MyLymeData is a
Patient-Powered Research Project
It was conceived by patients, is run by patients, and will
address the issues that Lyme disease patients care about.
It was conceived by patients, is run by patients, and will address the issues that Lyme disease patients care about.
Lyme Patients Are
Experts In Their Illness
Patients have more at stake in diagnosis and treatment of Lyme disease than anyone else involved in their healthcare. They are more dogged in the pursuit of their interests over time. MyLymeData lets patients learn from each other and provide data that can drive research to improve patients’ lives.
New Technology Allows
Patients To Take The Lead
The last treatment study funded by the National Institute of Health for Lyme disease recruited patients over 15 years ago. No new studies are in the pipeline. But, the waiting game is over. Today, thousands of patients can join together, pool their data and look to see which treatments are working best.
MyLymeData expects to gather more data about Lyme disease
than any research study has done before and build a patient-centered research community.
than any research study has done before and build a patient-centered research community.
That’s what patient-powered research is about!
MyLymeData lets patients lead the way to help find a cure.
Add your Lyme data to MyLymeData today!
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