Accelerating Kids' Access to Care Act: Improving Healthcare for Children Across State Lines

More than half of U.S. children depend on Medicaid or the Children’s Health Insurance Program (CHIP) for healthcare coverage, but this coverage is restricted to providers within their home state. For children with complex medical conditions, like brain tumors, this limitation often blocks access to specialized care available only out of state.

The Accelerating Kids’ Access to Care Act, passed by the U.S. House of Representatives on September 17, seeks to change that. Currently, out-of-state providers must undergo a time-consuming screening and enrollment process in a child’s home state Medicaid program, delaying access to life-saving care. This bill would create a streamlined pathway for providers in good standing to enroll in multiple state Medicaid programs, allowing children to receive faster, more timely care without all the red tape.

The Pediatric Brain Tumor Foundation, along with other childhood cancer advocates, has been championing this legislation for two years. Now, efforts are focused on ensuring the bill moves forward in the Senate. The Act has garnered bipartisan support from sponsors Senators Chuck Grassley (R-IA) and Michael Bennet (D-CO), and Representatives Lori Trahan (D-MA) and Mariannette Miller-Meeks (R-IA).

If passed, the Accelerating Kids’ Access to Care Act will improve children’s access to essential health care, while eliminating administrative burdens for providers and states. You can help push this critical legislation forward, by supporting advocacy efforts through the Pediatric Brain Tumor Foundation. Join the cause by signing up at curethekids.org/advocate. Your voice can help ensure children get the care they need when they need it most.

Related Updates

Groundbreaking Voice of the Patient Report for pediatric low-grade glioma (pLGG) published by Pediatric Brain Tumor Foundation

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Groundbreaking Voice of the Patient Report for pediatric low-grade glioma (pLGG) published by Pediatric Brain Tumor Foundation

“This report lays groundwork to improve the experience of people living with this disease,” said Dr. Sanjay Gupta, CNN’s chief medical correspondent, one of the country’s leading neurosurgeons, and a member of PBTF’s Board of Directors. “I believe it shines a much-needed spotlight on the wide-ranging and extensive challenges that this type of tumor causes for patients and their families, and I am hopeful that this moment is a significant milestone for this community.”

Ursula Burns, Former Xerox CEO, and Jordan Wertlieb, EVP and COO of Hearst, Appointed to Pediatric Brain Tumor Foundation’s Advisory Board as Inaugural Members

Press Release

Ursula Burns, Former Xerox CEO, and Jordan Wertlieb, EVP and COO of Hearst, Appointed to Pediatric Brain Tumor Foundation’s Advisory Board as Inaugural Members

The Pediatric Brain Tumor Foundation today announced the appointment of Ursula Burns and Jordan Wertlieb as inaugural members of the organization’s new Advisory Board. Burns and Wertlieb offer their exceptional business acumen and experience to PBTF, the largest patient advocacy funder of pediatric brain tumor research.

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