TOUCHED BY LYME: My conversation with “Lyme Time Podcast with Ali”
Alicia White suffered from bizarre, often painful physical symptoms for years. Consulting numerous doctors, the…
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.
Alicia White suffered from bizarre, often painful physical symptoms for years. Consulting numerous doctors, the…
Bonnie Crater, co-founder of the Center for Lyme Action–a lobbying group seeking more federal funding…
LymeDisease.org is one of the foremost Lyme patient advocacy organizations in the United States. We…
The federal Tick-Borne Disease Working Group held another online meeting Tuesday. Its upcoming Report to…
Prior to this past Tuesday, the last time the public tuned in for an online…
The following question from somebody named Tom showed up in my inbox today: Do you…
Dorothée Lorang, a filmmaker who lives in Nantes, France, has two children. One of them,…
The House of Representatives today approved a package of spending bills that includes $20 million…
Dana Parish is a singer, songwriter, and author who, along the way, has also turned…
I wrote the following article, which appeared in the July 2020 issue of the “Townsend…
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