It's great to make people more aware of bad mental habits and encourage better ones, as many people have done on LessWrong. The way we deal with weak thinking is, however, like how people dealt with depression before the development of effective anti-depressants:
- Clinical depression was only marginally treatable.
- It was seen as a crippling character flaw, weakness, or sin.
- Admitting you had it could result in losing your job and/or friends.
- Treatment was not covered by insurance.
- Therapy was usually analytic or behavioral and not very effective.
- People thus went to great mental effort not to admit, even to themselves, having depression or any other mental illness.
The only "anti-stupidity drugs" we have are nootropics. But the nootropics we have weren't developed as nootropics. Piracetam was, I think, developed to treat seizures. L-DOPA was developed to treat Parkinson's. No one knows who started using ginkgo biloba or what they used it for; it was used to treat asthma 5000 years ago. Adderall derives from drugs used to keep soldiers awake in World War 2.
And none of them are very good against stupidity. AFAIK, to date, not one drug has been developed by understanding and targeting the causes of different types of stupidity. We have the tools to do this--we could, for instance, sequence a lot of peoples' DNA, give them all IQ tests, and do a genome-wide association study, as a start.
We don't research these things because society doesn't want to research them. People don't conceive of stupidity as a disease that can be cured. We need, somehow, to promote thinking of stupidity as a mental illness. As something drug companies could make billions of dollars off of.
We must stop glorifying intelligence and treating our society as a playground for the smart minority. We should instead begin shaping our economy, our schools, even our culture with an eye to the abilities and needs of the majority, and to the full range of human capacity. The government could, for example, provide incentives to companies that resist automation, thereby preserving jobs for the less brainy. It could also discourage hiring practices that arbitrarily and counterproductively weed out the less-well-IQ’ed. ...
When Michael Young, a British sociologist, coined the term meritocracy in 1958, it was in a dystopian satire. At the time, the world he imagined, in which intelligence fully determined who thrived and who languished, was understood to be predatory, pathological, far-fetched. Today, however, we’ve almost finished installing such a system, and we have embraced the idea of a meritocracy with few reservations, even treating it as virtuous.
-- David Freedman [no, not David Friedman], "The War on Stupid People," The Atlantic, July/Aug 2016
Disclaimer: I have autism. I sometimes worry that despite functioning pretty well in society, some day, people will say "hey, these people have problems integrating with society sometimes! We should cure all the autisms!" and I'll be forcibly "cured" and have my personality (autism is a way of thinking, sometimes, so I think that this counts as part of someone's personality) altered against my will.
Compare with the deaf people, which is BOTH a culture and a disability. Same thing goes on here. I believe that a way should be found to prevent people from being born deaf/with autism (preferrably via curing in the womb, not via abortion, but if people want to abort because their unborn child is deaf/has autism I think they should be allowed to do that because it places a higher burden on the parents). I don't believe you should forcibly (or via social pressure) intervene in people who, for their entire lives, have been deaf/have autism in order to cure them. You should make the means available to them, but it's their decision.
From what I've read, most of the protest in the deaf community currently is deaf parents insisting they have the right to deny treatment and audible education to their children--which they want to do because it will be too late for the children to get the treatment themselves when they're adults. If it were possible for their children to get the treatment and learn spoken language once they grew up, and potentially leave the deaf community, parents would have less motivation to deny treatment to them as children.