This is a special page to honour some of the brave children diagnosed with DIPG.
A place where you can meet other DIPG families and read the stories of courage as they journeyed from a DIPG diagnosis with their child. As this is a reasonably new site and feature we are looking for any DIPG families who would like to include their child on this page,
It would be our privilege to honour them here, please just use our contact form or email email@example.com with your text and a couple of photos.
We are more than happy also to profile current fighters and include any of your fundraising links for self-pay treatment and support.
THANK YOU to all the parents for sharing their precious children with us here and taking the time to write such heartfelt accounts for others to understand.