Tick Boot Camp

Episode 318: Healing in Harmony - an interview with Micaela Hoo

Micaela Hoo is a 28-year-old freelance content creator, social media manager, Global Lyme Alliance (GLA) peer mentor, and entrepreneur from Los Angeles, California. She is the co-creator of My July, a clean skin care brand.

Born in the eastern United States Lyme belt, Ms. Hoo’s childhood was interrupted by persistent illness, learning difficulties, issues with word recall, and heightened sensitivity. She made frequent trips to doctors and medical centers without securing a diagnosis.

Ms. Hoo’s health did not improve when her family moved across the county to pursue professional opportunities on the west coast. Frustrated by the medical community’s failure to diagnose the source of her chronic symptoms, she turned to social media where she was told she “sounds very Lymie”.

As a graduation present, her dad offered to pay for a visit to a highly regarded California based Lyme Literate Medical Doctor (LLMD). Her gift included an IGeneX Lyme disease test that answered the multiyear medical mystery.

If you would like to learn more about how Lyme disease inspired a digital creator and entrepreneur to build a social platform that bravely represents “what it looks like when you do not feel well”, then tune in now!

PS Randi Goodman from Think Lyme special guest co-hosted this interview with Rich from Tick Boot Camp!

Episode 317: Lyme Support - an interview with Doctor Christine Arseneau

Dr. Christine Arseneau is a 38-year-old pharmacist who spent 6 years training at a hospital before managing an integrative compounding pharmacy where she now works today. She is the founder of Lyme Support which serves clients suffering with Lyme disease and tick-borne infections, is certified in Clinical Cannabinoid Pharmacy, and has a Functional Medicine Certification in Health Coaching.

Despite moving around a lot as a child because her father was in the Army, Dr. Arseneau was a straight A student and excelled at everything she did. Although her life seemed perfect from the outside, she never felt important or valued as a child since her mother had narcissistic tendencies and anxiety resulting in her emotionally abusing Dr. Arseneau.

Dr. Arseneau was bit by a tick and became sick at 9 years old, but she didn’t begin to have major health issues until she was 27 with things like meningitis, a rare form of cancer, debilitating fatigue, and pain. Finally, at the age of 29, she was diagnosed with Lyme disease, Babesia, and Bartonella.

Dr. Arseneau treated using Byron White Formulas (A-L Complex and A-Bart), Low Dose Naltrexone (LDN), plant medicine (psilocybin and ayahuasca), and more.

If you’d like to learn how a determined pharmacist refused to stay sick and overcame chronic Lyme disease to now help others heal, then tune in now!

PS Amanda Millie special guest co-hosted this interview with Matt from Tick Boot Camp!

PPS get Dr. Arseneau has a free virtual training for anyone struggling with chronic Lyme disease, pain, fatigue, and chronic complex health challenges titled How I Cured My Chronic Lyme Disease: The #1 Thing You Need to Know That Doctors Aren’t Talking About.

Episode 316: Reclaiming Embodiment - an interview with Dana Papadopoulos

Dana Papadopoulos is a 30-year-old not-for-profit Media Director residing in Charlotte, North Carolina.

Ms. Papadopoulos was transformed from an active, healthy, athletic child and young adult to a chronically ill 18-year-old woman. Then, for almost a decade, she battled a series of seemingly separate symptoms including anorexia, extreme GI issues, gastroparesis, POTS, EDS, fibromyalgia, ovarian cysts, hypotension, anemia, PCOS, leaky gut, and more.

Despite treating with over 50 medical doctors and medical centers, including the world-renowned Cleveland Clinic, she continued to suffer from poor health while collecting an array of diagnoses. Finally at the age of 27, a local chiropractor diagnosed her with Lyme disease utilize blood testing.

Her Lyme disease diagnosis became a blessing in that it permitted her to locate a focus for healing. After treating for one year, she successfully abated her symptoms and moved into a new apartment. Sadly, the new apartment had mold that reignited Lyme causing her to lose functionality.

Today, she is preparing to revisit Bee Venom Therapy (BVT) by rebuilding her gut, utilizing routine detox tools, exercising, and performing breath work and chanting.

If you would like to learn more about a young woman had to rebuild trust in herself, get back into her body and listen to body signals to overcome the challenges caused by Lyme disease, then tune in now!

PS Katie DePaola, from IGC Coaching School, special guest co-hosted this interview with Rich from Tick Boot Camp!

Episode 315: Grace Walk Farm - an interview with Amber Benge

Amber Benge is a 39-year-old young woman from Hickory, North Carolina who is now a sustainable farmer growing her own food and medicine at Grace Walk Farm. She’s a trained victim advocate and her professional background is in working with women who have addiction issues and are victims of sex trafficking.

Ms. Benge was bit by a tick when she was 5 years old during a family vacation. She got a bullseye rash, became sick, but Lyme disease went undiagnosed for the next 34 years.

