METABOLICNeglect

How Profit-Driven Medicine Failed a Generation's Health

A Life Trajectory

Early 1980s

Birth & Early Conditions

Born in rural America with multiple congenital conditions. Environmental exposure risks and Western diet set the stage for decades of struggle ahead.

Adolescence

Neuropsychiatric Symptoms Emerge

Significant neuropsychiatric symptoms develop. At age 14, diagnosed with autism spectrum disorder and Bipolar I with mixed states.

1990s-2000s

The Pharmaceutical Cascade Begins

Heavy psychiatric pharmacology: mood stabilizers (lithium, valproate), antipsychotics (risperidone, olanzapine), sedating antidepressants, beta blockers. The medications are powerful—but come with real, cumulative costs.

Over Time

Organ & Metabolic Damage Accumulates

Hypothyroidism. Hypercalcemia. Hypertension. Severe kidney infection. Recurring kidney stones. Liver steatosis and fibrosis (MASH). Each treated as isolated—never as systemic failure.

Years Later

Hyperuricemia & Gout

Symptom patterns traceable back nearly a decade, finally named: hyperuricemia and gout. The solution? Two of the oldest, cheapest drugs: colchicine and allopurinol.

Present Day

The Moment of Clarity

After decades of expensive, patent-protected drugs and predictable organ damage, stabilization finally comes from ancient, pennies-per-dose medications. This was not unfortunate. This was systemic.

The Medication Cascade

Lithium / Valproate

Mood Stabilizers

Powerful psychiatric medications with known risks: thyroid dysfunction, metabolic disruption, kidney stress, tremors, weight gain.

Risperidone / Olanzapine

Antipsychotics

Second-generation antipsychotics. Side effects include metabolic syndrome, weight gain, diabetes risk, hyperlipidemia, hormonal disruption.

Antidepressants

SSRIs / Others

Sedating antidepressants added to the regimen. Can contribute to emotional blunting, weight changes, and further metabolic strain.

Beta Blockers

Cardiovascular

Prescribed to manage emerging hypertension and anxiety symptoms—treating downstream effects rather than root causes.

Levothyroxine

Thyroid Hormone

Needed to counter hypothyroidism induced by years of mood stabilizers. Treating the side effects of other treatments.

Colchicine / Allopurinol

Ancient Medicines

Finally: two of the oldest, cheapest drugs in existence. Colchicine (ancient Greek) and allopurinol (1960s). Stabilization at pennies per dose—after decades of profit.

The System Design

Symptom Suppression Over Prevention

The medical economy incentivizes treating symptoms as they emerge rather than preventing disease upstream. Each new symptom becomes a new prescription, a new specialist visit, a new revenue stream. Prevention doesn't generate profit—management does.

Profitable Medication Lifecycles

Pharmaceutical companies don't maximize human health—they maximize shareholder value. Research follows ROI curves, not suffering curves. Patent-protected drugs generate profit. Off-patent interventions languish, no matter how effective.

Chronic Disease as Business Model

Health insurers don't earn revenue by eliminating illness—they earn it by managing billable care. Chronic disease becomes not a failure but a feature: stable, predictable, infinitely renewable. This is why Medicare for All faces such resistance—it challenges the very architecture of a medical economy that relies on chronic disease dependence.

The Neglected Biology

ATP Breakdown

Energy metabolism produces purines

Adenosine Signaling

Cell signaling & inflammation

Xanthine Oxidase

Oxidative stress & vascular injury

Uric Acid

Kidney damage & systemic inflammation

For decades, researchers have understood that purine metabolism plays a profound role in human physiology. Xanthine oxidase—the enzyme targeted by allopurinol—contributes to oxidative stress, vascular injury, kidney damage, and systemic inflammation.

Evidence linking uric acid and xanthine oxidase activity to cardiovascular disease, kidney disease, metabolic dysfunction, and inflammatory processes has existed for years. Yet clinically, allopurinol remains "the gout drug you give middle-aged men when things get bad enough."

Why? Because the pathway doesn't lend itself to blockbuster drug economics. Cheap molecules, off-patent therapies, preventative framing—these are structurally disadvantaged in a marketplace that rewards lifelong dependence on high-margin pharmaceuticals.

Two Economic Models

Current System: Profit First

  • Chronic disease management generates stable revenue
    Patients require lifelong medications, regular appointments, specialist referrals
  • Patent-protected drugs maximize profit margins
    Research focuses on patentable molecules, not foundational biology
  • Prevention is economically disadvantaged
    Preventing disease eliminates future revenue streams
  • Upstream interventions lack profit incentive
    Cheap, off-patent, multi-system approaches don't attract investment

Better System: Health First

  • Prevention reduces long-term costs
    Healthier populations require less intensive interventions
  • Foundational biology gets research priority
    Investment in metabolic health, inflammation, purinergic pathways
  • Environmental & dietary interventions supported
    Address root causes before pharmacological dependency
  • Universal care aligns incentives with outcomes
    A philosophical reconfiguration: system benefits when population health improves, not when illness persists
"If we want medicine worthy of human dignity, we must realign incentives so that curing disease, preventing metabolic collapse, and supporting foundational biological health are not economic liabilities but central priorities."We Can Do Better

My trajectory is not inevitable. It was constructed by a system that treats human beings as revenue streams, chronic illness as a stable business model, and broad-impact foundational biology as an afterthought unless it can be packaged profitably. What is constructed can be rebuilt.