Vaccination Mark of the Beast
The ‘coming’ mark will most likely involve a ‘subdermal’ application of the next wave of vaccinations, that will include a form of ‘digital data memory’ indicating date and time of vaccination. This ‘mark’ of vaccination will involve a sub-dermal outline or image representing a ‘branding’ that can be scanned and revealed by ultra-violet lite at a retail checkout point scanner. Just as many people have a physical vaccination ‘mark’ on their arm from getting shots in the 1960s, the coming vaccination mark will be subtle and reside ‘inside’ the human body affecting and indicating a genomic change in the recipient. This is an abomination viewed by God and causes the recipient to lose ‘Imager Status Before God’ and results in eternal damnation. The vaccination ‘mark’ has to be easily accessible by scanners and retail checkout points, hence the recipient will have the option of receiving the vaccination ‘patch’ either on their hand or forehead for ‘scannability.’
Revelation 13:16-17 And he causeth all, both small and great, rich and poor, free and bond, to receive a mark in their right hand, or in their foreheads: And that no man might buy or sell, save he that had the mark, or the name of the beast, or the number of his name.
And the beast was taken, and with him the false prophet that wrought miracles before him, with which he deceived them that had received the mark of the beast, and them that worshipped his image. These both were cast alive into a lake of fire burning with brimstone.
And the smoke of their torment ascendeth up for ever and ever: and they have no rest day nor night, who worship the beast and his image, and whosoever receiveth the mark of his name.
And I saw thrones, and they sat upon them, and judgment was given unto them: and I saw the souls of them that were beheaded for the witness of Jesus, and for the word of God, and which had NOT worshipped the beast, neither his image, neither had received his mark upon their foreheads, or in their hands; and they lived and reigned with Christ a thousand years.
5G + Biometric Facial / Hand Scanning + Digital / Cashless Transactions + Mark of Approval / Authorization = Tomorrow’s Economy (2020-2027)
Biometric scanning used for migrant/border control, secure identity verification and approval, government benefits, domestic and international travel security, economic inclusion of everyone, buying/selling transactions and fund transfers, instantaneous speed of transaction and convenience, VAT/taxation collection, mobility, social credit score and ranking, population movement and tracking, monitoring political and religious ‘extremism’ (terrorists). ‘Mark, number or name’ for verification and approval.
‘Any foreign material(s) should NOT be injected into the human body that causes any kind of change in genetic makeup or structure of a human being. This could be five (5) genetic ‘manipulation’, ‘enhancement’, ‘cutting’, ‘modification’, or ‘alteration.’
And the first went, and poured out his vial upon the earth; and there fell a noisome and grievous sore upon the men which had the mark of the beast, and upon them which worshipped his image
Both American vaccines use messenger RNA (mRNA) to combat the virus. That is an advanced genetic therapy that uses the virus’ own genetic material against it. Kendrick, however, warns that the technology isreally new and untested, meaning no one really knows how it could affect human health, since it literally hijacks the cellular reproduction mechanism. “We really do not know what these things might end up doing after a prolonged period of time.”
COVID-19 vaccines: The new technology that made them possible. FIVE (5) of the vaccines currently in clinical trials are mRNA vaccines; though they are made from different recipes, they use the same underlying concept.
By Yasemin Saplakoglu – Staff Writer December 11, 2020 LiveScience.com
The COVID-19 pandemic served as an unexpected proof of concept for mRNA vaccines.
COVID-19 has really “laid the foundation” for rapid production of new vaccines, such as mRNA vaccines, to fight future pathogens, said Maitreyi Shivkumar, a virologist and senior lecturer in molecular biology at De Montfort University in Leicester, England. “With the technology that we’ve developed for SARS-CoV-2, we can very easily transfer that to other emerging pathogens.”
Here’s how mRNA vaccines work, and why they could make such a difference for vaccine development.
Tapping into a natural process
mRNA vaccines are inspired by basic biology.
Cells store DNA that holds coded instructions for making proteins. When a cell needs to make a protein, it copies the appropriate instructions onto a messenger RNA molecule — a single strand of genetic material. A cellular machine called a ribosome then runs along this code, reads it, and shoots out the correct building blocks to make the protein. Proteins are the essential workers of the body, forming the structure of cells, making tissue, fueling chemical reactions and sending messages: Without them, everything would shut down.
