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This organization is a 501(c)3 tax-exempt organization, and your donation is tax deductible within the guidelines of U.S. law.

Behind every diagnosis is a family that needs us.

Nearly 30,000 Americans wake up every day managing a bleeding disorder that could cost them their health, their independence, and their future — unless someone fights for them. That someone is HFA. And that someone could be YOU.

The problem
A diagnosis that changes everything — overnight
When a family learns their child has hemophilia or another bleeding disorder, they enter a world of expensive treatments, insurance battles, and lifelong medical management. Without advocacy, many can't afford the therapies that keep them safe.

The solution
HFA stands between patients and a broken system
For 30 years, HFA has had a seat at the table — before Congress, the FDA, and the CDC — fighting for safe therapies, fair coverage, and the rights of every family in the bleeding disorders community.

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Hemophilia Federation of America
999 N. Capitol Street NE Suite 301
Washington, District of Columbia 20002-6096 US
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