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Good morning MS community 🤗. I was diagnosed in July with relapsing ms and have had it for four years before diagnosis. I am due to start my injections once the nurse has visited to show me correctly how to do the injection. I had worries about medication (family all have died of liver cancer or p...

Hello everyone. Kesimpta injection two today. Number 1 I was tired and Woolly headed and 48 hour headache. Injection 2: completely and utterly exhausted. Can barely keep eyes open. Can’t concentrate. Head feels really thick. Anyone else have this? Does it improve after the loading doses!?? Than...

Hello! First experience of DMTs. My MS team have just prescribed Plegridy. What’s everyone’s experience on this one? Open to all the good, bad and ugly feedback. Thanks in advance!

Hi, My name is Lidia...and I have RRMS(still being tearfull about it) I have seen recently my neurologist. I have complaint about fatigues, headaches, pains and weakness of one side...following to my complaint he has taken me for physical exam and told me that my left side is weaker but not greatly....

Hey yall, I've been on Kesimpta for half a year now, first injection went kinda smooth with barely any side effects, ever since I never noticed anything from the injection. Well, until now. I injected a dose on tuesday this week... everything went well, but today I noticed swelling and redness aroun...

Injection no 3 done yesterday. So far no side effects, no injection site reactions. I'm loving it. Anyone thinking of starting this treatment, it's fab. Also very easy to do, painless. A damn sight easier than Copaxone. I hated that. I just hope it does what it's meant to and stops progression.

Had a Plegridy injection last night and I feel like I was hit by a truck. Chills, body aches, some nausea, and a headache. I just want to sleep. Not necessarily looking for advice, just want to complain (if you have some that's still fine, though lol). If the medicine hadn't been controlling my MS...

Yay. My first Kesimpta injection is all done. So far I'm feeling absolutely fine with only a tiny red pin prick where the needle went in. Compared to Copaxone, which was horrendous, this was painless. Didn't feel the needle go in at all. I would recommend this treatment anyday. Just hope the second ...

Hiya, I've been on plegridy for around 6 years now, and I'm really struggling with it now. I'm ill for about 3 days every other week, and I'm having one of my most debilitating MS episodes so far. I'm thinking of a switch, what does anyone think of Tysabri or Gileniya? I don't know if I'll be offer...

I have had M S. For many many years now R&R and I wouldn't go near medication, my Neurologist said please Kim, your brain heavily scarred so probably started drugs 10 years ago, first 2 tablets, then injections and now Ocreluzimab past 4 years...no relapses, no side effects so don't be frightened! T...