Links to European neurofibromatosis laygroups.
On-line discussion group for people with neurofibromatosis 2.
Drug therapies for the treatment of two genetic disorders: neurofibromatosis type 1 (NF1) and neurofibromatosis type 2 (NF2). Find overviews, clinical trials and news.
A non-profit organization for people with NF and their families.
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.
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.
Details of many ways to volunteer to help the Neurofibromatosis Clinics Association.
Dedicated to improving the health and well being of individuals and families affected by the neurofibromatosis (NF).
Health /
Conditions_and_Diseases /
Genetic_Disorders
|