The depths of depression (by S. Kay)

Diane Farris Gallery, April 2010

 

My wife would have been 55 years old today, if she didn’t die of cancer in 2018.

It’s three years later and I’m still grieving. I don’t know how to get over it. (You don’t)

How do you recover from a loss that rips you apart? When your dreams and goals and plans for the future have been stripped away? Memories and self are sucked into a black hole of grief, where nothing seems real any more, and nothing escapes.

I have a history of depression (as you might have guessed), but that pales in comparison to what Sandra went through with severe Bipolar I Disorder. It often take 10 years or more to get a proper diagnosis. Meanwhile, “here’s your Prozac” — which never ends well. Antidepressants can result in hypomania or full-blown mania in undiagnosed bipolar disorder, leading to excessive spending and risky hurtful behaviors.

Sandra was an early adopter of proto-blogging, back when the content was highly personal and the writers were known as online diarists (pre-Facebook, pre-Live Journal).

In April 1994, Sandra wrote this stunning first-person piece on what it’s like to be mired in a relentless depressive state, while anticipating the death of her father (from cancer).

 

The depths of depression (by S. Kay)

I just can’t seem to control my emotions, no matter how much I understand them and their causes. I can intellectualize, study, analyze to a fine point, but still not change my behavior. Logic is no help. I have such a degree of understanding that part of me watches my reactions and explains them perfectly even while I fall apart. But so far I still can’t control myself.

 

 

In therapy … I learned how to express myself more, how to communicate to others what I feel (as described by the little logician) and to experience emotions to their full extent instead of quashing them. Feel the feelings. OK.

Sometimes this helped – in releasing old hurts and also riding out cravings. It was good for some applications, and really, repression isn’t a great way to deal with pain anyway.

So I know what to do with feelings as they arise (ie. nothing), and also understand why I feel them. The problem? They’re overwhelming.
Everything is too
extreme, too frequent and too spontaneous. It just flows and flows.

 

 

To use a water metaphor, it’s as though scalding hot water gushes into a bathtub. I know it comes from the water tank, and I know I have to let it drain instead of plug it up and have it overflow, but the tap is stuck all the way open. I can’t turn it off or even adjust it to a steady trickle, and the source never cools off because it’s fueled by crisis after crisis beyond my control. Like my father’s impending death, the current most worrisome situation.
I tell myself that I know what I’m supposed to do to cope, I’ve read the books, I know the techniques of dealing with grief now and that if I can get through this without losing it, without drinking or drugs or binging of any kind, that I’ll be free to live the rest of my life. This is one of the hardest things I’ll ever go through. It’s sort of a test, a challenge.

 

 

As with other periods of extreme depression, turmoil and pain, I long for a respite. However briefly, I wish I could escape the pain because IT WON’T STOP, it’s a constant wrenching, anxious, physically disturbing pain that is omnipresent. Erupting in tears frequently. I don’t mind that – I’m told it’s a healthy release and anyhow, I can’t stop it.
Yeah, I know it’s a hurtful situation and that all my family feels pain in the face of his death (anticipatory grief) but mine is further magnified by the depression that was already there. Transforming angst into torture. Taking a little dark gray matter and forcing it to expand, to overrun all my brain’s functions, sort of like cancer itself. It seems to want to swell even beyond the capacity of my cranium, forcing tears out of my eyes and pimples on my face. I touch my forehead gingerly, feeling it may explode, that poisonous brains will gush out of my scalp. It’s dizzying, the amount of raw emotion that seems so tangible, so physical.

 

 

How to live like this? Just suffer, suffer, suffer. No way to end it, no help available either by self-medicating or outside medical help. Therapy may be just another crutch anyway. Just suffer. Feel the feelings, understand them, but don’t bother trying to control them. Suffer – live, function as best I can. Eat, watch TV, speak when spoken to, try to sleep. Do what little I can to help my father. Read books and magazines, tears staining the pages despite practicing this most distracting, immersing and escapist of activities. I can’t escape, can’t hide, can’t numb.Television, even, is just a salad dressing, an emotional flavouring that doesn’t disturb the substance of the ever-present gnarl of pain.
Perhaps, without conscious attempts at obliteration, my mind will just shut itself down. But I doubt it. I’ve always been present and aware through the most harrowing episodes. Forced to live through it. Suffer, suffer, suffer. It’s SO exhausting. I expect it’ll last awhile, too.

