Dying, as it turns out, is incredibly boring. I expressed this thought to my boyfriend earlier today who pointed out that some people are bored with living too. That is much worse, I imagine. I am rarely bored. I always feel like I have a million things to do and not enough time to do them.

I’ve thought about checking out, and then people follow up and ask if I mean checking out of life permanently or checking out of hospice and I don’t know. I realize that I feel good enough to check out of hospice because I’m in hospice, with constant fluids and pain medication and electrolytes. There were times last week when I didn’t think I would make it to surgery, I was so weak and exhausted and in pain. Now everything is controlled, and I feel better, but on the outside I would be weak and sick again.

So far, one doctor and at least one nurse don’t like me. Someone likened it from going to first class to economy. I’m not used to making so many enemies now that I’m not in my 20s and I’m not drinking.

It’s strange to be the healthiest person in hospice. If I stopped taking my potassium and electrolytes and fluids, I wouldn’t be able to walk or control my lower body and eventually my heart would give out. It will probably take about a week or so to die. But I’m not there yet, so it’s odd. I want to sneak out to see the cats and do stuff. I’m also not well enough to be among the rest of the living, though. I’m in between.

I need to check out or check out. I probably need to do the permanent check out but I am scared. I have been resistant to home hospice but now I’m in a Libra conundrum of indecisiveness.

 

After the doctor had tried the debulking surgery but then discovered too many tumors and closed me back up, I kept falling asleep from medication and exhaustion. Each time, I woke up, I’d have to remember that the surgery didn’t go well. “Your tumors are still all there,” I had to tell myself. “There is nothing you can do.”

It seemed so surreal to be sitting here in recovery with no hope of getting better. I had to keep reminding myself that I wasn’t leaving to go home, but to hospice. I’d hopefully crossed out hospice on my calendar when I scheduled my surgery.

The surgery revealed lots of small tumors threaded throughout my bowels. That explains why my symptoms were so terrible, but the scans didn’t show much. The tumors had been hiding.

“You can’t open her back up and take them out?” a friend asked this morning as a last resort.

No. It’s not an option.

Today was hard. Today I was more cognizant and had to admit defeat. Today, on my way to hospice, I stopped by and visited the cats and my apartment for the very last time. (Cats are allowed at the facility but cats don’t like to travel.) I hurriedly packed some clothes and said goodbye to three very specific pieces of my heart. In between this, I sobbed at my boyfriend.

I don’t like being like this, so sad. On my way to the hospital, when I was optimistic about the surgery, I chattered away about fun stuff I’d done while doing chemo or going through treatment. As we passed by Lincoln Center’s film center, I recalled that I’d spent all day watching a season of Breaking Bad leading up to the premiere of the series’ last season and how fortunate I was to be bald to be Walter White for Halloween. I’ve tried to have fun no matter what and now all I can do is cry, particularly at my boyfriend, who I will hate leaving. I would have done anything for a few more months with him, and I hate that I have to go. I wanted forever and I should have been more specific, because my forever was only six months. I could have an abdomen full of tumors and be stapled together while being told that I don’t have very long to live and he smiles at me and I feel like the luckiest person in the world. All he has is a gaunt lady who looks at him and bursts into tears.

I don’t want him to remember me this way. I don’t want anyone to remember me like this.

I would like to go sooner rather than later, but I’m afraid to pull the trigger and stop the electrolytes and go. It will be quick.  I physically can’t go on much longer. There were times when I didn’t think I would make it during those two weeks until surgery. My body is giving out.

In the end, my heart will stop, but it feels broken now. I don’t want to leave the cats. I don’t want to leave my boyfriend. I don’t want to leave my mom. I don’t want to leave my friends. This is very different than how I felt in May of 2018, when my boyfriend at the time wanted me to die so he could be with his Pilates instructor in London (it worked out for him in the end even though I didn’t die then). Then I didn’t care whether I lived or died because I felt broken. This time, I don’t want to go, and I know that makes me much luckier. My life is so much better than the way it was.

My friends decorated by room with photos. I’ve had a good life. I can’t comprehend that it’s going to stop so soon. How did this happen?

I’ve been taking comfort in everyone’s kind words. I made it to 42, my friend Anne pointed out. “According to Douglas Adams, 42 is the answer to life, the universe, and everything. So nice job getting this far. The enemy’s gate is down.”

