RT @MolecularCell: A specific form of cPRC1 containing CBX4 is co-opted to mediate oncogenic gene repression in diffuse midline glioma http….

GOOD LUCK to Steve Young marking a poignant 10th anniversary year following the passing of his son Alfie to #DIPG in 2015. Tomorrow is the last of his challenges for Abbie's Army with a 15,000 ft skydive 🪂 Please help to fight here 👇

A HUGE thank you to @Alleyns_Junior for your wonderful support in memory of Sophia who sadly passed away in February 2024 at just 5 years of age. 💗 Read her story #DIPG #ResearchMatters

RT @ellielexx: This important study wouldn’t have been possible without the incredible UK DIPG research charity @AbbiesArmy and the phenome….

A small project grant has been awarded to Dr Ashley Vardon, @unibirmingham and will support pre-clinical research into engineering a new immune cell therapy for GD2-positive paediatric solid tumours. #DIPG #DMG #ResearchMatters.

RT @michelle_monje: Delighted to share our most recent #CancerNeuroscience study, led by brilliant postdoctoral fellows @RDrexler and@ADrin….

RT @Tsinghua_Uni: #InnovativeTsinghua uncovered the H3.3K27M–CREB5/ID1 axis that keeps fatal pediatric #DIPG cells in a stem-like, aggressi….

In August 2017, 6-year-old Isla woke up unable to walk. After months of scans, treatments, and surgeries, her family received the devastating news #DIPG We're on a donation dash to the end of the month please support research at

HUGE congratulations to Steve and Sally, who climbed Ben Nevis to honour 10 years since the passing of Steve's son Alfie to #DIPG. This is challenge 2 of 10 in a milestone year, which would also be Alfie's 21st Birthday 💗 Donate at

Awareness day may be over but throughout May you can still be a Superhero🦸‍♀️ for children with #DIPG Get involved at

RT @TBranchflo92956: Awareness Day is here. In the UK, around 40 children are diagnosed every year. Nearly one child every week. We owe the….

#DIPG Awareness Day is here. In the UK, around 40 children are diagnosed every year. Nearly one child every week. We owe them more than statistics!.In their memory we fight for research and a cure 💗 Donate and be a Superhero for kids

Zoé fought #DIPG bravely for over 3 years with treatment in the UK and in Mexico. Despite every effort DIPG remains a uniformly fatal diagnosis. We’re asking if you can donate just £1 to help fund research, and bring hope to families

We're asking for just £1 it doesn't go far these days. But £1 can fund #DIPG research. £1 can give hope. And £1 from thousands of people? .That’s a movement. Join in

RT @AbbiesArmy: Join us this May and support at Just £1. One Small Act. One Huge Impact. This May including #DIPG….

Do you have a superpower to use in the fight against the most deadly brain cancer #DIPG? Team Elias recently climbed Ben Nevis raising £1200, in memory of Elias Petteford Hearne who passed away at the age of just 5. 💗 Join in

Join us this May and support at Just £1. One Small Act. One Huge Impact. This May including #DIPG Awareness Day, we’re calling on everyday heroes to unite in the fight against this devastating brain cancer !

Huge well done to Summer Lees and Alice Herbert who completed the AJ Bell Great Bristol Run 10K 2025! The girls ran for Summer's sister Harlyn who is currently fighting #DIPG with her photo on their vests every step was inspired 💗

RT @AbbiesArmy: May is an Int brain tumour awareness month. including an all important #DIPG Awareness day on May 17th. Grab your cape, ra….

Earlier this year, Charlie's battle came to an end. He passed away at 12 years old. The heart-breaking reality for families facing a #DIPG diagnosis. His brother Jake runs this weekend in the Leeds Half Marathon pls support him here 💗