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 “waiting game” that comes before any longer trip getting started. I wish we could just leave right now. Visions of the beach, and lounging beside the pool seem like they’ll take forever to become reality.
Aaaaaand my chest is tight. I’m uncomfortably nervous and anxious. Something just feels...well…”off”.
What would have been Megan’s 35th birthday was a few weeks ago, on July 24th. I would venture to say that, for most widows and widowers, birthdays are one of the hardest days to remember. They are associated with memories of fun times, friends and family celebrating that person’s day, and yet another year “in the books”. To have that annual event suddenly take on a different meaning and a different remembrance affects all of those who knew and loved that person.
Megan’s came and went this year with what has been typical since her death. I’m grumpy most of the day, but we do something to remember her, keep occupied, and have an enjoyable day in her honor. Cliche as it is, yes, it IS” what she would have wanted”. Multiple people ensure they post to facebook about how they miss her, and say “Happy Birthday” on her wall. Heartfelt paragraphs about things they remember doing with her, or “breathe easy” are digitally pushed to her in the afterlife via keyboard, somehow. There may have been a few less posts this year than last on that day, but still, her friends remember her birthday.
A few days later though, and facebook is silent. Memories tend to fade when you don’t have automated reminders popping up, don’t they? As far as the internet is concerned, life moves on until the next year, when suddenly it seems like everyone is thinking about her again.
I don’t have that option. I think about Megan...every...single...day. It’s a matter of HOW MUCH I think about her that changes, and August 6th was a doozy.Read more
Sarah, Shelby and I are in Texas this week for the 4th annual get-together of her and Drew’s closest friends. This is the second time I’ve attended, and Shelby’s first. I’ve met these people before. They are all already friends of mine, albeit not as close as Sarah is to them, but friends nonetheless.
There seem to be a lot of similarities between Drew and I. We were entirely different people, but I hear every day from Sarah of things that I do or mannerisms I hold that are “just like him”. His friends have welcomed me with open arms just the same; knowing that I’m a different person, but able to sit down, have a beer, and shoot the breeze through the night with me as if I’ve always been part of the group.
There is one thing though, an event, that both Drew and I experienced in much the same way. Meeting Sarah’s parents.Read more
My mother, daughter, and girlfriend have all lost their own mothers at a young age, all to different illnesses. Each of their moms had to stare their own mortality square in the eye, and hope for the best for their daughters. They did everything they could to love and protect their little ones in the time they had, but ultimately, they had no choice but to leave them to grow up without their biological mother.
Tuberculosis, Cancer, and Cystic Fibrosis. Those are the diseases that took my mom, Sarah, and Shelby’s mothers, each before their daughters were even ten years old. Though each is of a different generation and time in their life, they have all needed to learn how to become a mother after losing their own biological mother. They each picked up surrogate mothers along the way. Friends of the family, adoptive parents, neighbors, teachers, and other relatives were all able to form part of the village it takes.
But none had their biological mothers. I can’t begin to fathom that.Read more
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.