The time has finally come to clean up the basement of my house. When I say that, I don’t mean that I need to go through and organize some of Megan’s things. I mean that the entire basement, full of god-knows-what from Megan, myself, and Shelby needs to be perused, bit by bit.
When we moved to this house (for the second time, long story) 4 years ago, we had already accumulated the detritus of 10 years of living together. Boxes upon boxes of paperwork, medical records, cables, doohickeys, whatzits, and general “stuff” tend to pile up and get shoved into a dark corner of a house to be dealt with another day.
Today (the past month or so, actually) is another day.Read more
In the spring, before Megan died, she and I decided to have a deck built on the back of our home. Nothing too fancy. It was to be a 12 foot by 12 foot square, with a new sliding glass door leading to it. We had wanted to have one on our house for years, and we were finally going to get it done.
We shopped out for a few different construction companies to give us a quote, and by about this time in 2014, we have chosen one and signed a contract.
Megan would decline in health and be admitted to the hospital a few weeks later. She came home one time that summer, after the deck was started, and sat on a half-completed platform, with no railings. She was bundled in a blanket in the 85 degree heat, being so emaciated that she could barely generate body heat.
That was the first, last, and only time she ever sat on that deck.
It was just a little walk. As we pulled up to the trailhead on Canaan Valley National Wildlife Refuge, there were very light snow flurries. We were at 4100 feet above sea level, and had plans to hike along the western ridgeline at Dolly Sods, the highest plateau east of the Mississippi.
Sarah, Shelby, and I took a trip this past weekend to the area. Shelby had been here once before, I had been here at least 15 times, and Sarah had never been. I wanted to show them both a few of the varied landscapes and terrains that are unique to this place, and I figured a day hike of a few hours would suffice.
10.5 miles later, I quite possibly had learned more than they did.Read more
So I bought a table.
It was only forty dollars, and it’s a little round glass patio table. Shelby and I spent an hour or so unpackaging it, laying the parts out, and assembling it. I know this sounds completely mundane, even boring, but bear with me. This table symbolizes something.
It’s not sentimental, really. It wasn’t something that Megan always wanted, or an item that had been passed down to her from a grandparent or family member. It truthfully is “just a table”, sitting on the deck at my house.
However, it’s a table that Megan will never sit at. It’s on a deck that she never got to relax on. She didn’t get to help Shelby put it together, and watch her do most of the work. Megan had absolutely zero bearing on the decision to buy this particular table. It’s not hers, and it never will be, and that’s why it is important.
My wife suffered from a long-term illness, Cystic Fibrosis. When I say “long-term”, what I actually mean is “life-long”. There wasn’t a day that I knew her where she didn’t have some sort of symptom or complication directly due to her condition. Even after her transplant, every day was filled with special medications, dietary and activity concerns, and the constant knowledge that the bottom could drop out at any time.
As blunt and morbid as it may seem, her death brought closure. It brought a bit of simplicity to everyday life. Make no mistake, I would much rather have her here, complexities or not, but that is a separate issue in my mind.
It’s been over a year since I attended my first Camp Widow. In less than two weeks, Sarah and I will be travelling to Tampa again to attend this year’s installment.
I’d be remiss to say that we weren’t incredibly excited. Not only do we get to see, converse, and connect with widowed friends that we don’t regularly see otherwise, we also get to leave the not-so-cold winter environment in Ohio and travel to Florida, together, for a few days in the warmth. It’s been a frequent topic of our conversations for the last month or two, and it is not just because of the fact that it is a mini vacation for us.
This past weekend, I remembered why.
There was once a time when I assumed that Shelby would grow up more quickly than her peers. Since she was born, she’s dealt with her mother being sick, going through major surgeries, and ultimately, dying. That a sobering thought when you’re the parent of a little girl, who really just wants to go to school, play with her toys, and do fun things. She would have to grow up fast.
She barely had the chance to be a “normal” girl. Megan was only in a truly healthy state for about two years; the rest of the time was spent between hospitalizations and recovery from her transplant. I cannot begin to describe how terrifying it must have been for Megan, knowing that she was going to be leaving Shelby to grow up without the only normal she had known.
I was ill-equipped to raise her alone...Megan knew it, and I knew it. I haven’t the slightest idea which Disney princess is currently popular, or what the newest trend is in 8 year old fashion. While I’m the one that can help her with her school work and take her hiking, I don’t have her friends parents’ names, let alone contact information. I barely know her shoe size, and I’m still constantly trying to figure out what foods she likes today versus yesterday.
You don’t realize how important the little things are until you don’t have them. It could be something as simple as sitting on the couch, watching TV until you fall asleep with your partner, and it is taken for granted. Then you lose that person.
I’ll admit that I was eased into some of the more technical aspects of the widower role, being that Megan had spent so much time in the hospital over the years. There were plenty of times where I was a temporarily single father. Making sure Shelby got to school and was fed and clothed was never something I struggled intensely with after Megan died.
Even so, there were plenty of things I still took for granted when Megan was here, and some of those things are surfacing over the past few weeks.
Megan’s priority in life was Shelby. The fact that it is so unlikely that a Cystic Fibrosis sufferer can even have a child naturally made Shelby that much more valuable to both of us. Her “peanut”, as we call her, completed Megan.
During her hospitalization, Megan and I had to have “the talk”. We knew the odds of her coming home, and we were smart enough to talk over her wishes should she not be around. Sure enough, her most important wish was for Shelby to be happy, healthy, and smart. We had also talked of me moving forward, and that she wouldn’t want me to be alone. Putting two and two together, I read this as her wishing me to be with someone that was good for Shelby.
Little did I know (and surely wasn’t looking for) that a few months after her passing, a few women would sit down beside me at Camp Widow. One of those women would move her life 1400 miles to be with me. It’s been a year since Sarah sat down at that table in the hotel bar and grille. There hasn’t been a single day we have not talked in some form since then.
What should I write about today? Nature? No, I am beginning to sound like a broken record, and I haven’t hiked in the past week. How about Sarah? Well, I’ve got a good subject for NEXT week, but that doesn’t help me right now..
OK, how about Megan’s disease? I mean, I went through a lot with that, but really, it just sucks. It would be hard to write an entire post about it right now, because I don’t have too much to say that hasn’t already been said. Any recent grief triggers come up that I can reflect on? Well damn...no. Problems that are related to being a widower? Not particularly, and Sarah’s post actually covered that on Sunday for both of us, so I don’t want to rehash it. Yes, the past week or two has been stressful, but things are resolved, and we've talked them out, so it's not at the forefront of my mind.
My mind is blank right now.