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JMJ

Why alternavita?

I believe scientists should help bridge the gap between mainstream medicine and natural science to achieve safe, low cost, and effective medicine. I’m a proponent of neither side (mainstream or alternative medicine) as they have become today but I am not neutral. I am against the majority of synthetic drugs, including vitamins, and supplements. I am also against genetic manipulation, DNA/RNA destructive research, products derived from no known natural configuration mutant amino acids (BPC 157), checkpoint blockade toxicity chemotherapeutics (mab drugs), pharmaceuticals, and supplements, synthetic immune suppressants, immune suppressants (food based), and pharmaceuticals targeting systemic immune system over natural oral immune therapeutic treatments which work via the GALT. I am the third way, alternative life.

bio:

I am a wife, mother and graphic designer from the
US. After losing my health and career in graphic
design I began an intense journey back to my own
beginnings seeking resolution and understanding of
my own health conditions, the most notable MS
(multiple sclerosis). I eventually recovered thanks to
natural immune therapy gcmaf and the pioneering work of Dr. Nobuto Yamamoto , Dr. Marco Ruggiero, Bravo Yogurt™, the work of Cedars Sinai, Dr. Mark Pimentel, Dr. Henry Lin and many others. Since my recovery I have sought to make their work known to the general public. I have written several books and have published many websites. Over this period of many years, while embarking on this teaching mission I have
met thousands of patients, many health professionals and professors throughout the world, many of whom follow my writing. I am currently
healthy and enjoy my life, family and profession to the fullest, forever
grateful to these pioneers in gut and immune research.

Special thanks to Dr. Peter Duesberg

(tireless advocate for the scientific method)

I was born two months premature, very low birthweight, and was not breastfed. This increased my risk for SAM (severe acute malnutrition), (immature microbiota not rescued by diet), and gut/immune deficiency significantly, problems that plagued me throughout childhood and the majority of my life. There is not enough space to list the ‘conditions‘ that I endured throughout my life due to early onset gut/immune deficiency but among the most severe was blindness (since fully recovered, no noticeable differential from healthy eyes), and an autoimmune syndrome. I am 56. From day one I wasn’t expected to survive, there were not nearly the advances for preemies that are available today, I only hope to serve as an inspiration.

My total recovery time on various natural oral immune therapy products took 18-24 months, IBD 4-6 months.

14 years of patient guidance and advocacy toward the most effective treatments on earth

Through my learned understanding of oral immune therapy, and common gut conditions that can arise from primary risk factors like mine, I have helped guide thousands upon thousands of patients through the oral immune therapy treatment process, showed them how they can achieve faster results through my publications, and how they can continue to maintain lifelong gut/immune, and metabolic health with minimal effort.

Natural oral immune therapy is both old and new (Sabin, Metchnikoff among others), and today newly produced natural oral immune therapy products made from bovine colostrum are being marketed almost daily, I also cover these new products from time to time, and show how they differ from minimally processed and unadulterated bovine products so consumers can make an educated choice.

I get it, I’ve been there, I also overcame it, with understanding. I eventually became bubble girl, intolerant to everything (thanks to Dr. Mark Pimentel I learned the real dangers of food group avoidance like going gluten free, more elimination only results in more elimination, and more immune intolerance). In fact, I couldn’t even be in the grocery store because the air conditioning fumes bothered me. I couldn’t walk down a city street. I have been in some polluted cities where the air was so dangerous, I barely made it home, and became violently ill. I’ve been in some mold infested buildings from which, I later suffered for years. I’ve had toxic shock numerous times. I couldn’t take a single drug, OTC included, or take one sip of alcohol, and I could barely eat a single food.

The greatest kindness you can render any man is leading him to truth.

