Medical gaslighting, myths, barriers to care, and limitations to our understanding of how MS functions... 🔬 #MSHistoryMakers Alison Thomson, Roxy Murray and Rawda caught up to talk about the importance of EDI in MS research. 🎙️ Listen now: mssoc.uk/4gCtYWc

Core stability muscles, or postural muscles, are the deep muscles in your abdomen, pelvis and back. It is important to have good core muscles to help you maintain a good posture. Good posture can help prevent pain, pressure sores or reduced mobility. pulse.ly/ekchdjkzin

If you have MS, it’s likely you’ve experienced that overwhelming feeling of tiredness that defines #MS fatigue. We put your questions on fatigue to occupational therapist, Kate Hayward. 🔗 Head to the link below to find out more. pulse.ly/ow8nmf2rdh #MultipleSclerosis

Around 75% of those living with MS are women. Most people living with MS will go through the menopause after their diagnosis. PhD student Imogen is aiming to improve support for women experiencing menopause and MS. Learn more about our #MSHistoryMakers: mssoc.uk/3AsivZ4

We caught up with Jay, diagnosed with MS in 2019, to hear about how she navigates movement and her MS on a not-so-easy day We’re supporting We Are Undefeatable, a major campaign to inspire people living with long-term health conditions to get more active mssoc.uk/3JjvT1W

📢 The government have announced changes in their Autumn Budget that will impact access to healthcare and financial support for people living with MS. We’re breaking down the two key areas that could make the biggest difference for our community.👇 #MSSociety #Budget2024

Dale share's his experiences on work, MS and finding a purpose. #MS #MultipleSclerosis #MSAwareness #MultipleSclerosisAwareness #InvisibleIllness #ChronicIllness #Health #AutoImmune #AutoImmuneCondition

On Wednesday the Chancellor Rachel Reeves delivered the autumn statement setting out the UK Government’s tax, borrowing and spending plans for the next 12 months. ➡️Read more about what it means for people affected by MS: mssoc.uk/4e9Mp2k #Budget2024 (1/2)

The benefits system can be complex – if you ever need help finding out about how it works and what benefits you are entitled to then you can contact our MS Benefits Advice Service: ☎️0808 800 8000 💻mssoc.uk/4e34nn7 #Budget2024

Rae, diagnosed with relapsing MS in 2004, is a writer and theatre maker from Birmingham. 🎭 This autumn Rae’s autobiographical play 'Bright Places' is touring England. We caught up with Rae during rehearsals to find out more about the show: ⏩ mssoc.uk/3C7ZfRr

Meet Dr Rebecca Sherrard Smith, just one of our amazing #MSHistoryMakers. She tells us why MS research is a subject close to her heart. And how she’s aiming to deepen our understanding of the underlying causes of MS. 👉 Read more about her research: mssoc.uk/4eiy8Av

Sex, intimacy and MS: a guide for men – UPDATED and BACK IN STOCK. You can order copies through our shop, where you can also find our guide for women. #MS #MultipleSclerosis #ThisIsMS #MSTrust #MSSex pulse.ly/x1xc2ehqze

"If I don’t get involved, I can’t make a change." 💬 Tony was diagnosed with MS in 1990. He's taking part in the groundbreaking Octopus trial and tells us why trials are so important for the future of MS treatment. Read about #MSHistoryMaker Tony ➡️ mssoc.uk/4fdxoxN

We’re closer than ever to stopping MS for everyone. Will you help change the future of MS by supporting our Christmas appeal? Find out how you can make history and #StopMS ➡️ mssoc.uk/3NYWswc #MSHistoryMakers

In this webinar, Nikoma and Simone will be having a discussion about how MS can affect intimacy in relationships. And how couples can navigate these challenges.🧡 They’ll be open about their experiences of #MS, relationships and intimacy. Sign up ➡️ mssoc.uk/4fcHbE8

Disclosure is key to managing #MS at work - Suzanne "Telling colleagues was hard as I didn’t want to be treated differently. But it was the right decision, people were understanding and I was able to keep working." Read Suzanne's story: pulse.ly/j5znij44qv

Mary lives with secondary progressive MS (SPMS) in West Yorkshire. Recently, she and her husband took a trip around Scotland by train. 🏔️ Mary tells us about their adventures and her experiences of travelling by train with a wheelchair 🚂 mssoc.uk/3NZrSCX

Submit your poster abstracts for #iDR25! 📢 Whether you’re a patient group representative, researcher or industry professional, you’ll get the chance to showcase your work to professionals in the drug repurposing field. 👉 Find out more: ow.ly/f0im50U0eqh

🚨 New Episode Alert! 🚨 This week on BeeWellWithMS, I chat with top UK MS Nurse, Amy Harbour. From managing MS symptoms & patient support to compassionate care & holistic health, Amy’s insights are a must-hear. 🎧 beewellwithms.com 👉 Listen now & share!

Please help build a picture of treatment, care and support for people affected by neurological conditions throughout the UK and the Republic of Ireland. Complete My Neuro Survey 2024. #MyNeuroSurvey #MS #MultipleSclerosis #MSAwareness #MSTrust pulse.ly/tcnfxbgwx2