New England Hemophilia Association
About
The New England Hemophilia Association is a Dedham-based nonprofit serving people with inherited bleeding disorders, such as hemophilia and von Willebrand disease, and their families across all six New England states. Its mission is to build an inclusive regional community that empowers members through education, support and advocacy. The association offers current, reliable information about bleeding disorders and helps individuals and families learn to advocate for themselves, from public policy to daily life.
Founded in 1957, NEHA brings families together through programs held throughout the region, including camps, retreats, conferences and social connection events. It describes its community as a Wicked Strong family and invites supporters to join as members, donate or volunteer their time. Its staff includes a program and engagement manager, a marketing and communications director, an advocacy coordinator and a Latino community consultant, and a board of directors oversees the organization.
What to Know
- All membership dues go directly to supporting the local bleeding disorders community.
- Community members can contact the board of directors directly with questions or suggestions.
- It is a member of Dedham Square Circle.
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