Our Mission:
We help educate others as well as work towards treatments and a cure for Fanconi Anemia.
We also aim to provide education and support services to affected families worldwide.
What is Falconi Anemia?
Fanconi anemia (FA) is a rare genetic disorder. Though considered primarily a blood disease, FA may affect all systems of the body.
Most FA patients develop bone marrow failure and require a stem cell transplant.
FA patients are at high risk of developing cancers decades earlier than the general population.
“
The Fanconi Anemia Research Fund is the single best orphan disease research support group in the world. It is a model for demonstrating how a small group of dedicated families can speed the pace of scientific progress and bring realistic hope to patients with an otherwise fatal disorder.
”
- David Nathan, MD, President Emeritius, Dana Farber Cancer Institute, Boston, Mass. Winner, 1990 National Medal of Science
Get Involved
Fanconi anemia research needs funding to move forward. Great advances in understanding this disease have been made, but more needs to be done.
See how you can help.
upcoming EVENTS
See what events we have upcoming. Learn about how you can participate in the cause.
Volunteer opportunities
There are more ways to help and participate than simply donating. Learn about Volunteering.
Make a Donation
Help fund the cause with a charitable donations to the Fanconi Anemia Research Fund.
Putting Your Donations to Work
The Fanconi Anemia Research Fund provides funds for research grants, helps produce scientific publications, convenes an annual international scientific symposium, and provides invaluable support to families affected by FA.