Lyme Disease Association Inc. Board of Directors 2023
Patricia V. Smith, BA
President
Patricia V. Smith, a Monmouth University graduate, is in her 26th year as President of the all-volunteer run national non-profit Lyme Disease Association (LDA). She is a member of Columbia University’s Lyme & Tick-Borne Diseases Research Center Advisory Committee and a member of the Environmental Protection Agency’s (EPA) PESP Partnership to promote avoidance of tick exposure. She is also serving on several panels for LymeX, the public-private partnership between the Cohen Foundation and HHS.
She served two terms as a public member of the HHS Tick-Borne Disease Working Group (TBDWG) in Washington, DC, where she co-authored the TBDWG Group Report to Congress 2018 and the TBDWG Report to Congress 2020 and wrote several minority reports contained in those documents. In her second term, she co-chaired the “Training & Education, Patient Access to Care” Subcommittee and co-authored its report, and was a member of the Inventory Subcommittee. In her first TBDWG term, she co-chaired the Subcommittee and co-authored its Report of the Disease Vectors, Surveillance, and Prevention Subcommittee 2018.
She was appointed in 2016 as a member of the US Army Medical Research and Materiel Command (USAMRMC) Tick-Borne Disease Research Program (TBDRP) as a member of the Congressionally Directed Medical Research Program Programmatic Panel, where she served 4 years. She has twice testified before Congress– in Washington, DC, on Lyme disease. Ms. Smith is also former Chair, (NJ) Governor’s Lyme Disease Advisory Council. She was EPA’s PESP 2011 Lyme prevention conference session co-chair with CDC. In 2011 she presented a Lyme session to the New Jersey Education Association’s Annual Meeting. She is a member & former officer of ILADS, International Lyme & Associated Diseases Society, a professional medical and research organization. She was a member of the on-line journal, Contagion Infectious Disease Today, Chronic Lyme Expert Panel on video.
Pat is former President/12-year member of the Wall NJ Board of Education where she earned state board member-certified status. She is a former officer of Monmouth County School Boards Assn. and was a member of the Federal Relations Network for New Jersey School Boards Association/National School Boards Assn. During her LDA presidency, Ms. Smith has led the effort to raise funds for researchers nationally, with 123 research grants awarded ─ research acknowledged in 62 scientific journals. She has organized 22 continuing medical education (CME) accredited Lyme scientific conferences for doctors and researchers with international faculty, held in different areas of the US, most jointly sponsored by Columbia University, the past 2 virtual. She has spoken at many conferences on Lyme including those presented by the University of New Haven (CT), the California Lyme Disease Association (now LymeDisease.org), Midcoast Maine Lyme Education and Support, Colorado Tick-Borne Awareness Association, Lyme Connections, Lyme Society, Inc., and International Lyme & Associated Diseases Society, ILADS. She presented Project Lyme’s Zoom Meeting on the IDSA Guidelines in 2020, to PA Lyme Resources 2022, to Nebraska Department of Public Health Officials in 2022, and LymeMind in 2022. In 2023 she has presented to NJ school nurses. She has been a speaker at hundreds of public, school, business, & government events.
Ms. Smith led the LDA in its effort with a partner organization, to endow the Columbia Lyme & Tick-Borne Diseases Research Center in New York, which opened in 2007. She developed the ABCs of Lyme Disease pamphlet for parents and educators (updated in 2019 and translated into Spanish in 2020) and co-authored an article in it, and she also developed the LymeR Primer brochure now featuring 20 tick-borne diseases, the Tick Mark bookmark, and helped design LDA Tick Awareness cards. More than 2.5 million education items have been distributed.
Ms. Smith has testified for and secured passage of state and federal bills for Lyme research and physician’s right to treat. She has been invited to state capitals including CT, MA, MD, MN, NH, NJ, NY, PA, RI, to present oral testimony and education on Lyme and has provided written testimony in many others. Based on her written testimony, LDA was included in ground breaking Maine legislation as a website resource on Lyme disease on Maine’s DPH website. She was invited to testify on two occasions before the NY Assembly Health Care Committee and also before the Rhode Island (Governor’s) Lyme Disease Advisory Commission and has spoken before the California Lyme Disease Advisory Council. Over time, she has personally met with many State Health Commissioners and with Governors in NH, RI CT on Lyme issues and with then Governor Pataki’s office on many occasions along with several NY state legislators. She has also presented before the Pennsylvania House of Representatives Majority Policy Committee and was an invited speaker for Lyme forums hosted by a member of the Massachusetts House of Representatives and the Majority Caucus Administrator for the Pennsylvania House of Representatives and the Minnesota State Senate Health Committee.
She has twice been invited to present to CDC Vector-Borne Diseases Division, Ft. Collins (2007, 2013); met with then CDC Director Dr. Julie Gerberding/5 Congressmen in DC; organized & led a team that met with HHS Asst. Sec. of Health with CDC/NIH officials teleconferenced in; met with military leaders in DC; and briefed the Senate HELP Committee Members and House Subcommittee on Health. She met several times with US Army CHPPM/Public Health Command at Aberdeen Proving Grounds. She met in DC with the NIH Program Director and research coordinator and presented educational Power Points on Lyme to employees at the Environmental Protection Agency (2008, 2014), to the Dept. of Energy, and to Homeland Security in 2014. In 2014, she helped develop language for a federal bill on Lyme and led the nationwide effort which successfully passed the bill through the House. In 2021, another Lyme bill she provided input into was introduced into the House. Language she has provided to Congressmen has been adopted into Appropriations Report language for many years. Ms. Smith spoke at a number of press conferences with Senator Charles (Chuck) Schumer (NY)–now Senate Majority Leader–including one in 2014 on the doxycycline shortage for Lyme patients. In 2012, she testified before the House Foreign Affairs Committee, Africa, Global Health & Human Rights Subcommittee on issues affecting Lyme patients. In 2013, she testified before the House Energy & Commerce Health Subcommittee on HR 610 to establish a federal Lyme & Tick-Borne Diseases Advisory Committee. She co-authored an article which was read into the Congressional Record on Lyme disease research priorities from the patient perspective. In 2015, she spoke at the American Association for the Advancement of Science in DC on patient research priorities. In 2016, she spoke before the Women in Government’s annual conference. In 2016, she led the negotiations with House leadership for the Lyme language subsequently passed in the 21st Century Cures Act which creates a federal working group on tick-borne diseases with patient and advocates reps at the same table as government officials.
Chosen Jackson NJ’s Chamber of Commerce 2008 Woman of the Year, she has also received commendation from the NJ legislature, a Special Congressional Recognition certificate from RI Cong. Langevin, and had a flag flown over the US Capitol by request of NJ Cong. Chris Smith in honor of her Lyme work. Ms. Smith helped to organize and presented at educational forums held by 3 congressmen (Langevin, Pitts, C. Smith). She has received awards from Dr. Brian Fallon, Columbia, from various Lyme groups, and was given the Courage in Advocacy Award in 2015 from Connecticut based Lyme Connection and Focus on Lyme Excellence in Advocacy (AZ) award in 2017. Other activities include providing input into a NJ law requiring teacher education for staff who teach students with Lyme disease, performing school in-services for educators on Lyme disease, and working with parents of students who are classified due to Lyme disease. Working with author Amy Tan, she created LDA’s LymeAid 4 Kids, a fund for children with no health coverage for Lyme, a fund that has awarded $450,000+ for uninsured children to date.