FPA Submits Response to NIH HEAL Initiative® Request for Information about how scientific research can address the urgent public health challenges of opioid use disorder, overdose, and chronic pain
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 programs of
Spring 2024 YPC Scholarship Recipient — Adrienne Burg
The Young Patients Committee (YPC) assists in fulfilling the mission of FPA by representing the interests of neuropathic facial pain patients under the age of 40. In 2021, YPC launched
Spring 2024 YPC Scholarship Recipient — Jennifer Hoeksema
The Young Patients Committee (YPC) assists in fulfilling the mission of FPA by representing the interests of neuropathic facial pain patients under the age of 40. In 2021, YPC launched
Updates on the FPA’s Research Initiative
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
A journey of a thousand miles begins with a single step…
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