St. Augustine

The greatest misfortune in my life is that while I have helped thousands of strangers all around the world I was never able to reach those closest to me (even by example), it continues to be the source of my deepest sorrow, and loss. It is what keeps me motivated to continue to publish the most effective treatments in the world brought to you by the world’s leading scientists, researchers, thinkers, and leaders despite almost zero monetary gain, and at great cost to the benefit of my own family. I am confidant that helping others avoid my suffering by following the leaders in their fields will someday prove to be the most efficient, beneficial, and hopeful course to follow for society but regardless I will always remain grateful for my own benefit to have found them. They gave me back my life.

The greatest scientific breakthrough of the modern era

These leading scientists hail from all over the world but I will say that without the tax dollars of the American people this research would likely not have seen the light of day, and American’s are the last to reap its benefits. The affects are so great in scope to re-writing a nation’s course, this knowledge continues to be suppressed, oppressed, and ignored. No matter, it shall forever remain the greatest scientific discovery of the modern era.

What a long strange trip it has been. From Gcmaf to Immuron® (projected earnings Immuron® by 2025, 45 billion), you should worry, unlike Gcmaf and Bravo Yogurt™, Immuron® patented a natural substance. What Immuron® is going to do when the hyperimmunized golden calves drop dead, I don’t know (research on hyperimmunized calves also given pharmaceutical drugs), although I suppose there are so many non breastfed, C sections, SAM (severe acute malnutrition) children who will not live a normal lifespan, I guess desperate times call for desperate measures.

In 2005, only 10% of children in the US were breastfed. Only 40% of the world’s children were breastfed in 2005.

Infant Formula Statistics

This greatly increases the risk of SAM (severe acute malnutrition).

I review supplements and products based on my own experiences with them and to ensure for readers that they do what they claim to do by meeting gold standard medical claims.

alternavita

alternavita monthly magazine©

natural science for a healthy lifestyle

Alternavita Monthly Magazine-© is a web and print publication featuring popular posts from the blog Alternavita as well as new recipes, how toʼs, products, tips and resources designed for the average reader who desires a healthy lifestyle with relative ease and effort, no extremes and most importantly, one that shows clear evidence as produced by valid scientific method leading edge clinical science.

Mission Statement:

80% Rule

80% safety, GRAS (Generally
Regarded As Safe) and well
tolerated in the majority when
used as directed

80% efficacy (the medical
threshold for certainty and gold
standard of care)

80% ease of use and
compliance (can the majority
reasonably achieve this)

80% accessibility/cost (can the
majority reasonably access this)

And finally, highly effective, cross condition and proponent of the scientific method, and open source science as both were the method and the mission employed which achieved the greatest advances to mankind throughout history.

Scientific Apostasy

Most people are not aware these methods have been eclipsed in use in favor of science by opinion and dictated by profit in the last century in school, university, Govt. institutions and the media creating a systemic imbalance of information and resulting in over 99% of current research papers being invalid (Harvard Study).

It will take a huge amount of effort to return to previous validation methods which have been used throughout history to ensure scientific data is based on objective measures.

 

life motto: “all truth, even scientific truth is not relative, it has an objective measure that must be met”.

“Beauty is truth, truth beauty,
that is all ye know on earth, and
all ye need to know”
John Keats

Posts are now published from Alternavita Monthly© magazine will be available on the blog for thirty days after which time they can be purchased as digital content. This health info is not going out of style, you should purchase, print and keep in a binder for your own health, and the only real thing to watch is consensus building toward natural oral immune therapy.

 

Important health info: start here for patient education.

Coming soon, H2S SIBO test. As loyal readers know I have written extensively in the past about the dangers of H2S (a dangerous gas with properties that induce nerve paralysis at very low PPM) , and H2S SIBO, thanks to Dr. Henry Lin of Cedars Sinai, an expert on H2S SIBO. I personally believed H2S SIBO was far more damaging other forms of SIBO. It led to one of my earliest advocacy efforts for effective, safe and easy treatments for neutralizing this dangerous gas, termed rocket fuel for cancer by leading universities. I personally highly respect Cedars Sinai for their leading public stance in the US, helping to advocate against increasing nonsensical labels for diseases with a common root in the gut/immune system which can lead to thousands upon thousands of cross conditions, and for their top notch clinical investigative units. The work of Cedars Sinai will greatly reduce useless, and expensive testing, and will enable quick diagnosis of these acute severe gut/malnutrition conditions (SAM) in infants, children, and adults.

