Updates on the FPA’s Research Initiative

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
The FPA Patient Registry

The FPA Patient Registry

The MAB Corner – By Wolfgang Liedtke, MD, PhD Dear members of the Facial Pain Association, I’d like to give you my take on the FPA patient registry, which is in