https://www.usatoday.com/in-depth/graphics/2020/12/17/how-to-build-strengthen-a-strong-immune-system-and-deal-with-stress/

How to strengthen your immune system this winter

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A balanced immune system is key to protect your body from illness

Dec. 22, 2020

In a year upended by COVID-19, it seems as if our immune systems have received more attention than ever before. But many unhealthy behaviors brought on by the pandemic make it harder for our bodies to fight off infections. Here are some tips on maintaining a balanced immune system that can protect you this winter:

Strengthening your immune system

The first line of defense is a healthy lifestyle. These factors can put you at risk:  (See link for article)

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**Comment**

A great general article and reminder how we can make ourselves tough targets for disease.

For more:  https://madisonarealymesupportgroup.com/2020/04/16/viruses-immunity-dr-waters-fix-your-soil-and-the-seeds-cant-grow/

https://madisonarealymesupportgroup.com/2020/08/07/the-shunning-of-nutritional-science-and-self-care-in-the-public-covid-19-narrative/

https://madisonarealymesupportgroup.com/2020/08/21/how-government-cures-drive-out-real-cures/

Article for natural remedies for strengthening the immune system:  https://vitalplan.com/blog/5-natural-remedies-youve-never-heard-of-and-why-you-should-try-them-now

https://rawlsmd.com/health-articles/mycoplasma-the-most-common-lyme-coinfection

Understanding Mycoplasma: Symptoms, Testing, and Treatment | RawlsMD

Mycoplasma: The #1 Lyme Coinfection + How to Outsmart It

by Dr. Bill Rawls
Updated 12/9/20

Mycoplasma is the stealthiest of all stealth microbes. It may be a major player in many chronic diseases associated with aging, but remarkably, most people — including most doctors — have limited awareness of it.

If you have Lyme disease, fibromyalgia, chronic fatigue syndrome, autoimmune disease, or possibly any other chronic illness, however, mycoplasma is a microbe you should know about.

Mycoplasma: The Master Manipulator

Mycoplasma is a parasite, meaning it can’t live without a host. And it’s the smallest of all bacteria: 4,000 of them can fit inside a single red blood cell in your body. By comparison, only 10-15 average-sized bacteria would fit in the same cell.

Unlike other bacteria, mycoplasmas don’t have a protective cell wall, creating an interesting survival strategy: They can shape-shift and fit into areas where other bacteria can’t go. For example, it also allows them to slip inside cells of the host. The lack of a cell wall makes mycoplasma resistant to some commonly prescribed classes of antibiotics like penicillins, which normally work by interrupting a bacteria’s cell wall so that when the bacteria divides, it falls apart.

More than 200 known types of mycoplasma (and probably many yet to be discovered) can infect animals and plants. There are at least 23 different varieties of mycoplasma that can infect humans. A few of them are considered harmless normal flora, but most have the potential to cause disease.

image split in three: tick, flea, and mosquito

Mycoplasma is spread by biting insects (ticks, mosquitoes, fleas, biting flies), sexual contact, contaminated food, and airborne droplets. Most everyone has been exposed to some form of mycoplasma. Several mycoplasma species have been closely associated with many chronic degenerative diseases like multiple sclerosis and Alzheimer’s disease, according to publications like the International Reviews of Immunology and the British Journal of Medical Practitioners, respectively.

Even beyond its tiny size, shape-shifting qualities, and proliferous nature, mycoplasma is a master at manipulating and outmaneuvering the host’s immune system. Half of its genetic makeup is devoted to that exclusive purpose.

While it has little ability to cause direct harm, it can use the host’s immune function to its advantage: Mycoplasma generates chronic low-grade inflammation and steals vital nutrients from the body.

In fact, everything that this stealthy microbe needs for survival — vitamins, minerals, fats, carbohydrates, and amino acids — must be scavenged from the host; it makes nothing itself. Mitochondria, which are the energy powerhouses of cells, are prime targets to sustain the microorganism, which helps explain why fatigue is always a factor in mycoplasma infections.

Mycoplasma favors infecting the cells of tissues that line different areas of the body. Common sites of infection include:

  • Nasal passages
  • Sinuses
  • Lungs
  • Lining of the intestinal tract
  • Genital tract
  • Vesicles inside the brain
  • Synovial lining of joints

They also commonly infect white blood cells, red blood cells, and brain tissue. Different mycoplasma has a preference for certain tissues, but all mycoplasma species possess the ability to infect any type of tissue and all organ systems.

