The Facial Pain Association (FPA) is committed to serving everyone affected by neuropathic facial pain, including people outside of the United States. Our international resources page provides customized information and support for people living with facial pain around the globe. We are better together, and we are dedicated to helping you find resources and support no matter where you live.
If you don’t have access to a Facial Pain Association in your area, we can offer guidance to start a new organization – one that meets the needs of the local community, wherever that may be. Read More
We currently have several international support groups and a patient guide that has been translated into other languages. We welcome anyone who needs these resources to make use of them
There are a handful of associations dedicated to the support of those living with facial pain in other countries, and we collaborate with them to make sure we are all delivering the support you need. Together we can offer better resources to more people.
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