TNA -- Facial Pain Association (formerly the Trigeminal Neuralgia Association)

TNA – The Facial Pain Association, a non-benefit, 501(c) (3) volunteer association, was established in 1990 by a gathering of trigeminal neuralgia patients significantly thankful for recuperation from years of crippling agony. The association now helps a large number of patients around the globe. TNA has risen as the world's driving asset for data and medicinal services direction for all individuals experiencing neuropathic facial agony. Both patients and social insurance experts advantage from its projects of instruction, patient backing and research. Controlling the affiliation is a volunteer administering board and a Medical Advisory Board of exceptionally talented specialists in neurosurgery, neuroscience, general medication, and dentistry. More than 2,560 patient phone calls every year and more than 14,500 patient email every year. 1-800 phone numbers, utilized by 5,200 guests every year. Far reaching site, www.fpa-support.org, the main asset on TN and related facial torment conditions for patients and their families, specialists and other restorative experts, policymakers and the general population, accepting over a large portion of a million visits every year. A broad TNA Support Network over the US and around the globe serving more than 10,000 patients. TNA Patient Registry, containing 13,000 patient profiles, for use by specialists. Get us at different national wellbeing proficient association gatherings every year.