One Million without Power!

Right now, one Million without Power in America! One Million. Is this fake news? I don’t think so:

Shepard Smith joins the Halftime Report with information about the search and rescue efforts in Mississippi and Louisiana following Hurricane Ida. For access to live and exclusive video from CNBC subscribe to CNBC PRO: https://cnb.cx/2NGeIvi

Hurricane Ida made landfall in Louisiana on Sunday as a Category 4 storm with winds of 150 miles per hour, one of the strongest storms to hit the region since Hurricane Katrina, the National Oceanic and Atmospheric Administration said. Ida has since been downgraded to a tropical storm and is expected to move farther inland over southeastern Louisiana and into southwestern Mississippi later this morning, the National Hurricane Center said. Maximum sustained winds have decreased to near 60 mph (95 km/h) with higher gusts. Late Sunday, President Joe Biden approved a major disaster declaration for Louisiana, unlocking federal funding for recovery efforts. The storm is expected to weaken rapidly over the next day or so, and the NHC said Ida is expected to become a tropical depression by this evening. The NHC warned that a life-threatening storm surge is expected for Grand Isle, Louisiana, to the Alabama/Florida border, including Lake Pontchartrain, Lake Maurepas, and Metropolitan New Orleans.

The NHC said winds will likely damage trees and trigger power outages as Ida continues to move inland over southeastern Louisiana. Heavy rainfall is expected through Monday across southeast Louisiana, coastal Mississippi as well as southwestern Alabama, and could trigger “considerable to life-threatening flash and urban flooding.” As of early Monday, more than 1 million Louisiana utility customers are without power, according to PowerOutage.us. On Sunday evening, New Orleans said the entire city lost power after “catastrophic transmission damage.” Ida made landfall on the anniversary of Katrina, the dangerous Category 3 storm that devastated Louisiana and Mississippi 16 years ago, killing more than 1,800 people and causing $125 billion in damage. The strength and path of Ida will be a significant test of New Orleans’ post-Katrina flood defenses, including levees, flood walls and gates that were built to provide storm protection. Katrina had caused levee breaches and catastrophic flooding in New Orleans.

Ida has also triggered concerns about the city’s hospitals, which are already overwhelmed with Covid-19 patients and have little room for evacuated patients. In Galliano, Louisiana, the struggle to care for patients as the storm roared ashore was exacerbated after a part of the roof of Lady of the Sea General Hospital blew off. President Joe Biden has declared a state of emergency for Louisiana and Mississippi, a move that authorizes the Department of Homeland Security and Federal Emergency Management Agency (FEMA) to coordinate all disaster relief efforts. “The storm is a life-threatening storm,” the president said during a briefing at the FEMA headquarters on Sunday. “Its devastation is likely to be immense. Everyone should listen to the instructions from local and state officials.” Louisiana Gov. John Bel Edwards on Sunday afternoon requested a presidential major disaster declaration from Biden after the storm slammed into the state’s coast. “Hurricane Ida is one of the strongest storms to ever hit Louisiana,” Edwards said in a statement. “It is our goal to assist our local agencies and the citizens of the state as quickly as possible, and we have pre-positioned search and rescue teams, boats and other assets to begin helping people as soon as it is safe.” Damaging winds will spread into southwestern Mississippi on Sunday night and early Monday, likely causing widespread tree damage and power outages, and heavy rainfall and is expected across the central Gulf Coast, the Hurricane Center said. » Subscribe to CNBC TV: https://cnb.cx/SubscribeCNBCtelevision »

Subscribe to CNBC: https://cnb.cx/SubscribeCNBC » Subscribe to CNBC Classic: https://cnb.cx/SubscribeCNBCclassic Turn to CNBC TV for the latest stock market news and analysis. From market futures to live price updates CNBC is the leader in business news worldwide. The News with Shepard Smith is CNBC’s daily news podcast providing deep, non-partisan coverage and perspective on the day’s most important stories. Available to listen by 8:30pm ET / 5:30pm PT daily beginning September 30: https://www.cnbc.com/2020/09/29/the-n… Connect with CNBC News Online Get the latest news: http://www.cnbc.com/ Follow CNBC on LinkedIn: https://cnb.cx/LinkedInCNBC Follow CNBC News on Facebook: https://cnb.cx/LikeCNBC Follow CNBC News on Twitter: https://cnb.cx/FollowCNBC Follow CNBC News on Instagram: https://cnb.cx/InstagramCNBC https://www.cnbc.com/select/best-cred… #CNBC #CNBCTV

Holocaust survivors send open letter to the MHRA demanding an end to the Covid-19 Vaccine roll-out because they are seeing another Holocaust unfold before their eyes

Truth11.com


Holocaust survivors send open letter to the MHRA demanding an end to the Covid-19 Vaccine roll-out because they are seeing another Holocaust unfold before their eyes
Tap News / Weaver

Holocaust survivors and their descendants have delivered a letter to the European Medicines Agency (EMA), and the UK’s Medical * Healthcare product Regulatory Agency (MHRA) demanding a halt to the Covid-19 vaccine roll-out following the FDA’s decision to grant full approval to new batches of Pfizer COVID-19 vaccines.

