Just wondering if any of you have had feeling of a tight rubber band around your ankle? I have been experiencing this on and off a little over 2 weeks? Is this a relapse? I’m so new to this as I was only diagnosed with rrms in april this year. I have had symptoms on and off for over 5 yrs wi…

Hi, I just need a rant!, I was going to my Dr for 10 yrs complaining of numbness, tingling etc but because I have a severe anxiety disorder he kept saying I was only thinking this was happening but I knew I could feel it, fast forward to December 2017 I had a brain scan cos my optition saw somethin…

Hi guys, I am the only one in my whole family and friendship group to be diagnosed with a condition that is long term/degenerative, and I’m really struggling with support from them. I don’t have any physical/physiological symptoms as of yet (thank God) but I struggle a lot with fatigue.…

Hi all, I’m new here I was diagnosed in 2003 with relapsing and remitting, but I keep as positive and productive as normally can. I’ve never been on a site like this, but always like to offer and receive support. Kind regards Scott

I’m new here, I’m 30 and have had MS for ten years, it started off as aggressive RRMS, now SPMS. I have been unable to work for the past 5 years. My friends are meeting the usual milestones in life, promotions, getting married, having babies, I’m just stuck in the same spot. I can’t help bu…

I have recently been diagnosed with RRMS and at the moment highly active. Neurologist suggested Tecfidera or Fingolimod. MS specialist nurse brought Ocrelizumab to the table. I decided on ocrelizumab but my symptoms have worsened and ocrelizumab can take 6 months to be fully effective so natiluzima…