immersed in the world of baseball. The following is a guide that will help you step up to the bat and enjoy this adorable game, rega...

Hey everyone , so I have been thinking a lot recently to start playing sports for fitness & fun but been worried as being on my feet for short period of time is tiring and I get leg spasms and of course the limited coordination. Has anyone picked up a sport since having ms? 🤗

Hello! I here new and I very need your idea. Is a question such, Or extreme sport can become a helper, or vice versa strong emotions and agitations at employments by it can provoke intensifying? I engage in windsurfing, very happy from it, but on does not really know as a nervous system reacts on it...

Hi all i got a question. I was diagnosed 2 years ago at 24 i woke up one day and both of my leg just didn't work. I use to do a lot of contact sport. Now I got medication and I am better but the question remain Can I restart to do kickboxing? I know sport is good for ms but is it ok to restart comb...

I've just managed to book myself a ticket to see Dylan in Hull in October because / and for the first time ever ..... I booked to sit in the accessible seating bit (based on the fact I have a parking permit, a bus pass and PIP mobility payments and obs a SPMS diagnosis) but I still felt a bit 'she...

Looking for advice, I was diagnosed with MS in 2012 in high school. I have been managing well and have been taking the Copaxone for years and have been great with it. I had a period of time I was not taking anything because of insurance problems. I love the sport of volleyball have been playing it ...