The Facial Pain Association (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 educational […]

About Us / About the Job  The Facial Pain Association (FPA) is a registered 501(c)(3) nonprofit organization founded in 1990. Our mission is to serve those with neuropathic facial pain, […]

We are excited to announce that the Facial Pain Association is a Platinum member of the National Organization for Rare Disorders, Inc. (NORD). Being a part of NORD’s membership network […]

The holidays can be a joyous time filled with parties and family gatherings. Unfortunately, the holidays can also be a time of increased loneliness and isolation. This can be especially […]

I will never forget the first time I dialed Claire Patterson’s number back in 1990. She sat at her kitchen table, laying the foundation for an organization that would go […]

As we stand on the threshold of a new year, I want to take a moment to reflect on the strength of the facial pain community. You offer one another […]

GuideStar is the world’s largest source of information on nonprofit organizations. It gathers and provides access to the most comprehensive, up-to-date, and accurate nonprofit information available. GuideStar’s mission is to […]

Advocacy— it’s part of our mission at the Facial Pain Association, but what does it mean? Well, this year, it means a whole lot more. As a community, we have hit […]

The Facial Pain Association marks its 35th anniversary this year. Thirty-five years of providing educational resources, connections to medical professionals, and support to those affected by facial pain. I am […]

John TempleVice Chairman, FPA Board of Directors What is a DAF? Donor-advised funds are 501(c)(3) charitable funds that aggregate charitable donations. Most national investing platforms such as Vanguard, Fidelity, and […]

A few months ago, I visited my dentist, who is familiar with neuropathic facial pain. Near the beginning of the appointment, she introduced a student who would be assisting. As […]

Shorter days and cooler weather often make this time of year difficult, especially for those with facial pain. Focusing on what we can do to help others can be an […]

January 5, 2023: The Facial Pain Association’s Phone a Pain Pal Holiday Help Line has concluded after a three-week pilot program. The FPA would like to thank the 30+ generous […]

We are grateful for everyone who supports our mission. When you give your time as a volunteer, use your voice to raise awareness, sponsor a fundraiser, or make a donation, […]

There are 300,000+ of us in the U.S. with trigeminal neuralgia and this past year approximately 15,000 more joined our group if the epidemiological estimates are correct. Add to these numbers […]

New beginnings often bring excitement, anticipation, and sometimes trepidation. As we begin our journey into 2023, I have to say I’m grateful to be part of the Facial Pain Association, […]

The Facial Pain Association is the largest patient organization supporting all people affected by neuropathic facial pain, leading the world in resources for information and healthcare guidance. Through educational programs, […]

Friends, By now I hope you’ve heard about our upcoming virtual conference on April 28-29, 2023! This is a fantastic opportunity for support and education, providing valuable learning opportunities, connection with […]