Meet the Young Patients Committee!

Welcome to the YPC Blog! We wanted to create a space for communication with all young patients in a more casual setting. We’re going to treat this space as a
Rare Disease Day 2025

Rare Disease Day 2025

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
From the Board Chair: 35 Years of the FPA

From the Board Chair: 35 Years of the FPA

About 35 years ago, Claire Patterson, working with Dr. Peter Janetta, the pioneer of microvascular decompression surgery, created what is now called the Facial Pain Association. Over the years, the