Messages To a Young Patient Newly Diagnosed with Facial Pain
Whether you are in the process of finding a diagnosis for your facial pain or just received your official diagnosis, we know how life-changing, overwhelming, and scary it can be.If All You Did Today Is Survive, We Are Proud of You.
The holidays have wrapped up, and we have entered a new year. Social media is full of people including friends and family talking about all they accomplished last year andMeet 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
The FPA Receives Rare Giving Grant
The Facial Pain Association is pleased to announce that we have been awarded a Rare Giving Grant through the EveryLife Foundation for Rare Diseases. In October, Brandi Underwood, the FPA’s
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
