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Hi , i am 40yrs old and have recently been diagnosed with MS where I had a flare last year, what am confused upon is medication .. how to decide if I really need to be on medication or maintaining a good healthy lifestyle can help me sail through .. very confused and afraid and have no idea how thes...

Regarding to my last post I went to the A&E to get checked out and guess what? It turned out I had Covid 19+ pneumonia and a lower respiratory tract infection😭I genuinely forget I’m immunospurssed sometimes because that combination truly made me laugh out of shock. No wonder I felt so sick AND ou...

Hi - this is a tricky question so not sure how many responses I will get ! Anyone happen to be on a biologic drug for psoriasis or athritis and been prescribed an MS drug that has not conflicted with the biologic ? If so what has worked? I’m newly diagnosed and wish to remain on the biologic but ...

Apparently for pregnant women and older adults only. I'm not an expert, though I wonder why immunosuppressed people are not included like they are for Covid and Flu. Does anyone know? https://www.nhs.uk/vaccinations/rsv-vaccine/

Hey all, I’ve been on Ocrevus for almost five years now with almost no problems - until this year. I had my most recent treatment in February, and since March I’ve been struggling with persistent UTIs, which have spread to my kidneys and uterus, and more recently had to be hospitalised for pelvic in...

I've been diagnosed with MS for 4 years now, first presentation was in 2015 however and it's taken til this year (2024) to find a good treatment. I say good treatment because not only do I have MS but I have other diagnoses too and all other treatments have worsened my symptoms of other conditions. ...

Hey everyone, I've tested positive for covid today. I found out that if you've got MS and/or you're immunosupressed you can get antiviral medication to help overcome covid faster and to help prevent it getting severe. I wasn't told about this from my MS team so thought I'd mention it here for people...

Hi, I was diagnosed with RRMS in April following a relapse where my hand and arm suffered partial paralysis. One month later and I’m much better. I am now at the point of talking treatments with my neurologist but he only gave me two choices: plegridy and a more agressive immunosuppressant which sou...

Has anyone had Coronavirus that won't clear while on immunosuppressants? Coronavirus on me for the second time in about three months, again had Paxlovid, this time it hasn't cleared the coronavirus. two weeks after Paxlovid still testing positive and have symptoms. Any advice on what to try or w...

Good morning, Anyone on tec find they had a constant cough/wheeze/bubble in their chest? I think this is the 3rd time since the start of March and with only a few weeks of having no symptoms. I was never really ill before tec and was aware of the risk of immunosuppression but this is taking the p*s...