The most common mycoplasma, Mycoplasma pneumoniae, has a preference for lung tissue. Initial infection with M. pneumoniae typically causes pharyngitis (sore throat), cough, fever, headache, malaise, runny nose — all the common symptoms of a basic upper respiratory infection.

man wrapped in blanket, coughing

If the person’s immune system is not full strength, the infection can progress to bronchitis and even pneumonia (about 20% of pneumonias). The type of pneumonia caused by mycoplasma, often called “walking pneumonia,” is rarely severe enough to result in hospitalization, though it can drag on for weeks or even months.

But even when those respiratory symptoms are cleared, it may not be the end of the story. That’s because after mycoplasma enters the body, it also infects white blood cells. And once inside a white blood cell, it can be carried to all parts of the body, infecting tissues and organs.

The potential for widespread infection is very much influenced by the status of the host’s immune function. If immune function is optimal, the microbe is contained after the initial infection, and no long-term harm occurs. Approximately 30-70% of people carry at least one species of mycoplasma without having symptoms. It essentially becomes like normal flora of the microbiome, which are the non-threatening microbes found on the skin, in the gut, and body cavities.

But most mycoplasma species aren’t normal flora, and they are just waiting for an opportunity to gain a foothold. If immune function slips for whatever reason, chronic, systemic infection becomes possible. Mycoplasma begins stealing vital nutrients and causing a wide range of symptoms that are unrelated to the initial infection. The general breakdown of tissues by stealth microbes like mycoplasma accelerates the aging process and is likely a primary factor in many, if not most, chronic degenerative diseases.

Stealth Characteristics of Mycoplasma

Stealth microbes are a stronger force together than when alone. In other words, mycoplasma may not be a problem unless another stealth microbe (or microbes) is present. Lyme disease may be a good example of this phenomenon.

image split in half: borrelia and mycoplasma

Mycoplasma is a common Lyme coinfection: It’s present in 75% or more of Lyme disease cases. Mycoplasma is known to be carried and spread by ticks, but it is also possible that mycoplasma is already present in the body when a bite from a tickcarrying borrelia — the primary bacteria associated with Lyme — occurs.

Immune dysfunction caused by the new tick-borne infection or possible other coinfection allows mycoplasma to proliferate and cause multi-systemic symptoms throughout the body. Many symptoms that occur in Lyme disease can be caused by mycoplasma, too.

Body Systems Affected by Chronic Mycoplasma

woman in bed, face in hand, tired

Mycoplasma infection may be localized to certain areas of the body (such as the lungs), or it can be more widespread and systemic. Parts of the body where symptoms can manifest include:

  • Joints: Mycoplasma commonly infects the synovial lining of joints, the lining protecting the joints. Ninety percent of people with rheumatoid arthritis test positive for mycoplasma in the synovial fluid.
  • Muscles: Muscle pain from breakdown of muscle fibers is common with systemic mycoplasma infection.
  • Heart: Mycoplasma can lead to inflammation of the heart, such as endocarditis, myocarditis, pericarditis.
  • Nerves: Mycoplasma scavenges fats from the myelin sheath covering nerve tissue. Not surprisingly, mycoplasma (and other microbes, including chlamydiaand borrelia) has been linked to multiple sclerosis and other neurodegenerative diseases, including ALS (Mycoplasma fermentans is most common) and Parkinson’s disease.

    Nerve involvement can be associated with neuropathic pain like burning and tingling in the hands and feet. Brain inflammation, contributing to insomnia, brain fog, depression, and anxiety, is common with systemic mycoplasma infection.

  • Immune system: Mycoplasma is a top candidate for explaining autoimmunity; it stimulates host self-damage, and it can live inside cells while simultaneously turning off the ability of the immune system to recognize the cell as abnormal.
  • Lungs: Mycoplasma in the lungs contributes to respiratory symptoms like sore throat, cough, fever, headache, malaise, runny nose, bronchitis, and pneumonia.
  • Digestive tract: Intestinal mycoplasma infection destroys villi — fingerlike projections in the small intestine that aid food absorption — and compromises the intestinal barrier. This allows accelerated damage by lectins in grains (especially wheat), beans, soy, nightshade vegetables, and dairy.

