This year, the Facial Pain Association is proud to celebrate 35 years of dedication to our mission — improving the lives of those affected by facial pain through support, education, and advocacy. Thanks to your generosity, we have built a compassionate community, filled with people who understand one another. We have provided critical resources, including educational materials and connections to experts who can help. And we have increased awareness of neuropathic facial pain, including trigeminal neuralgia and the other debilitating conditions that impact our community.
But while we honor the work that has been done, we also look to the next 35 years — a future filled with even greater hope, understanding, and progress.
A key part of that future is the upcoming launch of the Facial Pain Registry. It’s more than just a database, it’s a transformative initiative that we hope will drive research, improve treatments, and elevate the voices of everyone living with facial pain. Our hope is that by gathering comprehensive patient data, researchers and industry partners will see viable opportunities to focus on neuropathic facial pain, bringing scientific advances to a community who desperately needs them.
But the potential impact of the registry extends beyond research. Our hope is that it will:
• Inform the way we provide support and help us connect patients with better resources.
• Enhance educational tools, providing those living with facial pain with the knowledge they need.
• Amplify our advocacy efforts, ensuring that policymakers, medical institutions, and the broader community
Join us in building the future. Your donation today will fuel the next generation of progress in research, support, education, and advocacy.
Together, we can make an even greater impact. Donate now and help shape the future of facial pain care.
