TOUCHED BY LYME: Their message is clear. Patients want to get well.
I made these remarks by telephone to the Nov. 17 meeting of the federal Tick-Borne…
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.
I made these remarks by telephone to the Nov. 17 meeting of the federal Tick-Borne…
The Tick-Borne Disease Working Group is supposed to bring together 14 people—scientists, doctors, health officials,…
I delivered the following public comments by phone to the federal Tick-Borne Disease Working Group…
Carl Hamrin was born in Sweden, emigrated to the United States, and became a US…
The Center for Lyme Action (CLA), a nonprofit organization dedicated to increasing federal funding for…
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…
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