Hi all, hope your doing well.. I was diagnosed with RRMS October 2025. I’ll be receiving my first kesimpta delivery next week and a few days after be having the ms nurse train me in regards to how to administer it, I feel anxious?

Hi, I was diagnosed officially in June but investigations began last summer when I was off sick from work for 6 weeks. My teenage kids know about some of my symptoms but I have always downplayed how much they effect me to protect them from worrying. I haven’t told family or friends about my diagnosi...

Technically that's not quite true, but it's close enough, and I felt it appropriate not to miss quote the one and only Mark E Smith RIP My point is, I definitely don't have as many as I used to, and from reading other's posts I get the impression I'm not alone in this. Well, those fairweather frie...

Today I meet my new neurologist tomorrow I hope that things go well today and that I get my infusion today because I was supposed to get my infusion September 14th right now I'm having a relapse and I'm having pain really badly and I can't feel my hands,legs or my feet....

What things annoy you the most? With your Ms Mine is chewing loudly, untidiness, stupid annoying moaning sounds, annoying people..!!!

So, I've picked up the pocket book of the same name. By Claire Chamberlain. Let's skip the bit where it was given to me in 2011 😳 😔 😆. As I venture to read a page a day. Along side my usual I know I'm crazy singing antics while in doors.😂 I do firmly believe that we are not alright! But at times...