In the Media
05/18/2023
Passing Down Lyme Disease
Isabel Rose's article on congenital Lyme disease featured in the East Hampton Star.
In the Media
05/18/2023
Isabel Rose's article on congenital Lyme disease featured in the East Hampton Star.
In the Media
09/21/2022
Harvard conducted an online survey to gauge what the public does and does not know about Lyme disease and ways to prevent it, also asking questions to see whether they act on that knowledge. They received 4,099 responses.
In the Media
05/16/2022
Project Lyme mourns the passing of pediatric Lyme specialist, Dr. Charles Ray Jones. This is a profound loss for the Lyme community and for those whose lives he touched. In particular, his dedication to healing kids with Lyme and co-infections gave countless children a future.
In the Media
02/24/2022
Nearly a half-million persons contract Lyme disease annually in the US; learn how the new medical codes in ICD-11 recognize persistent, congenital, and potentially fatal complications from this illness.
In the Media
10/07/2021
Since 2018, Project Lyme has granted over $1 million to Bay Area Lyme Foundation to support their rigorous scientific agenda. Project Lyme is excited to have contributed to many multi-year research projects which Bay Area Lyme manages. A portion of the money Project Lyme raised at our 2020 Gala was used to fund a recent study with Flightpath Biosciences, Inc. Yesterday, they announced a newly licensed antibiotic that selectively kills Lyme Disease spirochetes. They are developing a narrow-spectrum antimicrobial therapeutic that can kill the bacteria causing Lyme disease without destroying the gut microbiome or contributing to the global Antimicrobial Resistance problem which has been associated with increased risk of chronic diseases.
In the Media
09/28/2021
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.
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.
In the Media
09/17/2021
Life was going well for Nicole Bell and her husband Russ, both successful engineers and entrepreneurs… until Russ started experiencing symptoms of cognitive decline. They visited doctor after doctor and were told it was Alzheimer’s disease, but the root cause turned out to be something they never expected—tick-borne disease. In her soon-to-be-released memoir What Lurks in the Woods (October 2021), Nicole describes her harrowing investigation into her husband’s mysterious illness in hopes that it will help others who are dealing with bizarre chronic symptoms to find the cause before it’s too late. Nicole graciously sat down for a (virtual) interview with Project Lyme about her book and her heartfelt message to the chronic illness community.
In the Media
07/15/2021
Changing climate conditions help drive up number of cases, as infecting insects thrive in warm, humid environments. Researchers and advocates say the lack of funding for tick-borne diseases contributes to major knowledge gaps surrounding the disease.