Immunodeficiency syndromes

Various immunodeficiency syndromes, such as IgA deficiency, common variable immunodeficiency, AIDS and others, are complicated by miscellaneous infection complications, including SIBO.

SIBO is often misdiagnosed and generally underdiagnosed. Clinical symptoms might be non-specific (dyspepsia, bloating, abdominal discomfort). Nevertheless, SIBO can cause severe malabsorption, serious malnutrition and deficiency syndromes. Prognosis is usually serious, determined mostly by the underlying disease that led to SIBO.

Therapy for SIBO must be complex, addressing all causes, symptoms and complications.

 – Cedars-Sinai Medical Center

SIBO-caused conditions include:

irritable bowel syndrome

fibromyalgia

chronic pelvic pain syndrome

chronic fatigue syndrome

depression

impaired mentation

impaired memory

halitosis

tinnitus

sugar craving

autism

attention deficit/hyperactivity disorder

drug sensitivity

an autoimmune disease, for example MS or SLE Lupus

and Crohn’s disease.

 

For any infectious or parasitic disease to start, it is always a requisite that the host suffer IMMUNODEFICIENCY. At the same time, infectious and parasitic diseases themselves cause additional IMMUNE SUPPRESSION and more MALNUTRITION. This immune suppression is SECONDARY to the accumulation of free radicals, especially oxidizing species, that occurs during and after infectious and parasitic diseases.

Clinical Aspects of Immunology and Biochem J.

Currently available treatments for IBD, which target the systemic immune system, induce immunosuppression, thereby exposing the patient to the risk of infections and malignancy.

The interplay between the gut and the systemic immune system determines the final effect on target organs, including the bowel mucosa.

Inflammatory bowel diseases (IBD) are associated with an altered systemic immune response leading to inflammation-mediated damage to the gut and other organs.

Clinical & Translational Immunology (2016)
Gastroenterology and Liver Units, Department of Medicine, Hebrew University-Hadassah Medical Center, Jerusalem, Israel

Among most mammals, the placenta is not effective at transferring antibodies to the fetus: antibodies are transferred immediately after birth via the colostrum.

In fact, the WHO recommends that immunization or treatment be orally administered due to economic, logistical and security reasons. Furthermore, this route offers important advantages over systemic administration, such as reducing side effects, as the molecules are administered locally and have the ability to stimulate the GALT immune responses (Levine and Dougan, 1998; Neutra and Kozlowski, 2006; Bermúdez-Humarán et al., 2011).

2017

Creation of a Regional Human Milk Assembly: A Model to Influence Practice and Policy Change in the NICU.

BACKGROUND:

The 2011 Surgeon General’s Call to Action to Support Breastfeeding highlights a need for optimizing lactation-based education for all health professionals; however, few schools of nursing and medicine offer lactation-based curriculum. In an effort to address these gaps in education and care, the director of the lactation program at a large urban children’s hospital developed and instituted the annual regional Human Milk Assembly (HMA), a half-day collaborative meeting of the hospital’s regional and referral hospitals’ neonatal intensive care unit (NICU) nursing staff, to address lactation-based educational and training needs of all participating institutions.

RESULTS:

Thirty-one of the 50 hospitals surveyed responded to the electronic survey for a total of 34 individual participants. Seventeen of the 22 (77%) of best practices were implemented at rates of over 50%.

In 1997, the American Academy of Pediatrics (AAP) published the policy statement Breastfeeding and the Use of Human Milk. Since then significant advances in science and clinical medicine have occurred.

