17/05/2026
Today is DIPG/DMG awareness day and The Institute of Cancer Research is sharing Daniel’s story. Please read it in the link. Diffuse midline glioma is the cancer that kills most children. It currently has no treatment plan and children diagnosed with this brain cancer have months to a year life expectancy. Daniel had 7 months from diagnosis. As well as supporting children with cancer practically we also help fund research which will hopefully bring treatment options for future children. We must fight it. We do this on Daniel’s birthday every year. Daniel should be celebrating his 23rd birthday this coming Friday. Losing our incredible boy is a pain we can’t describe. The grief is exhausting but we keep going, trying our best to live. Today we think of all the children and young adults taken by this monster cancer. There are far too many 💔
“We would like DIPG to no longer be a death sentence”
Daniel Caplan was 17 when he died in November 2020, just seven months after being diagnosed with an aggressive brain tumour, diffuse midline glioma (DMG)/DIPG.
There are currently no effective treatments for DIPG. Daniel was determined to raise money for brain tumour research to give others hope and the chance of treatment he didn’t have.
In his memory, his parents, Alison and Brian, set up the Doing it for Daniel Foundation to fulfil his wish.
The Foundation has generously supported our Diffuse Midline Glioma /DIPG research, making a hugely positive impact on the work being undertaken by Professor Chris Jones and his team to bring about effective treatments, sooner.
We are so grateful to them for their incredible support, which is helping us to work towards a brighter future for families like theirs.
To mark DIPG Awareness Day, we’re sharing Daniel’s story’: https://www.icr.ac.uk/research-and-discoveries/cancer-blogs/detail/science-talk/every-child-diagnosed-with-brain-cancer-should-have-a-chance-at-life-alison-s-story