Right here goes 13 a day and counting

So during the heatwave it's a bit weird but I can sense how hot it is outside and comparing to how cool inside and it's setting my tingles off. Anyone else experiencing this?

It was my birthday yesterday, and honestly, I’m struggling. The depression has been heavy, and with everything MS has brought into my life, plus motherhood and everything else, I feel overwhelmed in ways that are hard to explain. Yesterday didn’t feel like a day worth celebrating — not because I do...

I miss mowing my lawn. I miss washing my car. I miss driving. I miss going to work. I miss standing in lines. I miss all the things that a lot of people complain about. I miss smiling. I miss laughing. Just a emotional day. Its so hard to watch people do the things you were able to do, but no longer...

I need some advice and reassurance, I was diagnosed in May with RRMS after I had left sided weakness (first ever symptoms I thought it was a stroke). I have been fine for a whole month then on Tuesday my left leg and left hand spasmed and I ended up laying on the floor for 2 minuets and it stopped. ...

Ladies, I need advise.. As I am a organised woman just wanted to know in advance if you can breastfeed with Ocrevus I am due to give birth early December but my infusion will not start again until 2 weeks after giving birth. Any help will be much appreciated on this, I Thankyou! X

I was told by a neurologist a few years ago that as a patient with MS gets older they tend not to need immunosuppressants. Has anyone else heard this?

I guess after 40 u have to care more for ur self and being im permanently sick no cure its a must

Hi all, I was recently diagnosed, and I was wondering how other party animals manage it. I’ll be starting a B-cell depletion treatment, and I’m a little worried about how I’ll navigate going to clubs and kissing a lot of people while on an immunosuppressive treatment.