Give the Gift of Education
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
My Clinical Trial Experience
Anne-Marie Clarke is a retired Family Court Judge. She loves to travel. She is grateful for the help she has found for dealing with trigeminal neuralgia (TN) through Facebook and
My Rhizotomy Journey
Hello, my name is Stephanie Blough, and I am honored to share my experience with trigeminal neuralgia (TN) and the successful surgery I had that has left me pain and
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,