    Mycoplasma may contribute to leaky gut, or increased intestinal permeability. Severe mycoplasma intestinal infection can lead to nutritional deficiencies and weight loss. Infection of the gastric mucosa (stomach lining) can cause chronic gastritis with nausea and stomach discomfort.

  • Ears: Mycoplasma infection has been associated with hearing loss and ringing in the ears.
  • Eyes: The eyes may be impacted by mycoplasma with such issues as conjunctivitis, eye swelling, and vision loss.
  • Reproductive system: Research suggests mycoplasma has been found in ovarian cancer tissue. It may also contribute to interstitial cystitis, a bladder condition marked by severe pain and urinary frequency.
  • Blood: Mycoplasma has been found in the bone marrow of children with leukemia.

Diagnosing Mycoplasma and the Limitations of Testing

When it comes to testing, PCR (polymerase chain reaction) is the most accurate method for testing mycoplasma. It’s cost-effective and evaluates for the presence of mycoplasma’s genetic material, a test that’s easy, sensitive, and quick test to obtain at most laboratories.

However, PCR testing has limits because it only tests for a handful of mycoplasma species and primarily focuses on diagnosing acute respiratory or genital mycoplasma infections — not chronic, low-grade infections.

Female forensic technician collecting biological specimen in DNA

Another problem with diagnosing mycoplasma is that conventional science does not recognize chronic mycoplasma infections as being significant. Even though mycoplasma is commonly found in association with chronic degenerative diseases, it’s also found in one-third to two-thirds of any population without causing symptoms. In other words, it is assumed that mycoplasma just happens to be there but isn’t really a contributing factor in disease.

This type of thinking is simply a reflection of not understanding how stealth microbes operate. Mycoplasma does not cause disease unless it has an opportunity to do so. Individuals with a healthy immune system can harbor mycoplasma and suffer few ill effects. If immune function is disrupted by environmental factors or a coinfection with other stealth microbes, however, mycoplasma can definitely contribute to chronic disease.

When testing for mycoplasma, it is best to order a complete PCR mycoplasma panel, which will include:

  • M. fermentans
  • M. genitalium
  • M. hominis
  • M. penetrans
  • M. pneumoniae
  • M. synoviae
  • Ureaplasma urealyticum

But these are only the commonly-known species of mycoplasma; other lesser-known species could also be present.

Another problem with testing is that other stealth microbes can be associated with chronic infections with similar symptoms of mycoplasma infection, adding confusion to the clinical picture of what’s making a person ill. The list of knowns includes:

  • Yersinia enterocolitica
  • Chlamydophila pneumoniae
  • Chlamydia trachomatis
  • Campylobacter jejuni
  • Babesia
  • Bartonella
  • Ehrlichia
  • Anaplasma

Laboratories that test for mycoplasma include Medical Diagnostic Laboratories (MDL)and Armin Labs. Your healthcare provider may have additional recommendations for you.

But complete testing for the full range of all stealth microbes can cost hundreds or even thousands of dollars. Possibly the best course of action is assuming mycoplasma and other stealth microbes are there.

Stealth microbes only cause problems when immune function is suppressed. Addressing the causes of the underlying chronic immune dysfunction that allowed mycoplasma to flourish in the first place is the most effective solution for overcoming chronic infections.

Conventional Medical Solutions

The nature of mycoplasma makes it very resistant to conventional therapies. Many antibiotics target cell walls; since mycoplasma doesn’t have one, several classes of antibiotics are ineffective against the microbe. Some other antibiotics (doxycycline, erythromycin, clarithromycin, or azithromycin), block internal functions of bacteria and have some activity against mycoplasma, but activity is limited by the fact that mycoplasma bacteria only live inside cells where antibiotics have minimal penetration.

When it comes to chronic mycoplasma infections, the best approach is supporting the body’s natural healing potential.

Natural Solutions for Mycoplasma

Natural herbal therapy is the best therapeutic alternative for chronic mycoplasma. Herbs (especially medicinal mushrooms) work by:

  • Suppressing cytokine cascades
  • Reducing inflammation
  • Restoring normal immune function
  • Suppressing a wide range of covert pathogens

Consider the following herbs to get you started:

Cordyceps mushroom

Cordyceps (Cordyceps sinensis)

Native to Tibet, cordyceps is a medicinal mushroom that reduces cytokines and normalizes immune system functions. It is highly protective of cells, which reduces invasion by microbes.

