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Systemic Lupus Erythematosus Protocol

    

“Systemic lupus erythematosus (SLE) is a chronic autoimmune disease characterized by the production of autoantibodies and the deposition of immune complexes, affecting a wide range of organs. Genetic factors, environmental factors and hormonal factors are believed to contribute to the occurrence of SLE. However, the pathogenesis of SLE is complex and remains unknown. Breakdown of self-tolerance plays a critical role in the occurrence and development of SLE. Innate and adaptive immune responses against self-antigen induce the production of autoantibodies and the deposition of immune complexes in tissues leads to the activation of complement, accumulation of neutrophils and monocytes, and self-reactive lymphocytes [1]. Despite the improvement in the survival of SLE in the past decades, further improvement in the disease prognosis is hampered by organ damage caused by disease itself and adverse events related to conventional therapies. The in-depth study of disease pathogenesis is helpful to find new therapeutic targets and new biomarkers of SLE. In this review, we summarized recent advances in immunological pathogenesis and related targeting treatment of SLE.”   Immunological pathogenesis and treatment of systemic lupus erythematosus

"Recent advances in genome-wide association studies (GWAS) across autoimmune and immune-mediated diseases have augmented our understanding of pathogenic mechanisms underlying these diseases. This has further highlighted their heterogeneous nature, both within and between diseases. Furthermore, varying responses to therapy have also served to underline the importance of this heterogeneity in the manner in which these diseases are diagnosed and treated. Here we discuss our current understanding of the shared pathways of autoimmunity, including the tumor necrosis factor (TNF), major histocompatibility complex (MHC), interleukin 23 receptor (IL23R) and protein tyrosine phosphatase non-receptor type 22 (PTPN22) pathways. In addition, we summarize effective specific therapies tested across major autoimmune diseases, highlighting the insight they have provided into disease mechanisms and their implications for potential future improvements."    Heterogeneity of Autoimmune Diseases: Pathophysiologic Insights From Genetics and Implications for New Therapies

"For people genetically predisposed to lupus, a deficiency of vitamin D may be a catalyst for developing the disease, say scientists at the Oklahoma Medical Research Foundation. Vitamin D could be beneficial to lupus patients and people who are at increased risk of developing the disease, such as their family members, With vitamin D supplements, doctors might be able to reduce the chances of an autoimmune attack,”  Life Extension, Note MANY autoimmune diseases seem IMO to have this characteristic please keep your vitamin D levels above 60 ng/ml

"A geographic association with northern latitudes has been observed for rheumatoid arthritis, multiple sclerosis and Crohn's disease, other autoimmune diseases that may be mediated by reduced vitamin D from decreased solar exposure and the immune effects of vitamin D deficiency.”   Lower rheumatoid arthritis rates linked to vitamin D   Note most Americans are woefully deficient in Vitamin D

"In populations that consume natural diets of mostly unprocessed fruits, vegetables and grains autoimmune diseases are almost nonexistent. You do not see much rheumatoid  arthritis in China because they eat differently than we do."   Prevention

“This study is the first to indicate that excess refined and processed salt may be one of the environmental factors driving the increased incidence of autoimmune diseases, Junk foods at fast food restaurants as well as processed foods at grocery retailers represent the largest sources of sodium intake from refined salts. They found that mice fed a diet high in refined salts saw a dramatic increase in the number of Th17 cells in their nervous systems that promoted inflammation. They were also more likely to develop a severe form of a disease associated with multiple sclerosis in humans.”   Scientists Officially Link Processed Foods To Autoimmune Disease

 

 

"The immune pathogenesis of SLE and targets of SLE treatment (treatment targets are marked by red boxes). NETosis neutrophil extracellular trap formation, PMN polymorphonuclear neutrophils, DC dendritic cell, BDCA blood dendritic cell antigen, BCL B-cell lymphoma, IL interleukin, IFN interferon, TNF tumor necrosis factor, APRIL a proliferation-inducing ligand, BAFF B-cell activating factor, BCMA B-cell maturation antigen, TAIC transmembrane activator-1 and calcium modulator ligand interactor, ICOS inducible co-stimulator, ICOSL inducible co-stimulator ligand, HLA human leukocyte antigen, BCR B-cell receptor, BTK Bruton’s tyrosine kinase, MHC major histocompatibility complex, TCR T cell receptor, CXCR5 CXC chemokine receptor type 5"

Above the mechanisms of SLE pathogenesis are detailed. IMO the tissue based immune complexes are the KEY problem in SLE and must be addressed FIRST. Clearly tissue based pathologic Immune Complexes  play an IMPORTANT role in SLE, however unclearly understood.  Immune Complexes play this pathogenic role in  ALL Autoimmune Disease as well as SLE. Once these immune complexes are destroyed I believe much of SLE and Most other Autoimmune Disease will then go away.     