Around three decades ago, scientists realized that they could synthesize mRNA in the lab, deliver it into human cells and use the body to make any protein they wanted, such as proteins that could help fight a range of diseases in the body from cancers to respiratory illnesses. In 1990, researchers at the University of Wisconsin and biotech company Vical Incorporated figured out how to make mRNA that could direct mice cells to create proteins, according to Business Insider.
In the 1990s, Hungarian-born scientist Katalin Karikó started building on this work, but ran into major roadblocks, the biggest being that the mice’s immune system would deem synthetic mRNA foreign and destroy it, sometimes even creating a dangerous inflammatory response. A decade later, while working at the University of Pennsylvania, Karikó and her collaborator Dr. Drew Weissman, figured out that they could create an invisibility cloak for synthetic mRNA by swapping out a piece of the mRNA code for a slightly altered one, according to STAT News. That tiny edit allowed synthetic mRNA to slip right into cells without rousing the immune system, a finding that the researchers published in multiple papers starting in 2005, according to STAT News. These results caught the attention of two key scientists: one who later helped found Moderna and another who helped found BioNTech.
Neither company initially set out to develop mRNA vaccines against infectious diseases, but eventually started to expand into that field with mRNA flu, cytomegalovirus and Zika virus vaccines in development or clinical trials. But then a deadly virus presented a unique opportunity to test, in large groups of people, just how powerful the technology could be.
On Jan. 10, Chinese researchers first published the genetic sequence of the novel coronavirus on a preprint online; within a week, Weissman and his team at the University of Pennsylvania were already developing synthetic mRNA against the virus and both Moderna and Pfizer licensed this team’s formulation from The University of Pennsylvania, according to a perspective posted on Sep. 3 in the journal JAMA.
Within 66 (6) days of the sequence being published, Moderna, in collaboration with the National Institute of Allergy and Infectious Diseases, developed a vaccine and kickstarted the first U.S. clinical trial to test it against COVID-19.
Five of the vaccines currently in clinical trials are mRNA vaccines; though they are made from different recipes, they use the same underlying concept.
Both Moderna’s and Pfizer’s vaccines are made up of synthetic mRNA that carries the code for the spike protein. The mRNA is enveloped inside a fatty nanoparticle that acts as a Trojan horse, infiltrating human cells and delivering the spike-building instructions without awakening the immune system. Once cells have gotten hold of the mRNA, they create the spike protein, which in turn triggers the immune system to produce an arsenal of cells to fight the spike protein and thus protect the body against SARS-CoV-2.
‘Mimicking a viral infection’
The vaccines developed by Moderna and Pfizer are likely so successful because they’re “mimicking a viral infection,” by activating two major immune responses in the body, said Dr. Otto Yang, a professor of medicine in the division of infectious diseases and of microbiology, immunology, and molecular genetics at the University of California, Los Angeles.
The better-known response involves antibodies: The cells expel the spike proteins they make; these trigger the immune system to create antibodies against them, Yang told Live Science. Antibodies are found in blood, tissues and fluids — but they can’t access a virus that’s already inside the cell, “so the immune system evolved a way to deal with that,” Yang said.
That response involves killer T cells, also known as CD8 T cells. These killers scan cell surfaces — cells display small pieces of all the proteins they make on their surface — and destroy the ones that are infected by a virus. SARS-CoV-2 vaccines can also wave a warning flag for killer T cells: after the mRNA prompts cells to make the spike protein, cells display processed fragments of it on its surface.
This gives mRNA vaccines an advantage over more traditional vaccines such as those for flu or rabies, that are made from killed versions of the actual pathogen or their target proteins. Killed virus vaccines can’t get into cells, so they trigger antibodies but not the killer T-cell response, Yang said.
But mRNA vaccines aren’t the only ones that trigger both these immune responses; the University of Oxford vaccine, made from a weakened cold virus called an adenovirus that infects chimpanzees, also does, Yang said. This adenovirus is genetically modified to not be able to replicate in the body and to include the genetic code for the spike protein. These vaccines also prompt the cells to create the proteins themselves, rather than providing already-made ones; and because the cells make the proteins, they display fragments of them on their surfaces.