Suggested dosage: 1-3 grams (1,000-3,000 mg) of whole mushroom cordyceps powder or 400-800 mg extract (standardized to >7% cordyceptic acid is preferred) two to three times daily.

Side effects: Mild nausea can occur, but in general, side effects are rare, even with higher doses. Allergic reactions are rare.

Chinese Skullcap purple flowers

Chinese Skullcap (Scutellaria baicalensis)

When combined with other herbs, Chinese skullcap has potent synergist properties. Additionally, it has strong antimicrobial and immunomodulating properties that are beneficial for suppressing mycoplasma and protecting tissues and organs infected with the microbe.

Suggested dosage: 400-1,000 mg two to three times daily. Root extract standardized to >30% baicalin is preferred. Note: American skullcap does not offer the same antimicrobial properties and should not be substituted.

Side effects: Gastrointestinal upset can occur, but side effects tend to be rare, even at high doses.

white Bidens flowers

Bidens (Bidens pilosa)

The herb offers potent antimicrobial and anti-inflammatory properties against mycoplasma, affecting mucous membranes of the body.

Suggested dosage: Bidens is most potent when prepared as an alcohol tincture. The dose may vary depending on the company, but tinctures are an excellent way to begin at a low dose and increase drops as tolerated.

Side effects: Some plants can be contaminated with heavy metals, so make sure you purchase the product from a reputable company that takes steps to minimize exposure. You should not take this plant if you are diabetic, as it can cause fluctuations in blood glucose or insulin levels.

Houttuynia white flower

Houttuynia (Houttuynia cordata)

Native to India and Nepal, houttuynia is a potent antiviral with activity also against mycoplasma.

Suggested dosage: The dose may vary depending on a company’s preparations.

Side effects: The herb can have a fishy smell but is otherwise well tolerated.

budding Anamu stem

Anamu (Petiveria alliacea)

Found in tropical, Amazonian regions of Central and South America, anamu offers excellent antimicrobial coverage for mycoplasma.

Suggested dosage: The daily dose of powdered herb is 1,000-2,000 mg twice daily.

Side effects: Note that anamu will give urine and feces a strong garlic-like odor. Generally, the herb is safe and well-tolerated, but it should be avoided in pregnancy.

Mullaca leaf berry

Mullaca (Physalis angulata)

Mullaca is another Amazonian herb with antimicrobial qualities to fight mycoplasma, and it works well as a complement to anamu. It can be found online as a loose powder (add it to smoothies or make your own capsules) or a tincture.

Suggested dosage: The daily dose for powdered herb is 1,000-2,000 mg twice daily.

Side effects: The herb is generally regarded as safe, however, it should be avoided during pregnancy or breastfeeding.

The Bottom Line

In addition to herbal therapy, the optimal path to recovery from chronic mycoplasma involves eliminating artificially-processed foods in favor of whole, nutrient-dense meals, reducing exposure to toxins, and managing chronic stress — all of which disrupt immune function and pave the way for stealth microbes to flourish. By minimizing these factors and implementing a comprehensive herbal therapy protocol, you can begin to curb chronic mycoplasma infections and support your body in the healing process.

Dr. Rawls is a physician who overcame Lyme disease through natural herbal therapy. You can learn more about Lyme disease in Dr. Rawls’ new best selling book, Unlocking Lyme.
You can also learn about Dr. Rawls’ personal journey in overcoming Lyme disease and fibromyalgia in his popular blog post, My Chronic Lyme Journey.

