Medical Observation Journal Author: Jonathan Olvera Subject: Vibration Ellipse, Bone Polarity, and Fluid Conductivity in Systematic Pain (Apergy)

 

Medical Observation Journal

Author: Jonathan Olvera
Subject: Vibration Ellipse, Bone Polarity, and Fluid Conductivity in Systematic Pain (Apergy)

Date: 08/19/2025


Observation

During systematic pain episodes—referred to herein as apergy—patients may present with sensations linked not only to nerve conduction but to vibration ellipses arching across serous apertures within bone cavities. These apertures appear to mediate the relationship between fluid polarity and terminal conductivity in tissues.

Fluid and Polarity Measures

Preliminary notation demonstrates that pain sequences can be represented through incremental polarity shifts:

00 +01 +01 +02 00-1 1.0

These values, when graphed in celtic-spherical sequences, suggest repeating fluidic loops that correspond with protein generation, phosphate transfer, and reticulum activity.

Cellular Observations

  • Cellulose reticulum and Golgi structures are responsive to polarity change at +01 increments.

  • Conductivity within serous cavities may be traced through phosphate exchange, approximated as:

    • CI Cell Unit (+01 / –0)

    • Ch – Nitrogen (12–05)

    • Pho Mass (42 × 13 → 15)

    • U Phot–A–5 (13 / 05)

    • PeP Unit (30 × 5 × –09)

    • m Base [N] (83 × –09 × 15 /X)

Structural Notes

DNA composition may be modeled as an apergic fluid sequence—protein-generative under conductivity shifts. Phosphates, reticular units, and peptide complexes demonstrate consistent ellipsoidal vibration patterns.

Reference Notation – R Unit

Line U P OX OxygenMetals ID IderiSohine AI AdiLen Phire PhosphateIrile ILuRe LinLenUniCereine Pre L PreLinGet 4 PEP PhArUn

Interpretation

  • Systematic pain (apergy) correlates with bone cavity fluid polarity shifts.

  • The serous apertures function as resonance points, arching vibrations in elliptical sequences.

  • These ellipses may be measurable as DNA-fluid conductivity events, observable across Golgi and reticulum phosphate structures.

  • Pain therefore may be mapped as a fluidic polarity circuit, suggesting a diagnostic model where conductivity and vibration predict or reflect systemic pain.

Conclusion

Initial observations indicate that pain pathways in bone cavities are not only neurological but electro-fluidic in nature. The interplay of vibration ellipses, serous apertures, and phosphate conductivity may provide a foundation for both diagnostic imaging and therapeutic intervention.

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