Systemic acidosis is a scourge on the body, causing widespread affliction due to inhibited eliminative organ function (kidneys, intestine, skin, and lungs) and resulting in chronic lymphatic stagnation.

The relationship between our embryonic trunk, the transverse colon, and pituitary function is intrinsic. Systemic involvement and energy flow obstruction in the transverse colon affect pituitary hormone production and may lead to endocrine dysfunction.

Suppressed thyroid function inhibits the body’s ability to eliminate toxins through the skin. The skin is a crucial elimination channel in cases with adrenal dysfunction and impaired kidney function; symptoms associated with psoriasis, eczema, and other chronic inflammatory skin conditions may arise without it.

The inflammatory effect of systemic acidosis, transverse colon obstruction, and endocrine dysfunction ravage mental stability. Parathyroid involvement hinders calcium utilization, while adrenal insufficiency hinders crucial hormone and steroid production and kidney function. Glandular imbalances may present as symptoms associated with a variety of mental disorders.

Chronic inflammatory skin condition cases exhibit significant psychiatric comorbidities. Studies analyzing the connection identify a strongly correlated relationship with shared inflammation as a factor. Psoriasis is linked to anxiety, depression, bipolar, schizophrenia, psychosis, and other personality and eating disorders. In one comparison between non-affected individuals and those with psoriasis, an elevated risk factor of 41% for schizophrenia was observed.

Research offers no causative explanation for the link between comorbidities. The relationship is undefined despite acknowledging shared inflammation. Neither the inflammatory effect of systemic acidosis on the body nor the eliminative function of the lymphatic system receive consideration.

The “mental health crisis” is not a crisis—systemic acidosis is a crisis. Pharmakeia is a crisis. Mental disorder is an inflammatory condition.