Grief: Home Again

When Cathy was in hospice, we didn’t talk a lot about the Big Inevitable Thing that was about to happen. It was too upsetting for her. We had, however, done some preliminary planning many years ago, and this was codified during her treatment. I knew, then, what she wanted; we both decided on cremation for ourselves for a number of practical reasons. However, neither one of us wanted to hold on indefinitely to the other’s remains and so we decided to do something with them.

I won’t tell you what I want done with mine; you’ll just have to come to the funeral. Cathy’s solution was not nearly so interesting; she was fine with having her ashes scattered. Several locations were mentioned, but we always came back to Austin, where her heart’s home was.

This came up again during hospice. I asked her if she’d thought about it, and she said, “Maybe Town Lake?” She used to row there in college and kept it up for a while afterward as an exercise regimen. She loved it and always wished she could get back to it.

It was a solid choice. But I had another idea. “What about at Cliff Drive?” I countered.

Her eyes lit up. “Yes,” she said. “Do that.”

When I met Cathy, she and her sister Barbara were living in a small, heavily shaded neighborhood just off of Lakeshore Drive in Austin. Their place was an old garage apartment, part of a quad, originally built in the 1940s as a stone wall garage with the apartment over it. Sometime in the 1970s the garage got walled in and finished so that it was now an apartment with a nearly identical floorplan to the original one above it. What was cool about it was the wrought iron spiral staircase that connected the two living spaces. It was very bohemian and oh so very, well, South Austin. I started calling it The Bungalow of Love (shades of Lou Reed).

The Bungalow of Love was inextricably tied into our lives in Austin. We fell in love while Cathy lived there. Later, after I moved in, we got engaged there. We got married while living there. Dinner parties. Our first Thanksgiving together. It was her favorite place to live. Mine, too. It seemed absolutely right to bring her back home.

In the intervening years, the property owner had completely landscaped the front yard and the central courtyard between the four freestanding apartments. Behind our old digs, there was now a gravel path that flanked the house and led to a beautiful limestone fountain, two seating areas. In the center of the circular path, which winds around to the fountain and over to an open air patio space, there is a Chinese elm. It’s completely in the shade of the two leftmost apartments. The whole area is clearly meant to be a meditation space. The landlord graciously volunteered the elm tree for Cathy’s final resting place.

It was absolutely perfect. She would have loved it.

A mixture of old friends and family stood with me. I didn’t know what to say. I had one thing planned, and I did that first. Cathy had told our niece that she wanted a particular Tom Petty song played at her funeral. Our niece assumed that something so important would be a thing we all knew about, and so she didn’t say anything. Unfortunately, Cathy didn’t tell anyone else.

I thanked everyone for coming, and then played “The Waiting.” 

It made me laugh. Cathy had a very dry sense of humor, and I know this was supposed to be a joke to make us all laugh. I don’t know if anyone else did, but I appreciated the effort. Some folks spoke after that, and said very nice things. I wanted the people who weren’t at the funeral to be able to speak if they were so moved.

When no one else had anything to add, I played another Tom Petty song, from one of Cathy’s favorite Tom Petty albums. The song was “Wildflowers.”

I knelt down in the soft earth and I buried my wife by the tree. I covered her ashes up and packed the soil tightly over them. I spent more time doing that than I needed to, because I knew when I stood up, it would be over. My charge would be done. Nothing more left to do. Cathy was out of my hands now. I had kept her, loved her, cared for her, and grieved for her. And finally, I brought her home.

I know those ashes aren’t Cathy anymore. They aren’t the things that made her. They aren’t her heart, her soul, her dry sense of humor, her huge sense of fairness. It was merely, as Yoda once pointed out to Luke Skywalker on Dagobah, “this crude matter.” But bringing her remains home, to reside in the place she loved so much, and nourish a tree that, I guarantee, if she could have planted herself, she would have...well, I can’t speak for Cathy, not anymore. But I felt a sense of peace within myself when I stood up. I took a deep breath, smelling the fresh earth, the air, pregnant with rain, and the wet limestone fountain with water softly splashing into the stonework basin. I held that breath and let it go. It felt like a sigh of relief.

