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MoldCo

The science

Research & Evidence

Useful evidence beats certainty theater. MoldCo separates damp-building evidence, CIRS-field literature, clinical interpretation, and patient education.

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How mold affects the body

Inflammatory, environmental, and individual.

Mold-related illness is not framed from one symptom or one lab. MoldCo looks for patterns across symptoms, exposure history, biomarkers, susceptibility, and response over time.

  • Indoor dampness and mold are strongly linked with respiratory and allergic outcomes in mainstream public-health literature.
  • CIRS-field literature describes a broader inflammatory pattern after water-damaged building exposure.
  • MoldCo keeps evidence lanes distinct instead of collapsing them into one oversized claim.

Our biomarkers

Markers are context, not verdicts.

The right marker can clarify a body-side question. No marker should be presented as a standalone diagnosis.

  • Inflammation

    TGF-beta1, MMP-9, C4a, ferritin, and VEGF can help frame inflammatory and vascular patterns.

  • Hormone and fluid balance

    MSH, ACTH, cortisol, ADH, and osmolality add neuroendocrine and fluid-balance context.

  • Susceptibility

    HLA-DR/DQ testing can add genetic risk context, but it does not diagnose current illness or exposure.

Our clinical approach

Care uses a pattern, not a single proof point.

MoldCo starts with a symptom and exposure story, then uses testing when it can clarify the plan.

  1. Start with the patient's symptom pattern and environmental history.
  2. Use home, body, or genetic testing only when the result can change the next step.
  3. Treat within clinical scope while keeping emergency, primary-care, and remediation boundaries explicit.

Our testing methods

Each test has a job.

The testing hub is the launch surface for detailed SKU pages. Research explains the method boundary.

  • Blood biomarkers

    Body-side inflammatory and regulatory markers; not building contamination.

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  • Home dust testing

    Settled-dust mold species context; not a personal diagnosis.

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  • HLA-DR/DQ

    Genetic susceptibility context; not current exposure or illness.

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