MS Society UK
@mssocietyuk
We’re here to provide support for people living with multiple sclerosis and drive research into better treatments. Together, we are strong enough to stop MS.
Did you know you can donate your brain & spinal cord to #MSResearch? It’s vital for finding better treatments. 🧠 We spoke to a Research Nurse at the MS Society Tissue Bank so you don’t have to. Find out more: mssoc.uk/3GSNNM6 #WorldBrainDay

Meet Dom 👋 He’s lived with MS for 43 years. Since retiring, he’s focused on volunteering for the East Berkshire group. He reflects on the challenges of keeping the group going. And shares how it’s given him a purpose! Read Dom’s story: mssoc.uk/3U7s32d #MSCommunity

Have you heard of the Spoon Theory? 🥄 For people with MS, managing energy can feel like counting spoons. In this blog, Amy shares how she uses spoon theory to pace herself and make room for rest. Read her perspective on living with MS fatigue: mssoc.uk/4kUjx1i

Fatigue affects people in different ways, and it may change from week to week, day to day, or hour to hour. It’s one of the most common and invisible symptoms of MS, but that doesn’t make it any less real. 👉 Learn more: mssoc.uk/4f2NAm0 #MSFatigue #InvisibleSymptoms
Having MS means living with invisible symptoms, and we know everyone’s MS is different. You don’t owe anyone an explanation for how you manage your MS. 💬 What would you add to this list? Tell us in the comments. Find out more about MS symptoms: mssoc.uk/4kbfEVf

Join us for our using a wheelchair to gain independence webinar! We’ll be joined by Pete Donnelly, a wheelchair user of 19 years ♿ He'll chat to us about wheelchair skills and types of wheelchairs. 📆 Thursday 14 August ⏰ 6.30pm Find out more: mssoc.uk/4o3ZGiZ

Yesterday we celebrated World Brain Day! Problems with thinking can be common for people living with MS. If you’ve noticed cognitive problems, your MS team may be able to help. And there are small changes you can make to improve it 🧡 Find out more: mssoc.uk/46UX1Sr
A marketing manager diagnosed with multiple sclerosis three years ago has pledged to raise £30,000 for research into the condition. Jason Winter, who has treatment at K&C, works for @TTGMedia who have chosen @mssocietyuk as their charity for the year: ekhuft.nhs.uk/news/jason-s-f…
Tomorrow, we'll be sharing the Alliance's Digital Tools Workshop 🧡 The webcast will discuss how technological tools could speed up research. From wearable devices to the technology delivering treatments. We'll share the live stream on our Facebook page from 4pm. #MSResearch

Today we’re celebrating #WorldBrainDay! 🧠 We met with Rory Türkmen-Smith, the Engagement Manager at the MS Society Tissue Bank. He took us on a tour to show us the vital work they do to help us understand more about the brain and MS. #MSResearch #MSAwareness
Join us for our monthly Progressive forms of MS peer group! This will be a chance to chat to others and share tips. We’ll discuss ways to help you manage your wellbeing, mental and physical health. 📆 Tuesday 22 July ⏰ 6pm Find out how to register: mssoc.uk/4lxnABJ

Some people living with MS might experience pain at some time. But drug treatments and therapies can help. Lhermitte’s sign is a sudden brief pain or buzzing sensation. It can be triggered when you bend your neck forward, or cough or sneeze. Read more: mssoc.uk/4eXhRmo

Patients will be connected to specialist charities as soon as they've been diagnosed with a long-term health condition, starting next year. This new service means expert advice, emotional support and practical help from day one, alongside NHS care. More: gov.uk/government/new…
Are you a good listener? Could you spare one or two hours a week to provide support to those affected by MS? If so, the MS Helpline team would love to hear from you! 📞 Find out more information about becoming one of our Befriending Volunteers: mssoc.uk/46cUP8P

Join the Progressive MS Alliance for a new webcast on Wednesday 23 July all about digital tools 🖥️ The workshop will cover the hope for technology to speed up MS research. And deliver better treatments. We’ll be showing the live stream on our Facebook page at 4pm. #MSResearch

Join our free virtual webinar! 💻 You'll find out more about applying for Personal Independence Payment (PIP), or Adult Disability Payment (ADP), and the best way to prepare for your application. 📆 Thursday 24 July ⏰ 6.30pm 🔗 Register now: mssoc.uk/4lgtKWS

In April, we announced the launch of the Northern Ireland MS Research Hub 🔬 We chatted to Professor Denise Fitzgerald to talk about the Hub’s goals. And the benefits of collaboration between clinicians and scientists. Find out more: mssoc.uk/463SI79 #MSResearch

Hot weather making your MS symptoms worse? 🥵 Our free 'I have MS' card can help explain your condition if you're feeling unwell or need support while out and about. Order or download yours here 👉 mssoc.uk/4jw7xmP
