Zack Jones is a 48-year-old professional guide, trainer, trip designer, and photographer residing in Frankfurt, Germany. He is the “Zack of all Trades” with his current company and “recently added smitten father to an amazing baby girl to the CV”.

Mr. Jones described his life before Lyme as “pretty good and at the same time full of blissful ignorance”. While on a trip to Honduras, he and a travel companion began to suffer from neck and back pain that progressed to fever, intense body aches, and diarrhea that rendered him “barely able to function”. After treating with an infectious disease doctor, he returned to work but suffered from 5 years of lingering mental health issues.

Ten years after his initial symptoms, he traveled to Chile for work where he suffered relapsing mental health issues including anxiety attacks, depression, and insomnia. Thereafter he began to suffer physical symptoms including jaw pain, fatigue, neuropathy, bone pain and air hunger.

After treatment with “30 to 40 medical professionals for one symptom or another” he was tested for Lyme disease and co-infections through Armin Labs in Germany and IGeneX labs in the United States.

Today, Mr. Jones is in the midst of treatment utilizing genetic testing from traditional naturopath Bob Miller to guide him through the use of herbals, the Wave 1 bio resonance device, and the Patricia Kane protocol.

If you would like to learn more about how a professional guide and trip designer is mapping his treatment plan through genetic testing, then tune in now!

Jeni Quante is a 29-year-old Registered Nurse (RN) and chronic illness patient advocate from San Antonio, Texas. She has earned high regard from the Lyme disease community for producing creative educational content on social media platforms including TikTok and Instagram.

Ms. Quante was born with Congenital Lyme disease, but the undiagnosed illness did not become debilitating until the age of 14. Her disability activated her medically educated and trained parents who dedicated all their resources to advocating for their daughter. In total, the family visited “well over 100” doctors before she was diagnosed by a primary care physician. Her diagnosis took more than 12 years.

Despite debilitating symptoms, Ms. Quante graduated from college and nursing school, earning a BS, BSN, OCN, and RN. She also dedicated time to “engaging others in the chronic illness community and found some wonderful lymies who kept her going through the hell”.

This far, her 3-year treatment plan has included the use of several western and eastern treatment modalities, including, hyperthermia, SOT, herbs/tinctures, detox work, disulfiram, and biofilm busters.

If you would like to learn more about how Lyme disease played a role in transforming a Registered Nurse into a highly regarded chronic illness and social media advocate, then tune in now!

Axel Roelants is an entrepreneur and former athlete from Belgium. He is the co-founder of 4Gold, an athletic supplement, health, and performance company.

In 2016, Mr. Roelants suffered a broken neck in a dirt bike accident. Shortly after the injury, he began to suffer from a diverse and progressive set of classic Lyme disease symptoms that his doctors attributed to his traumatic injuries.

Trusting his intuition and relying on his entrepreneurial and athletic skill sets, he built a team of doctors, therapists, and friends to help him to “look at [his] disease like a project”. After much trial and error, one of the team members suggested his “strange health issues” should be evaluated by an ILADS doctor in Belgium where he tested positive for Borrelia Miyamotoi.

Mr. Roelants’ healing journey included the use of IV antibiotics, disulfiram, samento and banderol from NutraMedix, Meyers’ Cocktails, ozone therapy, and detoxification. Unfortunately, his discipleship in the church of the athletic “suck it up” culture caused healing setbacks because he “over exercised” and pushed through treatments too quickly.

If you would like to learn more about how a professional athlete and entrepreneur utilized his professional skill sets to heal from Lyme disease, then tune in now!

Ali Lazowski is the 31-year-old John’s Hopkins University educated founder and CEO of Bare Life. Bare Life is a company that creates “crave worthy and easy to enjoy plant based and gluten free foods, inspired by Ms. Lazowski’s journey with chronic Lyme disease”.

Undiagnosed Lyme disease symptoms began to interfere with Ms. Lazowski’s goal driven life during her junior year in high school. Beginning with “utter exhaustion, horrible headaches, brain fog, [difficulties] focusing, and a constant low-grade fever”, her illness progressed to include “joint pain”.

She suffered in constant pain without a diagnosis for 8 years despite treating with “north of 30 different doctors”. Finally, at the age of 25, she granted permission to “cry… with relief” when a blood test indicated that she was positive for Lyme, Babesia and Anaplasmosis.

Treatment with a Lyme Literate Medical Doctor included various antibiotics and antibiotic cocktails. The 3 “game changing” healing plan interventions were: 1. working with a psychologist to learn how to read her body signals, 2. dietary changes that removed dairy, gluten, and refined sugar, and 3. Cord stem cell therapy.

If you would like to learn more about how Lyme disease inspired Ali Lazowski to create great tasting gluten, dairy, and refined sugar free chocolate, then tune in now!

