>CDF is a suppressed truth, and the truth is dangerous. As an ancient control mechanism over humanity, it manifests as both a physical and spiritual affliction. It is the cause of most disease, mental and emotional issues, and enables Samsara to grind on. A physical and spiritual protocol is offered to obtain health, happiness and true free will.
The 1,000 Year Reign
"I believe I know a great secret. When the work of restoration is completed, we will not even remember the tyrannies, the cruel barbarisms of the Earth we inhabited... the vast body of pain and grief and loss and disappointment within us will be expunged as if it had never been."
The Three Magi
"You are a priest forever after the order of Melchizedek."
- Psalm 110
The Nazorean
"Yea, I tell thee truly,
The paths are seven
Through the Infinite Garden,
And each must be traversed
By the body, the heart and the mind As one"
- Essene Gospel of Peace
The NAC Protocol (Updated February, 2023)
Morning
1200mg NAC
Oregano Oil (min. 40mg Carvacrol)
Black Seed Oil (1 teaspoon)
Night
600mg NAC
Oregano Oil (min. 40mg Carvacrol)
Black Seed Oil (1 teaspoon)
Continue daily for a minimum of two months and count out 3 weeks with no die off symptoms prior to moving to the next step.
Maintenance Protocol
__________
Morning
600mg NAC
500mg Slo Niacin (nicotinic acid)
100mg Pterostilbene
250mg Pomegranate Extract (40% EA)
Black Seed Oil (1 teaspoon)
Night
500mg Slo Niacin
100mg Pterostilbene
250mg Pomegranate Extract
Black Seed Oil (1 teaspoon)
After every 3 weeks on the maintenance protocol, take 1 week off. Continue to use black seed oil during the off cycle.
Fungal die off symptoms may include :
>Tiredness, exhaustion, muscle soreness, increased chest or nasal discharge, cold or flu like symptoms, cold sores, headaches, rash, acne, irritability, change in stool frequency, volume or color; increased urination, bloated stomach, cramps, increased gas.
OREGANO DOSING GUIDE
For each morning and night dose you need a minimum of 40mg Carvacrol. Do not buy a product unless it is listed. Most products are steam distilled but you will want to confirm that.
If your chosen oregano oil contains a higher amount of carvacrol (60mg+ per cap) you'll want to start with 1 cap morning, 1 cap night. If each cap contains less than 40mg, take 2 morning 2 night.
POMEGRANATE DOSING GUIDE
You want a minimum of 100mg Ellagic acid for each morning and nightly dose. If you buy a Pomegranate extract that has 40% Ellagic Acid, that means a 250mg capsule contains 100mg Ellagic Acid.
>Peribsen discusses shared dreams and CDF
View: https://m.youtube.com/watch?v=O_q7vPmas14
>Peribsen discloses the fungal cancer link

Thread by @SPeribsen on Thread Reader App
@SPeribsen: My suspicion is the root of cancer will prove to be HGT (horizontal gene transfer) from fungal pathogens via extracellular vesicles. There are many moving parts to this theory that require testing of cou......

>Archives:
