There were so many reasons for Megan to be proud of Shelby. From her sheer intelligence, to her love for reading, to even her quirky weirdness. She appreciated that Shelby had a love for nature, at least tiny animals and flowers. We would take Shelby camping at least once a year, but due to Megan’s condition, that was the limit.
We took one “backpacking” trip as a family. Shelby was about 5 years old, and carried nothing but a few stuffed animals and granola bars in her pack. Megan had received her transplant, and thus was just healthy enough to schlep some weight and contribute to a one mile hike into the wilderness of West Virginia to camp.
I was proud of Shelby at that point for her enthusiasm. We hiked in a thunderstorm, to a small patch of territory in the middle of nowhere, and she loved it. There was no apprehension about not having four walls, light at the flick of a switch, or running water. She, like me, actually wanted that lack of modern conveniences.
Since Megan’s death, Sarah, Shelby and I have taken a few more “easy” trips. Each has had the same effect of me being proud of Shelby, although I’ve had to be proud for both Megan and I. She’s still been carrying a very small load, considering there were two adults to shoulder most of the baggage for her.
A big first happened this past weekend though. Shelby and I took our first trip together, just the two of us, and she started carrying some of her own baggage.Read more
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 making her cough.
Megan is never far from Shelby or I’s memory. If I had a nickel for every time Shelby began a sentence with “Remember when mom...” I’d be a millionaire. She hasn’t seemed to look any deeper into Megan’s death than humorous stories or zombie jokes though. I mean, she’s only 11. Her mom has been gone for almost 4 years now, and her biggest concerns are getting to ride her bike and the newest novel in the book series she’s reading being released to stores.
It makes me wonder when the other shoe is going to drop.Read more
`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 much older, and had much more time with her, Sarah had to “make do” with memories she only had as a little girl, and recollections of her older siblings.
Shelby, too, lost her mother at a young age. She was only seven when Megan died. She remembers quite a bit, but again, she was nowhere near adulthood when any memories she could form ceased. She relies heavily on myself, grandparents, and her uncle for the stories that she may have been a part of, but still too young to realize they were something to remember.
As we sat down to partake in the yearly birthday cake, I (somewhat in jest) asked Shelby if she remembered Megan’s birthday. She did not, other than she knew it was in summer (her guess was a month off). I wasn’t disappointed, for she’s still just a little girl. It is not like she has a date planner or had any part in actually NEEDING to remember the exact date of her mother’s birth.
After some good natured ribbing, and finishing our cake, Shelby asked a question to Sarah.
“Did you ever forget your mom’s birthday?”Read more
Four years have come and gone since the last time Megan was present for Shelby’s birthday. By February 17, 2014, Megan had already been diagnosed with rejection, although she hadn’t been admitted to the hospital as of yet. Shelby was turning seven, and four days prior, Megan and I received the results from her bronchoscopy.
We rented out one of those “inflatable gym” spaces for Shelby, and invited all of her friends to join. It was a madhouse, to say the least...screaming, jumping, running around, laughing, and smiles from ear to ear. I distinctly remember the both of us having nervous thoughts in the back of our minds about Megan’s health, but suppressing all of them in order to give Shelby the birthday she wanted. She would have no clue, no inkling of something amiss on this day.
Going through some old texts and emails last week, I came across a conversation that Megan and I had just a day or two before the party…
Megan: Should we talk to Shelby about it?
Mike: Yeah, but let’s do it together. I don’t know how to start the convo with her, but we need to anyway.
Megan: Yeah. I don’t like this.
Mike: Me either.Read more
In my 37 years, I’ve seen my share of loss. I’ve lost all of my grandparents, aunts, uncles, cousins, friends, fellow Marines, a brother-in-law, cats, dogs and other pets, co-workers, and obviously, my wife. There has been illness, accidents, age, war, heart-attacks, and a sprinkle of stupidity involved. It happens. Death happens. I know of no one my age that hasn’t experienced some sort of loss to death at some point in their lives. The first loss can symbolize a loss of innocence. A loss of the childlike optimism that nothing bad ever befalls us. It’s reality surfacing for the first time in our lives.
For some, that could happen at a very early age. Others may be adults before it happens. Regardless, death is something that we humans are aware of. We are conscious of our mortality very early on, and the first loss of someone or something close to us brings with it clarity.
However, there is a secondary loss currently beginning to clarify in my life. Something I was aware that I would lose one day, but that I will never be prepared for. You would think, after so many years with Megan’s Cystic Fibrosis, that I would be better suited to be mentally cope with something long-term and inevitable…
...Shelby growing up.Read more
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
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.