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There are striking similarities between chronic Lyme disease, long COVID, ME/CFS, and other chronic inflammatory conditions.
Dr. Bruce Patterson and his team have developed a novel protocol to treat these chronic sufferers and his approach has been found to have excellent results in nearly 500 patients who were treated with the same therapy.
This event will cover a variety of topics including the research Dr. Patterson has conducted into these chronic conditions, an explanation of his treatment protocol, and how your doctor can learn to adapt it in their own practice.
*Disclaimer, all opinions shared during this presentation are those of the presenters and not Project Lyme. This discussion is for educational purposes only, and you should always confer with your doctor before beginning any new treatment protocol.
Dr. Bruce Patterson, MD received his undergraduate training in molecular biology from the University of Michigan in Ann Arbor. He then received his MD at Northwestern University Feinberg School of Medicine followed by a residency in pathology. During the early stages of the AIDS epidemic, Dr. Patterson began investigating cellular reservoirs of HIV-1 using molecular and in situ cell-based technology patented in his laboratory and used today around the world. Dr. Patterson determined that enough HIV virus was present in infected individuals to account for the massive destruction of the immune system. This paradigm-altering work was published in Science in 1993 and featured in Scientific American, Rolling Stone, and on the Discovery Channel. Dr. Patterson has authored over 150 manuscripts and book chapters focusing on single-cell biology and diagnostics. Dr. Patterson was formerly Associate Professor of Pathology and Infectious Diseases and Director of Virology at Stanford University. He currently serves as CEO and founder of IncellDx Inc., a growth-stage company that has translated his research discoveries into state-of-the-art single-cell diagnostics in Cancer, Immuno-Oncology, and Infectious Diseases, especially COVID.
Our mission is to eradicate the epidemic of tick-borne diseases through awareness and education, support of cutting-edge science, and advocacy for solutions to end the suffering. As a national Lyme disease non-profit, we aim to impact patients’ lives through our work.
December 23, 2024
MAL meet-ups occur a couple of times a month and are geared towards mothers raising children with Lyme, or mothers with Lyme themselves. It serves as a support group where you will discuss a common theme each meeting, share stories of your own struggle caused by Lyme, as well as hear advice from other mothers going through the same things as you. Join us by registering through the webpage!
November 20, 2024
The goal of this webinar is to teach patients how to effectively advocate for change on the Federal, State, and local levels of government. Our presenters will discuss multiple topics including but not limited to: ways to engage with political representatives through letter writing, proclamation requests, how to participate in the upcoming Center for Lyme Action Fly-In and how to advocate for change hyper-locally, such as planning 5k's, social media fundraisers.
November 19, 2024
Illness invalidation, by medical professionals or others, is a common experience for patients with Lyme disease. This talk will discuss recent scientific articles in Lyme and other illnesses about the patient effects of invalidation. It will also discuss the gendered history of invalidation and how it influences the medical encounter today.