It seems just basic medicine to treat SLE with HIGH vitamin C and MMS to try to destroy these tissue based pathologic immune complexes. 

      

Immune Complexes and SLE

"If immune complexes [antigen-antibody couples] deposit themselves in the tissues, the complement system will arrive and bring about an inflammatory response which in turn leads to tissue destruction. This is  the beginning of autoimmune disease. ... Enzyme therapy can cause interruption of the self damaging complement cascade by breaking up pathologic immune complexes. This breaks the vicious circle which otherwise results in continual deteriorate of the involved tissue."   Doctor Anthony Cichoke MA DC  Note "vaccination" can cause an increase in these destructive immune complexes by THOUSANDS of times. IMO any "vaccination" damaged child needs Enzyme Therapy

“Your body is not going to attack itself unless you have done something to it.”    Doctor Trent ND , Yeah like get a "vaccination" full of crap to include auto-immune triggering animal viruses, human DNA, excess immune complexes and other auto-immune triggers

"Bovine serum is frequently used as a growth medium as a part of the vaccine manufacturing process. It has been the major source of contamination in vaccines. [10] The most prevailing bovine contaminants are:

• bovine viral diarrhoea pestivirus
• parainfluenza virus type 3
• bovine herpesvirus 1
• bovine enterovirus type 4
• bovine orbivirus (bluetongue)
• bovine polyomavirus
• bovine parvoviruses [10, 11]"

Vaccines are Unsafe

"Circulating Immune Complexes are the antigen (bad guy) plus antibody (policeman) pairs that clog up the bloodstream, can plug the kidneys and even implant in tissue so that the body recognizes itself as being contaminated and attacks itself.  That last one is the very definition of autoimmunity.  They call it something different in medical texts to cover up the fact that they caused it with vaccines and don’t want anyone to know about it.”   Patrick Jordan    Note allergies usually proceed autoimmune disease, Jordan shows us the cascade of disease initiated by vaccination and ending in autoimmune disease or death.

"According to Dr Shyh-Ching Lo, senior researcher at The Armed Forces Institute of Pathology and one of America’s top mycoplasma researchers, this disease agent causes many illnesses including AIDS, cancer, chronic fatigue syndrome, Crohn’s colitis, Type I diabetes, multiple sclerosis, Parkinson’s disease, Wegener’s disease and collagen-vascular diseases such as rheumatoid arthritis and Alzheimer’s. I have all the official documents to prove that mycoplasma is the disease agent in chronic fatigue syndrome/fibromyalgia as well as in AIDS, multiple sclerosis and many other illnesses."  Donald W. Scott MA

There has been an explosion of auto immune diseases concurrently with the "vaccination era". Above we can see why.

   

A Prime Cause of Autoimmunity

“Autoimmunity is born in the gut. That’s where it comes from – your gut wall. That happens because your gut flora is abnormal. In order to heal any autoimmune condition – whether it’s multiple sclerosis, rheumatoid arthritis, osteoarthritis, lupus, alopecia, psoriasis, or anything else that has got an autoimmune component – you have to focus on healing and sealing your gut lining with the GAPS Nutritional Protocol. And you have to focus on... normalizing your gut flora. You have to drive out the pathogens from the gut flora and replace them with the beneficial flora. Then a lot of healing will happen."   Doctor Natasha Campbell-McBride

“Once your gut lining begins to deteriorate, these disease-causing agents can be easily absorbed into your bloodstream and circulated throughout your body. Some of them have affinities for certain proteins, and will attach themselves to them. When that happens, it changes the three-dimensional shape of that protein molecule. When your immune system comes across this foreign-looking protein, it will attack it and begin producing antibodies against it.”    Doctor Natasha Campbell-McBride

Please go to the Autoimmune Protocol to view the numerous man made causes of autoimmunity. These roots of autoimmunity must be identified and corrected to treat SLE or any autoimmune disease.

