When our son Blake was diagnosed with Fanconi anemia in 2013, our world instantly changed. He was two years old and we didn’t have many medical concerns. Never in a million years would we have predicted all that Blake and our family would go through.
Stories
There’s nothing quite like the fierce determination of parents who have a child affected by Fanconi anemia. Our founders had three daughters with FA and to this day, the majority of our funding comes from FA family communities. One such family community from Colorado has been working on this cause for nearly 20 years and has raised an outstanding $3.1 million for FA research.
Stories, Fundraising
