Three months after my discharge from the Marine Corps, at 22 years old, I met my wife Megan, on December 10th, 2002. The very next day, I was drawn like a moth to a flame into dealing with a long term, terminal illness. Megan had Cystic Fibrosis, and after 8 years or declining health, she received a double lung transplant, and a new lease o life. Our daughter Shelby was born in 2007. In early 2014, those recycled lungs, which had brought our little family three years of uncomplicated health and happiness, finally began to give out. She died from chronic organ transplant rejection on November 19th, 2014 while I held her hand and let her go. I'm a single father and widower at 34 years old, and no one has published a manual for it. I don't fit the mold, because there is no mold. I "deal with it" through morbid humor, inappropriateness, anger, and the general vulgarity of the 22 year old me, as if I never grew up, but temper it with focus on raising a tenacious, smart, and strong woman in Shelby. I try to live as if Megan is still here with us, giving me that sarcastic stare because yet again, I don't know what the hell I'm doing.
On February 5th, 2015, I wandered into a Hotel in Tampa, Florida, not quite sure if I was supposed to be there. I had lost Megan less than three months prior, and I hadn’t honestly accepted the fact that I was now a Widower. In the year leading up to it, I had spent more time sitting next to my dying wife than anything else.
Like many of us, I was searching for answers to hypothetical questions. “Who am I now?” and “What am I supposed to do?” served only as constant reminders that, well, “I don’t know” was the only answer.
Almost three years later, and the questions, and the answers, are still the same. What has changed, and what I’ve learned in that time is that we will never know the answer, but we are always inching closer to it.