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SS Big Red's avatar

I just hate, so vehemently, that people, even so-called scientists, use studies to back their claim without truly evaluating the studies! Peer-reviewed studies are suspicious right off the top, but are considered sacrosanct, and those that might disagree risk condemnation from those peers, just for doing what scientists (and intelligent truth seekers) should do - THINK CRITICALLY! So much of today’s funding is received not for the merit of the study, but who you know, how your thesis fits in with the political zeitgeist, and how good you are at manipulating stats, because anyone who knows about stats knows they can be very misleading. Don’t get me started on control groups (although granted, because of ethical situations, sometimes it just isn’t possible).

So many people suffer because of this practice - not just scientists with good ideas and the passion for furthering discovery, but those waiting forever breakthroughs in orphan diseases, for example, or those that are prescribed medications that are truly harmful, because they have been through a shoddy evaluative process pressured by money, greed, massive egos and just plain bad people.

Sorry for the rant. I’ve experienced this firsthand, not just in the academic community, but as a proponent and patient of CCSVI, a legitimate condition, with solid evidence in existence for over 150 years. Treatment is a form of angioplasty, proven to be just as safe as a tonsillectomy and in practice, cheaply (about $2000 per procedure, at most, without complications that is) since the early 1970’s. That’s 50 years of common practice, performed widely in hospitals all over, which can legitimately aid in devastating diseases such as Multiple Sclerosis. The main reason CCSVI has been debunked (by only one particularly flawed study that even the conductor of it agrees to the flaws), compared to a body of supporting research? The go-to “treatments” for MS are called disease modifying therapies. Not cures. Not even treatments. Drugs that are the most devastating to your body, they knock out your immune system, have horrendous side effects, which “may” slow down the progression of the disease by a few percent, and cost hundreds of thousands to the patient. It is a multi-BILLION dollar industry, where the goal is to keep a patients’ treatment choices limited to a few of these drugs, keep them around long enough to profit, but never better enough to stop taking them, to support egocentric, close-minded neurologists and drug companies (who fund medical schools, who lobby governments, and who have free advertising through the MS Society, which is not a true charity or support group, but a cleverly-hidden group that continues to support this insidiousness, by literally brainwashing newly-diagnosed, terrified people into taking these drugs, and choosing to shove donations at studies they deem important (in other words, more of the same)). CCSVI isn’t even a neurological issue, but a vascular one which does not fall under the neurologists’ speciality! It has the potential to directly affect the well-being of untold people who suffer from a variety of formerly-considered purely neurological illness, more than just MS, but one study, reported on heavily by a paid journalist with an agenda, supported by aforementioned egocentric neurologists (with their own studies to push), billion dollar profits by a few drug companies (some who only make these disease modifying therapies), medical schools, the international MS Society (a “charity” that pays their national CEO’s 500k salaries to push agendas)… whew! You get my point.

And the public is not encouraged to or taught about critical thinking, so advocates are a handful of poor sick people and some scientists (with solid data) that have to fight Goliath and have their licenses revoked by the FDA, their studies cancelled by the “for purchase” supervisory bodies.

This is an example of what can happen if Joe and Jill Public don’t think critically.

I’m sorry for the extremely long post on your thread. Your frustration with the treatment and study of psychopathology mirrors my frustration with the brain disease one.

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Sheez's avatar

Well written, though everything is subject to opinion, except true science. Even that changes as we progress. The world and people in it change and hopefully advance. Perhaps not as quickly as we would like.

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