Prof @HarvardAnthro works on sci+tech+med+ hackers// Faculty Associate @HarvardHistSci & @BKCHarvard // Curator of @HackCurio // words these days in email …
Well, that's exciting, "Wearing Many Hats: the Rise of the Professional Security Hacker" is no longer vaporware or alpha but now out as a dedicated @datasociety report, covering the history of hackers going pro https://t.co/00KPgawcQK
Yesterday, this guy was quietly appointed to EPA's Science Advisory Committee on Chemicals 🤬
This is the group that peer-reviews EPA's risk evaluations for things like asbestos, PFAS, phthalates, lead and every other nasty chemical
Really bad news
https://t.co/OwNfdHkbY2
For nearly 50 years the standard of care for joint sprains has included rest, ice, and ibuprofen not bc rigorous evidence showed that worked, but bc that made intuitive sense and seemed to help. Now there's good evidence those actually impede recovery.
Add it to a long list of medical reversals, whereby a practice that was once widely adopted is later shown to be ineffective or even harmful.
Promising theories, observational evidence, underpowered studies, and early experimentation can generate important hypotheses. But they do not eliminate the need for rigorous randomized trials, regardless of the financial or professional incentives to move faster.
Once ineffective or harmful care becomes embedded in standard practice, it is very difficult to overturn. There is a role for regulatory flexibility and clinical experimentation when patients have unmet medical needs. But neither eliminates the need for rigorous evidence to ensure that the medical system is actually helping patients.
It's official: without climate change, the ongoing Eastern United States heat wave is "virtually impossible"
Climate scientists performed an autopsy of this week's weather and determined that it could not have happened in the past 500-years w/o the burning of fossil fuels
Swiss farmers planted flowers between their crops and watched pest damage drop by over half. The UK is now running the same trial across 15 farms. The reason this works is embarrassingly simple.
A Swiss study on winter wheat found that fields with wildflower strips had 40 to 53% fewer leaf beetle pests than fields without. Crop damage dropped 61%.
The mechanism is simple. Wildflowers feed hoverflies, lacewings, parasitic wasps, ladybugs, and ground beetles. Those insects eat the aphids, beetle larvae, and caterpillars that farmers would otherwise spray for. A few meters of wildflowers hosts an unpaid pest control crew that would jump at the chance to whoop some aphid ass.
In apple orchards where no insecticides had been used for five years, plots with wildflower alleyways had 9.2% damaged fruit. Control plots without flowers had 32.5%.
The UK is now running a five-year trial across 15 farms placing 6-meter flower strips through the middle of fields, not just at the edges, because the beneficial insects can't reach the center of a large field otherwise.
This works the same way in a backyard vegetable garden as it does on a commercial farm. Plant native flowering species near your tomatoes, beans, and squash. The pests still show up, but the predators show up too.
Study doi: 20151369
This is absolutely terrifying
The Nino 3.4 forecast temperature anomaly mean is now at 4C, when even the biggest historical super ninos have seen less than 3C
I really have no idea what this is going to bring over the next 12 months, but it will be very, very, grim
New reporting reveals that executives from America’s three biggest egg producers began colluding to keep egg prices high in 2022.
Executives from Cal-Maine Foods, Hickman’s, and Versova spoke of the phone phone and messaged to coordinate bids and trading on eggs.
While these producers blamed avian flu, they were actively and illegally collaborating to keep the price of eggs high.
https://t.co/0P7sYpbFMx
These pesticide approvals will outlast anything else that Trump has done because they are forever decisions
Releasing forever chemicals is a forever decision because there’s no going back
The lasting damage is cemented once that pesticide is applied
https://t.co/2PDQwzpDZx
The reason the Democratic Socialists are winning:
Bernie was supposed to go against Trump. Establishment dems pushed Hillary.
Biden was a compromise who enacted progressive policies.
