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In 2014 my Nan was diagnosed with Motor Neurone Disease. At the time I had no idea what the disease was and after some research I found that it is an incurable, muscle wasting disease which eventually prevents the ability to grip, walk, speak, swallow and breathe. 

The Motor Neurone Disease Association is the only national charity in England, Wales and Northern Ireland focused on MND. The charity aims to improve care and support for people with MND, their carers and families, fund and promote research that leads to new understanding and treatments and brings them closer to a cure,  and they campaign and raise awareness for the needs of people with MND.

All donations would make a huge difference, thanks!