The TMJ Association
The TMJA is staffed by a volunteer CEO, two staff members, and dedicated office volunteers.
Terrie Cowley, TMJA President and Co-founder, is a longtime TMJ implant patient whose personal and intimate knowledge of the plight of patients motivates a commitment to resolve any disconnect between scientific research findings and current treatment practices. Terrie has been tireless in alerting policymakers and members of Congress, the media, federal health and research agencies, implant manufacturers and dental and medical educators to the needs of patients, as well as promoting research aimed at developing evidenced-based diagnostics and treatments. Terrie received a BA in political science from Millsaps College and also attended Harvard University, where she studied at the Kennedy School of Government.
Deanne Clare, TMJA Administrator, has been vital in helping the organization fulfill its mission and objectives for over 20 years. Among many critical operational responsibilities, she executes the daily operations of the office, maintains TMJA’s website and social media, oversees production and dissemination of publications, and has coordinated the Association’s past eight international scientific meetings. Deanne is passionate about advocating for and advancing the needs of patients, as well as the development of safe and effective treatments and public awareness of chronic overlapping pain conditions. Deanne holds a Bachelor of Science in Business Administration from Marquette University.
Christin Veasley, Co-founder and Director of the Chronic Pain Research Alliance, an initiative of The TMJ Association, has lived with chronic pain since surviving a near-fatal accident in her teens. Her health experiences led her to pursue a Bachelor of Science degree, time conducting neuroscience research at Johns Hopkins Medical School and to the research advocacy community. Her life’s work has been to advocate for the acceleration of rigorous multidisciplinary pain research and the translation of research findings into meaningful change for people with chronic pain – with a special emphasis on pain conditions that are common in women and frequently co-occur. She has been a passionate advocate at the Congressional and federal agency levels for bringing about public awareness of the profound impact of chronic pain, the urgent need for an increased federal research investment to address this public health crisis and the long-overlooked value of including patient perspectives in all aspects of the research continuum. For over twenty years, she has served in several nonprofit management and leadership positions. She holds advisory positions for numerous critical pain initiatives within federal agencies, such as the NIH, CDC and FDA; academic pain research studies; and various collaborative alliances and public-private partnerships working to promote pain research, treatment and education. Chris has authored journal articles, op-eds, book chapters, continuing medical education programs for health care providers, patient tutorials and self-help guides. To promote awareness, she speaks openly about her experience with chronic pain and its profound impact on her life. Chris has been a presenter at over 30 medical, research and policy conferences, as well as federal agency meetings, and has been interviewed for print, television and radio media.
We would not be able to do what we do without our team of dedicated office volunteers. They assist us with our day-to-day office operations which include; proofreading, scientific literature searches, mailings, filing, and maintaining our website and computer systems. Our sincere thanks to Lisa Baker, Maureen Black, Claudia Clare, Laurie Friedrich, Lina Lee, Greg McQuestion, Karen McQuestion, Steve Pusztai, Janet Rakowski, Carol Jo Shonka, and Anthony Uljanec.