Motor Neurone Disease Association

MND is a rapidly progressive and fatal disease that affects around 5,000 people in this country alone at any one time. In the UK, five people a day die from MND.

Life expectancy for most people is just two to five years, and around half will die within 14 months of diagnosis.
MND leaves people unable to walk, talk or feed themselves. People with MND can still think and feel but their muscles refuse to work.

The MND Association is the only national organisation in England, Wales and Northern Ireland dedicated to supporting people affected by MND and funding research into the disease, so that one day we will achieve our vision of a world free of MND.

We support 18 Care Centres; provide a free equipment loan service, a national information service called MND Connect (08457 626262), a network of 25 Regional Care Development Advisers and the support of over 350 trained volunteer Association Visitors.

But promoting research and providing care are expensive commitments and it is essential to have a firm, financial base in place to support them. We rely on voluntary donations of which legacies are a vital part.

Of course, decisions regarding Wills and legacies are very personal and not to be taken lightly. This is why we have produced a Legacy Information pack.

To request your pack you can call us on 01604 611860, visit our website at www.mndassociation.org/legacies or email legacies@mndassociation.org.

Thank you.