Established more than 30 years ago, The Neil Frick Resource Center (NFRC), formerly HANDI, provides valuable information and support for individuals with inheritable blood and bleeding disorders, their families, and healthcare professionals. Find resources, connect with the community, and access vital information about treatment centers, support groups, and more.
The Neil Frick Resource Center (NFRC), previously known as HANDI (the Hemophilia and HIV/AIDS Network for the Dissemination of Information), has served the bleeding disorders community for over 30 years. Initially established during the HIV/AIDS epidemic, HANDI provided essential support and information, funded by a CDC grant, to individuals and families.
Under Neil Frick’s leadership for more than 26 years, HANDI expanded its reach, offering guidance on diagnosis, treatment, and support. In honor of his remarkable legacy, HANDI has been renamed the Neil Frick Resource Center (NFRC), ensuring Neil's advocacy continues to benefit the community for years to come.
Information resources developed by the Neil Frick Resource Center (NFRC) for aiding consumers and families affected by inherited bleeding disorders as well as for healthcare providers and the general US public.
NBDF does not give medical advice nor engage in the practice of medicine. NBDF under no circumstances recommends a particular treatment for specific individuals and in all cases recommends that you consult your physician or local treatment center before pursuing any course of treatment. All requests for information submitted to the Neil Frick Resource Center (NFRC) are kept strictly confidential.
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