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  1. Support
  2. Neuroblastoma Parent Education Conference
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Conferences

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

Neuroblastoma Parent Global Symposium 2020

Neuroblastoma Parent Global Symposium 2020

Neuroblastoma Parent Global Symposium 2020 Read more

Published: 12th August, 2020

Updated: 1st February, 2021

Author: Anne Denman

2019 Neuroblastoma Parent Conference

2019 Neuroblastoma Parent Conference

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

Published: 10th November, 2019

Author: Anne Denman

2018 Neuroblastoma Parent Education Conference

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

Published: 11th November, 2018

Updated: 19th July, 2019

Author:

2017 Neuroblastoma Parent Education Conference

2017 Neuroblastoma Parent Education Conference

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

Published: 13th November, 2017

Updated: 19th July, 2019

Author: Nick Pryce

2016 Neuroblastoma Parent Education Conference

2016 Neuroblastoma Parent Education Conference

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

Published: 14th November, 2016

Updated: 19th August, 2019

Author: Nick Pryce

2015 Neuroblastoma Parent Education Conference

2015 Neuroblastoma Parent Education Conference

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

Published: 16th November, 2015

Updated: 19th August, 2019

Author: Nick Pryce

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Showing 10 of 6

Latest

  • Ellie-May’s cutting 10 inches

    Ellie-May’s cutting 10 inches

    Chloe was diagnosed with high-risk neuroblastoma at just 2 years old. Chloe is now 10 years old and in February 2020 her parents were given the devastating news that she had relapsed for the second time with her disease progressing in February 2021. Let’s help Chloe fight this even by donating £1 can help!

  • Poppy's Campaign

    Poppy's Campaign

    Poppy was diagnosed with high-risk neuroblastoma at just four years old. Her family are fundraising for further treatment, either to get their daughter into remission or to try and keep the cancer away if her frontline treatment does go to plan.

  • ShinadeMiami support ting Chloe

    ShinadeMiami support ting Chloe

    It would be such a blessing to help support Chloe cause. Help Chloe which another chance with life.

  • Lily’s Big Bridge Walk with Mia scooting behind her

    Lily’s Big Bridge Walk with Mia scooting behind her

    Lily and Mia are raising money for their brave cousin Chloe Balloqui who needs cancer treatment abroad.

Most read

  • Lily-Mae, Ireland’s Tiny Dancer, supports Solving Kids’ Cancer

    Lily-Mae, Ireland’s Tiny Dancer, supports Solving Kids’ Cancer

    Lily-Mae from Galway, Ireland will be celebrating her 12th birthday this April, but for her parents Judith and Leighton every day is a blessing.

  • Corey is thriving after neuroblastoma battle

    Corey is thriving after neuroblastoma battle

    Family donate almost £150,000 to neuroblastoma research

  • Solving Kids' Cancer welcomes Alexandra Lane to the Board of Trustees

    Solving Kids' Cancer welcomes Alexandra Lane to the Board of Trustees

    Alexandra Lane was formally voted on and welcomed to our Board of Trustees this week. We are thrilled to welcome Alex to the team.

  • BEACON study opens in Europe

    BEACON study opens in Europe

    The much-anticipated BEACON study amendment is now open and recruiting patients.

  • Steve Richards to step down as Chief Executive

    Steve Richards to step down as Chief Executive

    CEO to leave Solving Kids' Cancer after three years in the role.

  • Chloe’s Journey

    Chloe’s Journey

    Chloe was diagnosed with high-risk neuroblastoma at just 2 years old. Chloe is now 10 years old and in February 2020 her parents were given the devastating news that she had relapsed for the second time with her disease progressing in February 2021.

  • Solving Kids’ Cancer appoints new Chief Executive Officer

    Solving Kids’ Cancer appoints new Chief Executive Officer

    Solving Kids’ Cancer, a national neuroblastoma charity, has appointed Gail Jackson as its new Chief Executive Officer.

  • Charities fund new clinical trial

    Charities fund new clinical trial

    Solving Kids’ Cancer, with Neuroblastoma UK, has awarded a grant of £609,762.40 to enable the SIOPEN High-Risk Neuroblastoma Clinical Trial 2 (HR-NBL2) to open in the UK, it is anticipated to open in early 2021.

  • Exploring the Statistics Behind Neuroblastoma in the UK

    Exploring the Statistics Behind Neuroblastoma in the UK

    A closer look into the National Cancer Registration and Analysis Service (NCRAS) 2021 report on cancer in children, teenagers and young adults.

  • First Three Months

    First Three Months

    Gail Jackson, CEO, launches her blog. Reflecting on personal resilience, our work and joining Solving Kids' Cancer as COVID hit.

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Solving Kids' Cancer UK
Coram Campus
41 Brunswick Square
London
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.