When I was 20 weeks pregnant, my doctor recommended an amniocentesis so we could find out what was causing concerns during my pregnancy. They took amniotic fluid for testing, and that's when my husband and I learned our daughter had a rare genetic disorder called Fanconi anemia (FA). We found out that we were both carriers, something we had never known.
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Your Story Matters
At FCF, we believe in the power of stories to connect, inspire, and inform. Whether you or a loved one lives/lived with Fanconi anemia, your experience is an important part of our shared community. We’d love to hear about it. Use our easy-to-follow form to submit your written story or video story.