@AussieDIPG

Advocating for change to the most fatal childhood cancer to affect Australian children - DIPG. Together we can make a change. #DIP4Good #cureDIPG

Joined August 2023
Silent Warriors - Episode Fifteen - Remembering Maddy facebook.com/share/v/yxL7Eon…
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Silent Warriors - Episode 14 - Remembering Giang facebook.com/share/4eHfaNm3K…
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Silent Warriors - Episode Thirteen - Dr Fatima Valdes Mora facebook.com/share/B5qXQ1ptP…
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Silent Warriors - Episode Twelve - Mark DeSouza facebook.com/share/1g6kPyPx7…
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Silent Warriors - Episode Eleven - Dr Charlie Teo facebook.com/share/p/LkaoXzE…
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Silent Warriors - Episode Nine - Miracle Mikayla facebook.com/share/4j67dy3Df…
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Silent Warriors - Episode Eight - Ruby Pringle facebook.com/share/mv35dYnJi…
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Silent Warriors - Episode 5 - Remembering Evie Whipps facebook.com/share/ocZUM76bj…
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Silent Warriors - Episode Four - Remembering Alex Jenkins facebook.com/share/yvyRY76Mo…
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Silent Warriors - Episode Three - Remembering Ryley Kemp facebook.com/share/zmybWGwbr…
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Silent Warriors - Episode Two - Remembering Zoe Tran facebook.com/share/5RcsaqRkw…
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Silent Warriors - Episode One - Remembering Talin Tye facebook.com/share/p/gBR3Y3w…
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Go Grey in May Brain Cancer Awareness Month 🩶 Meet Mighty Maddy 🦸🏻💜 DIPG Warrior - Fighting with all her might for 3 years! #memoriesinmay #RUNDIPG #DIPG #mightymaddy
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Go Grey in May for Brain Cancer Awareness 🩶 This month we will share photos of many beautiful children who have lost their lives to DIPG/DMG or are currently still in the fight. Please see them, Remember them! Mia 🩷🩶 Ryley 💙🩶 #memoriesinmay #gogreyinmay #DIPG #RUNDIPG
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Australian DIPG Families retweeted
Congrats to the scientists, doctors and families who helped secure $20M from the Fed Gov't for childhood brain cancer research. @Mark_Butler_MP said research was a key weapon in battling #braincancer and $KZIA is proud to be a part of this fight. shorturl.at/exBTY
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Australian DIPG Families retweeted
DIPG is a type of malignant brain tumour, and one of the most aggressive of all childhood cancers. There’s no known cure or treatment options. Angie’s daughter Eve was diagnosed in March 2021 and given 12 months to live.
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