Education. Support. Advocacy.
Since 1957, the New England Hemophilia Association has proudly assisted families in Connecticut, Massachusetts, Maine, New Hampshire, Rhode Island, and Vermont with a bleeding disorder through education, support, and advocacy.
Become a 2019 Member
We are proud of the strides and growth we’ve made by touching the lives of thousands of individuals through our programs and services, at our meetings, with print materials, and social media. With your help and support, we can continue to do great things. 100% of all membership dues support the New England bleeding disorders community.
Check out NEHA’s wide-array of award-winning programs designed to meet the needs of the entire bleeding disorder community. Register for an event in your area today.
Get involved in building our Wicked Strong family by becoming a member, making a donation, or volunteering your time. NEHA and the bleeding disorder community couldn’t do it without you!
Want to learn more about bleeding disorders? Here you will find current and reliable information on inherited bleeding disorders, such as hemophilia and von Willebrand disease.
NEHA is committed to empowering individuals with a bleeding disorder and their families to advocate for themselves. This includes learning to advocate for oneself in a medical environment as well as advocating for change in policies at the state and national level. Join our advocacy efforts today.