Motor Neurone Disease (MND) can leave people locked in a failing body, unable to walk, talk, eat and eventually breathe. It has no cure. For far too long the story of MND has been the same. Too many people facing MND alone, too many families torn apart – too many people losing loved ones before their time. But at the MND Association we’re fighting back. We’re focused on improving access to care, research and campaigning for people living with or affected by MND in England, Wales and Northern Ireland.
Our powerful network of volunteers, members, partners and staff provide information and support for people with MND, their families and carers. We fund and promote research that leads to new understanding and treatments, and brings us closer to finding a cure. We campaign and raise awareness so the needs of people with MND are recognised and addressed by wider society.
MND is relentless. And so are we.
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