Important Virus Update

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BOOM!

O'Keefe wasn't kidding!

I told you it was going to be a HUGE week for Patriots.

And we are just getting started!

TRUTH PREVAILS!

GOD WINS!

w-thumbs!^
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Ey5zUARVIAY3jiH



PRESIDENT TRUMP ALWAYS KNOWS AND IS ALWAYS RIGHT.

This is why Dems-DS and their libtard sheep hate him so much!

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Wall Street, Corporations Team Up with Soros-Funded Group to Pressure States Against Election Reforms

Wall Street firms, multinational corporations, and giant law firms are teaming up with the Brennan Justice Center, which is heavily funded by billionaire George Soros, to pressure states against reforms to their election process.

After Georgia lawmakers passed sweeping reform legislation to protect the state’s elections, including requiring photo identification to vote, corporate executives have blasted the move and many are suggesting they will boycott the state by moving business elsewhere.

Now, Fortune 500 corporate executives, Wall Street firms, and attorneys at some of the nation’s largest law offices are reportedly working with the left-wing Brennan Justice Center to pressure state lawmakers from passing similar election reforms.

The corporate coalition is seeking to sue states for passing such reforms while also threatening to pull their business endeavors from states that do pass reforms.

https://www.breitbart.com/politics/...-to-pressure-states-against-election-reforms/


This is what panic looks like!

Any company who opposes election reform that creates integrity and prevents cheating is anti-American!

It's time to start boycotting these companies by not buying their products and services.


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PRESIDENT TRUMP CONTINUES TO FORCE EVERYONE OUT OF THE DARKNESS AND INTO THE LIGHT

He is the master of getting darkness to show itself and did it during his entire first term.

And it's all part of the plan to show The People the TRUTH.

AND WHO JUST RECENTLY CAME OUT OF THE DARK SHADOWS?

The Corporations, who are now showing their true colors speaking out against election laws and voter ID!

And The People are seeing it and speaking out, even boycotting them.

WHO ELSE HAS BEEN FORCED OUT OF THE SHADOWS?

Dr, Fraudci, the CDC Director and the pharmaceutical companies who are pushing their vaccine agenda!

But things aren't going according to plan for them.

The People are rising up and saying they are not taking the vaccine.

Now they are all flip-flopping light fish out of water.

One minute the vaccines are okay, the next minute they are not.

Even Fraudci recently admitted he is confused what numbers are dropping so much in Texas and elsewhere.

Fraudci is even saying you still have to wear mask even if you get vaccinated.

None of what they are doing and saying makes sense.

And The People are seeing it all.

AND WHAT ELSE HAS BEEN FORCED OUT OF THE SHADOWS?

The use of blackmail in their relentless pursuit of Matt Gaetz.

This shows The People the invisible enemy's use of blackmail of politicians and other officials to get their agenda filled.

CNN recently published a report that was Gaetz denied a meeting with Trump.

This is false and all designed to weaken Gaetz' position.

This is a "hit" by CNN and the DS.

But the fake stories and "leaks" are not working.

A recent poll shows overwhelming support for Gaetz by the Constituents.

And this is all he needs.

And The People are all rising up showing their support for him too.

Darkness is being forced to light everyday!

The evidence is everywhere.

It's up to you to see it!

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'The People' continue to see it all!

CORPORATIONS TRYING TO DICTATE WHAT LAWS SHOULD BE CREATED

The People do not need the corporations, the corporations need them.

The People are already boycotting these companies.

Boycotting works!

Just ask Coca Cola whose sales are already plummeting!

The people creating the election laws are protecting The People and returning the power to The People.

REMOVAL OF PEACE DEALS AND TENSIONS IN THE UKRAINE

Biden is holding back $150 million in Military aide from the Ukraine.

It's already been approved by Congress.

He's asking Ukraine to conduct certain "reforms".

He wants no investigations, them to destroy all documents and make it all go away, and then the funds get sent. [quid pro quo]

This is exactly what he did previously under Obama.

Do you think Trump set this up?

Do you think he already knew Biden was going to do this?

BIDEN IS TRYING TO BRING THE U.S. INTO WAR

Trump set up to remove troops from Afghanistan by May 1st.

Now Biden is saying they won't be withdrawn until September 11th.

WHY did they pick 9/11?

Are they planning something? ["false flag"]

Biden is trying to create tension between Ukraine and Russia.

Is Putin going to bring troops in and start war?

