Their diagnoses were just the beginning: How tech app, community tap into co-founders’ own chronic illnesses

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WICHITA — An app launched to help patients take control of their chronic illnesses has origins in its co-founders’ own journeys in dealing with the day-to-day physical and emotional tolls of their ongoing health conditions, as well as efforts to better communicate with doctors.

“I personally struggled with trying to remember all the symptoms,” said Maddie Shonka, a lupus and narcolepsy patient who co-founded Wichita-based Co-Immunity Technology Solutions and its non-profit arm, Co-Immunity Foundation. “How accurately you describe your symptoms dictates your treatment plan and diagnosis, especially for diseases that don’t have labs or tests that correlate.”

The startup’s first tech tool, the app CoVstat — the name of which reflects CEO Shonka and co-founder and COO Kyle Manera’s Czech heritage, with “stat” meaning “to get up through difficulty” — was designated to help eliminate frustration and anxiety before appointments.

Click here to begin exploring Co-Immunity and CoVstat.

Participants currently can track their symptoms for free, but a subscription option is coming soon.

“We want to be the Disney of health care,” Shonka said, describing her hope that users can live a full life, doing what they love, but recognizing they’ll have to push themselves.

“I think it’s important that this culture of chronic illness where you can’t achieve anything is combated because it’s not true,” she continued. “You just have to do things differently.”

CoVstat allows people to choose a specific medical area to track their symptoms based on their needs. “When you have a chronic condition at our age, it can sometimes take longer because the test results people are looking for don’t always flag the same as those who are diagnosed at 40,” Maddie Shonka said. “It’s rare to be diagnosed with these rheumatology diseases in your 20s and younger.”

Regretting ‘right’

Before her diagnosis of lupus and narcolepsy with cataplexy in high school, Shonka would wake up at 6 a.m. for cheer practice and fall asleep stretching. When she’d go to her first class, she would fall asleep within the first 20 minutes. She’d even have to nap before driving five minutes home. 

“I got swine flu in fourth grade that triggered the narcolepsy, and I had mono in sixth grade that triggered lupus,” Shonka explained.

Her health problems, however, began much earlier, she said.

Shonka’s mother had a traumatic three-day labor where they both almost died. Shonka had pneumonia for the first time at 8 weeks old. Also suffering from chronic asthma, she had to wake up every night for breathing treatments.

“I knew I always wanted to be a doctor growing up,” Shonka said. “I was a super nerd who read medical terminology for fun.”

She also knew something was wrong in sixth grade. She remembers asking her doctor to run tests for lupus, a chronic autoimmune disorder. This search continued in Wichita until she was a sophomore in high school.

After traveling to the Mayo Clinic, she finally received answers 18 months later. Shonka learned she had narcolepsy the summer before her senior year of high school and lupus in December of that year.

“When I was finally diagnosed with lupus, I didn’t have a normal reaction,” Shonka said. “My mom was sitting there crying. I started celebrating because I was so happy I was right, and then it hit me.”

During her senior year, Shonka completed an EMT course through which she learned more about the initial prognosis of her new diagnoses.

“When I was studying for my practicals, I was reading about how one of the causes of a collapsed lung was lupus,” Shonka said. “It took me a few months to really hit me. This is a diagnosis that can and already impacts my life. Maybe I didn’t want to be right about it.” 

Shonka and her family had been looking for signs of lupus for years, but the diagnosis with narcolepsy came as a surprise.

“The narcolepsy affected me more,” Shonka said. “It came out of nowhere. I felt like I had slept my life away. Having a name for it made me really angry.”

Watch an interview below between Maddie Shonka and Chris Rehkamp, UMKC Tech Ventures Studio, then keep reading.

Changing the stigma

Shonka initially launched the Co-Immunity Foundation in July 2019 while attending Wichita State University, where she studied health care administration and management.

“I was really sick my freshman year of college,” Shonka said. “There were about two months where I couldn’t drive, walk, or talk. I was supposed to go to KU, and here I am watching all my friends partying. It’s really crazy to live this double life where you look normal, but at the same time your reality is completely different.”

Starting the non-profit seemed like a way to cope and help others, she said.

“I rely on gut feelings a lot,” Shonka said. “I just had this feeling that I needed to do this, and that the timing was right.”

Shonka attended E-Launch — a program at Wichita State designed to help foster entrepreneurship and commercialize ideas — interviewing several patients with chronic illnesses. Her first interviewee (and eventual co-founder), Manera, had just been diagnosed with hypothyroidism.

“When I started the tech company, he was in the pilot program,” Shonka said. “He’s an aerospace engineer and is definitely more technical than I am. I was shocked when he said ‘yes.’” 

She then launched a Sur(THRIVE)al program as a virtual support group on the non-profit side of Co-Immunity to unite people by age and not disease, she said.

Sixty-five participants from across the country joined Shonka in the program this year starting in September. They were split into middle school, high school, college, “adultish” for people 22 to 30 and adults older than 30.

“Our tagline is ‘chronic illness sucks, and that’s okay,” Shonka said. “Our goal is to acknowledge the ‘suck’ of chronic illness, but instill an attitude of resilience in people.”

“A lot of times you doom scroll on Facebook,” she continued. “I was reading this forum of everything that could go wrong with me, and it made me panic.”

The program runs for 12 months. Participants are challenged to do a chapter of the survival guide on their own to establish their feelings before talking once a month in a group.

“In the middle of COVID, I realized a lot of people were struggling,” Shonka said. “I had written a workbook that walked through the seven stages of grief. I decided to make that the foundation for support groups.”

People with all kinds of conditions are welcomed to the groups, she said, which share perspectives and resources on what has worked for various members. 

“We talk a lot about pushing yourself and balancing your disease,” Shonka said. “Everyone has an excuse to not participate.”

Whether working with the nonprofit community or tech startup sides of the endeavor, Shonka continues lean on her own experience, she said.

“I used to run half marathons in Disney with my mom when I was 17 years old,” Shonka said. “Doing a half marathon at all is a big feat. I use the marathon as a metaphor. There were metaphors where I had a personal record, and there were metaphors where I was completely flared and I limped the last four miles, but I finished.”

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