The Darker Stuff

In the first post I mentioned my mom went to the vet with me as my Emotional Support Mother. Boycat has dental issues and I needed to get him checked out and prescribed antibiotics, but the last time I took a cat to the vet the cat didn’t survive. I was gunshy basically.

Like statistically I knew it wouldn’t happen again, but emotionally I wanted someone with me. Because on top of the pain I was in and the worry about the cat I was angry.

Esso should have been there. I was incandescently angry that they weren’t here to help — to drive because I was in pain, for the emotional support (although being fair, they would have been much more afraid that something bad would happen), and because that’s what a spouse is for.

Saturday, the whole time I was pacing the ER, I was worrying about the pets. The dog needed to be walked. The dog needed meds. One of the cats needed meds. They all needed feeding. My mom doesn’t drive and I don’t trust my neighbors well enough for any of them to have a key.

I’m angry again.

I get angry at myself for being angry that esso is dead. I think about all the time I helped them with surgeries and sicknesses and all the time I took off work for them and the hours and hours of sleep lost and I get angry because I know it’s not a contest. There is no “I owe you one” and I wasn’t keeping score. But I can’t help feeling betrayed that we went through so much together and now I have to do this on my own.

Maybe it’s not really anger and more like heartbroken.

I feel like the friends that did help me are now all judging me. My house is a mess. There are (empty) boxes everywhere because every time I think “I’ll just break down a couple” I get so overwhelmed by it all, and I know it’s not overwhelming.

That’s the fun of my brain. I know exactly when I’m being completely irrational but I can’t get around this invisible wall in the way and I can’t articulate how I can’t get around it, and I spend a lot of time standing in the middle of my kitchen sort of awkwardly flapping and yelling “JUST START” in my head.

Anyhow, my disaster of a house is set up the way I understand it, and it doesn’t make sense to other people. I have to have my doors locked/unlocked particular ways. I have to have things in specific places. And people had to come in and touch stuff.

My old roommate came one day to take care of the pets after work because I couldn’t remember if I’d arranged with the dog walker. He and his spouse came by, fed everyone, and hung out with the dog. After, I got messages from him telling me that “almost everything was unlocked and all the lights were on” and that he locked the deadbolt on the front door for me.

I don’t use it. It’s upside-down and sticks and I lost the key for it. I should replace it with one that’s set the right way (and has a key) but I haven’t. It’s so low on the list of things that HAVE to be done and it affects so little of my life that I honestly never think of it.

There was frantic texting when the dogwalker DID show up (I had scheduled it but in my defense…. neurodivergent memory AND post-surgical painkillers make it hard to keep track of things). My friends came back, unlocked the lock, and we got all the keys sorted out.

But I feel like they’re at home now, discussing the terrible state of the house and my life and judging me and probably pitying me.

But not, you know, helping.

I am feeling very alone and tired and sore and in a couple more days I’ll be back to work like nothing ever happened and have to pretend that I’m not so heartbroken, and I’m already tired of it.

It’s Thursday the 18th about 7:15 pm. I’m setting this to post tomorrow morning to spread out the activity. When this posts, I should (hopefully) be back home from having the drain removed and face down for some more sleep.

The Surgery

I think technically it was still Saturday when the surgery started. I feel like it was around 11pm or Midnight and somewhere in the zone between 3 and 5am I was in recovery. They told me I was doing good, and I checked in with my mom. I think. I know I remember talking to a nurse about mom calling, and I feel like I said “I’m texting with her now” but then it got hazy again. I ended up in a very nice room all by myself.

The hospital has one section that’s for post-surgical stuff. Each floor is for different types. The neurosurgery floor isn’t as hot a spot as the floor for the general surgery so it was quiet.

The first day of recovery was miserable. The room was too hot, I couldn’t get comfortable, every time I dozed off someone else came in to check on me. I know people complain about it, but I get it. It’s to make sure I’m not dying or reacting or anything, and you sometimes have to be woken up for it.

