Most if not all individuals presenting with Autism show significant oxygen metabolic dysfunction. Typically these indviduals present:
- Multiple indications of liver dysfunction/damage
- High levels of Red Blood Cell dysfunction/damage
- Chronic Immunological / Inflammatory challenge
- Cognitive/behavorial dysfunction likely related to brain hypoxia
- Significant acid/alkali dysregulation
- Chronic Hypotension / Low Blood Pressure
It seems likely that a significant fraction of the durable symptoms of autism result from the capillary switch mechanism documented by Manfred von Ardenne.
Here is a pathology model based on the capillary edema model:
- In an pre-autistic child;
- Chemical stress triggers a traumatic decrease in blood oxygen desaturation;
- Desaturation results in hypoxia in capillaries throughout the body;
- Which triggers capillary endothelial swelling;
- In many systems throughtout the body, brain, bone marrow, pancreas, liver, etc.;
- Swelling creates durable (permanent) flow restriction through affected capillaries;
- Which permanently inhibits nutrient and oxygen delivery to tissue beds served by the capillaries;
- Which inhibits repair of core healing systems;
- Which prevents systemic healing;
- Which when severe enough reaches a point-of-no-natural-return;
- Which makes the condition permanent.
Note that we have observed variance in agglutination tendencies in autistic children which suggests that simple agglutination does not explain the why healing is permanently prevented in many autistic cases.
This model proposes that the zeta shock, triggers agglutination, which in turn switches on capillary edema, which is the long term reason why healing fails. The capillary edema mechanism is exhaustively discussed in Oxygen Multistep Therapy, by Manfred von Ardenne (text at this link).
The goal of this protocol section is to suggest an OMST therapy model which targets these issues. For background research, please see the appropriate references:
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