Cosmic Death Fungus: A Primer On An Ancient Enemy
Table Of Contents
I. Overview
1.1 Introduction ...........................................................
1.2 Defining The Enemy ...........................................
1.3 Common Yeast
1.3.1 Candida & Saccharomyces ...................
1.3.2 Alternative Metabolism .....................
1.3.3 You Are The Food ...........................
1.4 Aspergillus .............................................................
1.5 Cryptococcus ........................................................
1.6 Conclusions ............................................................
II. The Fall Of Man
2.1 Taforalt: Origins ...................................................
2.2 Taforalt: Migration ..............................................
2.3 Familial Candidiasis
2.3.1 How Errors Occurred ...........................
2.3.2 Immunodeficiencies ...........................
2.3.3 The Pharoah's Curse .......................
2.4 From Womb To Childhood
2.4.1 APECED .........................................................
2.4.2 Miscarriages & Defects ...........................
2.4.3 Thymus: Immune Failure ......................
2.5 Conclusions ..............................................................
III. Origins Of Disease
3.1 Inflammation ...........................................................
3.1.1 Candida: A Common Trigger ...............
3.1.2 Mycotoxins ..................................................
3.1.3 CDF Associated Interleukins .................
3.2 Connections With Common Diseases
3.2.1 Tooth Decay ..................................................
3.2.2 Cancer ..............................................................
3.2.3 Sclerosis ..........................................................
3.2.4 Heart Disease ................................................
3.2.5 Diabetes & Weight Gain ...........................
3.2.6 Joint Pain, Back Pain, Arthritis .............
3.2.7 Diseases Of The Brain ...............................
3.2.8 Accelerated Aging .......................................
3.3 Conclusions ................................................................
IV. The NAC Protocol
4.1 Introduction and Backstory ................................
4.2 Methodology .............................................................
4.3 The Protocol .............................................................
4.4 Brushing and Upper Respiratory ....................
4.5 Common Die Off Symptoms ...............................
4.6 Common Experiences ...........................................
4.7 Diet Considerations ...............................................
4.8 Conclusion .................................................................
V. The Maintenance Protocol
5.1 Introduction .............................................................
5.2 Methodology ............................................................
5.3 Die Off Symptoms ..................................................
5.4 Common Experiences ..........................................
5.5 Conclusion .................................................................
VI. History, Mythical & Religious References
6.1 Origin Of The Tribes .................................................
6.2 Egypt
6.2.1 Egypt: The Ennead ............................................ 100
6.2.2 Egypt: The Pharoahs ........................................ 113
6.3 Sumerian Legends ...................................................... 134
6.4 Abrahamic Legends ................................................... 140
6.5 Scandinavian Legends ...............................................147
6.6 Irish Legends ................................................................ 151
6.7 Greek Legends .............................................................
6.8 Interplanetary Ordeal ...............................................
VII. Science Behind The Protocol
The NAC Protocol
7.1 NAC ...................................................................................
7.1.1 Primary Benefit & Methodology ....................
7.1.2 Antibiofilm Activity ............................................. 182
7.1.3 Protocol Synergy .................................................. 186
7.1.4 Safety Studies ......................................................... 188
7.2 Oregano Oil ................................................................... 191
7.2.1 Primary Benefit & Methodology .................... 192
7.2.2 Antibiofilm Activity ............................................. 195
7.2.3 Antifungal Activity ............................................... 198
7.2.4 Protocol Synergy .................................................. 201
7.2.5 Immune Modulation ............................................ 203
7.2.6 Safety Studies ......................................................... 205
7.3 Black Seed Oil ................................................................ 209
7.3.1 Primary Benefit & Methodology .................... 210
7.3.2 Antibiofilm Activity ..............................................
7.3.3 Antifungal Activity ..............................................
7.3.4 Protocol Synergy .................................................
7.3.5 Immune Modulation ..........................................
7.3.6 Safety Studies ........................................................
The Maintenance Protocol
Table Of Contents
I. Overview
1.1 Introduction ...........................................................
1.2 Defining The Enemy ...........................................
1.3 Common Yeast
1.3.1 Candida & Saccharomyces ...................
1.3.2 Alternative Metabolism .....................
1.3.3 You Are The Food ...........................
1.4 Aspergillus .............................................................
1.5 Cryptococcus ........................................................
1.6 Conclusions ............................................................
II. The Fall Of Man
2.1 Taforalt: Origins ...................................................
2.2 Taforalt: Migration ..............................................
2.3 Familial Candidiasis
2.3.1 How Errors Occurred ...........................
2.3.2 Immunodeficiencies ...........................
2.3.3 The Pharoah's Curse .......................
2.4 From Womb To Childhood
2.4.1 APECED .........................................................
2.4.2 Miscarriages & Defects ...........................
2.4.3 Thymus: Immune Failure ......................
2.5 Conclusions ..............................................................
