Categories
Athena Scalzi

Ask Me a Question!

Athena ScalziHey, everyone! Today I thought I’d mix it up and have a Q&A. I’ve been writing on the blog for over a month and a half now, and I thought to myself, these people read my posts, but how much do they really know about me? Obviously, you probably know at least some stuff, considering how much my dad has posted about me in the past, or if you follow me on Twitter or Instagram then you probably know a considerable amount! But I thought it would be fun to open up more and have y’all learn some trivial information about me.

So, if you would like to know something, leave me a question in the comments! Please leave only one question, but it can be about any topic! You can ask me about writing, my home life, my favorite ice cream flavor, or even something philosophical or political — but note, since this will be for just one entry, my response will probably only be a paragraph, at most. I plan to pick a handful of questions and answer them all in a post sometime next week. Fair warning that your question may not be picked, but I will definitely read all of them.

And as always, have a great day!

-AMS

Categories
Uncategorized

Internet Speed Update

This will sound slightly ridiculous, but I can’t tell you how nice it is to have reasonable internet speeds after close to two decades of having to make do with substandard bandwidth relative to the rest of the county. When I moved to Bradford in 2001, the only local internet provider had speeds of 9600 baud, and since then every internet connection I’ve had was a compromise — slow and/or metered and/or susceptible to clouds or rain. Prior to this upgrade I could either have fast internet or unmetered internet but I couldn’t have both, and I spent a non-trivial amount of time doing the daily internal calculus of how I was going to access the internet with which gadgets and for how long, and whether it would affect what the other people in the house were doing.

Now for two weeks I haven’t had to do that, and it has been delicious. Again, an internet speed of 40mbps down/3Mbps up isn’t great, either in itself or relative to speeds available in non-rural areas. But it is enough — enough that I don’t have to do any of the connection calculus that I’ve been doing on a daily basis for literally years. I can just use my connection, like I can use my plumbing or my electricity. You turn on the tap, and there it is. A long-standing resource issue has been effectively solved, and I can use the brain cycles previously occupied dealing it for something else.

And yes, it’s been a genuine resource issue; more than most people, my life and livelihood are tied into my ability to get on the internet and use it. Or, more accurately, more than most people until recently, as the plague times we’re living in have made it clear to everyone that internet access is no longer a luxury or nice to have when you can get it; it’s an actual necessity for work and for school and for communication, for better or worse. The rural internet gap is no joke. I could get around it, sort of, because I have the money to do so; not everyone who’s been in the same sort of rural internet desert as I’ve been in has the same (imperfect) options I’ve had.

Intellectually I’m annoyed at how pleased I am at my increase of internet speed; emotionally I don’t care what I’m feeling about it intellectually. What a pleasure it is to simply to have enough bandwidth, for now, anyway.

— JS

Categories
Big Idea

The Big Idea: Karen Osborne

Sometimes, good things can emerge from bad circumstances. Author Karen Osborne’s newest book, Architects of Memory, is a prime example of that. What started as a medical emergency spiraled into a novel about facing one’s fragility. Read on as the author shares her emotional journey from pain to novel.

KAREN OSBORNE:

An orthopedist once saved my life with a phone call. 

Two weeks before, he’d slapped a walking boot on my broken foot and told me I’d be on crutches for a while. The break had been painful, but the pain I felt that day was worse—a ravening agony, like someone had shoved a knitting needle made of molten lava up my femoral artery. 

He took one look at my swollen calf, frowned behind his Claus-congruent beard, and told me to drive to a specific hospital where the radiologists had special training in vascular issues. He called ahead—I skipped triage and was delivered almost immediately to an ultrasound room in the vascular department, where a technician tried her very hardest to keep an adequate poker face as she stared at the massive time bomb in my leg.

The orthopedist had not been my first stop. I’d appeared in his office without an appointment, literally crying in pain. I’d previously been to two urgent care doctors and my GP, who all told me that I’d probably just pulled a muscle or was experiencing referred pain, that I was too young for a blood clot. I believed them—they were doctors, and I was not—but I couldn’t shake the crawling sense of doom that was making a slow apocalypse of my composure. That day in the ER was the very first time I really understood that you could know down to your bones that something was wrong with your body and the world. I did have a blood clot, and it would have killed me if left to its own devices. 