My friend Seanan says, “You are the most alive person I know, and I am beyond glad to know you.”

My friend Anna said, “You’ll live on for much longer than you know, in one form or another. You are so loved.”

I’ve received countless messages of love.

I asked my boyfriend what he thought happens after we die. He says you live on in other people’s memories, and I won’t be forgotten.

Still, the end looms close, and I feel like I’m not ready.

Every now and then, the worst thing happens. Yesterday was one of those times. When the surgeon opened me up, he found a lot of tumors that didn’t show up in the scan, so he closed up the incision.

That’s it. I’m done. There is nothing more to be done. We fought hard, but it’s time to go. I am in a lot of pain from the surgery and the tumors; I can feel the tumors cramping. I can’t control my bowels. I am exhausted and have a hard time fixing electrolyte imbalances.

It’s time for hospice. I knew this was an option going in, but I needed to exhaust all my options.

When I woke up from surgery yesterday, I was told the news. My boyfriend and two of my friends were there and my abdomen hurt so I couldn’t react. I still can’t do any gut-wrenching sobs. I am sad, but have to remain somewhat stoic.

I can’t laugh either, and in these situations, it shouldn’t be a problem, but I have the friends that I have, and so that is, thankfully, an issue.

I have a bunch of logistical and practical matters I have been working on, but I’ve wrapped those up, for the most part. I’m going to blow off some things.

Even now, when they talk about stopping the electrolytes and fluids, I hesitate. I still don’t want to die, but it is time. I had a good run.

I submitted Ziggy’s photo to a social media group for fat cats. It hasn’t been approved by the admins, so I’m not sure what this could mean. It’s possible a) he is not “chonky” enough, b) perhaps he’s too handsome, and they think maybe he’s a professional model c) my caption isn’t clever enough and doesn’t use enough umlauts and mention enough of the cutesy cat words, like “peets” or “himb” or “boi.”

Yesterday I was ghosted by a lampshade. Again. Since June of 2018, when my ex moved out, I needed some home decor items, but with my abbreviated timeline, buying new furniture seemed silly. I managed to find a floor lamp on the street, but it has a very specific lampshade that is stained. Last year, I tried to get a free lampshade that someone was giving away on NextDoor. After I rearranged my entire morning to be in Williamsburg, I went to her apartment and called. And called. And called. When I arrived at my train stop, I got a text back that she wasn’t looking at her phone. The first time I was ever ghosted was by a lampshade.

I tried again, and I planned to pick up a lampshade on Sunday in Kip’s Bay. I would be nearby at Rolf’s for the Christmas decor with friends in town. However, when I messaged Lamp Shade to confirm, it had been picked up already. “This is the second time I have been ghosted by a lampshade,” I noted.

Of course, I’m skipping over my big worry. Tomorrow is my debulking surgery. In an attempt to relieve some of my symptoms,  a surgeon is going to try to remove some of the tumors. Three are in my liver, and two are in my bowel. They’re not completely sure if they can get to the bowel tumors. There’s also a pancreas tumor that is inoperable. I have some sort of mammary thing happening, but they don’t think it’s cancer.

It’s not a small surgery. They will reopen my Whipple scar and then cut further down my abdomen. It’s a 30-day recovery.

I’m not afraid of the surgery and the staples and the scars. I’m worried it won’t work. There’s a chance it might work and there’s a chance it might not. Regardless, it’s my last chance. The PRRT didn’t work. It’s doubtful the Keytruda worked.

I was originally planning to go to hospice later this week, and instead, I’m having surgery to try to stay just a little bit longer. My time’s running out. I’m always tired and in pain. I just want a little bit more time.

I took three oxycodone today. I keep falling asleep writing this. I need to get up very early for surgery. Goodnight. See you on the other side of this surgery.

 

At the regular Thursday night Ladies Night during the spring of 2005, one of my friends waved to me near the dance floor. He smirked and said, “Word on the street is that Josie Rubio was seen buying a Kelly Clarkson CD at Best Buy today.”

Earlier, I had found myself at the Best Buy near my office in Columbus, Ohio, with Breakaway, the latest Kelly Clarkson CD in my hands. I couldn’t possibly buy (or perhaps even find) the CD at one of the cool record stores near the Ohio State campus, and this seemed like a good spot to make an illicit purchase. Until I hear a familiar voice behind me. “Hey, Josie, what are you buying?”