Vaccines like the Oxford vaccine also show great promise in the future of vaccine development, experts told Live Science. And such vector vaccines have been studied extensively when compared to mRNA vaccines, according to the JAMA perspective. But the Oxford vaccine, developed with AstraZeneca, showed less efficacy than the mRNA vaccines did; in late-stage clinical trials, the Oxford vaccine was 62% effective at protecting against COVID-19 in participants who were given two full doses and 90% effective at protecting those who were first given a half dose and then a full dose, according to findings published on Dec. 8 in the journal The Lancet.
It’s not yet clear why, but one major possibility is that the Oxford vaccine could be overwhelming the immune system when people are given an initial full dose. In addition to the spike protein, the adenovirus also has its own proteins. Because all of these proteins are foreign to the body, the immune system creates defenses against all of them. “There’s no way that the immune system has any sort of guidance that ‘OK, I’m only supposed to make a response against spike,'” Yang said. On the other hand, the mRNA vaccines are more targeted, telling the immune system to respond only to the spike protein.
But before we can say that mRNA vaccines are fundamentally better than other options, Yang said, scientists need to see detailed data from the trials, rather than gleaning information from “snippets from press releases.” It’s also not yet known how long mRNA vaccine-induced immune responses will last. That being said, mRNA vaccines are the “first technology that allows us to [make killer T cell responses] without giving a whole live virus,” Yang said. Though rare, live but weakened virus vaccines have a slight risk of causing a more serious disease, whereas mRNA vaccines, as far as we know, do not, he added.
mRNA vaccines do not integrate into our DNA (the DNA is stored in a cell’s inner core called the nucleus, a place that the synthetic mRNA doesn’t go) and the mRNA generally degrades after a few days, Shivkumar said.
In the first day that Pfizer’s vaccine was administered to several thousand people, two people who had a history of severe allergic reactions had anaphylaxis-like symptoms, prompting the U.K.’s regulatory agency to warn people with severe allergies to avoid getting that particular vaccine. But experts say the general population shouldn’t be anxious about getting this vaccine and it isn’t totally unexpected as allergic reactions can occur with a number of vaccines, Live Science reported.
“I do not believe that mRNA vaccines pose any significant greater chance of a severe allergic reaction than other vaccines,” said Justin Richner, an assistant professor in the department of microbiology and immunology at the University of Illinois (who previously, as a postdoctoral fellow, collaborated with Moderna on their as-of-yet unapproved mRNA vaccine to fight the Zika virus), noting that the safety data from the mRNA vaccine trials looked very similar to other vaccines. “If anything, I would predict that there is less likely to be an allergic reaction in the mRNA vaccines as the production does not require eggs like other vaccines,” he said. (Most flu-vaccines are made using eggs so they can contain bits of egg protein, according to the CDC).
Swap the code
Another huge advantage of mRNA vaccines is how quickly and easily they can be developed.
“The beauty of the mRNA platform is that you can easily swap out the genetic code,” Richner said. In theory, if scientists know what proteins to target on a virus to stop it from infecting human cells, such as the spike protein for SARS-CoV-2, they can use the same platform that was developed for other vaccines such as the COVID-19 vaccine and just swap out the code for the spike protein with the code for the new protein.
The real problem lies in finding the correct target, Richner said.
Because scientists had previously conducted research on similar coronaviruses — those that caused severe acute respiratory syndrome (SARS) and Middle East respiratory syndrome (MERS) — they knew early on that the spike protein was probably the optimal target, Richner said. But they may not get so lucky with other viruses, as previous failures, such as with HIV, have revealed.
mRNA vaccines are cheaper, easier and faster to develop, and in theory, scale up more easily when compared to traditional vaccines. That’s because older vaccine technologies rely on growing the virus or the proteins in the lab, Shivkumar said. Traditional vaccines are often grown in eggs or cells and then weakened or killed.