 

 

It begins in the brain, figuratively and literally. A sensation of hollow darkness encased by a taut, achy shell that threatens to explode, surrounded by an aura of prickly numbness. My eyes sting, my sinuses are at the ready. My mouth is dry, my jaw is tight and sore from reflexive clenching that I force myself to stop whenever I realize I’m doing it. My throat is constricted, an ever-present lump of tears at its base emitting adrenaline through anxiety. My lungs rasp from smoking too much. My heart struggles to keep up, speeding up and slowing down as emotions demand, and it often spasms in protest, sending little painful shocks to my chest. My shoulders and back ache, knotted with tension that never gets released, muscles that never get massaged, just exercised by tears and fears. My stomach is alternately bloated with excess depression, nauseated by pain, or empty and ravenous. My uterus cramps itself trying to hide, my genitals irrelevant. My legs and arms sometimes tense and cramp but only if the rest of my body is similarly wracked, otherwise they’re slack, mere instruments for motor reflexes. My hands flutter nervously, wanting to touch, to feed, to change the channel.
Mostly though, all is irrelevant, all is secondary to the churning, billowing stem of depression. A new organ, a seething growth sending dull, achy, prodding fingers through my gut as it tries to expand. It forces me to knot up my face with silent screams and burning tears, then abates to leave me trembling and shattered. Clammy with residual emotion, exhausted by the metamorphosis, the
invasive states of emotion. It oozes through me, trailing fear, sadness, anxiety and leaving despair as an afterglow.

 

 

Strangely, there is room for flashes of elation, of laughter, in the range of emotion. All is allowed except serenity, all feelings can be experienced as long as they are raw, primal torrents. It’s an alien consciousness, taking away all of myself to replace me with a fountain of negative and positive extremes, blanketed with angst. I’m someone else, someone who produces nothing but sickness. The best I can be is bored and tired, spent after spewing for hours, days, weeks at a time. Hoping that by surrendering it’ll grow monotonous, yet it never is because that’s not what it’s about. It must constantly generate more emotion, more extremes – a perpetual machine, an eternal flame. As hell is described.
Nothing to do but over-react to every little detail of existence as prescribed: with illogical, uncontrollable, unbearable emotions. Collapse, then do it again. Suffer, suffer, suffer.

 

 

 

The Most Boring Nightmare Ever

Last night, I had a nightmare where I was looking at a stack of my mother’s banking records. I woke up very startled and yelled “NO!!!”

Now you may think, “that’s not very scary!” and you’d be right if you didn’t have any context. My mother died on July 4. Tragically, I couldn’t get there in time to see her. The day before she died, I wrote:

My elderly mother is dying. She lives on the opposite coast and is the definition of a patient at high-risk for coronavirus infection. She has lung disease (COPD), two types of cancer, and is on oxygen 24/7. Her neighbor wasn’t able to reach her on Wednesday and called 911. She refused to leave her home. She desperately needs medical attention and professional care. Yesterday the neighbor convinced her to go to the hospital. Now, as the only child, I have to plan for her death. She won’t recover, she won’t ever live on her own despite her stubborn and obnoxious and admirable efforts to do so. It’s heartbreaking, and it’s too much for me to handle.

Since then I’ve traveled across the country four times, which has involved flying on 16 different planes. All while wearing masks and being in situations where adequate social distancing was not always possible. I’ve had to stay in my childhood home, where I haven’t lived in decades. I sorted through 50 years of my mother’s accumulated possessions, as well as her medical and financial records. I encountered unexpected letters, obsessive listings of grievances and household items and charitable donations, various collections/accumulations, and even my kindergarten drawings. It’s been quite confusing, like living at least two separate existences. Recollection of memories from my real life was impaired while I was there.

Then I returned home and observed the second anniversary of my wife’s death. It’s incredible that my life has been empty and meaningless for that long.

So the dream was really about disorientation and death.

 

Meanwhile, after months of covid denialism, anti-science propaganda, and anti-mask ridicule, SARS-CoV-2 took ironic revenge and infected the president of the United States.