Harris doesn't energize the base
Centrists don't energize the base
Leftists ENERGIZE THE BASE
🚨🚨We found out EPA approved ANOTHER PFAS pesticide yesterday
That makes 3 PFAS pesticides never before used in the United States approved IN ONE DAY
Just days after pesticide companies got immunity at the supreme court
This was the plan all along
https://t.co/TBNTbiVL2i
Bad news #1:
I have an autoimmune disease. My stomach is eating itself.
Bad news #2:
2–5% of people have this, too. Likely more, because it hides.
Good news:
I'm going to try and solve it. Will share all.
As a kid, I ate sugar cereal, drank sugary soda, and gobbled down fast food. I had a few healthy years in my early 20s but then became a young father of three and began building a business.
Juggling that stress and grind, I let my health slip and gained 40 lbs. Within a few years I’d fallen into a deep, chronic depression.
Somewhere in that timeline, my body began developing an autoimmune process affecting my thyroid and then my stomach lining.
It’s called Autoimmune Gastritis (AIG).
My hypothyroidism got diagnosed when I was 21 years old with a routine blood draw. That enabled me to begin proactive management, supplementing levothyroxine and Armour Thyroid. They are the hormones my body should be producing on its own but wasn’t.
By taking these pills daily, my body was able to operate as though my thyroid was functioning properly. What I didn’t know was that something else was going on inside my body: my stomach had begun attacking itself. But there was no routine test to find out and I didn’t have any symptoms.
I just discovered it in May. I'm unsure how long I've had it. AIG causes irreversible damage: nutritional deficiency, anemia, and over a long horizon, elevated cancer risk. When AIG is discovered today, standard medical care concedes defeat, stating that nothing can be done except managing the condition, no matter how awful or lethal the effects.
Looking back over the past few years, I can now see the early signals we were picking up in measurement but hadn’t connected the dots. For 11 years, I’ve had low ferritin, without anemia. We continually tried to raise my iron levels with food and supplementation but nothing would work.
We chased the obvious solutions first. A plant-based diet means all my iron is the hard-to-absorb, non-heme kind. Hard training, sauna, and hyperbaric oxygen all raise the body's demand for iron. But none of them explained the core failure: despite me taking iron orally, trialing every formulation, and using every timing trick, none of the iron would stick.
What I didn’t fully appreciate until recently is how many stones my previous providers had left unturned. The low ferritin kept getting explained away but not fixed.
I overhauled my medical team earlier this year. It was the rebuild to lay the groundwork for Immortals Care, our $1M a year protocol. With greater capacity, we revisited everything.
On the surface, my low ferritin was easy to dismiss by most standards of care. My hemoglobin and hematocrit were normal. Ferritin measures stored iron, while hemoglobin measures circulating iron, and because the body drains its reserves first to keep hemoglobin normal, you can be fully iron deficient with a perfectly normal hemoglobin and hematocrit.
This is why my low ferritin kept getting dismissed: the numbers that define anemia looked fine, so no one asked why my iron reserves wouldn't refill.
My team pressed on that question. They first turned to a colonoscopy. I was 48 years old and overdue. It was good health hygiene to have while also serving a specific purpose of searching for a hidden source of blood loss such as a polyp or even cancer in my bowels. Either one of those would be an explanation of why the iron kept disappearing.
At the same time, they began connecting the dots. Iron absorption depends on stomach acid, so one theory was that my stomach acid was disrupted. They also knew that thyroid and stomach autoimmunity often travel together, so often that the pairing has a name: thyrogastric syndrome.
Put against my 27+ year history of autoimmune thyroid disease, the pieces pointed to a single hypothesis: my own immune system was attacking my stomach.
To our surprise, my colonoscopy came back clean. A perfectly healthy colon, better than 95% of colonoscopies of men, according to the gastroenterologist. That ruled out the first concern and worst possible outcome: slow continuous bleeding from colon cancer, or pre-cancerous polyp.
