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Good Morning gang! Few things here: 1. Immediately change your neurologist if he/she doesn't cooperate to help you feel better. There's no time to waste. He/she needs to be in your team. He/she needs to be open to answer any and all questions, because there are no stupid questions. Don't find any ...

Hello! I was diagnosed in 2015, although the first onset was in 2013. Still trying to wrap my head around it all after 5 years! Havent had a full blown relapse since April 16 but have the odd numbness etc. How do you finally come to terms with having this illness and not constantly worry about what ...

https://youtu.be/gWWeRoLCdFE Part TWO

https://youtu.be/THeLVhU53ow Part one

Hello, I have a question here for anyone that reads it and is willing to answer, to get to know all of us better. Where are you from originally? I was born in Michigan and lived in New York for a large portion of my life. I went to high school in Virginia Beach and went to undergraduate in New York...

I'm curious to know if there are many East Asian MSers slipping under the radar in the UK or even across the world perhaps? In the UK, it's not a surprise if a friend, or a friend of a friend of a friend has MS - I guess you can call it the 'Six Degrees of Multiple Sclerosis'. It's that common beca...

Join Roxy, Heather, Maytee, Katt and Dave as they agree and disagree with hot MS topics, opinions and share their multiple sclerosis diagnosis stories. Did you have a difficult diagnosis? Why not share the lessons you learned with the Community in the comments below 👇 https://www.youtube.com/watc...

I’m looking to meet fellow MSers for coffee & connection in Edinburgh City Centre… I’ve been living with MS for 5 years & find it really hard to get connected with those that get it. In person as perhaps I’m a bit old fashioned & benefit most from real life connection..

Im in northern CA looking to make some friends people to talk to im finally feeling up to trying this app and just seeing whos out there and whats going on