New England Hemophilia Association

Founded in 1957, The New England Hemophilia Association (NEHA) is dedicated to improving the quality of life for persons with inherited bleeding disorders and their families through education, support, and advocacy.

NEHA creates programming with the conviction that education, support, and advocacy can improve quality of life, prevent disability, and enable persons to live active, fulfilling lives. NEHA currently offers a range of programs and services throughout the six New England states. Led by a volunteer Board of Directors, and managed by a small group of professional staff, the organization is well positioned to lead this community into the future.

Visit NEHA at www.newenglandhemophilia.org to learn more!