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My name is SCHULZ ALICE and i am 46 years old . I was born on 19/01/1974 in Carinthia (Klagenfurt)Austria . I grew up there till the age of 20 when i started having Vision problems,Fatigue and weakness,Bladder and bowel dysfunction,Sexual dysfunction,Cognitive problems. Since i was still young i nev...

Hi i am new to this site i am 53 and was diagnosed with RR ms when i was 19 only got told about this site recently nice to find people in the same situation and now what its like hope everyone is fine and safe at this unsure time. I am at the moment ok just sat waiting like some of you to start new ...

gf.me/u/x7wuvv I have Ms / nmo and it is very severe with repeated attacks of optic neuritis and leg weakness At this point I am desperate to try anything Please can people donate Thank you

Hi everyone, I have just read something about brainstem lesion. In 2018 before I started any treatment, I had a brainstem relapse that caused numbness on face and tongue, and reduced hearing. I am quite worried about this, as I believe if you have a relapse in that area, it is a part of the brain...

I just feel right now like the closer I am to an answer, the further away I am. I have been sick for 5 years and have had multiple diagnoses - Vitamin B12 deficient, COPD, Asthma, Vertigo, Adrenal Stress, Arthritis, Depression, just general aging. The thing is no matter what meds I took, it seems ...

Hi my name is Erika Iam 32 years old, I was diagnosed in 2012, am taking tysabri. I got married two years ago( I have a 14 year old son now, doctor said am stable and am good to start planning on having a baby but for that I would have to change my treatment to Ritaxon, I’ve read it’s good to start ...

How much of your immune system do you think is not suppressed? If you know about some research or info I'd love to read. Perhaps 20-40% I'd guess is active seeing as treatment is labeled as causing a low immune system.

I used to get a massage every month as I have chronic pain in my back, with covid Ive not had one for ages but Im concerned because I cant never have a massage ever again. But I'm concerned, you obviously cant social distance when having a treatment unless they are wearing ppe?? Anyone else get tr...

Hi everyone hope all are keeping safe .Just had a letter from the my M.S. Nurse Informing me my Ocrevus Infusion has been rescheduled to July ( original one cancelled due to virus) I was also told I may be more susceptible to the virus and also may be unable to accept a vaccine for the Virus should ...

Hi all, Seeking advice. Has anyone been taken off Tecfidera due to developing lymphopenia? If so, which DMT did you try next, and did your lymphocyte count remain stable with your next choice of treatment for RRMS? Anyone had the same adverse effect happening repeatedly despite trying differ...