It is what it is.

It Smells Like Gunpowder

It’s so loud, and I’m so tired. The hospital called 3 hours ago to say my mother had died at 11:40pm EDT. This was rather shocking (to say the least), because I wasn’t there. I was preparing for the trip, but her condition deteriorated so suddenly. And she died alone.

I can’t express much of anything now. This wasn’t supposed to be the grief to plumb for [my current grief writing group…] it was supposed to be my spouse (21 months ago) and my cat (2 months).

It’s so loud, and it’s July 4th. After calling a few people, I don’t know what else to do. What else is there to do except go out into the cold San Francisco night in a black hoodie to watch 15-20 separate displays of fireworks. I’m not sure how I feel about this yet. Is it a spectacular way to say goodbye and honor her passing? It’s certainly surreal, and it adds to my disbelief. But I walk up a steep hill and stand in the middle of the street anyway. I finally start crying at an overwhelming display of bright light and noise.

It’s so loud, and it smells like gunpowder.


NOTE (piece above written using this part of a writing prompt): “Today’s prompt focuses on the senses, particularly how certain smells connect with your grief.”

 

Prequel

July 3 at 7:39 AM

My elderly mother is dying. She lives on the opposite coast and is the definition of a patient at high-risk for coronavironus infection. She has lung disease (COPD), two types of cancer, and is on oxygen 24/7. Her neighbor wasn’t able to reach her on Wednesday and called 911. She refused to leave her home. She desperately needs medical attention and professional care. Yesterday the neighbor convinced her to go to the hospital. Now, as the only child, I have to plan for her death. She won’t recover, she won’t ever live on her own despite her stubborn and obnoxious and admirable efforts to do so. It’s heartbreaking, and it’s too much for me to handle.

Neuron Ink

IPRG cell

Sandra1 already had seven tattoos. Most of them were small. Lining her right outer thigh were six separate designs, the largest of which was about three inches in diameter. The seventh tattoo was more conspicuous, a First Nations bird on her right forearm, just above the wrist.

On her birthday in 2007, she wanted to get a new and unique neuron tattoo. Most of us are familiar with rods and cones, the classic retinal photoreceptors that transduce light into electrical impulses. Lesser known among the neurons in the retina are intrinsically photosensitive retinal ganglion cells (ipRGCs). These neurons express melanopsin, a light-sensitive protein involved in the production of melatonin, a hormone that regulates circadian rhythms (including the sleep-wake cycle). The ipRGCs project directly to the suprachiasmatic nucleus in the hypothalamus, the brain’s circadian pacemaker.

Sandra had a deep interest in circadian rhythms because of their significance in bipolar disorder (she had bipolar I disorder). Disruptions of the sleep-wake cycle are a prominent aspect of this condition. Before the existence of the f.lux® program that limits the amount of blue light emanating from your screen at night, before the studies demonstrating that electronic devices can suppress the production of melatonin (thereby altering your circadian clock), Sandra went out and bought yellow light bulbs for the lamps in the house. “But I can’t read in this dim yellow light!” I complained.

In preparation for the ipRGC tattoo session, I sent her several articles illustrating these rare neurons, which comprise only 5% of all ganglion cells in the retina. She chose an illustration from a 2005 Nature paper.

ipRGC in Nature.jpgModified from Fig 3a (Dacey et al., 2005).  (Left) Drawing of a giant ipRGC cell (arrow indicates axon). The cell was recorded from the in vitro retina (“retina in a dish”) and then filled with a substance to visualize it.  (Right) Electrical responses (voltage traces) of this cell to a specialized light stimulus.

Most stereotypical neurons have a long axon, but this giant ipRGC does not (see arrow in Fig. 3a). Sandra wanted the tattoo to look like a standard neuron (and she enjoyed the idea of an axon running down her arm), so she had the artist embellish the drawing with an extra branch. She also had horrid arachnophobia, and did not want anyone to mistake this work of art for a spiderweb.

The results were quite impressive.

tattoo_003_cropped
Then,

In 2007, [science writer] Carl Zimmer posed a question on his blog: are scientists hiding tattoos of their science? It turned out that many of them were, and they were willing to share their ink with him and the world.

