We Missed Out

This is a Really Real . . . well, a lot of things, post.

TW: Suicidal Thoughts Mentioned. Death Mentioned.

I’m sitting at an antique kitchen table, the light overhead the only one illuminating the expansive and open area.

Wonder Woman is asleep in a recliner in the connected living room. The Mountain Goats are playing quietly on the portable speaker that she was thoughtful enough to bring with us.

I almost fell asleep on the couch, cuddled up under my favorite blanket that I brought from home. Unfortunately I can’t fall asleep without my CPAP. But time slipped away as I laid there with my eyes closed.

Now the music has ended and I hear Wonder Woman snoring ever so quietly. The tap tap tap of Siah’s nails against the old linoleum floor. I wish she would relax and lay down some place, the constant noise of her nails makes me anxious.

I’ve wanted to write all day, but couldn’t quite figure out what to write about. I didn’t want to interrupt our quiet time together anyway.

My brain has been quiet for over 24 hours. The dreams and nightmares I had last night just quietly passed by, without the anxious reaction that they normally cause.

I didn’t realize how loud my brain has been since I went to my dad’s house, nearly a month ago. First there was worry about caring for him, and then there was the trauma of his death.

I mentioned to Wonder Woman earlier that I felt more connected to her than I have in awhile. Not because anything was wrong with us, or because we’ve done anything differently, but because trauma takes up so much emotional space that it’s hard to find room to truly connect.

I would notice how loud it was and how much space it was taking up when it was distressing. The times when my Facebook posts were quick and terse and scary. The times when I wasn’t sure I’d make it through this. At those times the noise is apparent.

But during the times when it’s just there, when I feel like it’s quieted down and is just gently simmering in the background, I didn’t realize how much space it was still taking up.

I suspect that some day I’ll look back on this vacation and see that it’s still taking up a lot of space.

But right now it seems quiet. It’s quiet enough that I can lay still and awake on the sofa with my eyes closed. I don’t feel the need to fill every moment with, something, until I pass out full of medications at night.

But there’s still a quiet thought in the background. Something completely unrelated to my current trauma, but a reminder that past traumas are always with me.

I walked into a game and toy store that sells wooden toys and puzzles and games. It’s a store that we came to last time we were here and I was so glad to see that they were still open, they had just moved one street over. I was talking to the owner, a woman who talks about so many different things because she’s just happy to have company for a few minutes. I told her, “My son is nearly 21 now, but this is exactly the kind of place I would have brought him to when he was a kid.”

Back when Parker was alive.

I wish we could have come to a town like this. I wish we could have experienced the long drive through the mountains to get here. I wish we could have seen the sun set over the rolling hills in the distance. I wish we could have seen how different the colors are, just from the difference in elevation.

I wish.

And I feel guilty for thinking about Parker, and thinking about old times, and thinking about how things were . . . while I’m on this amazing vacation.

But those times make me appreciate what I have now.

Don’t get me wrong, we’re still pretty poor, and it takes family help for us to experience these sorts of things, especially when it’s been a month since I last worked.

But this is a different sort of poor. This is the kind of poor where I can afford to buy something I forgot when I was packing for the trip. The kind of poor where we can stop for something to eat on the road instead of packing a cooler.

I’m sad that Parker died without experiencing this kind of poor with me.

I’m sad that Kidlet grew up without experiencing this kind of poor with me.

My bottle squeaks as I open it and Wonder Woman jumps awake to make sure I’m okay. I feel bad that I woke her up from that peaceful evening nap.

But she’s already fast asleep again.

It’s so quiet here. The music has stopped playing, the dog is finally resting on the carpet, and I can hear the bugs outside. I hear the wind gently blowing through the long grass in the field just beyond the little cottage we’re staying in.

This is a kind of peaceful that I don’t get to experience often.

And my brain is quiet.

I wonder if Wonder Woman jerked awake because she was afraid that she’d left me alone too long.

But the suicidal thoughts are quiet.

