Alison Haywood

We are fundraising as part of Team Timmy as we want to help The Lily Foundation find a cure for Mito for Tim and all those effected.

Fundraising for The Lily Foundation
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Christmas , 25 December 2018
Inspired by his strength, Team Timmy are joining together to help The Lily Foundation beat Mito by funding vital research and supporting all those families affected by this cruel disease with no treatment or cure. Together we will change this!

Story

Timmy is an inspiration. He first became ill when he was 4 years old. After many tests he was diagnosed with Mitochondrial Disease. We all have Mitochondria in everyone of our cells. They create the energy we need to function properly. In children like Timmy, theirs do not work properly. Mitochondrial Disease is a life limiting, degenerative, evil illness. Currently there is no real treatment or cure. Timothy is now looked after by specialist Mitochondrial Disease teams in Sheffield and Newcastle. Sadly there isn't a treatment or cure for Mitochondrial Disease, Timothy takes a Mito cocktail.. it contains various vitamins which are thought to help his symptoms. Hes fed through a tube into his intestines and uses a wheelchair to get around. He is amazing, he never ever complains.. hes a true warrior! The Lily Foundation support the family and fund vital research to find a cure for Timmy an all those effected. Please donate to we can help them reach their goal quicker.

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About the campaign

Inspired by his strength, Team Timmy are joining together to help The Lily Foundation beat Mito by funding vital research and supporting all those families affected by this cruel disease with no treatment or cure. Together we will change this!

About the charity

The Lily Foundation

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The Lily Foundation funds research into Mitochondrial Disease and other metabolic disorders. It also raises important awareness and supports those families who are affected with metabolic disorders.

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