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Fibrolamellar Cancer Foundation
About
<p>FCF, a public 501c3 nonprofit organization based in Greenwich, CT, was founded in 2009 by 27-year-old Tucker Davis, who lost his life to Fibrolamellar on Rare Disease Day in 2010, after an 18-month fight. FCF has funded nearly $10 million in research across more than 24 major institutions in the U.S. and internationally. 100% of all donations go towards research. All FCF’s overhead and administrative costs are paid by the Charles A. and Marna Davis Foundation and Stone Point Capital. For more information, visit www.fibrofoundation.org</p>
Press Releases
Two Different Rare Diseases Before Age 20: Chansen Savakinus’ Rare Disease Day Message
Released on February 25, 2022
Making Noise to Find Cures. Fibrolamellar Cancer Foundation Raises Awareness for #RareCancerDay 9/30/21
Released on September 28, 2021
Rare Disease Awareness Day Critical As Patients Struggle During COVID Times
Released on February 26, 2021
Rare Cancer Isn’t Uncommon: Courtney Homer’s Story
Released on September 30, 2020
Fibrolamellar Becomes Lead Example for Rare Cancer Awareness Day #RareCancerDay
Released on September 25, 2020
Chan Zuckerberg Initiative Awards Fibrolamellar Cancer Foundation First Ever Rare As One Network Grant
Released on February 6, 2020
October 1st Declared As Rare Cancer Day
Released on September 29, 2019
Fibrolamellar Global Summit Determines Research Funding As #GivingTuesday Top Priority
Released on November 22, 2017
Fibrolamellar Cancer Foundation Helps Lead Liver Cancer Awareness Month
Released on October 11, 2017
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