Advocacy

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 our voices during Facial Pain Awareness Month and Rare Disease Day to sharing our lived experience with researchers seeking to understand facial pain and find better treatments.

As the FPA continues to meet you where you are today, we press forward for progress. By partnering with organizations committed to advocating for legislative changes, funding allocations, and policy reforms, we can amplify our collective voice and have a greater impact.

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