They also found that I had a clotting disorder known as Factor V Leiden. FVL is a funny little genetic twitch that tells the platelets in my blood to keep right on singing “Come On Eileen” like they’re bartending at Coyote Ugly when they should be staggering on home after the last rendition of “Closing Time.” People with FVL have to worry about blood clots forming all the time: after surgery, after broken bones, or when they’re minding their own business walking down the street.

Recovery was $600/day of blood-thinning tablets, injections, and near-daily lab visits. It was also a major hit to my mental health: since I’d almost been gaslighted out of going to see the orthopedist, every minor pain in my leg for the next decade sent me into an anxiety spree (which the support groups actually said was completely normal). 

Pre-clot, I’d wanted to be a freelancer, but post-clot, that was completely out of the question. See, this was 2006 in the United States of America, and FVL was a pre-existing condition that put you on the no-fly list if you didn’t have employer insurance. The diagnosis stapled me to a job until I died. Want to live, Karen? Pay for it. Your worth is in your wallet.

If you’ve never had issues with American healthcare, say a prayer to whatever level of divine pasta monster you believe in that you never will. I can’t imagine what would have happened if I’d been freelancing for my paper instead of on staff. It’s a story told over and over again around here: she didn’t think she could afford the bill, my friends would have said. So she didn’t go.

A lot of us with pre-existing conditions ugly-cried when the Affordable Care Act became law. And we just haven’t been all right since the election of 2016, when the “businessman” holding the nation’s highest office started farting off about tearing it down whenever possible. 

I had just started Architects of Memory. I was angry. I imagined my protagonist Ash uninsured and staring down a healthcare system that wouldn’t give her the time of day. I gave her a quintessentially American problem: I put a time bomb in her blood and sent her off to a world where she couldn’t get treatment because she had a pre-existing condition, just to see what would happen. She’d recognize the steaming humanitarian crater that is the healthcare system of the most developed country in the world.

At least Aurora pays for your hospital bills if you get hurt on the job, she’d say. At least the CEO believes in science.

Science fiction is the literature of ideas. But ideas live in minds, and minds are meat like the bodies they run. They are linked together with an unassailable bond. When we love, we feel butterflies. When we lose, our heart aches. Ideas are married to the bodies in which they are born. Creativity is not some heavenly state divorced of care; it is a chronology of pain and nausea and viscera and breathing and moving and being. And so is science fiction. 

But Ash doesn’t have the luxury of money or time or health—the secrets of Tribulation are coming for her, whether or not she wants them. Life doesn’t wait. Everyone’s a terminal case. It’s only a matter of time. Until then, it’s a matter of if you want to be like the doctor who dismisses your crying patient, saying “it’s just anxiety”—or the one who listens and makes a call. 

Writing Architects helped me get through a time in my life when I felt like I was collecting chronic diagnoses like extremely crappy Pokemon, but at least I was allowed to actually go places. Since COVID was revealed as a disease that causes serious, fatal clotting, I’ve basically walled myself up as much as I can with a partner that plays church services for a living. The walls of my house are pretty much my world. Going for a walk feels like going EVA.

That’s the funny thing. I gave Ash her world and her problems. She gave it all right back to me. We’re all Ash now, facing down our squishy, delicate bodies, going no no no no, not symptoms, it’s too early for symptoms. Every twinge says: is this the day? Is it now? Is this it? Can I afford to go to the ER? I’ll be fired if I go, so should I go to the office instead? It’s care for those who can pay and everyone else can have prayer and oleandrin.

One of my first readers said they didn’t understand why an organization like Aurora doesn’t have more resources to deal with the problems at Tribulation. Look at how many ships they have, he said. They shouldn’t need to pick the bones of old wrecks to function. 

They shouldn’t, I agreed, but they do. Kinda like us.

And organizations like that never forget that you, too, have bones.

—-

Architects of Memory: Amazon|Barnes & Noble|Indiebound|Powell’s

Read an excerpt. Visit the author’s blog. Follow her on Twitter.

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