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Good evening all, I’ve been on ocrevus since 2019 and only this year my neuro has told me that my body fights the DMT and is likely creating antibodies against ocrevus. Due to this I have to have ocrevus every 6 months and not push it any longer. I looked back at my b cells from when I started a...

I’m in mourning for my brain this week as I’ve had to make the decision to go for medical retirement after 11 years of continuing to work with MS chewing away at my cognitive function. Recently been retested at neuropsychological service and the decline was shockingly apparent. Even having the OT co...

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I'm just sharing some thoughts here and I'm curious about other people's opinions! So, we may all know that Christina Applegate did a red carpet in the past couple days with a cane that had "FUMS" all over it. Which I respect but it's not for me. The "MSWarrior/Fighter" and the " FUMS" mentality isn...

Hello I am a mum of two boys . My m.s is very active and I'm on alot of medication. My oldest son is going through assessments for asd and adhd. But I really struggling to come with my health aswell as my son... any advice would be great

Has anyone noticed black tea to ease ongoing sensations? I’ve had pins and needles in my hands since diagnosis this feb and only once experienced full return of feeling in my body (not sure why and only for a number of hours), after accidentally drinking a iced peach drink with black tea (I usually ...

i was with my partner for 16yrs she got diagnosed with ms about 7 yrs ago .as the ms progressed we were starting to always fight and between work and looking after her and the fights i burnt myself out and we called it a day as i couldnt take the arguing anymore.the first few months were really hard...

Hi there, has anyone applied for or has successfully got a medical exemption certificate for the covid 19 vaccines ? Please pm me if you can! Kindest regards and happy new year everyone, #fightms