Focus – Opinions and Features

Perinatal transmission of Lyme disease: A qualitative study investigating the research priorities of patients with Lyme disease in pregnancy has just been published in PLOS ONE, a peer-reviewed, open access journal. By Catherine Kinsella This recent Canadian study articulates... Read More »

By Alain Mass, MD Nearly one in six children between the ages of 2 and 6 years old (17.4%) has a diagnosed mental, behavioral or developmental disorder. More than 17 million children in the United States have or have had a diagnosable mental illness. Mental disorders are either... Read More »

By Nancy Dougherty Infection-associated chronic illnesses such as Long COVID, myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and chronic Lyme disease share similar symptoms and may share important biologic mechanisms, too. Dysautonomia, or autonomic nervous system... Read More »

By Rachel Leland The top picture was taken in a parking lot, when my mom and I were traveling out of state for medical treatment in 2008. There was a little bit of snow and I was so excited, because I had spent the last three years in my bedroom…far away from any sort of snow to... Read More »

By Fred Diamond On this week’s Love, Hope, Lyme podcast, Center for Lyme Action Co-founder Bonnie Crater talks about how the Lyme community can influence the federal government to provide more funding for Lyme disease research. The annual Virtual Lyme Fly-In, where people get a... Read More »

By Jen Johnson Anyone who has ever been faced with an unsettling ERMI test knows that when you find yourself living in mold, there are no easy options for getting into a clean environment. Older homes are moldy. Newer homes are moldy. Rentals are moldy. Even AirBNBs and hotels... Read More »

By Anna Brennan I had already given birth four times before I found out that I had chronic Lyme. Looking back, I think my children’s diagnoses were inevitable. Just like the other children in our neighborhood, my kids sat in piles of leaves in the fall. They played in tall grass... Read More »

By Catherine Kinsella, CanLyme What happens when growing numbers of patients are unable to receive a diagnosis and adequate treatment for Lyme disease? They keep looking for solutions, both individually and collectively. This in-depth article by Cox and Levesque in Zoonotic... Read More »

By Fred Diamond On this week’s Love, Hope, Lyme podcast, Global Lyme Alliance (GLA) CEO Laura MacNeill shares some developments in Lyme disease diagnostics, treatment, and mental health care that her organization is supporting. When I was doing the research for my book “Love,... Read More »