The survivors have charged the authorities with failing to adequately inform populations of vaccine risks, and violating the right to free informed consent under the Nuremberg Code.

The Covid-19 injections are currently under what is known as conditional marketing authorisation in Europe, and temporary authorisation in the UK meaning they are authorised for emergency use only because of the fact they will remain in phase three clinical trials until 2023.

The…

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To Gaby: 28 August 1957 – 2012

You were a rare and beautiful flower !

Dear Gaby,


today 55 years ago you were born. When I heard the good news in the early hours of that day in 1957 I cried with happiness for you and your Mum. I wish you were still here so I could congratulate you for the good life that you lived, despite fate having given you a massive hurdle to overcome. But you did it !!! You put us all to shame with your zest for life. This zest for life you shared with the great German writer Johann Wolfgang von Goethe whose birthday you shared too. Here is what he wrote and you will understand, because you felt the same:

“I have come to the frightening conclusion that I am the decisive element. It is my personal approach that creates the climate. It is my daily mood that makes the weather. I possess tremendous power to make life miserable or joyous. I can be a tool of torture or an instrument of inspiration; I can humiliate or humor, hurt or heal. In all situations, it is my response that decides whether a crisis is escalated or de-escalated, and a person humanized or de-humanized. If we treat people as they are, we make them worse. If we treat people as they ought to be, we help them become what they are capable of becoming.”

Wasn’t that you? You spread the “good climate” and shared your attitude to life with the rest of us. Your birth and your life was a gift to us from the creator as the meaning of your name is “God gives Strength”. When we chose your name we must have subconsciously foreseen what would become of you.Your life was a gift to us. Thank you for having been Gabriele, our Gaby. We love and remember you for the rest of our lives.

A beautiful life

This is a blog that Peter wrote in 2012 and I copied it in memory of Gaby and Peter.

The Doherty Report

Opening with 70% of adults vaccinated, the Doherty report predicts 1.5K deaths in 6 months. We need a revised plan

August 25, 2021 3.46pm AEST

https://theconversation.com/opening-with-70-of-adults-vaccinated-the-doherty-report-predicts-1-5k-deaths-in-6-months-we-need-a-revised-plan-166659


Joel Carrett/AAP

“Governments cannot keep making unrealistic promises about easing restrictions at 70% and 80% adult vaccination, a plan that relied on optimistic scenarios in the first place, and one that now bears little relation to the real world. It is irresponsible to build public momentum and hope around targets that are unlikely going to be enough. Australia needs the National Cabinet to come clean and accept that the changing circumstances require a change in the plan.”

BBC Radio Host Died of COVID Vaccine Complications, Coroner Confirms

I’d prefer to risk dying from the sickness rather than from complications of these vaccines, even if the risk of severe side effects of these vaccinations is minimal. With my medical history I fear I could be of considerable risk of at least some side effect! After all I am 87. Most likely I am going to die in the not so distant future anyway.

The Most Revolutionary Act

An award-winning BBC radio presenter died as a result of complications from her first dose of AstraZeneca’s COVID vaccine, a coroner concluded.

Lisa Shaw, 44, who worked for BBC Radio Newcastle, died at the city’s Royal Victoria Infirmary in May — a little more than three weeks after her first dose of the vaccine developed by University of Oxford.

According to the BBC, the inquest — a judicial inquiry to ascertain the facts relating to an incident, such as a death — heard Shaw had been admitted to hospital after doctors investigating her complaints of headaches found she had…

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The Ivermectin Blackout

There is a blackout on any conversation about how Ivermectin beat COVID-19 in India.

THE Gangster Princess

This lack of coverage speaks volumes- the media SHOULD be on this like white in rice, but all we’re hearing crickets. A majour lifesaving drug that is 1) readily available; 2) inexpensive; and 3) minimal side effects is silenced. Could it be that majour medical institutions don’t want to bite the hand feeds them? Or…

“If you were wondering why Ivermectin was suppressed, it is because the agreement that countries had with Pfizer does not allow them to escape their contract, which states that even if a drug will be found to treat COVID-19, the contract cannot be voided.”

