Pediatric Brain Tumor Foundation Expands its Support for Families with the Addition of Scott Kennedy
When children with cancer need treatment, time is of the essence. But often they face burdensome, unnecessary delays or are being treated with therapies that are ineffective and toxic. There are two pieces of critical legislation aiming to change that. However, they first need to be passed by Congress before year-end:
On Wednesday, October 19, the Pediatric Brain Tumor Foundation and other pediatric cancer advocates will come together to remind legislators that children and families deserve better treatments and access to care. There are two ways you can join us on the Pediatric Day of Action and ask your representative to co-sponsor the bills or thank them if they already are a co-sponsor:
If your representative hasn’t co-sponsored the STAR Reauthorization Act and Accelerating Kids’ Access to Care Act, tag them in a tweet asking them to co-sponsor. Here’s a preview of what your tweets could say:
If your legislator has co-sponsored these bills, tweet them on the Pediatric Day of Action to thank them for their support.
The U.S. Capitol switchboard can easily connect you with your Representatives and Senators.
“Hi, I’m [your name], one of your constituents from [your town or city]. I want to urge you to protect the health of childhood cancer patients and survivors in any end-of-year package by co-sponsoring two bills:
First, we need to make sure that pediatric cancer research is funded for another five years, which is why I want you to support the Childhood Cancer STAR Reauthorization Act.
Second, kids often travel out-of-state for care, to see a specialist, or participate in a clinical trial. For kids on Medicaid, this process can lead to unnecessary delays in care due to administrative red tape, which can cause a child’s condition to worsen. Please co-sponsor the Accelerating Kids’ Access to Care Act to allow kids time-sensitive access to the doctors they need to become survivors.
[Please feel free to share why these issues matter to you and your loved ones.]”
More information about both bills can be found in our September Legislative Update, including their co-sponsors. If you have any questions about a specific bill or this month’s Pediatric Day of Action, please reach out to Mike Henry, our Director of Advocacy, at [email protected].
PBTF is committed to making kids with brain tumors a national health priority, and these pieces of legislation hold the potential to provide families with much-needed relief and drive new scientific discoveries. You can make your voice heard and help us educate Congress about the need to pass this legislation by signing up to be an advocate with PBTF. Sign up to receive future advocacy alerts and join our efforts at www.curethekids.org/advocate.
Getting families where they need to be without worrying about the cost of transportation.
The Pediatric Brain Tumor Foundation (PBTF) and Uber are joining forces to provide essential support for families navigating the challenges of pediatric brain tumors.