The information contained in the Organizational Database (ODB) is provided for informational purposes only. There is no implied endorsement by NORD. NORD does not promote or endorse participation in any specific organization. The information is subject to change without notice. Every effort is made to ensure that the details for each entry are as current as possible.
22 SE 5th Ave
Gainesville, FL 32601 USA
The TNA - The Facial Pain Association is a national, non-profit organization dedicated to providing information, mutual aid, support, and encouragement to people with trigeminal neuralgia (TN) and their families. Trigeminal neuralgia (or tic douloureux) is a disorder of the trigeminal (fifth) cranial nerve that causes intense, episodic pain in facial areas connected to the trigeminal nerve. Founded in 1990, FPA is also committed to increasing public and professional awareness of the disorder and reducing the isolation of those affected. The association serves as a resource and information clearinghouse for data and medical efforts on behalf of treatment for TN. It also encourages medical research into the causes and treatments for this disorder. The association's Medical Advisory Board consists of key specialists in the medical and surgical treatment of TN, dentistry, and pain management. FPA also has a network of local support groups that enable affected individuals to share experiences, receive encouragement, and obtain current information on the disorder's treatment. In addition, the association promotes patient advocacy and conducts an educational outreach program to medical and dental practitioners, and in addition, to the general public.
The National Organization for Rare Disorders (NORD) web site, its databases, and the contents thereof are copyrighted by NORD. No part of the NORD web site, databases, or the contents may be copied in any way, including but not limited to the following: electronically downloading, storing in a retrieval system, or redistributing for any commercial purposes without the express written permission of NORD. Permission is hereby granted to print one hard copy of the information on an individual disease for your personal use, provided that such content is in no way modified, and the credit for the source (NORD) and NORD’s copyright notice are included on the printed copy. Any other electronic reproduction or other printed versions is strictly prohibited.
NORD's Rare Disease Information Database is copyrighted and may not be published without the written consent of NORD.