From the latest headlines to community events, keep your finger on the pulse of the Lyme world. Learn about groundbreaking research and what’s new in patient advocacy. Stay informed to make the best possible health decisions for yourself and the people you care about.
In the Media
09/20/2021
Project Lyme is excited to announce our new public service announcements (PSAs). This multi-platform campaign spotlights patients’ firsthand experiences to educate the public about the rising threat of Lyme disease.
Education
03/14/2023
At 17 years old, Grace Burns started having episodes where her legs grew numb and she lost consciousness. She developed other symptoms, including fevers, arthritis, migraines, nausea, nerve and muscle problems, and brain fog. After 3 years of seeing many doctors who told her that her symptoms were “just in her head,” Grace finally saw Lyme expert Dr. Steven Phillips, who diagnosed her with neurological Lyme disease plus co-infections. Now on her path to recovery, she is spreading awareness about the delay in answers and why the medical system needs to change.
Education
03/09/2023
Most people recognize Bob Forster as an adventurer who posts on Facebook about his experiences mountaineering and back-country skiing in exotic places from Alaska and Canada to Argentina, Russia, Japan, Europe, and beyond. These outdoor activities are so physically demanding that those who don’t know Bob and see his updates are shocked to find out that he has chronic Lyme disease, often wondering, “How could that person be sick?”
Education
02/13/2023
Art is a critical storytelling device. Patients can use art to share experiences in a unique way, opening a door to understanding for non-patients. Jiatong Lu, a fine artist based in New York City, has accomplished that with her project “Nowhere Land”. She uses photography to capture the realities of Lyme disease and is sharing them to raise awareness.
Education
01/04/2023
Supportive Oligonucleotide Therapy (SOT) for Lyme Disease is a cutting-edge treatment for infections, including Borrelia Burgdorferi. This article serves to educate and help you decide if it may be right for you.
Education
12/08/2022
Dapsone is a sulfur-based drug originally used to treat leprosy. Its anti-inflammatory qualities and ability to attack persister cells make it a good option for treating persistent Lyme disease.
Education
11/30/2022
A low-histamine diet has benefits for many people, given its reliance on fresh, natural foods. However, it also directly applies to tick-borne disease patients suffering from Borrelia burgdorferi and other co-infections. Read this article to learn more about the benefits of this diet.
Education
11/23/2022
Supportive Oligonucleotide Therapy (SOT) for Lyme Disease is a cutting-edge treatment for infections, including Borrelia Burgdorferi. This article serves to educate and help you decide if it may be right for you.
Advocacy
11/16/2022
Deborah Findley’s son, Andrew, grew up with serious health problems, including autism, Lyme disease, and other conditions. When he turned 18, Deb and her husband attempted to get a conservatorship, but to their surprise, California’s Department of Developmental Services filed a competing request.
Advocacy
10/28/2022
Mindy White is an independent singer/songwriter from Nashville, TN. She suffers from Chronic Lyme Disease and loves finding inspirational stories of others persevering through their illnesses to do what brings them joy. She has lived with CLD for 5 years now, which has brought on a slew of other illnesses including POTS, Fibromyalgia, Neuropathy, and Hypothyroidism. Prior to that, she was a successful recording and full-time touring artist.