Founded in 1952, the Association is an independent not-for-profit voluntary health organization, incorporated in the state of New York, and classified under Section 501(c)(3) of the Internal Revenue Code.
To benefit patients, HANY maintains cooperative relationships with the federally-designated Regional Comprehensive Hemophilia Treatment Centers and other care facilities within our 14-counties service area.
HANY does not charge fees for the services it provides, but depends on voluntary contributions to support its programs. The Association is an organization of and for persons with bleeding disorders and their families helping each other.
Our Mission is:
To assist persons with hemophilia and related blood disorders through direct services and aid, and through programs of education and advocacy.
To encourage, promote, and support scientific research toward improved treatment, medical care, and cures of hemophilia and related bleeding disorders and their complications.
To educate the public regarding bleeding disorders and the problems thereof, and to promote the procurement of voluntary blood donations for the general welfare of the community at large.
You can impact several lives by joining our Footprints journey and becoming a fundraiser.
Leave your footprints!
Giving makes life worth living!
Hemophilia Association of New York
131 West 33rd Street, Suite 11D, New York, NY 10001
CHARITY FOOTPRINTS, INC.
We're committed to making this world healthy, generous & happy by promoting fitness and encouraging charitable giving. Let's get started and #GetFitGiveBack.