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Hello MSers, I haven't posted in a while but I wanted to talk about COVID19. Is anyone else worried about not receiving their treatment? I'm on ocrevus and doctors have stopped my treatment as it can suppress my immune system, however, they have also confirmed that the ocrevus inside my body will ...

Over the last couple of months I seem to have developed a new symptom. I now feel like the inside of my body is shaking but the outside of my body is not! I spoke to my MS nurse and they did not seem overly concerned with this. however, I notice it more and more and it is beginning to drive me slig...

I’ve recently just been diagnosed and have been given the option of which medication I could try out the most promising one is Tecfidera but has some unpleasant side effects and I was just wondering if you are on this medication, how long did the symptoms last or do you still have them?

I hate this disease (and I'm trying hard not to fill this with expletives). I have been with my partner 4 years after 16 years in a pretty miserable relationship. We are very much in love and had (and that really hurts me to say) a fantastic sex life. However, my interest in sex had been declining ...

I've had symptoms for the past 8 years but was only officially diagnosed in February. I thought I was handling it ok - wasn't looking to change anything I'd been doing just maybe not push myself as hard - then Covid-19 hit. Again was ok at the start but now my fatigue is hitting me earlier and earli...

Finding a way to get the human nervous system to grow back the myelin, the nerve covering that MS attacks and causes the symptoms, be they minor or major, we all experience is the next huge hurdle. - I link to a total science paper here: https://www.cell.com/cell-reports/pdf/S2211-1247(20)30611-2.pd...

I am one of those people who has all MS symptoms, but especially loss of eyesight. Anyhow I got a jpb. mostly home work, translation, etc. I told them I have MS but did not tell them I am registered blind. I have done this job for about 4 months. In face to face situations I can fake it, and mostly...

Sorry long post!! Finally got a diagnosis in March this year. Been a long haul from 2013. In the last 4 days I've had excruciating pain in my face and a banging headache. Back in 2013 it was optic neuritis I was diagnosed with but I ended up with more symptoms and everything got worse over the years...

<p>I was diagnosed with MS in 2009. </p> <p>My complaint is my neurologist. She says I have no need for medication at this time and never calls or has me schedule an appointment. She doesn’t listen to my symptoms. I asked many questions and she didn’t answer any.</p> <p>What can I do?...</p>

I need some advice on disclosing my symptoms #symptoms