ILADS announces the launch of a new research database for healthcare providers treating Lyme and related diseases: One Health Lyme
Evidence and Research-Based Lyme Treatment Recommendations
ILADS board of directors has determined that the upcoming conferences at East Stroudsburg University (April 17-18, 2020), Richmond (April 25, 2020), and Budapest (June 4-6, 2020) shall be rescheduled for later dates due to the corona virus situation.
Plan on attending our fall meeting in Washington, DC where discussions will be very timely and relevant. Abstract submissions are now open for the fall meeting. The theme of the fall meeting is: COMPLEXITIES OF HOST PATHOGEN INTERACTIONS RESULTING IN DISEASE.
We appreciate everyone's support and understanding during this global health crisis.
2020 ILADS Annual Conference in Washington, DC
Complexities of Host Pathogen Interactions Resulting in Disease
Save the Date!
September 10-13, 2020 | Washington, DC
Please join us for the International Lyme and Associated Diseases Society (ILADS) 21st Annual Conference. This year’s conference will be held September 10-13, 2020 at the Washington Marriott Wardman Park in Washington, DC.
2019 ILADS Annual Conference
Chronic Disease = Chronic Infections?
October 31 – November 3, 2019 | Boston, MA
News from the Board
Chevy Chase, MD – March 26, 2020 – The International Lyme and Associated Diseases Society (ILADS) is launching a new registry and crowd-solving platform, One Health Lyme, which will provide valuable resources to healthcare providers who are treating patients with Lyme and related diseases. In the planning stages for a while, the launch of the One Health Lyme initiative is being pushed forward expeditiously in response to the COVID-19 pandemic. One Health Lyme will give Lyme healthcare providers a unique opportunity to track and communicate the impact of COVID-19 on this specific group of patients. The unique immunological lesions of these patients will help us gain insights of general importance in the battle against COVID-19. Similar to initiatives operated by specialty societies that treat autoimmune diseases, this project will collect data from physicians about patient experiences and treatments. The goal is to create a vast repository of information about lyme…Read More >