A little background to our why....



This is Keeley, the heartbeat of our family. Keeley was diagnosed with a DIPG brain tumour at the age of 16. She fought a horrendous battle which involved her loosing alot of her everyday bodily functions like walking, talking, sight & swallow. Keeley greeted every day of her battle with the biggest smile and her constant saying while she was sick was "don't take anything for granted"

As Keeley got weaker and realised she wasn't going to get better, she gave us one parting wish. With tears in her eyes, she asked us to fundraise and help other sick children....

We have thought about how we could best honour Keeley's wish and recently we have taken the plunge to launch a charity in Keeley's honour,
The Keeley D Foundation 🦋💕

This is a  non-profit organisation with the sole aim of offering practical help to families of children being treated for a terminal cancer diagnosis in a palliative care environment.

We soft launch our foundation on May 11th and hope you can come along to honour the wish of Keeley, who left this world only wanting us to help others

Contact us

Interested in working together? Fill out some info and we will be in touch shortly. We can’t wait to hear from you!