The “only 6%” gambit: The latest viral COVID-19 disinformation

Surgeon David Gorski writes:

It’s always weird to try to get blogging again after an absence due to a health issue with a member of the family and other pressing issues that were more important than my little side hobby and thus crowded it out. True, the absence was only a week and a half, but it’s weird nonetheless. Sometimes, it’s hard to pick a subject. Fortunately (or unfortunately), over the weekend I started seeing memes and content on various social media that went something like this about “only 6%,” as shown by this collection of memes from @BadCOVID19Takes:

Many of them reference this blog post by one of the most idiotic right wing pundits out there, The Gateway Pundit:

The CDC silently updated their numbers this week to show that only 6% of all coronavirus deaths were completely due to the coronavirus alone. The rest of the deaths pinned to the China coronavirus are attributed to individuals who had other serious issues going on.

Jim Hoft, a.k.a. The Gateway Pundit, then went on to quote a Tweet by someone going by the handle Mel Q (@littllemel):

Mel Q's "only 6%" Tweet
Mel Q’s “only 6%” Tweet

Unsurprisingly, Mel Q was overjoyed to have had her Tweet retweeted by President Trump:

It was very disturbing indeed that President Trump chose to amplify this disinformation that “only 6%” of deaths attributed to COVID-19 had actually died of COVID-19 “alone” and that “only 9,210” had died from COVID-19. (Of course, these figures are a bit old, from when “only 153,504” died of COVID-19. The toll today is widely thought to be north of 180,000, which, according to the brain dead “logic” of people like Mel Q, would mean that “only” close to 11,000 people died of “only” COVID-19.)

This claim was rapidly amplified by COVID-19 denialists (those who deny that COVID-19 is deadly and that we need to take the pandemic seriously, instituting social distancing, masking, and in some cases lockdowns to control it), for example:

We’ve met Nick Gillespie before, when he spewed nonsense about the right-to-try and drug approval by the FDA. I’m not surprised that he swallowed disinformation about COVID-19 whole and then regurgitated it unthinkingly.

Amplification of the “only 6%” gambit also included Tweets by various conservative actors and celebrities, like Kevin Sorbo:

Unfortunately, even after Twitter deleted Mel Q’s Tweet, the “only 6%” hashtag is still going strong on Twitter.

I’m sure we’d all agree that this would be awesome if it were true! If “only 6%” of those who died with COVID-19 have actually died because of the coronavirus instead of dying of something else “with” the coronavirus at the same time, then it really would be true that the disease is much less dangerous than previously thought. Sadly, this claim is a huge truckload of fetid dingos’ kidneys piled on with a thick layer of bovine excrement. It’s a misrepresentation of the figures in this chart. Whether it’s unintentional or intentional can be debated. (Actually, to me it can’t. I know we’re not supposed to attribute to malice what can be explained by stupidity, but in the case of COVID-19 deniers I’ve learned that malice and stupidity are usually both involved.)

Overall, the message was similar to previous messages by COVID-19 deniers:

  • That COVID-19 death tolls are being intentionally exaggerated by the media and government for nefarious purposes, in this case the “true” toll is “only 6%” of the toll usually cited.
  • That “only” the sick and the old are at risk.
  • That you don’t have to worry about COVID-19 if you don’t have one or more of the comorbid conditions listed.
  • That, because “only 6%” died of “only COVID-19,” lockdowns, social distancing, masks, etc., are unnecessary.

I sensed an astroturf campaign, much like the one that tried to promote hydroxychloroquine based on hilariously awful “science” not too long ago. But what’s behind it? Much in the manner that the campaign to promote hydroxychloroquine based on risibly bad epidemiology two weeks ago, this astroturf campaign to downplay the risk of COVID-19 (“only 6%” of what you thought it was!) is based on a laughably incompetent and awful interpretation of CDC statistics, with a dash of conspiracy theory thrown in (the CDC “quietly updated the COVID number,” as though the CDC was trying to hide something), because there’s always a conspiracy theory. Adding to the conspiracy theory was Twitter’s deletion of the original Tweet by Mel Q that had been retweeted by President Trump.

Also, note the “Q” in Mel Q’s Twitter handle. That’s not just any “Q.” It’s clearly a reference to QAnon, an utterly bonkers far right conspiracy theory that claims (among many other things) that a network of Satan-worshiping pedophiles—and cannibals who apparently eat the children after abusing them!—are running a global child sex-trafficking ring and are (not coincidentally) trying to take down U.S. President Trump, who, unsurprisingly, has refused to denounce QAnon as the dangerous nonsense that it is.

Worse, the idea has spread from the wingnutosphere into mainstream news. I’ve lost count of the number of stories in mainstream news sources that basically parrot (or at least don’t push back very much against) the idea that the CDC has somehow admitted that “only 6%” of those dying with COVID-19 died of COVID-19, although, fortunately, that changed as the weekend wore on, Trump retweeted the claim, and Twitter took down Mel Q’s Tweet. Unfortunately, that didn’t stop “only 6%” from going viral and trending on Twitter:

I also saw it all over Facebook, even in a Star Trek group that I joined a long time ago.

So what’s behind this “only 6%” gambit? Basically, on August 26, the CDC updated its breakdown of COVID-19 deaths in the US, and one of the tables has deaths categorized by what are described as “comorbidities.” Where did the “only 6%” figure come from? If you peruse the table first, as I did, you’ll have a hard time figuring it out, but then I looked at how the table (Table 3) is described on the CDC website:

Table 3 shows the types of health conditions and contributing causes mentioned in conjunction with deaths involving coronavirus disease 2019 (COVID-19). For 6% of the deaths, COVID-19 was the only cause mentioned. For deaths with conditions or causes in addition to COVID-19, on average, there were 2.6 additional conditions or causes per death. The number of deaths with each condition or cause is shown for all deaths and by age groups. For data on comorbidities, click here to download.

If you peruse the table itself, you’ll soon see that it doesn’t show that “only 6%” of COVID-19 deaths were due primarily to COVID-19 and that, among those with comorbid conditions who died, there were 2.6 additional conditions or causes. The only way one might make such an misinterpretation is either through a profound misunderstanding of how this table was compiled or through willfully lying about the significance of the figures in this table. For one thing, looking at the table you’ll see things like “cardiac arrest,” “septic shock,” “multiorgan failure,” and “respiratory failure.” These can all be sequelae of severe COVID-19 infection that ultimately lead to death; so it would be shocking if they weren’t on the table:

To understand how the CDC table was tabulated, let’s elaborate on the Tweet above. You have to understand that it was compiled from standardized death certificates. It’s been a long time since I’ve had to fill out a death certificate—thankfully!—but I still remember how they work. On the death certificate form, there is a space for the immediate cause of death and then several lines for underlying causes. In brief, death certificates are filled out by the medical certifier (who can be the physician who had treated the patient before death), who provides his best medical opinion regarding the cause of death. Part I of the death certificate includes the proximal cause of death, or what directly caused the death, and Part II lists conditions that contributed to the death:

For example, if a patient dies of respiratory failure due to acute respiratory distress syndrome (ARDS), which was the result of pneumonia, which was the result of COVID-19, the proximal cause of death was the respiratory failure, but contributing causes were ARDS and COVID-19, with the one farthest up the chain being the underlying cause of death under Part I. If the patient had hypertension or asthma, that would go under Part II. As I like to say, if you suffer a cardiac arrest due to blood loss after being shot, the cardiac arrest might have been the proximal cause of death, but you still died of a gunshot wound. Still, that didn’t stop the Twitter brain trust from asking idiotic questions like:

https://twitter.com/mypersonalia/status/1300013312957087745?s=20

The answer is no. Anyone who has even the most rudimentary understanding of how death certificates are filled out would laugh at just how ignorant the person asking this question must be.

Sometimes these underlying causes contribute to the death. For example, if you have hemophilia and suffer a stab wound that leads you to bleed out and die when someone with normal blood clotting probably would have survived, then you still died of a stab wound, but the hemophilia was a contributing cause of death.

It’s really not that difficult to understand. Former fellow ScienceBlogs blogger Mark Hoofnagle Tweeted this:

And another, simpler, explanation:

And a couple of examples Tweeted three weeks before the “only 6%” disinformation campaign began:

It is true that sometimes determining the most important underlying cause isn’t always straightforward, but in the vast majority of COVID-19 cases it is. If someone with hypertension, obesity, and type 2 diabetes catches COVID-19, then develops pneumonia, then develops failure of multiple organ systems, and finally dies of respiratory failure, the proximate cause of death is respiratory failure, but the underlying cause of death is COVID-19, without which the respiratory failure never would have happened. Yes, it is well-known that certain conditions greatly increase your risk of dying if you contract COVID-19. These include, among several others:

  • Age (the chance of dying of COVID-19 begins to increase dramatically after age 50 and becomes truly frightening by age 80)
  • Obesity (BMI > 30)
  • Being male
  • Cancer
  • Chronic kidney disease
  • COPD (chronic obstructive pulmonary disease)
  • Immunocompromised state (weakened immune system) from solid organ transplant
  • Obesity (body mass index [BMI] of 30 or higher)
  • Serious heart conditions, such as heart failure, coronary artery disease, or cardiomyopathies
  • Sickle cell disease
  • Type 2 diabetes mellitus

These are contributory factors, but if you have one or more of these conditions when you contract COVID-19 and later die, it’ll very likely be the COVID-19, not your underlying health condition, that killed you. The underlying health condition(s) might have played a role in making you sicker, but it’ll be the virus that does you in.

