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We combine cutting edge personalized healthcare tools with published research literature and the clinical experience of hundreds of practitioners so that you can own your own health.a healthier youLET’S CREATEMetabolic…
Helminthic Therapy & CIRS: Could This Be The Missing Link?
CIRS otherwise known as “chronic inflammatory response syndrome”, is a condition defined by Ritchie Shoemaker, MD. CIRS pertains predominantly to the inflammatory response induced by biotoxins, namely mold. There is…
Naviaux Cell Danger Biology & The Future of Personalized Medicine
The research of Robert K. Naviaux, MD, PhD regarding the cell danger response (CDR) is groundbreaking and is leading to a new system’s biology view. This new system’s biology has…
Summer Training Sessions 2019 – New Approaches to Complex Illness
Summer Training SessionsNew Approaches to Complex Illness Presented byMichael McEvoyEducator and Founder of Metabolic Healing Are you working with patients or clients with complex illness? The Summer Training Sessions hosted…
The Estrogen Detox Handbook
This informative e-book details how abnormal estrogen activity can be a hallmark factor in cancers, auto-immune conditions, and many female gynecological issues. This e-book outlines how genetics, epigenetics (gene expression), methylation…
Estrogen & Phosphatidylcholine: Are You Deficient?
Estrogen is a necessary cofactor in the biosynthesis of phosphatidylcholine. Women with low estrogen may be at risk for phosphatidylcholine deficiency. Choline & Estrogen: Menopausal Links In summary: In females,…
What To Do With Your 23andMe Raw Data
Get more than ancestry out of your 23andMe test results. Explore your genetic strengths and weaknesses and biohack your way back to health. Turn your 23andMe Raw Data File into…
Defining The RCCX Phenotype
The RCCX gene cluster on chromosome 6 is one of the most complex regions of the human genome, and one that is likely a major player in chronic disease susceptibility.…
Gilbert’s Syndrome, UGT1A1: More Than Meets The Eye
Gilbert’s syndrome is a condition involving a defect in a phase 2 glucuronidation gene known as UGT1a1. The result of this causes elevations in the levels of unconjugated bilirubin. The…
RCCX Practitioner Course
RCCXUnravelling the Genomic Instability of Complex Illness INTRODUCINGRCCX & Complex Illness:Introduction to Theory, Phenotype & TherapiesAn in-depth training course for health professionals The RCCX gene cluster located on chromosome 6…