Facial Pain Association
The Facial Pain Association is the largest patient organization supporting all people affected by neuropathic facial pain, leading the world in resources for information and healthcare guidance. Through educational programs, personal support, and advocacy efforts, the FPA supports patients, their loved ones and caregivers, and healthcare professionals who diagnose and treat people affected by facial pain.
The Facial Pain Association's mission is to serve those with neuropathic facial pain, including trigeminal neuralgia, through support, education, and advocacy.
Visit us at https://www.facepain.org
Advocacy 101: What is Advocacy and Why Does it Matter?
By
Facial Pain Association
FEATURING
Julienne Verdi
By
Facial Pain Association
FEATURING
Julienne Verdi
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