It’s okay now. It’s going to be all right. I’m going to make it. And Cathy is home. 

I added one more song to the playlist at the last minute. Another Tom Petty song. Perfect for the occasion. He wrote it for the soundtrack to the movie She’s the One. It’s called “Angel Dream (no 2).”

We stood around after that, hugging, talking, comforting one another, and eventually, laughing. Old friends and family. The tree took it all in. I hoped later, that night, during the rain that fell in thick drops, the Chinese elm whispered to Cathy everything that was said while we stood around the tree, and I hope something I said made her laugh and say, “Oh, Honey.”

Grief: Leftover Thoughts on a Year of Mourning

 
Here are a few miscellaneous thoughts, scattered hither and yon, that I decided to combine into a single post. None of these were “enough” for me to post them individually. Maybe all together, it’ll add up to something.

The Bobby pin

I came across a bobby pin today. It was on the floor in my bedroom and I spied is as I was putting my shoes on. On automatic pilot, I scooped it up in my hand, thinking, “Cathy’ll need this for something, I’m sure...” and then I stopped, and I just stared at the bent strip of wire in my hand. Even as I was thinking it, I knew I’d blundered into the classic trap. Now, with the reality of the situation covering me like a thunder shirt in a rainstorm, I stared at the bobby pin, looking for, what? A strand of hair? Some clue to tip me off that Cathy wore it at some point?

There wasn’t any. It was just a bobby pin. Likely one that didn’t even make it into her hair. But on that day, it pinned me down and it took a while to get out from under it.

Grief: The Last First

Widows and widowers speak to one another very differently than people who have not experienced a loss. I say this with no judgement. It’s just that there is a frankness, a matter-of-fact tone, that you can deploy and it won’t be “taken the wrong way,” or “misunderstood.” It’s kind of refreshing, since most everyone else is ninja-creeping around your feelings, throwing you kind eyes, and nervous because they don’t know what to say, and then saying the wrong thing anyway. This isn’t a dig; I used to do the same thing. Everyone does, until the unthinkable happens.

I mention this because I was having a conversation with one of my friends, who has become closer in the midst of this, because we share similar trajectories. Anyway, we were knocking around our collective grief, playing air hockey with it and letting it clatter around between us. I brought up how much I was dreading October, but not the rest of the year. She nodded. “You’ve already done it once before,” she agreed. 

I told her that October 15th would be my last first. The first of this without Cathy, or the first of that without Cathy, happened in rapid succession last year: Our wedding anniversary, my birthday, Halloween, her birthday, Thanksgiving, and Christmas (all big deals in our home) happened between 3 days and 3 months of her passing.  

An old pic, rediscovered

About the only thing that kept me going was my seemingly eternal, acrimonious relationship with cruciferous vegetables. It gave me a purpose to hate broccoli. It’s the only way I got through it all. And for most of this year, I was able to navigate the flow of the seasons, the holidays, real and manufactured, and other perennial events that mark the passage of time. I knew, however, that October would be rough. Her (and my) favorite month, piled high with meaning: my birthday, our anniversary, and Halloween, all within a two-week period. Now there’s one more to add to that list: her death. A signpost, first in a series, like Burma Shave ads, running me all the way to the end of the month, and oh, just TRY and be happy during your favorite month now, sucker, I double dog dare you. 

But a funny thing happened when the first of the month rolled around. I made the calculation that I had given up quite enough to cancer. It had taken so much from me. And I didn’t want to have to surrender any more. It’s been nearly a year. Cathy’s passing would be acknowledged. It would be impossible to do otherwise. But I’ll be damned if I am going to give up the rest of it. All that other stuff was mine long before cancer took her away from me. It doesn’t get anything else from me.

Grief: Rage, and the Dying of my Light

I’ve been putting this off for a while. Months.

