You're not just human - you're a cyborg. Explore the 3.3 million genes that shape your health.
In medical school, I learned that, up until about 100 years ago, doctors prescribed cigarettes as a treatment for asthma¹. Equally perplexing is the lobotomy (a procedure in which the corpus callosum, a structure which joins the two hemispheres of the brain), is severed. Not only was this common practice, but it won a Nobel Prize². Consistent with this madness, heroin was once used to treat morphine addiction³.
It’s natural to think these doctors were really dumb, though, of course, they weren’t. They simply knew less. That’s why I often wonder about what I’m doing (or not doing) now, that will make me look dumb to people in the future. Science and medicine continue to achieve extraordinary things. For instance, there is the ROSA ONE Brain System⁴ for performing neurosurgery, CRISPR for editing genes⁵, and Google Deep Mind’s AI making rapid progress⁶ in both disease diagnosis and drug development.
We’re good, but we’re not that good. I say that because medicine as a profession overwhelmingly ignores the human microbiome, which happens to contain 3.3 million genes⁷, as compared with our own 20,000 genes. Ignoring its impact on physical and mental health, quality of life or susceptibility to disease, won’t age well. It’s a modern day ‘cigarette for asthma’.
In the last 100 years, we've lost 30% of Microbial Diversity.11
In the 1600s, Antonie van Leeuwenhoek⁸ peered into a handmade microscope and saw bacteria for the first time.
The best part of 400 years later, Australian scientists Barry Marshall and Robin Warren, demonstrated it was a bacterium, H. pylori, and not stress, that caused stomach ulcers⁹. Data 1, Dogma 0.
Thousands of years before the discovery of microbes including H. Pylori, however, Chinese Medicine was using faecal preparations¹⁰ to treat gut infections—what we now call FMT (faecal microbiota transplant). Sounds revolting but works brilliantly!
Dogs will never need FMT. Their sniffing, licking, and generally disgusting behaviour is innate behaviour that reinforces microbial diversity¹¹—for them (and us). Our ancestors, not so distant, used to gain diversity from dirt, shared meals, and unfiltered environments, whereas now, many seem more interested in antibacterial sprays and sterile packaging.
As our tools have improved, so too has our language¹². We now separate microbiota (the bugs) from the microbiome (their genes and the environment they contribute to). This has allowed us to evolve from carpet-bombing interventions to those more sniper-rifle—like, such as narrow spectrum antibiotics, prebiotics, probiotics, postbiotics, and curated exposures.
In the last 100 years, we’ve lost 30% of microbial diversity¹³, representing erosion as opposed to evolution. Indeed, the best way to think of your gut microbiome is as a garden-like ecosystem. When it’s healthy, it’s:
Most of the genetic material in your body isn’t yours. The vast majority belongs to trillions of bacteria, viruses, and fungi that call your body home. Despite what you may think, a bit like the 10-year-old at my house, they actually run the joint!
Top 10 Functions of the Microbiome
These are varied and complex²⁹, but at the top of the list come antibiotics, highly processed and sugary foods and foods stripped of nutrients, excessive alcohol, chronic stress, environmental toxins and living “too cleanly” for our own good.
When the ecosystem breaks down, it’s called dysbiosis³⁰—too many bad bugs, not enough good ones. The effects can be quantified using comprehensive microbiome and stool testing (including sequencing, metabolomics, or functional panels) which often reveal certain patterns:
Microbiome results can explain a person’s symptoms or can be harbingers of impending illness. They can explain why someone’s gut is dysfunctional, even when their blood tests are normal. More importantly, they guide more precise, targeted interventions.
I’ve had inflammatory bowel disease since I was 17 — and until fairly recently, not one gastroenterologist mentioned the microbiome. That tells you something about where mainstream medicine still stands. But now, having seen firsthand the impact of restoring microbial balance in my patients, it’s the first place I look when the clinical picture doesn’t add up.
When the gut ecosystem loses diversity³⁷, resilience³⁸, or microbial signalling³⁹, symptoms follow. That can happen gradually, or suddenly — after a course of antibiotics⁴⁰, a bout of food poisoning⁴¹, or travel-related exposure⁴² to unfamiliar microbes. Evidence⁴³ shows that microbial disruption from travel can occur within 24 hours, and while the microbiome may begin reverting⁴⁴ to baseline within a week, full recovery often takes weeks to months — and sometimes doesn’t happen without support.
Restoring microbial balance is more than theory. With the right inputs, it can build back. I’ve seen it — repeatedly in clinical practice, and personally. Some of the maladies that may be driven, or exacerbated by dysbiosis include:
A healthier gut means better digestion, as well as feeling stronger, thinking clearer, and living better, longer.
Understanding what’s happening in the gut allows for a more structured, targeted approach to treatment. One such framework is the 4 R’s — a method that can be used and adapted to a patient’s unique findings.
The 4Rs serve as a flexible, data-driven approach that may involve general practitioners, allied health, and when needed, specialist input.
1. Remove
The first step is to eliminate what does not belong. This may include using targeted antimicrobials to reduce bacterial overgrowth or parasites, removing aggravating foods, and addressing inflammatory drivers⁵² such as alcohol, chronic stress, or environmental toxins. This is a deliberate and test-informed intervention to disrupt the patterns sustaining dysfunction as opposed to a detox.
2. Replace
When digestion is impaired due to factors like low pancreatic enzyme output, bile insufficiency, or prolonged inflammation, nutrient absorption is compromised. Digestive processes may be supported with pancreatic enzymes⁵³ or bile acid replacement where clinically indicated. Micronutrient deficiencies⁵⁴ identified through testing are typically addressed at this stage. The focus is on restoring physiological function.
3. Reinoculate
With dysbiosis and digestion attended to, the third R aims to improve microbial diversity. This involves reintroduction of depleted species with specific probiotics, informed by stool testing. Interventions usually include specific probiotic strains, prebiotic fibres, and fermented foods⁵⁵. The aim is to restore ecological balance, since microbial resilience⁵⁶ depends on both diversity and function.
4. Repair & Rebalance
The gut lining is metabolically active and immune-responsive. When compromised, it permits translocation of antigens, pathogens, and toxins. Nutritional support may include glutamine, zinc carnosine, polyphenols, omega-3 fatty acids, or immunoglobulin supplementation⁵⁷. Additional strategies to restore circadian rhythm⁵⁸, autonomic tone, and inflammatory balance⁵⁹ are also considered, depending on clinical context. In complex cases, this phase often deploys experts within a multidisciplinary collaboration.
This article began by questioning what aspects of current medical thinking might seem misguided in hindsight. One strong candidate is the widespread neglect of the human microbiome. Having explored its importance, how it becomes disrupted, and how it can be repaired, readers who want to go further will find Your Best Gut: The 28 Day Guide to Transform Your Life by Dr. Paul Froomes an extremely helpful next step.