We talk of future trips and visits overseas and she says “But you have to stay alive that long.”

We’ve eaten at a restaurant within a local resort and Wonder Woman mentioned that she could see us vacationing in a place like that when we’re old and want everything close by.

“But you have to stay alive that long.”

I feel guilty that she even has to say that. I feel guilty because I know those thoughts tear us both apart. They aren’t just scary for me, they are scary for everyone around me.

But they are quiet right now.

I shiver slightly as the cool night air blows through one of the still open windows. I don’t want to get up and close it because I don’t want to disturb her again.

We’re both experiencing a sort of peace here that we rarely get.

I know there’s always the possibility that the peace will be broken before we leave. I don’t get to decide when trauma will speak up and remind me that it still exists.

But right now I’m going to sit here and enjoy the sound of the bugs, and the feel of the cool breeze coming in the window. And I’m going to listen to Wonder Woman peacefully sleeping.

And I’ll deal with everything else, when it gets here.

Lost Stability

This is a Really Real Trauma Post.

And a Really Real Mental Health Post, because the two go together.

TW: Mention of Suicidal Thoughts. Mention of Completed Suicide.

These have been long lately, thanks for those who are reading along.

First for the good news.

I’m wearing headphones and not freaking out, for the first time since that shot rang out.

I also turned off the hallway light tonight after we got home, without waiting for something to jump out from behind the shadows.

Slowly, I’m healing.

I’m taking note of the little things because maybe they’ll help me stop focusing on all of the bigger things.

Today I talked to my psychiatrist, she started off talking about raising my antidepressant, which we had been talking about a month or two ago.

I told her that was no longer the concern. The minor depression I had still been feeling when I was stable before wasn’t anywhere near as important as the current desire to end my life.

Or the sleep deprivation and nightmares.

And I realized, that’s part of what’s pissing me off so fucking much. Not only did this traumatize me, bringing with it, the previous traumas in my life.

Not only did this make me wobble in a really big way.

It did it when I was in a place of pretty solid stability. Yes, I was still slightly depressed. Yes, I was having problems focusing on work or other projects. Yes, it wasn’t perfect, but I was stable.

My feet were planted on solid ground and we were just making minor adjustments.

Today after PHP I laid in bed, unable to nap, but unwilling to be up. When Wonder Woman started mentioning going for a walk I got so angry with her. A rage that made me want to scream and yell at her. A rage that made me snap at her via text because I couldn’t trust myself to talk to her in person.

I haven’t felt that sort of rage in a long long time. I hate that side of me. I hate that it even exists.

I remember when I was finally fighting through the trauma of Parker’s death I sat on the kitchen floor and kicked the side of a shelving unit in. Using all of my force to release the rage brewing inside of me. So deep and solid with nowhere else to go but out. I started by drawing lines on my skin and by the end I was digging the pen in with all of my force. I remember that day, and I remember it being the day I measured my successes against. At least I wasn’t that bad anymore.

Today when I was talking to my psychiatrist, I told her I needed to be back on Abilify. The same medication I fought so hard to get off of because it makes me eat the house.

But I’m back to needing to be fat and alive rather than skinny and dead.

And it fucking sucks. I was so proud of myself for being able to brush away any suicidal thoughts that I had, even without the help of that medication. I was so proud of myself for being able to ignore them, or distract myself from them.

And now they are back with a vengeance. That rage turned inward taking away my will to exist.

I just want to go to sleep and never wake up, unless waking up means this never happened.

I see myself with a gun to my head, I hear the gun shots that no longer sound like bangs in the back of my head but now sound like the pops that they truly are.

The sound of gunshots in the back of my head were always the first sign of a suicidal downswing. Hearing how those sounds have changed, and seeing that it truly would be a viable way out, if I had a gun. Now I not only relate a way out to pills, but also to guns. They are ways that I know will work, I’ve seen it first hand.

And I was stable.

I was stable.