Ms. Benge was sick for decades after her family vacation and she was misdiagnosed with chronic fatigue syndrome (CFS). In her early 20’s, she battled infertility, had multiple miscarriages, had preterm births for both of her children, and finally had to have a hysterectomy at age 24.

In her late twenties, Ms. Benge developed severe arthritis in her hands and feet and had her gallbladder, tonsils, and adenoids removed. During her mid-thirties, things really fell apart and she was constantly sick and had to quit her job as a counselor at a drug rehab center for women.

Ms. Benge was finally diagnosed with Lyme disease and Bartonella this year when she was 39 years old by a naturopath through bioresonance. Her husband and youngest child both also tested positive for Lyme.

Ms. Benge and her family treated with DesBio homeopathy. This included 15 different supplements, a very strict diet (no gluten, dairy, caffeine, or sugar), along with a very intensive detox program.

If you would like to learn more about how a strong woman is fighting back Lyme disease after over 30 years of being sick, then tune in now!

PS Bianca Michele special guest co-hosted this interview with Matt from Tick Boot Camp!

Episode 314: Lyme in the Limelight - an interview with Daisy Ilchovska

Daisy Ilchovska is a 36-year-old nutritional therapist, researcher, and author from Bournemouth, England. She is the founder of Optimal Health Nutrition, a virtual clinic established to help people overcome health challenges through evidence-based strategies.

At the age of 26, Ms. Ilchovska was diagnosed with an autoimmune disease and doctors told her to expect to be permanently disabled in less than a decade. Shortly thereafter, she suffered a tick bite causing her to health to deteriorate from a myriad of neurological symptoms.

After working with a half dozen conventional doctors, she discovered that she had to take responsibility for developing her own treatment plan because none of her doctors knew how to treat her. She overcame Lyme through her own research and seeking out hypothermia treatment in Germany.

Her recent work includes publishing a research paper in the December 2020 issue of Autoimmunity Reviews, publishing a book titled “Lyme in the Limelight” in 2022, and contributing a chapter on Lyme disease and autoimmunity in the 3rd edition of Infection and Autoimmunity to be published in early 2023.

If you would like to learn how Lyme disease inspired a young researcher to study nutritional intervention, Lyme disease, and autoimmunity, then tune in now!

PS Christina Kantzavelos, Lyme literate therapist, special guest co-hosted this interview with Rich from Tick Boot Camp!

Episode 313: ChroniLyme - an interview with Christèle Dumas-Gonnet

Christèle Dumas-Gonnet is the 48-year-old co-founder of ChroniLyme, a patient advocacy association dedicated to improving diagnosis and treatment of chronic Lyme disease, based in Lyon, France. She is also a member of the European Lyme patient engagement collective PREFACE (Patient Resource Facilitator Europe).

Shortly before the end of her university studies, she began to suffer from fatigue, aches, pains, and “a white fog that prevented [her] from concentrating”. For the next 20 years, her health slowly and steadily declined requiring her to seek treatment from “dozens of doctors” and hospitals.

In 2014, she was hospitalized for “left side paralysis that lasted several days”. During her hospitalization, she underwent several diagnostic tests including a spinal tap and a brain MRI. Despite the “highly positive results” for “Lyme neuroborreliosis” from the spinal tap, the hospital released her with a single diagnosis of “atypical migraines”.

For the next two years, she was not treated due to her silent diagnosis resulting in a rapid health decline. Her illness prevented her from performing any social or professional activities and she was deemed fully disabled by the French government.

In 2016, she sought treatment with a general medical practitioner known as “Doc Lyme” who diagnosed her with and initiated treatment for Lyme disease. Following the diagnosis, Ms. Dumas-Gonnet collected her medical records and discovered that she had unknowingly tested positive for Lyme disease two years earlier.

Her experience with diagnostic and treatment nightmares typically faced by Lyme patients caused Ms. Dumas-Gonnet to use her education and training to advocate for patients in France and across Europe.

If you would like to learn more about how Lyme disease inspired a patient to build two Lyme advocacy organizations and to appear before the French National Assembly and Senate, then tune in now!

Episode 312: Redefining Wellness - an interview with Dr. Jaban Moore

Dr. Jaban Moore is a Doctor of Chiropractic and founder of the Redefining Wellness Center located in Kansas City, Missouri. The mission of Redefining Wellness Center is to educate people about the root causes of chronic illness to help them to find true healing.

The foundation of Dr. Moore’s passion for restoring health through a multi therapeutic approach was informed by witnessing his mother struggle with chronic illness and health decline during his childhood.

Later, during his time at chiropractic school, he began his own rapid health decline. His search for answers for why he was suffering from extreme fatigue, joint pain, and low testosterone began by utilizing his access to a wide range of doctors at medical conferences. After many misdiagnoses, he attended a conference for functional medical doctors where he accepted a recommendation to test for Lyme disease.

