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Hello, my name is Michael Russell and I was diagnosed with Multiple Sclerosis in 2009 after a five-year-long medical journey of tests, therapy, and doctor visits. Being diagnosed at age 54 and looking back at my physical changes over the years MS may have begun in the mid to late ’80s. Before being...

Hello, my name is Michael Russell and I was diagnosed with Multiple Sclerosis in 2009 after a five-year-long medical journey of tests, therapy, and doctor visits. Being diagnosed at age 54 and looking back at his physical changes over the years he feels MS may have begun in the mid to late ’80s. Be...

I was diagnosed over the summer of this year and I let the people closest to me know a few weeks later. My family have been a great support practically and my friends treat me the same way as always. But I’m struggling that no one is asking how I am or how I’m getting on with my MS since my diagnos...

Fertility, contraception, pregnancy, symptoms, relapses, treatment… with MS, family planning isn’t a simple ‘yes’ or ‘no’ decision, there are a lot of moving parts. “We limit ourselves. We are limitless if we want to be. It’s a social construct of people looking at us and feeling like “why have you...

Hope everyone is doing well. I’m going to a movie to watch John. Have a blessed night.

Hi Ms family 👋 I may be going through my first real replapse (possibly new lesions) as I have new symptoms that have lasted more than 48 hours 😬. One new symptom is feeling cold water on parts of my body randomly when they are completed dry. I am on Ocrevus and have been since January. My question...

Hi, I posted before about meet ups or im also happy to chat as a group or whatever I'm in central South East London (SE1) I was diagnosed late 2022. all the info is in my bio, we don't have to chat about MS but its nice to connect with people nearby that have similar experiences in this MeSsy diseas...