Story
Little Noah Mitford went into heart failure and passed away shortly after his second birthday. Noah had a devastating genetic disorder called mitochondrial disease which was responsible for seizures, delayed development and his inability to deal with even simple winter bugs. Since Noah's passing in 2012, over £38,000 has been raised for charity by friends and family in his memory.You can see a little video of Noah's story here
http://m.youtube.com/watch?v=ef5jJ-DuSlc
- This year we're doing some big challenges in aid of the Lily Foundation - a wonderful charity that supports families and funds research into mitochondrial disease. A crazy team cycled the length of Ireland in May and another team are taking on the Great North Run in September.
- Noah's mum and dad, godparents Keri and Brian and dear friends Stuart and Louise are doing the great North Run in September. This is a huge challenge for all, particularly for his parents Nick and Ashleigh who want to get fit as their personal tribute to Noah this year!
You can find out more about the Lily Foundation by following the link below. The little animation provides a great explanation of mitochondrial disease.
http://www.thelilyfoundation.org.uk/mitochondrial-disease/
Donating through JustGiving is simple, fast and totally secure. Your details are safe with JustGiving – they’ll never sell them on or send unwanted emails. Once you donate, they’ll send your money directly to the charity. So it’s the most efficient way to donate – saving time and cutting costs for the charity.