This MS Awareness Week, Shift.ms have partnered with MS Society, MS Trust, Neurotherapy Network, Overcoming MS, MS Together and MS-UK to launch the #MSUnfiltered campaign. Together, we're dropping the filter and getting real, shining a light on those not-so-glam symptoms. Have you had any symptoms...

Hello all, on this sun-drenched-friday-afternoon. But in spite of the weather, i'm so angry. Just now my partner told me that the newest workshops we are setting up, are given to another teacher. By him, btw. I have made such an efford to prepare the whole technical side, not to mention i have the p...

Hi all, I have a question. Is there anybody on a treatment that is working well for them and they can see and feel a good improvement in their situation. Personally I'm not on any medication at the moment only a daily vitimum d supliment tab. KESIMPTA OR OCREVUS ANY GOOD?? Good days and bad days ar...

Hey 👋 Welcome to the Shift.ms community! Drop a comment below and let us know where you're from 👇 Whether you've got MS questions, you're seeking advice, or you just want to chat to other MSers, we've got you covered 💚 Take a minute to hear Sarah's MS story and learn how she gets the most out ...

We’ve just launched Shift.ms polls! Take part in the first poll below👇 *Bonus points if you can leave a comment and let me know: are you happy with how long it took?

Hey everyone, does anyone lift? I actually started lifting before my diagnosis but after I started having symptoms, in my attempt to be healthier to see if things got better on their own (turns out going to the gym is good to have better balance, but you will still pee yourself at night on occasio...

Evening all, For the past week I've been suffering from a really stiff and painful lower back that spreading up. Back feeling super tense and achy. Could this be MS linked muscle stiffness or is it just poor posture? It's come on really suddenly and just can't shift it... any advice?

Hi all, I’m struggling to find a comfortable shoe/boot/trainers. I need support but heavy footwear doesn’t suit me

Morning 👋 I’ve had RRMS since 2011 and it’s only ever caused sensory impairment to my hand. Until a year ago when my walking started to be impacted, occasionally. That ‘occasionally’ is now pretty much all of the time and I use a stick. Consultant thinks I’ve probably moved to SPMS (was not in my...

Hello everyone! Newly diagnosed with MS here, I got a gum sore the other day that has yet to resolve itself. The first few days couple days were okay, but, now it's quite painful, brushing teeth on that side hurts, so I avoid that side where the sore is, I tried a topical "freezing" protective-lay...