My husband is dead. It’s been almost 6 months. And he’s still dead. I walked into our, well, my, technically, bedroom tonight and I could smell him. And I sobbed. He didn’t even really have a particular smell. He didn’t wear cologne even though I kept buying it for him. He used whatever soap I purchased, so I guess we smelled pretty similar. His shampoo wasn’t super aromatic. But I swear I could smell him. So maybe he did have a scent.
I miss him. And yet, it’s almost as if he were never here. I often wonder how in the world did it all happen. Why did we meet? How did we fall in love? How did we come to marry and have children? And how on Earth is he gone? At 37 years old. I’m 13 days older than Ash and he always joked I would die first, naturally, because I’m so much older. But that didn’t happen.
He started getting sick in 2014. I also happened to get pregnant at the very end of 2013 so, at first, I felt like he was stealing my thunder a little bit, what with all the throwing up and not getting out of bed. That’s what I was supposed to be doing. He had countless doctor appointments and multiple hospital stays before he finally ended up with a diagnosis. Primary Sclerosing Cholangitis. It’s an auto-immune disease that affects the liver and bile ducts. I’m sure you could have guessed that if you have been reading my writings for a while. There is no cure. He may need a liver transplant 10-15 years down the road. Ash’s doctor was world famous. One of the best in his field. We were scared back then but he assured us, most people that have PCS die with it and not from it. Most people.
Ash and I changed our lives. Our marriage had been more than a little shaky for a while. At times, I did not deserve him. At times, he did not deserve me. But once he was diagnosed, back in 2014, our perspectives changed quite a bit. We learned to accept each other. We worked at it every day. And it worked. We changed. Ash had to quit drinking, you know, because of the whole liver disease thing. He started a clinical trial, we had to travel a couple hours north once a month to his doctor to check in and they were some of the most fun days in our relationship. We learned to communicate with each other again. We fell in love all over again. I guess, in a way. Life changed, for the better, if you can believe it.
In April, 2018, we were back at Ash’s liver doctor, just for a routine check up. And the words that came out of that doctor’s mouth was some of the best news we’d ever gotten in our lives. He said “I don’t know what you’re doing, but keep it up. Your numbers are incredible. We don’t see this with this particular disease much.” In September, 2018, he was diagnosed with Stage IV Terminal Cholangiocarcinoma. Bile Duct Cancer. Terminal. That’s how fast it happened. He went from what we liked to joke as a “medical marvel like Ross Gellar” to a dying man. How does that happen? Why does that happen?
I just miss him. I miss kicking his ass at Mario Cart. I miss all our date nights. I miss holding his hand. I miss just driving around doing nothing with him. I miss the way he could make me laugh. I miss his amazing smile. I miss his positive attitude. I miss how he always knew when I was about to start my monthly business based on my attitude. I miss hearing his voice. Jack has Ash’s old cell phone and the voicemail on it is still Ash’s voice. I call it, at least a few times a week, just to hear that “Hey, it’s Ash’s voicemail. Leave a message.” Simple. To the point. Just like Ash wasn’t. Ha! (It’s funny because it’s true.) Either way, I miss him. Hell, I miss the shit that I hated and thought I’d never miss. But I do. Grief is annoying like that. It reminds you that even the bad shit wasn’t really that bad. In my case anyway.
The kids are so incredible. They are so resilient. So in the moment most of the time. Sure, they have their breakdowns. But they are less frequent. I’m so envious of their strength. They are growing and learning and they are just amazing.
I don’t know the point to any of this, other than I went in my room, could smell my husband, sobbed and felt the need to write. So I did. And it’s helped in the way that only it can. My own personal therapy. Remembering him is a gift, one that I hope to only love one day.



