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
