Sentenced to Life

Please note that this was written two weeks ago and I feel better.

Last week I had a much needed ECT. When I awoke from the short procedure, I felt strange. Usually, I have a terrible migraine, I’m confused and fatigued, but this time I was alert, I knew what had just happened and there was no sign of a migraine. Good, right?

During the two-hour drive home, I kept thinking that it was amazing that I didn’t feel like crap. I looked over the papers the hospital gave me and saw that I had a short, 42-second seizure, which is good — the shorter, the better. But something was bothering me.

It’s now been several days since the ECT. I don’t feel as different as I’d like. I don’t have much energy, I’m not as optimistic as usual and at times I’m just sad. I hate to say it, but I don’t think this treatment worked. It’s happened before — the ECT leaves me feeling no different or actually worse, but it’s rare. It scares me, because getting treatments is the main part of my treatment plan. I rely on them to feel better.

This is just a very sad reminder that I’ve been sentenced to life with major depression/anxiety, and there is no cure. I’m treatment resistant, meaning most medications won’t help. Therapy, ECTs and behavioral modification are the only things keeping me from slipping back into a depressive episode. And I’ve worked too hard to go back.

I don’t mean to be gloomy. Maybe it’ll take a week before I feel better. Maybe I’ll have to work harder on self-care and turning to healthy coping mechanisms. I hope to hell I don’t, but maybe I’ll need another ECT before the next one scheduled in eight weeks. Maybe that one will work.

It’s just hard not to feel betrayed right now. I hate getting ECTs, but I continue to get them because I know they help make me a better mom, wife and friend…they usually help, anyway. But this time was different — I feel bamboozled. I went to all that trouble for what? To still feel out of gas and like there’s nothing to look forward to? I hate my brain! Even if I do (most) everything right, my efforts are thwarted. It just doesn’t matter, my brain’s gonna do what my brain’s gonna do. And that, my friends, is depressing in itself.

I’ll give it a few more days. I’ll do my best, practice self-care, go to therapy. I’ll drudge on, but I have a feeling I’ll be making another trip to San Antonio sooner than expected. And that’s OK, if the next time works.

But what in the hell will I do if it doesn’t?

I can’t really entertain that thought, because it’s so suffocating. I feel the urge to stomp my foot like a child and scream, “It’s not fair!” Because it sure the fuck isn’t.

It’s just not fair.

All About ECT (Electroconvulsive Therapy)

I’ve had a lot of questions about ECT (electroconvulsive therapy) lately, so I thought I’d talk about it more today.

I’ve been doing ECT treatments since 2019, after I stayed at the Menninger Clinic for six weeks. My doctors all agreed that I was treatment-resistant, meaning most depression medications would be ineffective in helping me, and ECT has a high success rate.

I’ve had about 30 treatments, and I can honestly say they have changed my life for the better. I have more energy, more patience, I’m not sad as often, and I’m able to function pretty well for a girl with no serotonin, lol.

I now do my treatments at the Laurel Ridge Treatment Center in San Antonio; there are no doctors who do them in Corpus Christi where I live.

When I arrive at the treatment center, I fill out paperwork on how I’ve been feeling and whether I’ve been suicidal. I talik to the nurses and PA, discuss the depression symptoms I’ve experiencing then they move me to a bed. A nurse then puts in an IV and they give me medication for nausea, just in case. Next, they wheel my bed into the treatment room where an anesthesiologist, a doctor and nurse are waiting. They attach electrodes to my forehead and temple, then add a blood pressure cuff and pulse oximeter. Usually at this time, my blood pressure gets higher and my pulse races because I’m scared, even though I have no reason to be.

The docs chat with me for a bit and then they put me under anesthesia. After I’m out, they put a bite guard in my mouth and give me the oxygen mask. The nurse starts up the ECT machine which will send electric pulses to my brain, triggering a brief seizure. They also give me a muscle relaxant, so I’m not moving a whole lot. Once the seizure is started, they wait for my brain to stop it. My brain works hard to stop it as fast as it can, but sometimes the docs have to administer medication to stop it. The shorter the seizure, the better the outcome I usually have. This past ECT I had a 42-second seizure but I’ve also had ones that last up to a minute or longer.

