My wife lived with MND for 5 years. During that time she received a lot of help from our local branch of MNDA and from the MNDA funded team at John Radcliffe. Hence my decision to leave a legacy.

No cure has been found

A cruel, evil disease. A cure has to be found soon to prevent the devastation it brings with it

My husband died from MND in 2013. We had 3 years of great help from the Association & NHS

Linda Piper

We have benefited from support from the MND Association

I am now in a wheelchair. Anything that will help find out more about this disease must be done

The reason that I have decided to leave a gift to MNDA is because a very good friend of mine recently died from MND after a very short time of being diagnosed (about a year) it was awful seeing him go down hill so rapidly and I feel very strongly that mnda needs lots more funds in order to do scientific research with the hope of finding some sort of cure or at least, a drug that will slow it down dramatically especially for the vigorous strain that Geoff was unfortunate enough to get.

I lost my partner of 42years to MND age 62. Also my nephew age 64 to MND

I've pledged a gift in my Will in loving memory of my dear husband, who died 8 years ago from this horrid disease, hoping it will help to find a cure

anonymous

Mark Brazier

Catherine

Mrs Pollard

Hillary

Wendy Buchan

Emma

David Sweet