It’s been exactly one year today since I first went down hard with Covid. Six days before Christmas. The feeling I most remember is that I had been looking forward to the holiday for what felt like one million years. It was going to be a restful, peaceful end to a crap year. That was obviously my first mistake.
I’ve been thinking about this one year milestone for a long time, dreading it really. Not that the day necessarily means anything, but the best I can understand is that my mind and body must have fully believed that we’d all be better by now. And by we, I mean all the parts of me, but also the world, I guess.
Now that the day is here, it’s just another day, you know? The anticipation of it was worse because I think in the end, I know that I won’t fully be better for a long time. Neither will the world.
As I was sitting down to write whatever it is my brain felt like sharing on this Weird Day, I read through an old post I wrote after three months of being sick. I was so exhausted and so angry and so out of grace.
Now that it’s been a year, I can feel that I’ve come through the worst of the anger. I related it recently to the stages of grief. Like I can literally feel myself coming down the side of resignation and just.. acceptance, I guess.
I’ve dealt with the loss of friendships and others being irreparably changed. I’ve watched other friendships blossom and grow and strengthen.
I’ve seen people close to me do things I can’t un-see and say things I can’t un-hear. I’ve felt extraordinary anger at our former administration for leaving us to fend for ourselves, which has been proven even more true with every piece of historical context that comes out. I’ve seen my own personal lived experience be treated as a political weapon.
I’ve been told I am trying to “inoculate the world” by a stranger on the internet and that I’m “only thinking about myself” by people I personally know. I’ve been told I wasn’t as healthy as I thought I was before I got sick, implying that it’s somehow my fault I’m still in the space I am.
I’ve been told I’m “scared of Covid” and I’ve also heard a deafening silence from those who used to support me. I’ve been told I can’t argue for what I’m feeling and living.
I don’t tell you this to try and elicit sympathy. I tell you this to show you what it is I’m now resigned to. I certainly can’t change people, and I’ve also learned it’s not worth it to engage with those who have made up their mind.
What I can do is continue to share my personal, lived experience for myself and in honor of those who don’t feel comfortable sharing.
I am officially a Covid long-hauler. When I was just three months out, I felt weird calling myself that. Like I hadn’t been at it long enough to warrant the title. But I’m going to confidently say that one full damn year gives me the right to claim it.
If you don’t know someone suffering from this or haven’t read any stories about it, I fear that your impression of people like me is that we just get a little winded going up the stairs.
Along with many others who have reached out to me and many other stories I have read, this is like comparing a paper cut to having a limb amputated.
I do get winded going up the stairs, in part because I haven’t been able to work out in a year. The most I can do is walk the dog every day and I JUST last week started going to yoga.
Before I got sick, I had been doing CrossFit 3-5 times per week for close to 7 years.
But over the course of this last year, each month brings on an onslaught of symptoms. Some months better than others and I’d like to say I’m on a generally upward trend. Maybe?
I break out in full body night sweats. My ears alternate between feeling super plugged and ringing out of nowhere. Bruises and scrapes take weeks to heal.
For the most part, I still can’t smell anything except what I can only describe as organic matter. Dog poop, body odor, sewer drainage. My sense of taste is still completely jacked. I can taste food as long as its super salty, but a lot of food just tastes like dust. I’m convinced I don’t even know what things taste like anymore really. I’ve just gotten used to this new version of my taste buds.
The fatigue is still pretty intense. It’s definitely improved since those first awful weeks of being sick, but I’m still exhausted every day. I have to say no to a LOT of things, because I just know I won’t have the energy. Or if I do have the energy, I’ll be wiped out for the rest of the day.
It’s hard to answer the question “How are you doing?”. It’s my favorite question because it shows so much kindness, but I vacillate between wanting to just say “fine” because it’s easier and sharing my entire life story because I don’t want to downplay how I’m feeling.
Some days are in fact, fine. Not often great, but fine. I appear normal and functioning. Although I do often get told that I’m not the same as I used to be. To which I always want to answer — ARE ANY OF US REALLY?
