Parents, Who Do You Trust? The Government or Your Child’s God-Given Immune System?

Parents, Who Do You Trust? The Government or Your Child’s God-Given Immune System?

Situation Update ~ Juan O Savin, Michael Jaco, Scott McKay, Charlie Ward

Choose willful curiosity over willful ignorance. Educate yourself, integrate the knowledge, then apply it through action. This is alignment with the truth of Source & your inner essence.

They are not Elites, they are a Global Cult, that wants to eradicate God

15.22 Questioner: You also said that you offered the Law of One, which is the balancing of love/light and light/love. Is there any difference between love/light and light/love?

Ra: I am Ra. This will be the final question of this time/space. There is the same difference between love/light and light/love as there is between teach/learning and learn/teaching. Love/light is the enabler, the power, the energy giver. Light/love is the manifestation which occurs when light has been impressed with love.  Law of One

Juan o Savin, Charlie Ward, David Nino, Anne Vandersteel; Military in Control

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Latest News From Charlie Ward

Latest News from Charlie Ward

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Simon Parkes, Charlie Ward and Nicholas Veniamin

This is a wonderful positive video.  We have been living in a world of distortions,  creating   fear, anger, stress  greed controlling our thoughts, emotions and actions.  We seem to forgotten how love is the one emotion that will overcome all.  In your own way, cultivate love in everything you do.  Jesus said love your neighbor as you love yourself. According to the Law of One, our purpose on earth is to learn to balance  love and wisdom and be of services to others.  Within us all is the Christ Consciousness and together we will be a  collective consciousness.    Healing  starts with the mind and the realization of the power within, a change from traditional thinking.   It is  just you, your higher self with help from Infinite Intelligence.   The more divine energy of Love you generate, the more healing takes place not only for you,  but collectively we can heal our world.    It is time for people of all religions, cultures and nations that together  we can change our world by returning to God in your own away   From your heart, pray, meditate and contemplate and bring God back into your life. We all have free-will  to choose by  loving others as you love yourself, treat others as you would like to be treated, help those who need help. As our world transforms into greatness realize the divine power within  and be part of the great awakening.   It is our time!!!!!




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FDA Panel Supports Use of Pfizer Vaccine in US Amid Concerns of Side Effects


December 10, 2020 Updated: December 10, 2020

WASHINGTON—A 23-member vaccine advisory panel voted on Dec. 10 to support the emergency use authorization (EUA) of the COVID-19 vaccine created by Pfizer-BioNTech.

The final decision and official authorization will likely be taken up quickly by the Food and Drug Administration (FDA), ultimately triggering a massive distribution effort.

The agency held an all-day public hearing before the committee voted 18–4 in favor, with one abstention, on the question: “Based on the totality of scientific evidence available, do the benefits of the Pfizer-BioNTech COVID-19 Vaccine outweigh its risks for use in individuals 16 years of age and older?”

The one abstention, Dr. Cody Meissner, professor of pediatrics at Tufts University School of Medicine, said the data doesn’t support the inclusion of 16- and 17-year-olds yet, but he agrees with the rest of the statement.

“We know about the safety of this vaccine up to 60 days,” Meissner said. “It’s hard to see a vaccine injury after 60 days. I think the safety is pretty well demonstrated. I’m comfortable.”

The U.S. government has pledged to distribute 2.9 million doses of the vaccine to the public within 24 hours of FDA approval.

President Donald Trump signed an executive order on Dec. 8 giving Americans priority access to COVID-19 vaccines. The ultimate decision on who gets the first doses rests with governors, Trump said the same day. The administration is encouraging governors to prioritize seniors and individuals who work with seniors.

The vaccine is purported to immunize against COVID-19, which is the symptomatic disease caused by the virus SARS-CoV-2. The likely regimen is for individuals to receive two doses, administered 21 days apart.

The FDA has jurisdiction to approve a new product under an EUA if a “chemical, biological, radiological, or nuclear agent can cause a serious or life-threatening disease or condition.”

The benefits of taking the product also need to be proven to outweigh the risks; the vaccine needs to show a certain efficacy; and there must be no “adequate, approved, and available alternative to the product for diagnosing, preventing, or treating the disease or condition.” The product would initially remain experimental and unlicensed.

The United Kingdom approved Pfizer’s vaccine last week and began administering doses on Dec. 8.

But UK health officials were quickly left scrambling to reassure the public after two people had anaphylactic reactions to the vaccine, while a third reported a possible allergic reaction.

Updated guidance was issued late on Dec. 9 from the UK’s Medicines and Healthcare Products Regulatory Agency.

“Any person with a history of anaphylaxis to a vaccine, medicine, or food should not receive the Pfizer BioNTech vaccine. A second dose should not be given to anyone who has experienced anaphylaxis following administration of the first dose of this vaccine,” said Dr. June Raine, chief executive of the agency.

The FDA said it’s aware of the reports of anaphylactic reactions and will continue to monitor the situation. Moncef Slaoui, who is spearheading vaccine efforts in the United States, said on Dec. 9 that people with known severe allergic reactions should probably avoid the vaccine for now.

FDA officials suggested during the public hearing that a secondary study be conducted to test the vaccine specifically on individuals who have severe allergies. Officials also suggested that over time, children as young as 5 years old would be expected to be approved for the vaccine.

This week, reports from Pfizer’s clinical trials also revealed that four participants had suffered Bell’s Palsy, which is the temporary paralysis of one side of the face, caused by a neurological reaction.

“Symptoms appear suddenly over a 48- to 72-hour period and generally start to improve with or without treatment after a few weeks, with recovery of some or all facial function within six months,” according to the website of the National Institute of Neurological Disorders and Stroke. “In some cases, residual muscle weakness lasts longer or may be permanent.”

The most common side effects reported in Pfizer’s clinical trials included injection site reactions (84 percent of people), fatigue (62.9 percent), headache (55 percent), muscle pain (38 percent), chills (31.9 percent), joint pain (23 percent),  and fever (14 percent). Reactions were more severe after the second dose and in participants under 55 years.

Vaccine providers are required to report any serious adverse effects or vaccination administration errors to the Vaccine Adverse Event Reporting System, hosted by Health and Human Services.

Vaccine manufacturers are immune from liability for any adverse reactions.

This is the first time a vaccine has been developed for a coronavirus as well as the first time the FDA has approved  a product that uses modified RNA (mRNA) technology.

The mRNA’s purpose is to direct the body to make certain proteins. The immune system is then supposed to respond to those proteins by issuing a protective response if it encounters the COVID-19 virus.

Kathrin Jansen, Pfizer’s senior vice president and head of vaccine R&D, said mRNA vaccines can induce broad immune responses and can be “boosted repeatedly.”

During the public hearing portion of the FDA’s advisory meeting, presentations were a mix of praise for the speed and efficacy of the vaccine, and concern for yet unknown adverse reactions, as well as how to deal with hesitancy from the public to take the vaccine.

A poll published on Sept. 6 found that 21 percent of Americans would get a free vaccine as soon as possible, while 21 percent said they wouldn’t get the vaccine at all, and 58 percent said they would consider a vaccine but would wait to see how it had worked for others.

The FDA will consider granting an EUA to a vaccine created by Moderna on Dec. 17.

Follow Charlotte on Twitter: @charlottecuthbo
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