Reach LymeDisease.org’s Audience Of Engaged Viewers

LymeDisease.org is a 501(c)(3) nonprofit organization that was founded in 1989, making it one of the oldest Lyme organizations in the nation. We fight to make the patient voice stronger, to support patient-centered research, to create legislative change, and to create a future where Lyme patients can receive the treatments they need to get well.

LymeDisease.org is the largest communications network for Lyme disease and the most trusted source of information by patients. 73% of our traffic is driven by Google searches. We consistently rank among the top 3 in searches for Lyme disease, Lyme disease symptoms and the like—neck and neck with the CDC.

We believe that there is strength in numbers.

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3 MILLION

Unique visitors a year

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500,000

Page views a month

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TOP 3

Google search for “lyme disease”

TAP INTO A POWERFUL AUDIENCE WITH LYMEDISEASE.ORG SPONSORSHIPS

LymeDisease.org’s audience includes patients, physicians & researchers

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#1 TRUSTED

Source of patient information

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LARGEST

Communications network in Lyme disease

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LEADER

In Lyme Disease Big Data

An Authority On Lyme LymeDisease.org Member Community is THE one place to refer anyone wanting to get accurate info about Lyme Disease. It's now more like an authority that people go to other than the CDC. We need to support you in order to keep all the issues regarding this disease relevant and in the minds of all. LymeDisease.org Member Community is THE one place to refer anyone wanting to get accurate info about Lyme Disease. It's now more like an authority that people go to other than the CDC. We need to support you in order to keep all the issues regarding this disease relevant and in the minds of all. Part Of The Conversation  I joined LymeDisease.org to be part of the conversation to promote research, to gain info and share info (groups, Lyme Times), to be educated in order to affect policy, and to support outreach and help for those Lyme patients in need. No part of this mix is unimportant.  I joined LymeDisease.org to be part of the conversation to promote research, to gain info and share info (groups, Lyme Times), to be educated in order to affect policy, and to support outreach and help for those Lyme patients in need. No part of this mix is unimportant. Leader in Lyme Big Data LymeDisease.org Member Community is THE one place to refer anyone wanting to get accurate info about Lyme Disease. It's now more like an authority that people go to other than the CDC. We need to support you in order to keep all the issues regarding this disease relevant and in the minds of all.  I think it's terribly important that anyone with Lyme and/or the coinfections be a part of documenting what's happening with Lyme disease, and where it's being contracted and what's working to aleviate, if not cure it. This is why I've joined the LymeDisease.org Member Community. Dedicated To Education  I joined to be part of an organization dedicated to expanding the knowledge base of the public and of health professionals, politicians and more, to the dangers, prevention, diagnosis, treatment of tick borne diseases.  I joined to be part of an organization dedicated to expanding the knowledge base of the public and of health professionals, politicians and more, to the dangers, prevention, diagnosis, and treatment of tick borne diseases. Trusted Source  I joined to be part of an organization dedicated to expanding the knowledge base of the public and of health professionals, politicians and more, to the dangers, prevention, diagnosis, treatment of tick borne diseases.  I'm very grateful for all that LymeDisease.org has done and the trusted information available to us. There are 3 of us in our family currently in treatment. Before our diagnosis, I thought Lyme was something you tried to keep your dog from getting. UpDates On
Scientific Advances LymeDisease.org Member Community is THE one place to refer anyone wanting to get accurate info about Lyme Disease. It's now more like an authority that people go to other than the CDC. We need to support you in order to keep all the issues regarding this disease relevant and in the minds of all. LymeDisease.org does so many functions, does them well, includes all members with a sense of shared values, becomes more and more the town crier of scientific advances in tick borne disease when traditional media is either mute or propaganda driven. UpDates On Scientific Advances A Sense Of Community LymeDisease.org Member Community is THE one place to refer anyone wanting to get accurate info about Lyme Disease. It's now more like an authority that people go to other than the CDC. We need to support you in order to keep all the issues regarding this disease relevant and in the minds of all.  The most important part of being a LymeDisease.org member is feeling a sense of community and realizing the necessity for collaboration in order to move forward. A Sense Of
Community