Living with Motor Neurone Disease (MND) comes with challenges, and one challenge can be eating and drinking due to muscle weakness 🥪🥤 Rhea Sutcliffe our Motor Neurone Disease (MND) Care Co-ordinator at Marie Curie Hospice, Bradford suggests ways to help. 🔗 For more information visit mariecurie.org.uk/information 📞 If you need support now, call our free Support Line on 0800 090 2309 #MNDAwarenessDay #MND #MotorNeuroneDisease | Marie Curie UK
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Living with Motor Neurone Disease (MND) comes with challenges, an…
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Imagine being told you have around 1,000 days left to live. You are then told it will take 375 days for vital home adaptations. For Nikki, Katy and many people with MND, this is not a hypothetical. It is real life. You can help change it. 👉 mndassoc.org/unlockthedoor | MND Association
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Imagine being told you have around 1,000 days left to live. You are the…
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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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With your help, more people living with MND could have the chance to take part in groundbreaking research. We know the lengthy process can rob you of precious time you could be spending with your loved ones. Our new first-of-it's-kind MND Association Research Nurse Network will help connect more people living with MND and our pioneering researchers. Learn more: mndassociation.org/network | MND Association
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Rob Burrow: Living With MND – a brand new BBC Breakfast documentary. An intimate film about a love, support and determination. Tuesday 18th October, BBC Two at 7pm ⬇️ | BBC Breakfast
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This is Jennie's story. She is living with MND. Join us this month and help #TakeOverMND so we can be there for more people like Jennie. Find out more here: mndassoc.org/jennie | MND Association
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