My team had exercised great foresight though, anticipating this possible outcome. In addition to a colonoscopy, they’d ordered an upper endoscopy to be performed at the same time. The combined procedure is a bi-directional endoscopy. Probes would look at my entire intestinal tract, up from below and down the throat.
Additionally, we had several blood biomarkers measured ahead of the procedure to try and pick up on any signals that would give the gastroenterologist guidance for what to look for while doing visual inspections.
Fifteen minutes before the procedure, my blood results returned, finding elevated levels of anti-parietal-cells-antibodies (APCA). They came back at roughly five times the upper limit of normal (103, against a ceiling of 20 Units/mL). It was a positive result confirming the suspicion of AIG being the culprit behind my low ferritin, the other type of gastritis, driven by a bacterial infection, was already ruled out, as we knew I am negative to H. pylori.
Even before this finding, my team had ordered five biopsies to be taken from three regions of my stomach.
The biopsies were the critical piece. Had they not been ordered, the bi-directional endoscopy would have been completed and AIG remained undiagnosed as there were no visual signatures of the condition in my intestines.
Two days later, the results of biopsies came in, showing clear signs of early autoimmune gastritis: early atrophy confined to the acid-producing lining, with the rest of the stomach still spared. My team had anticipated this, methodically tracing every line of evidence.
We now had a formal diagnosis. I have autoimmune gastritis AIG. My stomach is eating itself.
So this was never one problem. It was three, linked to one another: the iron deficiency, the autoimmune gastritis driving it, and the autoimmune thyroid disease alongside it. Iron and thyroid feed each other both ways, low iron impairs the conversion of thyroid hormone into its active form, and an under active thyroid impairs how the body uses iron. Each made the other harder to fix.
Autoimmune gastritis affects an estimated 2–5% of people, and likely more, because it hides and is challenging to diagnose. It's usually silent for years, surfacing only once the stomach has atrophied enough to do real damage: iron deficiency first, then B12 deficiency, then anemia from both, and over a long horizon, raised stomach-cancer risk. In one study of people with precancerous gastric lesions, roughly 18% carried the autoimmune antibodies, and only about 1% had ever been diagnosed.
And the earliest clue, low ferritin, is the one standard medicine waves through. Low iron stores get normalized and rarely investigated at all when anemia hasn't shown up yet. That blind spot is what hid mine for a decade.
The good news: the iron deficiency is now corrected. I received a 1,000 mg Monoferric iron infusion. This was chosen for two reasons after considering multiple formulations. First, it can safely deliver a full dose of iron in a single infusion (1,000 mg), while older options like Venofer require several separate appointments to reach the same total.
Second, certain other IV iron formulations can cause a drop in blood phosphate levels, an important mineral for bones and energy. Monoferric is much less likely to do this, which matters given how closely we track long-term metabolic and bone health parameters.
As mentioned earlier, current medical standards treat AIG as something to be managed, not resolved.
It's worth noting that many of you give me a hard time, inviting me to "live life" and engage in self-destructive behaviors like a "normal person". I'm cool with the playful ribbing. Also, had I not taken care of my health during the past five years, my situation could potentially be very serious.
You too may have a lurking health issue that is undiagnosed and could increase in severity from unhealthy life choices, without your knowing. The absence of symptoms is not the presence of health.
A gentle nudge that minding your health, no matter your situation in life, is good decision making.
My team and I are going to try and solve my AIG. This is how we’re approaching it:
First, routine monitoring keeps the disease in view: ferritin and iron, B12, the pepsinogen I/II ratio, gastrin, and chromogranin A. Gastrin is the dial to watch. If it climbs, the disease is advancing, and the risk of gastric neuroendocrine tumors climbs with it.
Second, we’re doing advanced characterization of the disease. We’ll do a repeat biopsy to read the immune infiltrate, deep cytokine profiling, and T-cell subset analysis, to see which pathways are actually firing.
That testing drives the intervention plan, including the experimental approaches we intend to develop.
