To end neurofibromatosis (NF) by funding research, increasing public awareness, supporting patients and families, and encouraging the establishment of NF clinics.

CTF extends grants to scientists for studies into the causes of and treatments for neurofibromatosis types 1 and 2, Schwannomatosis and related disorders (NF). Primary research funding supports young investigators, drug discovery seed grants, pilot clinical trials, and a national consortium of research institutions got preclinical testing of promising compounds. For kids with NF, CTF hosts a summer camp where they are able to develop friendships and have an outlet for discussing questions and collective concerns. Support groups and other programs are coordinated by CTF chapters and affiliates. In addition to newsletters, CTF also produces guides and brochures for patients and their families on NF topics.

Research & medical programs
Public education
Grants
Fundraising