Since 1977, serving the people of North Carolina
Hemophilia of North Carolina was formed in the 1970s by a diverse group of parents, patients, spouses, health care professionals and others with an interest in promoting awareness, providing support and disseminating information to the community. Today HNC has over 700 member families and provides services and support to all persons with bleeding disorders.
HNC keeps patients and care givers aware of the latest news of interest on topics ranging from medical and insurance issues to programs and activities from which they may benefit. The Concentrate newsletter also provides updates on HNC projects and opportunities.
Additional activities include:
Hemophilia of North Carolina is a 501(c)(3) non-profit organization.
Copies of HNC's IRS Form 990 (Return of Organization Exempt from Income Tax) are available:
Financial information about this organization and a copy of its solicitation license are available from the North Carolina Solicitation Licensing Section, phone 1-888-830-4989. The license is not an endorsement by the State.
As a non-profit advocate for the bleeding disorders community, Hemophilia of North Carolina avoids any affiliation with the pharmaceutical, home care, or specialty pharmacy industries or any other for-profit corporation. Corporate logos and/or links to corporate sites displayed on posters, flyers and the HNC website only recognize sponsorship of specific events or projects. HNC never endorses treatment products, manufacturers, home care services or individual medical providers.