Yesterday would have been Megan and I’s thirteenth wedding anniversary. It has been the fourth since she died. We didn’t quite make it to a decade together as husband and wife, but we at least got to have the experience of buying our own home and becoming parents. We got to have a formal wedding, with a service in a church and a catered…
Long Term Illness
Edited Memories
As Sarah, Shelby and I near the time to depart for our summer vacation, I am reminded of just how different things were, and I am finding some appreciation of the very fact that as a widower, those differences weren’t always convenient. We’re traveling to my favorite place on earth, the Great Smoky Mountains, at the end of July. Megan and I…
The New Crew
Tomorrow, Wednesday, is officially the beginning of “Drewfest” 2018. It’s an annual summer get-together of Drew’s friends, usually taking place somewhere in Texas, with the specific goal of having a fun weekend together as if he was still around, yet remembering he’s not. It’s a great endeavor, and one that in and of itself should…
How-to: Mother’s Day
As Mother’s Day approaches, I always tend to think of Megan a bit more. Many everyday things become somehow intertwined with a memory or anecdote about her, simply because she was Shelby’s mother. Even mowing the lawn brings thoughts about the fact that she had to close all of the windows in the house due to the smell of fresh cut grass…
The Fact of the Matter
The fact of the matter is, I’m a 37 year old widower. By most standards, it’s quite unique. I wasn’t married to someone in a high-risk career. Megan wasn’t in her seventies, hell, she barely made it into her thirties. Statistically, I’m much more likely to be divorced than widowed at my age. The fact of the matter is,…
Half Life
Half a lifetime ago, it was esprit de corps. It was smoking breakfast, sleeping through lunch, and drinking dinner. It was hard working weekdays, and lazy weekends. It was little pay and long hours, and not caring about either. Half a lifetime ago, days went by as years. The soundtrack was Blink-182 and Korn. The beer was warm and cheap,…
A Mindful Conversation
It’s been far too long since I felt the sting of an icy wind hitting my face. Months have passed since I lazily stared into a campfire of my own creation, with nobody but my own self to discuss it with. I haven’t dunked into a mountain creek after a long march, and I haven’t been woken up by annoying crows, rather than an annoying alarm…
Maturity Rising
`Yesterday, the 26th, was Sarah’s mother’s birthday. Part of a tradition that she has done over the years is to have a small cake, and a bouquet of flowers, as a way of celebrating her, though she’s no longer here. It’s a simple gesture that means so much. She lost her mother when she was only nine years old. While her siblings were…
Holding a Hand
On a day-to-day basis, I’m fairly composed and not overly sensitive to things that remind me of Megan, her illness, or the fact that she’s gone. Shelby acheives honor roll like clockwork, and though it reminds me of how proud Megan would be, and I wish she was there, it’s an “it is what it is situation”, where I can be happy for both of…
Pre-survivor’s Guilt
It’s Monday night. After a long holiday weekend, and a single day of work, I’m off for a week. Sarah and I are traveling to Texas tomorrow, to meet with her friends and family and celebrate the memory of Drew, as they’ve done yearly since his death. The loose ends are tied up at work. Our bags are packed and we’re into the impatient…
Needing the Deads’ Voice
Just two weeks ago, I wrote of a friend that was, at the time, fighting for her life in the ICU, hoping for a lung transplant. She was on death’s door, and no one could guess if she would make it another week, waiting for a donor. I am happy to say, that, as of yesterday, she received her transplant. A call came in late in the night on…
Appreciating a Disease’s Lessons
The other day I received a text message from a friend of mine, who happens to have Cystic Fibrosis herself. This friend was there for Megan and I when Megan was going through her 6 month decline, and I can’t describe enough how she (and her husband) went above and beyond for us. They would visit at the drop of a hat, when I just needed an…