“After obtaining knowledge of the pathogen,” researchers can synthesize and have an mRNA vaccine ready for delivery in about a week, Richner said. “For traditional vaccine development, this process would take at a minimum one month and usually several months.”
mRNA is a chemical that can be made in a factory setting (such as in a test tube or tank) “relatively easily” once a pipeline is established, Richner said. “Manufacturing is going to be a big advantage going forward.” Pfizer recently experienced production delays, but those delays are only “because it’s the first time making an mRNA vaccine to this scale,” he added.
Still, this easy genetic swap isn’t a sole capability of mRNA vaccines, as the adenovirus vector vaccines also have this advantage. “The Oxford vaccine is more traditional, but it is, again, slightly sort of a jump from the traditional ones because it has the same backbone,” Shivkumar said. Prior to the pandemic, the group that was developing the Oxford vaccine was working on a vaccine against the coronavirus that causes MERS so “they actually just swapped in the SARS-CoV-2 sequence into that same backbone,” she said. But with the adenovirus vector vaccines, scientists still have to rely on the slower biological processes, namely, growing an adenovirus in the lab.
Theoretically, mRNA vaccines can tackle any virus — and one day, might even be able to tackle multiple pathogens at once, according to the JAMA perspective. But practically, we won’t know how universal these vaccines can become when confronted with a variety of new viruses. SARS-CoV-2 is “not a particularly difficult virus,” said Dennis Burton, a professor of immunology and microbiology at the Scripps Research Institute in California. There will likely be “more severe tests and then you’ll be better able to judge how universal RNA vaccines could be. Still, there’s “every chance” mRNA can be truly revolutionary, but we need more information before we can be sure, he told Live Science.
Either way, no matter how quickly genetic information can be swapped in and out of mRNA vaccines, “you can’t skip all the safety data,” Richner said. The “slowdown is always going to be the clinical trial,” Richner said.
Despite their promise, mRNA vaccines still have some limitations. For instance, right now, Pfizer’s mrNA vaccine must be stored at polar temperatures of minus 94 degrees Fahrenheit (minus 70 degrees Celsius). “Especially in developing countries and countries where it’s impossible to have minus-80 freezers everywhere, I think it’s still not ideal, so you would still need to rely on the more traditional vaccines,” Shivkumar said.
Moderna’s vaccine can be stored at freezer temperatures of minus 4 F (minus 20 C). The difference in storage requirements between the two vaccines likely comes down to the recipe that the company used to make them; the ultra-cold temperature may keep either the nanoparticle shell or the mRNA more stable, Yang said.
But if those mRNA vaccines could be stored and delivered at higher temperatures, with the impressive efficacy that they showed, “I can imagine that they will sort of be a game-changer globally,” Shivkumar added. In the future, Pfizer may be able to improve their vaccine to be more stable at higher temperatures, Richner said.
In the past, mRNA vaccines didn’t produce a strong enough response compared to more traditional vaccines, Shivkumar said. “Because with the mRNA you use such low levels and it degrades so quickly, the amount of protein produced will be relatively lower than if you were to be given either a protein or an attenuated virus,” she said. But clearly scientists have figured out how to make mRNA stable enough to trigger a strong protective response. While this would need to be checked with every pathogen, it’s clear the technology has “definitely improved,” Shivkumar added.
“It’s very exciting to have these mRNA vaccines,” said Dr. Octavio Ramilo, the chief of infectious diseases at Nationwide Children’s Hospital, Columbus, Ohio. But “it will be good to have more than just one strategy,” because you never know which one will stick, he said. Not all platforms will necessarily work as well for every pathogen, especially since each virus might have a unique strategy to hide from the immune system, he added.
It’s also important to understand how these vaccines will work in children and the elderly, Ramilo said. Though many of the trials have included elderly participants, children have been absent. Children can respond to vaccines differently than adults, Ramilo told Live Science.
Especially babies’ immune systems change “dramatically in the first year,” Ramilo said. The flu virus tends to impact children and the elderly more severely than other age groups, Ramilo said. But vaccines don’t work as well in those groups, he said. So having multiple platforms and understanding how they work “is going to be fundamental to leverage and to make them work in different situations,” he added.