Of course, the “only 6%” gambit is even more dishonest than it seems. Why? Because we have actual data published the same day as Table 3 telling us that. More importantly, the actual interpretation of the underlying data for the table shows:

In other words, COVID-19 is the underlying cause of around 92.3% of the deaths in the dataset, not 6%.

Also, the US isn’t the only country in the world with COVID-19. There are data from many other nations. As “Health Nerd” notes:

One important thing to note is that a lot of this is specific to the U.S. There are, oddly enough, quite a few other countries around the world, and they all have their own way of recording deaths. In some places, for example India, there has been a lot of criticism that the death reporting is shockingly bad and thus the country may be missing some or even the majority of their COVID-19 deaths. In other places, like Belgium, the death reporting is so good that it may explain the high COVID-19 death rates — they are simply picking up coronavirus deaths that other places have missed.

However, one thing remains true: most countries go to great lengths to ensure that deaths are correctly classified. Death reporting is incredibly important, and in most places it’s a detailed process that has to be checked carefully. In most cases, we can say with some certainty that deaths attributed to COVID-19 are, at best, a solid count, and at worst probably an underestimate. If anything, it’s likely that we are missing quite a few deaths that have been caused by coronavirus, but for whatever reason not picked up in our reporting systems, and thus the death count is actually higher than the reported figure.

And I say all of this as someone who has spent quite a bit of time studying COVID-19 death rates. I’ve now co-authored two studies looking at the fatality rates of COVID-19, and can say with some certainty that they are pretty good estimates, if probably a little low.

The bottom line is that the “only 6%” gambit is disinformation. It’s likely either astroturf or a product of the deranged minds of QAnon conspiracy theorists (or both). What’s most depressing is that we have a President who amplifies dangerous disinformation like this to a social media ecosystem of willing accomplices, allowing nonsense like this to go viral. As for the inevitable tone police trolls who will likely lament that I’m being way too sarcastic, insulting, and nasty, tough. Anything related to QAnon doesn’t deserve my civility.

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The Truth About Dentistry

Dentists seem to have the lowest standards of any profession. Horrifying. No wonder so many commit suicide.

From The Atlantic in 2019:

When you’re in the dentist’s chair, the power imbalance between practitioner and patient becomes palpable. A masked figure looms over your recumbent body, wielding power tools and sharp metal instruments, doing things to your mouth you cannot see, asking you questions you cannot properly answer, and judging you all the while. The experience simultaneously invokes physical danger, emotional vulnerability, and mental limpness. A cavity or receding gum line can suddenly feel like a personal failure. When a dentist declares that there is a problem, that something must be done before it’s too late, who has the courage or expertise to disagree? When he points at spectral smudges on an X-ray, how are we to know what’s true? In other medical contexts, such as a visit to a general practitioner or a cardiologist, we are fairly accustomed to seeking a second opinion before agreeing to surgery or an expensive regimen of pills with harsh side effects. But in the dentist’s office—perhaps because we both dread dental procedures and belittle their medical significance—the impulse is to comply without much consideration, to get the whole thing over with as quickly as possible.

The uneasy relationship between dentist and patient is further complicated by an unfortunate reality: Common dental procedures are not always as safe, effective, or durable as we are meant to believe. As a profession, dentistry has not yet applied the same level of self-scrutiny as medicine, or embraced as sweeping an emphasis on scientific evidence. “We are isolated from the larger health-care system. So when evidence-based policies are being made, dentistry is often left out of the equation,” says Jane Gillette, a dentist in Bozeman, Montana, who works closely with the American Dental Association’s Center for Evidence-Based Dentistry, which was established in 2007. “We’re kind of behind the times, but increasingly we are trying to move the needle forward.”

Consider the maxim that everyone should visit the dentist twice a year for cleanings. We hear it so often, and from such a young age, that we’ve internalized it as truth. But this supposed commandment of oral health has no scientific grounding. Scholars have traced its origins to a few potential sources, including a toothpaste advertisement from the 1930s and an illustrated pamphlet from 1849 that follows the travails of a man with a severe toothache. Today, an increasing number of dentists acknowledge that adults with good oral hygiene need to see a dentist only once every 12 to 16 months.

Many standard dental treatments—to say nothing of all the recent innovations and cosmetic extravagances—are likewise not well substantiated by research. Many have never been tested in meticulous clinical trials. And the data that are available are not always reassuring.

The Cochrane organization, a highly respected arbiter of evidence-based medicine, has conducted systematic reviews of oral-health studies since 1999. In these reviews, researchers analyze the scientific literature on a particular dental intervention, focusing on the most rigorous and well-designed studies. In some cases, the findings clearly justify a given procedure. For example, dental sealants—liquid plastics painted onto the pits and grooves of teeth like nail polish—reduce tooth decay in children and have no known risks. (Despite this, they are not widely used, possibly because they are too simple and inexpensive to earn dentists much money.)

…Fluoridation of drinking water seems to help reduce tooth decay in children, but there is insufficient evidence that it does the same for adults. Some data suggest that regular flossing, in addition to brushing, mitigates gum disease, but there is only “weak, very unreliable” evidence that it combats plaque. As for common but invasive dental procedures, an increasing number of dentists question the tradition of prophylactic wisdom-teeth removal; often, the safer choice is to monitor unproblematic teeth for any worrying developments. Little medical evidence justifies the substitution of tooth-colored resins for typical metal amalgams to fill cavities. And what limited data we have don’t clearly indicate whether it’s better to repair a root-canaled tooth with a crown or a filling. When Cochrane researchers tried to determine whether faulty metal fillings should be repaired or replaced, they could not find a single study that met their standards.

“The body of evidence for dentistry is disappointing,” says Derek Richards, the director of the Centre for Evidence-Based Dentistry at the University of Dundee, in Scotland. “Dentists tend to want to treat or intervene. They are more akin to surgeons than they are to physicians. We suffer a little from that. Everybody keeps fiddling with stuff, trying out the newest thing, but they don’t test them properly in a good-quality trial.”

* When physicians complete their residency, they typically work for a hospital, university, or large health-care organization with substantial oversight, strict ethical codes, and standardized treatment regimens. By contrast, about 80 percent of the nation’s 200,000 active dentists have individual practices, and although they are bound by a code of ethics, they typically don’t have the same level of oversight.

* Among other problems, dentistry’s struggle to embrace scientific inquiry has left dentists with considerable latitude to advise unnecessary procedures—whether intentionally or not. The standard euphemism for this proclivity is overtreatment. Favored procedures, many of which are elaborate and steeply priced, include root canals, the application of crowns and veneers, teeth whitening and filing, deep cleaning, gum grafts, fillings for “microcavities”—incipient lesions that do not require immediate treatment—and superfluous restorations and replacements, such as swapping old metal fillings for modern resin ones. Whereas medicine has made progress in reckoning with at least some of its own tendencies toward excessive and misguided treatment, dentistry is lagging behind. It remains “largely focused upon surgical procedures to treat the symptoms of disease,” Mary Otto writes. “America’s dental care system continues to reward those surgical procedures far more than it does prevention.”

“Excessive diagnosis and treatment are endemic,” says Jeffrey H. Camm, a dentist of more than 35 years who wryly described his peers’ penchant for “creative diagnosis” in a 2013 commentary published by the American Dental Association. “I don’t want to be damning. I think the majority of dentists are pretty good.” But many have “this attitude of ‘Oh, here’s a spot, I’ve got to do something.’ I’ve been contacted by all kinds of practitioners who are upset because patients come in and they already have three crowns, or 12 fillings, or another dentist told them that their 2-year-old child has several cavities and needs to be sedated for the procedure.”

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The Natural Cures They Don’t Want You To Know About!

