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2.0: Gabriella Miller Kids First Research Act, with Ellyn Miller
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This episode highlights H. R. 623, important funding legislation for a crucial program at NIH for childhood disease research. Ellyn Miller, CEO of Smashing Walnuts Foundation, joins us to share the history of this legislation as well as the work today and forward into this new year supporting this and other activity in the childhood cancer advocacy community. Ellyn's daughter Gabriella passed away in 2013 to DIPG, diffuse intrinsic pontine glioma, but she went out with a huge movement forward for pediatric research. Her enthusiasm and advocacy for other children was caught on tape that went viral and inspired the Gabriella Miller Kids First Research Act signed into law by President Obama in 2014 with her family members, including her little brother Jake, all present. Ellyn's storytelling is captivating, and the magic of Gabriellas legacy is palpable, and powerful in the telling. Visit: childrenscancercause.org advocacy action page to support this crucial legislation today.
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