The Facial Pain Advocacy Alliance is
the world’s only patient-led 501(c)3 nonprofit dedicated to
serving the chronic facial pain community.
Whether you are a patient or support person, family member or friend – you belong.
As veterans of chronic facial pain ourselves, we know that education and support lead to empowerment of the individual. In a world where our pain is little known and often misunderstood, it is vitally important for a patient to be well informed and well supported. Our mission is to provide a one stop, one-of-a-kind resource for all chronic facial pain patients, no matter where they are on their medical journey.