Families Powering Pediatric AML Research
Connecting families with promising pediatric AML research—and helping turn hope into progress.
When a child is diagnosed with pediatric AML, families need to know where to turn.
Families Powering Pediatric AML Research was created to help families find that information, understand the science in everyday language and connect with the people and organizations working to develop better treatments.
But information is only part of the challenge.
We've seen what can happen when families and foundations come together around promising science. They can help provide the resources, connections and urgency needed to move discoveries from the laboratory toward treatments for children.
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Promising Research Needs People To Power It
Think of pediatric AML research like a Formula 1 race car. The science may have tremendous potential, but getting to the finish line takes resources, expertise, collaboration and urgency.
Families help provide the fuel. They bring determination, urgency and a deeply personal reason to propel research forward.
A child is diagnosed → family needs information → we help them understand what's happening → they discover how little research some forms of AML receive → they learn families can do something about it → they can choose to become involved.
Different roles. Different strengths. One shared purpose.
No single source of support can move pediatric AML research forward alone. Funding is essential, but promising science needs more than funding.
The different colors represent the people, expertise and resources that must come together—researchers, clinicians, families, foundations & donors
Put Up An Umbrella™
Every child with pediatric AML deserves people standing with them. Help us make the umbrella bigger.
You don't have to be a scientist or a major donor to make a difference. Everyone has something to contribute.
Why Families And Foundations Matter
Pediatric AML is not a single disease. It is a collection of biologically different diseases—some so rare that only a handful of children may share the same form of AML.
For these rare diseases, small patient numbers can mean small research dollars. Promising discoveries can stall—not because the science isn't there, but because the funding, expertise and resources needed to turn those discoveries into treatments are not.
We Have Already Seen What Is Possible When Families Power Research
Project Stella has shown what can happen when families, foundations and donors rally around promising pediatric AML research. Now there is an opportunity to apply what we have learned to promising research affecting more children.
Looking For PROJECTSTELLA.NET?
Project Stella continues at Fred Hutch, supporting Dr. Soheil Meshinchi’s pediatric AML research. That has not changed.
What has changed is ProjectStella.net. The family-facing website that shared Project Stella stories, research reports and updates will now be part of Families Powering Pediatric AML Research.
Here, we will continue to share news and research progress from Project Stella, while also helping families understand pediatric AML and promising research underway across the pediatric AML community. [LEARN MORE ABOUT PROJECT STELLA]
FAMILIES POWERING PEDIATRIC AML RESEARCH
