Abbie's Army - Fight DIPG Brain Cancer

Today, May 17th is DIPG Awareness Day—a time to recognise the children and families we've come to know who have faced...or are currently facing the most devastating childhood brain tumour, and to reinforce why work to fund crucial research matters.

@allontheboard Can you help us shine a light 🙏

If you do only one thing today, please stand with the #DIPG community—patients, families, charities and advocates—it is their strength that continues to inspire action and accelerate change. Pls Read, share and donate... justgiving.com/campaign/super…

Only family led foundations truly understand the urgency of this which has driven us and everything we do for over a deacde!!!

Be a hero for #DIPG children today 💗 justgiving.com/campaign/super… #DIPG #DMG #ResearchMatters #DIPGHeroes

£1 each. Thats it. Because together we're mighty. Add your donations here justgiving.com/campaign/super… 💗

There are just 3 days to DIPG Awareness Day! Want to turn £1 into £10? And then into £100? Join the Superhero Squad Challenge! ✔️ Donate £1 ✔️ Ask 10 friends to do the same ✔️ Get them to do the same! A ripple effect if heroic giving that starts with YOU

As you can see from the video she is feeling as 'well' as possible. Long may it continue 💗 She's amazing! Read more about her hopes and dreams , please donate and share if you can gofundme.com/f/help-mimi-an… #DIPG #DIPGHeroes #ResearchMatters

using CAR-T cell therapy for 12 DMG patients, co-funded by Abbie's Army. Mimi (11) wants to raise £100,000 to help, which she sees as the cost of her place! She's undergone her second infusion, via an ommaya reservoir implanted under her scalp

Children fighting #DIPG never cease to dazzle us with their strength, when their life has been invaded, and turned upside down. This is Emilia , known as Mimi who we introduced in February, she is taking part in CARMIGO- a £1.2m clinical trial

A third of the fund will come to @AbbiesArmy so lease be a hero for Neve and donate on the link...no amount is too small to show that we care 💗 gofundme.com/f/nevies-brain…

Neve is missing her friends a lot and thought she wouldn't raise much....but the page is doing brilliantly! Courageously Neve is sharing her story to help us here at Abbie's Army, and we couldn't be more grateful to have such incredible, selfless support.

Can we all help beautiful Neve in her amazing and important mission? We were contacted a while ago by Neve's Mother Sian, about her lovely 16 year old daughter, who was diagnosed with H3K27M+ DMG in January this year.

DIPG = INCURABLE. I have been an advocate for Littles fighting the big fight for 10 yrs. You know what hasn't changed? It was INCURABLE then and it remains INCURABLE. That is so wrong, but we can change it. 💜🩷💚🦋 **please REPOST**

When a child is facing something as cruel and unfair as a #DIPG diagnosis....when their parents have to hear that their child's disease is incurable, we are constantly reminded of the change which is so desperately needed , by so many.

Huge thanks to Steve Sealey and the @Easthertsgc Captain's tour, who've raised a massive £2000 in Portugal Praia D'el Rey towards our #DIPG/DMG brain cancer research! A-MAZ-ING guys! 👏💗 #DIPGHeroes

Can YOU help? Join our fundraiser, be a hero for DIPG children! Every penny allows us to keep pushing and keep funding! justgiving.com/campaign/super… #DIPG #DMG #ResearchMatters #DIPGHeroes

Continued research and new clinical treatments are more than essential, they are hope. This May, we've committed to raising £252,000 to support a brand new clinical trial for DIPG starting later this year, utilising new drug delivery technology to the brain.