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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...

Hi everyone. I have RRMS but I believe I might be progressing to different type. This disease can be so frustrating at times. I can't get an appointment with my neuro until next month and my symptoms are increasing. I don't currently take a DMT - I had a bad reaction to Copaxone and haven't wanted ...

Hello! Me again. Injection 3 today and I did it in my stomach for the first time. MASSIVE bruise and it’s really painful! Does anyone else get this or am I just being inept? Thanks! X

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...

Finally after 2.5 years I've received a formal diagnosis. This was not a shock to me as my Neurologist had said after my first MRI it couldn't be anything else. Following my latest MRI the Radiologist found a new brain lesion described by my Neurologist as "tiny" and that he wasn’t convinced. My N...

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...

Hi, new here. End of April I started getting pins and needles in my feet and within 10 days they spread up to my chest which felt like someone was trying to squeeze the life out of me. Numb left hand, pins and needles, i was barely able to walk. Stifness in my torso. Then my eyes went wonky. Everyth...

Just writing to say hi. My name is Erin, I am 37 and was diagnosed 11.5 years ago. I started on Copaxone, then Tecfidera and now Kesimpta. Just here to give and get support and make some friends that have MS that understand what I’m going through. 😀

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.