TOUCHED BY LYME: Facebook chat with NY Lyme reporter tonight
Log in to chat with investigative reporter Mary Beth Pfeiffer, who wrote a series on Lyme in the Poughkeepsie Journal
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.
Log in to chat with investigative reporter Mary Beth Pfeiffer, who wrote a series on Lyme in the Poughkeepsie Journal
Lyme activist Trish McCleary tells how and why she founded “S-L-A-M.”
A new feature on the Centers for Disease Control’s website takes a narrow view of Lyme diagnosis.
Guest columnist Toni Bernhard’s recent blog about what not to say to sick people brought a huge response from readers. Here’s more on the subject.
Letter to a Lyme patient, written in the style of a famous essay by James Baldwin.
Last week, guest blogger Toni Bernhard told us what NOT to say. Here are her suggestions for things TO say to those who are sick or in pain.
Boston NPR radio station WBUR included a panel discussion of Lyme disease as part of its week-long series “Living with Lyme.” Guest blogger Jennifer Crystal attended the event, and writes this report.
Guest columnist Toni Bernhard, who blogs on the Psychology Today website, says even well-intentioned people may not know how to talk to the chronically ill.
Guest blogger Jennifer Crystal ponders how to make tick-borne diseases easier to pronounce and remember.
A minister’s experience gives rise to a new Lyme support group in Kentucky.
End of content
End of content