Surgeon David Gorski writes:

One of the biggest medical conspiracy theories for a long time has been that there exist out there all sorts of fantastic cures for cancer and other deadly diseases but you can’t have them because (1) “they” don’t want you to know about them (as I like to call it, the Kevin Trudeau approach) and/or (2) the evil jackbooted thugs of the FDA are so close-minded and blinded by science that they crush any attempt to market such drugs and, under the most charitable assessment under this myth, dramatically slow down the approval of such cures. The first version usually involves “natural” cures or various other alternative medicine cures that are being “suppressed” by the FDA, FTC, state medical boards, and various other entities, usually at the behest of their pharma overlords. The second version is less extreme but no less fantasy-based. It tends to be tightly associated with libertarian and small government fantasists and a loose movement in medicine with similar beliefs known as the “health freedom” movement. who posit that, if only the heavy hand of government were removed and the jack-booted thugs of the FDA called off, free market innovation would flourish and all these cures, so long suppressed by an overweening regulatory apparatus, the floodgates would open and these cures, long held back by the dam of the FDA, would flow to the people.(Funny how it didn’t work out that way before the Pure Food and Drug Act of 1906.) Of course, I can’t help but note that in general, in this latter idea, these fantastical benefits seem to be reserved only for those who have the cash, because, well, the free market fixes everything.

The idea that the FDA is keeping cures from desperate terminally ill people, either intentionally or unintentionally, through its insistence on a rigorous, science-based approval process in which drugs are taken through preclinical work, phase 1, phase 2, and phase 3 testing before approval is one of the major driving beliefs commonly used to justify so-called “right-to-try” laws.

* I can totally understand the patient impetus for these laws, given that I have had family members with terminal illnesses. Unfortunately, however, forces like the Goldwater Institute are taking advantage of the very human desire not to die and not to be forced to watch one’s loved ones die, all in order to push bad legislation. Indeed, the Goldwater Institute uses terminally ill patients desperate for their lives in much the same way Stanislaw Burzynski uses them: As shields and weapons in their battle against the FDA and state medical boards. That’s why, as I’ve morbidly joked before, being against right-to-try in the eye of the public is not unlike being against Mom, apple pie, the American flag, and puppies, hence the reluctance of even doctors doing clinical trials to publicly voice opposition. The most predictable attack against anyone who dares to publicly oppose these bills has been to portray opponents as not just callous, but as practically twirling their mustaches with delight and cackling evilly while watching terminally ill patients die without hope.

* Not surprisingly, libertarians are declaring this a big “win” for patient’s rights. It’s nothing of the sort. The flavor of the arguments can best be seen in two articles from Reason.com’s Nick Gillespie, who is clearly clueless about clinical trials. Basically, he took to Reason.com to gloat, referencing an article from over two weeks ago that he entitled The Upside of Ebola (Yes, There May Actually Be One). It’s about as blatant a move to take advantage of the Ebola outbreak to promote bad right-to-try legislation as I’ve ever seen. The subtitle exults:

A rising death toll, mass panic, scary mortality rate—what could possibly be good about the out-of-control epidemic? It may accelerate the adoption of laws giving patients more power.

Yeah, sure. Thousands of people are dying of a horrible disease in Africa while people in the U.S. are freaking out about the possibility of the virus causing outbreaks right here at home, and Gillespie sees these events, apparently more than anything else, as an opportunity to push his libertarian agenda with respect to medicine:

Ebola’s arrival and seeming spread in America is causing mass panic, tasteless Internet jokes, and incredibly poorly timed magazine covers. Can anything good come out of the disease, which has no known cure and a terrifying mortality rate of 50 percent?

Yes. To the extent it forces a conversation about the regulations surrounding the development of new drugs and the right of terminal patients to experiment with their own bodies, Ebola in the United States may well accelerate adoption of so-called right-to-try laws. These radical laws allow terminally ill patients access to drugs, devices, and treatments that haven’t yet been fully approved by the Federal Drug Administration and other medical authorities. The patients and their estates agree not to bring legal action against caregivers, pharmaceutical companies, and insurers.

You don’t have to be a doctrinaire libertarian—though it helps—to see the value in letting people with nothing left to lose experiment on themselves. They may get a new lease on life. The rest of us get meaningful information that may speed up the development of the next great medical intervention.

Actually, you do rather have to be a doctrinaire libertarian to have a reality distortion field as powerful as Nick Gillespie’s that leads him to write drivel like this. Ebola and right-to-try laws. Hmmmm. How is one thing not like the other (or not related to the other)? First of all, Gillespie’s rationale is a complete non sequitur, clearly designed to take advantage of the Ebola panic to persuade people that right-to-try laws are a good idea, even though such laws would not have had one whit of an effect on the odd patient in the US who might be infected with Ebola. After all, Ebola, as deadly as it is, is not a terminal illness. Second, I can’t help but note that existing FDA mechanisms got ZMapp to American Ebola patients rather rapidly, no need for right-to-try laws necessary. But excuse me. What Gillespie says is that Ebola and ZMapp are “forcing a conversation.” I suppose that’s true, but it’s the wrong conversation, a profoundly deceptive conversation, in which an advocate of right-to-try laws shamelessly takes plays on people’s fears of Ebola to promote these bad laws. Claiming that there is “no good argument against right-to-try” (wrong, wrong, wrong), Gillespie also shamelessly attacks straw men, representing the primary argument against right-to-try as giving patients “false hope.” There are lots of other reasons why these are bad laws.

But Gillespie is just getting warmed up:

But what’s already cruel is the FDA’s drug-testing process. It’s massively expensive and overly long, costing between $800 million and $1 billion to bring a drug to market and taking a decade or more to complete the approval process. There’s every reason to believe that the FDA approval process is killing as many or more people than it saves, especially as the FDA doesn’t allow approvals from Europe and elsewhere to stand in for trials here.

Uh, no. There is not “every reason to believe” anything of the sort. See? Once again, there’s the myth that there are all these fantastic cures out there that the FDA, through its bureaucratic inertia, is keeping from you. I am rather grateful, though, that Gillespie, through his link, makes his intent very clear. The article to which he linkes is entitled Kill The FDA (Before It Kills Again), in which, referencing the movie Dallas Buyers Club—which I finally saw on cable and was surprised to find that, leaving aside its historical inaccuracies about the AIDS epidemic in the 1980s, taken just as a movie it was at best just OK (I was seriously disappointed)—Gillespie proclaims that the FDA “continues to choke down the supply of life-saving and life-enhancing drugs that will everyone agrees will play a massive role not just in reducing future health care costs but in improving the quality of all our lives.” And what is his rationale? Wrap your mind around this:

As my Reason colleague Ronald Bailey has written, this means the FDA’s caution “may be killing more people than it saves.” How’s that? “If it takes the FDA ten years to approve a drug that saves 20,000 lives per year that means that 200,000 people died in the meantime.”

Completely missing from Bailey’s and Gillespie’s equation is the number of drugs that the FDA doesn’t approve because they don’t show efficacy and safety that could allow even more than those 20,000 people a year to die or even actively kill some of them. As conceded by even Bailey, it was the FDA that prevented, for example, approval of Thalidomide in the US and the rash of birth defects seen elsewhere in the world. Bailey’s argument is, at best, tenuous, at worse misleading. Gillespie notes:

A 2006 Government Accountability Office (GAO) study found that the number of new drug applications submitted to the FDA between 1993 and 2004 increased by just 38 percent despite an increase in research and development of 147 percent. The mismatch, said GAO, was the result of many factors, ranging from basic issues with translating discoveries into usable drugs, patent law, and dubious business decisions by drug makers. But the problems also included “uncertainty regarding regulatory standards for determining whether a drug should be approved as safe and effective,” a reality that almost certainly made pharmaceutical companies more likely to tweak old drugs rather than go all in on new medicines.

Notice how this is another non sequitur applied to right-to-try laws, given that the answer to this problem would be regulatory clarity, not state-by-state right-to-try laws. Think of it this way: What’s more uncertain? The FDA or having different laws in different states regarding “right to try”? Gillespie’s citing his previous article claiming that the FDA is killing you in an article promoting right-to-try is a very good indication what these laws are really about. They are not about helping patients. That’s how they are sold to desperately ill patients, but in reality libertarians like Gillespie and Bailey are using desperately ill patients in the same way that Stanislaw Burzynski is: As a powerful tool to sway public opinion against the FDA and towards their viewpoint.

There’s a reason that certain aspects of these laws are not as widely emphasized in the PR offensive in favor of right to try. It’s because they are pure “health freedom” and libertarian wingnuttery. For example, if you look at the Goldwater Institute template for right to try laws, which, unfortunately, has been the basis of every right to try law passed and under consideration, you’ll notice a number of highly problematic clauses. As I’ve discussed multiple times, there is the requirement that the drug or device has only passed phase 1 trials, which, given how few drugs that have passed phase 1 actually make it through to approval, is a really low bar, especially since most phase 1 trials involve fewer than around 25 patients.

