Omicron and the Balm of a Caring Community

January has been a long month. Seriously. I know I’m not the only one saying that, and that the last two years have honestly been such a time warp in general, but it is only the 22nd day of the month and I honestly feel as though I’ve lived several lifetimes this year so far.

Last Monday I woke up with a nagging headache. Not debilitating, but pretty uncomfortable. I’m no stranger to headaches in general, since I have a very finicky neck that doesn’t allow me to sleep in certain positions or do particular tasks that most people wouldn’t think twice about. Probably once a month, I end up with a pretty gnarly headache that requires a trip to my phenomenal chiropractor to fix (she shakes her head and says, “what have you done?” in a very gentle, caring manner that reminds me I am in good good hands and puts everything back where it is supposed to be and sends me on my way). So, honestly, that’s what I figured this was. I made my way through the day with Advil and the hope that it would resolve on its own.

But around midnight on Monday/Tuesday, I started to notice that I was thrashing about in bed quite a bit and that is really unusual for me. It only took a minute before I realized I was spiking a fever – this was chills, and the headache had kicked up a notch. I knew pretty much right away that this was Covid. I stuck it out until dawn and then took my temperature to confirm, texted a friend who I knew had access to home tests, and waited.

It was a rough four days. That headache was brutal. Not the worst one I’ve ever had, but definitely second in line. I couldn’t watch tv or read or really look at much of anything. I just laid on the couch staring into space and hoping it would abate sooner rather than later. Somewhere in the back of my mind, I remembered that when I first moved here last May, this was the scenario I feared most – that I’d get sick while living on my own and not be able to really take care of myself or the dogs. I’m here to say that, like most fears I’ve ever had in my life, this one didn’t play out the way my amygdala warned me it would.

I had friends near and far texting me all day long, checking in, offering help of any kind. The friend with the home tests also brought soup, Gatorade, bottles of water, cold medicine from her own stash, and Meyer lemons from her tree. Other new local friends offered food delivery, dog walks, and just general moral support. One of my neighbors, having spotted a friend dropping off supplies at the front door, texted one night to say her husband had just made a beautiful homemade dinner – could they fix me a plate and leave it at the door for me?

I was brought to tears with each and every one of these offers, and I accepted it all (well, not the dog-walking – my dogs would no more leave me behind at the house and go walk with someone else than they would chew their own leg off). Blissfully, the headache subsided by Day 3 and I remember lying on the couch, imagining my poor, stressed brain inside my skull, sending it waves of soothing light to recover. Every little thing I did prompted a two-hour nap. The last time I was this exhausted was after giving birth to Erin and that was only because I caught the flu while I was in the hospital so I brought her home and spent the first week battling a fever and trying to recover from a 40-hour labor.

I’m still recovering, but finally not sleeping 16-18 hours a day. I am able to do a few things here and there and then lie down for a bit to rest. There is some acute sense that if I don’t go slowly, there is a real danger of setting myself back, and I can’t help but wonder how people with children at home or elders to care for or lots of work to do that needs to be done manage this. It honestly brings me to tears to think about having to make a meal for someone else or go to a job feeling such extreme fatigue. I wish we lived in a world where we believed each other when we say we need rest, where we made sure to provide space and the necessities for that to happen. I recognize my massive privilege in this – that I was able to be cared for from afar by friends and family, that I am able to put off my work obligations as long as I need to, that I have a roof over my head and a soft bed in which to recuperate. I wish that for everyone.

It is so interesting that one of the first things people ask is “where did you get it” and then “were you vaccinated?” I am reminded that we have done a really good job of framing this pandemic in the same way we frame nearly everything in this culture – in terms of personal responsibility. I know that those two questions are some attempt to insulate ourselves – if we think we can crack the code, we can avoid getting sick. But I also know there is some judgment there because that’s what we’ve been taught. If you just didn’t do X, you wouldn’t be struggling with Y. I am so much more taken by the folks who ask “how can I support you” and “what do you need?” There is a radical form of community that can be created just by asking these simple questions and I am here to tell you, it feels amazing to be the recipient of it. On Thursday night, when I was so astonished by how absolutely tired a person could feel after sleeping most of the day, my phone pinged with an incoming email. As I read something from a friend expressing her deep care for me and her fervent wish that I recover quickly and thoroughly, I spent a few minutes going back through my day and replaying all of the text messages I’d gotten from a dozen or more friends and family members, checking in, offering help, saying they were sending love, and I made the conscious decision to hold that in my head and heart as the last thoughts before sleep – the notion that I was held in deep care and love by so many people from literally all over the planet. It was magic.

I’m now a week in and my sense of taste and smell is coming and going unpredictably, I struggle to catch my breath when walking the dogs on our normal, flat, 20-minute route through the neighborhood, and I still occasionally sit down after doing something  mundane like folding a load of laundry and feel a powerful need for a nap. My sleep is the sleep of the dead – deep, strange dreams and waking up feels like swimming up from the depths of the ocean, but I am grateful for the freedom to sleep when I need to and for friends and family who text or call or email to check in and let me know they’re rooting for me. That is medicine for my soul.