For Lyme Disease Awareness Month, Project Lyme asked our community to honor those Lyme and tick-borne disease doctors who are committed to helping patients recover, sometimes putting their own reputations at risk in the process. This blog answers the question, who is your Lyme hero?
read moreCenter for Lyme Action hosted their 2nd major event of the year. Featuring Congressional Representatives, Federal employees and renowned scientists, CLA educated the public about major issues and raised awareness about the growing prevalence of tick borne disease. This blog pulls key takeaways from the event and focuses on answering the central question: Is Lyme Disease the First Epidemic of Climate Change?
read moreKenzie Vath felt a shift in her body when she was about 10 years old. Since then, she has gone on a lifelong journey towards recovery. Being sick day in and day out is not easy, but after years of searching Kenzie has found a way to live with Lyme. In this blog she writes about finding the right treatment methods and support system and goes on to describe she works to help others do the same.
read moreProject Lyme Jr. Board Member Reema Shah joins a brave group of people who have told their stories to the world. Featured at the top of this New York Times article, Reema tells the world of her battle for proper diagnosis and treatment. Since NYT has begun charging for their articles, we downloaded the full text and embedded it below for you to read in case you do not have a subscription.
read moreMother’s Day can be a time to reflect on the mothers who nurture children with Lyme. While the following material, about the rare form of child abuse known as Munchausen’s Syndrome by Proxy, is disturbing in nature, we present it with the hopes of raising awareness for mothers, families, and the entire Project Lyme community.
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