TOUCHED BY LYME: “When the story of Lyme disease is written, it will be the story of patients standing up and being heard."
Highlights from the Tick-Borne Disease forum streamed live from NYC this morning.
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.
Highlights from the Tick-Borne Disease forum streamed live from NYC this morning.
The previously inexpensive drug is often prescribed for Lyme disease.
The court will examine the question of “burden of proof” in actions by the medical board.
RIP, Jeremiah Katches, from Colfax, CA, who died after a long battle with Lyme disease.
(Book review) “This is How I Save My Life: A True Story of Embryonic Stem Cells, Indian Adventures, and Ultimate Self-healing.”
A high school sophomore–and budding researcher–has discovered important information about ticks.
(book review) “Beyond Lyme disease: Healing the underlying cause of chronic illness in people with Borreliosis and co-infections.”
Making neither head nor tails of what the CDC website says about Lyme disease.
According to this northern California newspaper, “The misdiagnosis and lack of accurate counting of those with Lyme disease needs to stop now.”
Tell her about Lyme disease now.
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