I had forgotten that someone I knew from the goth clubs/nights worked in the automotive stereo department. I sheepishly showed him my Kelly Clarkson CD. He was out at the club that night, and apparently word was spreading about my love of catchy pop tunes.

I love “Since U Been Gone” so I slipped the disc into my car stereo right after I bought it and listened to it on repeat all the way back to work. It’s not even a guilty pleasure. It’s a good song.

Today there is a dance party celebrating its 15-year anniversary and release in November 2004. I remember watching and discussing the video with my former roommate.

I still love that song. In fact, it was one of last summer’s anthems, for obvious reasons. After the breakup, I had a very small Gwen Stefani “Used to Love You” phase of a few weeks, followed by a triumphant return to victory songs. I played “Since U Been Gone” a lot. A lot. My music snob ex would have hated it so I played it even more. I alternated between that song and Icona Pop’s “I Don’t Care.” I listened to the latter on repeat the day we went to the courthouse to dissolve our domestic partnership. I was so happy, the clerk congratulated me.

I was trying to think of my other favorite breakup songs, but I don’t remember most of them. I do know that I played “Ordinary World” by Duran Duran over and over again after my very first breakup at 15. I guess the tone of the song depends on the breakup. That one was definitely a “Since U Been Gone” parting of ways. Happy 15-year-anniversary to one of my favorite breakup anthems. I don’t regret making that purchase at Best Buy.

 

I was supposed to start dying next week in hospice, but instead, I’m getting surgery. It’s strange. I’m still preparing for death and dealing with a bunch of red tape for everything from cashing out some of my retirement funds to my disability payments. I had nonstop visitors for over a week and instead of a tearful final goodbye, at least this gives us a bye-for-now attitude, hanging hope onto the surgery that may or may not buy me a little bit more time.

There are many worse things than the prospect of too many visitors once you’re in the hospital for surgery and recuperating. I appreciate all the messages I’ve received about visiting, both when I’m in the hospital and after my surgery. I check into the hospital on November 11 and have surgery November 12, then I am in the hospital for four to five days. My mom is coming out to stay with me and take care of me November 20–29.

I’ve been through a similar surgery for my Whipple procedure, though this will be less invasive. Refreshing my memory about that time with old posts, recovery was tough and worse than the stem cell transplant. I spent a lot of time in pain and on pain meds. I also came across an old blog about my unofficial visitors policy when I was in the hospital recovering from my stem cell transplant in 2014, and my attitude then was: “I want to be alone.”

This procedure and the circumstances are much different, of course. I had to be really careful with my immunity after the stem cell transplant. Also, I knew I would live and get better afterwards. I’m aware this might not work or it could hasten hospice and will buy me a small amount of time at best.

However, I’m still the same person I’ve always been. When a few people mentioned to one of my friends that I don’t seem that sick, she compared me to my favorite animal, the cat. She had taken her 20-year-old cat to the vet, who told her that the cat was really sick and in bad shape. She didn’t know how serious the cat’s health problems were or how bad the cat felt. The vet explained that cats don’t always show their pain, and when they do, it’s usually at a point where it’s pretty bad. “Josie’s like a cat,” she said.

At this point I can’t hide how bad I feel sometimes with the pain and dehydration and fatigue.

Also, like a cat, when I am feeling bad, I would like to drag myself under a porch and disappear.

When I am sick, I’m not huge on people visiting me when I’m drugged up and won’t remember things with a bag of my bodily fluids hanging off my bed. I prefer to hang out with people on my terms, when I’m more in control.

The other thing is that I’m actually an introvert. I had a shrink in my 20s who was really into the Briggs-Meyers test, and I always test on the more social side of introvert. I want to be an extrovert and I believe through sheer force of will I have pushed myself to the border of introvert/extrovert. But I’m not naturally “on” and even if you say I don’t have to entertain you, I really feel compelled to do so. I sometimes get a little drained.

I am up for visitors, but, like I said years ago, “’If you happen to be around and want to drop by, that’s OK. But if you plan to come to New York specifically to see me in the hospital, please don’t.” It’s possible I might change my mind but for now, I think I will need some down time too.

I love and appreciate the help, and I will definitely ask for more help if I need it. It is very possible that I will. I would rather just see you, say, poolside than bedside, and I’m hoping I have the chance. I think I have a lot of the caregiving covered. Hopefully see you on the other side of this.