After being so open with all of my emotions and thoughts these last few years, I wanted to take a little break from being sad. It just got to be too much. Some of you more astute folks could read between the lines on the weekly updates I’d been sending out over The FaceBooks and asked after me. Maybe I gave you a platitude. Maybe I just said, “I’m hanging in there,” which is my go-to for moving on the conversation to the next topic. I just didn’t know what to tell folks who asked after me. “I’m still furious?” "Life is a tourniquet and my neck is turning blue?" No one wants to know how the monstrous depths of my anger. 

Because that’s what I am. Still.

I thought it might be worth a checkup on the ol’ mental health report card using the five stages of grief as our barometer. I got this list from one of my grief counselors, mostly as a way to check in with myself to see just how well I’m doing. Let’s follow along together.

 

Aftermath: One Month

 Cathy died a month ago today. As hard as the last two years have been, and this includes my own hospitalization and other assorted health problems, and as rough as this year has been, and as painful as the last four months have been, the last thirty days have been some of the most challenging days of my life. I went from the funeral straight to not having a vehicle for three weeks. The enforced shut-in was both oddly comforting and ridiculously stressful, in that it made me feel even more helpless an ineffectual. Running the gauntlet between our wedding anniversary, my birthday, Halloween, and Cathy's birthday sure as hell didn't help matters one little bit. 

All this to say, I am grateful that friends and family don't blithely ask me how I'm doing. Ordinarily I would be loathe to bypass the social niceties (the hi's and how are you's), but my patience is worn tissue paper thin right now, and things that ordinarily wouldn't bother me a bit are sending me into a red rage. But I can't yell in a stranger's face, "I feel like I'm trying to play the trombone with only one arm! How do you THINK I'm doing today!?"

That's how I feel: like I've been amputated. And phantom limb syndrome for me involves walking around the house like a mental patient, talking to thin air and anxiously waiting for an answer that will never come. 

Cancer: Aftermath

I feel like I have a lot to say, but I don't really want to voice any of it. Instead, I'll just dump my brain out and we'll see how it goes. 

The funeral was nice, insofar as funerals go. I think everyone honored Cathy with their words and their expressions of love and admiration for her. Several friends showed up, unannounced, just to pay their respects and be present. Most of my family was here, too. I managed to mostly keep it together. The church was kind enough to post the video on their Facebook page for the many people who could not attend. If you want to see it, it's still up.

For my birthday this year, my middle name was Duncan, because I Yo-Yo'ed up and down all day. Low points included missing my wife, and figuring out that my car wouldn't work and making plans to have it towed on Monday. Because, you know, insult to injury, and all of that nonsense.

Thanks to everyone who wished me happy birthday, and also to everyone who didn't, because there wasn't anything particularly happy about the day. You were quite right.

But I tried. I really did. And I'm going to keep on trying, because otherwise, what's the use? Don't answer that, it's rhetorical.

After the last two weeks, preceded by the last four months, my chest is starting to unclench and my breathing is back to normal. Somewhat. I keep getting into crying jags. I am still pacing the house. I'm still anxious, and scared. And sad. Just so heartbroken. I feel her absence, humming in the air like a high note that vibrates my sternum.

I'm going to look into grief counseling. After I fix the car. And pay the outstanding bills. And sign back up for health insurance (we were dropped.) And a half-dozen other things that suddenly need my attention. Somewhere in all of this, I need to have a real serious Come-to-Jesus meeting with myself about what happens next.

I have been incredibly lucky to have known from the age of 15 what I wanted to do with myself. And then I went and did it. Not a lot of people have that kind of clarity of vision, and I know it's a gift. But for the last twenty years, my goals have been intertwined with Cathy's goals. Oh, we had our side projects, too, but overall, we were always working on advancing our own desires and dreams as we helped the other person do the same.

Now I'm alone. And I have no idea what I want to do. For the first time since the age of fifteen, I have no direction, no heading, and no hand on the rudder. I hate the way this feels. I'll be taking some time off for a bit, so that I might figure out what the next phase of my life is going to be with the label "widower" attached to me like a barnacle I can't scrape off.

I'm tired. I'm tired of crying. I'm tired of getting hit with sudden waves of sadness, whack, in the face, like a creme pie made from depression and despair.

