Katie Hughes

In Memory of Jake

Fundraising for The Lily Foundation
£2,220
raised of £470 target
In memory of Jake Hughes
Throughout December we are asking people to donate so we can give the gift of hope to families affected by Mitochondrial Disease this Christmas across the UK

Story

Thanks for taking the time to visit my JustGiving page.

At 18 months old our beautiful boy Jake began having seizures. After many weeks at Great Ormond Street he was finally diagnosed in July 2015 with a rare mitochondrial condition called Alpers.

We were told it was life-limiting but had no idea of how much time we had with him so tried to make every day count. In between hospital visits he was reasonably well and remained our ever happy, loving little boy with a wonderful cheeky sense of humour.

Devastatingly Jake passed away a year later aged 2 and half having fought a brave fight with a battle he could never win. He slipped away peacefully in his sleep on 28th May 2016 held tightly by his devoted Mummy and Daddy.

We want to support the Lily Foundation this Christmas for their ongoing research into this devastating disease. Hopefully, one day, there will be a cure to stop other little ones being robbed of their future and stop parents going through the heartbreak we continue to go through.


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About the campaign

Throughout December we are asking people to donate so we can give the gift of hope to families affected by Mitochondrial Disease this Christmas across the UK

About the charity

The Lily Foundation

Verified by JustGiving

RCN 1122071
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.

Donation summary

Total raised
£2,220.00
+ £327.50 Gift Aid
Online donations
£1,700.00
Offline donations
£520.00

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