MSCroydon

Our volunteers provide information, support (practical + emotional) and events for people affected by MS.

[Multiple Sclerosis Neurologist dr Agne Straukiene @AgneStraukiene]

🚨 New Episode Alert! 🚨

This week on BeeWellWithMS, I chat with top UK MS Nurse, @amyharbour7. From managing MS symptoms & patient support to compassionate care & holistic health, Amy’s insights are a must-hear. 🎧 https://t.co/qNHiX9YFPw

👉 Listen now & share! #MultipleSclerosis #MSNurse #BeeWellWithMS #PatientCare

[MSTrust @MSTrust]

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
https://t.co/4QYemestEu

[Beacon for Rare Diseases @RareBeacon]

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: https://t.co/uDTZV2hDmH

[MS Society UK @mssocietyuk]

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 🚂 https://t.co/az3RkT8qbV

[MSTrust @MSTrust]

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:

https://t.co/JXbyzrDekD

[MS Society UK @mssocietyuk]

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 ➡️ https://t.co/H5iQgctNna

[MS Society UK @mssocietyuk]

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: https://t.co/hWvxe6NzCK

[MSTrust @MSTrust]

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

https://t.co/x5UbPQifOu

[MS Society UK @mssocietyuk]

"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 ➡️ https://t.co/IWa7j4GD1G

[MS Society UK @mssocietyuk]

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 ➡️ https://t.co/kpraWmSQ92

#MSHistoryMakers

[MS Society UK @mssocietyuk]

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
💻https://t.co/JwGGc9u1kc

#Budget2024

[MS Society UK @mssocietyuk]

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: ⏩ https://t.co/2qy9iijQaH

[MS Society UK @mssocietyuk]

On Wednesday the Chancellor @RachelReevesMP 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: https://t.co/UkXoATYCnR

#Budget2024 (1/2)

[MSTrust @MSTrust]

Dale share's his experiences on work, MS and finding a purpose.

#MS #MultipleSclerosis #MSAwareness #MultipleSclerosisAwareness #InvisibleIllness #ChronicIllness #Health #AutoImmune #AutoImmuneCondition

[MS Society UK @mssocietyuk]

📢 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

[MS Society UK @mssocietyuk]

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

https://t.co/21Z80bcw1q

[MSTrust @MSTrust]

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.

https://t.co/LJcDtdmcOQ

#MultipleSclerosis

[MS Society UK @mssocietyuk]

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: https://t.co/dkS7HEmgIc

[MSTrust @MSTrust]

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.

https://t.co/jdSywdoR4M

[MS Society UK @mssocietyuk]

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: https://t.co/OvS13gtQrK