I can't get her deathbed out of my head. I close my eyes and I see it. I see her, arranged, eyes closed, and I can smell her skin and feel her hair on my cheek when I cradled her in my arms and sobbed. I have twenty years of great memories, good times, happy occasions, and all I can think about is her final minutes.

I'm not ready to accept this new state of being. It's still too raw. Too maddening. I was afraid of this happening. Alone in this house, pacing around like a caged animal, alternating between repeating lists of things I have to do, over and over, and crying out for my wife in an empty room , because I don't think I can do it all by myself.

Maybe I'm just wallowing. I don't want to let go of the pain, because I don't want to let go of her. I'm just so angry at everything right now. Things are going to move on with or without me, and I know that. This will likely fade into a dull ache. I'll have an epiphany or two and reorganize (and maybe even reinvent) myself and as time marches on, so shall I, older, wiser, ready for what comes next.

Eventually.

Right now, I think I want to just wallow. And I don't want you to see me like this.

 

Cancer: An Obituary

Cathy Day lost her fight with ovarian cancer on 10/15/2020. She was 56 years old. 

Catherine Day was born in Dallas, Texas, the daughter of Richard Day and Diane More, and attended Vernon High School. After graduating in 1983, she attended the University of Texas, where she received a master’s degree in Speech Language Pathology. She taught in various public and private schools in California, Maryland, and Texas, helping learning-disabled children to read and speak, for two decades.

 Cathy was a lifelong student of the theater and she acted in plays throughout her school years. As an adult, she was active in community theater in Austin, appearing in Different Stages productions, and later with the Violet Crown Radio Players, of which she was a founding member. In Wichita Falls, Cathy was proud to call the Backdoor Theatre her creative home and she appeared in several productions, including “Sordid Lives” which earned her a Genesius Award for Best Actress in a Non-Musical Role, and “Dirty Laundry,” where she co-starred with her husband, Mark Finn.

Cathy met Mark in the Summer of 2000 and they were married in October, 2003. They later moved to Vernon as co-owners of the Vernon Plaza Theater where they lived and worked. Cathy was a member of First Presbyterian Church of Vernon and was active in the community as a founding member of Leadership Vernon, The Vernon Main Street Program, and the Vernon Farmer’s Market. She always had a smile and a laugh for everyone she met, and the memory of her kindness, her gentle nature and her warmth will be a comfort to her mother Diane; her step-father Pat More; her sisters: Susan, Barbara, and Erin; her brother Mike; her many nieces and nephews, and her husband, who survive her, but will never forget her.

 In lieu of flowers, the family has requested giving a donation to the Backdoor Theater in Wichita Falls in her name.

My thoughts are below. Fair warning: this is uncomfortable, and I don't recommend  you reading past the break unless you want my raw, unfiltered take on all of this. 

Cancer: End Stage

I don't know how much more of this I can take.  

Cathy took a turn this week, and it was bad. Last Sunday, I worked up the energy to come into the room, brightly, like I've been doing; I don't want her to see my anguish, and I know I'm not hiding it as well as I think I am. We've cried together enough. I'm trying to be a comfort to her. 

Ordinarily, she greets me with some variation of "There you are! Finally!" However, when I came in on Sunday, she was asleep. I let her be. She didn't wake up until around 9 pm. She looked surprised to see me, but couldn't really talk. I'd seen this look in her eyes before, and immediately thought about the double-up of medicines. 

But that wasn't it. She was just getting worse. Slower, weaker, more confused. 

Someone is always with her overnight; me or one of her sisters. We're all suspending our lives to help Cathy at the end of hers. I made plans to go on Thursday, because the doctor said we are getting close to the end. 

When I walked into the room, she was asleep again. This whole time, I've been able to see Cathy in and amongst the tubes and the gowns and the sickness. I could still see her, the person I've spent two decades with. 

Last night, all I could see was the disease and what it has done to my beautiful wife. The swelling, the discoloration, the distortion of her skin, the skin she diligently cared for her whole life. It was too much. I've been holding open this gaping wound over my heart since July and I didn't think I could rip it open any wider, but I was wrong about that. I cried over her, quietly, as she slept. 

