Hey all. Hope everyone is well. So once again fair warning this could end up being a long post so for that I am sorry. But I just have to get this off my chest because I am about at my limit here. So please don’t feel obligated to read this. It is more just so I have an outlet to get this out bef…

I’m Em! I am Irish and 23 years old 🙂 I am newly diagnosed with MS, in April of 2019. I was 22 at the time- I experienced sudden double vision in my left eye and after all the tests etc, they told me it was MS. It was a HUGE shock to me, but I was actually kind of relieved that I had a dia…

Hi all I caught a terrible infection, cold and flue, which knocked me down and having low white blood cell due to gilenya, I am suffering. What should I do. I have been drinking alot of herb teas with lemon and honey… does not help that much. I am in bed and worrying that it will trigger a …

Hi I am 10 years in with RR MS, and had 2 very successful doses of alemtuzumab, in January 2016 and January 2017. I responded very well to the alemtuzumab neurologically (despite being highly prone to any virus, cold or infection going in the 1st year) and in 2018 was in extremely good neurologica…

Hello ❄️ call me crazy but in weather like this i feel …

Dear all, this is what i am thinking of doing this summer. I want to get stem cell therapy done in Uk. I know the cost and the restrictions on it but just wondering can l pay some towards the cost to the NHS would l be accepted. Or if l want to get it done outside UK, would it be cheaper and wha…