“Super responders” are key to personalized Lyme disease treatment.
Lyme patients all hope to find the most effective treatment with the fewest side effects.
Lyme disease cases for 2017 are actually much higher than the CDC reported.
Canadian Lyme Patients to “Give Input” on Matters Already Decided.
We could potentially use the data from MyLymeData.org to build a research engine.
Many U.S. and Canadian Lyme patients are traveling to the Lyme Mexico Clinic for alternative treatments.
Most patients with late or chronic Lyme disease waited years for proper diagnosis with devastating consequences.
There are those who say you can’t have Lyme because it “doesn’t exist” where you live.
Who decides what constitutes scientific evidence for chronic Lyme disease?
Some claim that chronic Lyme disease is not a legitimate diagnosis.
Broader criteria are needed for chronic Lyme disease diagnosis.
Become a member and help us advocate for change, raise awareness and fund research that can improve patients’ lives.