A statement from the parents of Charlie...
When little Charlie was born our world changed forever. It was the best day...
Hope for Charlie’s Law
Hope for Charlie’s Law: Parents of 11-month-old Charlie Gard, who died in 2017, get...
£8500 Raised to mark our First-Year Anniversary
June 1st 2019 marked the Charlie Gard Foundation’s first-year anniversary and we made sure...
Team of brave fundraisers walk across fire...
On Tuesday 30th April 2019 over 1000 people descended on Newcastle Falcons’ Rugby grounds...
What is it like to live with,...
For Mother’s Day 2019 we invited one of our most inspiring mito mums, Zoe,...
WIN VIP TICKETS
Hugh Jackman: The Man. The Music. The Show – London O2 Box Hospitality for...
Butterfly Awards
On Saturday 27th October 2018 Connie and Chris attended a very special event called...
Mitochondrial Disease Awareness Week
Sunday 16th September 2018 marks the start of Mitochondrial Disease Awareness week, and to...
No other family should be put through...
By Sam Greenhill for the Daily Mail A new law in memory of tragic...
Charlie Gard’s parents want ‘Charlie’s Law’
By Catherine Burns Health correspondent, BBC News When Charlie Gard died, his parents said...
Launch Party
June 1st 2018 sees the official launch of The Charlie Gard Foundation, and we...
Our First Fundraising Event
AMay 4th 2018 saw our first ever Charlie Gard Foundation fundraiser event with our...
The launch of Charlie’s Law
Connie and Chris lost Charlie on 28th July 2017, but have bravely and tirelessly...
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