+ If gastrin and chromogranin rise: damp the gastrin drive (netazepide) and tighten endoscopic surveillance. If the profile is Th1 / interferon-driven: target JAK/STAT.
+ If it's Th17 / IL-17-driven: target IL-17 and STAT3.
+ If regulatory T cells are failing: rebuild them (low-dose IL-2, induced Tregs).
+ If it's antibody- and B-cell-driven and antigen-specific: engineered cell therapy (CAAR-T).
Which organizes into four tiers, from available today to frontier:
Tier 1, now: protect and support; zinc-L-carnosine, and acid replacement (betaine HCl with pepsin) under physician supervision. This is specific to my case and not something to self-prescribe, especially given the cancer-surveillance considerations above.
Tier 2, target the signaling , JAK/STAT, GSK-3, IL-17, and damp the gastrin drive (netazepide).
Tier 3, reset the cells, induced regulatory T cells (iTregs).
Tier 4, frontier: engineered T-cell therapy (CAR-T / CAAR-T), custom AI-designed antibodies, or synthetic proteins, that can specifically seek out inactivate or destroy the rogue immune cells attacking my stomach lining.
To be clear: there's no approved cure for autoimmune gastritis today. Medicine treats it as something to manage, not solve. Tiers 2 through 4 are investigational preclinical evidence at best, and in several cases therapies that still have to be built.
If you're working on autoimmune gastritis, antigen-specific tolerance, regulatory T cells, or CAAR-T for organ-specific autoimmunity, please reach out.
Modern medicine has normalized too many conditions that erode our health, function, and comfort, shrinking the goal to monitoring and management while a cure is rarely even attempted. Most of these verdicts were handed down decades ago, in an era that predates nearly all of our current tech and science, and they have gone largely unchallenged.
We want to change that. In the age of AI, multiomics, and custom-built DNA, proteins, and cells, no condition should be presumed incurable simply because no one has yet tried to cure it with today's stack.
I’ll end on a personal note.
We fill our days mostly on things that are trivial next to what we ultimately care about. We know, deep down, however, that in the noise of it all, health is easily forgotten until it’s the only thing that matters.
We spend a fraction of our lives truly sober to the preciousness of life. We feel it when someone we love dies, when a child is born, when we come close to death ourselves, or when a diagnosis marks our limit. In those moments, we are sobered, and the rarity of it all becomes self evident. Imagine the existence we’d build together if that clarity didn’t fade.
I wish all of you the very best. Care for yourself, care for others, care for the planet and care for our animal friends. Care for life as it’s the most precious gift there is.
It’s time to run a mold/mycotoxins, glyphosate and heavy metal functional medicine panels. Especially nickel from your plant based diet. High-nickel plant-based diet and high cacao = higher nickel exposure = immune and histamine activation = gastric inflammation. You never tested your cacao for nickel, only 4 other metals.
Mark my words, this is the SCOTUS decision from today you will remember years from now.
This is the one we need all hands on deck to overturn, along with Buckley, Citizens United, and McCutcheon.
NEWS: 29-year-old Democratic Socialist Melat Kiros will defeat 15-term incumbent Rep. Diana DeGette in the Democratic primary for CO-01. Kiros, a first-time candidate and former attorney, dominated the Denver assembly and tapped into anti-incumbent sentiment. Kiros was born four months after DeGette first took office.
They want us to believe buying a $700k starter home on a $60k income is the same as them buying a $70k house on $40k a year. Make it make sense. The housing market isn't just bad, it's literally the most unaffordable in history. Don't call us lazy, we're just priced out.
@alpashah001 I owe you an email about all this nonsense around Anthropology (the Vanderbilt/Wash U report), and, of course, your work is some of the best both for defending the empiricism of our field and for showing it in action.
The Vanderbilt report highlights that much humanities writing is "turgid" and hard to read, but why didn't they also highlight the dozens of empirically driven ethnographies that are a delight and easy to read? Here are a few https://t.co/FQZ5aIY39B