MS Society Surrey

Howard donated his tissue to the MS Society Tissue Bank. We sat down with his daughters, Hannah and Charlotte, to find out what they would say to someone who is thinking about giving to the MS Society Tissue Bank. 🧡

Dog Walk for Dosh! Join the MS Society Surrey team at the Big Charity Fund Raising Walk on Sunday May 17. We will supply t-shirts and fundraising support. Email Helen.Bell@groups.mssociety.org.uk for more information.

We did it. Together. After 10 years, the Stop MS Appeal has reached its fundraising target — raising £101.9 million to drive life-changing MS research. We want to thank you, our wonderful supporters for making this happen.

The UK Government has announced the PIP review steering group members. We’ll campaign to make sure the review understands the reality of living with MS so we can improve PIP. Get involved: mssoc.uk/4taCXV7

What’s one thing you wish more people understood about living with MS? We asked our community this question and this is what they said. Do these sound familiar to you? If you need support, our MS forum is here for you. 🧡 Find out how to register here: mssoc.uk/3PBvzQ2

If you need support over the festive season, we want you to know you’re not alone 🧡 Our MS Helpline will be closed from 5pm on 24 December and reopens at 9am on 2 January 📞 But our forum is open for anyone affected by MS 💻 Sign up to get support: mssoc.uk/3PBvzQ2

Muscle weakness is one of the most common symptoms of #MultipleSclerosis and makes everyday tasks like opening jars or walking difficult. Check out causes behind muscle weakness and tips that may help improve #MuscleStrength here:mymsteam.com/resources/musc…

Reserve your free place today bit.ly/4pDCbgC

Yinka’s MS Letter 💌🎥 “Life dealt a big blow to you with this diagnosis. You’re dealing with pain and spasticity, and you’re finding it harder to walk.” While Yinka faced an uncertain future, she tells us about adapting to life after her MS diagnosis. ⬆️ #MSLetters

🙌 Huge thanks to @katrinamurray71 for speaking up in Parliament this week on the need for faster diagnosis and better access to specialist MS care.

Asking an MS researcher your questions! 🎙️ 🔍 Why does MS research need more money? 🔍 What excites you about the ChariotMS clinical trial? 🔍 What are the most promising treatments being researched right now? Dr Tarunya Arun answers your questions. ⬇️

Join us for our Understanding your new diagnosis of MS webinar! We’re partnering with MS Together to cover what MS is, the support that’s available and looking after your physical and mental health 🧡 📆 Thursday 27 November ⏰ 6.30pm Find out more: mssoc.uk/47Hr9RB

📢 The Government has launched its review of the PIP assessment. The review will be led by Sir Stephen Timms MP together with disabled people and experts. We welcome the review, but it must stay focused on improving PIP — not cost-saving. Learn more: mssoc.uk/47UCKMY

Lyndsey tells us how there weren’t many treatments available when she was diagnosed with MS. But the treatment landscape is changing thanks to your generous donations. 🔬 She shares her reasons for leaving a gift to us in her will. Find out more: mssoc.uk/46vSDZM

Join us for our Finding your way: adapting to life with MS webinar! We’ll cover understanding your MS, what adapting looks like to you and strategies to manage adjusting to life with MS 🧡 📆 Wednesday 12 November ⏰ 6.30pm Find out more: mssoc.uk/47hgpsZ

For women living with MS, making the decision to start a family can be tricky 🤰 Actress Bianca Gruffudd shares her experiences of pregnancy. She tells us what she considered before deciding to have a baby. And how her pregnancy has impacted her. #MSCommunity

Did you know that eye problems are common in people living with MS? 👁️ People with MS can find that they suffer with optic neuritis, double vision or involuntary eye movements. Find ways to manage vision problems and MS: mssoc.uk/3KA7YQx