Hundreds of people sent in their science tattoos. The original chronicle of this collection is nearly impossible to reconstruct from Zimmer’s many blogs, hosted by ScienceBlogs, Discover, National Geographic, Typepad, etc. Fortunately, the best of these tattoos were collected in a book called Science Ink: Tattoos of the Science Obsessed. Sandra was invited to submit a photo of her Neuron Ink.

tattoo_003
Photo by Maurice Li.

In an entry called “Ganglion Cell”, Zimmer eloquently wrote:

It is sensitive to blue light, but it does not paint the blue of a bluebird. Instead, it sends its color elsewhere: to neurons that control the size of the pupil, to regions of the brain that set the body’s clock, to other regions that release hormones that make us sleepy and wakeful.

Sandra got two more tattoos after that, both in January 2016. One of these was the cover art from her book, Reliant.

Her very last tattoo was a daffodil to represent being a cancer survivor.

daffodil tattoo_small.jpg

About this, she said:

Daffodils are the official flower of the Canadian Cancer Society and daffodil pins are sold each spring to raise funds. They’re the first flowers of the year, pushing through winter decay to burst forth with hope and life. A daffodil is a good symbol.

At the two year post-treatment milestone, the oncologist told her that the chance of recurrence was less than 5%. There was reason for optimism, because the doctors said she was cured. But six months later, after experiencing right upper quadrant pain, Sandra was diagnosed with stage 4 cancer. There was an 8 cm tumour in her liver that was “missed” because her ten prior scans didn’t bother to screen the most likely sites of metastasis.

The irony of her final tattoo was not lost on me.

On her birthday this year, I decided to get the same ipRGC tattoo (sans axon). It was my first; I did not have any tattoos before this.

ipRGC tattoo_small

I wish she was there with me to see it.

Footnote

1 Sandra Dawson, my late wife. See There Is a Giant Hole Where My Heart Used To Be.

Involuntary Visual Imagery

I’ve become interested in the topic of involuntary visual imagery because of my own recent experiences. After my partner died of cancer, I’ve had periodic episodes of involuntary visual imagery (akin to flashbacks) of traumatic events leading up to her death. I’ve also had images of places appear for no apparent reason. The places themselves are neutral, but in the context of loss they become fraught with distress. {As an aside, I have vivid auditory imagery of popular songs which can play in my head with high fidelity.}

Today I was reviewing a paper, with a song playing in my mind in the background (Save a Prayer by Duran Duran, which I had heard a few days before). It’s a sad song, but I was managing the workload just fine. Then an image of driving onto the on-ramp of the Second Narrows Bridge appeared in my head and totally derailed me1. The view wasn’t from the car, like I was driving, but more from above (a bird’s eye view), like a detached observer fixed in mid-air. It reminded me of all the travel to a city I may not see again (especially of all the trips back and forth during the last months).

Last week, I was writing a report at work, and suddenly a vivid image of standing across the street from the BC Cancer Agency appeared. My partner had 6 weeks of radiation there in 2015. This was even more upsetting, for obvious reasons.2

Derealization

This isn’t a new phenomenon for me, although the current level of distress is novel. I have very strong memories of significant places, and sometimes an image of a specific location from my past springs to mind for no apparent reason. These visual images can be accompanied by a sense of derealization, a subjective alteration in my perception of the outside world. Revisiting these old places from childhood was disorienting:

I went on this trip once, back to my hometown after a long absence. Have you ever felt that your surroundings seem odd and distant, and that you’re completely detached from them? That the things and places around you aren’t real? This can happen to me, on occasion.

It did on this trip, perhaps because I’ve dreamed about those places so many times that the real places and the dream places are blurred in memory.

Visual imagery can be an elusive phenomenon to study scientifically, but there’s a solid literature that I’ll eventually review. A recent fMRI experiment examined the neural correlates of visual imagery vividnesss, and the authors reviewed 11 previous papers on the topic (Fulford et al., 2018). An early study found that visual imagery ability may be associated with flashbacks in post-traumatic stress disorder (Bryant & Harvey, 1996). I recently speculated that individuals with both (the inability to form mental images) and PTSD must not have visual flashbacks.

