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The Scottish Medicines Consortium (SMC) has announced cladribine (Mavenclad) will be available for people with ‘active’ relapsing remitting MS. Until now it could only be prescribed in Scotland for ‘highly active’ RRMS. #MultipleSclerosis #MSTreatments buff.ly/t5KsX82

It’s Carers Week! This year’s theme is ‘Caring about equality’, highlighting the inequalities unpaid carers face. If you care for someone living with MS, you might find that you neglect your well-being. Read our info on available support: mssoc.uk/455jPhF #CarersWeek

Are you joining us for one of our MS Walks? Our Ambassador Scott Mills tells us why he'd love you to join him on 14 June for our MS Walk Birmingham! Walk, roll or stroll to help raise awareness and funds for MS research 🔬 Find an MS Walk near you: mssoc.uk/4cAPrNS

Yesterday, we hosted a roundtable in Parliament with the MS Society UK to discuss how to support people with MS to thrive at work. We were delighted to be joined by Sir Stephen Timms (Minister for Disability), Danny Kruger (Shadow Minister) & colleagues. (1/5)

It’s Carers Week and we’re celebrating carers! Meet Simone 👋 She cares for her husband Nikoma who lives with MS. She tells us how they’ve adapted to his MS diagnosis. And shares her tips for looking after her wellbeing. Read more here: mssoc.uk/4jBVUtJ #CarersWeek

Soon, the Bill that paves the way for changes to disability benefits will come to the UK Parliament. 📩 Send a postcard to your MP calling for them to protect disability benefits. Disability benefits are a lifeline, not a luxury. Send a postcard 📢 mssoc.uk/3SLRAx2

Our MS Walk Birmingham is tomorrow 🧡 To all our supporters walking or rolling, we're wishing you the best of luck! And if you'd like to join us for a future MS Walk, we've got events happening all over the UK. Find out more: mssoc.uk/4cAPrNS #MSWalkBirmingham #MSWalk

It’s Carers Week, and we’re celebrating unpaid carers 🧡 Do you care for someone living with MS? It’s really important to look after your own mental and physical health. What do you do to unwind? Share in the comments and let's support each other! #CarersWeek

Join us for our monthly Move More with MS session. Facilitated by our Physical Activities Specialist Shahida. 🧡 You can discuss the benefits of keeping active and connect with others who also understand MS. 📆 Monday 16 June ⏰ 6pm 🔗 mssoc.uk/4e1Nzyp

On 5 July, we’ll be marching in the Pride in London parade, and we’d love for you to join us! 🧡 We’ll be marching with our community and colleagues. And we’ve worked with the parade team to improve the experience for our people! Find out more: 🌈 mssoc.uk/3S7QxqY

We’re wishing all the fathers in our community a very happy Father’s Day! Say hello to Gil 👋 He shares how he’s adjusted to living with MS. And how he hopes that his kids learn to live life to the full 🧡 Read Gil’s story here: mssoc.uk/45hAVJf #HappyFathersDay

Previous research has found no effects of vitamin D on MS. But a recent study has looked at how people with early signs of MS respond to high dose vitamin D supplements. And if it could have an impact on relapses and new lesions. Read more: mssoc.uk/441vkVj #MSResearch

Will you join us at Pride London on Saturday 5 July? 🌈 We’ll be joined by our community and colleagues as well as other neurological charities. And we'd love for you to join us too! Find out how you can march with us: mssoc.uk/3S7QxqY #Pride #PrideLondon

Is it hot where you are? ☀️ We know MS symptoms can get worse for many people when they're hot. And over 60% of people with MS say they experience heat sensitivity. Read community tips for staying cool in the heat: 🔥 mssoc.uk/4e6JsB0

Yesterday, the government took the first steps towards passing its Welfare Bill in parliament. The Bill's first reading takes us closer to cuts to disability benefits. ❌ Send a postcard to your MP ask them to stop the cuts: 📩 mssoc.uk/4l5xD0r #DisabilityBenefits

Did you join us at MS Walk Birmingham? We caught up with Scott Mills, Sam Vaughn and Teddy to see how they got on with their MS Walk! 🐾 We also chatted to Melissa, who has been living with MS for 20 years. Join us and find an MS Walk near you: ☀️ mssoc.uk/4cAPrNS