Our son Alex Ward was committed to public service and helping others. In February 2020 he was diagnosed with an aggressive form of MND, caused by a gene mutation. He rapidly lost the ability to walk, eat, speak, move, and finally breathe. In July 2020 he passed away, aged just 31. MND is more common than you think - affecting 1 in 300 people over their lifetimes.

We are raising funds for ground-breaking Gene Therapy research  into Motor Neurone Disease (MND) to help end MND. 

This funding is being done via the My Name's Doddie Foundation, a charity set up by Doddie Weir which is focussed on finding a cure for this cruel disease. They will expedite our funds being utilised in the best way possible and according to our wishes.

You can learn more about Alex here: www.alexwardfund.org