Happy Halloween! 🎃 Phoebe was diagnosed with relapsing remitting MS (RRMS) in 2020. She got crafty and shared with us her ‘Haunted House of MS’. 👻 In Phoebe’s house, she’s visited by symptoms like fatigue, spasms and double vision. Whether your MS has given you a trick or a treat today, we’ll be there to support you. 🧡 Find support for your MS symptoms on our website: https://mssoc.uk/3UQiJA1 | MS Society UK

I don’t follow the perfect diet. I follow the one that actually fits my life...and spoiler? *I'm still stable* Almost a decade after being diagnosed with Relapsing Remitting Multiple Sclerosis. Listen, I tried the whole “do it exactly right” thing: 🥦 Every checklist 🥕 Every MS Diet rule 🥬 Every supplement you could spell without vowels And every time I slipped up? I told myself I didn’t have what it takes. But here’s the truth I wish someone told me sooner: 💥 You don’t need a flawless protoc

Many people living with relapsing MS say making treatment decisions can be complicated. Deciding whether you want to treat your MS, or how, can depend on many factors. It’s as individual as you are. Our Treatment Stories is a series of honest accounts from people with MS about how they made that decision. Below is a trailer – watch our full, interactive films here: https://mssoc.uk/2LVDdTa | MS Society UK