Seven years ago, I wrote a grant that was mercilessly rejected (one of many); the only section of the proposal that the reviewers liked was on imagery. So I’ll retrieve that file, dust off the virtual cobwebs, and perhaps look at the approach with a fresh set of eyes (so to speak). A bleary set of eyes is more a more apt description…

 

ADDENDUM Jan 17 2019 (2:22AM): I didn’t mention that the image below came to mind while I was writing this post. These sorts of situations, when you’re preoccupied with doing something else like reading and writing, aren’t the most conducive conditions to voluntarily imagining a visual scene or recalling a visual autobiographical memory. And yet there it was, Phibbs Exchange, appearing without warning or conscious thought.

Question for the readers: Do any of you experience involuntary visual imagery, whether confined to visual images alone or incorporating other sensory modalities (e.g., hearing, smell, touch)?

 

Footnotes

1 We were in a long-distance relationship that involved travel between Vancouver and California. I’ve taken great pains to find images on Google Maps that are the closest to those conjured up by my mind.

2 She was told she was “cured” several months after that, which clearly was not the case. Imaging the liver in all those subsequent CT/MRI screenings was not part of their “protocol” (despite suspicious early results, and despite the fact that the liver is the most likely site of metastasis). So you can see why imagery of staring at that building was quite upsetting.

References

Bryant RA, Harvey AG. (1996). Visual imagery in posttraumatic stress disorder. J Trauma Stress. 9(3):613-9.

Fulford J, Milton F, Salas D, Smith A, Simler A, Winlove C, Zeman A. (2018). The neural correlates of visual imagery vividness–An fMRI study and literature review. Cortex 105:26-40.

WATCH

How to Reconstruct Your Life After a Major Loss

I titled this post as if this is something I’m doing (I’m not). Or that I know how to address in a didactic way (I don’t). Some of you may know that my partner died recently. “It hasn’t been long,” you say, a little over two months. And that’s true. “Go easy on yourself.”

I returned to work three weeks later. Was that too early? Within the first two days I was faced with e-mails and deadlines and meetings that were overwhelming, and the assumption was that I was operating at normal capacity. Far from it. I couldn’t (and still can’t) handle stress very well. I’d go home and cry, which would only worsen my grief.

Or maybe it wasn’t too early. Having structure and routine and simple tasks and a low stress environment might be a good thing. Although I’m finding it nearly impossible to keep up with the workload, I have accomplished a surprising amount. “Your resilience is inspiring,” a kind and supportive co-worker said, but they don’t see me when my grief is intolerable, because I stay home those days.

It has been exceptionally hard to write, and this has been true for over a year. My partner was diagnosed with stage 4 cancer on October 4, 2017 and died on October 2, 2018. “It was a long goodbye,” said one friend. Until it wasn’t.

My partner’s decline was precipitous and unexpected, or at least not predicted by any medical professional at the hospice. One nurse even said it was a gradual decline, which was clearly not the case, according to close observers. You see, a major issue was that we didn’t live in the same city. Although I traveled there five times in the last two months, I ended up plagued with guilt because we were supposed to have weeks together on my last visit. And we didn’t. Nothing went as planned (or at least, according to the doctors’ vague prognostic indicators…).

The National Institute of Nursing Research (NINR), part of NIH, has issued an important funding opportunity on End-of-Life and Palliative Care Approaches to Advanced Signs and Symptoms (PAR-19-045). I’ll write about that in another post. I know, I know, “out of scope” for this blog.

Grief make life seem pointless. Why go on? Why care about that grant I should be writing? It’s meaningless. When you lose everything, nothing else matters.

Derealization / Dying

Derealization is a subjective alteration in one’s perception or experience of the outside world. The pervasive unreality of the external environment is a key feature, along with emotional blunting. The world loses its vividness, coloring, and tone.

I’ve spent much of the last year walking around in a fog, hazy, underwater, under glass, where nothing is real. This isn’t happening.

My partner has end-stage cancer, and was transferred from Acute Care to the Palliative Care Ward about 3 weeks ago. I was standing there, just staring at her while she slept in a hospital bed, knowing where we were and who I was and yet, the scene was surreal. Detached from my real life. Like flowing curtains.

Then her psychiatrist walked in, and suddenly everything was real. I started sobbing at the horrible reality of what was happening, and what will happen.

