Advocacy Alert

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

This February 13th and 14th, make your voice heard at the Alliance for Childhood Cancer’s 2024 Action Days!

In a few months, much of the country will focus their attention on the race for the White House. By becoming an advocate with the Pediatric Brain Tumor Foundation and joining us on Capitol Hill at this year’s Alliance for Childhood Cancer Action Days, you can remind Congress that pediatric brain tumors don’t stop for an election.

Action Days give childhood cancer patients, survivors, caregivers, family members, and advocates from across the country the chance to meet with their home state legislators in-person, advocate for key policy issues currently before Congress, and make sure the voice of children with cancer is heard loud and clear. Training is provided on February 13 and meetings with legislators on February 14 will be scheduled for participants in advance.

A founding member of the Alliance for Childhood Cancer, the Pediatric Brain Tumor Foundation is proud to stand alongside advocates and speak with one voice about the most pressing issues facing the community. Learn how you can join us in urging Congress to pass legislation that would improve the lives of children with brain tumors by filling out the form below or emailing Director of Advocacy Mike Henry at [email protected].

Related Updates

Pediatric Cancer Neuropsychological Needs Assessment Act Introduced in New York Legislature

Advocacy Alert

Pediatric Cancer Neuropsychological Needs Assessment Act Introduced in New York Legislature

A new bill introduced in the New York State Legislature by Senator Shelley B. Mayer and Assembly Member Christopher Burdick will help remove some of the barriers standing between children with cancer and the learning accommodations they need to succeed in school. The Pediatric Cancer Neuropsychological Needs Assessment Act (NY State S.8750) would require insurers to provide coverage for neuropsychological assessments for children diagnosed with cancer that affects brain development or function.

The Pediatric Brain Tumor Foundation Welcomes Dr. Sanjay Gupta to Its Board of Directors

Press Release

The Pediatric Brain Tumor Foundation Welcomes Dr. Sanjay Gupta to Its Board of Directors

The Pediatric Brain Tumor Foundation (PBTF) is proud to welcome Dr. Sanjay Gupta, CNN’s chief medical correspondent, to the PBTF’s Board of Directors. Dr. Gupta will bring his wide-ranging experiences in medical practice and journalism, including as associate chief of the neurosurgery service at Grady Memorial Hospital in Atlanta, associate professor of neurosurgery at the Emory University School of Medicine, and chief medical correspondent for CNN, to bear as a valuable and expert advocate for pediatric brain tumor patients, survivors, and their families.

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