The New England Hemophilia Association is dedicated to improving the quality of life for persons with bleeding disorders and their families through education, support, and advocacy.


New England Hemophilia Association is the leading organization in New England dedicated to empowering individuals and families with bleeding disorders and building local and region-wide communities for them by providing diverse information sources, dynamic programming, individual and legislative advocacy, and emergency financial aid.


The New England Hemophilia Association, established in 1957, is a chapter of the National Hemophilia Foundation, and a chapter of the Hemophilia Federation of America.




Become educated on the different types of Bleeding Disorders.  You can also learn about the Programs and Services that we provide.




Learn about NEHA's Advocacy mission as well as the State Advocacy Issues and the National Advocacy Issues that are currently going on.

NEHA is grateful to these Corporate and Non-Profit Partners for their financial support in 2014.

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  There are a variety of ways that NEHA supports the local bleeding disorders community.  Learn about our Emergency Assistance Fund. 


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