TOUCHED BY LYME: One woman’s story of healing from chronic Lyme
Guest blogger Erika Arens writes about her eight-year journey with tick-borne illness.
Author | LymeDisease.org
Guest blogger Erika Arens writes about her eight-year journey with tick-borne illness.
Yesterday, the CDC officially announced that it “recommends that laboratory tests cleared or approved by FDA be used to aid in the routine diagnosis of Lyme disease.” This is a shame. Waiting for FDA approval suppresses innovation in Lyme testing and furthers the interests of those who have vested interests in the current flawed lab tests which miss as many cases as they detect. Neither of these is good for patients.
Guest blogger Caroline Trujillo shares her experience with Lyme-induced aphasia.
A concerned grandfather and I exchange emails.
LymeDisease.org asked chronic Lyme patients the same “quality of life” questions the CDC asks about other chronic diseases. Nobody had ever done that before.
The organizers of this juried show hope to start a dialogue about Lyme disease through art.
Guest blogger Karl Ford collected infected ticks while hiking the Appalachian Trail, but kept himself tick-free. “I wore permethrin-treated bug-net pants, a treated long-sleeved shirt and hat and had no ticks on my body at any time during the 140-day hike.”
The next step in the chilling story of Justina Pelletier is a court hearing in Boston on March 17.
Michael Kruse says he thinks people “should be looking at all of the evidence, not just the few studies that agree with an opinion that moves us emotionally.” Then he bases his argument on evidence that agrees with an opinion that moves him emotionally.
Children with Lyme disease experience many different kinds of pain, which don’t always fit neatly into categories on a medical chart.
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