People speak, I’ve no reply

I’m empty inside

But for the incessant screaming

Which refuses to subside

–Single Gun Theory, I’ve Been Dying

Less than a week later, she was transferred to hospice.

I’ve been dying a long time

Down on my knees

There’s no way out of here

I’ve been dying a long time

Can’t seem to pick up the pieces of my life

–Single Gun Theory, I’ve Been Dying

Single Gun Theory were an Australian band who sampled from myriad sources, including Robert Oppenheimer, Natalie Wood, spoken word samples recorded in India, Turkey, and Southeast Asia (e.g., Islamic call to prayer, recitation of the Qur’an, Indian female vocals), and The Twilight Zone.

Twelve months ago to the moment you destroyed yourself

Much as I told you you would

{sampled from The Silence, Season 2, Episode 25 of The Twilight Zone}

Nearly a year ago, Sandra was diagnosed with stage 4 cancer. I tried for 7 months to enroll her in a clinical trial, to no avail. I wrote about how hard that was, and what was wrong with the cancer clinical trials systems in both the US and Canada.

[That] post [was] my own personalized rant about the false promises of personalized medicine. … It [was] about oncology, for very personal reasons: misery, frustration, and grief. After seven months of research on immunotherapy clinical trials, I couldn’t find a single one in either Canada or the US that would enroll my partner with stage 4 cancer. For arbitrary reasons, for financial reasons, because it’s not the “right” kind of cancer, because the tumor’s too rare, because it’s too common, because of unlisted exclusionary criteria, because one trial will not accept the genomic testing done for another trial. Because of endless waiting and bureaucracy.

But somehow, I’ll have to go on without her. Sandra was very active in suicide prevention efforts on social media, as @unsuicide and with her Online Suicide Help wiki so there you go.

September 10 was World Suicide Prevention Day, and Dr. Erin Michalak of CREST.BD wrote a touching tribute to Sandra’s work.

Sandra Dawson’s Legacy

. . .

Most significantly, Sandra created the Unsuicide directory of online and mobile crisis supports, as well as a popular corresponding Twitter feed (@Unsuicide) with close to 25,000 followers. Her Unsuicide online supports are authentically grounded in her lived experience of bipolar disorder, but also unfailingly focused on helping people, regardless of their geography, to access credible and safe online and mobile support tools. In 2016, she was awarded the Sovereign’s Medal for Volunteers from the Governor General of Canada in acknowledgement of the impact of her work as an advocate for people facing mental health challenges and in suicide prevention.

Samuel Beckett, The Unnameable

It will be I? It will be the silence, where I am? I don’t know, I’ll never know: in the silence you don’t know.

You must go on.

I can’t go on.

I’ll go on.

Field: “Brain Optimization” for the Wealthy and Gullible

An article in New Beauty magazine alerted me to the latest brain wellness scam NYC’s Hottest Club Is Selling ‘Designer Brains’:

Imagine the best moments of your life. … Then imagine you could wake up and feel that way every morning. According to the founders of Field, a center devoted to “brain optimization” that will open in New York City this winter, it only takes 19 electrodes and some neurological tweaks to get there.

With a combination of neurotechnology and new age philosophy, Field’s founders describe brain optimization as the new frontier of wellness. Devon White, a performance consultant, expert in human behavior and one of the team’s four founding partners, compares neurological treatments to acupuncture.  …  “Most of us don’t have control over our brains—until now,” says White.

[NOTE: complete and utter BS]

Field has been described as a gym for the brain, a clinic/spa/laboratory hybrid and a luxury cognition center. But instead of deadlifts or massages, the space will offer transcranial magnetic stimulation (TMS).

This procedure involves placing an electromagnetic coil against the scalp to deliver magnetic pulses that alter electrical current flow. TMS is a valid brain modulation technique approved for specific medical uses, but there’s absolutely no evidence that it can make you relive the best moments of your life or improve your day-to-day cognitive function.

 

But actually, the illustration in the New Beauty article appears to be a cap for transcranial direct current stimulation (tDCS), a cheaper and easier to administer type of neuromodulation that works in a different  manner.