III. Origins Of Disease
3.1 Inflammation ...........................................................
3.1.1 Candida: A Common Trigger ...............
3.1.2 Mycotoxins ..................................................
3.1.3 CDF Associated Interleukins .................
3.2 Connections With Common Diseases
3.2.1 Tooth Decay ..................................................
3.2.2 Cancer ..............................................................
3.2.3 Sclerosis ..........................................................
3.2.4 Heart Disease ................................................
3.2.5 Diabetes & Weight Gain ...........................
3.2.6 Joint Pain, Back Pain, Arthritis .............
3.2.7 Diseases Of The Brain ...............................
3.2.8 Accelerated Aging .......................................
3.3 Conclusions ................................................................
IV. The NAC Protocol
4.1 Introduction and Backstory ................................
4.2 Methodology .............................................................
4.3 The Protocol .............................................................
4.4 Brushing and Upper Respiratory ....................
4.5 Common Die Off Symptoms ...............................
4.6 Common Experiences ...........................................
4.7 Diet Considerations ...............................................
4.8 Conclusion .................................................................
V. The Maintenance Protocol
5.1 Introduction .............................................................
5.2 Methodology ............................................................
5.3 Die Off Symptoms ..................................................
5.4 Common Experiences ..........................................
5.5 Conclusion .................................................................
VI. History, Mythical & Religious References
6.1 Origin Of The Tribes .................................................
6.2 Egypt
6.2.1 Egypt: The Ennead ............................................ 100
6.2.2 Egypt: The Pharoahs ........................................ 113
6.3 Sumerian Legends ...................................................... 134
6.4 Abrahamic Legends ................................................... 140
6.5 Scandinavian Legends ...............................................147
6.6 Irish Legends ................................................................ 151
6.7 Greek Legends .............................................................
6.8 Interplanetary Ordeal ...............................................
VII. Science Behind The Protocol
The NAC Protocol
7.1 NAC ...................................................................................
7.1.1 Primary Benefit & Methodology ....................
7.1.2 Antibiofilm Activity ............................................. 182
7.1.3 Protocol Synergy .................................................. 186
7.1.4 Safety Studies ......................................................... 188
7.2 Oregano Oil ................................................................... 191
7.2.1 Primary Benefit & Methodology .................... 192
7.2.2 Antibiofilm Activity ............................................. 195
7.2.3 Antifungal Activity ............................................... 198
7.2.4 Protocol Synergy .................................................. 201
7.2.5 Immune Modulation ............................................ 203
7.2.6 Safety Studies ......................................................... 205
7.3 Black Seed Oil ................................................................ 209
7.3.1 Primary Benefit & Methodology .................... 210
7.3.2 Antibiofilm Activity ..............................................
7.3.3 Antifungal Activity ..............................................
7.3.4 Protocol Synergy .................................................
7.3.5 Immune Modulation ..........................................
7.3.6 Safety Studies ........................................................
The Maintenance Protocol
The rabbit hole you are about to jump down is going to merge disciplines rarely seen together; esotericism, history, archaeology and science. This information is considered undisclosed, hidden, forbidden, avoided, sometimes challenged and frequently ridiculed. Cosmic Death Fungus (CDF) isn't one specific fungi. It is several genera of fungi that can shape shift at will, play with your immune system as food and cause a lifetime of illness and despair. Cosmic signifies that the fungi in question has a cosmic origin, otherwise known as Panspermia theory.
Death signifies the Entropy that CDF causes by continual damage to our DNA.
CDF can cause brain disorders, heart problems, tooth decay, cancer, diabetes, sclerosis, back and joint pain, anxiety, depression and accelerated aging. It is also responsible for multiple defects in our genome which predispose us to serious diseases, then we pass these defects on to our children. It doesn't stop at causing suffering and disease. It also influences our thoughts, behaviors and eating habits. It can prompt deviant or impulsive behavior, thrives on conflict and stress, and creates hormone imbalances for it's own benefit. It wreaks havoc throughout your body and works intelligently to get what it wants. You are it's food. You are not even fully human. In fact, you won't experience your true potential until you remove it from your body and heal the damage it has caused.
1.2 Defining The Enemy Typically fungi is classified as a mold or a yeast. Dimorphic fungi can be both, changing shape and purpose based on many different factors. This type of fungi is not symbiotic and provides no benefit to the host. Thermally dimorphic fungi can maintain mycelial form in the environment, but when entering the human body they become pathogenic. (source) Even perfectly healthy individuals can trigger disease by simple things such as taking antibiotics. (source)
1.3.1 Common Yeast : Candida and Saccharomyces This form of fungi can exist in single cell and hyphal form. Initial infection starts in the gastrointestinal tract, oral cavity and upper respiratory tract. Both create biofilms. Candida gets most of the attention and is the most widely studied as a fungal pathogen, but common bread and brewers yeast can also be pathogenic and cause disease. (source) Surprisingly, many supplements claim this yeast is beneficial for ingestion, even though it can filament and invade organ and tissue causing serious problems (source). It's also commonly used to fatten cattle (source) and can directly trigger diabetes. (source)