NO!

If he was going to do it he would have already done it.

Actions speak louder than words!

This is something else President Trump set up.

He wanted to expose it all for The People to see.

It worked.

And now their plan is failing.

They are literally self-destructing before the world's eyes!

AND NOW PROJECT VERITAS EXPOSES CNN AS A PROPAGANDA NETWORK

Their undercover work proved Gaetz was set up.

The People already stood up for Gaetz but now the masses are following this support.

THE FDA PULLS THE JOHNSON & JOHNSON VACCINE OVER 6 ALLEGED DEATHS

Dr. Fraudci and the CDC immediately came out and touted Pfizer and Moderna's.

This move is a "hit" on Johnson & Johnson.

This is them pushing their agenda, and pushing it aggressively.

They want as many people injected with the Pfizer and Moderna vaccine.

They are the only two mRNA vaccines.

mRNA vaccines contain AI technology that overwrites your DNA.

It makes you a Trans-human. [AI-human hybrid]

This is an irreversible process and allows them to control you through a rogue signal.

Whereas, J&J's vaccine is a viral vector vaccine use a modified version of a different virus (the vector) to deliver important instructions to our cells.

The benefit of viral vector vaccines is those vaccinated gain protection without ever having to risk the serious consequences of getting sick.

If you really want the vaccine for whatever reason just know you have a choice.

DEMAND JOHNSON & JOHNSON'S OR DON'T GET ONE AT ALL.
 

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Low iqanons are awake!

th



Waiting for for my next instructions, must be long distance.
 

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BREAKING: Water is now being pumped into all the tunnels below the U.S. Capitol building and National Mall


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BBBBWWWAAAAAAAAAHAHAHAAAAAAAAAAAAAAHHHH!!!!!:):):):)

My fat orange hero lost on Nov 3rd and I can't get over it. My QAnon sites kept posting failed prediction after failed prediction and I look like an idiot.
So now I post lies and made up shit every day so I don't have to face reality. :):)
 

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[h=1]Secure Arkansas[/h] [h=2]A Grassroots Organization[/h] <nav>
<form method="GET" action="https://securetherepublic.com/arkansas" class="search-box"> <input type="text" name="s" placeholder="Search" value="" class="form-control"> </form>
</nav><nav>
</nav> [h=2]Covid-19 RNA Vaccines & Risk of Prion Disease[/h] March 8, 2021 Coronavirus, Featured



Emergency Alert – Depopulation Agenda Going on Now!
Legislators, take the time to read this link below, please.
Covid-19 RNA Based Vaccines and the Risk of Prion Disease
— a research article by J. Bart Classen, MD in Microbiology & Infectious Diseases, ISSN 2639-9458.
Click here for the home page that this article came from.
From the Abstract in the link above:
Development of new vaccine technology has been plagued with problems in the past. The current RNA based SARSCoV-2 vaccines were approved in the US using an emergency order without extensive long term safety testing. In this paper the Pfizer COVID-19 vaccine was evaluated for the potential to induce prion-based disease in vaccine recipients.

The folding of TDP-43 and FUS into their pathologic prion confirmations is known to cause


  • ALS,
  • front temporal lobar degeneration,
  • Alzheimer’s disease and
  • other neurological degenerative diseases. The enclosed finding as well as additional potential risks leads the author to believe that regulatory approval of the RNA based vaccines for SARS-CoV-2 was premature and that the vaccine may cause much more harm than benefit
[Bullets added by Secure Arkansas to draw attention to potential risk factors.]
Attention:
The vaccine could be a bioweapon and even more dangerous than the original infection. Here’s a direct quote from the article.
The fact that this research, which could be used for bioweapons development, is funded by private organizations including the Bill and Melinda Gates Foundation, and Ellison Medical Foundation [2] without national/international oversight is also a concern.
This is another one of many reasons that Secure Arkansas DOES NOT support the Covid-19 vaccine. Analysis of the Pfizer vaccine against COVID-19 identified two potential risk factors for inducing prion disease in humans. Could this lead to a degenerative brain disorder?
(Remember our articles on prion-based disease in the deer population (CWD, or Chronic Wasting Disease) and mad cow disease?)
Prion diseases are dangerous, and there is a reason that so many people are questioning this controversial Covid-19 vaccine.
What are Prion Diseases? – from Johns Hopkins Medicine site:
Prion diseases comprise several conditions. A prion is a type of protein that can trigger normal proteins in the brain to fold abnormally. Prion diseases can affect both humans and animals and are sometimes spread to humans by infected meat products. The most common form of prion disease that affects humans is Creutzfeldt-Jakob disease (CJD).

