The Hemophilia Association of New York is a non-profit organization located in New York, New York, dedicated to supporting individuals affected by hemophilia and other bleeding disorders. Serving the community from its central location at 131 West 33rd Street, the organization focuses on providing valuable resources, education, and advocacy to improve the quality of life for those impacted by these conditions. Through a variety of programs and outreach efforts, it aims to foster a network of support for patients, families, and healthcare providers alike.
This organization plays a vital role in raising awareness about bleeding disorders, offering guidance on treatment options, and connecting members with essential services. By collaborating with medical professionals and community partners, the Hemophilia Association of New York ensures that individuals receive up-to-date information and assistance tailored to their specific needs. Educational workshops and support groups are among the key initiatives that help empower individuals to manage their health effectively and navigate the challenges associated with these conditions.
Beyond direct support, the Hemophilia Association of New York engages in advocacy efforts to influence public policy and improve access to care for people with bleeding disorders. The organization’s commitment extends to fostering a community where patients and families can share experiences and resources in a compassionate environment. For those seeking information or wishing to get involved, the association can be reached at 212-682-5510, providing a vital connection to ongoing support and community engagement in the New York area.