The low-simmering anxiety that would often ramp up around my period turned into All The Time Anxiety, which eventually resulted in a full blown panic attack. I fell into a deep depression for awhile, which culminated in an entire weekend where I couldn’t physically get out of bed and a scared shitless husband.
There are so many symptoms that I joke each month is like a bingo card waiting to be filled out. WHAT WILL IT BE TODAY? It’s so fun.
The fatigue is truly the thing that affects every minute of every day, but if I had to pick the absolute worst symptom, it’s the lingering brain fog. In the beginning, I literally couldn’t focus on anything. I was a total mess. But it’s morphed into a high percentage loss of short term memory. I can’t remember simple words. I listen to a podcast and am deeply moved, but then can barely remember what it was about five minutes after it ends.
This is the symptom that worries me the most. I am a Big Feelings Thinker who loves to write and read and listen and dive deep. But most of the time, I can’t remember what I have read or listened to or talked about. It feels like a core part of me has been ripped away.
Work has been really challenging. I honestly feel so fortunate that I was already working part-time before getting sick and that my company is so understanding, flexible and patient with me. And the fact that I’m not the primary breadwinner in our home has been a blessing so big I didn’t even understand it until I read stories about those who have lost their full time income.
I somewhat have the time and space to take care of myself. We have the financial means to afford tons of doctors visits, supplements out the wazoo, anxiety medication every month. I’m in counseling and have started massage therapy. None of these things are cheap. My husband has a good job with decent medical insurance, which has been a life saver. Like literally, a life saver.
I’ve been so incredibly, outrageously frustrated around the rhetoric that “if we were just healthier, we wouldn’t get sick”. Like steam comes out my ears.
Should we all eat healthier and exercise? Of course. Do most of us KNOW we should do those things? I imagine so. That doesn’t make them easier and it doesn’t magically grant the resources to everyone to do so. It also doesn’t fix the immediate issues that I and others who have been profoundly affected by this virus are dealing with.
I understand where folks are coming from when they say these things. I have a lot of grace. If I had gotten sick and recovered quickly, I honestly think I’d be one of those people thinking the same thing. It’s fair.
But it can’t be an excuse to disregard the suffering and loss of so many. There is way too much self-righteousness out there from folks who either haven’t gotten sick or did actually recover quickly.
Without even having to hear it directly, I KNOW what people are saying. I hear the questions about others who get sick or lose their lives. What were their underlying conditions? How old were they? Did they know that exercise and losing weight helps? How much fast food did they eat? How much did they drink? I know people disregard my experience as a one-off or that I must have done something wrong to be where I’m at today.
If you have felt this way, I encourage you to search out some stories of others in the same shoes as me. This article from the Washington Post is heartbreaking and important.
My family and I have spent hundreds, if not thousands of dollars, on trying to get me the help I need. I’m not a single parent relying on one income, I don’t have to go into an office every day, so I can take the time in the afternoon to rest if I need it. If I had to, I guarantee you I wouldn’t have any energy left for my family.
I’m one of the lucky ones.
If your initial instinct after reading this is to tell me that I’m obviously not thinking about the children or other people’s mental health or the suicide rate or small businesses going under, please save yourself the time. These are things I think about every single day. I do my best to balance my risk assessment and my Big Political Feelings with those of everyone around me.
But I also feel it’s important to share my story, to add another piece to the puzzle that is this weird life we are living.
If you are going through something similar or know someone who is, feel free to email me at melodymarie33@gmail.com. I’m so happy to chat and am generally an open book.
If you are going through something similar, what I can tell you is that there are some damn silver linings (to beat a dead horse cliche). I’ve been well-loved by some of my people. Like giant bear hug wrapped in a cozy blanket with a cold glass of Prosecco well-loved. I’ve learned a lot about myself in a very short period of time and I’ve learned how to unapologetically say no when I don’t have the space or energy. I’ve been given so much grace.
Thank you for being here with me. There’s approximately one million more things I want to say and share, but I’ll leave you with this. Please check in on those you know who have had Covid. Just to make sure.









