Conferences

The Solving Kids' Cancer Neuroblastoma Parent Education Conference has been held since 2012. You can click and view each conference below.

2019 Neuroblastoma Parent Conference

2019 Solving Kids’ Cancer Neuroblastoma Parent Education Conference. Read more

2018 Neuroblastoma Parent Education Conference

Our 2018 conference offered a concurrent session focusing on ways to deal with and manage the long-term side effects of neuroblastoma. Read more

2017 Neuroblastoma Parent Education Conference

Our 6th Annual Neuroblastoma Parent Education Conference – ‘Understanding the Landscape of Neuroblastoma Research’ Read more

2016 Neuroblastoma Parent Education Conference

Our 5th Annual Neuroblastoma Parent Education Conference was held at Latimer Place in Chesham Read more

2015 Neuroblastoma Parent Education Conference

Our 4th Annual Parent Conference was again held at Latimer Place, Chesham Read more

Neuroblastoma Parent Global Symposium 2020

Neuroblastoma Parent Global Symposium 2020 Read more

Neuroblastoma Parent Global Symposium 2021

Neuroblastoma Parent Global Symposium 2021 - 5th & 6th November Read more

Latest

100 Miles for Jessica

To help raise money for critical treatment for Jessica Butler
Lucy’s Skydive for Jude

I am taking on this challenge to fundraise to help get my son, Jude, to target to access the bivalent vaccine in New York
Raffle for Jude

Jude is 4. He lives in Sheffield with his family. He is battling cancer & needs pioneering treatment in America. We can help get him there…
Rock N Roll for Kayla

Kayla from Norwich is facing a huge challenge, so rock n rollers unite.

Beau's Campaign

Beau was diagnosed with high-risk neuroblastoma, an aggressive childhood cancer that has a 40-50% chance of long-term survival at diagnosis, in December 2020. Her family are appealing for your help to raise £317,000 by May 2022.
Flora's Campaign

In January 2021 Flora was diagnosed with Autism Spectrum Disorder, and just three months later her parents were given the devastating news she had high-risk neuroblastoma. Her family are appealing for your help to raise £252,000 by August 2022 for Flora to enrol on the Bivalent Vaccine clinical trial in New York that aims to stop her neuroblastoma from coming back.
Jude's Campaign

Jude is a Dinosaur and animal-loving three-year-old. In July 2021 Jude was diagnosed with high-risk neuroblastoma, a rare and aggressive childhood cancer that has a 40-50% chance of long-term survival at diagnosis.
Joseph Yeandle

We are devastated to share the news that beautiful Joseph has sadly passed away.
Maysaa's Campaign

Four-year-old Maysaa was diagnosed with high-risk neuroblastoma, an aggressive childhood cancer that has a 40-50% chance of long-term survival at diagnosis, in March 2021. Her family are asking for your support to raise £106,000 by August 2022 for Maysaa to enrol on the DFMO study in Charlotte that aims to stop her neuroblastoma from coming back.
Chloe’s Journey

Beautiful Chloe passed away on the 4th of February 2022.
Eden's Campaign

Six-year-old Eden was diagnosed with high-risk neuroblastoma, an aggressive childhood cancer that has a 40-50% chance of long-term survival at diagnosis, in April 2021.
Kayla's Campaign

Three-year-old Kayla was diagnosed with high-risk neuroblastoma in May 2021. Kayla’s parents are asking for your help to raise £221,000 by November 2022 for Kayla to enrol on the bivalent vaccine clinical trial in New York that aims to stop her neuroblastoma from coming back.
Peter's Campaign

11-year-old Peter was diagnosed with neuroblastoma in early 2019. Devastatingly he relapsed in August 2020 after being clear of disease for 6 months. Thanks to your incredible fundraising and support, Peter was able to enrol on the DFMO study in Charlotte at the end of January 2022.
Dulcie's Campaign

In December 2021, five-year-old Dulcie was diagnosed with high-risk neuroblastoma, a rare and aggressive childhood cancer that has a 40-50% chance of long-term survival at diagnosis.