The Field website is a masterclass in neurogibberish…

Your experience at Field is entirely personalized. We begin by creating a comprehensive model of you at your best as well as a deep understanding of your desired goals from the Field experience. This multi-dimensional assessment of who you are is complete with psychodynamic history, autonomic data, psychometrics, performance analysis, hormone and gene panels, and a qEEG reading of your brain.

…and elitism:

Field is a private membership club dedicated to transforming the way our clients use themselves and their brains. Our innovative and personalized application of cutting edge neurotechnology will revolutionize everything you know about personal development and high performance.

. . .

Membership during our first year of operation in Manhattan is limited.

As the world leaders in this technology-augmented approach to consciousness enhancement, we are intent on ensuring all-around excellence in the culture at Field, both for our team and our members.

During our charter year, we are working exclusively with superlative individuals interested in creating positive personal and global impact. The intention of Field is to vault these already remarkable clients into new domains of power, satisfaction, performance, and Flow.

…and from New Beauty:

…Field is open to “superlative individuals” who can afford the entrance fee. In addition to the upcoming physical location in NYC, the company is planning a 10-day intensive that combines neurological treatments with networking, body work and meditation. The experience costs $25,000 and participants are vetted for more than just money. The spots will be reserved for those with generally good mental health (not bipolar, schizophrenic or suffering from major psychiatric disorders), and, as Devon describes it, “good people.” The New York space also has a membership application process, making Field feel like a SoHo House for wealthy wellness junkies.

More like wealthy wellness monkeys, willing to pay for the privilege of being experimental socialites in a beauty spa of unproven neuromod technologies.

“Atheists Are Mutants,” says paper based on Yelp, Yahoo Answers, and the Bible

A surprising new paper in the journal Evolutionary Psychological Science claims that atheism1 is underpinned by “high mutational load” as indicated by (1) poor general health, (2) autism, (3) fluctuating asymmetry (attractiveness), and (4) left-handedness (Dutton et al., 2017). This is silly for a number of reasons. Let’s start with the preposterous rationale for the study, which is actually based on Christian blogs, Yelp, Yahoo Answers, and the Bible:

There seems to be a stereotype that religious people, and especially religious women, are particularly attractive and healthy. A number of popular articles and social media pages discussing this observation can be found online (Malloy, 2017; Hewitt, 2010, p. 99) including threads beginning with questions such as “Why are Mormon girls so hot?” (Yahoo Answers, 2008) and “OMG … why are Christian woman so extremely (physically) attractive?” (Yelp, 2010).2 Several passages in the Bible seem to suggest that those who intensely fear Yahweh are more disease-resistant (Deut. 7:15) and are more physically attractive (e.g. I Samuel 16:18). Those inspired by other gods or by Satan are, in contrast, autistic (Mark 9:25) and even left-handed (Matt 25: 41). Why should the authors of these books believe this to be the case? It could, of course, be a way of idealising the virtuous, but it is not clear that all of these features were the most pertinent for that purpose.

Really??? Has anyone heard about the stereotype that “religious women are particularly attractive and healthy”? And that the New Testament says autistic individuals3 and left-handers are “Satanic”??  This is so ridiculous that I thought the paper must be a spoof, similar to the articles that appear in the The BMJ Christmas issue.4

Oh, and then there’s the title of the article:

The Mutant Says in His Heart, “There Is No God”: the Rejection of Collective Religiosity Centred Around the Worship of Moral Gods Is Associated with High Mutational Load.

It’s really hard to go any further. Professor Shane O’Mara named it a contender for the worst scientific paper of 2017.

 

Footnotes

1 …and paranormal belief…

2 The first answer on Yelp is quite amusing:

I think you lucked out….go to a heavily Christian city in middle America and the church populace will look more like peopleofwalmart.com (is that the right site?). I don’t think their looks is attributed to religion, you just happened onto a group of good-looking women. It can happen anywhere.

3 The author of the gospel of Mark must have discovered autism, then.

4 I asked the journal about this, but didn’t hear back.

 

Reference

Dutton E, Madison G, Dunkel C. (2017). The Mutant Says in His Heart,“There Is No God”: the Rejection of Collective Religiosity Centred Around the Worship of Moral Gods Is Associated with High Mutational Load. Evolutionary Psychological Science. pp. 1-12. First Online: