curethekids.org Open in urlscan Pro
2606:4700:20::ac43:45ac  Public Scan

Submitted URL: http://curethekidz.com/
Effective URL: https://curethekids.org/
Submission: On April 04 via api from BE — Scanned from DE

Form analysis 3 forms found in the DOM

GET https://team.curethekids.org/give/461117/#!/donation/checkout

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  <p class="donate1-more">
    <a class="more1 -t:16" href="https://curethekids.org/donate/" target="" title="More ways to give">
							<span class="-a:1">			More ways to give					</span>					<i class="icon-directional-right-bold"></i>			</a>
  </p>
</form>

GET https://curethekids.org/

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</form>

POST /#gf_7

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A CHILD’S BRAIN TUMOR DIAGNOSIS IS OVERWHELMING. WE’RE HERE TO HELP.



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OUR MISSION

With a mission to Care. Cure. Thrive., the Pediatric Brain Tumor Foundation
leads the way in funding childhood brain cancer research to cure the kids,
supports families affected by this disease, and advocates for policies that help
patients, survivors and their loved ones.

About the Pediatric Brain Tumor Foundation


FAMILY EDUCATION & SUPPORT

Newly Diagnosed


NEWLY DIAGNOSED

Life After a Brain Tumor Diagnosis


LIFE AFTER A BRAIN TUMOR DIAGNOSIS

Support for Families


SUPPORT FOR FAMILIES


JOIN THE CAUSE. HELP US CURE THE KIDS.

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Whatever form your gift takes, you can be confident your generosity will help us
lead the way toward a future without childhood brain cancer. Learn more about
the different ways you can donate and make a difference.

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Join our efforts at the national and local level to educate policymakers and the
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OUR COMMUNITY'S IMPACT


THANKS TO SUPPORTERS LIKE YOU, THE PEDIATRIC BRAIN TUMOR FOUNDATION IS ACTIVELY
MANAGING MORE THAN $5.3M IN RESEARCH FUNDING TO ACCELERATE PROGRESS FOR KIDS
WITH BRAIN CANCER.

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STORIES

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Valentina: Living with Pediatric Low-Grade Glioma


VALENTINA: LIVING WITH PEDIATRIC LOW-GRADE GLIOMA

In June 2018, Valentina was diagnosed with a pediatric low-grade glioma with a
BRAF mutation. At the time, she was only one year old. Surgery was not an
option, so her family had two choices for treatment—traditional chemotherapy or
an experimental treatment suitable for her type of mutation.

Zoe: A Pediatric Brain Tumor Survivor’s Love of Books Opens the Door to New
Research Funding


ZOE: A PEDIATRIC BRAIN TUMOR SURVIVOR’S LOVE OF BOOKS OPENS THE DOOR TO NEW
RESEARCH FUNDING

Combining her love for reading and desire to give back to help kids with brain
tumors like her, Zoe created Books 4 Brains to raise money for pediatric brain
cancer research. Join her upcoming Books 4 Brains read-a-thon and support the
Pediatric Brain Tumor Foundation's research funding efforts.

I'm a dad and scientist who works in drug development. Here's why your support
matters.


I'M A DAD AND SCIENTIST WHO WORKS IN DRUG DEVELOPMENT. HERE'S WHY YOUR SUPPORT
MATTERS.

As Nathan's dad, I am forever grateful to the Pediatric Brain Tumor Foundation
community. And as one of the foundation’s internal research advisors and a
scientist who works in drug development, I also see there’s so much more work we
can do.


UPDATES

All Updates

Urgent Action Needed: Congressional Hearing on Accelerating Kids’ Access to Care
Act

Advocacy Alert

URGENT ACTION NEEDED: CONGRESSIONAL HEARING ON ACCELERATING KIDS’ ACCESS TO CARE
ACT

Recently, the Accelerating Kids' Access to Care Act gained significant momentum
in Congress when Charlie, a 12-year-old brain tumor survivor and advocate with
the Pediatric Brain Tumor Foundation, testified to the U.S. Senate Finance
Committee about the hurdles families face when seeking treatment for their
child. Now, to see it become law requires your immediate action.

February 27, 2024

2024 Action Days: Join Us in Urging Congress to Help Children with Cancer

Advocacy Update

2024 ACTION DAYS: JOIN US IN URGING CONGRESS TO HELP CHILDREN WITH CANCER



January 10, 2024

A Look Back: Celebrating the Community’s Impact in 2023

A LOOK BACK: CELEBRATING THE COMMUNITY’S IMPACT IN 2023

In 2023, the Pediatric Brain Tumor Foundation community answered the call to
create a brighter future for children with brain tumors and their families. Read
about what your support made possible in research, family support and advocacy.

December 27, 2023


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