TJ: Nazi Destroyer came about after Trump’s election, when TJ was 7-years-old. I had to explain to TJ why I was upset. We’ve talked about racism, white supremacy and systemic bigotry before. But this was the first time we talked about literal Nazis. She was quiet for a bit and then told me she had the solution. She would become a Nazi Destroyer.
CN: ABA, violation of privacy, ableist slurs
Today I had an um, interesting, encounter with an Autism Mom(tm).
With the federal elections of both Canada and the US approaching, not to mention the constant political maneuvering happening across provinces and states, a lot of things are happening at once. It can feel like a whirlwind, just getting your bearings about one issue before the next one suddenly crops up demanding your attention. The breakneck pace of the news cycle means that a lot of the resolution or lack thereof of one issue often gets missed.
It’s the perfect setting to employ several tricks of social psychology that make it possible for politicians (and salespeople and so on) to change the conversation without ever having to convince the electorate of the issue. I’ve talked about at least one of these social psychology manipulation techniques before.
Additionally, it allows them to employ several public relations tricks to encourage several extreme side groups, while also counting on the majority of the population to forget about it before it’s time to vote.
It’s called a Test Balloon.
Ford’s government recently proposed a series of cuts to what is covered by OHIP in the provincial budget. As justification for him depriving the population of Ontario of adequate healthcare, in particular those who happen to be poor, on social assistance including disability, or underage, were the claims that a significant portion of tests are unnecessary. He went on to claim that less than 4% of family doctors are responsible for ordering over 40% said tests, in a demonstration of how statistics and a lack of understanding can be used to obfuscate the truth.
Let’s start with the latter claim. While it may seem strange that such a small percentage of family doctors may be responsible for so many tests, it’s less surprising to those of us who deal with chronic illnesses.
Not All Family Doctors
(Posted with permission. )
It’s 2 am, when suddenly you find yourself unable to communicate clearly. Your words come out incoherent and hard to understand, including in text. What do you do?
The comment that influx of migrants and refugees disproportionately affects the poor is actually and demonstrably false. The biggest increase I saw to my ODSP came around when Canada accepted a large contingent of Syrian and Somali refugees.
In addition, historically, forced improvements to social safety nets to deal with the sudden influx of new users actually strengthen those safety nets and tend to improve services for existing citizens and users of those services.
Where it does affect the poor is when conservatives make cuts to those social safety nets, then blame it on refugees. It’s literally them taking food out of our mouths, then blaming it on the person starving next to us. It’s a diversionary tactic that allows politicians to redirect the anger legitimately directed at them [the service cutting politicians] towards a more vulnerable population by playing on existing, unacknowledged, ignored, and normalized social racism.
It’s practically a political cartoon of someone physically stealing something from you in front of you then pointing at another person saying, “hey, they look different than you, clearly they must have stolen it.” without even bothering to hide what they’re doing.
To blame an influx of refugees for a rise in white supremacist sentiments is literally to blame the victims of racism for the existence of racism. That racism was already present, it just wasn’t talked about or more accurately was claimed to no longer be a problem despite all evidence to the contrary, making it easy for anyone to harness those sentiments for political gain.
It’s victim blaming, and it’s racist.
For all the various experiences I’ve had as a disabled person, a long distance move is a relatively new one. I’m lucky in a lot of ways because the place I’ve moved to isn’t completely new. Although it has been 13 years since I’ve lived here, my parents have been here that whole time. As a result, I have access to certain resources that I wouldn’t have otherwise had. Among these resources is faster access to a family doctor – the same one that has served my family since I was a kid.
I’m lucky because that’s not the case for most people. There is currently a pretty significant shortage of Family Doctors or General Practicioners as they’re sometimes called. Your GP is meant to be the point person of your medical care. They’re responsible for managing the big picture of your overall health – receiving updates from all your specialists, all test results, providing referrals to specialists, and in many cases managing the vast majority of your prescriptions.
As part of my move, I had to transfer my prescriptions from Ottawa to here. Since I was using the same chain of pharmacies, I didn’t much foresee a problem. That’s because I didn’t know about a law that prevents pharmacies from transferring prescriptions that are categorized as narcotics. It’s part of the ongoing war on patients masquerading as the various wars on drugs. The problem is that narcotics are the recognized treatment for a variety of different conditions including ADHD. If I needed a refill of my medication, in this case Vyvanse, I would need to find a family doctor and get a brand new prescription.
CN: mentions of suicidal ideation
For the last little while, I’ve been struggling quite a bit. I’ve been trying desperately to fix the situation I was left in last year. I’ve been just barely getting by with help from friends, by taking out more debt, and by surviving off of stores I’ve had sitting by just in case.
Rather than getting any easier however, things have just been getting worse. My roommate had to move to BC for work and while I was able to find someone to take over his room, the rental agency had issues with him replacing my former roommate on the lease. I couldn’t very well leave my old roommates name on it, and my own financial situation means they are not willing to have it be in my name alone.
As such, I had to give my notice for the end of summer.
I knew the rental situation in Ottawa had gotten worse in the years I’ve been living at this place, but even so I was unprepared for the reality I am facing. The rent costs have skyrocketed to such a point, where $300 over what disability considers a reasonable housing allotment gets me a room in a house with six other people, and I can forget about the house being accessible, meaning I have no idea what to do with my wheelchair, let alone how to be able to live in a place I can’t physically navigate.
Essentially, the way things stand right now, at the end of August I am homeless.
On Saturday July 14th, I signed up to attend a community consultation on Strategic Priorities for the Ottawa Police Service for the coming years. I attended at the request of a friend, an anti-torture activist who is desperately trying to convince the police force to stop the new policy that would give a taser to every police officer in Ottawa.
I agreed to attend not just because she asked me too, but also because for some time I’ve been thinking of ways to improve accessibility in Policing. Also, because I wanted to be a white face bringing up racism against people of colour.
Institutional Racism in the force is a problem that is starting to be talked about by more people not directly influenced by it, as it should, and is a major issue that needs MORE attention than it is currently getting. A related issue however is Institutional Ableism.
A recent review of fatal police interactions in Canada shows that most people killed by police are disabled. Something like 72% of those killed in police interactions were shown to be mentally ill or to have substance abuse problems, which is itself also considered a mental health issue.
A while back, I wrote a post begging the Canadian Government to open it’s borders to Americans with Disabilities as refugees from a slow-motion genocide. Someone left a comment on that post to which I’ve been meaning to respond for a long time.
CYNTHIA: I had previously mentioned this to Michael.
Reluctantly, as a fellow Canadian, I cannot fully support this.
As you know, the United States has 10x the population of Canada. It is a first-world country.
There is no way that the math works for Canada to be able to support the complex heath care needs of Americans with pre-existing conditions. As you mention, the system is already at capacity when it comes to providing proper health care with disability support programs for Canadians. No system can function unless you have a large base of relatively healthy people paying into the system to cover the costs of those who are using it more.
Of course, in a situation of someone being a genuine refugee from any country, humanitarian considerations should come into play. That can’t be extended to American “medical costs refugees”, though, because it would break our system.
In the long run, Canadians need a system that is sustainable – and ultimately, that benefits all Americans as well. Americans are looking at us to see how our single-payer system is functioning. If it works relatively well, that increases political support for it. If it doesn’t, that increases the dire warning about “socialized medicine”. The most vulnerable Americans ultimately need an American health care system that works, and they are less likely to get it if the Canadian health care system breaks or if ordinary American voters stop fearing the consequences of repealing Obamacare because they think that free health care will always be available to them in Canada. Right now, that fear has managed to stop the repeal attempts, to the benefit of all Americans who will ever need health care.