1.3.2 Common Yeast : Alternative Metabolism Candida utilizes glucose sensing receptors to detect when sugar is consumed. (source) Attempting to eliminate sugar will not work, however. It can utilize alternative metabolism at any time. one regular way it feeds off of us is using the peptide toxin candidalysin to penetrate membranes and tissue then feeds off of what is available. (source)
1.3.3 Common Yeast : You Are The Food Depending on where in the body it resides, it can choose intelligently to utilize fatty acids, protein, glucose or LDH as food sources. (source)
1.4 Aspergillus This pathogenic fungi is particularly dangerous because it can be inhaled and quickly infect the lungs, brain and modify immune and gene expression. (source) Exposure typically happens in the home in a closed environment. This particular fungi can become systemic and be the cause of brain lesions, nervous system damage (source) and even autism. (source) Once inhaled, this human pathogenic mold uses aflatoxin and gliotoxin to suppress immune response and increase virulence. (source) In immune competent people it can remain in the lungs for years and heavily contributes to asthma. (source)
1.5 Cryptococcus This dimorphic pathogen is particularly dangerous to humans since it has an additional layer of defense using a chitin formed membrane similar to crustaceans. (source) This dangerous fungi with it's own mobile biofilm attacks various body systems, including the brain (source), lungs (source), prostate and central nervous system. (source) This insidious fungi primarily targets the brain and central nervous system via inhalation. It has several advanced techniques to enter the brain, including traversing the blood brain barrier inside of our own immune cells as a Trojan horse technique. (source)
1.6 Conclusion This was a quick overview covering the 3 specific genera we focus on: Aspergillus, Cryptococcus and Candida. We've shown how it goes well beyond a gut issue, can feed on more than just sugar, and can infect various body systems. The average person is infected with at least 3 pathogenic fungi, and the above mentioned are the most common. The failure of modern medicine is based on symptom management and ignoring fungi as an origin of disease. Even though there are decades of research linking fungi to all types of disease, the focus still remains on viruses and bacteria. Most studies focus on fungi as being a problem only when you are immune compromised. This is an abysmal failure in understanding of how fungal metabolites contribute to disease and suffering.
Section II : The Fall Of Man 19
2.1 Taforalt: Origins Taforalt, Morrocco These ancient cave systems were discovered in 1961, containing burial sites for early Homo Sapiens spanning thousands of years. As archeologists dug through layers representing different time periods, the period between 35,000 to 15,000 BC harbored a unique trait that other periods did not. This period showed the earliest evidence of dental caries in the population. (source) Claims were made that new agricultural practices lead to this evidence of dental caries, but evidence shows that these new practices came approximately 10,000 years later. (source)
Thee real cause of the dental caries was based on thousands of years of raising pigeons. These birds are known to harbor and spread several species of pathogenic fungi. (source) We also know that tooth decay and biofilm formation is the interplay between bacteria and fungi. (source) (source) We also know due to modern science that when constantly subjected to fungal pathogens, the body suffers from constant DNA damage. (source)
This mostly results from their metabolites and toxins used to suppress immune function. (source)
After many generations of exposure to multiple fungal pathogens from pigeon excreta and constant inhalation of spores, this genetic damage lead to mutations and the eventual formation of hereditary defects known today as Familial Candidiasis. (source) We believe that other familial defects will be discovered for Cryptococcus as well. These defects in our genome are specific to our response to fighting pathogenic fungi, and we believe these defects lead to the first evidence of dental caries as our immune response began to malfunction. This cradle of civilization was populated by the Amazigh people, a fair skinned and red haired population that later began their migration to Egypt, Europe and beyond.
2.2 Taforalt: Migration The Amazigh people who occupied Taforalt in Northern Africa had distinct features for the area, including light skin and red hair. The MC1R Genome has some roots in Taforalt and is featured heavily in the genetic breaks we will discuss later. Details of the Taforalt migration shake the current version of history and civilization at it's foundation. Yet the genetic records of the migrations have been verified. Also known as the Berbers, they populated what is now known as Europe, as well as Iran, Egypt and Russia. (source)
Migratory Path From Taforalt (bottom left)
The Berbers became the root of what we now call European civilization. They were Pharoahs of Egypt. They populated England, The Netherlands, Ireland and surrounding areas. It's therefore no great surprise that red haired people or people with genetic lines sharing these characteristics also have the most genetic breaks. Their ancestors in Taforalt spread these gene errors far and wide. We have further archeological evidence to share on this ancient Pharoah line in later chapters under The Pharoah's Curse. We've been gathering personal reports for over a year now online, and we've seen plentiful evidence that people from migration areas are more effected by fungal infections than others.
2.3.1 How Genetic Errors Occurred Gene mutations are the reason for these errors found in Familial candidiasis, and even a function of evolution itself. One good example would be fish subjected to PCBs in their water supply. the eventual gene mutations that make them more resistant to PCBs gets passed on via natural selection and becomes commonplace throughout the population. (source) Since Familial Candidiasis doesn't have an immediate impact on survival, this devolution was carried on and survived to modern day. Just as the mutations of fish created resistance to PCBs, the mutations in humans caused by fungus created mutations beneficial to fungal infection.
