
Since
1989

FOUNDER OF MIT - ACADEMY OF FUNCTIONAL MEDICINE & INTEGRATIVE THERAPIES -
Founder of Cryptostain® Microbiology/Microscopy Research
Senior Doctor Spinal Trauma Care Unit USAC Hospital CCHN: 006582/DNA-CCHN Director of M.BS Doctoral Studies USAC University Hospital Saigon VietnamSubsidiary/Affiliate Hospital - Ministry of National Defence Vietnam

COLLEGE OF MEDICAL EVANGELISTS (CME)
LOMA LINDA UNIVERSITY
SCHOOL OF MEDICINE
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WHO Global Report - 2014 - 2023
Alternative Medicine
Strategy - COVID 19


The United Nations Department of
Economic and Social Affairs (DESA)
World Health Organisation
Charter Resolution Decision 115620 20-6-30
The Open University of Complimentary Medicine
(ALMA ALTA) FACULTY OF MEDICAL STUDIES MEDICINA ALTERNATIVA INSTITUTE. (Rhodes)
PhD Lic. 98.4475 c. D.Sc Lic. 2000. 1212 R.


MEDICAL RESEARCH AUSTRALIA
Therapeutic Goods Agency
Schedule 1 defined as Subregulation 4 (2)
regulations of the Therapeutic Goods Act 1989.
Reg No: Y2550431 Item no: 142. Bona Fide Therapeutic Goods (TGA) Schedule 1 Research Association, (RIDDP) Statutory Rules 1990 NO 394
British Council of Complimentary Therapies
Licence Reg; 184/1904/2152/ MITBCCT/ 2000-2021.
Current Member - Directory of Practitioners
Immunotherapy using Acupuncture

Acupuncture Sequencing - A Micro Surgical Approach
DNA repair, the collection of highly-regulated mechanisms by which
a cell identifies and repairs DNA damage, remains one of the most
essential processes of human life.Without DNA repair mechanisms
cells lose the ability to transcribe important regions of their genome,
resulting in harmful mutations, which could eventually jeopardize cellular wellbeing.
Sources of DNA damage include double-stranded breaks and DNA
intra- and interstrand crosslinks, which can ultimately become
alternating factors in Interleukin 17 synthesis, leading to OA.
To study Sequencing Acupuncture in its role as a major rehabilitation modality, we now conclude this advanced art as integral to single molecule studies, having proven to greatly enhance understanding at the molecular level injury bypass mechanics.
Interferons can stimulate or inhibit up to 300 different genes encoding proteins involved in antiviral defense mechanisms,inflammation,
adaptive immunity, angiogenesis, and other processes.
Sequencing technique Acupuncture changes amniotic tissue, increases platelet rich plasma via continuing program of Acu injections.
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Regenerative Medicine
Dr Jeffrey Hunter has taught clinical and practical theory more than 30 years in both Sports Medicine and Pre/Post Surgical Rehabilitation Regen Therapies.
Regenerative Medicine boosts the body's ability to heal itself naturally.
Treatment with regenerative medicine can create living tissue in
the body that has been damaged from disease or degeneration
​
There are four components as to why a joint may be degenerative or injured:
- Mechanical / alignment
- An aging articulation
- Lifestyle (diet, weight, overuse, lack of movement, etc.)
- Trauma
Therefore all four components require attention in the evaluation stage of this process. The Aus Spine Reset method touches on all of the above components. This approach results in the best possible outcome, and a successful return to pain-free activity.
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Custom Treatment
There are many different conditions that cause joint pain and dysfunction. Over the years we have mastered the utilization of different regenerative therapy tools in combination with one another in order to best treat your unique condidition. This may include the use of Acu - Sequencing technique to change amniotic tissue, platelet rich plasma Acu injections, and other modalities.
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With real-time, high resolution Acupuncture we have observed DNA-protein interactions involved in DNA repair. Molecular activities and kinetics of Sequencing Acupuncture hastens rehabilitation of injured, both skeletal and connective tissues. DNA is tethered between puncture sites, as multiple stem cell labelled repair proteins are interacting with the DNA molecule. The kymograph in Figure 2 shows
the binding position of two DNA repair proteins that are involved in non-homologous end joining.








