Facial Pain Association

Description

The Facial Pain Association (FPA), a non-profit, 501(c)(3) volunteer organization, was founded in 1990 by a team of people who were profoundly grateful for recovery from years of disabling trigeminal neuralgia pain. The organization now assists thousands of others around the world. FPA has emerged as the world’s leading resource for information and health care guidance for all people suffering from neuropathic facial pain. Both patients and healthcare professionals benefit from its programs of education, personal support, and research.

Available Helps