The fungi we call CDF have many harmful metabolites that damage DNA and also the body's repair functions. Starting with Candida species, a toxic metabolite of concern is acetaldehyde. It damages the guanine enzymes responsible for repairing DNA (source) and also directly damages the DNA using reactive oxygen species. (source)
Aspergillus uses different mycotoxins based on the species, the most common being aflatoxin and gliotoxin, used to suppress immune response to increase virulence. These toxins also directly damage DNA. (source) (source) Cryptococcus is far more complex, and could be considered the evolution of CDF, having a mobile biofilm and over 30 different metabolites. (source)
Cryptococcus interacts with it's food using more advanced techniques, tailoring release of enzymes depending on environment. Urease is one of the known metabolites that can cause molecular damage, but it can use protease reactions and other techniques. (source) The DNA and nuclear damage these fungi cause are only part of the problem. When combined with genetic breaks, dysfunctional immune response due to genetic errors can cause a never ending autoimmune loop, where the fungus cannot be eradicated and it continues to damage host cells and DNA. Since the immune system cannot do the job on it's own, additional antifungals and strategies are required. At this point you've seen how it can damage our bodies and send us into a downward spiral. It doesn't require any preset conditions to damage your body.
2.3.2 Specific Immunodeficiencies
Searching the OMIM database (source) will show many entries related to Familial Candidiasis, the collection of genetic breaks we discuss here. This section will cover only a handful to demonstrate how relevant they are to chronic infections.
CANDF2 (Immunodeficiency 103) A defect in CARD9 gene, 342 variants. Primary immunodeficiency characterized by increased susceptibility to fungal infections. Predisposition to Systemic and Invasive forms.
CANDF3 Chronic fungal nail infections.
CANDF4 Vaginal and Nail Candidiasis. Immune defect. Immune response 15% or less versus normal.
CANDF5 (Immunodeficiency 51) Immune dysfunction in interleukin 17A,17F, 17A/F, 17E, responsible for responding to fungal infection. Frequent bacterial infections in the lungs. Connected to pancreatic cancer.
CANDF6 Gain of Function mutation in STAT1. Recurrent bacterial, viral, fungal, and mycoplasmal infections, disseminated dimorphic fungal infections, enteropathy with villous atrophy, and autoimmune disorders, such as hypothyroidism or diabetes mellitus. A subset of patients show apparently nonimmunologic features, including osteopenia, delayed puberty, and intracranial aneurysms. Laboratory studies show increased activation of gamma-interferon (IFNG; 147570)-mediated inflammation
CANDF7 A primary immunodeficiency disorder with altered immune responses and impaired clearance of fungal infections, selective against Candida. It is characterized by persistent and/or recurrent infections of the skin, nails and mucous membranes caused by organisms of the genus Candida, mainly Candida albicans.
CANDF8 Affiliated tissues include skin, and related phenotypes are macroglossia and seborrheic dermatitis
CANDF9 Important gene associated with Candidiasis, Familial, 9 is IL17RC (Interleukin 17 Receptor C). Affiliated tissues include skin, and related phenotypes are recurrent aphthous stomatitis and chronic mucocutaneous candidiasis
2.3.3 The Pharoah's Curse
(Pharoah Ramses II, son of Seti I) One of the landing points for the Amazigh people was Northern Egypt. Our research lead to a well hidden document from France that the Egyptian Antiquities would rather you not see.
Pharoah Ramses II was quickly moved to France after being discovered, as he was decaying from a fungus. This fungus remained active for thousands of years in his tomb. He lived as most Amazigh lived. Chased and tortured by the fungi we refer to as CDF. In the documents, later translated, they found all of the classic symptoms of FC. He had posture issues, his legs were bowed, he was balding, and the fungus literally consumed his nose. He wore a prosthetic nose to cover up this fact, which is also described in the documents.
There is a big connection to history and mythology here that we will expand upon more in coming sections. But for now, let's clarify that Ramses II followed Seti (Seth) and moved his people to monotheism. The decision to worship Seth over Osiris was indicative of the battle his people faced.
Osiris promoted bread and beer, and Seth fought against it. They knew even then how dangerous this fungus was. The following are quoted excerpts from the documents, translated to English. "for the skull: loss of material in the region of the cribriform plate of the ethmoid bone (evisceration gap); calcification of the falx cerebri, with atheroma of the carotid sinuses and temporal arteries; wear of the dental crowns in the upper and lower jaws, with geodes at the level of the root apex, due to abscesses; a kind of nasal prosthesis composed of exogenous elements, of circular or oval outline."