Prion diseases can’t be cured, but certain medicines may help slow their progress. Medical management focuses on keeping people with these diseases as safe and comfortable as possible, despite progressive and debilitating symptoms.
The damage caused by prion diseases may not show up right away, either. It could take a few years to be noticed.
The EUA (Emergency Use Authorization) prevents Covid-19 vaccines from being mandated already.
COVID-19 Vaccines are still considered experimental until fully licensed by FDA, CDC, and all state Health Departments CANNOT be trusted when it comes to your health.
Once again, we want to let you know that employers can’t require Covid-19 vaccination under an EAU (Emergency Use Authorization).
Historically, less than 1% of all vaccine injuries and deaths are ever reported to VAERS (Vaccine Adverse Event Reporting System).
People all over the world are questioning AND protesting vaccines.
No Immunization or Vaccination should EVER be mandatory.
Freedom of Choice is the right choice for all.
As always, you can find our email articles posted on our website: SecureArkansas.com. The Search box is a handy tool.
For more information about any topic, such as vaccines, just type it into the Search box on our website, and click Enter!
1837120052_stop-fluoride.png

Securing the blessings of liberty,
Secure Arkansas
securetherepublic.com/arkansas
info@securetherepublic.com


Volume 5 | Issue 1 | 1 of 3Microbiol Infect Dis, 2021COVID-19 RNA Based Vaccines and the Risk of Prion DiseaseClassen Immunotherapies, Inc., 3637 Rockdale Road, Manchester, MD 21102, E-mail: classen@vaccines.net.J. Bart Classen, MD*Citation: Classen JB. COVID-19 RNA Based Vaccines and the Risk of Prion Disease. Microbiol Infect Dis. 2021; 5(1): 1-3.Research ArticleABSTRACTDevelopment of new vaccine technology has been plagued with problems in the past. The current RNA based SARS-CoV-2 vaccines were approved in the US using an emergency order without extensive long term safety testing. In this paper the Pfizer COVID-19 vaccine was evaluated for the potential to induce prion-based disease in vaccine recipients. The RNA sequence of the vaccine as well as the spike protein target interaction were analyzed for the potential to convert intracellular RNA binding proteins TAR DNA binding protein (TDP-43) and Fused in Sarcoma (FUS) into their pathologic prion conformations. The results indicate that the vaccine RNA has specific sequences that may induce TDP-43 and FUS to fold into their pathologic prion confirmations. In the current analysis a total of sixteen UG tandem repeats (ΨGΨG) were identified and additional UG (ΨG) rich sequences were identified. Two GGΨA sequences were found. Potential G Quadruplex sequences are possibly present but a more sophisticated computer program is needed to verify these. Furthermore, the spike protein, created by the translation of the vaccine RNA, binds angiotensin converting enzyme 2 (ACE2), a zinc containing enzyme. This interaction has the potential to increase intracellular zinc. Zinc ions have been shown to cause the transformation of TDP-43 to its pathologic prion configuration. The folding of TDP-43 and FUS into their pathologic prion confirmations is known to cause ALS, front temporal lobar degeneration, Alzheimer’s disease and other neurological degenerative diseases. The enclosed finding as well as additional potential risks leads the author to believe that regulatory approval of the RNA based vaccines for SARS-CoV-2 was premature and that the vaccine may cause much more harm than benefit.*Correspondence:J. Bart Classen, MD, Classen Immunotherapies, Inc., 3637 Rockdale Road, Manchester, MD 21102, Tel: 410-377-8526.Received:27 December 2020; Accepted: 18 January 2021Microbiology & Infectious DiseasesISSN 2639-9458KeywordsCOVID-19, Vaccines, Diabetes, Immunity.IntroductionVaccines have been found to cause a host of chronic, late developing adverse events. Some adverse events like type 1 diabetes may not occur until 3-4 years after a vaccine is administered [1]. In the example of type 1 diabetes the frequency of cases of adverse events may surpass the frequency of cases of severe infectious disease the vaccine was designed to prevent. Given that type 1 diabetes is only one of many immune mediated diseases potentially caused by vaccines, chronic late occurring adverse events are a serious public health issue.The advent of new vaccine technology creates new potential mechanisms of vaccine adverse events. For example, the first killed polio vaccine actually caused polio in recipients because the up scaled manufacturing process did not effectively kill the polio virus before it was injected into patients. RNA based vaccines offers special risks of inducing specific adverse events. One such potential adverse event is prion based diseases caused by activation of intrinsic proteins to form prions. A wealth of knowledge has been published on a class of RNA binding proteins shown to participating in causing a number of neurological diseases including Alzheimer’s disease and ALS. TDP-43 and FUS are among the best studied of these proteins [2].The Pfizer RNA based COVID-19 vaccine was approved by the US FDA under an emergency use authorization without long term safety data. Because of concerns about the safety of this vaccine a study was performed to determine if the vaccine could potentially induce prion based disease.MethodsPfizer’s RNA based vaccine against COVID-19 was evaluated for the potential to convert TDP-43 and or FUS to their prion based