More disturbing are the financial aspects. The Goldwater Institute legislative language template (to which the Michigan legislation is virtually identical) allows drug companies to charge patients, with no provision to help patients pay for exercising right-to-try. Indeed, it specifically states that the bill “does not require any governmental agency to pay costs associated with the use, care, or treatment of a patient with an investigational drug, biological product, or device” and that insurance companies do not have to pay for costs associated with the use of such therapies. You know what this means? Insurance companies could refuse to pay for care related to complications that might occur because of experimental treatments. You use an experimental drug and suffer a complication? Too bad! Your insurance company can cut you off! Now, it’s unlikely that government entities like Medicare or Medicaid would do that, but insurance companies certainly will.

Basically, what this law says is: If you can afford it yourself, no help, you can have it. If not, you’re SOL. As I’ve pointed out, if there’s one thing worse than dying of a terminal illness, it’s suffering unnecessary complications from a drug that is incredibly unlikely to save or significantly prolong your life and bankrupting yourself and family in the process. Right-to-try encourages just that. What’s more compassionate? Attacking the FDA and degrading the approval process that requires drug safety and efficacy while dangling false hope in front of patients or standing up and protecting patients from the harm such a policy could cause. Let’s just put it this way: I predict that Stanislaw Burzynski will soon be sending antineoplastons to patients in right-to-try states if, as he keeps bragging, the FDA has allowed him to reopen his clinical trials. After all, his antineoplastons would qualify just fine under right-to-try laws if they’re back under clinical trial. Indeed, if there’s one thing the decades-long battle between the FDA and Burzynski tells us, it’s that the FDA actually bends over way too far backwards to allow manufacturers of dubious drugs to prove themselves.

Finally, the anti-FDA rhetoric, such as linked to by Gillespie, is a very good indication that the true purpose of right-to-try legislation is to neuter the FDA’s power to control drug approval, thus greatly loosening or even eliminating hurdles to the drug approval process. It is no coincidence that the strongest, richest, and most vocal proponents of these laws are the Goldwater Institute and libertarians like Nick Gillespie and Ronald Bailey, who, not coincidentally, think that the FDA is “killing us.” Those articles are a definite tell. It’s also clearly a strategy to get right-to-try passed in as many states as possible and get referendums passed by wide margins to pressure the federal government to weaken the FDA.

In the end, though, right-to-try laws are what I like to call “placebo” laws in that they make people who pass them and support them feel good but don’t actually address the problem that they are supposedly intended to address. Drug approval regulatory authority lies with the FDA; it could completely ignore state right-to-try laws. The FDA also has a compassionate use program and rarely turns down such requests. Admittedly, the application process is long and probably too onerous, but the answer to that problem is not state right-to-try laws. It’s to address the issue at the federal level. I’ve also said in an interview that, now that my state government has foolishly passed a right-to-try law, one of two things is likely to happen: Either nothing, because federal authority trumps state authority, or disaster for patients, doctors, and, yes, biotech and drug companies. Everybody, myself included, wants to help terminally ill patients. After all, I’ve seen too many of them. Right to try and similar misguided efforts, however, are not the way.

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The Problem With Challenge Trials

Marcia Angell writes: There are two specific problems with even the most carefully done challenge studies of a Covid-19 vaccine. First, we still know very little about this novel virus, including what hidden or longterm effects it might have on even young, healthy volunteers. And second, will a vaccine be equally effective in the elderly and chronically ill, those who are most vulnerable to Covid-19? Elliott acknowledges this problem, but I think it may be more serious than he implies.

But more generally, I worry about the erosion of our hard-won ethical consensus (starting with the Nuremberg Code) that people should not be used as means to an end if they might be harmed. There is also a risk of bribery or coercion in enrolling volunteers, even if they are officially unpaid. I believe this erosion of our ethical standards, even for a good cause, would be a very unfortunate precedent. We would then be on the proverbial slippery slope downhill.

Carl Elliott replies: First, if research subjects in the United States are sickened or injured in a trial, they may well face financial ruin on top of their illness. Most sponsors require subjects to pay for their own medical care, and virtually none guarantees compensation for pain, suffering, or the inability to work. Second, many of the current industry sponsors of vaccine trials have a record of burying, spinning, and rigging their research. (The list of such sponsors includes Merck, for which Lipsitch consults.) Third, even if a trial leads to a vaccine, we have been given no guarantees that it will be made available to those who can’t afford it, raising the possibility that the sacrifices made in vaccine trials will yield benefits primarily to the rich and well insured.

None of these problems is unique to challenge studies. What is unique about those studies is the extraordinary number of people willing to volunteer without being told about the fine print. This is a recipe for exploitation. Eyal and Lipsitch claim their priority in their article was “to explain how to select participants with minimal likelihood of dying,” yet in the study design they proposed, some subjects up to the age of forty-five would be exposed to the coronavirus after getting only a placebo vaccine.

Like Marcia Angell, I’m disturbed by the use of subjects as a means to an end, especially when the risks are unknown. If I left the door to Covid-19 vaccine challenge studies ajar, I can think of no one better than Angell to close it. In fact, we may need to close a lot more doors. In Phase I trials, researchers routinely use subjects as a means to an end, even when the risks are significant and the subjects are vulnerable. That slope was slippery and we have reached the bottom. We need to find a way back up.

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Should antidepressants be used for major depressive disorder?

From a 2019 meta-analysis in the British Medical Journal: Conclusions: The benefits of antidepressants seem to be minimal and possibly without any importance to the average patient with major depressive disorder. Antidepressants should not be used for adults with major depressive disorder before valid evidence has shown that the potential beneficial effects outweigh the harmful effects.

Wikipedia notes:

[Harvard psychology professor Irving] Kirsch’s analysis of the effectiveness of antidepressants was an outgrowth of his interest in the placebo effect. His first meta-analysis was aimed at assessing the size of the placebo effect in the treatment of depression.[7] The results not only showed a sizeable placebo effect, but also indicated that the drug effect was surprisingly small. This led Kirsch to shift his interest to evaluating the antidepressant drug effect.

The controversy surrounding this analysis led Kirsch to obtain files from the U.S. Food and Drug Administration (FDA) containing data from trials that had not been published, as well as those data from published trials. Analyses of the FDA data showed the average size effect of antidepressant drugs to be equal to 0.32, clinically insignificant according to the National Institute for Health and Clinical Excellence (NICE) 2004 guidelines, requiring Cohen’s d to be no less than 0.50.[8] No evidence was cited to support this cut-off and it was criticised for being arbitrary;[9] NICE removed the specification of criteria for clinical relevance in its 2009 guidelines.[10][11]

Kirsch challenges the chemical-imbalance theory of depression, writing “It now seems beyond question that the traditional account of depression as a chemical imbalance in the brain is simply wrong.” [12] In 2014, in the British Psychological Society’s Research Digest, Christian Jarrett included Kirsch’s 2008 antidepressant placebo effect study in a list of the 10 most controversial psychology studies ever published.[13]

In September 2019 Irving Kirsch published a review in BMJ Evidence-Based Medicine, which concluded that antidepressants are of little benefit in most people with depression and thus they should not be used until evidence shows their benefit is greater than their risks.

Marcia Angell writes in the New York Review of Books:

It seems that Americans are in the midst of a raging epidemic of mental illness, at least as judged by the increase in the numbers treated for it. The tally of those who are so disabled by mental disorders that they qualify for Supplemental Security Income (SSI) or Social Security Disability Insurance (SSDI) increased nearly two and a half times between 1987 and 2007—from one in 184 Americans to one in seventy-six. For children, the rise is even more startling—a thirty-five-fold increase in the same two decades. Mental illness is now the leading cause of disability in children, well ahead of physical disabilities like cerebral palsy or Down syndrome, for which the federal programs were created.

A large survey of randomly selected adults, sponsored by the National Institute of Mental Health (NIMH) and conducted between 2001 and 2003, found that an astonishing 46 percent met criteria established by the American Psychiatric Association (APA) for having had at least one mental illness within four broad categories at some time in their lives. The categories were “anxiety disorders,” including, among other subcategories, phobias and post-traumatic stress disorder (PTSD); “mood disorders,” including major depression and bipolar disorders; “impulse-control disorders,” including various behavioral problems and attention-deficit/hyperactivity disorder (ADHD); and “substance use disorders,” including alcohol and drug abuse. Most met criteria for more than one diagnosis. Of a subgroup affected within the previous year, a third were under treatment—up from a fifth in a similar survey ten years earlier.

Nowadays treatment by medical doctors nearly always means psychoactive drugs, that is, drugs that affect the mental state. In fact, most psychiatrists treat only with drugs, and refer patients to psychologists or social workers if they believe psychotherapy is also warranted. The shift from “talk therapy” to drugs as the dominant mode of treatment coincides with the emergence over the past four decades of the theory that mental illness is caused primarily by chemical imbalances in the brain that can be corrected by specific drugs. That theory became broadly accepted, by the media and the public as well as by the medical profession, after Prozac came to market in 1987 and was intensively promoted as a corrective for a deficiency of serotonin in the brain. The number of people treated for depression tripled in the following ten years, and about 10 percent of Americans over age six now take antidepressants. The increased use of drugs to treat psychosis is even more dramatic.

