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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

Posted this before, but it was so long ago it's been lost to the ether....

I am off to the London Marathon tody to support my friend Anjali Silva. Anji has MS and is doing the full 26+ miles using a rollator for support. She will be walking for approx. 8-hours. What an amazing warrior, never give up and always try to fight MS in any way you can. Anji is doing the marathon;...

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...

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...

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

Hello Shift.MSers. I was diagnosed with early PPMS (male, 28) in july, 4 months after breaking up with someone I still love. The break up was slow, painful, emotionally violent. Today I went for a drink with this person, mostly to share my MS diagnosis and my treatment plan with a newly approved...

Hi, I'm Sharon, was diagnosed back in November 2007 (nearly 11 years!). It's been a rollercoaster. There's been highs: one when I got back on my motorbike, another when I started a round the world trip. And many lows: like when I had to come home 2 months into the round the world trip and when I ...