Neuroblastoma Parent Global Symposium 2021

Neuroblastoma Parent Global Symposium
5th & 6th November 2021

Bringing together families affected by neuroblastoma from across the globe with those who work to treat, help, and support them.

Hosted online over two days, this FREE virtual event provides valuable content for families, neuroblastoma survivors, clinicians and other healthcare professionals, researchers and charitable organisations.

The event programme includes live and pre-recorded sessions, presentations from internationally renowned experts, networking opportunities, specialised conversation rooms and parent-driven Q&A. Live sessions will be recorded and available for on-demand viewing. Sessions will cover:
Information for newly diagnosed families
Overview of international clinical trial landscape
Drug development and emerging research
Supportive care management
Survivorship issues
Parent-driven conversation rooms will run in parallel to main sessions offering families the opportunity to come together, network and share their experience around a specific interest and topic. The event also makes available a library of video resources from the 2020 symposium.
Register for NPGS 2021
Register
Outstanding Initiative
"Thank you for the opportunity to contribute to this outstanding initiative. It was beneficial to learn from my colleagues who work in areas outside of my expertise – it was refreshing to attend such diverse talks that were communicated so well."
Christina Signorelli,
Kids Cancer Center Sydney
2020 NPGS Speaker
Amazing Experts
"This event highlighted how well connected the pediatric oncology world is. We are fortunate to have so many amazing experts around the globe searching for better treatments and cures for this devastating disease. Thank you for organising!"
Adam, Australia
2020 NPGS Attendee
Phenomenal Resource
“What a phenomenal resource for families to connect, share information, and build a global community!
Thank you for making this possible for families all over the world!”

Jessica, United States
2020 NPGS Attendee
THE ORGANISERS

Solving Kids’ Cancer UK is a parent-led charity, our vision is a future where no child dies of neuroblastoma or suffers due to its treatment. We provide emotional and practical support to families and our research focus is on clinical trials, seeking to explore new ways of treating neuroblastoma, providing hope and options for children and their families now and in the future. www.solvingkidscancer.org.uk

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 (7208646).

The Children’s Neuroblastoma Cancer Foundation (CNCF) is the premier source for neuroblastoma information and resources. Comprised of families just like yours, we are committed to finding a cure for neuroblastoma through research, education, awareness and advocacy. Visit www.cncfhope.org/ to find out more about the work of CNCF.

Children's Neuroblastoma Cancer Foundation (CNCF) is recognized as a public charity under Section
501(c)(3) of the US Internal Revenue Code.
Federal ID 36-4370725.

Solving Kids’ Cancer is not just our name, it’s our mission. We focus on aggressive childhood cancers with low survival rates—because Every Kid Deserves to Grow Up. Solving Kids' Cancer (SKC) helps accelerate clinical trials of next-generation treatments with an understanding of the global childhood cancer research landscape 
and current unmet needs. 
www.solvingkidcancer.org

Solving Kids' Cancer is recognized as a registered public charity under Section 501(c)(3) of the US Internal Revenue Code. Federal ID: 20-8735688.

Bringing together families affected by neuroblastoma from across the globe with those who work to treat, help, and support them.

Hosted online over two days, this FREE virtual event provides valuable content for families, neuroblastoma survivors, clinicians and other healthcare professionals, researchers and charitable organisations.

The event programme includes live and pre-recorded sessions, presentations from internationally renowned experts, networking opportunities, specialised conversation rooms and parent-driven Q&A. Live sessions will be recorded and available for on-demand viewing. Sessions will cover:

Information for newly diagnosed families

Overview of international clinical trial landscape

Drug development and emerging research

Supportive care management

Survivorship issues

Parent-driven conversation rooms will run in parallel to main sessions offering families the opportunity to come together, network and share their experience around a specific interest and topic. The event also makes available a library of video resources from the 2020 symposium.

Register for NPGS 2021

Register for NPGS 2021

Outstanding Initiative

Amazing Experts

Phenomenal Resource

THE ORGANISERS

THE ORGANISERS

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