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  1. About us
  2. Annual reports

Annual reports

2019 Annual Report

2019 Annual Report

Read more

Published: 11th November, 2019

Updated: 5th December, 2019

Author: Daniel Ingle

2020 Annual Report

2020 Annual Report

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Published: 7th December, 2020

Updated: 13th April, 2021

Author: Anne Denman

Annual Report 2021

Annual Report 2021

Read more

Published: 1st December, 2021

Author: Anne Denman

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Showing 10 of 3

Latest

  • Kathryn's RSR for Jude

    Kathryn's RSR for Jude

    To help Jude's family reach their fundraising target.

  • St Mary Magdalene - Y5 and Y6 Ticket Sales

    St Mary Magdalene - Y5 and Y6 Ticket Sales

  • Leah Ambler- Research Officer

  • Solihull Half Marathon for Jude Mellon-Jameson

    Solihull Half Marathon for Jude Mellon-Jameson

    For Jude

Most read

  • Beau's Campaign

    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

    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.

  • Joseph Yeandle

    Joseph Yeandle

    We are devastated to share the news that beautiful Joseph has sadly passed away.

  • Jude's Campaign

    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.

  • Maysaa's Campaign

    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

    Chloe’s Journey

    Beautiful Chloe passed away on the 4th of February 2022.

  • Eden's Campaign

    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

    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

    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

    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.

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WC1N 1AZ

Phone: 020 7284 0800

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Solving Kids’ Cancer UK is a registered charity in England and Wales (1135601), and in Scotland (SCO45094). It is a company limited by guarantee in England and Wales (7208648). The charity and company is currently operating as Solving Kids’ Cancer.