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My experiences with asthma.

As a child, I fell through the cracks and did not get the diagnosis of childhood asthma that I should have gotten. My inability to keep up with my peers began to manifest itself in junior high school when I could not keep up with them running laps around the gym, and it didn’t seem like any of my gym teachers cared enough to notice. An attempt to join my high school’s cross-country and soccer teams were thwarted by the fact that I could not for the life of me keep up with my peers at all — I was the only student on the cross-country team that year who “could not get over the mental block” required to run the mile (and wished that my coach would have realized that it was not a mental block preventing me from running the mile, but asthma), and was frequently having asthmatic exacerbations while attempting to train for the soccer team that only went so far noticed by my soccer coach as to reduce what was actually expected of me on the field. My parents did not find out until more than a decade later, after I had been forced to drop out of both teams due to an inability to keep up due to undiagnosed childhood asthma, that when I was enrolled in gym class and my gym coach discovered the severity of my asthma he let me ride the bench the entire period to get the needed credits for gym and gave me an A without informing my parents that there was any concern at all about me not being able to participate with my peers. Literally no one reached out to my parents at all.

While my classmates did gym activities, I sat on the bleachers doing homework and was given As for gym.

I wasn’t formally diagnosed with asthma until I began seeing my own primary care physician as an adult, and she was flabbergasted that it had taken this long for anyone to even question that I had asthma given the frequency and severity of my symptoms as well as the limits that they imposed on my life. Because various maintenance medications did not have the desired effects and my asthma was still as prevalent as it was, especially exertionally, I was referred to a pulmonologist (and eventually had to change to a new primary care physician and pulmonogist over the years). Although I am comparatively in a bit of a better place with my asthma than I was years, even decades ago, I still resent the fact that I was never diagnosed with asthma as a child and that I could not participate in the activities that I wanted to participate in because the coaches that were supposed to be responsible for my well-being could not even reach out to my parents to let them know that there were impediments to me successfully being able to be a part of the teams that I wanted to be on. (And at that, my gym coach letting me ride the bench for multiple gym classes gets more and more absurd the more that I continue to think about it, especially as I continue to get older.)

All in all, I feel like several key adults that were in my life when I was a child dropped the ball and failed me.

Actually, for more than just this reason, I feel like key parts of my secondary school education failed me.

Maybe my asthma wouldn’t have snowballed into what it became if these adults at school had contacted my parents about my exertional struggles sooner, cluing my parents in to the realization that I needed assistance to participate in activities that I wanted to participate in, and I would be more fit for it today.

But all I can do, more than a decade after graduation from high school, is sadly wonder about that though…

If someone says that they’re disabled…

Believe them. Please just do everyone a favor in general and take them at their word.

And for the record, the Google definition of disability, to make it even easier on people:
“a physical or mental condition that limits a person’s movements, senses, or activities.”

I can not begin to convey in here, let alone articulate, how many times I have seen — or heard — people playing “the disability police”, being the arbiter of whether or not someone is “disabled enough” or “truly disabled”. If you live in the United States, you probably already have a good idea how difficult it is for an adult to actually get disability benefits. Not getting them does not mean that they are not disabled. One’s worth is not defined by the job that they have, any jobs that they are capable of holding, or their lack of job.

Some people are disabled and can work. Some people are disabled and can not work.

Sometimes this fluctuates over the course of the disabled person’s life, depending on their disabilities.

This does not mean that they are not disabled, or that their disabilities have any less of an impact on them.

For able-bodied people to smugly suggest jobs that they think someone who is disabled should get, or “be able to work”, is so outrageous that I don’t actually have words for it other than the fact that it is so smug that I don’t ever want to be around when it actually happens. It must take an extreme amount of smugness to sit on your high, usually middle-class throne to make comments like that when you’re not disabled (and no, your intermittent conditions do not count if they are not disabling, so do not use them trying to gain clout with the community… I’ve seen this happen when these folks have their feet held to the fire, as they should), not having any of the lived experiences that come with disability. Do these folks not even hear themselves?

If a disabled person says that they can’t do something, please just take them at their word.

