A new group has been formed for young adults dealing with neuroimmune conditions such as chronic Lyme disease, chronic fatigue syndrome (ME/CFS), fibromyalgia, atypical MS, multiple chemical sensitivities, and mold illness. Read More »
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.
LymeDisease.org is a non-profit
501(c)(3) that serves the patient community through advocacy, education and research.
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