Andrew & Rosaleen's fundraiser for the MNDA
Fundraising for Motor Neurone Disease Association
Fundraising for Motor Neurone Disease Association
Story
After Andrew was diagnosed with MND/ALS earlier this year, we're now running and walking a combined 60 miles over August to raise awareness and funds for the Motor Neurone Disease Association (MNDA). MND is today incurable and life-shortening, we aim to help change that!
What is MND?
With MND, messages from the motor neurones gradually stop reaching the muscles. This leads the muscles to weaken, stiffen and waste, which can affect how you walk, talk, eat, drink and breathe. As stated, MND is life-shortening and there is no cure.
Who are the MNDA?
The MND Association focus on improving access to care, research and campaigning for those people living with or affected by MND in England, Wales and Northern Ireland.
Please donate whatever you can to support the important work the MNDA does for those living with MND, and their families/friends/carers. Also please join us for runs if you're up for it - we'd love the company.
Thank you for supporting us, now it's time to fly!
* Charities pay a small fee for our service. Find out how much it is and what we do for it.