REFERENCES
1. K Waites and D Talkington, Mycoplasma pneumoniae and its Role as a Human Pathogen, Oct 2004, Clinical Microbiology Reviews
2. Hakkarainen, Turrunen, Miettinen, Kaitik, and Jannson, Mycoplasmas and Arthritis, Ann Rheu Dis, 1992, Oct 5 (11): p. 1170-1172
3. Baseman, Joel, et.al., Mycoplasmas: Sophisticated, Reemerging, and Burdened by Their Notoriety, CDC, Journal of Infectious Diseases, Vol 3, No.1, Feb 1997
4. Leslie Taylor, ND, Mycoplasmas – Stealth Pathogens (Review article), Jan 2001
5. Razin, Yogev, Naot, Molecular Biology and Pathogenicity of Mycoplasmas, Microbiol Mol Biol Rev, 1998, Dec; 62(4): p. 1094-1156
6. J Rivera-Tapia, N Rodriguez-Preval, Possible role of mycoplasmas in pathogenesis of gastrointestinal diseases, Rev Biomed 2006 17: 132-139
7. Berghoff, W, Chronic Lyme Disease and Co-infections: Differential Diagnosis, Open Neurol J., 2012, 6, p. 158-178
8. Gilroy, Keat, Taylor-Robinson, The Prevalence of Mycoplasma fermentans in patients with arthritides, Rheumatology, Vol 40 (12), p. 1355-1358
9. Zhang et al, Mycoplasma fermentans infection promotes immortalization of human peripheral blood mononuclear cells in culture, Blood 104 (13), p. 4252-4259
10. Walter Berghoff, Chronic Lyme Disease and Co-infections: Differential Diagnosis, Open Neurol J, 2012, 6: p. 158-178
11. Buhner S H, Healing Lyme Disease Coinfections, Healing Arts Press, Copyright 2013 http://www.cdc.gov/pneumonia/atypical/mycoplasma/index.html
12. Libbey JE, Cusick MF, Fujinami RS. Role of pathogens in multiple sclerosis. Int Rev Immunol. 2014;33(4):266-283. doi: 10.3109/08830185.2013.823422
13. BJMP 2009:2(4) 20-28
14. Huang S, Li JY, Wu J, Meng L, Shou CC. Mycoplasma infections and different human carcinomas. World J Gastroenterol. 2001;7(2):266-269. doi: 10.3748/wjg.v7.i2.266
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For more:  
 
 
 
 

https://www.activistpost.com/2021/01/another-free-webinar-genetic-predispositions-to-emf-sensitivity-and-personalized-interventions.html

Another FREE Webinar: “Genetic Predispositions to EMF Sensitivity and Personalized Interventions”

By B.N. Frank

Last month the National Academies of Sciences reported that American Embassy workers in China and Cuba were injured by microwave radiation exposure.  The cause may not have been from weapons.

Microwave Sickness is also sometimes referred to as “EMF Sensitivity” or Electrosensitivity.  Many doctors don’t evaluate patients for this.  Of course, without an evaluation, patients won’t know whether or not they are suffering from it or not.  Got pets?  Exposure can affect them too! (See link for article)

______________________

**Comment**

The Webinar is January 7, 2021.  Register here:  https://us02web.zoom.us/webinar/register/

Topic: Genetic Predispositions to EMF Sensitivity and Personalized Interventions with Bob Miller
In this free webinar Bob Miller will show how genetic mutations in Calcium Voltage Channels, Glutathione, Catalase, SOD, IL-6 and others can lead to increased sensitivity to EMF, and how to create a custom compounded formula to compensate.
 
Time:  Jan 7, 2021 05:00 PM in Pacific Time (US and Canada)
 
This Webinar is sponsored by Functional Genomic Analysis, GOLD Sponsor of the EMF Medical Conference 2021.
 
EMF exposure can:  

For more:

https://www.cdc.gov/vaccines/covid-19/info-by-product/clinical-considerations.html

Clinical Considerations for Use of mRNA COVID-19 Injections 

(See link for entire article)

An important consideration for Lyme/MSIDS patients is the fact doctors have seen a reactivation of symptoms after vaccination:  https://madisonarealymesupportgroup.com/2017/12/02/scottish-doctor-gives-insight-on-lyme-msids/

 And to balance out the CDC’s continued denial of vaccine harm:  https://www.greenmedinfo.com/blog/attacking-ourselves-top-doctors-reveal-vaccines-turn-our-immune-system-against-us

Excerpts for Lyme/MSIDS patients from CDC website:

Immunocompromised persons

Persons with HIV infection or other immunocompromising conditions, or who take immunosuppressive medications or therapies might be at increased risk for severe COVID-19. Data are not currently available to establish vaccine safety and efficacy in these groups.

Persons with autoimmune conditions

No data are currently available on the safety and efficacy of mRNA COVID-19 vaccines in persons with autoimmune conditions.

Persons with a history of Bell’s palsy (a symptom of Lyme disease)

Cases of Bell’s palsy were reported following vaccination in participants in both the Pfizer-BioNTech and Moderna COVID-19 vaccines clinical trials.