PS Nicoleta Forbes special guest co-hosted this interview with Rich from Tick Boot Camp!

Debbie Kimberg is a 55-year-old author, activist, and director of International Expansion for Merchant Services at JP Morgan Chase from Dallas, Texas.

Ms. Kimberg, her mother, and her 3 children have been diagnosed with Lyme disease. Despite 3 generations of the family exhibiting classic Lyme disease symptoms, Lyme was not a consideration until after the youngest child, Sammy, was diagnosed.

Sammy’s Lyme journey began prior to birth, when a brain development issue was discovered on a prenatal ultrasound. He saw a neurologist at birth and then doctors and special education service providers diagnosed him with ASD, ADHD, Tourette's syndrome (TS), OCD, Autism and PANS.

At the age of 10, Sammy was also diagnosed with Lyme disease by a functional doctor. At the same time, Ms. Kimberg was also diagnosed. Finally, Sammy’s test results led doctors to test his 2 brothers and his grandmother.

For most of Sammy’s life, his family, doctors, and teachers believed his disability would limit his ability to work and require him to live in a long-term residential facility. However, in the past 18 months, Lyme and Bartonella treatment protocols have resolved his learning disabilities and ADHD. As a result, he is reading above grade level, attending school in the general education population, and studying for the ACT college entrance exam in anticipation of attending a 4-year college.

The Kimberg family’s lengthy congenital Lyme disease journey activated Debbie. She has participated in advocacy forums, podcasts, articles, and has authored a soon to be published book titled “Our Hijacked Brain: A True Story of Infection, Autism, ADHD and Psychiatric Issues”.

If you would like to learn more about how a Lyme advocate was born out of solving a multi-generational medical mystery, then tune in now!

Georgia Grace Ritchie Wood is a professional ski coach, yoga instructor, poet, and podcaster from Australia. She currently resides in Woodstock, Vermont, USA.

Ms. Wood was born with a kidney disorder that rendered her immune compromised. Her parents were advised that she would require kidney reconstruction surgery and should not engage in activities such as skiing or skydiving. Ms. Wood was also born with a passion to vanquish any and all limits and she developed an improbable passion for snow skiing.

Her will to overcome all challenges resulted in an invitation to join the Australian Ski Team. Ms. Wood represented her country in several international competitions and traveled to North America to train for the Olympics.

The rigors of international travel, Olympic level training, and North American ticks resulted in Ms. Wood suffering illnesses that rendered her bed bound. Unfortunately, a “devil inside of [her]” stole her Olympic dreams and a college scholarship. After several years of misdiagnosis, doctors discovered that Lyme disease was in fact the “devil inside” of Ms. Wood.

Today, Ms. Wood is a ski instructor and international Lyme disease advocate. Her highly regarded podcast, Blooming with Lyme, had become a staple in the Lyme community genre.

If you would like to learn more about the journey an international skiing champion took to overcome chronic illness to Bloom with Lyme, then tune in now!

Special Note: in this episode Ms. Wood read her poem “The Devil Inside of Me”. See the poem below:

There is a devil inside of me, I am his disguise. He's taking over, crept his way inside. Picking and pulling, punching and pounding Constant chatter, no good for the ears Only leaving me mad and in fear I’ve lost my way, being locked away The devil holds the key, Not quite sure I'll be able to break it free. Close my eyes I see the devil, Keep them open, and I’m left venerable. But worse of all, everyone else will see, What's really happening inside of me. Lack of control, now my current theme He's come in and ruined, every one of my scenes. Barely breathing, continuous aching “Stab me, slash me” now he’s screaming! There is a devil inside of me, I am his disguise. Locked in a jail, visible only to me Sick and tired, no way to break free Stripping me of my dignity, repetitively Trying to drown him in both pills and potions But the funny thing is, he’s just learnt to swim So why even bother when the devils just growing stronger? Barely breathing, lack of control He strikes again and oh so bold I’m trying to speak up, but in he cuts. Let me speak up, let me reach recovery There is a devil inside of me, I am his disguise. Someone please help me, someone please save me Cause these pills and potions aren’t doing a thing Barely breathing, where’ll he strike next? First to my family, friends you'll be up next. And slowly but surely, he'll bring them an end. Heart racing, head ponding He's constantly screaming “Slap me, stab me and finally shot me.” There is a devil inside of me, I am his disguise. No more is he just, that little side bloke He has taken over, sucking at all my hope Pills and potions, keeping him only entertained But sober him up and he’s right back for more games I’m trying to push through but I’m not sure if I can cope. He’s growing and expanding, and he’s made me his permanent home Where have I gone? And where is this mysterious key? He’s locked me away for no one else to see. There is a devil inside of me, though no more am I his disguise He has become me, and I have been locked deep, deep inside. I am not fighting myself, I am fighting a fight against that evil devil that’s taken over my inside.