I had two of the best nurses in the world the next couple of days. When I got a call from the hospital after getting home I made sure I named them specifically because they were just so comforting. We talked to each other like equals, they never made me feel like I was being unreasonable, even when I felt like I was being unreasonable, and they got my jokes.

Back to the first day post-surgery. I was hot, the room was hot, the blankets were wrinkled, my gown was askew, and all the seams were in the wrong places. Between the heat and the plastic pillow I was sticky with sweat.

I did badger them a little about getting cleaned up. I was able to do that myself though! And they kept turning the heat back and back and back and eventually brought me a little battery operated fan and that fixed almost everything.

At some point I said to someone checking on me that I needed to get the catheter out. I told them I’m asexual and the contact was incredibly distressing and I was sure I’d feel better once it was out.

I felt so much better once it was out. THAT fixed everything.

Tuesday I was up and walking and peeing like a grownup and feeling much better. I got to cut my pain meds way back — I was off the painkiller pump and down to a muscle relaxer and an oxy. Physical Therapy signed off and I got a referral for outpatient PT if I feel like I need it. So far I don’t.

I got home mid afternoon on Wednesday and slept a lot, but I got to do it in my own bed, in my own clothes, with my own cat. I think the pets might get a short post of their own.

It’s Thursday afternoon. I’ve been home a little over 24 hours and it’s fantastic how much better I feel each time I fall asleep.

Tomorrow I have an appointment to have the surgical drain removed. Next week I have follow-up number one. In October, I have the second and final follow-up.

I’m glad no one knows about this blog

It’s Thursday, September 18th. On Friday the 12th I woke up with a pain in my lower back. It felt like any other strained lower back and I assumed I slept in a bad position or something. I went about my day and it was mostly alright until that evening, when I had to take my cat to the vet.

I made my mom come with me because the last time I took a cat to the vet, the cat didn’t make it. Not through their fault and not because of neglect. He had a heart defect. Anyhow, she came with me for moral support. While we were there I complained to her about my back hurting, and how it was getting worse. I couldn’t sit comfortably. Driving to and from the vet was incredibly painful. But I thought it was just because I’m in my 50s and overweight and sit too much and planned to get high and sleep it off.

I skipped getting high and tried to sleep it off. Somewhere overnight Friday to Saturday I started throwing up. Could’ve been from pain, could’ve been since I’d forgotten to eat. I made a deal with myself that if I threw up again I would go to the ER because it all was adding up to sound like kidney stones (I’ve never had them so I couldn’t be sure, but where and how the pain was, it seemed sensible).

Well, I threw up again, and at about 7:30 in the morning I drove over to the ER.

I was there for hours before even being triaged. I kept telling them my pain was a 9.5 at least. I couldn’t sit down without pain so I paced the ER waiting room until I was seen. I had to stand for the vitals and initial bloodwork because I couldn’t sit at all. They put in an IV and gave me a little morphine and I continued to pace the waiting room.

Around midafternoon they wanted me to get a CT scan. I’m allergic to contrast dye and need days worth of pre-medication before I can have it, so they did a CT without contrast. And didn’t like what they couldn’t really see.

“They’d rather get an MRI now and look at it before deciding anything.”

Sigh. OK. I JUST re-pierced my ears, but this is important. I took out the earrings, went to the MRI (I’m walking/standing this whole time because even after two rounds of morphine I was still in a lot of pain) and got one more hit of morphine. Just before the scan started I had to stop. I threw up. “Was it the morphine? We have anti-nausea meds!” It took me a few minutes to make them understand that it was a pain reaction not a morphine one. The good news was that took enough time for the drugs to work and I had an MRI.

After the MRI they took pity on me and let me have some food. A little half cup of unsweetened applesauce, just the way I like it. And about five minutes after I finished, one of the PAs came in and said “Your next stop is neurosurgery.” and I was like “Oh cool, so you’ll drug me up and I can go home and start this on Monday, right?”

“….. they kinda want to do it now.”

“But I just ate something! I can’t do anesthesia now!”

A quick confer and they decided to talk to anesthesiology about how to proceed and then I said “Oh it’s ok. I’m gonna throw up.”

And I did.