Now the thoughts have a tight hold around my neck, squeezing tighter and tighter. The bed is my safe space. Holding the blanket tight around me means I can’t act on the urges.

The other day Wonder Woman, in reaction to a suicidal post, told me she knew that if I looked hard enough I could find what I needed around here. No matter how careful we are to keep things locked up, if I tried hard enough, anything in this house could be a tool for my death.

So when the thoughts are bad, I put myself in bed. As long as I don’t step foot out from under those covers I can’t do any harm.

And while I’m there the shots can ring out in the back of my head, and the urges can come all they want, but I can’t act on them.

But that same survival mechanism allows for the thoughts to twist and turn and get stronger and stronger and louder and louder.

Being in bed is both the best and the worst place for me.

I’ve started walking late at night with my old gym buddy. We are doing super short walks for now, but plan to build up our strength and stamina again. Maybe one day soon I’ll be back in the gym where you can’t tell the sweat from the tears. Maybe I’ll be back to working it out that way.

But for now we just walk our little circle around the neighborhood, sometimes talking, sometimes silently, becoming accountability buddies for each other.

Just like before.

Just like the last time I healed from finding someone dead.

This sucks, but sometimes I can see myself getting back to stability. Sometimes I can remember that I did this once, and I will do it again.

Sometimes.

The rest of the time I just have to fight to hold on. Live from one Starbucks trip to the next.

Just make it one more day.

One more hour.

One more minute.

One more second.

And to think, just a few short weeks ago, I was stable.

He took that from me with the same shot that took his life from him.

Suicide doesn’t end the pain, it just gives it to those who are left behind.

I guess there’s a reason for this rage that keep building up inside of me.

This isn’t fair.

But I’m okay.

Or at least, I will be okay.

Recording These Memories

This is a Really Real Aging Parents post.

I’m writing these so often because this time next year I believe he’ll be gone, and just like I look back on my mental health progression, I want to be able to look back on this time in my life, as well as the progression of his disease.

This one is long, apparently I have a lot on my mind tonight.

Dad has always kept his house at 80 degrees. I keep my at 68, plus have fans going constantly. One of my bigger complaints when I would come see him was that it was hot and humid and gross inside, not to mention outside. When I first got here, I turned the damn AC down to 72. Still hot by my standards, but at least I’m not dripping sweat. And I’m working my ass off here (literally, this is one hell of a weight loss and exercise plan.) Today Dad was cold, and he wheeled himself over to the thermostat, first time he’s noticed since he came home. “Turn this back up, no wonder it’s cold.” “Dad, you’ve been fine for 4 days at this temperature, we can get you a sweater if you’d like, but I can’t take care of you if I’m sweating so badly that you slip out of my arms.””Oh.”

Dramatic much?

He went back into his room to watch TV and when I came in a few minutes later, he was struggling with the comforter that he’d pulled off the bed. I asked again if he wanted a sweater and he said no, so I bundled him up.He had me take him into his closet a little while later and he picked out a sweater.

The hospice nurse came today, 3rd day in a row as they get him set up. Today was the care plan.He’ll have an aide 2 or 3 days a week to bathe him and help him shave, etc. They are going to figure out if using the chair in his shower works, or if we need to get a transfer bench that we can use over the regular tub in the guest bath. She said it was great that I’d gotten so much stuff, but said don’t buy another thing without asking them first. They cover most of it. Yesterday they brought waterproof pads and briefs and wipes and gloves. Today they brought him a hospital table, a cushion for his wheelchair, and something else. A fully electric bed will be here any day now.

I asked if a lift chair was possible, I can’t get dad in and out of his recliner, but a lift chair would make it possible to transfer him. She said no, but if you find one, we’ll reimburse you for the cost. We can even help you find one if needed.

The social worker will be out one day this week, she can help arrange respite sitters and connect us with other community resources. Most of his medications will be mailed to him now, without a copay, and if we have to pick something up at the pharmacy they gave us a card which will waive the copays there as well.