Marcia Angell follows up in the July 14, 2011 issue:

One of the leaders of modern psychiatry, Leon Eisenberg, a professor at Johns Hopkins and then Harvard Medical School, who was among the first to study the effects of stimulants on attention deficit disorder in children, wrote that American psychiatry in the late twentieth century moved from a state of “brainlessness” to one of “mindlessness.” By that he meant that before psychoactive drugs (drugs that affect the mental state) were introduced, the profession had little interest in neurotransmitters or any other aspect of the physical brain. Instead, it subscribed to the Freudian view that mental illness had its roots in unconscious conflicts, usually originating in childhood, that affected the mind as though it were separate from the brain.

But with the introduction of psychoactive drugs in the 1950s, and sharply accelerating in the 1980s, the focus shifted to the brain. Psychiatrists began to refer to themselves as psychopharmacologists, and they had less and less interest in exploring the life stories of their patients. Their main concern was to eliminate or reduce symptoms by treating sufferers with drugs that would alter brain function. An early advocate of this biological model of mental illness, Eisenberg in his later years became an outspoken critic of what he saw as the indiscriminate use of psychoactive drugs, driven largely by the machinations of the pharmaceutical industry.

When psychoactive drugs were first introduced, there was a brief period of optimism in the psychiatric profession, but by the 1970s, optimism gave way to a sense of threat. Serious side effects of the drugs were becoming apparent, and an antipsychiatry movement had taken root, as exemplified by the writings of Thomas Szasz and the movie One Flew Over the Cuckoo’s Nest. There was also growing competition for patients from psychologists and social workers. In addition, psychiatrists were plagued by internal divisions: some embraced the new biological model, some still clung to the Freudian model, and a few saw mental illness as an essentially sane response to an insane world. Moreover, within the larger medical profession, psychiatrists were regarded as something like poor relations; even with their new drugs, they were seen as less scientific than other specialists, and their income was generally lower.

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The 10 Most Controversial Psychology Studies Ever Published

From the British Psychological Society:

* 5. Loftus’ “Lost in The Mall” Study
In 1995 and ‘96, Elizabeth Loftus, James Coan and Jacqueline Pickrell documented how easy it was to implant in people a fictitious memory of having been lost in a shopping mall as a child. The false childhood event is simply described to a participant alongside true events, and over a few interviews it soon becomes absorbed into the person’s true memories, so that they think the experience really happened. The research and other related findings became hugely controversial because they showed how unreliable and suggestible memory can be. In particular, this cast doubt on so-called “recovered memories” of abuse that originated during sessions of psychotherapy. This is a highly sensitive area and experts continue to debate the nature of false memories, repression and recovered memories. One challenge to the “lost in the mall” study was that participants may really have had the childhood experience of having been lost, in which case Loftus’ methodology was recovering lost memories of the incident rather than implanting false memories. This criticism was refuted in a later study (pdf) in which Loftus and her colleagues implanted in people the memory of having met Bugs Bunny at Disneyland. Cartoon aficionados will understand why this memory was definitely false.

* 8. The Kirsch Anti-Depressant Placebo Effect Study
In 2008 Irving Kirsch, a psychologist who was then based at the University of Hull in the UK, analysed all the trial data on anti-depressants, published and unpublished, submitted to the US Food and Drug Administration. He and his colleagues concluded that for most people with mild or moderate depression, the extra benefit of anti-depressants versus placebo is not clinically meaningful. The results led to headlines like “Depression drugs don’t work” and provided ammunition for people concerned with the overprescription of antidepressant medication. But there was also a backlash. Other experts analysed Kirsch’s dataset using different methods and came to different conclusions. Another group made similar findings to Kirsch, but interpreted them very differently – as showing that drugs are more effective than placebo. Kirsch is standing his ground. Writing earlier this year, he said: “Instead of curing depression, popular antidepressants may induce a biological vulnerability making people more likely to become depressed in the future.”

* 9. Judith Rich Harris and the “Nurture Assumption”
You could fill a library or two with all the books that have been published on how to be a better parent. The implicit assumption, of course, is that parents play a profound role in shaping their offspring. Judith Rich Harris challenged this idea with a provocative paper published in 1995 in which she proposed that children are shaped principally by their peer groups and their experiences outside of the home. She followed this up with two best-selling books: The Nurture Assumption and No Two Alike. Writing for the BPS Research Digest in 2007, Harris described some of the evidence that supports her claims: “identical twins reared by different parents are (on average) as similar in personality as those reared by the same parents … adoptive siblings reared by the same parents are as dissimilar as those reared by different parents … [and] … children reared by immigrant parents have the personality characteristics of the country they were reared in, rather than those of their parents’ native land.” Harris has powerful supporters, Steven Pinker among them, but her ideas also unleashed a storm of controversy and criticism. “I am embarrassed for psychology,” Jerome Kagan told Newsweek after the publication of Harris’ Nurture Assumption.

* 10. Libet’s Challenge to Free Will

Your decisions feel like your own, but Benjamin Libet’s study using electroencephalography (EEG) appeared to show that preparatory brain activity precedes your conscious decisions of when to move. One controversial interpretation is that this challenges the notion that you have free will. The decision of when to move is made non-consciously, so the argument goes, and then your subjective sense of having willed that act is tagged on afterwards. Libet’s study and others like it have inspired deep philosophical debate. Some philosophers like Daniel Dennett believe that neuroscientists have overstated the implications of these kinds of findings for people’s conception of free will. Other researchers have pointed out flaws in Libet’s research, such as people’s inaccuracy in judging the instant of their own will. However, the principle of non-conscious neural activity preceding conscious will has been replicated using fMRI, and influential neuroscientists like Sam Harris continue to argue that Libet’s work undermines the idea of free will.

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How Do We Make Sense Of A Confusing World? (3-30-21)

00:00 Who’s carrying out the anti-asian crime wave?
07:00 Photographers encouraged to take photos of attractive women
22:00 Dennis Dale joins to discuss diversity, anti-asian violence, https://dennisdale.wordpress.com/
54:00 2020 election
1:02:00 Many Capitol rioters unlikely to serve jail time, https://www.politico.com/news/2021/03/30/jan-6-capitol-riot-jail-time-478440
1:48:00 Leslie Ellis: The creative power of dreamwork, https://relationalimplicit.com/ellis/
1:59:00 Trans resistance has come out of nowhere, https://www.unz.com/isteve/nyt-in-2021-organized-resistance-to-world-war-trans-2013-seems-to-have-come-out-of-nowhere/
2:01:00 Arkansas passes bill restricting access to medical treatments for transgender children, https://www.washingtonpost.com/dc-md-va/2021/03/29/arkansas-passes-bill-restricting-access-medical-treatments-transgender-children/
2:10:00 My snake nightmares, https://www.lukeford.net/luke_ford/bio/l7a.html
2:22:00 Porn and society
2:38:00 Votescam: The Stealing of America, https://twitter.com/klejdys/status/1376891125777186822
2:47:00 Mind Fixers: Psychiatry’s Troubled Search for the Biology of Mental Illness
2:50:30 Trickster: The Many Lives of Carlos Castaneda, https://www.audible.com/pd/Trickster-The-Many-Lives-of-Carlos-Castaneda-Podcast/B08JJMVXXM

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Relational Perspectives on the Body

Here are some excerpts from this 1998 book:

* One’s image of oneself or one’s self-representation originates in one’s bodily sensations and is a reflection of one’s body image.

* According to the Dictionary of the American Psychological Association: “affect n. any experience of feeling or emotion, ranging from suffering to elation, from the simplest to the most complex sensations of feeling, and from the most normal to the most pathological emotional reactions. Often described in terms of positive affect or negative affect, both mood, and emotion are considered affective states. Along with cognition and conation, affect is one of the three traditionally identified components of the mind.”

* conation n. the proactive (as opposed to habitual) part of motivation that connects knowledge, affect, drives, desires, and instincts to behavior. Along with affect and cognition, conation is one of the three traditionally identified components of mind. The behavioral basis of attitudes is sometimes referred to as the conative component.

* embodied cognition: the thesis that the human mind is largely determined by the structures of the human body (morphology, sensory and motor systems) and its interactions with the physical environment. This concept emerged from work in late 20th century linguistics, philosophy, and cognitive psychology.

* A potentially useful concept here is ’embodiment’: the processes whereby our physical bodies incorporate traces of previous experiences. … Embodiment may be physical, cognitive or emotional and refers to the processes whereby a person’s life experiences are literally incorporated into their body.