She's been having pain when she uses the bathroom, and it's very likely a urinary tract infection, which can cause fogginess. They put her on antibiotics with a shrug; it couldn't hurt, they said. But they are all certain it's disease progression, a euphemism I've come to despise. 

She moaned in her sleep, all night. As usual, they woke her up every two hours to see if she was resting. I couldn't help ease her pain. I could do nothing, except wipe her mouth when she coughed up phlegm. She assured me I was doing a good job. It's harder and harder to understand her. 

This morning, she was a little more alert, relatively speaking. They gave her the scheduled meds, including the antibiotic, crushed up, and mixed with pudding, Michael Scott style. She didn't eat last night. I just want her pain to go away. I don't want her to die confused and in pain. 

Before I left, I put on Downton Abbey for her. She was watching it as I packed up to leave. There was a scene where someone turned on the phonograph and asked for a dance. Others followed suit, like one does in Downton Abbey.  I leaned over to kiss her forehead and tell her I love her and she said, "I need you do do something for me." 

"Okay, sure, what'cha need?"

"I want you to tell the doctors..." she drifted away for a second. 

"Tell the doctors what?" I prompted. 

She snapped back and locked eyes with me. "Tell the doctors I've forgotten how to dance. They need to teach me. I forgot how."

Somehow I managed to smile from behind the curtain of tears and said, "I'll teach you, baby. It's easy. I know all the steps. It's going to be all right."

She nodded, satisfied, and tried to touch my hand. "Don't cry, honeybee." Her arm was swollen and she had trouble moving it. I took her hand instead. 

I don't know how much more of this I can take. 

2010. She would hate me sharing this picture,
but I think it's beautiful. This is Cathy.

Hospice: Our New Normal

 Cathy has been in Hospice for five weeks now. It feels like forever. I am struggling with watching Cathy's gradual shutting down. She is at the point now where she is bedridden; her leg muscles can't support her and so any scenery changes she wants to make are done with nurses and a wheelchair. Her short term memory continues to fade, as well. People, faces, events and things are all crystal clear to her. But she can't keep up with her phone. In bed. She can't quite remember from day-to-day how to work it, either. She learns it in the morning, but by the evening, she needs help again. Hospice keeps telling me it's "disease progression." It's getting on my nerves. She's not sick, she's hungry. 

Cancer: Hospice, Week 4

 (Warning: Language)

What a shitty week. 

Sonya wasn't too happy about us leaving Cathy behind at the Hospice Center. This is her as I was driving out of the parking lot. Her way of saying, "You left a man behind, dude!" 

Trust me, Sonya. I know. And I'm not happy about it, either. 

Cathy continues to hang on, her heart beating strong, her mind struggling to connect, to understand, her lungs working, her muscles flexing. She's willing. But her body is slowly killing her. It's the worst kind of torture to see her slipping in increments that could be measured in centimeters, and there's not a thing anyone can do about it. 

What makes this doubly galling is that Cathy's own body is cutting off her food supply. And Cathy has never been one of those people with hang ups about food or eating. She loves to eat, and she loves good food. She's always appreciative of anyone who cooks for her. Our first date, I made her chicken parmesan, and she was so impressed, she married me three years later. 

Cancer: Hospice Supplemental

 

Most long-time readers here will recognize the name of Sonya, our affable pit bull pooch with the winning personality and a bevvy of entertaining tricks. She's ten years old now, and she's lost a little bit of bounce, but only a little. We've been pretty lucky in terms of dog maintenance; she hasn't cost an arm nor a leg, and aside from the occasional itchy eye from high pollen days, she's reasonably healthy. 

Last year, we took her to a specialist in Wichita Falls because (and I didn't know this) apparently pit bulls have those big, fleshy mouths that continue to grow as they age. The teeth get covered up by the gums and that's what causes the stinky-mouth, and left untreated, can rot teeth, forcing an extraction. We didn't want that, but Sonya's mouth was definitely in bad shape. 

