The British Columbia Neurofibromatosis Foundation is committed to empowering and improving the lives of individuals and families affected by Neurofibromatosis. The BCNF provides information and support services, promotes awareness and funds research to improve treatment and find a cure.
The BCNF erves people with Neurofibromatosis (NF) and their families. Provides information for health professionals, promotes and supports scientific research, hosts an annual medical symposium, publishes a quarterly newsletter, and has a resource lending library. Also offers support groups for people with NF, their significant others, and caregivers. Also provides scholarships for youth with NF to attend the NF INC. summer camp in Arizona. A contact registry is available for members.