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Hi all Newbie here Was diagnosed a couple of weeks ago waiting for a date to start Ocrevus. Its been a crazy two years. I was told I had a stroke two years ago but then a couple of weeks ago neurologists confirmed it was MS showing itself for the first time. I already greived through having a “stro...

Hello, I was diagnosed with MS in 2023 after 5 long years of trying to get answers from my GP. Unfortunately it wasn't found until my body was in quite a bad way. I ended up bed bound and with a catheter for 3 months. Throughout my time in hospital all I wished, is that I'd be able to walk again bu...

Just wanted to say HI!!! newbie here…

I'm having symptoms; tingling and numbness in leg spreading to both. Pin s and needles in foot, trigeminal neuralgia, tripping over and bruising toes, increased bumping in to things. I've had a physio confirm not trapped nerve and x ray and bloods confirming not a cancer. (I had breast cancer 2 year...

Hi, I believe I have rrms, currently newly diagnosed. Have left leg spasm that goes completely rigid and is very painful since taking quinine tablet it has help leg spasm. They prescribed this before I was diagnosed as were weren’t sure what we were dealing with. I now left with pins and needles in ...

Hello everyone, I'm new here and just wanted to say hello 👋 I was recently diagnosed with PPMS in January and it's been a struggle since. I cannot walk without my walker, it's been very prevalent in my arms and hands (I have a very difficult time doing the most basic tasks with my hands). It's be...

How does everyone feel after their infusion? I always feel horrendous, frankly. Like I’ve been in a car crash, fatigue, pain, gastric issues, headaches. Anyone else? Been on it four years so no newbie.

Hi my name is Aly, I was just diagnosed with RRMS and are going to start taking Tysabri IV infusions. Is anyone else being infused with Tysabri and how is that working for you? How do you feel on it?