  

"Vaccination" and SLE

Results of Kids infected with "Vaccination" Inflammation

In SLE like many Autoimmune Diseases which present with tissue embedded pathologic immune complexes, IMO, "vaccination" is often a LARGE FACTOR in the pathogenesis of the disease. These diseases are often not your body malfunctioning but are diseases caused mainly by "vaccination". "Vaccination" is often CREATING these immune complexes as your body is forced to try and mop up all the toxin and other damage the "vaccination" has caused.

All of the oxygen based therapies should be used to treat SLE IMO.

  

Please REJECT "Vaccination"

"If immune complexes [antigen-antibody couples] deposit themselves in the tissues, the complement system will arrive and bring about an inflammatory response which in turn leads to tissue destruction. This is  the beginning of autoimmune disease. ... Enzyme therapy can cause interruption of the self damaging complement cascade by breaking up pathologic immune complexes. This breaks the vicious circle which otherwise results in continual deteriorate of the involved tissue."   Doctor Anthony Cichoke MA DC  Note "vaccination" can cause an increase in these destructive immune complexes by THOUSANDS of times. IMO any "vaccination" damaged child needs Enzyme Therapy

“Tissue origin vaccines contain extraneous protein in addition to the [rabies] antigen that can lead to autoimmune disease,”  Insert from Pfizer’s Rabies vaccine, Note this is true for MANY vaccines

Chronic Diseases are the Inevitable Result of Vaccinations

“The study, Self-Organized Criticality Theory of Autoimmunity, produced a wide variety of tests on animals to examine the fact that, as they stated: Repeated immunization with antigen causes systemic autoimmunity in mice otherwise not prone to spontaneous autoimmune diseases. They concluded: Systemic autoimmunity appears to be the inevitable consequence of over-stimulating the host’s immune ‘system’ by repeated immunization with antigen, to the levels that surpass system’s self-organized criticality. In other words, they found that not only is vaccination a possible or even probable cause of autoimmune disorders, but that: Chronic diseases are the inevitable result of vaccinations!”

Please investigate the practice of "vaccination" and IMO reject it as a deadly scam. IMO this is possibly the best gift you can give your immune system; or more importantly the immune systems of your children and grandchildren. There is little question that vaccination is a cause of many inflammation produced allergies and autoimmune diseases.

Doctor Moulden, Patrick Jordan and others explain how ischemia, chronic inflammation allergies often follow the barbaric practice of "vaccination" in a deadly cascade. After "vaccination" ischemia, chronic inflammation, leaky gut and allergy often is induced often followed in turn by delayed hypersensitivity, serum sickness and finally autoimmune disease. Of course autoimmune disease as bad as it is is often not the WORST effect of "vaccination", there is autism and death.

Vaccine Exemptions Under Dire Threat

 

 

 

 

 

 

 

 

This File was last updated on 30 June 2020 08:57 PM

YOU are the ONLY one responsible for your life and health; others may be indirectly responsible for your death; once you realize this your life will get MUCH better and also in ways other than your health. Healthy Protocols is designed to help YOU PREVENT most disease in YOUR body. The Disease Prevention State is the beginning basis for all Disease Treatment. The information provided throughout this site should not be used during any medical emergency or for the diagnosis or treatment of any illness. Call 911 for all medical emergencies. A licensed integrative physician should be consulted for diagnosis and treatment of any and all illnesses you can not handle yourself (soon very few). You and your doctor should reach an informed consensus on diagnosis and treatment. It is incumbent on YOU to know enough about your illness to do this. Blindly following  some doctors orders will in the end sink you IMO. Links to other sites are provided for the targeted information indicated and links should not be regarded as an endorsement of all additional information that those other sites may provide although these sites are in general very good to excellent or I would not use them. Trust but verify. Trust government at your own risk. IMO toxic depopulation  politics is the cause of MANY of our health and our death problems. Trust yourself because YOU have become knowledgeable enough to trust.  All Rights Reserved © Healthy Protocols