"The radiochromo densitographic study revealed in particular that the cervical spine and the skull present an aspect reflecting a post-mortem fracture of the spine, certainly straightened during the mummification. As for the jaws, all methods then combined or confused, their examination makes it possible to affirm that it is about an individual carrier of numerous and important dental lesions, due to cavities often complicated by septic bone lesions, that in a very old man, reached of a very alveolysis. marked and an osteitis of the mandible linked to an abscess formation towards the chin." "And this is how we were finally able to reach an approximation: height, by bone measurements: 1.72 m, age, by the state of the bones and teeth: 80 years, race, by the diameters, indices, angles and cranial or facial profiles: a type a priori Berber.
There remained the hair, of exceptional interest because of its state of conservation fine, supple, slightly wavy in places, of a blond-red pulling on the yellowish. Oval in section, and overlapping all the other anthropometric observations, they are characteristic of the hair of a cymotrichous leucoderma, close to prehistoric Mediterraneans, such as a Berber, with white skin and not a Nubian, with black skin. , contrary to what had been maintained"
2.4.1 APECED Autoimmune polyendocrinopathy-candidiasis- ectodermal dystrophy (APECED) is an immune disorder due to the genetic breaks we've discussed. It allows fungal infection of the ectoderm layer in the womb and results in failure of t-cell tolerance, autoimmunity against various organs, lifetime predisposition to candidiasis and damage to the Thymus, which regulates T cell function and differentiation. (source) Other features of this genetic disorder are hypoparathyroidism, and primary adrenal insufficiency (Addison's disease). (source)
This can manifest as tongue thrush, nail fungus, balding, auto immune skin disorders, and various other candida related symptoms. This genetic break via mutation is painted as a rare condition, but we believe it is much more common than expected.
2.4.2 Miscarriages & Birth Defects candida is usually the primary culprit when associating fungi with miscarriages. (source) It kills our children before they are born. But it doesn't stop there. It also attacks male sperm (source) and even becomes more virulent during pregnancy. (source) If the child survives this process there is now a possibility of birth defects and permanent neurological damage if they carry the infection post birth. (source) Mainstream thinking claims that candida is harmless and only causes yeast infections and nail fungus. They were certainly wrong on that as well.
2.4.3 The Thymus: Early Immune Failure
The Thymus plays a critical role in our body's defenses against pathogenic fungi. It is the origin point of new T- cells and also where the cells are differentiated. For most people this organ shrinks and becomes atrophied early in life, right around puberty, but the damage starts much earlier. (source) It is one of the most common targets of pathogens, (source) and fungi in particular. This causes dysfunction in critical interleukins 17 and 22 in response to fungal pathogens, and is also tied to the genetic breaks under Familial Candidiasis. (source)
Section III: Origins Of Disease
3.1 Inflammation "Inflammation is the cause of all disease."
Stop right there. Nobody questioned where the inflammation was coming from. Furthermore, if it's from a commonly occurring source, we can address the real problem. In order to impose a unified theory where CDF is the primary cause of inflammation, thus the primary cause of most disease, you would need to show that there is a chronic issue regarding exposure, and a chronic issue in the way the immune system handles the response. The next few sections will dive a bit deeper into how CDF causes inflammation, and how it can be connected to various disease states in the body.
3.1.1 Candida: A Common Trigger
Candida Albicans does immense damage to the body and is a constant source of inflammation. A primary cause of chronic inflammation from Candida is from it's metabolite, Acetaldehyde. When it metabolizes glucose it produces this toxic substance, which constantly damages your DNA and is carcinogenic (source). Acetaldehyde directly induces pro inflammatory cytokines (source). When you combine it with immune defects from Familial Candidiasis, now you have an out of control situation. The immune system cannot remove the infection, and it continues to damage your DNA and cause inflammation indefinitely. This form of autoimmune loop has been linked to various diseases that we discuss in coming sections.
3.1.2 Mycotoxins Candida isn't the only source of chronic inflammation. The other abundant source is Aspergillus. Before we explain these toxins, keep in mind that it is in your food (source) and you breathe in the spores regularly, (source) usually from your home environment. Aspergillus Fumigatus produces Gliotoxin. This potent toxin triggers inflammation, destroys brain cells, eats holes in your brain and is connected to diseases like Multiple Sclerosis (source). Aspergillus Flavus produces Aflatoxin. This is also prevalent in the food we eat. This toxin damages DNA, is also considered carcinogenic, damages the immune and central nervous system. (source)
3.1.3 CDF Related Interleukins
Immune dysfunction against CDF is a potent source of chronic inflammation and autoimmune disease. As mentioned earlier, a common target of CDF is the Thymus, since it plays an essential role in adaptive immune response. Our immune response is neutered at a young age. Thymus function crashes. Most have their tonsils removed, which is full of both b and t cells used by adaptive immune response. Then the relentless attack against our DNA begins. Involution of the thymus is one of the most ingenious attacks by CDF. It's connection to APACED and Familial Candidiasis has been made previously (source). Chronic inflammation due to chronic infection and genetic breaks show the same responses.
