Natalie Torres is a 27-year-old life coach, entrepreneur and model from Houston, Texas. Ms. Torres was infected twice with Lyme disease, first at the age of 12 and then she was reinfected at the age of 23. She was working as a fashion model based in New York City (NYC) when her doctor diagnosed with Lyme disease. After receiving a Lyme diagnosis, Ms. Torres granted herself permission to engage in self-care and to make healthy lifestyle changes which became the foundation for a career change. Ms. Torres’ healing journey introduced her to various eastern and western healing modalities including antibiotics, psychedelic mushroom micro dosing, mineral detoxing, Kambo, Kundalini yoga and breathwork. If you would like to learn more about why a fashion model left the bright lights and the big city to answer a spiritual calling to coach healing, then tune in now!

Mimi Maclean is a 49-year-old Ivy League educated entrepreneur, Lyme disease platform curator and dual podcast host from Los Angeles, California. Ms. Maclean, her husband and one of their 5 children have been diagnosed with Lyme disease. Ms. Maclean was infected with Lyme disease 6 years ago when she was bitten by a tick while visiting the east coast. Upon returning home to California, she sought medical treatment for the tick bite and made the regrettable decision to forego prescribed antibiotics. If you would like to learn more about how a tick bite and Lyme disease transformed an entrepreneur and mother of 5 into the founder of the Lyme 360 platform, podcast and community, then tune in now!

Johanna Laliberte is a 35-year-old registered behavior technician, life skills coach and small business owner serving the special needs community in Bergen County, New Jersey. Ms. Laliberte’s Lyme disease experience began during her childhood when her mother was diagnosed with chronic Lyme disease. Ms. Laliberte was herself diagnosed with chronic Lyme disease approximately 5 years ago. She is currently on a professional leave to dedicate full time to a unique IV and nutritional therapy protocol. In response to the concern that most Lyme disease stories are told after the healing journey has ended, Ms. Laliberte offered to share the physical and emotional challenges of her experience immediately after commencing treatment. If you would like to learn more about why a second generation chronic Lyme disease patient is bravely sharing the ups and downs of her treatment experience, in real time, then tune in now!

Michelle McKeon is a Certified Mold Specialist, teacher, Board-Certified Nutrition Specialist (CNS) and the founding owner operator of Lyme and Cancer Services and Balancing Pathways. She is also the director of LifeSpan medicine’s Lyme Nutrition Program. After a 5-year diagnostic journey that started with a tick bite on Fire Island, New York, she treated with some of the top Lyme Literate Doctors (LLMDs) in the US including Dr. Kenneth Leigner, Dr. Richard Horowitz and Dr. Sheryl Leventhal. She also treated at the renowned Klinik St. Georg in Germany. Ms. McKeon’s diagnostic and treatment journeys granted her insight into a diverse set of treatment tools which she converted into Lyme disease recovery frameworks. If you would like to learn how a Lyme disease experience inspired a pivot from a teaching career to a career dedicated to building businesses designed to end the suffering caused by Lyme disease, then tune in now!

Mariko Sato is a sales representative for an IT Company and a professional Samba dance entertainer from Tokyo, Japan. Ms. Sato’s Lyme disease journey began when she was bitten by a tick when she traveled to Brazil to study Samba. She was diagnosed with Lyme disease by a DNA Connections test administered by the Japanese Wellness Clinic Kagurazaka. Ms. Sato tested positive for Borrelia Burgdorferi, Babesia and Bartonella. If you would like to learn more about how a professional entertainer from Tokyo, Japan contracted Lyme disease, then tune in now!

Christina Kovacs is a 32-year-old Lyme disease blogger, advocate and lobbyist from Kentucky. Ms. Kovac’s Lyme disease journey began shortly before she left college at the University of Louisville. For the next 5 years, Ms. Kovacs’ health continued to decline and she visited with over 100 doctors in 8 US states. Finally, she was referred to the real life “Doctor House,” Dr. Michael Bernui, who diagnosed her with Lyme disease. If you would like to learn more about Christina Kovacs’ 100 doctor Lyme disease journey, then tune in now!

Olivia and Holiday Goodreau are the dynamic mother-daughter team from Denver Colorado that co-founded the LivLyme Foundation and the Tick Tracker App. The Goodreau family’s Lyme disease journey began when Olivia was bitten by a tick at the age of 7. Olivia’s classic Lyme disease symptoms were misdiagnosed by 51 doctors over 18 months. Since her diagnosis, Olivia has become one of the Lyme disease community’s most aggressive advocates resulting in her meeting with Governors, Senators, a President and world leaders. She has also partnered with some of the Lyme community’s most famous doctors including Dr. Neil Spector and Dr. Richard Horowitz. If you would like to learn more about how Lyme disease transformed a 16-year-old woman and her mother into advocates, educators, app builders, and co-founders of a foundation that provided treatment grants to 49 patients and awarded 4 major university research grants, then tune in now!

Sam McLaren-Fahey is a 31-year-old Citizenship Assimilation program manager and the creator of the acclaimed trauma survivor podcast: “Your Survived. Now What?” Ms. McLaren-Fahey’s traumatic Lyme disease experience began at the age of 24 when she suffered symptoms including complex migraines, weight and hair loss, panic attacks and severe neurological symptoms. On one occasion Ms. McLaren-Fahey’s neurological symptom prevented her from processing how to use a cooking spatula and she attempted to turn an egg with her bare hand. Ms. McLaren-Fahey’s Lyme disease was misdiagnosed by 13 different doctors over 2 years. If you would like to learn more about the Lyme disease journey of popular podcast host Sam McLaren-Fahey, the tune in now!

Christa Nannos is a 30-year-old American actor, writer and Lyme disease educator from Los Angeles, California. Ms. Nannos was bitten by a tick when she was 9 years old. Her Lyme disease remained mostly dormant until she was exposed to parasites while on a mission trip to Guatemala. During the following 10 years, she was misdiagnosed with mental health illnesses, Candida, SIBO, Overactive Bladder Syndrome, IBS and more. Despite being mistreated by the medical community and suffering from debilitating physical symptoms, Ms. Nannos focused on maintaining a positive mindset and used laughter as a healing tool. If you would like to learn more about how a comedic actress and writer is using laughter as a Lyme disease healing tool, then tune in now!

Christine Lydon is an Ivy League educated American Medical Doctor (MD), Author and Attorney (JD) living in Rossland, British Columbia, Canada. Ms. Lydon moved to Canada, with her son, to attend law school. Both Ms. Lydon and her son began to exhibit classic symptoms and were diagnosed with Lyme disease by the well know Lyme Literate Doctor (LLMD) Daniel Cameron. Unfortunately, Ms. Lydon’s Lyme disease diagnosis was questioned by the Canadian medical and legal communities and her son was temporarily placed in the Canadian foster care system which prevented him from receiving Lyme treatment. If you would like to learn more about how a doctor-lawyer suffering from chronic Lyme disease was failed by the Canadian medical and legal systems, then tune in now!