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Honesty..... People tell me to be honest about where I am with my ms. I try to do that, but my problem just now is being honest with myself. I am struggling with work. My colleagues are very supportive and they say that they understand, but my thinking is how can they understand when I don't unde...

I started Lemtrada June of 2018, completed May of 2019. It wasn’t an easy treatment. Ms for me began in 1995 (17 years old). Around 29 years of interferons…betaseron and then avonex. Then I stopped dmt’s and tried just diet…..bad idea.🤦🏼‍♂️. With my ms progressing and shouldering from RRMS to ...

So after all the welfare meetings, I was given severance on medical grounds by work, they were very good tbh, kept me in the loop as we couldn't go further really with "reasonable adjustments". So last Tuesday was my last day as they are paying me my notice in lieu along with all my leave which I h...

New here and newly diagnosed PPMS. Still trying to figure out how to take this, and except that my life will never be what it once was or what I dreamed it would be.

New here and newly diagnosed PPMS. Still trying to figure out how to take this, and except that my life will never be what it once was or what I dreamed it would be.

Hi I have PPMS, diagnosed last year. I've just been sent a letter offering me this treatment. Does anyone have any advice or experience that they can share?

Can anyone help with a definitive answer about whether ppms should or shouldn't take a vit c supplement? There's so much conflicting advice! I've read that it can trigger symptoms due to boosting the immune system, but when I recently started ocrevus lots of people were recommended it to prevent inf...

Hi All, I'm new to this forum and glad I've found it as there are many others out there with very little activity. Anyway as the title suggests... I have Primary Progressive MS that was diagnosed in late 2022. However, I also have CML which is Chronic Myeloid Leukaemia which was diagnosed in 2017, ...

If you’ve been diagnosed after a ‘big’ relapse but have experienced ’odd’ symptoms in the past but didn’t know what it was, was this ms then? Does this also mean potentially progressing to PPMS happens quicker because it’s taken a couple of years/ or longer to actually diagnose ms? Hope this makes s...

Feeling soooo much better having now emptied out a wee bit. Last went Monday but not much, then today was immense. Had to share this sorry, not had great bowels since Dx ppms. Also stopped drinking milk in my tea and coffee this week , swapped for oat milk and spearmint tea. Thank you for reading. �...