Åland, a province of Finland, issues stamp highlighting tick research
I must admit that until recently, I’d never heard of Åland. It turns out, the…
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 must admit that until recently, I’d never heard of Åland. It turns out, the…
Deborah Findley’s son, Andrew, grew up with serious health problems, including autism, Lyme disease, and…
Subcommittee reports from the federal Tick-Borne Disease Working Group are now available for you to…
Dr. Rochelle Walensky, the director of the US Centers for Disease Control and Prevention, has…
When Fred Diamond fell in love with a woman who had Lyme disease, he didn’t…
Joanne Drayson is a Lyme patient/advocate in the UK. She and I have been Facebook…
People being treated for Lyme disease often have to change what they eat. Eliminating sugar…
Depression, anxiety, and other mental symptoms are frustratingly common in people with long-term Lyme disease….
Pamela Weintraub is a science journalist, Lyme disease survivor, and author of the groundbreaking book…
There has been an outpouring of emotion in the wake of the recent death of…
End of content
End of content