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Hi my name is Hayley! I thought I would be brave and put up a first post. I have recently been diagnosed with Remitting MS (November 2020), its been quite a journey that began with the complete loss of feeling in my left leg in summer 2019. Things spiralled from there and lots of MRI, blood tests an...

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...

At 33 years old smack dab in the middle of Alberta Canada which happens to be the MS hot zone of the world. I am noticing there is almost nobody from Alberta on this website which is very confusing to me! Anyway... I have been suffering for well over 10 years and I've seen hundreds upon hundred...

What do you compare it too, and where does it hurt.

Hello. I am UK based. I have been diagnosed with Remitting Relapse and take Tysabri monthly. I have been taking Tysabri for a year now and had to get an MRI scan done. I did it. Got told my scan is alot worse than last year. I have new active liesions. JCV is negative. Had to get a lumber puncture...

Good evening, Has anyone experienced pressure in their tongue and slight discomfort in their jaw? It's like I can't 'relax' my tongue? It's so hard to explain. This just started getting worst and I'm getting massive headaches now due to it. Thoughts? Thanks a lot, Amanda

Hello all. I have stumbled across this and looks very friendly and supportive. I have not yet been diagnosed but am under investigation. I have had to give up work 3 months ago (I was self employed) as I knew I wasn’t firing on all cylinders and something wasn’t quite right. My doctors / neurol...

Its been a year, since my first relapse which led to diagnosis. Blue lighted to hospital with Nystagmus, severe Dizziness and numbness all over. Was left on a trolly in A&E for two days in the worst hospital i've ever been to (not mentioning names). I work away so at first there was no-one who c...

Hi, my name is james. Probably have a million questions for you all. Just where to start. Started tecfidera 4 days ago. Even though there is no diagnosis of ms as of yet. Its still a "strong suspicion." So, we went along with the dmd. I will further introduce myself as time goes on. I have a questio...