And if another new virus comes along years from now, we’ll hopefully have learned lessons from 2020. The pandemic served as a “proof of concept” that mRNA experts had been waiting for, Yang said. The fastest vaccine developed to date prior to the COVID-19 pandemic was the Mumps vaccine, which took four years to develop and license it in 1967. Not counting the years it took to develop the vaccine, the Ebola vaccine was the fastest ever tested in clinical trials — which took less than a year — during the Ebola outbreak across West Africa. That is, until the world was faced with a deadly pandemic.
Just nine months into the pandemic, the fact that new vaccines are already finished clinical trials “is pretty impressive,” Yang said. “When you’re talking about a vaccine possibly being FDA-approved only a few months after it was first tried in a human that is amazingly fast.”
“I’m not sure that it could actually be much quicker than this.”
Night Watchman Note; ‘THE GRAND DADDY SIGN’. ‘THAT WICKED’. That is what ‘watchmen or women’ do. Jesus made clear that when He actually does come for His disciples, His wise and faithful servants would be aware of the time because they would be watching. They would know the season of the times by WATCHING those things ‘coming to pass or occurring’ as Jesus said they would. The ‘BENCHMARK SIGN(s)’ always point towards Israel / Jacob. God’s prophetic timepiece. The FALSE PEACE COVENANT confirmed by the Prince/Beast among MENA (the many) is the ‘key sign’ of the times or the season of the times. Yes, we are in that period. The Prince/Beast will likely confirm and enhance the current ‘normalization’ agreement with Jacob to be a ‘peace’ agreement, to be extended to 7 years from the current 5 years, to include some agreement permitting the rebuilding of the third temple in exchange for ‘some portion of Jerusalem.’ The current ‘investment’ period for the Palestinians stands at five (5) years. This will likely occur AFTER the Bride, Disciples or True Church is removed from the earth via the Rapture / Harpazo / Redemption / ‘Twinkling’.
Confirmation for Seven (7) Years
Daniel 9:26-27 And after threescore and two weeks shall Messiah be cut off, but not for himself: and the people of the prince that shall come shall destroy the city and the sanctuary; and the end thereof shall be with a flood, and unto the end of the war desolations are determined. And he shall confirm the covenant with many for one week: and in the midst of the week he shall cause the sacrifice and the oblation to cease, and for the overspreading of abominations he shall make it desolate, even until the consummation, and that determined shall be poured upon the desolate.
‘Current Plan’ (Satan’s Plan = Five (5) years financial investment period for 180 (6+6+6) ‘infrastructure projects’ costing $50 (5) Billion to cut poverty by 50% (5)).
U.S. President Donald Trump’s “Peace to Prosperity” plan, which he unveiled at the White House on Jan. 28, 2020, calls for Israel to retain 30 percent of the West Bank (territory that the parties to the conflict had already agreed would remain under Israeli control, in accordance with the 1995 Oslo Accords), with the remaining 70 percent reserved for an eventual Palestinian state. The plan states that there would be a freeze on Israeli settlement-building in that area for four years—and land swaps to provide the Palestinian state with land comparable in size to the territory of pre-1967 West Bank and Gaza, and a capital in eastern Jerusalem.
It includes a $50 billion investment fund for 179 infrastructure and business projects in that state, designed to create more than one million jobs, cut the poverty rate by 50 percent and reduce unemployment from 31 percent to a single digit.
US President Donald Trump has predicted that Saudi Arabia will be among up to 10 further countries preparing to ‘normalize’ their relations with Israel.
The meaning was obvious: The country [Saudi Arabia] is tired of waiting for Palestinians to make peace and is preparing to move on. The message to foreign capitals, perhaps to Washington in particular, is equally clear: The time is coming when a deal may be done.
Prophetic Discernment: Two ‘Scenarios’. I am not ‘dogmatic’ about either one. Other scenarios could come into play. THE POINT … is how close we are!
Trump may still yet get the Beast to agree for ‘MENA’ the ‘CURRENT’ plan, SHORTLY, in the few remaining days left in the ‘Last Trump’ or ‘Last Trumpence’ Presidency. Saudis may be ‘nervous’ about the Biden election and want to get the ‘deal done and finished’ while Trump is in the twilight of his presidency.