* reflexive behavior: responses to stimuli that are involuntary or free from conscious control (e.g., the salivation that occurs with the presentation of food) and therefore serve as the basis for classical conditioning. Compare planned behavior; voluntary behavior.

* The term cathexis is used to describe an investment of libidinal energy in an object or an idea. Sentimental attachment to a keepsake, a family heirloom, or a photograph would be an example of cathexis. Patriotism and other impassioned identifications with groups and systems of belief are also forms of cathexis. The word is derived from the Greek verb “to occupy” and is a translation of the German word Besetzung, “occupation.” The image suggests that the libido is sent out to “seize” the external object, as an army would seize and occupy a city.

* In attempting to understand the relationship between subject and object, psychoanalysis describes “objects” that have been cathected, invested with libidinal energy. These objects can be other people (the “object of one’s affections”) or anything else (including abstract concepts like “freedom” or “justice”) that serves as a focal point of desire.

* In psychoanalytic theory, the term “subject” refers to the sum of the physiological and psychological operations that sustain a human individual as a “person”. The human subject has both mental and bodily dimensions.

Psychoanalysis is critical of the Cartesian vision of the subject as a centered, autonomous “I” whose self-awareness can be taken as a foundation for philosophical inquiry. For psychoanalytic theorists like Freud and Lacan, the subject’s autonomy and self-awareness is constantly undermined by impulses from the id and steered by the pressures of the superego. In this sense, “individual” is an inaccurate synonmym for “subject” because the Freudian model of the subject is divided into at least three conflicting parts.

* mentalization: n. the ability to understand one’s own and others’ mental states, thereby comprehending one’s own and others’ intentions and affects. It has been theorized that this ability is a component of healthy personality development and is achieved through a child’s secure attachment to the parent. The concept has had particular application in the understanding and treatment of borderline personality disorder (BPD), characterized in this context as a disorder marked in part by an inability to mentalize due to poor attachment in early life.

* I remember that when I was in analytic training I would frequently hear (or tell) a joke along these lines: Students would say that, if you told a Freudian supervisor about a case organized around problems related to intimacy, then you would be told about the meaning of this in terms of the patient’s conflicted sexuality. If, on the other hand, you told an interpersonal supervisor about a case in which the patient’s sexuality played a central role, then you would likely be told to look at the underlying difficulties in the patient’s capacity for intimacy. There was, I believe, much truth to this joke. Both groups used theoretical structures, metapsychologies, to guide their analytic listening; and, whereas the Freudians tended to highlight bodily phenomena, particularly sexuality, as at the core, the interpersonalists tended to put interpersonal events at the center and to view sexuality as derivative of such interpersonal experience as intimacy. What was surface for one analyst was depth for the other.

* Sexual disturbances and problems [are conceived] as pointed reflections of wider and more general difficulties in living, reflections of the person’s outlook and orientation vis-a-vis himself as a physically independent unit and his concomitant outlook upon others. A person’s sexual behavior is then seen as a manifestation of his orientation rather than its cause.. . . Sexuality lends itself more readily than any other behavior to symbolic expression of attitudes toward oneself, others, and life itself.

* …four reasons why sexuality is a central organizer of childhood experience. First, because bodily sensations, processes, and events dominate a child’s early experience, bodily events are drawn on and elaborated imaginatively so that the child can construct and represent a view of the world and of the important people in it. Second, since sexuality involves both an interpenetration of bodies and desires and contact with the bodies’ boundaries and openings, it is ideally suited to represent longings, conflicts, and negotiations in the relations between self and others. Third, bodily, and especially sexual, experience entails powerful surges that are used to express the dynamics of conflict and interpersonally generated affect. Fourth, the very privacy, secrecy, and exclusion in one’s experience of one’s parent’s sexuality make it perfectly designed to take on meanings concerning a division of interpersonal realms, the accessible vs. the inaccessible, the visible vs. the shadowy, surface vs. depth. Sexuality takes on all the intensity of passionate struggles to make contact, to engage, to overcome isolation and exlusion [p. 103].

* I remembered one woman supervisor from whom I had learned a great deal, who told me repeatedly as we would listen together to a patient’s free associations to “think body, think sex, think dirty.”

* The interpersonal position stresses the formative impact of parental character.. . . the emotional life of the child is filled with and shaped by the contours of parental character and is constructed out of actual interactions. The parents’ issues become the child’s issues; the kinds of interaction they make possible determine the metaphors that ultimately are utilized by the child to constitute the intrapsychic.

* This book, Relational Perspectives on the Body; emerged out of this call for renewed attention to the place of the body and somatic experience within a relational paradigm. Psychoanalysis (across all of its various schools) has increasingly moved in a relational direction. Simultaneously with this shift from a drive-centered to a relational theory, the profession of psychoanalysis has undergone a demedicalization, which may have further shifted the attention of psychoanalysis away from the body. Nonmedically trained analysts may well have felt less sure of themselves in attending to and studying bodily based and psychosomatic phenomena. It is the intention of this book to bring the focus of psychoanalysis back to the body, to the bodily rooted self, to bodily based communication, to bodily and affective experience, and to somatic and psychosomatic phenomena, now all viewed in a relational context.

* In this chapter, I bring together these two broad areas of study: the role of the body in the psychoanalytic enterprise and the self-reflexive function of the mind: the clinical body and the reflexive mind. I focus our attention on the place of the body in the mind’s self-reflexive functioning, and the effects on the body when self-reflexive functioning is impaired. Extending this to the realm of the intersubjective, I will consider the mutual impact of the mind and the body on each other as the psychoanalytic situation entails two individuals jointly processing, experiencing, and reflecting on psychosomatic phenomena.

* Self-reflexivity (the capacity to experience, observe, and reflect on oneself as both a subject and an object) is at the very heart of the clinical psychoanalytic process, and in this chapter I explore the body’s role in self-reflexive functioning as well as the body’s involvement when self-reflexive functioning fails. The construction of a bodily self requires self-reflexivity, and self-reflexivity emerges through intersubjectivity. On the other hand, under normal conditions, intersubjectivity (and for that matter any subjectivity) is always embodied. Trauma is responsible for disruptions in the development of self-reflexivity, intersubjectivity, and embodiment.

* Self-reflection ordinarily connotes a cognitive process in which one thinks about oneself as if from the outside, that is, as if examining oneself as an object of thought. The way I am using self reflexivity here, by contrast, includes the dialectical process of experiencing oneself as a subject as well as of reflecting on oneself as an object. It is not, therefore, exclusively an intellectual observational function, but an experiential and affective function as well.

* [Sheldon] Bach (1985, 1994) suggests that a good deal of narcissistic and borderline pathology, including such structurally related conditions as perversions, addictions, eating disorders, and psychosomatic disorders, may be best understood in terms of the patient’s inability to maintain appropriate tension between these two perspectives on the self. When immersed in a state of consciousness of subjective awareness, the self is experienced as the agent, in Kohut’s (1977) words, as “a center of initiative and a recipient of impressions” (p. 99). At the extreme, this may lead a patient to experience grandiosity and a sense of entitlement and be unable to experience the self as an object among other objects or a self among other selves. When immersed in the state of consciousness of objective self-awareness, the patient can view himself or herself only as an object among other objects and cannot experience the sense of agency or vitality that comes with being a subject, a distinct center of thoughts, feelings, and actions. Although some patients (with certain forms of pathology) are more apt to maintain one side of this polarity over another (for example, overinflated narcissists tend to maintain states of subjective awareness, whereas depressives tend to maintain states of objective selfawareness), nevertheless, according to Bach, the real problem with all of these patients is that they have persistent difficulties moving back and forth between the two perspectives on the self and integrating them into their representational world.

Bach (1994) proposes that it is an important developmental achievement for a person “to integrate his sense of wholeness and aliveness (subjective awareness) with his parent’s and his own developing perspective on himself as one person among many others (objective self-awareness)” (p. 46). Accordingly, psychopathology is understood as a person’s inability to tolerate ambiguity and paradox, to deal with metaphor, or to maintain multiple points of view, especially about the self.5 Instead, in psychopathology, we find polarization, splitting, either-or thinking, manic and depressive mood swings, and sadomasochistic role reversals.

* Because one cannot simultaneously regard oneself as an object and immerse oneself in one’s own subjectivity, except perhaps during mystical experiences or states of ecstasy, and because these two modalities for self-knowledge can result in highly discrepant self-images, the capacity for reflexive self-awareness necessarily produces psychological tension and conflict, especially about one’s conception of oneself.

Auerbach, following Bach, goes on to elaborate narcissism as an attempt to escape the conflicts that result from self-reflexivity. He writes, “Kernberg’s narcissists, in their shameless grandiosity and entitlement, overemphasize subjective self-awareness; Kohut’s narcissists, in their shame ridden hypersensitivity, vulnerability, and submissiveness, overemphasize objective self-awareness.”

