Patient Registry

        Now, more than ever, your participation in the patient registry by completing a survey is an opportunity to contribute to scientific research and expand what we know about TN and related facial pain. It could yield significant benefits, and influence treatment in the future. Please join us in this effort, and build hope for the future. Together, we will end the pain!

        The TNA Patient Registry has been converted to a newer, more efficient data structure.  Your input is very important to us and to our efforts to promote awareness of and support for this rare disorder.  Please take a few moments to complete the "Face Pain Survey" online by using the links provided, or if you would prefer, you may print the form and return it to our national office (click here)

Privacy Policy—we do not sell, rent, or lend the e-mail addresses of our subscribers.

Updated 2-2-07