Your Energy Oil Crisis - No One Talks About - Part 1

Rheece Hartte

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YOUR Energy Oil Crisis - How This Shows Up in Disease

Is this You or someone You know?

Cancer - Every cancer cell shares one trait - broken energy metabolism. When mitochondria can’t burn fuel properly, cells are forced into fermentation.

Neurodegeneration - Memory declines, thinking slows, and plaques form as brain energy collapses. Another example of energy failure at the cellular level.

Diabetes - Mitochondria lose their ability to handle glucose efficiently, driving insulin resistance and unstable blood sugar.

Joint Pain & Inflammation - When rancid fats accumulate in tissues, oxidative stress and inflammation flare up, making joints stiff and painful.

Fat Loss Resistance - Damaged mitochondria struggle to burn fat for energy, leaving people stuck no matter how hard they diet or exercise.

Hypothyroid (Hashimotos) - If mitochondria are damaged by oxidized linoleic acid (LA), even normal T3 levels won’t translate into good energy. This creates a “functional hypothyroid” state — labs may look fine, but the person feels tired, sluggish, cold

What

Mitochondria failing to produce clean energy because cardiolipin is damaged by excess linoleic acid (seed oils).
Cells switching from oxidation (burning fuel cleanly) to fermentation (a backup survival mode).

Why

Because the fats we’ve been eating for decades (seed oils, processed foods) oxidize easily and damage the delicate machinery inside mitochondria.

Once oxidation and rancidity set in, the body can no longer power itself properly — leading to disease.

When

It starts silently, often years before symptoms show.
For most people, damage accelerates in midlife (40s–60s), when decades of high linoleic acid intake finally overwhelm the system.

Where

In the arteries - cholesterol turns rancid, leading to plaques.
In the brain - energy collapse drives memory loss and plaques in Alzheimer’s.
In the cells - cancer arises when mitochondria can no longer burn glucose and are forced into fermentation.

If the damage compounds & accelerates in mid-life could that be why we see some people age faster and get dis-ease in their bodies earlier than others?

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