After the seizure, I’m sent to a recovery area. It usually takes about 20 to 30 minutes for me to wake up. After I’m looked over by the nurses, I’m free to go home. I usually have a killer headache, so I get something to eat, take my migraine meds and sleep on the way back to Corpus Christi.

I can see how reading this would surprise some people — one person described it as barbaric after I explained the treatments, but it is not barbaric. For someone like me, it’s life-saving, and even though I don’t like getting them done, I’m grateful for treatments.

ECT helps as many as 80-85 percent of patients who receive it and is the most effective treatment option for those who are treatment-resistant.

Most people have an initial course of ECT then do maintenance treatments every now and then. I haven’t gotten to the point where I don’t need them, so I go every four to eight weeks. I’m working on stretching out the treatments, and maybe one day I won’t need as many.

I hope I haven’t shocked you — haha, get it? If you’d like to know more, please leave a comment on email me heatherannloeb@gmail.com

Low Battery Mode

Note: I wrote this blog a couple weeks ago and have since had an ECT treatment.

It started yesterday — irritability, moodiness and the urge to overeat. I attributed it to lack of sleep; Eli had woken up at 3 a.m. and hadn’t gone back to bed, which meant I didn’t go back to bed. I thought if I just get some good sleep I’d be fine, but this morning, I could feel it — thick fog around my brain, heavy weight on my shoulders, more irritability and wanting to just go back to bed.

I thought, “Great, I’ll have to get another ECT before I’m ready.” I’m trying to go at least eight weeks without one. I was totally preparing to power down to my Low Battery Mode when I thought to myself that I should get on the treadmill and spur some endorphins. It was the first time I’d ever worked out for my mental health and not to lose weight. I didn’t stay on the treadmill long (my kids drained my Air Pod batteries) but I instantly felt better, not all the way better but better. Not bad for a girl with no serotonin.

I still have the urge to binge and to get in bed for the better part of the day. That’s where my Low Battery Mode comes in, like I talked about on my Spoon Theory post. I only have so much energy, even when I’m not feeling depressed. Unfortunately, that means I’ll have to depend on my husband more and housekeeper. I say unfortunately because my husband already has a lot on his plate and I never want to be a burden. So, I’ll ask for help when I need it. I’ll take more breaks than usual. I’ll force myself to drink more water and back off the Diet Cokes. I’ll get a pedicure. I might even take a (short) nap. I’ll do what I have to do to feel better, because I HATE getting ECTs. It should be a last resort on my treatment plan, not just a quick fix. I hate feeling like I’m waving a white flag in defeat to my depression. I want to fight, I have to fight it. I just can’t let it win. And if it turns out that I do really need an ECT, I’ll concede because that’s what’s best for my family and me. But I still want to fight. I’ll have to fight my brain and not give into unhealthy coping mechanisms that seem so much easier to do than healthy ones.

Last night, I wanted pizza for dinner. We don’t usually eat pizza, we usually cook or get takeout from Asian restaurants. But I wanted pizza. I thought that it would just be a treat because I had a bad day and sometimes you just have to treat yourself. But when you’re dealing with an eating disorder, it’s a slippery slope. And I sure did slip. I purposely ate too much and then binged on my kids’ candy stash. I felt so sick, and despite feeling so badly, I still planned on getting donuts in the morning before dropping off the kids at school.

It’s the instant gratification that I’m always seeking. I hate being uncomfortable, so I turn to my bad habits for that temporary release.

But today is a new day. Instead of feeling overwhelmed and anxious about my mood, I actually feel optimistic. I didn’t just say, “Fuck this day!” and give myself carte blanche to binge, etc. I made myself get on the treadmill. I made myself sweat and think about how much better I would feel afterward. And that, my friends, is progress. It’s a huge step for me. I KNOW what to do to stay healthy, I blog about it all the time, but honestly this is one of the first times I’ve actually taken my own advice. It’s hard when your brain is telling you to do the opposite, but I did it. I won a battle against my obstinate brain.

I might still have to power down a bit, but that’s OK. It’s self-care. It’s a survival mechanism, a healthy one.

So, I’ll keep on fighting and surviving — it’s what I do best.

I Hate My Brain

Ever have a long day and think to yourself you deserve a treat? So you get ice cream and start to feel better? That sounds normal to me. My problem is that I think I deserve a treat multiple times a day. I constantly want to feel good. To feel happy. I compulsively eat to get that high and, enjoy that “treat.” Then I feel sick. After I’ve recovered, I look for another treat, forgetting how sick I felt earlier. It’s a vicious cycle.

I do this a lot but especially when the kids are away at my mother-in-law’s. I tell myself that I need to relax, enjoy the quiet and that I need to feel good. Last night, even after I had a big dinner, I sat there thinking of what I could eat that would make me feel good. And I even tried many things, despite being uncomfortably full already. M&Ms didn’t work. Neither did peanut butter crackers, ice cream or SweeTARTS.

But there is nothing I can eat that will make me truly happy.

Now, I’m trying to give myself a break because I am in need of an ECT treatment, which is scheduled for Friday. Usually the week before treatment I run out of gas, and I try to cope however I can. BUT this doesn’t just happen in the weeks leading up to treatment. This happens all the time, even when I’ve just had an ECT.

So I pose this question, “Why do I feel the need to be happy all the time?” Honestly, that question was asked by my therapist last week. She following up with, “Can’t we sit with other emotions? Nobody is happy every minute of the day.”

And she’s right. We don’t need to be happy every minute. I think my problem is that I HATE being uncomfortable, so I’ll do anything to push those negative emotions aside. Emotions like anxiety, stress, anger or sadness. It’s clearly not working for me to ignore these problems, and even if overeating has helped in the past, it sure as hell is not working now.

This may sound strange, but I think I need to acknowledge and honor whatever feelings I’m having. Maybe I need to grab my journal whenever I’m feeling negative emotion, talk about what’s going on and then release that feeling. I don’t know.

All I know if that I need to stop coping by bingeing. It’s made me gain a bunch of weight and really, aren’t I just eating my emotions?

Sometimes I really hate my brain, which I hold responsible for my debilitating-at-times depression and anxiety. I hate that it doesn’t respond to other treatments. I hate that my mental health is so precarious, and I resent that I have to be so careful as to not disturb it. I hate that happiness seems so fleeting at times. I’m not a big fan of my eating disorder either.

I don’t like to say hate; It forces a dichotomy with the idea that I should love and respect myself. I’m trying really hard to love myself, even almost 30 pounds heavier and a handful of mental disorders. But I feel betrayed by my brain. I know I need to reconcile those ideas. I know there is more benefit in loving all of me. I’ll get there. Despite everything that my brain has thrown at me, I’ve only become stronger. Take that, asshole.

And there are times that I think God made me this way because He thought I could handle it. I can, and I will. I remember this quote: “Your talent is God’s gift to you. What you do with it is your gift back to God.” I don’t mean to sound haughty, but maybe He knew I would use my voice and (hopefully) help others through my writing. That’s why I can’t stop blogging so much about mental health; there are so many who feel alone and haven’t found their voice yet. I certainly don’t mind lending mine in the meantime.

I guess my brain is just as much a blessing as a curse.

In a Nutshell: My Week in Review

I hope y’all are doing well. It’s been awhile since I posted an update, so here goes. First of all, I want to wish everyone who celebrates a Happy Easter. We’re Jewish but we still do an Easter egg hunt and the Easter Bunny drops off goodies in their baskets.

This past week was a little trying for me. I’ve had an ECT appointment scheduled for next week, which is the eight-week mark. I really thought I could push past eight weeks but I’ve noticed I’m more irritable and my temper is shorter than normal, so I should probably just do it. It’s hard for me to admit that I need one because I hate them so much. I really dislike going under anesthesia; it makes me anxious and scared. My pulse quickens and my blood pressure goes higher than normal, and I have to use all the strength I have not to start bawling and begging to get me out of there. I know it doesn’t make sense — I’ve had almost 30 treatments, and I’ve never had a bad experience. But that’s just how it is. Anyway, I’ll try not to focus on that this week; I’ll just think how much better I’m going to feel and what a difference it’ll make.

In other news, tomorrow (Monday), one of my latest columns will be printed in the Corpus Christi Caller-Times. They’re letting me write some more mental health columns, and I’m hoping it turns into a regular columnist job — it would be a dream of mine. So if you’re not too busy, go to Caller.com tomorrow and check it out.

That’s it for now. I hope you guys have a happy, healthy week.

Stay in the light.

Favorite Products That Help Me Keep My Chill

I’ve really been focusing on self-care lately. My goal is to space out my ECT treatments to eight to 12 weeks, so in between sessions I need to step up my self-care game. That includes exercising more and eating a healthy diet. It also includes taking advantage of the little things at home that add up to a lot when you’re trying to take care of yourself. Remember, self-care is not selfish — it’s necessary.

Below you’ll find my favorite things around the house and products that help me keep my chill and decrease anxiety.

My favorite books — I don’t get to read much these days but when I do, I usually go for a book I’ve already read. There’s no mystery, no twists and turns to upset my anxiety, just my favorite characters and their stories. I’d also add The Red Tent to this list — that’s another of my faves but not an easy read. You’ll also see The Big Activity Book for Anxious People, which always helps me feel better. It’s not a boring workbook, it’s a hilarious take on how to calm down and I love it.

Lauer Under Eye Patches — I found these on Amazon , and I really like them. They’re inexpensive but feel so good under my eyes after a long day. They feel cool to my skin, and I think it helps minimize some of my lines. It definitely helps with puffiness.

Not Your Mother’s Butter Masque (Green Tea and Apple Blossom) — I follow the Curly Girl Method for my hair, so after using my conditioner on my curls, I put this hair mask on and it makes me hair feel so hydrated and helps with the curls. The mask is inexpensive and can be found in a number of places. I use Target and Amazon.

OPI Nail Colors — I went more than a year without going to a nail salon, so I quickly learned to do my own manicures. Every few days, I change the color and it makes me so happy to see all the bright colors. I recommend getting a cheap manicure set and buying your favorite colors. Definitely get a Base Coat and a Top Coat, too.

Sephora’s The Peeling Mask — This a disposable face mask that you do for just a few minutes, but I love how relaxing it is to lie down with this mask on after the kids are asleep. It brings a touch of luxury to my day that’s usually not luxurious at all. The mask is under $10; I usually find it for $4.

Candles — In the past I’ve never been able to tolerate candles, because fragrance can cause migraines, but I’ve been able to use more, sometimes every day. I love waking up in the morning and lighting a candle while I’m getting the kids ready for school. It’s calming and certain smells can definitely reduce the amount of stress you feel and decrease anxiety. My fave candle right now is Cactus Blossom from Bath & Body Works. The three-wick candle usually sells at $24.50, but they have sales quite a bit.

Slippers — When we moved to the new house, my feet started hurting from all the back and forth I was doing while organizing. I put on a pair of Ugg slippers and rarely take them off. They are so comfortable! Sometimes I forget I’m wearing them and accidentally leave the house in them. I love that they have a strap around the back and how cushy they are. They are expensive but in my opinion, they’re worth it. I love putting my comfy clothes on at the end of the day and sliding into my slippers. I feel it helps me relax better.

Soft Touch Foot Peel Mask — This is another Amazon find. I bought it after I saw a video of a woman peeling off dead skin after using the peel mask. It was so satisfying. What you do: put the mask footie on your feet and leave on for an hour. Then you wash your feet off and in a couple of days your feet will start to peel. Not only is it fun to peel them, but it leaves your feet so soft. I used these every few months. It was especially helpful because I couldn’t go to the nail salon for a pedicure. It’s affordable too — about $20 for a two pack.
Udderly Smooth Hand Lotion and Body Cream — The lotion is no joke. I use it on my hands (and sometimes my feet) and it makes them feel so soft, and I hope it’s helping all the wrinkles on my hand. I have old lady hands. But this stuff goes on and makes your hands soft like buttah. It costs $16 for a 12-oz pack of two.

Dr. Teal’s Pink Himalayan Bath Foam, Body Lotion and Salt Scrub – I LOVE the smell of the pink himalayan salt. It smells so good, and I instantly relax in the tub when I use the bath foam. There’s nothing like taking a long hot bath, using the bath foam and the salt scrub. Followed by the lotion. It makes me feel like I’m at a spa. None of the products are expensive. You can find them at HEB, Target and Amazon. I heard the lavender fragrance is good, too but that’s an instant migraine trigger for me.

Last but not lease — Karribi Paint by Number Kit — I thought doing a paint by number piece would be relaxing and help me to focus on something other than my anxiety. I love putting my headphones in and painting these kits. There are several kits that have birds, so I bought all of those. It’s relaxing, it gives me some uninterrupted “me time” and I get a beautiful bird painting afterward. I highly recommend this for anxiety and stress. It looks like Amazon no longer carries this particular kit, but there are tons of paint by number kits for adults.

I am in no way being paid for these endorsements — I just wanted to share what goes into my self-care routine. If you want to add anything, please feel free and drop it in the comments. I’m wishing you all good health and peace. Thanks for reading.

Stay in the light.

I’ve Gained 26 Pounds

Last Friday I had an ECT treatment. I hadn’t been there in four weeks, so they asked to weight me (to calculate how much anesthesia I get). Usually, I avoid the scale. The number shouldn’t matter to me, but it does. Big time. I looked down after I stepped on the scale, and I was shocked. I’ve gained 26 pounds since the pandemic — 26 POUNDS! I’m almost 200 pounds, which I swore to myself I’d never be again. I mean, who has weight loss surgery and doesn’t lose the weight? Me, apparently.

I have all the reasons in the world to lose weight and be healthy, mainly my kids. I want them to see me be healthy so that they can be healthy. I want to lose the weight because I want to live a long time. It would benefit my mental health greatly if I maintained a healthy lifestyle. But I don’t.

Even after my ECT, while feeling happy and more stable, I had the intense urge to overeat and binge. And I did. The ECT is supposed to reset my brain. Last week, I was so depressed and even had suicidal ideation, so I needed the ECT. But the ECT can only take me so far. I’m responsible for making health decisions for myself. And I need to hold myself accountable. At some point, I have to make the effort to be healthy without expecting something or someone else to help me.

I don’t know what drives me to overeat or binge. It sort of makes sense when there’s conflict in my life, and I feel the need to be comforted by food. But right now, there’s no conflict in my life. There’s no logical reason for me to shove food in my face. It bothers me so much that I don’t know why I binge, and I’m not sure it would even help if I did know. It’s just frustrating. And I know it’s a hard time because of the pandemic, but we’re not getting back to any kind of “normal” I know any time soon. So, it has to be now. I have to make changes now. But honestly, I don’t know if I will. I don’t know what it will take.

I bought a treadmill that will be delivered this week. I bought a food journal to help me track my water and meals. I have a brand new pair of running shoes to use for exercise. Conditions are favorable for change. My brain, my stubborn brain, is the only thing holding me back. Even now, as I’m typing this, I want to eat, to be comforted. To lose myself in the taste and texture of something delicious. I fear my urge to escape the real world will be permanent, as it manifests in other ways, too like abusing my anxiety meds. And again, I don’t know why or what I’m trying to escape. I have a great life — better than most — and I’m so grateful for everyone in my life and everything I have. So, I really can’t tell you why I want to escape.

At one time, I thought it was emotional pain that was holding back — trauma from my past. But I feel like I’ve dealt with that. I’ve talked to my therapist about it extensively. I wrote a blog about it that I will never share. I got if off my chest, but still the pain resides. At least, I think so. Why else would I be trying to fill this unrelenting void?

I so want to be able to wake up in the morning and not immediately think about what I’m going to eat. To plan my next meal, as I’m licking off my current meal’s crumbs from my lips. I live meal to meal, snack to snack, and I hate it.

I hope this week I can make changes to my daily life and incorporate healthy habits. I pray for strength and guidance. I pray for what feels like a miracle.

Next week is National Eating Disorders Awareness Week. It may not seem like a big deal, but there are 30 million Americans who suffer with an eating disorder. There are so many people suffering right now, who are suffering more because of the pandemic. Only 1/3 of people receive help for their eating disorder. Eating disorders have the second highest mortality rate of any mental illness, with nearly one person dying every hour as a direct result of their eating disorder.

If you are struggling with an eating disorder, please know that you are not alone. It’s a challenging time for us, but it’ll be OK.

We will be OK.

In a Nutshell: My Week in Review

I’m proud of myself this week. I had to move up my ECT (to this past Friday) because I quickly became depressed after the last one, which was four weeks ago. I hate getting them, but I knew I needed it. I went into survival mode last week (and had to cancel plans) and made it to Friday.

I was more nervous about this one, but I don’t know why. When we got to Laurel Ridge, I started pacing in the waiting room. Luckily, there was only one girl ahead of me, so I didn’t wait long. But when a bed was available, the nurses couldn’t get my IV in. This made me incredibly nervous. I was afraid that they would do a bad job with the IV, then I wouldn’t get all the anesthesia I needed. I know that’s not likely, but that was the thought racing around my head. One of my favorite nurses finally got it, but to be honest I had shed some nervous tears. I tried to chat about my kids to take the focus off, and it helped.

When I went into the room, everyone was really nice and accommodating because of my anxiety and I had a good seizure — 72 seconds long. I was told the shorter the seizure, the better, but looking at my records, all my seizures are kinda long, over a minute. One was two minutes long — after that seizure, I was doing very well and was able to go nine weeks without an ECT. So, who knows. I am keeping a notebook where I’m documenting my symptoms a week leading up to an ECT and immediately after. I think it would be helpful to find patterns or correlations.

Enough about that. My birthday is this coming Saturday, so I’m looking forward to that.

That’s really all I got for now. Y’all have a good week, and stay in the light.

Cancelled Plans and Spoons

I’ve had to cancel plans with three different friends this week. I HATE cancelling plans — it makes me feel so guilty, because I feel like I’m letting my loved ones down. I know I can’t help it — and my friends are very understanding — but I still feel guilty and less of a friend.

At least now I can tell them the truth — I’m too depressed to leave the house. Before I went to The Menninger Clinic, I didn’t tell the truth, and I probably seemed like such a flake who didn’t care about spending time with her friends. But now, I’m honest. I said that I was having intrusive thoughts about suicide (not suicidal thoughts per se) and I just didn’t have the energy. I call it survival mode. You see, I’m getting an ECT treatment on Friday, so I just have to make it until then. The ECT should reset my stupid brain and maybe I won’t be so depressed and fatigued. I’m hoping that I won’t have as many migraines after this treatment, too. For some reason, my migraines have ramped up the past few weeks, and it’s been really annoying. I hate being limited by my illnesses, and on that note, I’m reminded of an article I read about the Spoon Theory by Christine Miserandino, who suffers with lupus. She writes about the physical and mental toll an invisible, chronic illness can take. And I relate.

While describing what it’s like to have a chronic illness, Miserandino grabbed spoons and used them to represent finite units of energy. Healthline.com writes this of Miserandino’s theory, “Energy, for many of us with chronic illness, is limited and depends on many factors including stress levels, how we’re sleeping, and pain. Miserandino then walked her friend through the friend’s normal day, taking spoons, or energy, away from the friend as the discussion went on. By the end of the day, her friend wasn’t able to do as much as she wanted. When she realized Miserandino went through this every single day, her friend started crying. She understood, then, how precious time was for people like Miserandino, and how few ‘spoons’ she had the luxury of spending.”

