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.
Today, Megan would have been 37 years old. This is the fourth birthday since her death, and I can confidently say that they have gotten a bit easier. I’m not a ball of snot and tears, or missing her any more than I already do.
She’s s imply “in focus” today. There is no other way to describe it but “in focus”. On any given day, something occurs that makes me think of her. Shelby says something that sounds like her. It may be a five minute, fleeting memory, but regardless, she is in my thoughts. Four years of processing those moments have blunted the sharp edge of grief. Her birthday is no different, other than the fact that those moments occur throughout the day in a reliable, predictable sense.
The elevated awareness that she’s dead does, in fact, make today a bit more stressful overall. Her birthday doesn’t make any one individual thought of her “worse” per se, but the accumulation of them tends to just wear me out by nightfall. That in mind, I’ve decided I don’t care about being worn out. We’re physically in my favorite place on earth right now, and I’m welcoming the overwhelming flood of stimuli that will have me in bed by 9:00 PM.Read more
Something that Megan and I did every year or two was get family photos taken. While we had thousands of “candid” pictures, taken from our phones or old point-and-shoot devices, we were never posed, and neither of us were exactly professional photographers. We would make the appointment, pack up a few various pieces of clothing, and head to JCPenney for an hour or so of awkward positions and goofy smiles, followed by standing in a department store looking through each and every shot, choosing the six best, and deciding on a package. The photos are done well, and I like them, but the experience of producing them was not exactly the most enjoyable memory. If we could have had them without all of the other hassle (and money), they would have been perfect.
We still have some of those photos hanging on our walls. Shelby truly lives up to her “Peanut” nickname in most of them...being about 2 feet tall and 25 pounds at the largest. (for the record, I too have added about 30 pounds since then, so the “growing together” has a literal meaning). The memory of her simply being that size is the most enjoyable to me.
Megan has a beautiful smile in all of them. She was, simply put, photogenic, and she knew how to apply a good “picture smile”. For Shelby and I’s part, we did our best to smirk.Read more