Former sports stars Rob Burrow, Stephen Darby, Doddie Weir and Ed Slater are all living with MND. As they campaign for greater awareness, on #BBCBreakfast they reunite to discuss living with the condition ⬇️ https://bbc.in/3LH018m | BBC Breakfast
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Former sports stars Rob Burrow, Stephen Darby, Doddie Weir and E…
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Join the community that believes MND can be beaten. Sign up to become a Cure Finder today. | MND Association
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We need your help more than ever to find a cure for MND. Become a Cure Finder today and see how your support helps researchers on the front line. | MND Association
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🧡 Hear real stories of people living with and affected by motor neurone disease. 🧡 Learn about the work MND Association are doing to end this awful disease. 🧡 Listen and subscribe to the latest podcast episode. | MND Association
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The MND Register of England, Wales and Northern Ireland is a research study funded by the MND Association. It's purpose is to collect information about every person living with MND. The information will help plan the care for people living with MND and tell researchers more about what might be causing the disease. Information such as gender and ethnicity can be used to look for characteristics of people more likely to develop MND. People with MND can take part in the study via the project websit
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LifeArc’s MND translational challenge aims to transform how MND is detected, treated and managed, with the ultimate goal to make the condition treatable by 2030. To find out which research has the most potential to help people living with MND now and in the future, LifeArc would like to put people with MND and those closest to them at the heart of the research decision-making process. To do this they are creating an MND Insights Group and survey team, which we’re excited to be supporting, togeth
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𝐓𝐮𝐫𝐧𝐢𝐧𝐠 𝐭𝐡𝐞 𝐓𝐢𝐝𝐞 A documentary highlighting, promising, pioneering MND research by a team at University College London. The team is funded by the MND Association, LifeArc and the My Name'5 Doddie Foundation. It features Jo and Lucy, who are both living with MND, who share an honest insight into how the disease has impacted their lives. | MND Association
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Alex was diagnosed with MND over 3 years ago. When he sent us this …
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