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TOUCHED BY LYME: CDC ignores ethics, attacks “chronic Lyme”

JUN

2017

...p of the article she planned to write. This is how CDC employees conduct research into Lyme disease treatment? They solicit input from only one side of a highly contentious medical debate, they dangle the incentive of a prestigious... Read More »

Early diagnosis of Lyme disease is essential; better treatments still needed

DEC

2016

...rld evidence to improve patient care. MyLymeData, which allows patients to input information about their individual experiences with Lyme disease, has enrolled more than 6,500 patients. This makes it the largest ever study of Lyme... Read More »

Bias and group-think contribute to faulty treatment of Lyme disease patients

JUL

2020

...omment on articles indexed in the agency’s database of biomedical literature.] Ensure that the CDC-controlled curriculum development team represents the broad scientific perspective on persistent Lyme disease. Merely seeking stakeholder... Read More »

The haunting legacy of Lyme, Connecticut

JUL

2024

...LymeData Chart Book. https://www.lymedisease.org/mylymedata-lyme-disease-research-report/ 10. “Why Lyme disease treatment sometimes doesn’t work.” LymeDisease.org https://www.lymedisease.org/lyme-treatment-sometimes-fails 11. CDC... Read More »

The complexities of IACCs: what do “long haul” diseases have in common?

OCT

2024

...e IACC Initiative here). Understanding shared mechanisms Cross-condition research is not meant to replace specific research for individual diseases but to balance it. Each condition requires independent research to fully understand its unique traits,... Read More »