Regardless, the CDC, WHO, government and MSM have blood on their hands. Read on my friends…

India’s Ivermectin Blackout

BY TYLER DURDEN

Ivermectin Wins in India

News of India’s defeat of the Delta variant should be common knowledge. It is just about as obvious as the nose on one’s face. It…

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No, Guardian, Ivermectin Not Discredited by Elgazzar Retraction

Oh yes, Science matters!

Science Matters

97178-ivermectin

The hits against Ivermectin keep on coming.  Dr. Colleen Aldous and Dr. Warren Parker explain this latest smear campaign in their article Ivermectin — front-line doctors vs bureaucrats.  Excerpts in italics with my bolds.

Given the safety profile of Ivermectin, there is nothing to lose and there’s a good possibility of saving many lives and slowing the pandemic

The Ivermectin battle of ideologies on safety and efficacy pits a group of doctors who deal with dying patients every day against bureaucrat academic clinicians. These academic clinicians have dismissed all evidence, favouring a single, large randomised trial that is entirely appropriate for novel drug development but not for pandemics.

This is akin to a person suffering a heart attack and refusing to be taken to hospital in a Toyota, choosing to wait for a Rolls-Royce.

If science is pure, there should not really be a debate, but there is, and…

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FDA Approves First COVID-19 Vaccine

https://www.fda.gov/news-events/press-announcements/fda-approves-first-covid-19-vaccine

FDA NEWS RELEASE

Approval Signifies Key Achievement for Public Health

Immediate Release:August 23, 2021

Today, the U.S. Food and Drug Administration approved the first COVID-19 vaccine. The vaccine has been known as the Pfizer-BioNTech COVID-19 Vaccine, and will now be marketed as Comirnaty (koe-mir’-na-tee), for the prevention of COVID-19 disease in individuals 16 years of age and older. The vaccine also continues to be available under emergency use authorization (EUA), including for individuals 12 through 15 years of age and for the administration of a third dose in certain immunocompromised individuals.

“The FDA’s approval of this vaccine is a milestone as we continue to battle the COVID-19 pandemic. While this and other vaccines have met the FDA’s rigorous, scientific standards for emergency use authorization, as the first FDA-approved COVID-19 vaccine, the public can be very confident that this vaccine meets the high standards for safety, effectiveness, and manufacturing quality the FDA requires of an approved product,” said Acting FDA Commissioner Janet Woodcock, M.D. “While millions of people have already safely received COVID-19 vaccines, we recognize that for some, the FDA approval of a vaccine may now instill additional confidence to get vaccinated. Today’s milestone puts us one step closer to altering the course of this pandemic in the U.S.” 

Since Dec. 11, 2020, the Pfizer-BioNTech COVID-19 Vaccine has been available under EUA in individuals 16 years of age and older, and the authorization was expanded to include those 12 through 15 years of age on May 10, 2021. EUAs can be used by the FDA during public health emergencies to provide access to medical products that may be effective in preventing, diagnosing, or treating a disease, provided that the FDA determines that the known and potential benefits of a product, when used to prevent, diagnose, or treat the disease, outweigh the known and potential risks of the product.

FDA-approved vaccines undergo the agency’s standard process for reviewing the quality, safety and effectiveness of medical products. For all vaccines, the FDA evaluates data and information included in the manufacturer’s submission of a biologics license application (BLA). A BLA is a comprehensive document that is submitted to the agency providing very specific requirements. For Comirnaty, the BLA builds on the extensive data and information previously submitted that supported the EUA, such as preclinical and clinical data and information, as well as details of the manufacturing process, vaccine testing results to ensure vaccine quality, and inspections of the sites where the vaccine is made. The agency conducts its own analyses of the information in the BLA to make sure the vaccine is safe and effective and meets the FDA’s standards for approval. 

Comirnaty contains messenger RNA (mRNA), a kind of genetic material. The mRNA is used by the body to make a mimic of one of the proteins in the virus that causes COVID-19. The result of a person receiving this vaccine is that their immune system will ultimately react defensively to the virus that causes COVID-19. The mRNA in Comirnaty is only present in the body for a short time and is not incorporated into – nor does it alter – an individual’s genetic material. Comirnaty has the same formulation as the EUA vaccine and is administered as a series of two doses, three weeks apart. 