They are sending out a speech therapist and a physical therapist. I can ask tomorrow about occupational therapy, because I forgot. The goal is to maintain his current abilities and quality of life.

I was shocked when they said they could provide a mechanical lift for transfers when he can no longer help us with that process. I hope he doesn’t live that long.

The nurse recommended we get him a laser pointer for those times when he can’t find words. He can point from across the room and show us exactly where something is. I wonder if one day we’ll have a picture board for him, just like I had with my son before he could talk.Today I could tell he was depressed. The reality of this situation is setting in.

He told me I talk too much, asked me if I ever stopped yakking (nope dad, I never stop, sorry). I’m sure it sounds incredibly loud when you’re used to a silent home with no one around.

He was restless, moving from one room to another, calling for help when he couldn’t push himself anymore. He never did settle on anything to do, eventually asking me to help him to bed even though it was only 730.And he was wiped, once again dozing off before he could help me pull him up the bed. He was dead weight in my arms.He asked for his night meds, said he was just done for the night. He choked while taking them, trying to gasp for air. It was one of the scarier things I’ve been through with him, as I quickly raised the head of his bed getting him more upright. He eventually cleared it, but he’s been coughing ever since.Losing the ability to swallow is one of the symptoms of his illness, aspirating foods or liquid will often cause pneumonia. Pneumonia is regularly the cause of death with his condition. I sit in the kitchen hearing him dose off and wheeze a bit, then wake up with a little cough and clearing his throat. I could call the hospice nurse, but it would just wake him back up when she got here in an hour (he’s so far out from anything), and it’s not like they can do anything anyway.I have the number in my phone though, and I’ll be listening to him through the monitor all night, stirring with every cough. I will call if it becomes too bad, because maybe they can do something to make him a bit more comfortable.That’s the purpose of all of this. That’s the reason I’m here instead of letting him spend his final days in a home. I’m here because no matter how difficult our relationship has been, he deserves to spend however long he has left, at home, or at least as much time as I can give him.

Wednesday his dog comes home. It’s been almost 2 months since he’s seen her and he misses her so much. I’ve hated that we had to wait this long but I needed to have a routine down, before adding another mouth to feed.

And for the first time since he came home I just burst into tears reading back over this. My dad is dying and I’m watching it happen before my eyes. Maybe it’s just a few bad days, maybe this is our current new normal. There will be lots of new normals before this is over.

I hope I’m here when it ends, and not my son. I hope he doesn’t have to find him dead in his bed like I found Parker. But I’ve already talked to him about it. We know it’s a possibility.

Hopefully he’s still in his own home, with his dog, when that day comes.

Side Effects

This is a Really Real Mental Health post.

And a Really Real Medical Health post.

TW: Talk of weight, mention of suicidal thoughts, talk of marijuana use, talk of narcotic pain medications. (Also, side note, sorry I haven’t been as good about TW, I will go back to using them more frequently.)

This is super long, way longer than most of my posts (twice the length it seems), but, writing helps, and I have a lot to say this time. I totally understand if it’s too long to get through, thanks for reading this far.

I need medications to stay stable.

Medications come with side effects.

Side effects make it difficult to continue taking the medications.

I need medications to stay stable.

The Abilify really really helped me. It kept the suicidal thoughts tame enough that I could handle them most of the time. An extra 50 lbs later (more than 50, who am I kidding), I couldn’t continue taking it anymore because my weight and the fact that I gained it all back, was making me suicidal. It seemed dumb to stay on a medication to control my suicidal thoughts when the side effects were making me suicidal.

Around the time we were taking me off of Abilify, I started using medical marijuana. A few different doctors and my therapist had mentioned that it might help with this and that, and I figured it wouldn’t hurt to try.

It helped a lot once I found the right strains, I found that keeping a very low buzz was just enough to make me able to focus on work, I got more done in that few weeks than I had in awhile. It was easier to do the things that needed to be done, but at the same time I was facing a lack of motivation. I felt less anxious. I was sleeping better. My pain was almost completely controlled.

