Dedicated to advancing the understanding and treatment of neuropathic facial pain, the Facial Pain Association (FPA) provides non-financial support of research efforts, including letters of support, community survey data, patient
Advocacy— it’s part of our mission at the Facial Pain Association, but what does it mean? Well, this year, it means a whole lot more. As a community, we have hit
Worrying about your next pain flare and how people may perceive you when experiencing facial pain is common in the facial pain community. Due to their nature, facial pain episodes
Advocacy lies at the core of our mission. Through educational resources and volunteer support, the FPA empowers the facial pain community to advocate for themselves and one another. From using
Kenneth F. Casey, MD Have you heard that white potatoes are bad for you? Or that going out in the cold without a jacket will make you sick? Medical misinformation
By Jeffrey Fogel, MD, Member of the FPA Board of Directors Dr. Jeffrey Fogel is an FPA Board Member and pediatrician who was diagnosed with trigeminal neuralgia (TN) in 2008