TOUCHED BY LYME: Same-old, same-old from the CDC
The agency stubbornly adheres to its party line, denying care to suffering Lyme patients.
Author | LymeDisease.org
The agency stubbornly adheres to its party line, denying care to suffering Lyme patients.
Dr. Lyle Petersen of the CDC wrote an editorial for the Poughkeepsie Journal in response to the remarkable series of articles by Mary Beth Pfeiffer on Lyme Disease. In his letter, Dr. Petersen restates the IDSA/CDC perspective patients have long heard. Lyme disease is easy to diagnose and treat, but for those with chronic Lyme treatment is both ineffective and dangerous. He proposed that we work on preventing Lyme disease and early diagnosis and treatment—both laudable goals, but not at the expense of treating seriously ill patients. My response to his letter, which I posted on the Poughkeepsie website (and encourage you to respond there as well) follows.
How the Lyme community stepped up–with donations big and small–to buy a sophisticated microscope and support the groundbreaking research of Dr. Eva Sapi. (Pssst: still time to donate!)
Liz Schmitz, of the Georgia Lyme Disease Association, discusses important new research indicating that yes, folks, there is indeed Lyme disease in the southern US.
California unveils a new way to display tick and Lyme information. Will it help those who need it most?
Dr. Leana Wen discusses how PCORI–Patient-Centered Outcomes Research Institute–hopes to change how medical research is approached in the US.
Guest blogger Jennifer Crystal explores something almost every Lyme patient comes up against at some point in their health journey.
What everybody needs to know about tick protection.
The “real housewife” and “real Lyme patient” posted the following information about her Lyme status for Facebook fans.
Watch her inspirational 30-minute documentary for free on-line
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