Rare Disease Day 2024
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 educationalDr. Liedtke Reflects on Joining the American Clinical and Climatological Association
The FPA congratulates Dr. Liedtke on his election to the American Clinical and Climatological Association “Wow I’m in!” — it immediately hit me when I recently opened an e-mail fromA Message from the CEO
Every January, many people look forward to the new year with hopes and dreams, goals and objectives. The Facial Pain Association (FPA) is no different. We have spent the lastFrom the Board Chair
We are a community because we share some very important things: We either share the experience of having this terrible pain or helping someone who does; we share the needFacial Pain Association Co-Signs Letter Urging White House Women’s Health Research Initiative to Prioritize Headache Disorders, Including Neuropathic Facial Pain
UPDATE: October 23, 2024 Sprint for Women’s Health Announces Awardees, Featuring Project on Quantifying Neuropathic Pain The Advanced Research Projects Agency for Health (ARPA-H) has unveiled the awardees of the