* “emotion is essentially psychosomatic”. Thus, when the psychological aspect of an emotion is ejected, the physiological part is left to express itself, leading to “psychosomatic explosions.”

* this development of “self-awareness of one’s affects as signals to oneself,” or, as he more dramatically calls it, of “owning one’s own soul”, that is the key step in the development of adult affect.

* Writing about dissociation resulting from trauma, Bromberg defines pathological dissociation as “a defensive impairment of reflective capacity” (p. 519). Conversely, as patients make the structural shift from dissociation to conflict, this movement is seen clinically “as the increasing capacity of the patient to adopt a self-reflective posture in which one aspect of the self observes and reflects (often with distaste) upon others that were formerly dissociated” (p. 525).
So, in the work of all the leading theorists of trauma and dissociation, just as in our survey of current work on psychosomatosis and alexithymia, we find an emphasis on the disruption of self-reflexive functioning at the heart of the pathology and the resumption of self-reflexive functioning as central to the cure.

* A long-established principle of psychoanalysis is that the analyst needs to form an alliance with the patient’s observing ego, which is split off from the patient’s experiencing ego.

* To become self-aware, a person must break the identification with any single aspect of self and engage in the internal dialogue of the multiple voices of subjectivity. Self-reflection, from this point of view, is based on the capacity for internal division and dialogue, healthy dissociation, standing in the spaces between realities, the transcendent,
oscillating, or dialectical function. Self-reflection is based on the ability to link up experiences, whereas trauma leads to dissociation as a result of “attacks on linking”.

* …one of Jung’s central contributions was the view of the unconscious as striving to compensate and correct for a one-sided conscious attitude.

* In summary, somatic symptoms, while pointing out the archaic connection with the primary object, highlight the failure or the inability to own the body and the mind. The body and the mind are not separate entities. Cartesian dualities have biased psychoanalytic thinking about the connection between the body and the mind, thus offering a schematic and fragmented perspective on their interrelationship. Rather, mind and body are better understood as operating within a dual track, a “Siamese twinship,” a “mind-body” that is one although it seems to be two (Grotstein, 1997).

Some specific conceptualizations by patients about the ownership of the body and the mind may be helpful to clinicians when listening to their patients from this framework. First, some patients actually physically tighten or tense their bodies in order to give the body boundaries, for fear that a relaxed body state would be equivalent to fusion with the powerful object. For example, Malcolm, a 45- year-old man, was preoccupied with tight, firm “butts,” both his own and that of the woman with whom he was involved. In the transference, he was preoccupied with the degree of firmness of the analyst’s “butt.” If two firm “butts” come together, there was no fear of fusion; but if one “butt” was not firm, even if his was, body boundaries would
disappear and he would fuse with the powerful object, the woman.

Second, affects that are localized in the body in a concrete way are real and therefore preferred. John, a 30-year-old single man suffering from ulcerative colitis, displayed the alexithymic trait of being unable to name affects and claimed ignorance when attempting to elaborate on his feelings. Inner life was practically nonexistent during the early stages of treatment. Only while talking about his illness did John become alive, as if the diseased body existed in ways his mind did not. To John, the body’s affliction was a sign of life.

Third, the psychic body exists if one does not admit loneliness. If loneliness or need for another person is acknowledged, psychic structure crumbles. Margaret, a 32-year-old woman, spent much of her time in analytic sessions caressing and stroking herself, particularly when the analyst was actively engaged with her (interpretations). Her attention was less on the interpretations offered by her analyst than on strengthening the boundaries of her own body. Fantasied relations with men were available to her 24 hours a day; she was never left in a state of loneliness or need for another person. Her ultimate desire to
remain in mother’s womb, and later to remain in analysis for the rest of her life, was the solution that warded off psychic disintegration.

Fourth, there can be a temporary mind-body dissociation when the body is experienced by the patient as failing him. Sam, a 48-yearold man, felt that his body had been weak since childhood. He described posture problems and not feeling balanced on his feet. He felt that his backbone could not keep him erect. During the analysis, Sam attempted various strenuous physical activities to try to correct this sense of his physical body. Each activity would start with hope and end in despair. His feelings about his weak body affected his feelings about his mind: weak body, weak mind. Unfortunately, during the course of the analysis, Sam developed a slowly degenerative physical condition that took away any hope of his having a strong body and, with it, a strong mind. Sam might have progressed if he could have separated the weak body from the strong mind. Instead, his anger at his weak body preoccupied him, and his mind was filled with attacks on his weak body. His mind was also filled with fantasies of his being an Olympic skier or a famous basketball player. He had two minds, one belonging to the weak body and split off from the other mind, which was full of potent, hopeful fantasies.

Several female patients who were experiencing physical difficulties felt that the body was their enemy, motivated to defeat them, that it was a “foreign body” with a mind of its own. Here we note a feeling of betrayal of the self by the body. This can, however, be a temporary state. Alice, a 52-year-old woman, and Margaret, 32 years of age, were enraged with their bodies when they experienced serious difficulties in their pregnancies and were unable to have their own children. They were particularly envious of their analyst’s body for being able to produce not only one baby but two (twins). They each had two bodies—their real bodies, which did not function as promised by their mothers, and their fantasied bodies, which worked perfectly and allowed for childbirth. For Alice, going through her pregnancy and childbirth in the analytic sessions led to her being able to buy a kitten to nurture. Margaret, who carried in her womb a baby who had to be aborted, was unable to mourn the loss. She continued to remain heavy—“pregnant”— even after the adoption of several children.

Fifth, the body realm is often used to avoid relationships. It serves to keep internal object relations a secret and ongoing while there is an actual avoidance of establishing new, real relationships. Andrew, a 41-year-old socially withdrawn single man, complained of an unusual sensitivity to temperature changes in the analyst’s office. He would remove his jacket and put it back on several times during a session. Andrew was convinced of the “biological reasons” for his condition, ignoring the analyst’s attempt to address his social isolation. Only at home, in the privacy of his bedroom, was he successful in regulating the temperature, which he maintained unchanged through the entire year. His preoccupation with his cold or warm body served as a buffer against relating. He ignored the analyst’s interventions and devalued both personal and professional relationships.

Sixth, psychosomatic concerns are often defenses against sexual and aggressive impulses, wishes and fantasies. Julia, a 27-year-old graduate student, tended to develop severe migraine headaches during sessions that she described as “heavy” or “difficult.” She would sit up on the couch, reach for her purse, and get her medication. She would then apologize, spending the rest of the session attending to her headache by pressing her temples with her hands or massaging her head. The analyst became a passive, useless observer, lacking the “touch” to soothe his patient’s pain.

John, whom we mentioned earlier, relates to his body as a physical object devoid of any meaning or fantasy elaboration. The early stages of his analysis were devoted to scientific descriptions of the vicissitudes of his illness. He reported his wife’s being unable to tolerate his demands for bodily attention, and his grieving about his illness in the middle of the night. Being alone with and within his body was too painful. He wanted the analyst to become familiar with the illness that perturbed his body and, keep him away from the contents of his mind; he hoped that the analyst would become la mere calmant (Fain, 1971).

A premature baby, John was placed in an incubator for several weeks. His mother, fearing that she might get too attached to him and then she would have to deal with a painful loss, refused to visit him in the hospital. She was convinced that her child was not going to survive. She refused to name her child, and only at the hospital’s insistence did the father name the child so he could obtain a birth certificate. Although John lived, his mother never overcame the fear of losing him. She became overprotective of John’s frail body. She used enemas, vitamins, and oils to assure herself of her child’s survival.

As an adult, John truly felt that he could not live without the assistance of others. He demanded from his analyst a complete recognition of his bodily illness. He wanted the analyst to care for his body, to listen to its noises, and to observe its movements. To John, the condition of his body was a matter of life and death. He was not sure whether he was going “to make it,” as his mother felt toward him.

* Several years into her analysis, my patient Iris said to me, “Our work will be done when I have had enough time with you, when I have been as comfortable in my body as one can be in an old sweatshirt.” When I asked her to tell me how that might feel, she said, “I would be able to be fully in my body, in your presence, and able to move freely around your room and touch and see things from my real self without fear. I would be able to give up the fear that comes with constantly overthinking and evaluating whether I really have or deserve your availability. I would be able to take for granted that it is fine with you that I can take you for granted.”

* Nearly all my patients suffer from some degree of disconnection from their bodies and, therefore, from their truest feelings and core sense of self. Patients complain of not being able to breathe naturally or to feel entitled to take up space or to move about the world propelled by authentic feelings and needs. They suffer from a deep conviction that they cannot occupy their bodies while maintaining mutually safe and intimate contact with the people they need most. I believe that these dissociative conditions are often the cumulative developmental sequelae of various forms of parent-child misattunement.

