A year lost

“…Wherever you are is called Here,/And you must treat it as a powerful stranger”

“Lost” by David Wagoner

It’s been a year. 

Today. Today makes one year.

And while I celebrate surviving that year, I have to name it Lost. Taken or Stolen might also work but that victimizes my situation and I am not here for that–that allowance would keep me stagnant in anger and helplessness. I cannot be about that anymore.

Lost. Lost speaks truth on so many levels. Most obvious of those, ground floor entry so to speak, the impact of my battle with Long Covid sapped my energy and muddled my brain’s acuity leaving me with only faded and blurred watercolor memories of the last year. So many things happened–events, trips, the life of my family–and while I was physically present I was also encapsulated in a bit of a Long Covid forcefield shielding my mind from the details, the weight, the value and thus the fullness of anything.

Lost. Second floor. Abandoned by my sensibility. For most of the year, my emotions neutralized themselves. I felt no surges of excitement, sadness, anger, anxiety, joy…which sounds sort of great in some ways, right? No anxiety for the person who has always struggle with anxiety is pretty fantastic, yeah? And I guess in some ways it was a nice departure. My body was dealing with an erratically racing heart as well as so much inflammation and overwhelm that it could not also manage inflamed emotions. Rationally, I get that. But honestly, I just felt radically empty most of the time which is why I assume the year doesn’t exist in vivid memory. Without emotions to tie to events, to anchor them inside of me, they just sort of float off into the distance leaving a vague shadow behind.

Lost. Third floor. And this cannot be overstated and is far from the cliche it sounds like: I lost myself. What does that mean?

Well, it is hard to quantify and qualify in a way that relates the compounding weight of the truth of this statement. Most obviously, in losing my ability to be fully present, to feel vibrancy of any shade of emotion, to think without roadblocks emerging between each and every thought, to participate in conversation without confusion, to remember even the simplest but most important details (this list goes on a while, I’ll stop here), it was impossible not only to be myself but to remember what it felt like to be myself. I want to emphasize that. I wasn’t just less than myself due to illness–I have been there before. I suffer with other chronic “stuff”. But I was lost inside of myself–I could not remember what it felt like to be the person I was before that positive test. Not on any given day did I feel fully me. And not on any given day could I harness the hope of finding that person because my energy had to be focused on simply getting through the day in the shape I existed. Exhausted already, I further laid waste to my energy supply in creating a mask that would hide the truth from those around me.

The things by which I identify myself–cooking, reading, writing, exercise, smiling, ridiculous optimism–had to be either relearned,  modified, or set aside. 

Cooking, my favorite way to show my love to others, transitioned into a chore. On my worst days, just the thought of standing in the kitchen and thinking through steps in a recipe, left me frozen in how to proceed. I could not desert cooking completely, but my skill and joy in it certainly deserted me.

As a reader, I found myself having to adopt new reading practices in order to maintain. Gone: my pencil in hand adept at skillful annotation and noting depth and nuance in a text. Adopted: a letting go of disappointment in myself for just reading the story without deeper investigation because I knew that reading in any form was good for my brain’s recovery.

As a writer, well, if it wasn’t mandated for work, it probably didn’t happen. I could not face my loss for words, my confusion mid sentence, my inability to see a piece through. A singular email at work could take me an hour to construct; I had no energy for personal writing. I lost my confidence in staring at a blank screen with a  brain that felt equally blank and hid behind my illness rather than writing my way through it. 

In a fleeting attempt to maintain some semblance of my former reality in the face of so much loss, I tried to reinsert my pre-Covid, relatively intense, exercise regimen (even if watered down a bit). I quickly learned that I could no longer exercise during the work week if I wanted to be able to function in the world. I had to live inside of what my doctor called “the energy envelope” which meant instead of HIIT training and weightlifting, I was walking…and not during the work week. My physical strength began to mirror my eroding mental strength bewildering me further in who it was my body would allow me to be.

The rest of the list here–smiling…optimism–existed mostly because I reached deep inside to exude a picture that would bring about fewer questions about how I was really doing. A reach that left me fatigued beyond measure.

Lost. Top Floor. My coping strategies evacuated with everything else that comprised who I had previously been. All those years of managing chronic illness while also maintaining my strength of perseverance…all those skills honed over years even in situations like Long Covid where no answers or cure were clear…none of them could be called to mind and put into practice. I tried. Believe me, I really tried. But, honestly, that perseverance took so much more energy than I had inside of me. Something as simple as starting an anti-inflammatory diet (something I have done successfully before) required more thought than I could see through to fruition. Eventually, I stopped trying to cure my Long Covid symptoms. I preached patience to myself because it was the only tool in my arsenal that I could muster. I allowed myself the grace to wait rather than shaming myself for not fighting harder. 

So I waited. Impatiently patient. Resigned to maybe never seeing “me” again. Accepting of the need to rebuild from scratch.

And then, I guess you could say I snuck up on myself, because I never saw or felt “old me” resuscitating herself. And yet, she did.

And so here I am, a year later and I am cautiously optimistic that I am on the other side. In the last month of this year, I have read a book with the complexity of thought that mirrors (almost) the way I might have before…the inflammation that has flooded and plagued my legs and hands has receded…the cardboard has retreated from its post as a blockade between my thoughts leaving them feeling connected, even if only by a thread…I have found myself more fully present, laughing effortlessly, enjoying small moments and not needing to take a nap because of the effort…I have felt like myself for the first time in nearly a year and for that, there are no words. It’s not perfect. There are still hurdles to clear and some days are harder than others. But this moment brings honesty to two things I lost sight of this last year.

Gratitude and Hope.

 

 

neutrality wavers

“See, I’ve been having me a real hard time…”

A couple of days ago, I cried.

The tears weren’t prolific or anything, but as they welled up and overflowed their banks, I couldn’t help but consider them glorious and restorative gifts…only, not in the way you might expect.

If you know me, a tearful moment doesn’t sound like some kind of triumphant occasion since one of my finest skills is feeling all of the feelings, all of the time…to a fault. I am not a daily cry or a cry in front of other people kind of human, but when overwhelmed by any particular emotion, joy…anger… frustration…sadness…love…awe, tears populate my eyes and from there travel as rivulets running. These tearful moments are sort of how I know I’m living in and connecting with the people and the world around me. They are sort of how I know myself.

Well, that used to be true. Until I contracted a relatively mild case of Covid in January 2021 with no prior comorbidities, and the workings of my brain became a bit of a mystery for the long haul.

“I just kept hoping, I just kept hoping/The way would become clear”

My long hauler symptoms have been extensive and, at times, debilitating over the last six months. Irregular heartbeat, intense fatigue, frightening brain fog, weekly and ever intensifying migraines, daily headaches, weird aches and pains, sore throat, hoarseness, tinnitus, dizziness, weakness, chest pain…this list could go on.

Perhaps the most troubling lingering symptom of all evolved as a strange neutrality. Me. The emotional cornucopia… neutral. Let me explain what I mean by “neutrality”…

“So please don’t take my feelings”

I became sort of inert, feeling no strong emotions one way or the other. Like an extinguished candle. And it was so hard to explain this to anyone because I was struggling in so many ways, it was hard to pinpoint this issue. And then, people kept saying they knew how I felt…which was strange because I wasn’t feeling much. In some ways, this neutrality was kind of nice because my lifelong anxiety dwindled significantly. On some level I just couldn’t muster the energy for it. That vacation from being driven by an overthinking  brain and an overzealous set of nerves was actually a delight. Not me at all, but kinda great.

Yet in other ways, this neutral stance was painful. I would be at events that I knew were important to me, that should have felt exciting, exhilarating and joyful and I, well I was just there…present but not…smiling but vacantly…not even sure how much of the moment I would be able to remember without the lingering vibrance of the emotion. I felt so far away from everyone and everything even when they were right next to me. I often found myself surprised by people’s reactions to my words because even my ability to communicate with emotion and sensitivity had been marred. At times, I would become overwhelmed by how badly I had been feeling or by work or just by the world at large and I would want to cry to release some of that tightly wound energy, but I couldn’t do it. That one outlet seemed to have barricaded itself from accessibility. At other times, I would be in conversation speaking about emotional topics, about how strongly I feel on an issue or how passionate I am about education and while my words were all true to who I know myself to be, they felt false in speaking them because inside they seemed hollow, detached. And so that is how I have been walking through the world since Covid, hollow and detached.

“So I just kept going, I just kept going/And hoping I’m growing near”

For a while, I embraced the idea that this was my brain’s way of protecting itself. It was dealing with too much in my extended recovery so maybe adding in emotion would have been debilitating. Actually, I felt it was pretty awesome of my brain to extend that gift. I knew with certainty that when the school year was over and I had the chance to fully rest, all of that neutrality would erode to reveal the emotions it had been shielding me from.

Except, it didn’t. It lingered.

And the longer it did so, the more I realized that this wasn’t just me trying to save myself from overwhelm; this was damage done to my body, to my brain, by Covid. When I considered the work I had to muddle through to relearn how to think through the incredible Covid induced brain fog, I realized that my emotional void very much connected to that situation…maybe even lost in the dense pillows of fog circling and settling…awaiting the sun to clear them away.

“And it feels so nice to know I’m gonna be alright

Please don’t take this feeling

I have found at last”

My brain is different than it was 6 months ago. It is healing–my tears this week are proof of that for sure, but no one can tell me to what point I will heal…because no one really knows. And I just have to try to not let that defeat me. I have to take what my body gives me and know that this recovery road is less than perfect but I am still on it.

So I am just going to say this…take it or leave it…it has become my lived experience and thus, my truth. Even a mild case of Covid can have life altering impacts beyond what anyone can tell you they might be. Be safe. Do what you can to keep yourself and those around you healthy. This is my current plan, because, let me tell you what terrifies me. The possibility of catching Covid again. Terrifies me beyond what I can type on this page. Because I am still sick. Because my brain hasn’t fully healed. Because I am just starting to feel like myself again six months after a mild case and I don’t want to lose that progress or worse. Because my pulse ox still dips into the upper 80’s and I would like for that to repair fully before my system is attacked again. I have had Covid once and I don’t need to re-live that misery (I’m sorta still living it). I’ve done all I can to keep myself and my family well. I should be safe. And yet, in this world, as people continue to tell me that Covid is no big deal, that it is a fiction, that it is nothing to worry about–essentially denying my lived experience, in this world still, I am not safe.

Lived experience can be different from our own and still be accepted as a truth, still carry weight, still be worthy of our attention. Maybe that is an overly empathic stance, but to me, it is the only way we learn to see each other with respect in this world…it is the only way we begin to act for each other  rather than just for ourselves, elevating our own singular story instead of the varied and valuable experiences of those around us. Hibernating in the blankets of that which makes us comfortable only endangers us. And so I tell this story of my experience with Covid. Not for sympathy because while a momentary comfort, sympathy doesn’t fix anything. Nope. I tell this story to add it to the collective tale of this pandemic. Because this outcome isn’t often written about. Because maybe it will help someone realize Covid is not worth the risk. Because maybe I just needed to get it out into the world.

“So, I just kept dreaming, yeah, I just kept dreaming’…Tryna figure out why”

(All lyrics from “This Feeling”, Alabama Shakes)