From information desert to Lyme news hub: why membership matters
When my family fell into the Lyme world in 2005, there were almost no books…
Author | LymeDisease.org
Dorothy Leland is a longtime advocate and researcher focused on Lyme disease education, policy awareness, and patient support. She has contributed to numerous publications and works closely with medical professionals and organizations to improve understanding and treatment of tick-borne diseases.
When my family fell into the Lyme world in 2005, there were almost no books…
As Dave Martz lay dying, an idea serpentined around his mind and would not loosen…
By Fred Diamond When I was researching my book “Love, Hope, Lyme: What Family Members,…
Sign the “Stop the BOP” petition here. by Crystal A. Frost The daily life of…
A Celebration of Life for Pat Smith will be held September 7 in Neptune, New…
On September 12, the California State Board of Pharmacy is expected to vote to eliminate…
By Fred Diamond Many listeners of my Love, Hope, Lyme podcast ask me to go…
Navigating the uncertainty of potential Lyme disease, mold exposure, or a combination of both can…
On July 11, a committee of the National Academies of Sciences, Engineering, and Medicine held…
By Christina Campbell “I wish I could just stay home and rest.” “But what do…
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