I’ve been battling multiple sclerosis since 2003. I have student loans that I’m eating help with everyone wants to help out by lowering your payment, but that doesn’t necessarily help me out. Does anyone have any ideas?

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.

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...

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

Right here goes 13 a day and counting

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. ...

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?

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?