And I was eating the house again, because, munchies are a real side effect of marijuana. What’s the point of stopping a med that makes me eat too much, just to replace it with a med that makes me eat too much.

So I stopped it.

But now the lack of focus is back, the anxiety is back, the difficulty sleeping is back. My pain is back, too.

I’m on a few different medications for pain. The one I take every day is an anti-inflammatory. It helps, but not enough.

Earlier this year my primary put me back on Oxycodone, not necessarily daily, but on an as needed basis. It helps, a lot, but also I’m hesitant to take it. I didn’t need it at all when I was using marijuana. But now that I’m not using that, I’m instead falling back on the Oxycodone. It scares me. I was on it daily (actually, multiple times a day) a few years ago. I absolutely feel like dependency on medication isn’t always a bad thing (I’m dependent on my psych meds), and I absolutely feel that withdraw is something that happens with a lot of meds (stop taking a psych med cold turkey and you’ll see what I mean . . .actually, don’t do that.) Dependency on narcotics feels like a whole different ballgame. Maybe it is, maybe it isn’t. I don’t really want to go there, so I use it super sparingly.

I’m falling back on my Ativan more often, because it controls the overwhelming anxiety. Ativan is another one I’m super careful with. A thirty day script will often last me 6 months or more. But right now, because of the whole 2020 thing, I need it more often, and I don’t like that.

Oh, and I should mention my antidepressant and those side effects. It causes nausea. It’s bad enough that some nights I actually get sick a few hours after taking it. We’d like to increase it because it could probably work a bit better. But increased doses cause more nausea. What is worse, living with low grade depression constantly, or being miserable after taking the medication to treat it.

I’m stuck in this trap. All of the medications have side effects. Figuring out which side effects are worse than the ailment they’re treating is a constant conversation within myself and with my doctors.

I’m frustrated. I want solutions that don’t cause more problems.

I need medications to stay stable.

Medications come with side effects.

Side effects make it difficult to continue taking the medications.

I need medications to stay stable.

Hulk Smash

This is a Really Real Mental Health post.

Anger.

Coursing through my blood.

Irritated.

Through every fiber of my being.

The whole day just snowballed against me. The littlest things setting me off.

Except, it was all internalized. Nothing was said other than a quick “I’m grumpy today.” But beyond that, the anger just stayed in my head.

Spinning round and round, like a tornado, finding more things to suck into the vortex. I just wanted to scream and lash out, but I also knew that wasn’t rational. I knew it wasn’t actually anything that was happening around me.

I was just angry.

The inside of my skull was so so loud. Scripting fights, scripting explosions, scripting a loss of control.

But I controlled it, kept it deep inside.

We got home and I climbed in bed.

I kept trying to think of DBT skills that would help, and I could feel them, just outside of my reach, just beyond my grasp.

I was afraid to get up and go for my book, because it felt like the anger would eat me alive. It felt like I would lose the battle to keep it all inside.

So I stayed in bed. Fuming at everything and nothing.

Finally I dosed off, powerful angry dreams haunting me in my sleep. I woke up a few hours later, Wonder Woman asking if I wanted to get up so that I could sleep that night.

I opted to get up long enough to take meds (mother fucker, they had to be put together again), take a few ativan and a meletonin, and go back to bed for the night.

I slept straight through.

Today I’m not so angry. Today I can look back from a place of calm and see what went wrong.

The Abilify is totally out of my system now, a few weeks after I stopped taking it. And for the first week or two, I was smoking medical marijuana. It did a great job at lowering my reactivity off of the medication, but then I realized it was making me eat the house. Which was the whole reason I went off of Abilify.

So I stopped that too.

And now I’m left wondering if this anger could become my new normal.

Anger makes people die.

Today I’m tired, melatonin and a higher than normal dose of ativan will do that.

I’m tired. But I’m not angry anymore.