The person living the experience, the disabled person, should be able to describe in sufficient detail what their limitations are, and it should go without saying that since they live with those limitations every day — at least as a general rule of thumb insofar as them being disabled, having that disabling condition — that they should be believed when they discuss them. We as a society should more automatically believe them.

It would make disabled people’s lives so much more easier as a whole if people just simply did this.

Comparatively speaking, very few people lie about being disabled. Far more people are telling the truth.

Why did you put down the Vita?

Because that’s what you did, Sony. You put it down like Susan the horse from Doctor Who.

When I found out that Sony was going to discontinue the Vita last year and that they were not going to manufacture any more games for it, I was extremely perplexed for a number of reasons, some personal.

Not only is the Vita a reigning household favorite for the simple fact that it is a mobile console, meaning that we can take it with us as needed — and as wanted — wherever we are, and wherever we want to go, but it was Sony’s most recent mobile console. And if they were going to discontinue it, Sony wouldn’t have a mobile console, meaning that the only game developer to have a mobile console… would be Nintendo, with the Nintendo Switch. This meant that Sony would be conceding the entire mobile console market to Nintendo. Was this really the most tactical thing for them to do when there was no word of a new mobile console even waiting in the wings? Not so much as a peep of anything new in development? Seriously, Sony?

We here at the Bub Club, as I like to put it, take our consoles seriously. We take our mobile consoles even more seriously. (And the fact that I call them mobile consoles pays homage to the fact that I am a Doctor Who fan, or a Whovian as some people like to put it. Sometimes I straight up call them mobiles. Sometimes I straight up call cell phones mobiles. That’s the overwhelmingly British lineage in me talking from across the pond, courtesy of Ancestry and 23andMe. I knew there was a reason that I liked the shows that I did as much as I did.) We don’t throw consoles away when they still function, and we replace parts and consoles when they don’t function to make them still function. We frequent pawn shops as needed, and we still have a functioning Nintendo 64 and Super Nintendo. Who says blowing into a cartridge isn’t fun for the whole family? I mean, I’m an asthmatic, so I have one of my kids do it for me, but I mean, my kids know what blowing into a cartridge is like because I’m a good parent and my goal is clearly raising them right here…

Frankly, though, I got a lot of enjoyment out of games that came out on the Vita, and Bub has enjoyed a lot of them as well. So for Sony to completely discontinue the Vita like this and take themselves out of the mobile console market is, at least to me, incredibly foolish. This concedes the whole mobile console market to Nintendo. Do they even care that this affects their bottom line and their revenue, or does it not bother them?

Christmas break 2019, in a nutshell.

· get a 256GB microSD card for the boys’ Nintendo Switch as an early Christmas present
· find for some reason that it does not consistently want to load past a certain point
· have to load the entire Nintendo Switch from scratch because it almost fails, but for some reason… does not
· able to recover everything with the 128GB microSD card, which is nearly 100% full with Bub’s games
· have to fix an issue with this website’s hosting, which I should finally be done with

Seriously, with the errors that the Nintendo Switch had begun to give me at one point, I thought that I would have to replace it because it had begun to fail. But then miraculously, after doing everything to save it that I had already done all over again, it begins to work with the smaller microSD card when it hadn’t even been doing that before. Mobile consoles help keep Bub from having meltdowns because they can go wherever he goes, especially when I know that we’re going to have to commute somewhere and stay there for awhile… I can just bring the charger with us if needed, find a power outlet, and explain the situation to anyone who would like me to explain the situation to them. Because I honestly do not mind doing so. Trust me, I don’t…

The only reason I haven’t brought it with us when Bub has come with me to neurology appointments is because I do not want to exacerbate, or set off, someone’s epilepsy, migraines, or other neurological condition while we are sitting there in the waiting room and have him get upset because he knows that we packed the console and games with us and that he was not being given access, even if it was for reason.

I am just fine “giving myself migraines” for my own child, but won’t do something like that to someone else.

The fact that we got a microSD card that actually seems to function on the day of Christmas, though, has been absolutely great! I didn’t begin to load it until the afternoon of Christmas, though. But that was because I didn’t know about it until the afternoon of Christmas. The one that wound up… wanting to work on everything but the Nintendo Switch itself was one that I knew about before Christmas, if this makes sense.

I suppose we can use the other microSD and adapter to keep files backed up from the computer.

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