“Our scientific and medical experts conducted an incredibly thorough and thoughtful evaluation of this vaccine. We evaluated scientific data and information included in hundreds of thousands of pages, conducted our own analyses of Comirnaty’s safety and effectiveness, and performed a detailed assessment of the manufacturing processes, including inspections of the manufacturing facilities,” said Peter Marks, M.D., Ph.D., director of FDA’s Center for Biologics Evaluation and Research. “We have not lost sight that the COVID-19 public health crisis continues in the U.S. and that the public is counting on safe and effective vaccines. The public and medical community can be confident that although we approved this vaccine expeditiously, it was fully in keeping with our existing high standards for vaccines in the U.S.”

FDA Evaluation of Safety and Effectiveness Data for Approval for 16 Years of Age and Older

The first EUA, issued Dec. 11, for the Pfizer-BioNTech COVID-19 Vaccine for individuals 16 years of age and older was based on safety and effectiveness data from a randomized, controlled, blinded ongoing clinical trial of thousands of individuals. 

To support the FDA’s approval decision today, the FDA reviewed updated data from the clinical trial which supported the EUA and included a longer duration of follow-up in a larger clinical trial population. 

Specifically, in the FDA’s review for approval, the agency analyzed effectiveness data from approximately 20,000 vaccine and 20,000 placebo recipients ages 16 and older who did not have evidence of the COVID-19 virus infection within a week of receiving the second dose. The safety of Comirnaty was evaluated in approximately 22,000 people who received the vaccine and 22,000 people who received a placebo 16 years of age and older.

Based on results from the clinical trial, the vaccine was 91% effective in preventing COVID-19 disease. 

More than half of the clinical trial participants were followed for safety outcomes for at least four months after the second dose. Overall, approximately 12,000 recipients have been followed for at least 6 months.

The most commonly reported side effects by those clinical trial participants who received Comirnaty were pain, redness and swelling at the injection site, fatigue, headache, muscle or joint pain, chills, and fever. The vaccine is effective in preventing COVID-19 and potentially serious outcomes including hospitalization and death.

Additionally, the FDA conducted a rigorous evaluation of the post-authorization safety surveillance data pertaining to myocarditis and pericarditis following administration of the Pfizer-BioNTech COVID-19 Vaccine and has determined that the data demonstrate increased risks, particularly within the seven days following the second dose. The observed risk is higher among males under 40 years of age compared to females and older males. The observed risk is highest in males 12 through 17 years of age. Available data from short-term follow-up suggest that most individuals have had resolution of symptoms. However, some individuals required intensive care support. Information is not yet available about potential long-term health outcomes. The Comirnaty Prescribing Information includes a warning about these risks.

Ongoing Safety Monitoring

The FDA and Centers for Disease Control and Prevention have monitoring systems in place to ensure that any safety concerns continue to be identified and evaluated in a timely manner. In addition, the FDA is requiring the company to conduct postmarketing studies to further assess the risks of myocarditis and pericarditis following vaccination with Comirnaty. These studies will include an evaluation of long-term outcomes among individuals who develop myocarditis following vaccination with Comirnaty. In addition, although not FDA requirements, the company has committed to additional post-marketing safety studies, including conducting a pregnancy registry study to evaluate pregnancy and infant outcomes after receipt of Comirnaty during pregnancy.

The FDA granted this application Priority Review. The approval was granted to BioNTech Manufacturing GmbH.

Related Information

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The FDA, an agency within the U.S. Department of Health and Human Services, protects the public health by assuring the safety, effectiveness, and security of human and veterinary drugs, vaccines and other biological products for human use, and medical devices. The agency also is responsible for the safety and security of our nation’s food supply, cosmetics, dietary supplements, products that give off electronic radiation, and for regulating tobacco products.

India’s Ivermectin Blackout: Censorship of Peer-reviewed Analysis

This is so interesting. Please, take the time to read it and then think about it!

The Most Revolutionary Act

By Dr. Justus R. Hope

Global Research News

News of India’s defeat of the Delta variant should be common knowledge. It is just about as obvious as the nose on one’s face. It is so clear when one looks at the graphs that no one can deny it.

Yet, for some reason, we are not allowed to talk about it. Thus, for example, Wikipedia cannot mention the peer-reviewed meta-analyses by Dr. Tess Lawrie or Dr. Pierre Kory published in the American Journal of Therapeutics. See this.

Wikipedia is not allowed to publish the recent meta-analysis on Ivermectin authored by Dr. Andrew Hill. Furthermore, it is not allowed to say anything concerning www.ivmmeta.com showing the 61 studies comprising 23,000 patients which reveal up to a 96% reduction in death [prophylaxis] with Ivermectin. See this.

One can see the bias in Wikipedia by going on the “talk” pages for…

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