Anger is the most likely to make me lash out. Anger pulls me apart. Anger feels like it’s going to split me at the seams.

Anger is wrong. Anger is the one emotion I wish I could stop feeling, forever.

Anger.

Six Months

This is a Really Real Mental Health post.

So, I’ve been really torn about writing this. It seems silly to celebrate something that most people just, do. But it also feels like a really big deal, to me.

As of this week I’ve been working for 6 months.

I’m fighting the urge to minimize. Fighting the urge to say “I did it, but . . . “

But, the truth is, this wasn’t possible for a long long while. This wasn’t within the realm of my abilities. I could barely make it to doctors appointments, and then I could barely keep up with school work, and then I could barely keep up with volunteering. I wasn’t sure I’d ever be able to work again.

And now, I struggle, I take mental health days, I’m not always at my best, but I’m holding down a job.

I’m working like a real adult.

And still, in the back of my mind there is the not-so-quiet voice telling me, I’m only kind of doing it. I work from home, I work for family, it’s just part time.

It’s not a real job.

I haven’t done anything special.

But also, I have.

Working is scary. Working is hard. Working leaves room for failure and mistakes.

Sometimes, working sucks.

And yet, I am.

I’m doing the thing.

It’s taken me a long while to get here, but I’m doing the thing.

Where’s My Roller Coaster?

This is a Really Real Mental Health Post.

It’s been 2 weeks since I’ve written. Now granted, time is going super fast, so it feels like less than that, but it really has been 2 weeks. I wrote daily for a long time, I wrote at least twice a week for a long time. Now I’m lucky if I write every couple of weeks.

Part of it is Covid. Nothing exciting is happening in my life. It’s the same shit, different day, different week, different month.

But a bigger part of it is that I’m just stuck in this low grade, constant, depression.

I miss my roller coaster. The monotony of day to day life with mental illness was broken up by constantly changing levels of mania and depression.

Good news: we stopped the rapid cycling.
Bad news: we stopped the rapid cycling.

Mental health was an obstacle course before. Making it through this episode just long enough for the next one to kick in. It was exhausting, but it was interesting.

Now my mental health is a long marathon. Just keep functioning at some constant level, reserving energy for the long haul.

The benefit to the obstacle course was that the adrenaline, kept me going, The hypomania and the influx of serotonin that it brought, kept me going.

That said, I read the posts I made in years past and I know that it wasn’t all that comfortable riding the roller coaster either. The suicidal thoughts were worse (and more dangerous) during mixed episodes. The hypomania brought along poor decision making. The lows were so dark, so so dark.

But, this version of stability is its own type of difficult.

I mean, I should be thankful that I’m stable. The suicidal thoughts are fleeting. I’ve held a job for close to 6 months. I’m not constantly in crisis.

But I’m also depressed enough that I’m often doing the bare minimum. Just enough to get me through to the next day. I can’t seem to find the will or the energy to do more.

I have enough work available to easily pull 20-30 hours a week. Yet, some weeks I’m lucky if I do half that.

And it isn’t that I don’t want to. I sit here stuck. I want to work, I know what I want to work on, but I just can’t find the energy to actually do it.

And it’s not just work, so it’s not just that I’m avoiding that.

I have a list of cards to make for friends. The list was made in April and May. It’s July. I’m still only part way through this list.

Side note for those that requested cards, they will make it to you eventually, I promise.

I sit here, aimlessly scrolling facebook. I want to craft, I want to game, I want to do SOMETHING, but I can’t find the will or the energy to start.

This is hard. A different kind of hard than constant crisis.

I miss my roller coaster.

Just hold on

This is a Really Real Mental Health Post.

TW: Talk of suicide, including plan. Talk of weight/weight loss/weight gain.

There’s so much in my brain and I don’t know where to start. This ended up being super super long, but I need to get it out. Words of encouragement and understanding would be greatly appreciated.

Last night was really, really hard.

