The NF Network (formerly NF, Inc.) was founded in 1988. We are the leading national organization advocating for federal funding for NF research and building and supporting NF communities. "We seek treatments and a cure for neurofibromatosis by promoting scientific research and improved clinical care, and by providing outreach through education and awareness, offering hope and support to those affected by NF". The NF Network’s goal is to eradicate the health issues, pain, isolation and uncertainty that the diagnosis of NF inflicts.
The NF Network programs and services include:
Active pursuit of NF treatments and a cure
Highly successful advocacy program for Congressional funding of NF research through a grassroots initiative involving NF advocates in all 50 states.
Working closely with members of the House and Senate to seek funding for NF research through the National Institutes of Health (NIH) and the Department of Defense Congressionally Directed Medical Research Program (CDMRP);
Providing seed grants for NF researchers
Opportunities for participation with NF researchers, clinical trials, clinicians at scientific meetings and medical conferences.
Building and supporting NF communities
Coordination of state and regional efforts to maximize impact at the national level
Creating awareness of NF and its effects to health care professionals, government authorities and the general public.
Patient outreach through physician referrals
Provide peer support through chats, walks, gatherings, blogs, etc.
Educational meetings and webinars
Publication and distribution of NF educational materials to individuals, physicians, educators, media, etc.