The process is straightforward; they use a laser to cut off the excess tissue and cauterize it. This was a little more than Cathy and I could pull off last year, so we made plans to do it in 2020. 

Fast Forward to August, with the world on fire and my life in turmoil. I've got a dog with a stinky mouth, and she's in the dumps because she can't find her human, Cathy, anywhere. I've also got Cathy, pining away for her sweet baby. I've squirreled some money away for Sonya's health needs, and I thought this would be a great way to kill two birds with one stone. 

Cancer: Hospice, Week 3

I'm running hot and cold. Some days, I've got full functionality and can do normal things and feel like an adult, and other days, I'm clutching my stomach and staggering around like I've been junk-punched by a silverback gorilla. The worst days are the ones that start out as normal and end up junk-punched. 

Cathy is still in hospice. I don't want the word "still" to have any undue emphasis, like I'm disappointed. Quite the contrary. Rather, the emphasis should be on "in hospice," meaning, she's not home yet. Yet. 

I'm still trying to find a scenario where she gets to come home. I don't have a solution yet, but I'm working on it. In the meantime, I find that a routine is settling in with us, almost like the schedule of a long-distance trucker. I'm on for three, off four four. But those three are 18 hour days a piece. This is exhausting, and the whole family has been rocked back and forth, up and down, and we are all frazzled. 

I don't want anyone to think that I am not grateful for the assistance; I am. It's been really nice having someone, anyone, in the house when I get home. But I want everyone to know that I am absolutely festooned with feminine energy right now. Covered up, even. I'm pretty sure I've started to ovulate. Everyone's cycle is all linked up, now. Mine, the dog's, everyone. 

I've been sitting on some short takes and little incidents that have stacked up in the last few weeks, and I want to share a few, if only to take my mind off of the grind of the days. 

Cancer: Hospice Week Two Update

I'm going to start this with a strange little coincidence. Cathy was moved into the hospice care center in Wichita Falls about ten days ago. They got her in and comfortable and settled and I hung around outside while nurses and orderlies swarmed over her and did stuff. 

As I was sitting outside, I noticed the tiles in the building were all donated--you know what I mean, where you pay a certain amount and sponsor an oblong tile in the name of a loved one, or just as a donation from a family or an organization. These tiles (bricks?) run two-up all around the walls, like wainscoting, down every wall and across each doorway. Outside each room, however, there is a larger plaque, presumably reserved for larger donations, or to sponsor a room. Here is the plaque outside of Cathy's room.

It says "The Hoblitzelle Foundation" for those of you who can't make it out. I read it and a chill ran down my neck. Let me explain why.

Cancer: Hospice

We tried.
We really did.
Cathy tried hardest. 
But in the end, the pain won out. 

I took her home from the hospital on Wednesday, with the understanding that in order to qualify for this eleventh hour clinical trial that had just opened up, Cathy would need to be able to eat without throwing up. She had to keep food down. Or, well, you know, broth. Soup. Liquid. 

Her family was waiting for her when we got home, and they helped her upstairs and get settled. It was nice having folks around, and Cathy seemed cheered by their presence, if a little tired. She tried to eat something, but gave up. The heartburn and nausea were back. 

We tried to get home health to come out, but a snafu with the hospital showed our visits had been canceled because the social worker thought we were going to Oklahoma City. That was frustrating, to say the least, and so I spent an hour on the phone lining up meds for Cathy to be administered tomorrow. All she had to do was get through the night.

She got about one hour of sleep. The pain and the cramps were just too much. I didn't do much better, but I napped a bit, and then started calling people at 7:30 to get her some help. I was on and off the phone for roughly four hours. In the middle of all of it, Cathy said, "Call hospice." 

When everyone showed up, it was all within a ten minute window. The house was full of health care folks, and it took a bit of sorting out. In the end, this is what we decided: the Hospice people have an actual facility in Wichita Falls, and by checking her in there she'd have constant care. They would get her stabilized and comfortable, and then we could send her home for home care in a couple of days. 

Back into the car we went, and drove back to Wichita Falls. I've come to really resent that drive.

