Patient advocates register their objections to the restrictive guidelines that damage real lives.
By Dorothy Kupcha Leland
& Sandi Bohle
Entrenched mainstream medical positions drive patients to continue protesting.
By Lyme Times Staff
NGC posts “trustworthy” practice guidelines.
By Lyme Times Staff
By Dan Cameron, MD
Symposium attendees tackle the “wicked problem” of Lyme and national research priorities.
By Lyme Times Staff
Lorraine Johnson speaks to a distinguished group about the power of “citizen science” to improve patient outcomes.
By Lyme Times Staff
“Democratization of Science” means doing research differently and including the patient perspective.
By Pamela Cocks, MPH, MLS
Stanford MedX conference publicizes the promise of Big Data for patients.
By Lyme Times Staff
LDo launches a groundbreaking research project to help solve the Lyme riddle.
By Lyme Times Staff
Over a decade of survey experience informs LDo’s concept for a patient registry.
By Lyme Times Staff
Patients know the difference between “normal tired” and “too tired to breathe”.
By Jennifer Crystal, MFA
Authors who once called for a major effort to combat the Lyme disease epidemic weigh in again.
By Pamela Cocks, MPH, MLS
How we estimate the number of Lyme cases seriously impacts critical policy decisions.
By Lyme Times Staff
New tick-borne disease discovered in Northern California parks.
By Kris Newby
Health policy debates can hinge on how researchers count the number of Lyme cases.
By Lyme Times Staff
Psychiatric symptoms of neuroborreliosis misdiagnosed by mainstream medicine.
By Virginia T. Sherr, MD
Johnson critiques a Cochrane evaluation of extended antibiotic treatment.
By Lorraine Johnson, JD, MBA
Yolanda Foster, Avril Lavigne, and John Caudwell make news.
By Dorothy Kupcha Leland
A Parent’s Survival Guide.
By Sandra Berenbaum &
Dorothy Kupcha Leland
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