Volume 5 | Issue 1 | 2 of 3Microbiol Infect Dis, 2021disease causing states. The vaccine RNA was analyzed for the presence of sequences that can activate TDP-43 and FUS. The interaction of the transcribed spike protein with its target was analyzed to determine if this action could also activate TDP-43 and FUS.ResultsAnalysis of the Pfizer vaccine against COVID-19 identified two potential risk factors for inducing prion disease is humans. The RNA sequence in the vaccine [3] contains sequences believed to induce TDP-43 and FUS to aggregate in their prion based conformation leading to the development of common neurodegerative diseases. In particular it has been shown that RNA sequences GGUA [4], UG rich sequences [5], UG tandem repeats [6], and G Quadruplex sequences [7], have increased affinity to bind TDP-43 and or FUS and may cause TDP-43 or FUS to take their pathologic configurations in the cytoplasm. In the current analysis a total of sixteen UG tandem repeats (ΨGΨG) were identified and additional UG (ΨG) rich sequences were identified. Two GGΨA sequences were found. G Quadruplex sequences are possibly present but sophisticated computer programs are needed to verify these.The spike protein encoded by the vaccine binds angiotensin converting enzyme 2 (ACE2), an enzyme which contains zinc molecules [8]. The binding of spike protein to ACE2 has the potential to release the zinc molecule, an ion that causes TDP-43 to assume its pathologic prion transformation [9].DiscussionThere is an old saying in medicine that “the cure may be worse than the disease.” The phrase can be applied to vaccines. In the current paper the concern is raised that the RNA based COVID vaccines have the potential to cause more disease than the epidemic of COVID-19. This paper focuses on a novel potential adverse event mechanism causing prion disease which could be even more common and debilitating than the viral infection the vaccine is designed to prevent. While this paper focuses on one potential adverse event there are multiple other potential fatal adverse events as discussed below.Over the last two decades there has been a concern among certain scientists that prions could be used as bioweapons. More recently there has been a concern that ubiquitous intracellular molecules could be activated to cause prion disease including Alzheimer’s disease, ALS and other neurodegenerative diseases. This concern originates due to potential for misuse of research data on the mechanisms by which certain RNA binding proteins like TDP-43, FUS and others can be activated to form disease causing prions. The fact that this research, which could be used for bioweapons development, is funded by private organizations including the Bill and Melinda Gates Foundation, and Ellison Medical Foundation [2] without national/international oversight is also a concern. In the past, for example, there were prohibitions for publishing information pertaining to construction of nuclear bombs.Published data has shown that there are several different factors that can contribute to the conversion of certain RNA binding proteins including TDP-43, FUS and related molecules to their pathologic states. These RNA binding proteins have many functions and are found in both the nucleus and the cytoplasm. These binding proteins have amino acid regions, binding motifs that bind specific RNA sequences. Binding to certain RNA sequences when the proteins are in the cytoplasm is believed to causes the molecules to fold in certain ways leading to pathologic aggregation and prion formation in the cytoplasm [2]. The current analysis indicates Pfizer's RNA based COVID-19 vaccine contains many of these RNA sequences that have been shown to have high affinity for TDP-43 or FUS and have the potential to induce chronic degenerative neurological diseases.Zinc binding to the RNA recognition motif of TDP-43 is another mechanism leading to formation of amyloid like aggregations [9]. The viral spike protein, coded by the vaccine RNA sequence, binds ACE2 an enzyme containing zinc molecules [8]. This interaction has the potential to increase intracellular zinc levels leading to prion disease. The initial binding could be between spike proteins on the surface of the cell transfected by the vaccine and ACE2 on the