MyLymeData is research done differently. It is the first national large-scale study of chronic Lyme disease. This study is different from all other Lyme disease studies because it’s patient-powered BIG DATA research.
LymeDisease.org will analyze data and provide information to the community through publication of white papers and peer reviewed articles. We will also partner with researchers and clinicians who are interested in research that puts patient interests at the center and seek to cure or improve quality of life. Our previous surveys have been published in peer-reviewed articles and used to inform healthcare policy issues affecting the community. Our last published survey has been downloaded over 4,000 times.
Take your first survey. The first survey is a little longer than most, but you should be able to complete it within 30 minutes. You can take a break and come back to it if you need to. After the first one, we will send you additional surveys (about quarterly) asking additional questions and tracking your progress. We will let you know what we discover.
And, spread the word! The more people that participate in this study, the more we will learn about Lyme disease and how to treat it. So tell your friends, post this on Facebook, and Twitter away. There’s power in numbers!
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Add your Lyme data to MyLymeData today!