It started with boredom. None of my usual activities were grabbing my attention. I tried pushing through and making myself start something anyway. Just start, just design one card, just complete one quest, just plan one dish.

Just start something.

But I wasn’t able to. So slowly I felt myself drifting towards bed. Once there I couldn’t even bring myself to turn on the TV.

Laying there my mind was wandering. Is this the medication change, it’s supposed to make me less flat and sometimes it just doesn’t seem to be doing that. It’s supposed to help me eat less, and I thought I was, but yesterday morning I had gotten on the scale, and I gained another 10 lbs.

Inching ever closer to my heaviest weight. A weight I swore I’d never reach again. I worked so so hard to lose so much. Even at 300 lbs I was proud of my body and what it could do. I felt accomplished at the gym. I was far more at peace with my body, even though I still had a lot to lose.

I spent months working towards bariatric surgery, for the 3rd time, and right as I cleared the last hurdle, they thought that emotionally it could be very dangerous for me to move forward. I walked away from the program on the day I was supposed to set a surgery date. I still don’t know if it was the right decision.

That was when this latest weight gain started. I had already stalled with losing, due to the medication increase, but then I started gaining. We increased the medication more, and I gained more. First I noticed 10 lbs, then a couple of months later there was another 10. Then in the first couple of months of quarantine it just kept going up and up and up.

And as much as the numbers suck, even worse is that I’ve lost my ability to walk as far as I used to. My pain is worse. I get out of breath just getting adjusted in bed. Walking up to my second floor apartment feels like running a marathon.

I don’t feel proud of what my body can do anymore. I spent almost 2 years celebrating accomplishment after accomplishment, and now I’m back to living in my desk chair barely able to hold myself up.

And last night it crashed down on me. Weight is such a huge trigger for my suicidal thoughts.

It started with a quiet whisper. “You failed again.”

Then a little louder. “You’re right back where you were, fat and useless, and no matter how hard you work, you’ll always end up back here.”

With a little more force, “You’ll never overcome this, it’s not worth trying anymore, it’s not worth living.”

In the back of my mind I started telling myself. Get up, get dressed, go for a walk. You don’t have to give in to this.

“See, you can’t even do that, can’t even bring yourself to work on this. You’re such a fat failure and you’re just taking up space. The world would be better off without you in it”

Then the quiet voice again. Please, just get up, put on shoes, and walk. You don’t even have to change out of your pajamas, just get out of bed and walk.

There was a back and forth battle between the voice that wanted me to die, and the quiet voice trying to stand up and help me live.

I came out to the living room and checked some pill bottles. I don’t have enough of this, this, or that . . of course we keep most of it locked up, but maybe, maybe if I take all three different ones.

I started hoping that Wonder Woman would go in the other room. Go into the bathroom, so that I had enough time to take what I had. I know she’d notice if I took the pills into my room, and she’d definitely notice if I took them right there. I just needed to take them and go to sleep. Hopefully I wouldn’t wake up.

It was a calm sort of suicidality . I wasn’t afraid, I wasn’t rushed, I was just waiting for the right moment.

Just waiting in bed and listening for the moment when she got up from the sofa.

Quietly waiting.

Instead I sent her a text. A that small voice fighting to live. “I’m calmly but intensely suicidal tonight.”

She asked how she could help. I didn’t have an answer.

Eventually, I heard her get up. I was waiting to hear the bathroom door. It would finally be my chance. But instead she turned off the lights and came to bed. We talked.

I told her my plan.

She locked up more meds, and I felt like a child in need of a babysitter.

And then I felt defeated. I felt, and still feel, like there’s no way out of this mess I’m in. This mess that is me.

We went to the store this morning. She reminded me that I had to stay alive to cook the food we were buying. I felt the voice slowly fading away. Slowly backing off.

I’m worried that these thoughts are because we’re lowing the medication. But staying on such a high dose is just going to exacerbate my weight problems. It’s nearly impossible to lose weight when the intense craving for food feels like a drug addiction. I can not adequately explain the drive to eat that has been occurring the last 6 months or more.

