Focus – Opinions and Features

The challenges facing the Lyme community are huge. Yet, working together, we’re making progress. In partnership with people like you, LymeDisease.org: * educates the public, the media, and lawmakers * publishes The Lyme Times * helps train physicians * supports... Read More »

  This is the first of a series of guest blogs by people who have enrolled in MyLymeData. By Sherrill Franklin My Lyme journey began in 2008. Ironically, a few days after placing tick repellent in our woods, I saw an engorged tick embedded in my hip. Having struggled through... Read More »

Last week, LymeDisease.org launched MyLymeData, a major research project aimed at collecting information that can transform the treatment of Lyme disease. Some people have questions about what MyLymeData is and how it will be used. The following is taken from the Frequently Asked... Read More »

LymeDisease.org today announced the launch of MyLymeData, a first-of-its-kind national patient-powered research project aimed at improving the quality of care for Lyme disease patients. The MyLymeData registry allows patients to pool their health information through a secure... Read More »

LymeDisease.org will soon launch a patient-powered research project called MyLymeData. It promises to be the largest study of chronic Lyme patients ever. Our latest issue of The Lyme Times explains all about it. You can read this issue online (for free) by clicking here. (Note:... Read More »

Lyme disease patients and advocates will demonstrate outside the Infectious Diseases Society of America’s (IDSA) Annual Conference in San Diego Oct. 9-10. All events will take place across from the San Diego Convention Center, 5th Avenue and Harbor Drive. (Right next to the... Read More »

The IDSA is holding its annual conference in San Diego this October, and LymeDisease.org,  the MayDay Project, and the San Diego Lyme Disease Support Group are teaming up to hold a protest there. Events will take place in front of the San Diego Convention Center, October 9th –... Read More »

From Buzzfeed, August 3, 2015 by Ana Saldamando There’s no way to explain illness to someone who hasn’t been ill. Like, seriously ill. It’s like saying “Enjoy your youth” to a teenager. And you can only say “I feel like I’m dying” so many times before it falls on deaf ears — and... Read More »

by Dr. Andrew Pugliese   A 15-year-old young lady came to see me last year with quite an interesting story. Six months prior to her visit, she was at summer camp, when she developed a fever, chills, myalgia and arthralgia. The patient also has a history of cranio-pharyngeal... Read More »