This is such a common thing now. Just say there's a conspiracy, and that's evidence enough for QAnon supporters. Throw Soros into the sentence and that's verification for them.
When you ask them for REAL evidence, they go, "OMG do your own research! Don't you know how to use Google?!"
So you use Google and produce evidence to the contrary of what they say, and they move on to, "Think for yourself!"
Science communication is one of the most essential jobs in the world today. Not just, "What scientists say" or "What science says" (because many people don't trust that), but "HOW SCIENCE GETS ITS ANSWERS".
The fallibility of scientists and doctors is an important part of the what needs to be communicated, but it's only when people understand how science works that they can trust and distrust in a healthy way.
I mean, the average person doesn't know about things like predatory journals or ethics in research, or even that there are different types of research. Ask people what 'double-blind' means and many will probably tell you it's when someone has two eyes that can't see.
I have a friend who was a high school science teacher and she doesn't know this stuff. She just taught the currently accepted facts in specific subdisciplines.
The loss of nuance, complexity and grey areas is a huge problem.
Many people can't have a proper conversation about vaccination, because we try to oversimplify the message for people who don't understand the technicalities, and in the process we evoke the distrust of those already primed for conspiracy theories.
We have to be able to say that large pharmaceutical companies have committed many crimes WITHOUT immediately following that statement with a logical fallacy.
Jacob Harbin is a nonspeaking autist who studies the Bible for guidance on life's challenges. Here's a blog post which he wrote last year. anchorofhopefoundation.org/single-post/20…
Nonspeaking autist Hari Srinivasan lectures on disability justice. #DisabilityRights#CRPD
Here's a short video by 17-year-old nonspeaking autist Jordyn Pallett in preparation for the Innovations in Education Conference 2020. In a few days, I will share one of Jordyn's full presentations at that event.
I am encouraging a boycott of autism research participation by autists and parents of autistic children, unless autistic people are involved in setting the goals of the studies. Don't participate just because it's about autism. The study design and ethics may be up to maggots.
People who participate in ethics committees are not necessarily trained in the #CRPD. In my experience, many of those people are clueless about the realities of human rights.
A simple example is that many of the supervisors and ethics people insist on researchers using person-first language in research papers, which is exactly what most autistic participants in English-speaking environments DON'T want. (This is, like, 'Autistic Culture 101'.)
Some months ago I shared a video of nonspeaking autistic author Lucy Blackman typing a conference speech. Today I am sharing Lucy's bio at the Brotherhood of the Wordless site. brotherhoodofthewordless.com/our-authors/lu…
My mother and I took more than two hours trying to sew a 3-layered mask from a 2-layer pattern.
We didn't finish.
Come 1 May, Cape Town is gonna have the largest number of fake niqabis the city has ever seen, thanks to modern women being klutzes at traditional skills.
IMPORTANT
Your mask is to protect OTHERS in case YOU are infected and you don't know it.
An infected person in an inferior mask (e.g. loose, single layer) places others at risk.
So if YOU want to be safe from others, you need to help THEM get access to good masks.
If you are sewing decent 3-layer masks for yourself, sew some for others and give them away for free. Encourage other people to do the same. To reduce the spread of the virus, we need to spread THIS idea virally. #Masks4All
I've figured something out. We don't necessarily another service organisation for autists in South Africa, although ALL the service organisations could do with massive improvement (and it doesn't all depend on funding increases).
We need a DISABILITY RIGHTS ORGANISATION.
We need this because existing service organisations are not equipped to deal with human rights violations and in particular, the nature of the abuse that many autistic children and adults experience at the hand of caregivers.
They are not well structured and equipped to lobby for change and they are DEFINITELY not geared towards prosecutions and victim placements.