Typically CDF will trigger Interleukin 6 (IL-6) and Tumor Necrosis Factor Alpha (TNF-a). Consistently higher response is seen with Candida (source) and Aspergillus. (source) Cryptococcus is unique because it can suppress IL-6 response (source) as a method of survival. So what exactly would chronic IL-6 and TNF-a response do to the body? Interleukin 6 is not only directly responsible for inflammation, but also for triggering the change from acute to chronic inflammation. (source). TNF-a induces inflammatory gene expression and apoptosis in healthy cells, also directly contributing to diseases like cancer. (source)
Now you have a direct path. All 3 CDF genre induce IL-6 and TNF-a. Chronic infection that the body cannot clear will create chronic inflammation. Chronic inflammation is viewed as the source of most disease. (source) Now you understand a cause of chronic inflammation and disease, but more importantly a true source. The next section will focus on common forms of disease, and the myriad connections that have been made to fungus. The evidence has been there for decades, hidden in studies waiting for someone to make the connections.
3.2 Connections With Common Diseases
3.2.1 Tooth Decay
Before we get directly into tooth decay, let's start with gingivitis. The interplay with fungus is once again required. The bacterium P. gingivalis, responsible for disease, has issues adhering to epithelial cells. Candida is commonly found in pockets of infection due to dental work like root canals, and it directly contributes to adhesion and virulence by triggering a pro inflammatory response. (source)
Candida also lays the groundwork for tooth decay through biofilms on the teeth. In biofilms that Candida forms, any cohabiting bacteria have shown dramatically increased virulence and pathogenicity. (source) The most recent science shows that Candida can utilize Candidalysin, it's peptide toxin, to penetrate tissue and begin adherence to create biofilms. (source)
Candida causes the initial penetration of tissue and adherence, then forms a multi-species biofilm with P. gingivalis. Without the presence of Candida, P. gingivalis has a hard time adhering to tissue. Fennel oil has been scientifically proven to be safe and effective against biofilm, bleeding gums, halitosis, mouth ulcers, and preventing tooth decay and is one of the solutions provided later in this document.
3.2.2 Cancer
One of the most recent and eye opening studies of cancer was released recently. The study included 17,000 people and 35 different types of cancer. Fungus was detected in the cancer cells of all 35 types. (source) To make matters worse, CDF sets up this condition using it's own metabolite, Acetaldehyde. (source) Because CDF is a systemic issue, it can set up cancer virtually anywhere in the body. More recently there has been a direct association with oral cancers as well. (source) Don't discount Aspergillus, however. One of the most frequently encountered, A. fumigatus, produces gliotoxin.
This toxin is directly carcinogenic and known to cause cancer of various types (source)
3.2.3 Sclerosis
Nothing puts young people in wheelchairs like Multiple Sclerosis. It's the #1 disability in younger people. The level of suffering compounds as loved ones must give up their incomes to care for them. Science is now catching on to what we've been saying. (source) The newest research is now making a link to Aspergillus exposure (source) and the onset of MS. Even back in 2010 they were raising the alarm (source) but nobody listened. Science calls it incurable, but we know much about this disease. Aspergillus can be responsible for infecting the brain causing the characteristic lesions (source) or it can be cryptococcus via infection of microglia cells, preventing their normal function of clearing abscesses of debris and toxins. (source) These reactive microglia can directly cause lesions via ROS generation.
It's also possible that both fungi, Aspergillus and Cryptococcus, can contribute to the disease concurrently. There is evidence that they can increase virulence while cohabiting. (source) Characteristic brain lesions in combination with damage of the myelin sheath around nerves are the telltale signs of MS. Remyelination is possible once the source of infection is fully cleared. (source)
3.2.4 Heart Disease
There is a misconception that high cholesterol causes heart disease. The truth on the matter is that high cholesterol is a symptom, not a cause. The body protects itself from mycotoxins in the blood by binding with a cholesterol or lipid. (source) The same process is used in the brain to protect it from free roaming mycotoxins. (source) Recent research has shown that cryptococcus uses a unique mechanism to trigger atherosclerosis via lipid peroxidation. (source) Not surprisingly, cholesterol drugs were originally tested as antifungals. On the flip side, many drugs derived from mycotoxins can directly trigger atherosclerosis as seen in the above source.
