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Hi, I'm new to the app. I was diagnosed with RRMS in August 2019 but my journey began in April 2017. I have been very fortunate and have had no relapses since beginning my DMD in October 2019 with my MRIs remaining "stable" since then. I have spent the last 4 days with a severe stomach bug, not...

Hello my name is Penny, was dxed in 2007 with RRMS and what a ride . I have 3 grown children and now 2 Grandchildren, published poet and I make jewelry and sell it to help find a cure for MS

So I have RRMS I find it so difficult because I know I do not have it as bad as people with progressive. Sometimes I just feel like it’s not real in peoples minds, I have head pain 24-7, people just think I can carry on. Just finding it hard at the min. I like to keep fit and use to run a lot but I ...

Hello! I’ve been diagnosed this year with highly active RRMS . My last relapse was July 2024 with a lesion showing as active at C1/C2 level of the spine. It was only sensory (pins and needles neck down) and slowly improved over the months. I still get pins and needles intermittently in the hands. ...

I've been diagnosed since 6th June 2023. Found out because of an accident that happened when me and my then 2 year old was playing a game. He headbutted me directly on my nose/between my eyes. I then started getting tingles in my face, my head and all down my right side. Led to several MRIs and the...

Hi,Im new here so apologies if its already been asked. I was diagnosed with RRMS 2years ago,currently on Kesimpta. Still getting used to spotting relapses- Daily life is tough. Constant dull pain,numbness to hands,painful feet,no balance,flickering eyes,hotness, the list is endless. I was just wonde...

Just a quick note to say hello. Had what I thought was shingles back in May. Fast forward a few months and some MRIs and lumbar puncture and onto a rrms diagnoses (pending one final blood test that we are waiting on). Had call with MS nurse and will meet her in three weeks to discuss what DMT to ...

Hi all, I’m all shiny and new to the app and thought I introduce myself. I was diagnosed with RRMS in April of 2019 (was actually April 1st….of all the days! 🙄) this was after my first relapse where I lost all feeling from my belly button to my toes a few months prior. Second relapse (optic neuriti...

Platform.. Tecfidera (Dimethyl Fumarate) Better efficacy.. ocrelizumab olatumumab Anti cdoz thermypy ?

Hi everyone x How do you handle not feeling supported mentally, emotionally or physically? I live on the other side of the Atlantic from my family. They don’t visit. I’ve made peace with it. If they ever say it I’m like whatever. My mother never really took my MS stuff seriously. But she met a...