Disclaimer: Reference herein to any specific organizations, or service by trade name, trademark, or otherwise, does not necessarily constitute or imply its endorsement, recommendation, or favoring by the Lyme Disease Resource Center. Descriptions are copied from individual web sites. Information is not intended to treat, diagnose, cure or prevent any disease. All content provided is for informational purposes only. Always seek the advice of your physician before making any treatment decisions.
is a nonprofit, international, multi-disciplinary medical society, dedicated to the diagnosis and appropriate treatment of Lyme and its associated diseases. ILADS promotes understanding of Lyme and its associated diseases through research and education and strongly supports physicians and other health care professionals dedicated to advancing the standard of care for Lyme and its associated diseases." www.ilads.org/
is a non-profit corporation that is a central voice for Lyme patients
across the nation through advocacy, education and research.
Since 1989, LymeDisease.org (formerly CALDA) has been revolutionizing
the Lyme disease arena in public policy, advocacy, and science." www.lymedisease.org/
"...formed by the merger of Lyme Research Alliance (LRA) and Tick-Borne Disease Alliance (TBDA), is a leading private nonprofit organization in the United States dedicated to finding a cure and accurate test for Lyme disease as well as educating physicians and the public about the dangers of Lyme. Today GLA has gained national prominence for its commitment to changing the course of Lyme disease by funding ground-breaking research, while expanding education programs for the general public and physicians." https://globallymealliance.org/
"A chilling tale of microbes, medicine and money,
this Oscar shortlisted film has changed the landscape of the Lyme epidemic,
bringing unprecedented awareness in an engaging and accessible way.
The definitive record of the Lyme controversy, UNDER OUR SKIN exposes a hidden story
of medical and scientific malfeasance and neglect...
The newly released Director's Cut includes 15-minutes of restored footage,
re-edited scenes and character updates. (100 min.)" http://www.underourskin.com/film/
"In this dramatic follow-up to the widely acclaimed
UNDER OUR SKIN, EMERGENCE takes the viewer on a journey from horror to hope.
We witness the emerging epidemic of Lyme disease as infection
and education spread globally.
We watch as the truth emerges about the disease’s persistence and reach,
about promising new research, and about
medical collusion and conflicts of interest
that continue to impede progress.
We revisit the characters from UNDER OUR SKIN as they emerge into better health,
reclaiming their lives and dignity,
and offering hope to the legions now suffering.
(65 min., © 2014 Open Eye Pictures)" http://www.underourskin.com/sequel/
represents physicians, scientists and other health care professionals who specialize in infectious diseases. IDSA’s purpose is to improve the health of individuals, communities, and society by promoting excellence in patient care, education, research, public health, and prevention relating to infectious diseases." www.idsociety.org/Lyme/
promotes tick-bite protection and tick borne disease prevention by engaging, educating, and empowering people to take action."
at Southampton Hospital educates the public, promotes collaboration in the medical community, and facilitates access to diagnosis and treatment of tick-borne diseases. http://www.southamptonhospital.org/services/tick-borne-disease-resource-center/default.aspx
was established as the first academic research center in the country to focus multidisciplinary research on chronic Lyme disease. In recognition that a growing number of patients experience ongoing or relapsing symptoms after having been treated for Lyme disease, in recognition that diagnostic tests often do not provide definitive information regarding the presence or absence of infection, and in recognition that there are multiple possible mechanisms by which symptoms persist, the mission of this center has a particular focus on identifying better diagnostic assays, better treatments, and a better pathophysiologic understanding of the mechanisms of symptom persistence." www.columbia-lyme.org/
"The Dean Center for Tick Borne Illness is a specialized clinical and research program for individuals with impairment and disability related to tick borne illness. The goals of the Dean Center are to improve the care and function of patients with Lyme disease and other tick borne illness by focusing on individualized treatment, ongoing education, and emerging science."
is designated by IRS as a public charity operating under 501(c)(3) non-profit status. Its mission is promoting awareness of and controlling the spread of Lyme and other tick-borne diseases (TBD) and their complications through education and other means; raising and distributing funds for Lyme and tick-borne diseases (TBD) research, education and other related Lyme and TBD issues; assisting underpriviledged patients in connection with Lyme and other TBD. " http://www.lymediseaseassociation.org/
is a project that seeks to give a voice to the entire Lyme community. Those currently battling for their health, those in remission, and those who have passed away as a result of it.
It is a work of art and an expression of our love and support of each other. It is our voice, crying out for help, pleading with our leaders and those that can change the future of lyme research, diagnosis and treatment to get involved, to hear us, to stand up and make a difference.
The Lyme Quilt is a continuous project that will continue to grow so long as there is a single person battling this horrific disease.
Eventually it will travel throughout the country serving as a voice for so many who are unable or who flat out can’t be there because of this debilitating disease."
Website resource created by Cindy Kennedy, Nurse Practitioner, Wife, Mother and Lyme Disease sufferer.
"If you have a friend, relative or coworker with an illness or disability that isn’t obvious, you may think you’re doing the right thing by saying he or she “looks so good.” You can’t even tell the person has a disability, and that’s a good thing, right? Wrong."
is to help everyone with a chronic illness or invisible disability, in order for them to live their lives to the fullest and not feel isolated and alone. We believe that our medical circumstances have put us in a unique and understanding position, so that we can help each other through similar difficult times. We hope the information and community on our site can aid people in leading better lives through knowledge, networking, friendship and most of all support." http://www.butyoudontlooksick.com/
encourages, educates and connects people and organizations touched by illness, pain and disability around the globe. Formerly known as The Invisible Disabilities Advocate, IDA was founded in 1997 and incorporated in 2004 as a 501(c)(3) non-profit." http://www.invisibledisabilities.org/
"Please take the time to read Christine Miserandino’s [author of 'The Spoon Theory'] personal story and analogy of what it is like to live with sickness or disability."
was founded in 1992. We advocate for environmentally responsible stewardship of land and natural resources in landscaping and horticultural practices of both professionals and the public. Through education, collaboration, and networking, ELA promotes the design, installation, and maintenance of landscapes that are guided by a knowledge of and respect for natural ecosystems." http://www.ecolandscaping.org/about/
promotes tick-bite protection and tickborne disease prevention by engaging, educating, and empowering people to take action." http://www.tickencounter.org/prevention/protect_your_yard
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