The right doctor changed everything for John Bush.
Since October of 2016, the Kenosha teenager had had a series of health issues, shifting his life filled with musical theater and academics to a life of constant doctor visits. Doctor after doctor told his family what they thought would relieve his pain, but nothing sufficed.
If he had waited four more months before seeing yet another doctor, he could’ve faced paralysis.
That’s the usual waiting period to see Dr. Casey Kelly, a Lyme-literate doctor in Chicago.
But when John’s mom, Laura Bush, called the office seeking treatment for her son, the receptionist had good news.
“You’re really lucky,” the receptionist said. “Someone just canceled a new patient appointment; can you be here tomorrow at 2 p.m.?”
Developing diagnosis
About a month after his colonoscopy and initial Lyme diagnosis, John had finished his 30 days of antibiotics, but his body continued to scream with pain.
“They’re going to tell me it’s not active in my body anymore,” John said to his mom when she made an appointment to see another doctor, a rheumatologist, who specializes in joint pains and autoimmune diseases.
His stiff muscles made it difficult to get out of bed each morning and the flu-like symptoms persisted.
Holding the songbook at church made his hands and neck ache with pain, a common sign of chronic Lyme.
It was supposed to be gone. That’s what his doctors kept telling him.
According to the Centers for Disease Control and Prevention, there are no accurate tests to prove that Lyme has been eradicated from the body.
John’s frustration grew with his doctors’ seemingly low knowledge of what was happening to his body. His first doctor thought it might just be mononucleosis.
Finding the book “Why Can’t I Get Better?” by Dr. Richard Horowitz changed John’s perception of Lyme.
Horowitz wrote rheumatologists often think the disease is depression and anxiety if the antibiotics fail. John felt the doctor visit was going to be useless.
The doctor’s explanation of John’s chronic pain resembled Horowitz’s prediction.
Laura Bush asked to see the Lyme doctor in the building.
“I am the Lyme doctor,” he replied.
They left quickly.
The right treatment
John shared his entire medical history with Dr. Kelly, leading her to believe he was bitten by a tick 11 years ago.
The body doesn’t always recognize the bacteria as an active disease when it’s first transmitted. That leaves it dormant for years — sometimes presenting itself as other health conditions — until it’s stirred up, Dr. Debra Muth, a Lyme-literate doctor in Waukesha, said.
John’s symptoms surfaced when he started taking doxycycline for his acne.
He had yet to be diagnosed with Lyme. The antibiotic went to work, not only on the bacteria causing his acne, but on the dormant Lyme-causing organisms in his body. As they died off, they unleashed toxins, creating John’s symptoms.
Throughout his life, John had been diagnosed with attention deficit disorder, obsessive-compulsive disorder, oppositional defiant disorder, motor impairment, concussions and a slew of stomach issues.
Kelly told John she thought those diagnoses were caused by the bacteria festering in his body, he said.
John was skeptical about the treatment until he spotted Dr. Horowitz’s book in the waiting room, which instantly calmed him.
John was in Chicago four days a week for three weeks for a mixed-medication plan.
That treatment included mass doses of vitamins, infusions of medicine and cleaning toxins from his blood using a UV light.
Living with Lyme
One January morning, months after his initial diagnosis and attempt at treatment, John realized he needed help walking one morning.
With a grimace plastered on his face, his stiff muscles walked into his basement to fetch his grandpa’s wooden cane.
His parents thought he was being theatrical at first, citing John’s involvement in local theater, but quickly saw the look on their son’s face and knew it was real.
Clutching his newly bought blue plastic cane, John steadied himself walking the halls of Bradford High School.
He felt his classmates’ and teachers’ eyes on it, not quite understanding why he had it while he was still trying to understand his disease, too.
“I didn’t want anyone to feel like they owed me anything,” John said, recalling how he attempted to minimize his suffering.
During choir practice, he danced with the cane through his muscle pains while he struggled with brain fog, making it hard to memorize the songs he loved performing.
“I didn’t want people to see me as disabled, which I was,” he said.
Looking back, he recognizes he was trying to fight reality.
Eventually, John had to drop most of his classes. School became too much.
The Lyme drained his energy and took a toll on his family’s finances.
“How do you go about something that’s difficult to begin with and how do you wrap the budget around it?” he said.
Finances
The insurance company wouldn’t cover the cost of John’s treatment.
After the first visit with Kelly, they left with about $400 worth of supplements. So far, his family has paid $12,000 out of pocket for his treatment.
“I don’t know how my parents are doing it, because it’s not cheap,” John said.
His initial medical routine included a strict diet with seven medications at breakfast, two at lunch, six at dinner and another six at bedtime.
After two weeks on the new routine, John ditched his cane.
Advocacy
Now, six months removed from his initial diagnosis, John speaks at Rotary clubs to share his story.
He wants to shift the conversation so others get treatment quicker at lower costs.
“It’s really important for people to realize that we have an epidemic in this country and in the state of Lyme disease,” he said.
Madison Area Lyme Support Group 