This revision cites substantial new research on the importance of breastfeeding and sets forth principles to guide pediatricians and other health care professionals in assisting women and children in the initiation and maintenance of breastfeeding. The ways pediatricians can protect, promote, and support breastfeeding in their individual practices, hospitals, medical schools, and communities are delineated, and the central role of the pediatrician in coordinating breastfeeding management and providing a medical home for the child is emphasized.

These recommendations are consistent with the goals and objectives of Healthy People 2010, the Department of Health and Human Services’ HHS Blueprint for Action on Breastfeeding, and the United States Breastfeeding Committee’s Breastfeeding in the United States: A National Agenda.

This statement provides the foundation for issues related to breastfeeding and lactation management for other AAP publications including the New Mother’s Guide to Breastfeeding and chapters dealing with breastfeeding in the AAP/American College of Obstetricians and Gynecologists Guidelines for Perinatal Care, the Pediatric Nutrition Handbook, the Red Book, and the Handbook of Pediatric Environmental Health.11

Human milk is species-specific, and all substitute feeding preparations differ markedly from it, making human milk uniquely superior for infant feeding. Exclusive breastfeeding is the reference or normative model against which all alternative feeding methods must be measured with regard to growth, health, development, and all other short- and long-term outcomes.

Most importantly, the immune modulatory agents used today for IBD do not achieve remission in many patients.

Not all IBD patients benefit from currently available drugs. Young people with IBD do not want to be on long-term drug therapy. Oral immune therapy, while not yet studied in large cohorts of patients, may provide an answer to this unmet need.

Clinical & Translational Immunology (2016)
Gastroenterology and Liver Units, Department of Medicine, Hebrew University-Hadassah Medical Center, Jerusalem, Israel

Malnutrition  is the leading cause of death worldwide in children under the age of five, and is the focus of the first World Health Organization (WHO) Millennium Development Goal. Breastfeeding, food and water security are major protective factors against malnutrition and critical factors in the maturation of healthy gut microbiota, characterized by a transient bifidobacterial bloom before a global rise in anaerobes. Early depletion in gut Bifidobacterium longum, a typical maternal probiotic, known to inhibit pathogens, represents the first step in gut microbiota alteration associated with severe acute malnutrition (SAM). Later, the absence of the Healthy Mature Anaerobic Gut Microbiota (HMAGM) leads to deficient energy harvest, vitamin biosynthesis and immune protection, and is associated with diarrhea, malabsorption and systemic invasion by microbial pathogens. A therapeutic diet and infection treatment may be unable to restore bifidobacteria and HMAGM. Besides re-feeding and antibiotics, future trials including non-toxic missing microbes and nutrients necessary to restore bifidobacteria and HMAGM, including prebiotics and antioxidants, are warranted in children with severe or refractory disease.

 

Diseases that benefit from gcmaf immunotherapy:

Cancer Autoimmune diseases Epstein-Barr Virus (EBV)
Hepatitis B virus (HBV) Herpes Simplex virus (HSV) Cystitis
Hepatitis C virus (HCV) Multiple sclerosis (MS) Urinary tract infection (UTI)
Autism Spectrum Disorders (ASD) Rheumatoid arthritis (RA) Endometriosis
Chronic Fatigue Syndrome (CFS) Lyme disease (Lyme borreliosis) IgA deficiency disorder
Myalgic Encephalomyelitis (ME) Mycobacteria infections Parkinson’s disease
Tuberculosis Fibromyalgia Human papillomavirus (HPV)
Lupus (Systemic lupus erythematosus, SLE) HIV AIDS Dengue fever
Pneumonia infection Warts caused by viral infection Norovirus
Malaria Influenza virus (flu) Herpes simplex virus (HSV)
Q fever (Coxiella burnetii) Polycystic ovary syndrome (PCOS) Chicken pox (varicella zoster virus)
Psoriasis Respiratory tract infections Ulcerative colitis, Crohn’s disease
Type 1 diabetes (T1DM), insulin-dependent diabetes (IDDM) Type 1.5 diabetes, Latent autoimmune diabetes of adults (LADA)

 

Diseases to which the immune system responds can be treated:

GCMAF

according to the methods of the invention. Infections, as used herein, are broadly defined to mean situations when the invasion of a host by an agent is associated with the clinical manifestations of infection including, but not limited to, at least one of the following: abnormal temperature, increased heart rate, abnormal respiratory rate, abnormal white blood cell count, fatigue, chills, muscle ache, pain, dizziness, dehydration, vomiting, diarrhea, organ dysfunction, and sepsis. Such infections may be bacterial, viral, parasitic, or fungal in nature. The method may further comprise combinatorial treatment with other anti-infective agents, such as antibiotics. Viruses susceptible to treatment according to the methods of the invention include, but are not limited to adenoviruses, rhinoviruses, rabies, murine leukemia virus, poxviruses, lentiviruses, retroviruses; including disease- causing viruses such as human immunodeficiency virus, hepatitis A and B viruses, herpes simplex virus, cytomegalovirus, human papilloma virus, coxsackie virus, smallpox, hemorrhagic virus, ebola, and human T-cell-leukemia virus. Bacteria susceptible to treatment include, but are not limited to gram negative bacteria and gram-positive bacteria, including but not limited to Escherichia coli, Staphylococcus aureus, Staphylococcus epidermidis, Streptococcus pneumoniae, Mycobacterium tuberculosis, Neisseria gonorrhoeae, Neisseria meningitis, Bordetalla pertussis, Salmonella thyhimurium, Salmonella choleraesuis, and Enterobacter cloacae, as well as bacterium in the genus Acinetobacter, Actinomyes, Bacilus, Bordetella, Borrelia, Brucella, Clostridium, Corynebacterium, Campylobacter, Deincoccus, Escherichia, Enterobacter, Enterr ococcus, Eubacterium, Flavobacterium, Francisella Glueonobacter, Heliobacter, Intrasporangium, Janthinobacterium, Klebsiella, Kingella, Legionella, Leptospira, Mycobacterium, Moraxella, Neisseria, Oscillospira, Proteus, Psendomonas, Providencia, Rickettsia, Salomonella, Staphylococcus, Shigella, Spirilum, Streptococcus, Treponema, Ureplasma, Vibrio, Wolinella, Wolbachia, Xanthomonas, Yersinis, and Zoogloea Parasitic agents that can be treated by the methods of this aspect of the invention include, but are not limited to Plasmodium, Leishmania, Trypanosomes, Trichomona, and including but not limited to parasitic agents in the phylums Acanthocephela, Nematoda, Nemtomorpha, Platyhelminthes, Digena, Eucestoda, Turbellaria, Sarcomastigophora and Protozoa including but not limited to species Giardia duodenalis, Cryptosporidium parvum, Cyclospora cayetanenis, Toxoplasma gondii, Trichinella spiralis, Tanenia saginata, Taenia solium, Wuchereria bancrofti, Brugia malay, Brugia timori, Onchocerca vovulus, Loa loa, Dracunculus medinensis, Mansonella streptocera, Mansonella perstans, Mansonella ozzardi, Schistosoma hematobium, Schistosoma mansoni, Schistosoma japonicum, Ascaris lumbricoides, Entrobius vermicularis, Trichuris trichiura, Ancylostoma brasiliense, Ancylostoma duodenale, Necator ameicanus, Strongyloides stercoralis, Capillaria hepatica, Angiostrongylus cantonensis, Fasciola hepatica, Fasciola gigantica, Fasciolopsis buski, Chlonrchis sinensis, Heterophyes heterophyes, Paragonimus westermani, Diphyllobothrium latum, Hymenolepis nana, Hymenolepis dimunuta, Echinococcus granulosus, Dipylidium caninum, Entamoeba histolytica, Entamoeba coli, Entamoeba hartmanni, Dientamoeba fragilis, Endolimax nana,

Lodomoeba butschilii, Blastocystis hominis, Giardia intetinalis, Chilomastix menili, Blantidium coli, Trichomonas vaginalis, Leishmania donovani, Trypanosoma cruzi, Sarcocystis lindemanni, and Babesis argentina. Fungal infections that can be treated by the methods of this aspect of the invention include, but are not limited to fungal meningitis, histoplasmosis, Candida albicans infection, as well as Blastomyces dermatitidis Histotplasma capsulatum, Cryptococcus neoformans, Sporothrix schenckii, Aspergillus fumigatus and Pneumocystis carinii infections. Angiogenesis-mediated disorders susceptible of treatment by the methods of the invention include solid and blood-borne tumors including but not limited to melanomas, carcinomas, sarcomas, rhabdomyosarcoma, retinoblastoma, Ewing sarcoma, neuroblastoma, osteosarcoma, and leukemia; diabetic retinopathy, rheumatoid arthritis, retinal neovascularization, choroidal neovascularization, macular degeneration, corneal neovascularization, retinopathy of prematurity, corneal graft rejection, neovascular glaucoma, retrolental fibroplasia, epidemic keratoconjunctivitis, Vitamin A deficiency, contact lens overwear, atopic keratitis, superior limbic keratitis, pterygium keratitis sicca, sjogrens, acne rosacea, phylectenulosis, syphilis, Mycobacteria infections, lipid degeneration, chemical burns, bacterial ulcers, fungal ulcers, Herpes simplex infections, Herpes zoster infections, protozoan infections, Kaposi’s sarcoma, Mooren ulcer, Terrien’s marginal degeneration, marginal keratolysis, traum, systemic lupus, polyarteritis, Wegeners sarcoidosis, scleritis, Steven’s Johnson disease, radial keratotomy, sickle cell anemia, sarcoidosis, pseudoxanthoma elasticum, Pagets disease, vein occlusion, artery occulsion, carotid obstructive disease, chronic uveitis, chronic vitritis, Lyme’s disease, Eales disease, Bechets disease, myopia, optic pits, Stargarts disease, pars planitis, chronic retinal detachment, hyperviscosity syndromes, toxoplasmosis, post-laser complications, abnormal proliferation of fibrovascular tissue, hemangiomas, Osier- Weber-Rendu, acquired immune deficiency syndrome, ocular neovascular disease, osteoarthritis, chronic inflammation, Crohn’s disease, ulceritive colitis, psoriasis, atherosclerosis, and pemphigoid. (See U.S. Patent No. 5,712,291)

Bone disorders susceptible of treatment by the methods of the invention include but are not limited to bone fractures, defects, and disorders resulting in weakened bones such as ostepetrosis, osteoarthritis, rheumatoid arthritis, Paget’s disease, osteohalisteresis, osteomalacia, periodontal disease, bone loss resulting from multiple myeloma and other forms of cancer, bone loss resulting from side effects of other medical treatment (such as steroids), age-related loss of bone mass and genetic diseases such as osteopetrosis. The polypeptides of the invention can be used alone or together with other compounds to treat bone disorders. Immune suppressed illnesses or conditions susceptible of treatment by the methods of the invention include but are not limited to severe combined immune deficiency syndrome, acquired immune deficiency syndrome, and at risk populations including but not limited to malnourished individuals and senior citizens. Also susceptible of treatment are diseases such as cancer and viral infections. An effect of this enzymatic activity is an immuno-suppressed state that can be overcome by treatment with the polypeptides of the invention.

GcMAF should be distinguished from T-cell lymphokine macrophage activating factor, also known as γ-interferon, which is generated by lymphokine-producing T-cells in small amounts, or is obtained by genetic engineering at pharmaceutical grade levels. IVIG is considered a systemic immune suppressing therapy.

There is no such thing as a safe, synthetic pharmaceutical, ALL chronic drug use contributes to liver failure, endocrine disorders, arthritis, inflammatory, autoimmune conditions, mental deterioration, AIDS, allergic conditions, rash, chronic malnutrition syndromes, IBD, checkpoint blockade toxicity, Cushing Syndrome, endotoxemia, oxidative stress, cancer, overwhelming infection syndromes, chromosome damage, genetic damage, and early death.

The following drugs are known to be contra-indicated in gcmaf or natural immunotherapy.

All kinds of Corticosteroids (Prednisolon, Prednisone, Betapred, Solu-Cortef, Solu-Medrol etc). So avoid Cortisone and steroids if possible.

Anti – inflammatory drugs should be avoided. (NSAIDs like Ibuprofen, Diklofenalk. Celebrex Aspirin etc should be taken in moderation.)

Morphine (Morfine) analogs, (Morfin, Tramadole, codeine, Fentanylplasters, Oxynorm, Oxycodon etc).

LDN blocks gcmaf

Birth Control

 

THIS BLOG IS FOR ADULT EDUCATIONAL RESOURCES AND PURPOSES ONLY. I DO NOT AND CAN NOT OFFER MEDICAL ADVICE, EXCEPT UNDER THE GUIDELINES OF UTILIZING FREE SPEECH AND MY OWN PERSONAL EXPERIENCES OR THE EXPERIENCES OF THOSE WHO CARE TO SHARE THEM AND ALLOW THEIR PUBLICATION OR THOSE THAT ARE ALREADY IN THE PUBLIC DOMAIN.

Alternavita is a participant in the Amazon Services LLC Associates Program, an affiliate advertising program designed to provide a means for sites to earn advertising fees by advertising and linking to Amazon.com.

This blog content and some images are not in the public domain and may not be used anywhere without the express written permission of the author. Sources are usually always posted at the bottom of posts as the reference to quoted material or reference material can be found in the library menu.

The owner of this blog is not compensated to provide opinion on products, services, websites, and various other topics.   I will only endorse products or services that I believe, based on my expertise, are worthy of such endorsement. Any product claim, statistic, quote or other representation about a product or service should be verified with the manufacturer or provider.

This blog does not contain any content which might present a conflict of interest.

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 “This statement has not been evaluated by the FDA. This product is not intended to diagnose, treat, cure, or prevent any disease”

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I don’t mind if you write but don’t expect any of your info to be saved for the sake of your privacy and security. I routinely delete personal emails after a certain time period. Subscriber info is stored.

August 2018: My personal email is no longer a valid contact.

This blog is an education resource.

Psalm 91 
You who live in the shelter of the Most High, who abide in the shadow of the Almighty, will say to the Lord, “My refuge and my fortress; my God, in whom I trust.” For he will deliver you from the snare of the fowler and from the deadly pestilence; he will cover you with his pinions, and under his wings you will find refuge; his faithfulness is a shield and buckler.
You will not fear the terror of the night, or the arrow that flies by day, or the pestilence that stalks in darkness, or the destruction that wastes at noonday. A thousand may fall at your side, ten thousand at your right hand, but it will not come near you. You will only look with your eyes and see the punishments of the wicked. Because you have made the Lord your refuge, the Most High your dwelling place, no evil shall befall you, no scourge come near your tent.
For he will command his angels concerning you to guard you in all your ways. On their hands they will bear you up, so that you will not dash your foot against a stone. You will tread on the lion and the adder, the young lion and the serpent you will trample under foot.
Those who love me, I will deliver; I will protect those who know my name. When they call to me, I will answer them; I will be with them in trouble, I will rescue them and honor them. With long life I will satisfy them, and show them my salvation.

 

 

 

 

 

 

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