The Facial Pain Association

The Facial Pain Association The world's leading resource for everyone affected by facial pain conditions. We serve everyone affected by facial pain.
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Our mission is to serve those with neuropathic facial pain, including trigeminal neuralgia, through support, education, and advocacy. Founded in 1990 as the Trigeminal Neuralgia Association, FPA is a registered 501(c)3 nonprofit organization.

Do you have neuropathic facial pain, such as trigeminal neuralgia, occipital neuralgia, anesthesia dolorosa or burning m...
06/05/2026

Do you have neuropathic facial pain, such as trigeminal neuralgia, occipital neuralgia, anesthesia dolorosa or burning mouth syndrome and live in the Midwest? The Facial Pain Association has support groups for you.

Join our support groups in Indiana, Kentucky, Michigan, Minnesota, Missouri, Ohio and Texas.

Share your story, ask questions about doctors and treatments, and make new connections!

Find a support group near you: https://www.facepain.org/find-support/about-support-groups/

Join us for a free live webinar with AdventHealth Orlando on Thursday, June 18 at 6:30 PM ET. Dr. Dharani Mudugal and D...
06/04/2026

Join us for a free live webinar with AdventHealth Orlando on Thursday, June 18 at 6:30 PM ET.

Dr. Dharani Mudugal and Dr. Melvin Field will cover how trigeminal neuralgia is diagnosed and distinguished from other facial pain conditions, medication options and their side effects, when surgery should be considered, and how their neurology and neurosurgery teams work together to coordinate patient care.

Questions from patients and caregivers are welcome, either in advance or during the webinar.

Register now by visiting https://us02web.zoom.us/webinar/register/4417794621241/WN_K1QLLCDsRCGJYuDP7bR-jg

Did You Know đź’ˇ The Facial Pain Association has a guide for living well with facial pain. Being an active participant in...
06/04/2026

Did You Know đź’ˇ The Facial Pain Association has a guide for living well with facial pain.

Being an active participant in your overall wellness will provide you with a sense of empowerment while you raise your quality of life. Taking steps to improve your sleep, nutrition and diet, oral and dental care, and physical activity may not rid you of facial pain, but they will likely provide great benefits and make you feel better overall.

Learn more here: https://www.facepain.org/managing-facial-pain/living-well/

Next week, we are celebrating the one-year anniversary of the Facial Pain Registry launching this June with Facial Pain ...
06/03/2026

Next week, we are celebrating the one-year anniversary of the Facial Pain Registry launching this June with Facial Pain Registry Week! During Registry week, we will share the latest in data discovery, behind the scenes with the researchers and doctors using the Registry and testimonials from people about why they feel it is important to add their data to a rare disease registry.

Share your Facial Pain Registry story on social media and tag the Facial Pain Association to be featured! Tell us why you joined the Registry and share your hopes for the future of facial pain research.

If you haven’t joined the Facial Pain Registry yet, you can help us reach our June 2026 goal of 1,000 participants by adding your data to the Registry. Join the Facial Pain Registry today by visiting https://www.facepain.org/facialpainregistry

Join us next week at 4:00 PM as we continue the 2026 Video Series with “Managing Ongoing Trigeminal Neuropathic Pain” pr...
06/03/2026

Join us next week at 4:00 PM as we continue the 2026 Video Series with “Managing Ongoing Trigeminal Neuropathic Pain” presented by Jeannine Conway, PharmD, Monique Montenegro, MD and Maram Taema, DDS

Although the video is not live, we encourage you to comment and ask questions. Your participation and feedback will help us gauge interest in a variety of topics to better serve the community with future webinars.

The video will premiere on the FPA’s YouTube Channel and on our website at: https://www.facepain.org/tag/webinars/

Registry Data Discovery: 35% of Facial Pain Registry participants report currently having trouble chewing, while 34% sai...
06/02/2026

Registry Data Discovery: 35% of Facial Pain Registry participants report currently having trouble chewing, while 34% said they have had difficulty in the past.

If you haven’t joined the Facial Pain Registry yet, you can help us reach our June 2026 goal of 1,000 participants by adding your data to the Registry. Join the Facial Pain Registry today by visiting https://www.facepain.org/facialpainregistry

June is Migraine and Headache Awareness Month đź’śJoin us this June to help raise awareness for headache and migraine disor...
06/01/2026

June is Migraine and Headache Awareness Month đź’ś

Join us this June to help raise awareness for headache and migraine disorders, including neuropathic facial pain.

The Facial Pain Association is proud to stand with other organizations in the fight to support, education and advocate for patients, their loved ones and healthcare providers in the headache and migraine space.

If you have a migraine or headache disorder, including neuropathic facial pain, tag the FPA in your awareness social media posts this June! Together, we can change the future of treatment and support for people with headache disorders.

Do you have neuropathic facial pain, such as trigeminal neuralgia, occipital neuralgia, anesthesia dolorosa, or burning ...
05/29/2026

Do you have neuropathic facial pain, such as trigeminal neuralgia, occipital neuralgia, anesthesia dolorosa, or burning mouth syndrome and live on the East Coast? The Facial Pain Association has support groups for you.

Join our support groups in New York, the Carolinas, Pennsylvania, New Jersey, Washington DC, Virginia, Maryland, Massachusetts, Florida, Georgia, or New England.

Share your story, ask questions about doctors and treatments, and make new connections!

Find a support group near you: https://www.facepain.org/find-support/about-support-groups/

The FPA's Peer Mentor program allows people living with neuropathic facial pain to connect with 1:1 support. Our Peer Me...
05/29/2026

The FPA's Peer Mentor program allows people living with neuropathic facial pain to connect with 1:1 support. Our Peer Mentors are trained volunteers who can be empathetic listeners, share their experiences, connect you to resources, and share tips for coping with facial pain that is unique to your journey.

You can learn more on our website: https://www.facepain.org/connect-with-11-support/

Address

7778 McGinnis Ferry Road, #256
Suwanee, GA
30024

Telephone

+18009233608

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