Kevin is originally a Nebraska native and now lives in Missouri. He was diagnosed with idiopathic pulmonary fibrosis in 2014. Kevin had a bilateral lung transplant in August 2020. Through his column, “Riding the Idiopathic Pulmonary Fibrosis Rollercoaster,” he strives to provide in-depth awareness for those traveling on their PF journey. Kevin’s passion is to make the words “pulmonary fibrosis” a widely known term so more people can get diagnosed and receive treatment sooner. He also provides awareness through his local Pulmonary Fibrosis Foundation website and Facebook page.My pulmonologists are talented jugglers. They must determine my medication dosages, keep my lab results within the standard ranges, and minimize medication side effects. After my bilateral lung transplant in August 2020, it took a year to find the…
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In my previous column, I described the roller-coaster ride of my lung transplant evaluation. On Aug. 7, 2020, six years after my diagnosis of idiopathic pulmonary fibrosis (IPF), I was officially placed on the transplant list. Waiting…
In May 2017, I began the roller coaster ride that was my lung transplant evaluation. I call it this because it had the usual climbs of positive developments, and the fast and dramatic drops. But it also had…
When I learned that the prognosis for idiopathic pulmonary fibrosis (IPF) patients is about five years after diagnosis, I started wondering how my disease would progress. I didn’t think my progression would follow the usual, defined stages. I believed…
The dynamic between an ill person and the loved ones who care for them should extend beyond the caregiver providing and the sick person receiving. The relationship should go two ways — thus, a care partnership. I define a…
When I was diagnosed with idiopathic pulmonary fibrosis with dendriform ossification in 2014, it was the second time I had a medical condition with an unknown cause. Three years earlier, I developed blood clots and had two pulmonary…
When I volunteered to coordinate the Pulmonary Fibrosis News initiative “30 Days of PF” alongside fellow columnist Charlene Marshall, I didn’t expect a tremendously emotional experience. I asked my wife, Dana, to write her pulmonary fibrosis (PF) story for…
I received my new lungs a year ago, on Aug. 14, 2020. Now it’s time for me to reflect on my quality of life. Initially, I evaluated my progress by how long I stayed in the hospital. Unfortunately, I…
On Aug. 14, 2020, around 10 p.m., my successful lung transplant was completed. Now I was in the daunting recovery phase. Before being discharged from the hospital, I had to meet three requirements: Walk 1,000 feet without supplemental oxygen.
In February of 2016, I joined the Greater Kansas City Pulmonary Fibrosis Support Group. As I attended more meetings, I realized PF awareness was important, and I wanted to make a difference. Because I had a unique case…
A couple weeks ago, my good friend Bert Maidment and I completed the American Lung Association’s Fight for Air Climb, an annual fundraising event. I had never before competed in an event like this. I’m not a runner…
After my idiopathic pulmonary fibrosis (IPF) diagnosis, I was in denial about having the disease. So, I had a video-assisted thoracoscopic lung biopsy in July 2014.
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