She was made comfortable, in a nice, spacious room, that looks like a nursing home room decorated by a mid-price hotel room. Hey, it beats the hospital. She was feeling better, and we were amiably chatting about I don't even remember what, when she grabbed her nausea bag and filled it. 

I jammed the button and yelled for nurses. They came running and took over as the crap in her stomach poured out of her. I've never been so scared, nor felt so helpless. 

They cleaned her up and changed sheets and all of that, and also gave her a powerful anti-nausea med in her port. Later, at midnight, she would get a drug that limits the production of stomach acid. But even after she threw up, she was feeling better. And I think we both realized at that point that what she did next was dependent on her stomach. She wouldn't be able to eat solid food anymore. And for now, liquids were working, but they may one day stop. And then the clock would start counting down. 

I read to her until she fell asleep. I watched her, until some time after midnight, and then I crashed in the chair. I woke up with a nurse in the room, and Cathy awake. "Hi, Honey!" she said. Perky. Like her old self. She was hungry, and wondered if they would bring her crackers. I told her no. But I get it; she's feeling better now. We had a long talk about stuff, interrupted only by a nurse who said her doctor had ordered some more drugs for her. He wanted to know if he should order a NG tube (that thing that went up her nose in the hospital).  I said no, she didn't want that. Cathy looked at me and said, "Well, maybe."

This is what we are currently weighing. With the tube, she's going to be able to hang on for a while. But she will have to stay in the center. She can't come home with the NG tube. If she takes that NG tube out, the timeline is shortened, but then so is her pain and discomfort. 

The drugs she is on right now seem to be working spectacularly. She has a day or two to mull it over. We've all decided that whatever Cathy wants, Cathy gets. That includes Ginger Beer, as I am under strict instructions to bring some back when I return. 

And that's all I know at the moment. She's resting and she's comfortable--well, as comfortable as she can be in a hospital bed. She's seen a lot of family and she's got more coming. She's making calls and talking to people. I don't know if this is a rally, but I hope it is. I hope we see a few of them. 

I know these posts are upsetting to a lot of you, and I don't want you to have these terrible images in your head as the last memories of Cathy that you have. I'm not going to show any more pictures of her fight with cancer. Instead, I'm going to show only pictures of the Cathy we all remember, the Cathy we know and love. This is one of the photos we took for our engagement announcement. Not a lot of people have seen it. I guess it was a little too mushy. But it's a really good picture. 

I will post again when something changes. Hopefully I can get Cathy home one last time. 
Thank you, everyone, for your friendship and your love. Thank you for your courage and for going through this with me. Thank you for everything, from me and from Cathy. You've all made an incalculable difference in our lives. 

Cancer: Three Days Later

Many of you aren't on Facebook and don't follow me there, so here is the update on our situation. Suffice to say, we are mostly out of the woods now, and Cathy is doing much better. Thank you all for your words of comfort, encouragement and strength and support during this hellish ordeal. It's been a long week. I feel like I've aged a month. But things look much much better.

Cancer: Three Days

Happier Times.

Two years ago, almost to the month, Cathy started cancer treatments. At the time, she had a rare and aggressive form of ovarian cancer, and they were calling it Stage 3, but with a look on their faces that suggested that number could change at any second.

We were terrified, if I may be allowed the largest understatement of my professional writing career. Petrified. But also, weirdly, galvanized. There was a sense—more from me than from Cathy—that this was a temporary state of being. An inconvenience to be conquered, and then monitored closely thereafter. We were getting older. Trade-offs being, now we have health problems. But even though the numbers of recurrence were scary, 48% chance of the cancer returning, we were committed to powering through this. The cancer, after all, showed up at the worst time. Super inconvenient. We were just getting our shit together, after, what? Fifteen years of marriage? But we had time to fix it.

Now we have seventy-two hours. 