Testing positive for Lyme disease gave rise to a journey of personal and professional development for Dr. Moore. After consulting several doctors and utilizing a wide range of treatments, he found relief and has been symptom free for over 5 years.

If you would like to learn how Lyme disease inspired a doctor to build a wellness center to educate people about the root causes of chronic illness, then tune in now!

Episode 311: Socially Serving - an interview with Sarah Lombard

Sarah Lombard is a 27-year-old social media marketing, management, and creation professional from Scottsdale, Arizona.

Prior to attending college, she enjoyed a very social teen life that included “the worst diet known to man”. She would “eat candy and cookies for lunch with some fries and coming home, starving, eating frozen dinners and spoons full of sugar”.

At the age of 17 she began to get sick. She suffered monthly infections, stomach aches, lethargy, lack of motivation and anxiety. Her symptoms forced her to seek treatment from so many doctors she “lost count”.

After being misdiagnosed with various illnesses and undergoing several procedures and tests, a co-worker recognized her symptoms and referred her to a Lyme Literate Medical Doctor (LLMD). A blood test confirmed her co-workers suspected Lyme disease diagnosis.

Post diagnosis treatment began with clearing her “gut from yeast and parasites” followed by the “Cowden protocol with liquid tinctures for 9 months”. She then turned to “Disulfiram but it’s an extremely hard regimen and it made [her] too sick to function so [she] had to stop”.

If you would like to learn more about how Lyme disease inspired a young woman to use her professional skill set to socially serve the community, then tune in now!

PS Ashley Marba special guest co-hosted this interview with Rich from Tick Boot Camp!

Episode 310: I Can't Wait - an interview with Vanessa Nolet

Vanessa Nolet is a 29-year-old young woman from Quebec, Canada. She is working on finishing up a bachelor’s degree in Healthcare Management.

Prior to getting sick with Lyme disease, Ms. Nolet had a great life filled with friends and sports. She worked at a spa while going to college and was exposed to Freon during an accident which changed her life.

Around this time, Ms. Nolet was bit by a tick and within a month she became very ill. She had chronic fatigue, whole body spasms, light sensitivity, body burning, ulcers, arthritis, irregular periods, autoimmune symptoms, and more.

She visited many doctors, specialists, and hospitals in Canada before going to America for help where she was finally diagnosed. Nobody could figure out why she was sick. Some doctors misdiagnosed her with conditions such as Fibromyalgia, other pain disorders, and Lupus.

Finally, at the age of 27, Ms. Nolet was diagnosed with Lyme disease in part thanks to Dr. Richard Horowitz’s Multiple Systemic Infectious Disease Syndrome (MSIDS) questionnaire. She was treated with Doxycycline, Rifampin, Azithromycin, Naltrexone, AGE, and more with a specialist in Canada.

If you would like to learn how a young woman from Canada fought for a root cause diagnosis and is now on the path to health, then tune in now!

PS Johanna Laliberte special guest co-hosted this interview with Matt from Tick Boot Camp!

Episode 309: Two Monies - an interview with Kahlil Fuller

Kahlil Fuller, stage name “Two Monies”, is a singer, songwriter, musician, and entertainer from Charlotte, North Carolina.

Shortly after graduating from North Carolina A & T with a degree in marketing he “noticed a huge rash on [his] left leg” while working out at the gym. He assumed the rash was from a harmless “bug bite” until he began to limp 5 or 6 days later.

Prompted by left leg paralysis, Two Monies called his primary care doctor of 15 years. Expecting his doctor to diagnose his “problem and… fix it” he was surprised to “be let go by his doctor” without a diagnosis.

The medical surprises continued for Two Monies when his next set of doctors diagnosed him with a “complex and controversial” medical condition named Lyme disease. His diagnosed illness moved him from a stable independent life to “stressed, depressed and anxious”.

Working with a Lyme Literate Chiropractor in North Carolina and a Lyme literate practitioner in San Francisco became a game changing experience for Two Monies. Treatment with herbs, Low Dose Naltrexone (LDN), probiotics, CBD oil, IV glutathione, infrared sauna, and IV antibiotics modulated his symptoms and expanded his quality of life.

If you would like to learn more about how two co-infections and Lyme disease gave Two Monies a bad rap, then tune in now!

The goal of the Tick Boot Camp Podcast is to help people liberate themselves and others from suffering caused by Lyme disease through validation, community building, belief that healing is possible, and modeling success. Listen to our Tick Boot Camp podcast using all major podcast streaming services such as Apple Podcasts, Spotify, and YouTube Music. Our podcast is also integrated with smart home devices, such as Amazon Alexa and Apple TV. Ask your device to "play the Tick Boot Camp Podcast!"