TOUCHED BY LYME: Game warden who died from Lyme to be honored in Washington DC
His name will be engraved in the National Police Officers Memorial.
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.
His name will be engraved in the National Police Officers Memorial.
Dr. Richard Horowitz will discuss MCIDS, a more inclusive description for chronic Lyme, at two conferences in San Diego May 5 & 6—one for doctors and one for patients.
Iowa girl creates a YouTube video to help people realize how serious Lyme can be.
Multiple Chemical Sensitivities can offer unique challenges to someone seeking a driver’s license.
Minnesota Lyme Association seeks feedback from state residents who have had long-term antibiotics for Lyme disease.
An 11-year-old Lyme survivor shares her story to help others.
This doctor finds about 20% of her autistic patients turn out to have Lyme disease, and for many of them, Lyme treatment helps their autism symptoms. She’ll speak in Sacramento March 21.
(Guest blog) Using art and writing to help ourselves and each other.
(Book review) “Sunlight Chair Yoga” teaches adaptive techniques for the ill and injured.
“The Devastation of Lives and Lies: Those with Lyme disease and related chronic infections respond to the Infectious Diseases Society of America’s (IDSA’s) request for comments,” is a 274-page document prepared by patients and sent to Congressional Members, Congressional Committees, CDC, State Legislators, the President, and the media.
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