3.2.5 Diabetes and Weight Gain
Diabetes derived from pancreas dysfunction is a hallmark of fungal infection. IL-6 and TNF-a are regular inflammatory reactions to fungal infection, and also show up in pancreatic cancer. (source) Damage is caused by inflammation of the pancreas, which is responsible for controlling blood sugar via insulin secretion and also releasing enzymes for digestion. (source) Eventually the body cannot regulate insulin correctly, and weight gain rapidly increases. (source) Cryptococcus (source) and Candida (source) are both known to attack the organ but background inflammation from mycotoxins is likely the major contributor. (source) Candida's production of acetaldehyde plays a major role, as well as brewer's yeast. (source) (source)
3.2.6 Joint Pain, Back Pain & Arthritis
All of these symptoms of suffering usually have the same cause; inflammation that is triggered by long term infection. IL-6 plays a significant part. Rheumatoid arthritis (considered an autoimmune disease) is directly linked to overactive IL-6 (source) and Osteoarthritis cartilage and tissue degeneration is as well. (source) Keep in mind that IL-6 is a hallmark of longterm CDF infection and the associated mycotoxins, covered previously. Lower back pain is a common trigger when carrying a longterm infection. Sciatica is a good example. IL-6 and TNF-a are commonly found, but also IL-17 and IL-22, specific to fighting fungal infection. (source)
3.2.7 Diseases Of The Brain
This information is going to be shocking to some people. Various brain related diseases all have common causes. Neuroinflammation gets blamed often, but once again, we question where it comes from. We're seeing multiple angles of attack. More than one species can work together to cause these issues, and even increase virulence in combination. (source) Amyloid beta plaqueing is associated with Parkinson's Disease (source), Alzheimer's Disease (source) and Multiple Sclerosis (source) to name a few. So how does this slime accumulate on the brain and in lesions, preventing the body from repairing itself?
Unfortunately there are multiple ways. The first is through mycotoxin mitigation, causing hypercholesterolemia and amyloid beta buildup (source). This is a similar defense mechanism that A.V. Constantini discovered in his research of Atherosclerosis, with lipids binding to mycotoxins in the blood stream mentioned earlier. The second method of amyloid plaquing is cryptococcus. This fungus is very advanced. One of the reasons Multiple Sclerosis is difficult to treat is because cryptococcus zombify microglia, which are the cells responsible for clearing debris and toxins from lesions. They then become reactive microglia (source) and directly produce amyloid beta, preventing the lesions from healing while also further damaging the brain with ROS/NOX2 (source) from glial dysfunction.
Cryptococcus is also known to directly infect astrocytes, (source) which normally assist in plaque removal. Once cryptococcus invades astrocytes, this not only weakens the blood brain barrier but increases plaquing. (source). The third method of infectious disease progression is yet to be defined publicly, but to summarize we believe it is a gene defect related to cryptococcus that is Familial, and interferes with normal ability to prevent NOX2 oxidation. More information will be available on this in future updates.
3.2.8 Accelerated Aging
How is aging defined? It's generally accepted that genome damage, telomere shortening and mitochondrial dysfunction are major contributing factors. We've already discussed how CDF is constantly damaging our DNA, and puts us into a state of chronic inflammation. Part of this cellular damage is also mitochondrial dysfunction. To get technical for a moment, a structure called a g-quadruplex is responsible for performing many genome repairs in the cell. When the body contains active fungal infections, DNA damage occurs. Also the ability of g-quadruplexes to repair DNA errors is impeded. CDF directly causes an oxidative reaction in the cell (ROS) and destroys the g-quadruplex. Additional damage to the genome happens via oxidative lesions to telomeres. (source)
3.3 Conclusions
We've covered alot of material in this section. We've shown how chronic inflammation is triggered, what pathologies are responsible, and how CDF genera contribute to the most common diseases. Considering the contribution of CDF and it's mycotoxins to chronic inflammation and the top diseases by mortality, the problem becomes so overblown that it's difficult to understand why we are in this situation. The death toll is minimized by focusing on pathologies featuring chronic overgrowth, like cyrptococcal meningitis. But what if we add up the numbers based on cancer, heart disease and the other diseases mentioned? What level of suffering and misdiagnosis will it take before this issue is given the gravity it deserves?