* During enactments of troubled relational patterns, analyst and patient will share or take turns feeling all kinds of disturbing experiences of psychosomatic disunity. These states of disconnection are powerful diagnostic tools that guide us to the places that need to be healed. I demonstrate through clinical examples that it is the analyst’s struggle to remain embodied consciously throughout these enactments that makes the patient feel, quite literally, held and, consequently, safe enough to
experiment with new relational patterns.

* When Freud removed his hand from his patient’s forehead and invited her to free associate, he empowered her mind but abandoned her experiencing body. He abandoned the body that remembers and carries meaning, and that, above all, seeks to connect her to others for the sake of connection. With the development of the structural theory, the primacy of the Oedipus complex and the call for abstinence, the actual body was eclipsed by the fantasized body and the intrapsychic fate of the sexual and aggressive drives. The touch taboo and the fixed postures of patient and analyst that we have inherited from the classical model inhibit not only what we do and say with our patients, but also even what we are able to imagine and feel? We have been taught to be quick to reflect interpretively, to impose rational order on bodily experience. We foreclose our opportunity to learn from the body and to connect it to both affect and abstract thought.

* Repeated failed attempts to connect with one’s caretaker can result in rage, frustration, and despair (Bowlby, 1973). Such despair becomes a dead space between mother and child and between mind and body, a space where defensive pathological thought processes proliferate. Andre Green (1993) explores this phenomenon and describes the child’s attempt to repair the psychic hole left by precocious body-psyche dissociation with compulsive sadomasochistic thought and fantasy. Eigen (1986) has provided a wealth of examples of the kind of “crazy” bodily imagery that can fill this dead space in psychosis. He says that in psychosis “what seems to be a spoiling process can be an attempt to put mind and body together in whatever ways are possible under the circumstances.”

Psychotic thinking is only one of many consequences of rage and despair about not having comfortable access to the mother’s body.
In our work we more often see patients who have responded to their mother’s psychosomatic disunity and unavailability with an avoidance of being fully alive. This fear is expressed through many symptoms, perhaps most commonly in psychosomatic, obsessional, or depressive illness. In all of these conditions there is a fear and avoidance of either loving or hating from an embodied place. The internal world is cut off from people, and the mind is cut off from affect and body.

In obsessional thought we try to control the past or the future with our minds by running away from the experience of the moment and from the body. Shabad and Selinger (1995) have described this flight from rootedness in the body and the spontaneous moment to an identification with vigilant mental activity as a counterphobic defense against disappointment by the environment.

In depression, the arms and hands, which would ordinarily reach out to touch and cling in hope, or gouge and penetrate in frustration, withdraw from the needed one and hang in limp despair. The mind of the depressed person is mostly involved in an attack on one’s own body and on one’s own body-based attachment needs.

* Both analysts believe that patients who are trapped in this cocoon of self-hatred must be helped to direct aggression toward the analyst in order to gain access to the interpersonal world. Bringing aggression, either loving or hating, into the relationship and bringing it into the experiencing body are major tasks of psychoanalytic treatment.

* working in the dissociative gap requires more than verbally based descriptions of the landscape on either side and of the terrors in the dark canyon below. It must include awareness of what it actually feels like in the body for both analyst and patient as they slip and fall and catch themselves and each other as they work in that gap. As Ferenczi (1912) said, “Conviction is felt in the body.”

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The Psychology Of The Silent Treatment (3-26-21)

00:00 Dooovid joins to talk about Jewish studies, https://twitter.com/RebDoooovid
08:00 Jonathan Pollard says Jews ‘will always have dual loyalty’ and would counsel young Jews to consider spying for Israel, https://www.jta.org/quick-reads/jonathan-pollard-says-jews-will-always-have-dual-loyalty-and-would-counsel-young-jews-to-consider-spying-for-israel
46:00 What You’re Saying When You Give Someone the Silent Treatment, https://www.theatlantic.com/family/archive/2021/03/psychology-of-silent-treatment-abuse/618411/
1:03:00 Desirable But Dangerous: Rabbis Daughters in the Babylonian Talmud, https://lukeford.net/blog/?p=138063
1:21:00 Kenneth Brown drives for California, https://www.youtube.com/watch?v=aMdS_BAp_lo
1:28:00 Unreleased Federal Report Concludes ‘No Evidence’ that Free Speech Online ‘Causes Hate Crimes’, https://www.breitbart.com/tech/2021/03/03/exclusive-unreleased-federal-report-concludes-no-evidence-that-free-speech-online-causes-hate-crimes/
1:44:00 Seasons of a Man’s Life, https://www.youtube.com/watch?v=ZLE2SITDUOM
1:48:00 Race and False Hate Crime Narratives, https://quillette.com/2021/03/25/race-and-false-hate-crime-narratives/
1:55:00 Amy Wax + Paul Gottfried on cancel culture and the society it destroys, https://www.listennotes.com/podcasts/cottogottfried/amy-wax-paul-gottfried-on-5JAUDSNMqWz/
2:03:00 Matt Yglesias’s Substack Generates $860k in Revenue Per Year, https://lukeford.net/blog/?p=138045
2:14:20 Covid Long-Haulers Fear for Their Future, https://www.youtube.com/watch?v=mRikNbf8aGU
2:17:00 The Dubious Origins of Long Covid, https://www.wsj.com/articles/the-dubious-origins-of-long-covid-11616452583
2:21:00 Treating Chronic Pain – An Interview with Frances Sommer Anderson, PhD, http://www.wheretheclientis.com/2010/02/08/treating-chronic-pain-an-interview-with-frances-sommer-anderson-phd/
2:23:00 Frances Sommer Anderson on Using Somatic Experiencing in Psychoanalytic Practice, https://relationalimplicit.com/anderson-septalk/
2:39:20 Michael Beckley: USA as a Future Rogue Superpower, https://www.youtube.com/watch?v=Sf5JSJE2l_A
2:56:00 Your Public Persona: Self-Presentation in Everyday Life, https://www.audible.com/pd/Your-Public-Persona-Self-Presentation-in-Everyday-Life-Audiobook/1629979686
3:00:00 Whiteshift by Eric Kaufman, https://twitter.com/GuiDurocher/status/1375403850102882306
3:18:00 China’s economy is not overtaking America’s, https://www.aei.org/research-products/journal-publication/chinas-economy-is-not-overtaking-americas/
3:28:40 The Power of Nations: Measuring What Matters, https://www.youtube.com/watch?v=Ip-i_m8aqEQ
3:41:00 How Americans Were Driven To Extremes, https://lukeford.net/blog/?p=138059

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Ann Coulter: Asian Women Are Too Damn Hot! (3-25-21)

00:00 ‘Morning Bull’ host Rob Lederman fired, ‘horrified’ by his words after exchange using racist language, https://buffalonews.com/news/local/morning-bull-host-rob-lederman-fired-horrified-by-his-words-after-exchange-using-racist-language/article_92048fb0-8cf5-11eb-aeb7-c3c325a473f7.html
10:00 Argue My Position (Ft. Aella Girl) – Women’s Rights & Wrongs, https://www.youtube.com/watch?v=hBOt3gYHB8E
11:30 The Rationalist community
12:00 Who is OnlyFans Aella? https://twitter.com/Aella_Girl
40:00 Internal vs external locus of control
59:30 PASSOVER | ‘Aren’t You Embarrassed?’, https://www.youtube.com/watch?v=TOdokxzWIuA
1:01:30 Asian Women Are Too Damn Hot!, https://anncoulter.com/2021/03/24/asian-women-are-too-damn-hot/
1:10:50 Beauty supply store owner speaks out after being attacked, https://www.youtube.com/watch?v=WQ0AsQP20XU
1:13:00 Why America’s Great Crime Decline Is Over, https://www.theatlantic.com/ideas/archive/2021/03/is-americas-great-crime-decline-over/618381/
1:17:45 Mike Cernovich, https://www.youtube.com/watch?v=xkXgH_A5fV0
1:27:30 Michael Changaris: The power of mindful touch, https://relationalimplicit.com/changaris/
1:59:00 People Spoon With Professional Cuddlers For The First Time, https://www.youtube.com/watch?v=SO2-tMzG43Y
2:03:30 David Allen: The implicit pressures that shape our clients, https://relationalimplicit.com/allen-2/
2:25:00 Apricot Sky/Venice update
2:26:00 Update homeless encampment in Venice Beach new skid Row, https://www.youtube.com/watch?v=rF-5hVfrqSY
2:29:20 Emotional Sobriety: The Path to Optimal Recovery (Dr Berger & Herb K), https://www.youtube.com/watch?v=F8szumvyni8

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