Gina's page

Gina Hall is raising money for The Maddi Foundation

Participants: Amy Coppen, Anna Furie, Emma Priest, Glyn Mummery, Claire Huartson, Victoria Copeland, Alex Thurgood, CJ Watson, Neil Miller, Steve Jones, Clive Madden, Eric Binks & Craig Brown

£1,220

raised of £800 target by

25 supporters

FRP Advisory LLP Three Peaks Challenge · 21 September 2018 to 23 September 2018 ·

The Maddi Foundation

Verified by JustGiving

RCN 1174374

www.themaddifoundation.com

We raise funds for SPG15 medical research to find a cure for this rare disease

Story

Thanks for taking the time to visit my JustGiving page - any amount is greatly appreciated and also means I will HAVE to complete the challenge!

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. They'll send your money directly to the Maddi Foundation.

Hope there's a Champagne bar at the end...

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25 donations

Kate Perry
6 years ago
Well done Gina, knew you could do it xxx
£30.00 + £7.50 Gift Aid
Graeme Young
6 years ago
I'm right behind you on this, I know you can scale all three. ðŸ˜
£100.00 + £25.00 Gift Aid
Anonymous
6 years ago
£50.00 + £12.50 Gift Aid
Caryn Littlechild
6 years ago
Good luck! The training will be worthwhile, Gina.
£10.00 + £2.50 Gift Aid
Ian Sutton
6 years ago
All the training will be worthwhile so I'm sure you will smash it!!
£25.00 + £6.25 Gift Aid

About the charity

The Maddi Foundation

Verified by JustGiving

RCN 1174374

www.themaddifoundation.com

The Maddi Foundation is a non profit charity which was founded by the family of a young teenage girl “Maddi” who in 2016 was diagnosed and started battling Spastic Paraplegia Type 15 (SPG15), a degenerative neuro disease. Symptoms present themselves generally in early teens causing paralysis in the limbs with progressive brain abnormalities resulting in loss of nerve cells, visual impairment and possible juvenile Parkinson's. This is a genetic type of motor neuron disease. To date there is no cure or treatment! Conditions this rare receive very little attention and funding so with your help we can try to change this so our children can have a brighter future. The Maddi Foundation aims to continue to support medical research to help cure this disease and also help other similar rare diseases.