Mahazareen Dubash, originally from India, is the primary caregiver for her 19-year-old son with FA. Now residing in Canada, Mahazareen has been an advocate for the FA community since her son’s diagnosis in 2010. She is dedicated to promoting medical...
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Kerrie Cazzari holds a BS in Mathematics and Computer Science from UNC at Chapel Hill. After a successful career in IT, Kerrie became an active advocate when her son was diagnosed with Fanconi anemia in 2001 at age six. She...
Sarah Borden, based in Milwaukee, Wisconsin, is a dedicated advocate for the Fanconi Cancer Foundation (FCF). Since 2017, she has been deeply involved in the FA community, attending Family Meetings and Scientific Symposiums, supporting her son Eli through a bone...
Will is a 30-year-old from Salisbury, Maryland, where he works remotely in data operations management. He was diagnosed with Fanconi anemia in 1997 at age 5 and was transplanted in 2020 during the height of the COVID pandemic at Sloan...
Evan Connelly, 22, is an individual with FA and a member of the FCF Adult Council. He holds a bachelor’s degree in Chemical and Biomolecular Engineering from the Milwaukee School of Engineering. With five sisters, one of whom also has...
Louise is a 23-year-old British photographer who was diagnosed with FA at age six and is now 11 years post-transplant. She works as a freelance photographer as well as market worker, drag king and nightclub safeguard. Louise strives to shift...