We are just over halfway through #DisabilityPrideMonth! We spoke to #MSWarriors, Carly and Ekow about what Disability Pride Month means to them both. They told us that no matter what your disability is, you should always have pride in yourself. We couldn't agree more 🧡 You can read our interview with Carly and Ekow, where they tell us about their MS journey and how they use their wheelchair's together here: https://mssoc.uk/4f5RgmB
MS Society
Non-profit Organizations
We’re here to provide support for people living with multiple sclerosis and drive research into better treatments.
About us
We’re the MS Society – a community of people living with MS, scientists, campaigners, volunteers and fundraisers. 130,000 people live with multiple sclerosis in the UK. Every one of them shares the uncertainty of life with MS. We understand what life’s like with MS, and we support each other through the highs, lows and everything in between. And we’re driving research into more – and better – treatments. For everyone. Together, we are strong enough to stop MS.
- Website
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http://www.mssociety.org.uk
External link for MS Society
- Industry
- Non-profit Organizations
- Company size
- 201-500 employees
- Type
- Nonprofit
- Founded
- 1953
- Specialties
- MS Care and Support, Fundraising for MS, and Research for MS Treatments and Cures
Locations
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Primary
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8 City North Place
Carriage House
Finsbury Park, England N4 3FU, GB
Employees at MS Society
Updates
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People living with MS in England, Wales and Northern Ireland who are currently receiving the drug ocrelizumab via an infusion can now be offered an injection that takes just ten minutes. Ocrelizumab is a disease modifying therapy (DMT) for active relapsing MS or early primary progressive MS. It can be taken as an intravenous infusion and after starting with two infusions close together, you can take ocrelizumab just every six months. Now you can also take it as an injection once every six months. This method will expand the choices available to many MS patients and will mean more people can receive this treatment in a way that suits them. We've updated our Ocrelizumab information page: https://mssoc.uk/4bHXczt
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"The thing I love most about volunteering is feeling like I’m giving something back and helping other people. To anyone thinking about volunteering, I say do it! You’ll make new friends for life and the satisfaction is contagious." Simon’s been volunteering with the Yeovil and Sherborne District Group since 2013. He tells us how joining his local group has given him friends for life and opened up new opportunities. Find out more about Simon and his experience volunteering with us: https://mssoc.uk/4cY0rE4
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"As a Support Volunteer, I often speak to people who are reaching out for help for the first time. As I know how difficult this can be, I’m able to listen, empathise and offer practical support whenever possible." Lynn is a Support Volunteer at our Hinckley and District Group. She tells us how she got involved, and how helping others has enriched her own life. Find out more about Lynn and how you can get involved in volunteering: https://mssoc.uk/3xRISqg
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Hey Marks and Spencer, Matalan and John Lewis & Partners - we had to improvise a little, what do you think? We're the MS Society, here for everyone affected by multiple sclerosis across the UK. #MSSocietyUK #MarksAndSpencer #JohnLewis #Matalan #Primark #MSAwareness
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Already over 13,000 of us have signed our open letter calling on Keir Starmer, our new Prime Minister, to commit to deliver change for people with MS. Thank you! There's still time to add your name - it's time to make MS a priority! 📢 Please sign our open letter today: https://mssoc.uk/4acNJiE
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"CBT has been like an awakening in me. It gave me some coping tools and has helped me lots." When Fiona started to struggle with her emotions she reached out and got some help. With the help of a CBT therapist she’s learnt tools and strategies to help her deal with the bad days. She spoke to us about her experience with CBT, and how it has helped to retrain her mindset. Find out more about Fiona's story: https://mssoc.uk/4cV5Coi
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What a great couple of days we had in Liverpool for #MSFrontiers 2024! From presentations by early careers researchers to lectures looking at the future of MS research. A massive thank you to everybody who attended and presented their research to make it such a great event.
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Wow! What a brilliant couple of days we have had at MS Frontiers 2024 in Liverpool! Yesterday kicked off with a keynote lecture by Professor Jennifer Graves, who discussed the impact of age on MS. We also presented the poster prizes along with 4 flash talks from researchers. Check out what we've been up to below 👇
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It’s official: Keir Starmer is our new Prime Minister and the Labour Party are forming the government. No matter how we voted as individuals, we all know that people living with MS deserve better. During the general election, we made sure MS was part of the conversation. Together, we sent thousands of emails to candidates across the UK. And over 11,000 of us signed our open letter to the Prime Minister. As Keir Starmer settles into his new office to decide his priorities, now’s the time to raise our voices even louder. We won’t stop until all our voices are heard.