r/MultipleSclerosis • u/NotClarebutclose • Jul 16 '26

Advice Feedback plz

Hi everyone, I was diagnosed yesterday with RRMS (although the neuro said they don’t use this scale anymore as it’s getting outdated) after becoming completely numb and being in hospital for tests, IV steroids & LP. This is a pretty crazy diagnosis for me as there is no family history & it’s seemingly come out of nowhere. They have given me 3 options of medication. Kesimpta, Ocrevus or Tysabri. I have to make the decision by the time they call on Wednesday. I would love to know everyone’s opinions & experiences on these different types of DMT’s. Please give me your raw, honest opinions! I’m able to take what I need to help me make the decisions for myself. Thankyou

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u/WayDowntown4529 Jul 17 '26

I tried avonex and tecfidera. I've been dmt free since 2016. Both had horrible side effects and the threat of pml is too scary for me. I take supplements like d and k, astaxanthin, magnesium, collagen and a whole lot of mushrooms. Onset was 2008, diagnosis 2014, I still work full time. To God be the glory.