-Georgia Wood, January 13, 2016

Greg Lee is the 55-year-old founder of the Lyme Research and Healing Center and GoodbyeLyme.com. He is a nationally recognized expert in the use of Chinese herbs and alternative medicine for the treatment of persistent infections.

Mr. Lee began his career as a systems engineer on NASA projects such as the Hubble Telescope, the Space Station, robotics, and climate modeling projects. The stresses of working on multiple space projects caused Mr. Lee to suffer from irritable bowel syndrome (IBS) which he managed with medications until he resolved the illness after treating with an acupuncturist.

The relief offered by the alternative treatment inspired Mr. Lee to change his career path. He returned to college to become a Master of Acupuncture and he also earned a Chinese herbal certification before opening a healing practice for chronic pain in Fredrick, Maryland.

Two concurrent events inspired Mr. Lee to narrow the scope of his healing practices focus on Lyme: first, many of the patients he successfully treated for fibromyalgia tested positive for Lyme disease, and second, his daughter was bitten by an infected tick.

If you would like to learn more about how you may benefit from herbals, alternative treatment, and the Lyme Research and Healing Center on your Lyme disease healing journey, then tune in now!

PS Greg has offered an exclusive free download to Tick Boot Camp listeners detailing the Top 5 Essential Oils for Lyme Disease!

Dr. Janis J. Weis, Ph.D. is a Professor of Pathology in the Division of Microbiology and Immunology at the University of Utah School of Medicine.

Dr Weis developed a professional passion for studying Lyme disease when she and her family lived in the east coast Lyme belt during the time she performed her post-doctoral training in immunology at Brigham and Women’s Hospital / Harvard University Medical Center.

Dr. Weis maintains an active research laboratory at the University of Utah studying the mechanisms and genetic regulation of Lyme arthritis development. She also serves as director of the Training Program in Microbial Pathogenesis, a National Institute of Health (NIH) sponsored training grant that supports pre-doctoral and post-doctoral trainees in this discipline.

Dr. Weis’ current studies are focused on understanding the inflammatory dysregulation associated with acute and chronic Lyme arthritis in mice. Recent studies have identified in Lyme infected immune deficient mice several features that are similar to features seen in patients with chronic Lyme disease.

If you would like to learn more about how the work of research Professor Dr. Janis Weis may provide the answers to how the Lyme bacteria may cause sustained inflammation and chronic illness regardless of the status or condition of your immune system, then tune in now!

Sarah Corlis is a mother of two children with Lyme disease from Alpharetta, Georgia. Growing up, she had a very active social life and used to work out all the time.

Sarah was a human resources manager until she was 34 years old when she took some time off to have her kids. A few years later, she returned to work as a realtor with a more flexible schedule for 6 years until she decided to work fulltime on her health and the health of her two children.

Some of Sarah's early Lyme disease symptoms included dizziness, nausea, jaw pain, headaches, terrible fatigue, depression, and anxiety, but doctors dismissed her symptoms and told her she was just anxious. Finally, Sarah was tested for Lyme disease by a functional medical doctor and was positive through both Labcorp and Vibrant Wellness tests.

Sarah has been treating using a variety of different tools for almost a decade. She has used antibiotics, herbals, FREmedica WAVE 1, Supportive Oligonucleotide Therapy (SOT) for Lyme and Bartonella, and most recently Ivermectin/Azithromycin for Babesia. Next, she is considering SOT for Babesia.

If you'd like to learn more how a determined mom "didn't lose hope, kept trying" and knew her and her children "could feel better", then tune in now!

PS Cassidy Colbert special guest co-hosted this interview with Matt from Tick Boot Camp!

Amanda Millie is a 35-year-old model, blogger and podcaster from London, England.

Shortly after Ms. Millie’s family immigrated from Africa to the UK, she was bitten by a tick on a school camping trip. She “picked off the tick and moved on with [her] life” because she was “unaware of what that bite meant”.

Around the age of 19, Ms. Millie “started getting intense fatigue” which she attributed to lifestyle changes she felt compelled to make to advance her career in the fashion modeling industry. Ms. Millie’s pursuit of food deprivation and high intensity exercise bolstered her modeling career and at the same time her undiagnosed Lyme disease symptoms, including, night sweats, headaches, brain fog, and hair loss.

The next decade of Ms. Millie’s life was punctuated by “a lot of doctors’ visits” and new symptoms. After visiting over 20 “private pay” doctors that caused her to collect several misdiagnoses, she was referred to a Lyme disease clinic in London. There, she was diagnosed with Lyme disease and prescribed a 10 step “personalized treatment protocol”.

Today, Ms. Millie has rebuilt her health by reorganizing her career and reconnecting with a healthy food and exercise regimen. If you would like to learn more about how Lyme disease forced a fashion model to return to her traditional lifestyle choices to support healing, then tune in now!