WASHINGTON, D.C. – Today, U.S. Senator Tim Kaine (D-VA) joined House Majority Leader Eric Cantor (R-7th) and Senators Mark Warner (D-VA) and Orrin Hatch (R-UT) to announce bipartisan, bicameral support for the Gabriella Miller Kids First Research Act. In December, H.R. 2019, sponsored by Congressmen Gregg Harper (R-MS), Peter Welch (D-VT), and Tom Cole (R-OK) overwhelmingly passed the House of Representatives with a bipartisan vote of 295-103. Senators Tim Kaine (D-VA), Mark Warner (D-VA), and Orrin Hatch (R-UT) plan to lead support for the companion bill in the U.S. Senate:
Senator Kaine said, “The Gabriella Miller Kids First Research Act is an important way to honor the memory of this remarkable young Virginian while recognizing the importance of pediatric disease research. I’m honored to support this effort and look forward to doing all I can to move it forward in the Senate.”
Leader Cantor said, “Gabriella Miller was an inspiring young girl from Virginia who was only 9 years old when diagnosed with an inoperable brain tumor the size of a walnut. Gabriella’s fight lives on with the bipartisan Gabriella Miller Kids First Research Act. Putting a priority on federal funding for pediatric medical research at the NIH will help overcome childhood cancer, autism and many other diseases impacting our children. Thanks to the hard work of Congressmen Gregg Harper, Peter Welch, and Tom Cole the House chose to put finding cures for our kids before financing political conventions. With the bipartisan support of Senators Kaine, Warner, and Hatch, I hope the Senate acts swiftly to do the same and sends Gabriella’s bill to the President’s desk to be signed into law so we can help more children.”
Senator Warner said, “I am pleased to add my support to this worthwhile effort to boost NIH research for pediatric diseases. By all accounts, Gabriella Miller was a profile in courage, and I can think of no better way to honor her legacy.”
Senator Hatch said, “There is no greater tragedy than the loss of a child, as Gabriella’s parents know all too well. Their story is heart-breaking and shows how much more we have to stop pediatric illness. Prioritizing research funding at the National Institutes of Health to combat life-threatening childhood diseases just makes sense. That’s why I’m so proud to back this legislation with my good friends from Virginia and thank my colleagues in the House for their hard work. Once we’ve introduced this legislation in the Senate, I pledge to do everything in my power to make sure this bill becomes law.”
The Gabriella Miller Kids First Research Act is supported by over 100 patient advocacy groups and has over 2,600 Citizen Cosponsors. Learn more HERE.