Pregnant people

Pregnant people with COVID-19 have an increased risk of severe illness, including illness resulting in intensive care admission, mechanical ventilation, or death. Additionally, they might be at an increased risk of adverse pregnancy outcomes, such as preterm birth.  There are currently few data on the safety of COVID-19 vaccines, including mRNA vaccines, in pregnant people.

Lactating people

There are no data on the safety of COVID-19 vaccines in lactating people or the effects of mRNA COVID-19 vaccines on the breastfed infant or milk production/excretion.

Children and Adolescents

Vaccine safety and efficacy data in this age group are limited. Children and adolescents younger than 16 years of age are not authorized to receive the Pfizer-BioNTech COVID-19 vaccine at this time.

Contraindications & Precautions

Anaphylactic reactions have been reported following vaccination with mRNA COVID-19 vaccines. Persons with a history of an immediate allergic reaction (of any severity) to an mRNA COVID-19 vaccine or any of its components might be at greater risk for anaphylaxis upon re-exposure to either of the currently authorized mRNA COVID-19 vaccines. An immediate allergic reaction to a vaccine or medication is defined as any hypersensitivity-related signs or symptoms such as urticaria, angioedema, respiratory distress (e.g., wheezing, stridor), or anaphylaxis that occur within four hours following administration.

CDC considers a history of the following to be a contraindication to vaccination:

  • Severe allergic reaction (e.g., anaphylaxis) after a previous dose of an mRNA COVID-19 vaccine or any of its components
  • Immediate allergic reaction of any severity to a previous dose of an mRNA COVID-19 vaccine or any of its components (including polyethylene glycol [PEG])*  They should not receive additional doses.
  • Immediate allergic reaction of any severity to polysorbate (due to potential cross-reactive hypersensitivity with the vaccine ingredient PEG)*
Precautions

CDC considers a history of any immediate allergic reaction to any other vaccine or injectable therapy (i.e., intramuscular, intravenous, or subcutaneous vaccines or therapies not related to a component of mRNA COVID-19 vaccines or polysorbate) as a precaution but not a contraindication to vaccination for both the Pfizer-BioNTech and Moderna COVID-19 vaccines. These persons should be counseled about the unknown risks of developing a severe allergic reaction and balance these risks against the benefits of vaccination. 

Observation periods following vaccination (for persons without contraindications to mRNA COVID-19 vaccines)

CDC recommends an observation period following vaccination with mRNA COVID-19 vaccines. Persons with a history of an immediate allergic reaction of any severity to a vaccine or injectable therapy and persons with a history of anaphylaxis due to any cause should be observed for 30 minutes. All other persons should be observed for 15 minutes.

Reporting of vaccine adverse events

Adverse events that occur in a recipient following mRNA COVID-19 vaccination should be reported to VAERS. Vaccination providers are required by the Food and Drug Administration to report the following that occur after mRNA COVID-19 vaccination under Emergency Use Authorization:

  • Vaccine administration errors
  • Serious adverse events
  • Cases of Multisystem Inflammatory Syndrome
  • Cases of COVID-19 that result in hospitalization or death

Reporting is encouraged for any other clinically significant adverse event even if it is uncertain whether the vaccine caused the event. Information on how to submit a report to VAERS is available at https://vaers.hhs.govexternal icon or by calling 1-800-822-7967.

In addition, CDC has developed a new, voluntary smartphone-based tool, v-safe. This tool uses text messaging and web surveys to provide near real-time health check-ins after patients receive COVID-19 vaccination. Reports to v-safe indicating a medically significant health impact, including pregnancy, are followed up by the CDC/v-safe call center to collect additional information to complete a VAERS report, if appropriate. 

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https://thevaccinereaction.org/2021/01/who-fauci-warn-covid-19-vaccines-may-not-prevent-infection-and-disease-transmission/

WHO, Fauci Warn COVID-19 Injections May Not Prevent Infection and Disease Transmission

 
 
 
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**Comment**
 
If you mistakenly believe getting this touted injection will solve all your problems and allow you to once again live freely, think again.  It was never about returning to normal.  
 
BTW: HHS is launching a $250M Propaganda campaign with massive ad blitz slated for January:  https://www.fiercepharma.com/marketing/hhs-readies-vaccine-confidence-campaign-massive-ad-blitz-rollout-january  Excerpt:
 
The Ad Council video leads with Anthony Fauci, M.D., director of the National Institute of Allergy and Infectious Diseases, who says: “My primary message to healthcare professionals is please get vaccinated. It’s important to protect yourselves, to protect your family, but as important symbolically as healthcare providers to show confidence in the vaccine so that other people in this country follow suit and get vaccinated.”
 
