MyLymeData Patient Registry Highlights
MyLymeData is a patient-driven registry and research platform that permits patients to quickly and privately pool their data. Enrolling thousands of patients permits researchers to evaluate care as it is provided in real world practice. It can also facilitate research by generating research hypotheses and recruiting patients for trials. Enroll in MyLymeData today to become a part of the solution.
19,000+ Patients Enrolled
Research projects & collaborations
MyLymeData is a research engine that seeks to work with researchers, biorepositories, and clinicians to accelerate the pace of research. We collaborate with researchers at the University of Washington and the University of California at Los Angeles as well as the Lyme Disease Biobank, a project of the Bay Area Lyme Foundation. UCLA’s efforts are supported in part by a National Science Foundation grant.
Most severe symptoms of persistent Lyme disease
- Fatigue 54%
- Sleep impairment 38%
- Muscle aches 38%
- Joint pain 38%
- Neuropathy 34%
- Cognitive impairment 28%
- Psychiatric 28%
- Memory loss 27%
- Gastrointestinal 25%
- Headache 19%
- Twitching 9%
- Heart related 9%
Co-infections are common in persistent Lyme disease
Registry By The Numbers
