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Our team has curated app, clinical trials, and organizations that help with trigeminal neuralgia so you know what resources to trust.
Ouchie is a free app available in the App Store and on Google Play that helps users manage chronic pain. With tracking,…
Flaredown is an app that allows users to track symptoms for a chronic illness. Users can enter in all symptoms, conditions,…
The Pain Tracker & Diary app was designed by MD and PhD Pharmacology specialists to help users track and manage chronic…
The Manage My Pain Lite app allows users to track and understand pain related to various conditions. Users can utilize the…
The iBeatPain for Teens app helps teenagers manage chronic pain and related symptoms. The app provides guidance to teens and…
PainScale is a free pain tracking app available in the App Store and on Google Play. It was created with consultation from…
The Feasibility Study of ExAblate Thalamotomy for Treatment of Chronic…
The (Botox) Mechanisms of Action in Altering the Molecular Environment in…
The study conducted by The Will Erwin Headache Research Center is aimed at…
The Neurophysiologic Signatures of Trigeminal Neuralgia Pain study is aimed…
The American Association of Neurological Surgeons is a scientific and educational association with more than 10,000 members that is dedicated to advancing…
FaceFacts.org features information and videos about a variety of chronic facial pain conditions, including trigeminal neuralgia. All of the written content is…
The Facial Pain Association website has a wide array of resources and information for people with trigeminal neuralgia. Users can easily find written information…
The American Chronic Pain Association (ACPA) offers “peer support and education in pain management skills to people with pain, family and friends, and health care…
The National Organization for Rare Disorders (NORD) “is a patient advocacy organization dedicated to individuals with rare diseases and the organizations that…
The National Institute of Neurological Disorders and Stroke (NINDS) aims “to seek fundamental knowledge about the brain and nervous system and to use that…
The Genetic and Rare Diseases Information Center (GARD) is “a program of the National Center for Advancing Translational Sciences (NCATS) to provide access to…
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