Cancer: The Devil Defeated

In the middle of all of this insanity comes the best good news we've had in a while: Cathy is through with her course of treatment on the Red Devil. That doesn't mean we are done with chemo, or done with cancer. Only that we are done with the horrible poison they were putting into her body for the past seven months. Or to put it another way: we're not out of the woods, yet, but the deranged mutant bear that has been pursuing us this whole time finally gave up the chase and we can take a minute to catch our breath before resuming the hike to get out of these woods.

Health Update: Cancer and Quarantine

Cathy and Sonya, rocking the matching sweaters.

It's been a while; too long, in fact, and I sincerely apologize. 

We're all friends here, so I'm just going to dive right in. 

I'm not in a good place right now. About two month ago, I realized that with the stress of the recurrence of Cathy's cancer so quickly on the heels of the successful surgery, and the subsequent difficulty of Cathy's chemo treatments on her (and by extension, me) this time around, I had slipped back into a state of depression. 

I wish I'd caught it sooner. This self-diagnosis was a result of some tangential health concerns popping back up and me realizing that I'd not been addressing them like I had been before. Mostly therapy stuff, but also some physical symptoms, too. 

Man, this whole ordeal has just sucked. 

Cancer: The Devil You Know

The water she has to drink
prior to the CT scan.

It's been a while since an update, and that's because we've been overwhelmed with the new chemo cycles and the crippling downturn of the entertainment industry this year. I'm used to not being busy due to high school football, but it's been worse than that, and for months instead of weeks. We are both dealing with life, the best way we know how. My way, for example, includes bourbon.

At the last visit to the oncology center, Cathy was chatting with one of the nurses she's gotten to know better and we found out that there's a cool, fun nickname for the melted Flavor-Ice looking stuff that she gets at the beginning of each new cycle.

They call it "red devil."

I wish I was being funny.

Cancer: A Long-Overdue Update

I met Cathy in 2000, which makes it easy to compute our anniversary and our wedding and all of those other days. Weirdly, in our relationship, I'm the one that tends to remember those things, so this works out great. Today is our 16th wedding anniversary, and I can't quite remember what the 16th year present is, but I'm going to call an audible and wish, instead, for a break from all of the crap Cathy's been dealing with.

This second brace of chemotherapy has been, in many ways, worse than the first round. Chief among them has been the nausea. Cathy didn't have severe nausea the first time around, not like this. Two weeks ago, I woke up to the sound of Cathy throwing up. It was horrible. I mean, any time you throw up, it's bad, but this was scary. I sat up with her the rest of the night, and every time she ran to the bathroom, I dutifully wetted some paper towels and waited for it to subside. It's a helpless feeling, to say the least.

We are also battling the new schedule, because it's a twice a month deal, but they have been calling her in for iron infusions and blood work. So, in effect, it's been more or less weekly anyway. We have tried five times to move the treatment days to Tuesdays, to no avail. The self-populating schedule making program that Texas Oncology uses will let you change one appointment date, but not all of them. Very frustrating, considering that I can do it was Google's calendar app and I'm not a medical facility.

We are trying to focus on the upside, which is this: Cathy gets a CT scan at the end of the month. They are looking now for any shrinkage, rather than waiting for six months. That means we'll know very soon if all of this horrible poison is working. If it's not, we get to try a different cocktail of chemicals. If it is working, however, we will soldier on through and get more anti-nausea meds and all of that fun stuff.

In the meantime, we are trying to live as best as we can. We have an evening planned for our anniversary, and I'm crossing my fingers that we'll get to go through with it.

Next week is my birthday. I'll be turning 50. I haven't decided if I'm going to write about it or not. But I know some of you like to do nice things for people, so if you want to do anything, you can either drop a few dollars into Cathy's GoFundMe account, or head over to Amazon.com and buy one of my books. My author page has all of the things currently available that I have stories or essays in, as well as things like Blood & Thunder: The Life and Art of Robert E. Howard, the Con-Dorks trilogy, and all of that other stuff. Recently some folks have re-discovered the Con-Dorks trilogy and have been saying nice things about the books.

Cathy's GoFundMe page.

Mark's Amazon Authors page.

That's it, really. I'm sorry the update is so short, and that it's not very funny. I just wanted to let folks know that we are still here.