I moved to Columbus right after retiring from 39 years of government service, eager for a new chapter. My greatest joy was walking my grandson to elementary school—a simple, fulfilling routine. The first year went as planned. Three times a week, I walked a mile, breathing in the crisp morning air, feeling strong. Then, something changed. A sluggishness crept in. I brushed it off as aging. But that fatigue didn't go away as time passed—it settled in, deep and unshakable.
I never connected how I felt to what my kidney specialist had warned me about before I moved: my kidneys were deteriorating. Back then, I felt fine. The warning felt distant, almost theoretical. Even when subtle signs appeared—water retention in my legs, hips, and abdomen—I dismissed them. Then, the morning after an anniversary dinner with my wife, I woke up in a hospital bed. It was the beginning of an 18-month ordeal that would redefine my life. My kidneys had reached their breaking point. I underwent emergency dialysis.
Emergency dialysis is a harrowing experience. There was no established access to the machine that now had to replace my kidneys. The only option was to insert a catheter directly through my neck, into my subclavian artery—or possibly even my aortic arch. The sensation of a tube so close to my heart was surreal. To say I was scared would be an understatement. But fear doesn't change reality. The only way to solve a problem is to go straight through it. So, I gritted my teeth and moved forward.
Looking back, I understand why my kidney specialist moved so fast to get me on dialysis. After just a few sessions, they inserted an intermediate access point—a catheter into my aorta. It was a temporary fix until they could create a fistula in my left bicep, a direct connection between a vein and an artery. That fistula would be my lifeline, but it needed time to mature. Until then, the catheter was my only access point for dialysis—three days a week, four hours per session. The reality of my new life settled in quickly.
At no point did I feel sorry for myself. Self-pity was never an option. My mission is clear: to mentor my grandchildren until they reach adulthood. That is the sole meaning of my existence, my life's work. The reasons behind it could fill another story, but I know this much—it's a calling from God. And when you're given a mission like that, you don't waver. You endure.
With a military and civil service background, I see dialysis as another mission—one with strict orders. Those who assist me, my doctors and nurses, aren't just medical professionals. They're my partners. They're not punishing me; they're keeping me alive. Their instructions—what I should eat and avoid—aren't suggestions. They're direct orders from higher headquarters. I follow them because the mission demands it.
But let's be honest—sometimes, the rules suck. Hard. But that's the job. Get over it and move forward.
I don't understand how some people treat these instructions as optional as if their choices won't have consequences. I've lost friends that way—people who sat right next to me in treatment, ignoring the rules, doing what they pleased between sessions, thinking they could cheat the system. But the body doesn't negotiate. The system always wins.
Would I love a beer? Absolutely. But that's verboten—off-limits. The potassium content alone could push my levels to fatal territory. It's not about willpower. It's about survival. And survival means following the damn rules, no matter how much they suck.
That's not to say I'm perfect—because I'm not. Dialysis doesn't allow for illusions. With weekly bloodwork, there are no hiding places. Every decision, every misstep, is exposed immediately.
I learned the hard way when my grandson had a birthday dinner at a Chinese buffet. I knew better, but it was easy to justify it at the moment—just this once. But the numbers don't lie. The next time my labs returned, my misstep was in black and white—undeniable.
But here's the difference—I own my mistakes. No excuses. And more importantly, I don't make the same mistake twice. Because in this battle, repetition isn't just failure—it's self-sabotage.
I'm on two transplant lists—one at Ohio State and another at the Pittsburgh VA Transplant Center. I've been waiting for two years, with credit for my first year on dialysis. My family has been fully supportive. My daughter and I have planned for every scenario. If I become incapacitated, my wishes are clear.
But dialysis takes its toll. The fatigue is relentless. Depending on how much fluid is removed, it can last four or 36 hours after treatment. The impact isn't random—it's measured in kilos. If they remove less than two kilos, I'll bounce back fast. More than that? The exhaustion is like a truck hitting me head-on. It's directly proportional—the more they take, the worse I feel.
Still, my biggest regret isn't the fatigue. It's missing church services. The guilt weighs on me. I should be there. I want to be there. And when I make it, I'm running on sheer willpower, pushing through the exhaustion, trying to keep a brave face for my congregation. But the truth is, I'm at war with my body whenever I walk through those doors. Faith is my foundation, but I still struggle with the feeling that I should be doing more—even when I know I'm already giving everything I have.
Dialysis isn't just a treatment. It's a way of life—a complex, grinding, relentless way of life. But I made a promise. And as long as I have breath, I will complete my mission.