I’m on the other side of the three year mark at this point. I can watch a movie where an actor is hospitalized, and not have to turn it off. I can hear a song that reminds me of Megan, and get a little choked up, then laugh it off. I can even pull all of our holiday decorations out from storage, observe the ornaments with Megan and I’s names on them, or pictures, or items we purchased together, curl my lip a bit, and remember the happy times we had at Christmas.
I can remember dates. Anniversaries, birthdays, transplant dates, and so on, and know that they’re coming. I can even find a private writing of Megan’s, written long before her passing, cry my eyes out reading it, and go about my day afterwards. A persistent cough that Shelby or Sarah may be experiencing only pales in comparison to the decades of it that Megan experienced, but it still makes me remember just the same.
These are called “triggers”. I know it. We all know it. It’s the songs, sights, events, smells, sounds and memories that don’t really “haunt” us, so much as they are just part of our day to day lives. Time does not make these go away, but rather, softens their outward impact. When that godforsaken “Let Her Go” song, by Passenger, gets randomly played, it has become somewhat humorous (that particular piece of music has followed me around since the day she died), albeit still thought provoking, to say the least.
On February 5th, 2015, I wandered into a Hotel in Tampa, Florida, not quite sure if I was supposed to be there. I had lost Megan less than three months prior, and I hadn’t honestly accepted the fact that I was now a Widower. In the year leading up to it, I had spent more time sitting next to my dying wife than anything else.
Like many of us, I was searching for answers to hypothetical questions. “Who am I now?” and “What am I supposed to do?” served only as constant reminders that, well, “I don’t know” was the only answer.
Almost three years later, and the questions, and the answers, are still the same. What has changed, and what I’ve learned in that time is that we will never know the answer, but we are always inching closer to it.
I’m going to (try to) keep this short, simple, and to-the-point. Megan’s birthday was yesterday...the third since her death. She would have been 36, which, for someone born in the early 80’s with Cystic Fibrosis, is twice the normal life expectancy.
The first thing I thought of when I opened my eyes in the morning yesterday was Megan’s birthday. It was the last thing that went through my head as I closed them in the evening. Her birthday cycled through my head off-and-on all day, just as it had been doing for the past few weeks.
It is what it is. It’s white noise.
18 Months. 564 days. A year and a half has now passed by without him. It doesn’t feel like that long ago, but then again it does. Some days it feels like yesterday that we were sharing kisses. Other days our life feels like a sweet distant and faint memory. Some days it’s not real at all, as though we just lost contact somewhere along the way. I imagine and dance with the idea he is away somewhere living out a happy and full life. Somedays I like to pretend ill see him again in this life. None of my day dreams change how much I miss him.
There is no longer much left in my house of the life we shared. His clothes, I have packed away. His toiletries, packed away. His tools, packed away. Out of sight but never out of mind. People rarely speak of him now, speak of us. I miss hearing his name being spoken. I miss hearing stories told about him, even if they make me cry. Tears are worth the sound of his name. How I wish for more than just memories.
His ashes rest in a pendant around my neck. The pendant is a reality check, I cannot pretend he is away when part of him is with me. Which part I wonder at times. These thoughts are sickening, sorrow filled, painful and yet to be peaceful. I want all of him with me. In life not dust. I long for him in the flesh. I long for the warmth of him, but instead of his warmth I wear a cold chain around my neck. Although it brings me pain to wear it, I do not feel as alone when he is with me.
I find myself smiling with life and without thinking about it the pendant becomes pressed to my lips. When I feel afraid, stressed, worried alone, the pendant is clasped in my fist. And I can speak to him, cry to him as he were here. It’s both comforting and depressing.Read more
(So, I wrote this last year on Mother’s Day. I tried and tried to write this week, and the more i did so, the more it read just like the below. So instead, I’ve decided to re-post it, with an update on what has changed, a year later. A year further from losing Megan, and another year growing with Sarah.
I’ve underlined in parenthesis my updated perspectives and thoughts. It’s an interesting examination of what a year can bring...or not bring)
I'm enjoying my last few months in Kona working at the restaurant. It is situated just a few feet from the water; the view is stupendous. The people are friendly and fun - this includes the staff and the customers. So it's really not a bad place to be in any regard. I often find myself gazing out over the ocean and the other quaint buildings in this little town - well, you can't help it, it literally fills your view wherever you are down there.
Father’s day around our house was never a big production. I was usually the first to wake up in the house on any given day, creep downstairs, make myself some coffee, and watch or read the news until everyone else started stirring. I preferred it to be that way. I didn’t relish any extra attention placed upon me.
I appreciated every card or “Happy Father’s Day” I got, and every coffee mug or shirt that Shelby and Megan gave me on that day, but Father’s Day was just another Sunday to me, and I was just happy to have my family with me.
Last year though, it was different. I didn’t have my entire family. I woke up from an empty bed and walked downstairs, trying to have a “traditional” father’s day, but it wasn’t happening. I didn’t even write about it on here last year.Read more
Finding ways to fill my time after Dave died was a huge challenge. I needed to stay busy and connected to others, but I wasn't any good for social situations, especially early on.