Jesse Colin Young “got brain back” after Lyme treatment
The singer/songwriter/founding member of the band “The Youngbloods” talks about his experience with Lyme disease.
This blog has several goals. First, to explore the personal side of Lyme disease and how it affects individuals and families. Second, to highlight useful information for people seeking answers about this complicated illness. Third, to help foster a sense of unity and shared purpose among the many diverse members of the Lyme community. Dorothy, who serves as President of LymeDisease.org, has a family member with Lyme disease. She is co-author of a book called When Your Child Has Lyme Disease: A Parent’s Survival Guide.
The singer/songwriter/founding member of the band “The Youngbloods” talks about his experience with Lyme disease.
Review of “Compendium of Tick-Borne Disease: A Thousand Pearls.”
Book review of “lyme light: a memoir” by Natalie London.
Many youngsters with chronic Lyme fill their time taking medicine and watching TV. But some find other ways to broaden their horizons.
Guest blogger Erika Arens writes about her eight-year journey with tick-borne illness.
Guest blogger Caroline Trujillo shares her experience with Lyme-induced aphasia.
A concerned grandfather and I exchange emails.
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.
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