Please remember, this isn’t a “vaccine.”
 
Here is a list of the lies that are being told to the American people through this video (Source):
 
  • LIE #1: “It’s important to note that none of these vaccines can give you COVID19 since they only express a protein from the virus that allows your body’s immune system to generate antibodies.”  FALSE. The fact is, the COVID19 SARS virus has never been fully identified, and the PCR test to test for COVID19 is inaccurate. Even if what they say is true about there not being a COVID19 virus in the vaccine, since they can only at this point identify fragments from the faulty PCR test, who is to say that a “protein” from the virus that affects the body’s immune system would not produce symptoms of COVID19 and test positive?Also, in Israel, which at the time of publication of this article has had the largest amount of people vaccinated with the experimental COVID vaccines, has reported that 240 people have come down with COVID right after being vaccinated. See: 4 People Died and 240 Got COVID19 in Israel After Being Injected with Pfizer Experimental mRNA Vaccine
  • LIE #2: “Because vaccines are given to millions of healthy people to prevent serious diseases, they’re held to very high safety standards. Both the FDA and the CDC have to ensure the safety and efficacy of the vaccines before they are recommended for use in the United States. The COVID19 vaccine, just like all others, are undergoing a rigorous process...”FALSE. The COVID19 vaccines are NOT approved by the FDA like every other vaccine currently in the market, and the typical time it takes to bring a vaccine to market is 5-7 years. (Source.)  The experimental COVID vaccines should NOT be compared to vaccines that have full FDA approval, but to other times a vaccine was rushed to market under emergency use authorization, and the last time that happened was in 1976 with the Swine Flu “epidemic.”  But the “epidemic” never panned out. Only one death and 13 cases were attributed to the Swine Flu, while 25 people died from the vaccine and another 500 or so developed Guillain-Barre syndrome. The vaccine was withdrawn from the market after 10 weeks.  https://healthimpactnews.com/2020/healthcare-workers-in-the-u-s-suffer-serious-reactions-from-illegal-pfizer-experimental-vaccine-others-fake-vaccination-on-tv/
  • LIE #3: “So far, we haven’t seen any trends of serious side effects.”  FALSE. They are trying to be clever by using the word “trends” so that specific cases of serious side effects, including DEATH, can be excused as “abnormal” or not a result of the vaccine.  But they got caught in their own lie here, as even the FDA has stated that they are investigating why so many people are experiencing anaphylactic shock after receiving the vaccine, focusing on the polyethylene glycol component of the vaccine. (Source.)  Not to mention that several people have now died after receiving the experimental vaccines, including one healthcare worker in Portugal, and apparently Nurse Tiffany Dover from Tennessee as well.  There were deaths in the vaccine trials as well, before the FDA EUA was issued. (Source.)

Facts About the Experimental COVID Vaccines they Do NOT Tell You

In addition to their lies, the people in this video are failing to give full disclosure about all the facts regarding these experimental COVD vaccines.

