Facial Pain Association (FPA)

The Facial Pain Association (FPA), formerly known as the Trigeminal Neuralgia Association (TNA), is a registered non-profit, 501(c)(3) volunteer organization, founded in 1990 by a team of people who were profoundly grateful for recovery from years of disabling facial pain.

The FPA is volunteer led and community focused.

The FPA is the largest patient organization supporting all people affected by neuropathic facial pain, leading the world in resources for information and healthcare guidance. Through programs of education, personal support, and advocacy efforts, FPA supports patients, their loved ones and caregivers, and healthcare professionals who diagnose and treat people affected by facial pain.

Mission:
To serve those with neuropathic facial pain, including trigeminal neuralgia, through support, education, and advocacy.

Vision:
To be the most reliable and comprehensive resource on facial pain conditions for patients, their families, and healthcare professionals.