Rare Disease Day 2023

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,

Happy New Year!

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 FPA: 2022 Year In Review

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

There’s Still Time to Make an Impact in 2022

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,

Phone a Pain Pal: The FPA Holiday Help Line

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