  1. These vaccines are NOT approved by the FDA.  This is stated multiple times in the vaccine guidelines that are supposed to be given to everyone. Therefore, it is illegal to require anyone to take them. They are 100% voluntary, because you are basically participating in the last part of their vaccine trials in order to get FDA approval.
  2. Emergency Use Authorization was issued by the FDA illegally, because other therapeutics to treat COVID19 are available.  Hydroxychloroquine and Ivermectin are two older drugs already approved by the FDA that tens of thousands of doctors have used successfully to treat and cure COVID19.  In addition, the experimental COVID19 vaccines used the faulty PCR test in their trials, and therefore should never have been approved until accurate testing was used. An Administrative Stay of Action was filed against the FDA, but they simply ignored it. See:  https://healthimpactnews.com/2020/stay-of-action-filed-against-fda-to-stop-approval-of-covid-vaccine-for-using-faulty-pcr-tests-in-trials/
  3. Warnings of Potential Infertility due to These Experimental Vaccines are NOT Being Issued by the FDA.  The UK guidelines for the Pfizer vaccine warn of potential infertility of women and also do NOT recommend pregnant women receive the vaccine, while neither warnings are issued for the same vaccine for Americans. See:  https://healthimpactnews.com/2020/unlike-uk-u-s-fda-allows-pregnant-and-lactating-women-to-receive-experimental-pfizer-covid-vaccine/  Also, the University of Miami is investigating the effects of the COVID-19 vaccines on male fertility. See:  https://www.local10.com/news/local/2020/12/20/study-investigates-effects-of-covid-19-vaccine-on-male-fertility/
  4. The other thing that the U.S. Government and Big Pharma never disclose, is the revolving door between both. Former FDA Chief Scott Gottlieb, for example, now sits on the Board of Directors for Pfizer. See:  https://healthimpactnews.com/2020/former-fda-director-gottlieb-now-pfizer-board-member-secures-1-95billion-for-covid-vaccine/  The CDC, FDA, and HHS have become primarily marketing branches of Big Pharma. And now, the U.S. Government is going to give the corporate media and Big Tech a quarter of a million dollars to try and brainwash you into getting the unapproved experimental COVID vaccine, which is a mere drop in the bucket of the $TRILLIONS of American wealth that has been transferred to Big Pharma in 2020 all in the name of the “pandemic.” Don’t be fooled by their lies! Turn off your TVs and stop watching these Hollywood-style actors and actresses posing as journalists spew forth this dangerous propaganda.
  5. Corporate Media is owned by Big Pharma.  While in years past the primary advertisers funding the corporate media were Wall Street conglomerates heavily invested in tobacco and the oil industry, today it is Big Pharma.  See: https://healthimpactnews.com/2020/brainwashing-the-masses-6-companies-own-almost-all-of-the-media-in-the-u-s-using-medical-doctors-to-sell-their-message/  Protecting their financial interest in the pharmaceutical trade is Big Tech, as now even Google is a pharmaceutical company, and they filter their search results to censor anything that challenges pharmaceutical products like vaccines. See:  https://healthimpactnews.com/2019/vaccine-scientific-denialism-the-vaccine-deep-states-control-over-public-policy-by-ignoring-real-science/

For more on the COVID-19 vaccine:

 

https://www.thedesertreview.com/news/dr-george-fareed-and-dr-brian-tyson-share-early-treatment-protocol/article

Dr. George Fareed and Dr. Brian Tyson share early treatment protocol

Updated

Dr. George Fareed, Imperial Valley frontline doctor fighting against the COVID-19 pandemic locally, has been fielding phone calls from across the nation helping those afflicted but unable to get early treatment from their medical establishments.

“I’m really busy, but I’m willing to help anyone,” Fareed said.

(See link for article)

________________________

Excerpt:

Fareed/Tyson COVID-19 Treatment Protocol
  • HCQ 200 mg tabs #16 (HCQ = hydroxychloroquine)
  • Zinc sulfate 22O mg (or elemental Zinc 50 mg) # 15
  • Azithromycin 500 mg # 5 (or Z pack) or
  • Doxycycline 100 mg # 10)
  • Ivermectin 3 mg tabs #8
  • Aspirin 325 mg tabs #30 
Day 1
  • HCQ 2 tabs twice a day
  • Zinc sulfate tab twice a day
  • (Azithromycin tab one per day or doxycycline cap twice a day)
  • Ivermectin 12 mg on day 1 only
  • Aspirin 325 mg 
Days 2-5 
  • HCQ tab 3 times a day
  • Zinc sulfate 3 times a day
  • (Azithromycin tab daily or doxycycline cap twice a day)
  • Aspirin 325 mg daily
  • Ivermectin 12 mg on day 3 if symptoms warrant 
  • Prednisone 60 mg daily x 5-7 days or
  • Dexamethasone 4 mg bid if wheezing /SOB
  • Budesonide 0.5-1mg/2ml vía nebulizer bid 
  • Vitamin D3 5000 iu daily
  • Pepcid 20 mg daily
  • Continue daily Aspirin 325 mg
Over the counter prevention:
  • Elemental Zinc 25 mg once a day
  • Vitamin D 4000 iu once a day
  • Vitamin C 1000 mg once a day 
  • Quercetin 500 mg once a day. If Quercetin is unavailable, then use Epigallocatechin-gallate (EGCG) 400mg once a day

Protocols for low, medium, and high risk patients are also included.

For more on COVID treatments: