TOUCHED BY LYME: When poor health and the holidays collide
Guest blogger Toni Bernhard discusses how a chronically ill person can ease the pain brought on by holidays.
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.
Guest blogger Toni Bernhard discusses how a chronically ill person can ease the pain brought on by holidays.
Looking to learn about Lyme disease? Start here.
New book from the author of “The Lyme Diet: Nutritional Strategies for Healing from Lyme Disease.”
NeedyMeds.org provides information about patient assistance programs for medicines and other health care costs.
Guest blogger Toni Bernhard takes issue with how doctors officially describe Chronic Fatigue Syndrome.
Guest blogger Jennifer Crystal reports on her emotional response to hearing her own doctor speak at ILADS.
Guest blogger Jennifer Crystal filed this from the 2012 ILADS conference in Boston.
The Poughkeepsie Journal continues its series on Lyme disease (“No Small Thing”) with a look at the vagaries of Lyme diagnostic testing.
LymeDisease.org’s IDSA Lyme protest rally, across from IDSA annual meeting at San Diego Convention Center on Oct. 20, 2012.
Challenge: how can a small group Lyme activists send a message to a huge group of ID doctors?
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