The following would take place AFTER the Rapture: Biden/Harris may work to ‘ENHANCE’ the plan by the literal splitting of Jerusalem along the 1967 lines. An ‘exchange’ of sovereignty to get a temple for the Jews and to give the Beast custodianship of al-Aqsa … that which he covets. The plan will be ‘ENHANCED’ (investment wise for the Palestinians) for Seven (7) years. Perhaps the investment amount will also be increased.
Then the following: Beast ‘ENHANCES’ the plan under Biden, by splitting Jerusalem along 1967 lines. In a ‘Give up Sovereignty, Get a Temple’ scenario. The plan finally gets ‘CONFIRMED’ or approved shortly, under Biden/Harris (Deceiver-in-Chief and Jezebel-in-Chief).
Either way, the Rapture / Harpazo / Redemption / ‘Twinkling’ is imminent.
Prophecy has a ‘window.’ That window is closing shortly and quickly. As is the door in the ‘Age of Grace’ for the world.
Pay ‘Eagle-Eye’ attention to the world geo-political news feeds to see if any type of ‘confirmation’ is forthcoming or made by the Prince / Beast/ 8th King / Son of Perdition / Future Antichrist / Man of Lawlessness. Also MbS, Man-by-Satan and the Confirmer and he that causeth the Abomination of Desolation in April 2024. Trump may surprise the world and suddenly proclaim that a deal has been reach or agreed upon by Saudi Arabia and at least nine (3×3) other Arab/Muslim countries from MENA. If nothing happens over the next 10 days, it is possible the entire covenant could be ‘strengthened and confirmed’ AFTER the rapture. This is a very real possibility. Be warned and hopeful.
Seven (7) References to ‘BE WATCHING or WATCHFUL.’
Matthew 24:42; Watch therefore: for ye know not what hour your Lord doth come.
Matthew 25:13; Watch therefore, for ye know neither the day nor the hour wherein the Son of man cometh.
Mark 13:35; Watch ye therefore: for ye know not when the master of the house cometh, at even, or at midnight, or at the cockcrowing, or in the morning.
Luke 21:36; Watch ye therefore, and pray always, that ye may be accounted worthy to escape all these things that shall come to pass, and to stand before the Son of man
Luke 12:37-39; Blessed are those servants, whom the lord when he cometh shall find watching: verily I say unto you, that he shall gird himself, and make them to sit down to meat, and will come forth and serve them. And if he shall come in the second watch, or come in the third watch, and find them so, blessed are those servants. And this know, that if the goodman of the house had known what hour the thief would come, he would have watched, and not have suffered his house to be broken through.
1 Thessalonians 5:2-4; For yourselves know perfectly that the day of the Lord so cometh as a thief in the night. For when they shall say, Peace and safety; then sudden destruction cometh upon them, as travail upon a woman with child; and they shall not escape. But ye, brethren, are not in darkness, that that day should overtake you as a thief. (Be Watching).
John 13:19 Now I tell you before it come, that, when it is come to pass, ye may believe that I am he.
John 14:29 And now I have told you before it come to pass, that, when it is come to pass, ye might believe.
Luke 21:31 So likewise ye, when ye see these things come to pass, know ye that the kingdom of God is nigh at hand.
Mark 13:29 So ye in like manner, when ye shall see these things come to pass, know that it is nigh, even at the doors.
Luke 21:28 And when these things begin to come to pass, then look up, and lift up your heads; for your redemption draweth nigh.
Revelation 1:1 The Revelation of Jesus Christ, which God gave unto him, to shew unto his servants things which must shortly come to pass; and he sent and signified it by his angel unto his servant John:
‘Increasing Like Labor Pains.’ ‘Fearful Sights.’ ‘Perilous Times.’ ‘Men’s hearts failing with fear.’ Great Convergence of Signs.’ REDEMPTION IMMINENT.
In His Service,
Night Watchman Ministries
Make Your Decision for Christ NOW!!!!!!! Time is Up!!!!!!!
Jesus Christ’s Offer of Salvation:
The ABCs of Salvation through Jesus Christ (the Lamb)
A. Admit/Acknowledge/Accept that you are sinner. Ask God’s forgiveness and repent of your sins.
. . . “For all have sinned, and come short of the glory of God.” (Romans 3:23).
. . . “As it is written, There is none righteous, no, not one.” (Romans 3:10).
. . . “If we say that we have no sin, we deceive ourselves, and the truth is not in us.” (1 John 1:8).
B. Believe Jesus is Lord. Believe that Jesus Christ is who He claimed to be; that He was both fully God and fully man and that we are saved through His death, burial, and resurrection. Put your trust in Him as your only hope of salvation. Become a son or daughter of God by receiving Christ.
. . . “That whosoever believeth in him should not perish, but have eternal life. For God so loved the world, that he gave his only begotten Son, that whosoever believeth in him should not perish, but have everlasting life. For God sent not his son into the world to condemn the world; but that the world through him might be saved. (John 3:15-17). For whosoever shall call upon the name of the Lord shall be saved.” (Romans 10:13).
C. Call upon His name, Confess with your heart and with your lips that Jesus is your Lord and Savior.
. . . “That if thou shalt confess with thy mouth the Lord Jesus, and shalt believe in thine heart that God hath raised him from the dead, thou shalt be saved. For with the heart man believeth unto righteousness; and with the mouth confession is made unto salvation.” (Romans 10:9-10).
. . . “If we say that we have no sin, we deceive ourselves, and the truth is not in us. If we confess our sins, he is faithful and just to forgive us our sins, and to cleanse us from all unrighteousness. If we say that we have not sinned, we make him a liar, and his word is not in us.” (John 1:8-10).
. . . “And he is the propitiation for our sins: and not for ours only, but also for the sins of the whole world. (John 2:2).
. . . “In this was manifested the love of god toward us, because that God sent his only begotten Son into the world, that we might live through him. And we have seen and do testify that the Father sent the Son to be the Saviour of the world. Whosoever shall confess that Jesus is the Son of God, God dwelleth in him, and he in God.” (1 John 4:9, 14-15).
. . . “But God commendeth his love toward us, in that, while we were yet sinners, Christ died for us. Much more then, being now justified by his blood, we shall be saved from wrath through him. For if, when we were enemies, we were reconciled to God by the death of his Son, much more, being reconciled, we shall be saved by his life.” (Romans 5:8-10).
. . . “For the wages of sin is death; but the gift of God is eternal life through Jesus Christ our Lord.” (Romans 6:23).
. . . “Jesus saith unto them, I am the way, the truth, and the life, no man cometh unto the Father, but by me.” (John 14:6).
. . . “For I am not ashamed of the gospel of Christ: for it is the power of God unto salvation to everyone that believeth.” (Romans 1:16).
. . . “Neither is there salvation in any other: for there is none other name under heaven given among men, whereby we must be saved.” (Acts: 4:12).
. . . “Who will have all men to be saved, and to come unto the knowledge of the truth for there is one God, and one mediator between God and men, the man Christ Jesus.” (1 Timothy 2:4-6).
. . . “For God did not appoint us to suffer wrath but to receive salvation through our Lord Jesus Christ.” (1 Thessalonians 5:9).
. . . “But as many as received him, to them gave the power to become the sons of God, even to them that believe on his name.” (John 1:12).
True Church / Bride of Christ Spared from God’s Wrath:
Romans 5:8-10. “But God commendeth his love toward us, in that, while we were yet sinners, Christ died for us. Much more then, being now justified by his blood, we shall be saved from wrath through him. For if, when we were enemies, we were reconciled to God by the death of his Son, much more, being reconciled, we shall be saved by his life.”
Romans 12:19. Dearly beloved, avenge not yourselves, but rather give place unto wrath: for it is written, Vengeance is mine; I will repay, saith the Lord.
1 Thessalonians 1:10. And to wait for his Son from heaven, whom he raised from the dead, even Jesus, which delivered us from the wrath to come.
1 Thessalonians 5:9. For God hath not appointed us to wrath, but to obtain salvation by our Lord Jesus Christ,
Romans 8:35. Who shall separate us from the love of Christ? shall tribulation, or distress, or persecution, or famine, or nakedness, or peril, or sword?
Jeremiah 30:7. Alas! for that day is great, so that none is like it: it is even the time of Jacob’s trouble, but he shall be saved out of it.
Revelation 3:10 Because thou hast kept the word of my patience, I also will keep thee from the hour of temptation, which shall come upon all the world, to try them that dwell upon the earth.