More than four decades ago, Lynn Frohnmayer was a mother searching for answers after learning that three of her five children had Fanconi anemia. There was no roadmap and no established network of families or experts. Information was scarce, treatments were limited, and the future her family had been given was devastating.
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Whether you’re an established investigator or an aspiring one, we welcome your proposals and are eager to support your journey towards making a difference in the lives of those affected by FA.
