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. HANY does not charge fees for the services it provides, but depends on voluntary contributions to support its programs.
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. BE PART OF US.
Our Mission:
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.
HANY serves persons with hemophilia and related congenital blood clotting disorders in the 14 southeastern counties of New York State (New York City, Long Island, Dutchess, Orange, Putnam, Rockland, Sullivan, Ulster and Westchester).
This publication may contain medical information taken from sources believed to be reliable. HANY provides this material for your general information only. HANY does not engage in the practice of medicine, nor does it advocate or recommend specific medical treatments. You should consult your physician or local treatment center before pursuing any course of treatment.
