TOUCHED BY LYME: Microscope you helped buy is now on the job
With the help of people like you, LymeDisease.org raised $150,000 to support the important work of Lyme researcher Dr. Eva Sapi.
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.
With the help of people like you, LymeDisease.org raised $150,000 to support the important work of Lyme researcher Dr. Eva Sapi.
Lyme survivors, advocates, and high profile speakers converged on this year’s event on Oct. 19.
Guest blogger Jennifer Crystal found “whooshing and zooming” of iOS7 a challenge to navigate.
Dr. Richard Horowitz’s new book looks at pain, fatigue, memory and concentration problems, sleep disorders and much much more.
“Revolt” performed at Oct. 5’s Lyme protest in San Francisco.
How a fire alarm, a message truck, a couple hundred folks with signs and stories, and a “Lyme rapper” came together at the IDSA annual conference.
If you’re joining us at the IDSA Lyme protest in San Francisco on Oct. 5, what message would you like to convey?
Official says: “We are sure that he had the infection (Lyme) — what role it played in his death is still being investigated.”
Cartoonist/Lyme warrior David Skidmore develops a line of cartoons to document the trials and tribulations of Lyme treatment.
After grueling treatment for Lyme disease, Logan McCulloch made a surprising choice.
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