It's wonderful to see the AMRC’s annual infographic and we're incredibly proud to see our collective efforts 💛💙

🚨 Calling our community - we need your help! 🚨 bit.ly/3IhHD8G

TODAY is the crucial Third Reading of the Rare Cancers Bill, which could be truly transformational for rare & less common cancers by improving clinical trials, creating strategic focus and by reviewing drugs regulations. Follow along here: Parliamentlive.tv

We are thrilled the Rare Cancer Bill passed its Third Reading in the House of Commons on Friday 11th July! The Bill now moves to its First Reading in the House of Lords (date to be confirmed) and we remain hopeful for its continued progress. Learn more: neuroblastoma.org.uk/news/rare-canc…

🚨Research Update! As part of our 2021 Grant Round with support of Children's Cancer Research Fund we funded £469K to explore how blood tests could be used in clinical trials to improve outcomes for children with neuroblastoma. Read full article here: neuroblastoma.org.uk/news/blood-tes…

We’d love to stay connected! 💛 Subscribe to our e-newsletter and be one of the first to hear about ground breaking research, inspiring community stories, upcoming events, and so much more ➡️neuroblastoma.org.uk/keeping-in-tou…

Join us in walking 100 miles this September in honour of the around 100 children diagnosed with neuroblastoma each year 🚶🏽‍➡️💛 Lace up your shoes, walk with purpose, and help bring hope to families facing neuroblastoma. Sign up ➡️ register.enthuse.com/ps/event/Walk1…

Today we joined #OneCancerVoice, a coalition of more than 60 charities uniting to urge the UK Government to deliver a bold, fully funded National Cancer Plan for England to save and improve more people’s lives. #NationalCancerPlan

As part of our 2024 Grant Round we part-funded an exciting new project to improve availability of scanning drugs, reduce hospital time and improve radiation dosage for children with cancer. Read the full article here ➡️ neuroblastoma.org.uk/news/new-proje…

September is #ChildhoodCancerAwarenessMonth. Every year, 250 children in the UK lose their lives to cancer - Around 15% from neuroblastoma. With your help, we can beat childhood cancer. Start with a gift today ➡️ neuroblastoma.enthuse.com/cf/childhood-c…

Neuroblastoma is an aggressive childhood cancer typically found in children under five years old. No child should lose their life to cancer but the only way we will find a cure is through funding research. 🎗️Join us in making change by donating today➡️ neuroblastoma.enthuse.com/cf/childhood-c…

Fundraising superstars Frances & Paul are walking the 630-mile South West Coast Path in memory of their granddaughter Cara 💛 They’ve already covered 450 miles + raised £8,308 for Neuroblastoma UK 🎗 Support them here 👉 justgiving.com/fundraising/fr… justgiving.com/fundraising/fr…

🌟Fundraising Superstars🌟 Zara and Lucy took on the Antrim Coast Half Marathon on 24th August to raise over £2000 for Neuroblastoma UK! We want to say a huge thank you for your hard work and determination.💛 🏃

Harper was diagnosed with Stage 4 High Risk Neuroblastoma at just one-year-old in 2023. Despite a relapse scare and some side effects from her treatment, two years on from her diagnosis Harper has no evidence of disease. Read Harper's story here ➡️ neuroblastoma.org.uk/personal-stori…

📢 Researchers investigating mRNA Vaccine to treat Childhood Cancer As part of Neuroblastoma UK’s 2024 Grant Round, Dr. Olga Piskareva, alongside an international team of researchers received £208,887 to conduct research into the mRNA vaccine. Read more: neuroblastoma.org.uk/news/researche…

We welcome the recent NHS initiative, Jess’s Rule, and hope its ‘three strikes and rethink’ approach will help future neuroblastoma diagnosis. Read more about the initiative here: bbc.co.uk/news/articles/…

A big thank you to Suzanna & her friends who took part in a 10K night walk for Neuroblastoma UK. The group of friends raised a fantastic £1100! 🌟 If you are interested in fundraising for Neuroblastoma UK then visit our fundraising hub for inspiration ➡️ neuroblastoma.org.uk/fundraise-for-…

After losing their son Ted to neuroblastoma in 2023, Rob and Yvette set up TedFest as an annual festival to celebrate Ted's birthday and help fundraise for Neuroblastoma UK. An inspirational response to an unimaginable loss. Thank you for supporting Neuroblastoma UK 💙 💛

Maria was diagnosed with Stage 4 Neuroblastoma in March 2019 at 13-years-old and after three years of treatment sadly died in 2022. Her mum, Leyla, shares her story… neuroblastoma.org.uk/personal-stori…

Yesterday's #SoundsOfThe70s on BBC Radio 2 featured a dedication to Lizzy B & a shout out to Neuroblastoma UK 🎗 for the amazing work they do... Bob mentioned the amazing donation sent from donfeldermusic of Eagles to auction for #NBUK... have a listen & thank you, Bob Harris 💙