And you can’t just quit food cold turkey.

I don’t have any answers. I don’t have any uplifting ending to this post. I don’t have any feel good words.

I just have me, feeling like I don’t want to continue to fight.

I just have me sitting here, getting my words out on the screen so that they don’t eat me alive.

Asshole Brain

TW: Suicidal Thoughts

This is a Really Real Mental Health Post.

My brain is an asshole sometimes.

Last night was one of those times.

Stuck in bed at 9pm, unable to fight my way out without help. Brain beating me up for everything I might have done wrong in the past months. Brain beating me up for my weight, my lack of motivation. Beating me up for existing.

Not wanting to exist any longer.

The suicidal thoughts were fleeting, but they were there, quietly humming in the background under a very loud chorus of self loathing.

I hate my body. I hate my brain. Sometimes it feels like I hate life.

Even though life isn’t all that bad, really. I mean, the world is going up in flames, but my own little bubble isn’t all that horrible, considering what my past has looked like.

Isolation is getting to me.

We were supposed to get out of the house today, taking a break from these four walls to visit someplace that wasn’t a necessity. Getting some fresh air. I was hoping for it, looking forward to it. And instead it’s going to storm.

I guess we’re staying home again.

These four walls are exhausting.

It doesn’t help that I’m hurting. Whatever is going on in my chest is this constant dull roar seeping it’s way into all areas of my life. While the hospital ruled out the most dangerous things, I’m still worried.

I’m still scared.

I’m still anxious.

I’m still feeling lethargic, unable to do much of anything before I’m exhausted.

Which makes me climb in bed.

Which allows asshole brain to speak up again.

Hello my old friend.

It’s almost, in a strange way, comforting to hear the quiet hum. Comforting in the worst sort of way.

It’s what I know. It’s what I’m used to. The constant roar of my trains of thought, underlined by the hum of wanting to die.

It’s also scary.

My doctor called in a med that, in high enough doses, could kill me. It took everything in me to speak up and tell Wonder Woman that she needed to take the pills when I pick them up, handing it out small numbers at a time, so that I don’t have access to it.

Another pill bottle in the safe.

I wanted to hold onto this one. Comfort myself with the knowledge that a way out was right there.

But that just makes the hum louder. It makes it more real.

It’s dangerous.

I have to be protected from my own asshole brain.

I have to be protected.

I have to be.

Four Years Ago Today

This is a Really Real Widow Post.

TW: Talk of Suicide including method and post death graphic stuff.

Four years ago today.

Four years.

My new normal started 4 years ago today.

I still replay the movies in my head. I remember waking up earlier than her.

I remember going in to wake her up so that I could bring her something back for breakfast.

I remember the way her skin felt, that eerie cold that didn’t feel quite right. I knew the second I touched her that she was gone.

I remember the rigidness of her limbs.

I just knew.

I remembered hearing the rustling of her pills the night before. I thought she was just taking her night time meds. The bag that held her medications was empty. She took every last one of them.

I remember sending a message to my closest friend and neighbor, asking her to get Draven out of the house while I was on the phone with 911. I didn’t want him waking up to the chaos. I wanted him safe from the new reality.

I remember making phone calls that changed lives forever.

I remember sitting in my desk chair lost, numb, unsure of how to process the way my life was changing.

I remember my mother sitting here, strangely she was up from Florida, strangely she was going to take me to breakfast that morning, strangely she came into the house as the first wave of paramedics did.

I was so thankful she was here.

I remember taking a drive, to Burger King, to get us out of the house as the coroner took Parker’s body out.

I remember ordering food that went uneaten.

I remember being thankful that Draven already had therapy that day, and that I was able to get in for my own appointment.

I remember crying more tears then I ever thought possible. The feeling of my eyes being so raw from wiping them.

I remember.

Four years.

Four years ago today.