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I was never given like an option on ocrevus or told about any other treatment that helps to stop relapses. my neurologist just kinda went "yea im gettin you started on ocrevus" and is gonna do an MRI after my next ocrevus infusion but ive heard and read about kesimpta and idk i think i would feel m...

Long story short Officially diagnosed 2020 but have had all the issues for over 25 years and neurologist can see old lesions dating back to this time Issues every couple of years then I went back to normal and I was a gym bunny and a runner ( half marathons) Then I had the covid vaccines and ever...

so what happened is in august i was complaining of the lights being too bright,parents took me to hospital, they did a CT scan and couldnt find the problem and then made me an inpatient, did an MRI and were like ah yup inflammation in her brain and transferred me to a diff hospital (atp bright light...

Hi everyone! It’s taken a lot to write this post but I feel I wanted to share. I have been fortunate enough to be diagnosed young and have not experienced many direct symptoms of MS (only tingling feet last year when I got diagnosed). I have recently started Kesimpta treatment and honestly my body h...

Just sat down and the sharp stabbing pains have started in my thigh at the back ....it feels like I'm being pricked with a needle then the shooting pain follows after going Down bk of my right leg and thigh.... the sharp stabbing pains are horrible coz after it happend in my right leg it also happe...

Just when I thought the leg vibrations, buzzing sensation in my right leg was over, it's back. Had them before but it seems to have started up again. My legs, what can I say. Since 2020 has not been the same. Nerve pain first, then the buzzing/vibration sensation, stabbing pain, stiffness and now bu...

Hello all, I was diagnosed in 2015 after a few years of symptoms. I had been on Copaxone 3 per week for some time, took a period of time drug free and was then restarted on Copaxone. I have been spoken to about switching to Kesimpta or Aubagio due to relapses in recent years. I was to avoid any m...

Has MS impacted your sex life? Sex, intimacy and pleasure is hugely impactful to quality of life but let’s be real, for any MSer, discussions about sex can be awkward. In episode 4, Roxy, Emma, Evie, Katt and Shereena talk candidly about MS and sex. Fatigue, numbness, loss of libido, over-sensi...

Is the MS hug/grip/corset feeling something that gets worse over time? Does anybody have this around their middle back? Last year, I started feeling what was a very slight tightness around my middle back. It was only occasional and typically only noticeable after dinner. It only lasted for about ...

I am literally a White CIS Male HAHAHAHAHAHA. Anyways... I don't know how to think or feel about it because it may be just one relapse or another one might be around the corner. I still get brain fog and fatigue at times but it doesn't count as a relapse so... I am DBTing, staying positive and tryi...