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Hi everyone, new to all this but thought I'd be brave and post! I was diagnosed just as covid kicked in and progressed very quickly unfortunately, I'm struggling a wee bit with all the massive life changes, gone from being a fiercely independent workaholic to having my husband help dress me, in a wh...

I started intermittent fasting a few months after my diagnosis,my diet switched to heavy on the veggies,and i run away from any stressfull people and situations ,i work out and keep a positive outlook,at this point no one even beleives i have m.s,i do not know if everyones outlook is the same ,a bit...

Is anyone else using this? There is a lot of research out there about how red and infrared light therapy can have positive effects on a range of different biomarkers. I am using a small red light panel for about ten minutes a day alternating between my chest and back each day. Whilst it is a nice ...

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...

VERY INTERESTING FACTS ! ! Dead Penguins - I never knew this! Did you ever wonder why there are no dead penguins on the ice in Antarctica ? Where do they go? Wonder no more ! ! ! It is a known fact that the penguin is a very ritualistic bird which lives an extremely ordered and complex life. Th...

If the title of this post jumped out at you, we should talk. I’m wondering if anyone else has experienced this full body long-term rash. It seems to be related to hyper T cell, which makes me suspicious of B cell depletion therapy like Ovrevus.

It seems everyone these days is on Ocrevus I’d like to try it but my HMO insurance doesn’t cover it (in the US). The closest my plan gets is Rutiximab. Not sure why other than cost (currently I’m on a generic version of Tecfidera) doing okay but fear it’s not “highly effective”. My HMO is convenie...

Hey there, newly diagnosed and awaiting starting treatment. I have been reading some of the posts here and it's really nice seeing others who understand how it feels to be in pain all the time and all the other feelings that come with MS. Thank you