The Hemophilia Association of New York, established in 1952, is a trusted organization dedicated to enhancing the lives of individuals with bleeding disorders through education, advocacy, and direct assistance. With over seventy years of experience and $2.5 million in research grants, they are committed to driving progress and finding solutions for those affected by hemophilia and related disorders.
By providing valuable resources, organizing fundraising events, and collaborating with advocacy groups, the association strives to support the bleeding disorder community in the 14 southeastern counties of New York. Their mission is to offer information, education, and financial aid to individuals with bleeding disorders, while also encouraging scientific research to improve medical treatments and develop potential cures.
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