Education Archives - Page 3 of 7

Education

05/30/2023

What Does AI Know About Lyme Disease

The arrival of ChatGPT, Google Bard, and other artificial intelligence (AI) chatbots has sparked a flurry of interest and concern, particularly in the field of healthcare. As many in the tick-borne disease community know, there is a lot of information floating around the Internet about Lyme disease and other tick-borne infections—and not all of it is accurate or helpful. So will today’s AI chatbots help clear up common misconceptions, or will they perpetuate misinformation that leads many people with Lyme and other tick-borne illnesses to stay sicker longer?

Education

05/09/2023

Lyme Disease Symptoms, Treatments, and Prevention | Backpacker Radio Episode #200

Project Lyme recently joined Backpacker Radio to discuss all things deer ticks and Lyme disease.

Education

04/18/2023

Medical Gaslighting – The Lyme Patient’s Experience

Project Lyme recently chatted with Ashley Baker to get a patient’s perspective on medical gaslighting. Ashley is a passionate artist, Lyme disease advocate, member of Project Lyme’s Junior Board, and also one of the stories featured in the new Lyme documentary I’m Not Crazy, I’m Sick.

Education

04/03/2023

Isabel Rose – Author, Advocate, and Mother

Isabel Rose is a recording artist, author, and mother whose personal experiences with Lyme disease have motivated her to become an advocate for tick-borne disease awareness and education. She has been a Board Member of Project Lyme since 2019. Currently, Isabel runs Mothers Against Lyme, an initiative of Project Lyme, which offers support groups for mothers in need with a focus on congenital and pediatric Lyme disease.

Education

03/14/2023

Delayed Diagnosis: The Cost of Missing Lyme Disease

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

Reframing How to Live With Chronic Lyme Disease

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

Nowhere Land: Photographing the Life of Lyme Patients

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

Whole-Body Hyperthermia for Treating Lyme Disease

Whole-body hyperthermia is a medically induced state used to treat Lyme disease. This article serves to answer questions from our patient community about this therapy. This article does not serve as an endorsement. You should always consult with a medical professional before moving forward with a new treatment.

Education

12/08/2022

Considering Dapsone For Persistent Lyme

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.