Lyme Disease Association, Inc., LDA, is proud to celebrate 30 years of advocacy and volunteerism to improve research, education, and patient support surrounding Lyme and tick-borne disease. Early Years By 1990, the total US reported Lyme disease case numbers were 7,943 cases – NJ was second in the nation for the highest number at 1,074 […]
About the Lyme Disease Association
In 1991, the Lyme Disease Association began as an informal group and then incorporated as Lyme Disease Association of Central Jersey, Inc. (LDACJ) in 1992 and then became Lyme Disease Association of New Jersey, Inc. (LDANJ) in 1993. It was formed by several patients and doctors─the Fordyce and Drulle Families were particularly instrumental ─who saw the need to organize and fund research and educate people. It had first a regional then state focus. In 1997, Pat Smith became President of LDANJ and it began to have influence far beyond NJ borders. She saw the increasing need for a national organization. Supported by entreaties from doctors and patients alike, the LDANJ Board of Directors in 2000 changed the name to Lyme Disease Association, Inc. (LDA) and changed the focus to a national one, which had a broader mission expanding research funding (LDA funded research has appeared in 53 scientific journal publications to date) and including patient support, e.g., LymeAid 4 Kids fund. At that time, LDA decided to remain an all volunteer organization without paid employees so that all monies would be dedicated to the mission. In 2013, 144 individuals volunteered 22,840 hours to assist with LDA programs. Additionally, LDA created a loose umbrella, LDAnet, where other groups could strategize and collaborate with LDA to impact Lyme disease issues nationally.