The National Hemophilia Foundation, based in New York, NY, is a leading organization dedicated to improving the lives of individuals with bleeding disorders. With a rich history spanning 75 years, they provide comprehensive medical care, educational programs, advocacy, and support for patients, healthcare professionals, and the community.
Through their initiatives, such as the Red Tie Society and the ACT Initiative, the foundation strives to promote health equity and advance research in the field. Their team of dedicated staff and board members work collaboratively with partners and stakeholders to ensure access to quality care and support for individuals with bleeding disorders.
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