~ The McCairn Protocol ~
(also called the Edogawa-McCairn Protocol)
• is an experimental, two-part treatment approach developed or promoted by neuroscientist Dr. Kevin McCairn, PhD, in collaboration with a hospital in Japan (Edogawa Hospital) & ran by Dr Kato
• It primarily targets symptoms associated with Long COVID & post-mRNA vaccine injury
• it focuses on issues like persistent spike protein, amyloid fibrin microclots, autoantibodies, inflammation, & related vascular/neurological damage edogawadfpa.com
2)
• The full protocol is typically an outpatient process spanning about 2 weeks at the Japanese facility, with pre-/post-testing (including microclot analysis via Thioflavin T staining & fluorescence microscopy through Synaptek Labs)
• Dr. McCairn’s work involves neuroscience research (previously on movement disorders like tics in primates) & analysis of blood samples for amyloid fibrils, abnormal clotting, & prion-like misfolding potentially linked to spike protein
• The protocol addresses what proponents call “spikeopathy” — persistent effects from SARS-CoV-2 or mRNA vaccines leading to microclots, endothelial damage, & chronic inflammation
• It is not a mainstream or FDA-approved treatment for these indications
• It is positioned as a proof-of-concept study with patient testimonials (e.g., dramatic improvements in energy, cognition, & function in some severe cases or similar)
• Efforts are underway to fund IRB-approved trials in the U.S. to study it more rigorously
• This protocol represents one investigational avenue in a broader field of microclot & spike-related research
• Unlike standard plasmapheresis (which replaces plasma with donor plasma or albumin), DFPA uses filtration to retain most of the patient’s own plasma while targeting specific larger molecules/pathological elements
~ Goal:
• Physically remove circulating microclots (often amyloid-positive fibrin structures) & inflammatory triggers that may impair microcirculation, contributing to fatigue, brain fog, etc
• Intravenous (or sometimes nasal/olfactory) administration of trophic factors, cytokines, exosomes, & growth factors harvested from the culture supernatant of mesenchymal stem cells (often from primary tooth pulp/dental pulp stem cells — autologous or allogeneic “baby teeth” derived) donated to the clinic
• No live stem cells are infused; instead, it’s the secreted “paracrine” signals (e.g., anti-inflammatory IL-10, neurotrophic factors like BDNF/NGF, VEGF, HGF, TGF-β)
~ Goal:
• Promote tissue repair, reduce inflammation, support vascular/endothelial healing, modulate immunity, & aid neurological recovery
• Often given daily for ~14 days alongside or after DFPA
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• For the latest, check sources like Synaptek Labs or updates from involved clinicians below:
• A hospital-led pathway for long COVID & vaccine injury presentations, pairing DFPA blood purification with cytokine analytics, amyloid detection, live blood analysis, & SHED-derived regenerative growth factor support
***Explanation of Stem Cell Growth Factor Treatment that Im receiving here in Japan via my own Research Trial Participant Consent Form Paperwork***
"Uninsured Medical Care: Intravenous Administration of Conditioned Medium Derived from Deciduous Tooth Pulp Stem Cells for the Enhancement of Vascular Endothelial Cell Function"
The purpose of this explanatory document is to ensure that you fully and accurately understand the details of this study, and to enable you to decide—based entirely on your own free will—whether or not to participate in this medical treatment
Please read this document carefully, listen to the explanation provided by your attending physician, and take sufficient time to reflect before making your decision regarding participation in this clinical program
Please be assured that your decision not to participate will in no way result in any disadvantage regarding your future medical treatment
Furthermore, should you have any questions or points of uncertainty—no matter how minor—please feel free to ask us at any time
Regarding "Voluntary medical treatment using intravenous administration of culture supernatant fluid from deciduous tooth pulp stem cells to enhance vascular endothelial cell function"
This time, we are pleased to announce the development of "Deciduous tooth pulp-derived stem cells for the purpose of enhancing vascular endothelial cell function."
Thank you for participating in our "Voluntary Medical Treatment Using Intravenous Administration of Culture Supernatant.”
Below is an explanation of this research
About the medication:
The medication used in this treatment was developed based on numerous research findings obtained at universities and other institutions
While its safety and effectiveness have already been confirmed in a limited number of patients, the number of patients tested is insufficient, and its safety and effectiveness cannot be guaranteed
Therefore, we ask that only those who agree with the purpose of this clinical trial and are willing to use the medication at their own risk participate
How to use medicine
The medication is administered intravenously, with 20-30 ml used per session
1. About Uninsured Medical Care
At our clinic, we strive to provide our patients with the latest available treatments
To this end, we conduct research into the characteristics of various diseases and work continuously to improve diagnostic and therapeutic methods within the field of regenerative medicine
Medical care provided by healthcare institutions generally falls into two categories: insured medical care and uninsured medical care
Uninsured medical care applies in cases involving treatments or medications that have not yet been approved by the Ministry of Health, Labour and Welfare
This category includes instances where patients seek access to cutting-edge therapies, or—in the context of dental care—where patients specifically request the use of high-quality materials sourced from abroad rather than domestic alternatives; in such cases, the full cost of treatment is borne by the patient
Currently, we are offering a form of "uninsured medical care"—specifically targeting healthy individuals such as yourself—that utilizes conditioned medium derived from human deciduous tooth pulp stem cells (hereinafter referred to as "the Agent")
• Early assumptions about COVID-19 vaccine components suggested that modified messenger RNA & spike protein would be rapidly cleared from the body, consistent with the known degradation pathways of natural RNA
• HOWEVER, multiple studies have identified these vaccine-derived components in human tissues & bodily fluids for unexpectedly prolonged periods after vaccination
• This persistence challenges initial expectations & raises important questions about the mechanisms enabling such long-term presence
• This review systematically examines the evidence for enduring COVID-19 vaccine components, including modified messenger RNA, spike protein, & lipid nanoparticles, in the human body long after administration.
• We evaluate the techniques used to detect these substances, highlighting the sensitivity & specificity of various assays, & summarize the specific tissues & fluids where these components have been found
• Special attention is given to methodological considerations that may influence detection & interpretation
• Furthermore, this review explores potential biological explanations for the prolonged presence of vaccine-derived material
• Possible mechanisms include altered RNA stability due to chemical modifications, slow clearance of lipid nanoparticles, & the formation of stable complexes or reservoirs within tissues
• The evidence for each hypothesis is discussed, with an emphasis on distinguishing between true persistence & assay artifacts