The Lyme Disease Association (LDA), an organization which expanded its focus nationally 28 years ago, is dedicated to Lyme disease education, prevention, research funding, and patient support. An average of 97 cents of every dollar raised by the Lyme Disease Association is spent directly for its programs.
The Lyme Disease Association, Inc. (LDA) formulated a response to FDA to be included in its comment period on its testing Guidance which will affect specialty lab Lyme tests. Groups […]
The LDA requested Lyme leaders to sign on to a letter against the Amendment in the Nature of a Substitute to HR 4701. Letter with signups was sent 7/7/14 to […]
March 16, 2015 Diane Steward, Committee ClerkLegislative Information Office100 State House StationAugusta, ME 04333 Testimony from: Lyme Disease Association, Inc. a national non-profit raising funds for research, education, […]
October 20, 2014 The Honorable Andrew M. CuomoGovernor of New York StateNYS State Capitol BuildingAlbany, NY 12224 Dear Governor Cuomo, I am writing on behalf of the Lyme Disease Association, […]
The Lyme Disease Association, Inc. held its 15th annual scientific conference, Lyme & Other Tick-Borne Diseases: Medical, Neuropsychiatric & Public Health Implications in the Providence Marriott Downtown, Providence RI, […]
Oral Testimony before US House of Representatives Energy & Commerce Health Subcommittee Patricia V. Smith, President, Lyme Disease Association, Inc. (LDA) November 20, 2013 Chairman Pitts and Committee Members, Thanks […]