The National Neurofibromatosis Foundation (NNFF)
Information sponsored by the National Neurofibromatosis Foundation for people with NF, and links.
http://www.nf.org/

Neurofibromatosis(Von Recklinghausen's disease)
A review of the most important aspects on physical examination, classification and treatment, for medical students.
http://www.medstudents.com.br/neuro/neuro7.htm

The Neurofibromatosis Association UK
Information about the UK Association, including family support, membership details and local group contacts.
http://www.users.zetnet.co.uk/neurofibromatosis/

Neurofibromatosis Clinic at M. D. Anderson Cancer Center
Information about neurofibromatosis and details of Center which provides diagnosis, treatment, patient education, and relevant research.
http://www.mdanderson.org/departments/neurofibrom/

Neurofibromatosis
Information page compiled by NINDS, the National Institute of Neurological Disorders and Stroke.
http://www.ninds.nih.gov/health_and_medical/disorders/neurofibro.htm

British Columbia Neurofibromatosis Foundation
BCNF is a membership driven organization, which empowers individuals with NF and their families to reach their full potential by providing support, education and research funding.
http://www.bcnf.bc.ca

Neurofibromatosis Association of Australia Inc.
Support group for people with neurofibromatosis. Has a medical and scientific advisory board and close affiliation with similar NF groups overseas.
http://www.nfaa.org.au/

NF2Crew
On-line discussion group for people with neurofibromatosis 2.
http://www.nf2crew.org

NexGenix Pharmaceuticials
Drug therapies for the treatment of two genetic disorders: neurofibromatosis type 1 (NF1) and neurofibromatosis type 2 (NF2). Find overviews, clinical trials and news.
http://www.nexgenixpharm.com

Neurofibromatosis Clinics Association, Inc.
A non-profit organization for people with NF and their families.
http://www.nfpittsburgh.org/

Race for NF Research
Dedicated to promoting awareness of Neurofibromatosis. It also contains the latest research as well as fund raising programs (Marathons, racing, walking, etc) that raise money towards NF research.
http://www.racefornfresearch.com

Understanding Neurofibromatosis
This information will explain what NF is, what causes NF, what your family will need to do about it, and who can help you. From the University of Chicago Comer Children's Hospital.
http://www.uchospitals.edu/peds-neurology/neurofibromatosis/

The Children's Tumor Foundation
Dedicated to improving the health and well being of individuals and families affected by the neurofibromatosis (NF).
http://www.ctf.org

Neurofibromatosis Resources - Photographs
Photos of cafe au lait spots and external neurofibroma tumors.
http://neurosurgery.mgh.harvard.edu/NFR/photos.htm

Just Ask!
Presents the personal aspects of living with the disease, including news, photographs and videos.
http://www.reggiebibbs.com

Texas Neurofibromatosis Foundation
Includes a list of events, fundraisers and outreach programs, as well as background information on the disease, and links to related resources.
http://www.texasnf.org