I feel this in my soul. Especially right now. I have to save every waking minute in order to do what is absolutely necessary, what I deem necessary, at least. This includes taking care of the kids and all their needs. This, to me, comes first. My remaining energy, if you can call it that, goes to taking care of myself. Many people would argue that it should be reversed, and I don’t totally disagree, but this is how it is right now. I hope to change it, because I know you can’t pour from an empty cup, and if I don’t start taking better care of myself, my cup will stay empty. I’m working on that, too.

It dawned on me this week that I could probably space out the ECTs more if I just put in the hard work of self care. I don’t mean getting a massage every week, although that would be nice right now, but I mean taking my medicine as I should, taking breaks and eating healthier. And actually sitting and exploring my emotions instead of burying them then stuffing my face. That happens a lot, almost every day. I also would like to increase my therapy sessions to twice a week — I have a lot to do, lol.

That’s OK though. I’m worth the work; I just need to remember that every single day.

Thank you to my friends who were so gracious about me. cancelling on them. I love y’all and appreciate your support.

Imaginary Brakes

Sometimes my anxiety runs rampant. I catch myself moving my foot as if I’m slamming the brakes in a car. I guess I want time to come to a screeching halt, as if I’m in the driver’s seat. But I’m not. It’s the out of control feeling I can’t stand. And though I have anxiety every day, Sundays are the worst, as documented here.

I’ve always hated Sundays from the time I was little, I guess because I NEVER wanted to go to school, especially on Mondays. I used to get a feeling of dread when I got older, too when I had a full-time job. The Sunday Night Blues or Case of the Sundays was always present, no matter what age or circumstance I faced.

And today, even though I don’t work outside the home, I feel it. The threat of responsibility looming is just too much to take and I feel the tightness in my chest and butterflies in my belly. It makes no sense to me — I don’t have anything unusual happening this week, nothing to be all doom and gloom about. But it’s there. At least, it’s consistent.

I try really hard to have a “countdown” methodology about anything — like countdown to Christmas, to the weekend, to my birthday, etc. So, as much as I’d like to look ahead to Valentine’s or my birthday, I need to be here, now. I look ahead at this week’s events, but that’s as much as I’ll let myself look.

It may sound silly, but as depressed as I am and how often, I get wrapped up in looking ahead and squander the perfectly good time I already have. I don’t want that. I don’t know how much time I have where I’m lucid and not depressed. I need to make hay when the sun shines, as my daddy says.

I still feel a nagging feeling in my belly, and I realize that I have an ECT treatment Friday. I wasn’t supposed to have it until March 5, but last week I felt the all-too-familiar signs of a depressive episode, so I moved my appointment up to stop it in its tracks. And even though I know it will make me better, I still get anxious and scared. Even though the past couple treatments have been pleasant. Even though…

Just thinking about it, I have a white-hot feeling pass from my head to my toes. It’s adrenaline, I think. And fear. I feel my foot try and stomp on the imaginary brakes and start to sweat.

Ugh, I’m not a stupid person. I should be able to address my fear and anxiety with the logic that I mentioned. Tears are threatening. I’m scared.

But come Friday, I will joke with the nurses. I will ask my favorite nurse to hold my hand while they put me under anesthesia. I will wake up 15 to 20 minutes later, not even knowing whether I’ve had the treatment. I’ll irritate David by (unknowingly) asking him the same questions over and over on the way home. I’ll get Chick Fil A on the two-hour drive and fall asleep until we reach home. I will be a better version of myself, a more patient and loving one. I’ll be free (for now) of self hatred and self judgement. And if that’s not the case, I’ll go back weeks later and repeat the same thing, always hoping to get the best version of Heather I can get, born out of fear and an induced seizure.

Whatever version, I know it will be a pretty perfect version of myself….just with amnesia and neurons that are unruly af. And hey, maybe the Sunday Night Blues will disappear for awhile. But I won’t countdown until they do. That, I refuse.