surface of an adjacent cell. The resulting complex may become internalized. Alternatively, the interaction could initially take place in the cytoplasm of a cell that makes ACE2 and has been transfected with the vaccine RNA coding for the spike protein. The interaction is quite concerning given the belief that the virus causing COVID-19, SARS-CoV-2, is a bioweapon [10,11] and it is possible that the viral spike protein may have been designed to cause prion disease.Another related concern is that the Pfizer vaccine uses a unique RNA nucleoside 1-methyl-3'-pseudouridylyl (Ψ). According to FDA briefing documents, this nucleoside was chosen to reduce activation of the innate immune system [12]. RNA molecules containing this nucleoside will undoubtedly have altered binding [13]. Unfortunately, the effect on TDP-43, FUS and other RNA binding proteins is not published. The use of this nucleoside in a vaccine can potentially enhance the binding affinity of RNA sequences capable of causing TDP-43 and FUS to assume toxic configurations.There are many other potential adverse events that can be induced by the novel RNA based vaccines against COVID-19. The vaccine places a novel molecule, spike protein, in/on the surface of host cells. This spike protein is a potential receptor for another possibly novel infectious agent. If those who argue that the COVID-19 is actually a bioweapon are correct, then a second potentially more dangerous virus may be released that binds spike protein found on the host cells of vaccine recipients. Data is not publicly available to provide information on how long the vaccine RNA is translated in the vaccine recipient and how long after translation the spike protein will be present in the recipient’s cells. Such studies pertaining to in vivo expression will be complex and challenging. Genetic diversity protects species from mass casualties caused by infectious agents. One individual may be killed by a virus while Volume 5 | Issue 1 | 3 of 3Microbiol Infect Dis, 2021another may have no ill effects from the same virus. By placing the identical receptor, the spike protein, on cells of everyone in a population, the genetic diversity for at least one potential receptor disappears. Everyone in the population now becomes potentially susceptible to binding with the same infectious agent.Autoimmunity and the opposing condition, metabolic syndrome, are well know adverse events caused by vaccines [14]. COVID-19 infections are associated with the induction of autoantibodies and autoimmune disease [15,16] making it more than plausible a vaccine could do the same. One author has found amino acid sequences coded by the spike protein to be identical to sequences in human proteins including proteins found in the CNS [17]. Autoimmunity can also be induced by epitope spreading when a foreign antigen, like the spike protein, is presented by an antigen presenting cell that also has self molecules attached to its MHC molecules. Finally, others working in the field have published additional support that COVID-19 vaccines could potentially induce prion disease. Authors [18] found prion related sequences in the COVID-19 spike protein which were not found in related coronaviruses. Others [19] have reported a case of prion disease, Creutzfeldt-Jakob disease, initially occurring in a man with COVID-19.Many have raised the warning that the current epidemic of COVID-19 is actually the result of an bioweapons attack released in part by individuals in the United States government [10,11]. Such a theory is not far fetched given that the 2001 anthrax attack in the US originated at Fort Detrick, a US army bioweapon facility. Because the FBI’s anthrax investigation was closed against the advice of the lead FBI agent in the case, there are likely conspirators still working in the US government. In such a scenario the primary focus of stopping a bioweapons attack must be to apprehend the conspirators or the attacks will never cease. Approving a vaccine, utilizing novel RNA technology without extensive testing is extremely dangerous. The vaccine could be a bioweapon and even more dangerous than the original infection.References1. Classen JB, Classen DC. Clustering of cases of insulin dependent diabetes (IDDM) occurring three years after Hemophilus influenza B (HiB) immunization support causal relationship between immunization and IDDM. Autoimmunity. 2002; 35: 247-253.2. King OD, Gitler AD, Shorter J. The tip of the iceberg: RNA-binding proteins with prion-like domains in neurodegenerative disease. Brain Res. 2012; 1462: 61-80.3. WHO, International Non Proprietary Names Program: 11889. 9/2020.4. Kapeli K, Pratt GA, Vu AQ, et al. Distinct and shared functions of ALS-associated proteins TDP-43, FUS and TAF15 revealed by multisystem analyses. Nature Communications. 2016; 7: 12143.5. Kuo P, Chiang C, Wang Y, et al. The crystal structure of TDP-43 RRM1-DNA complex reveals the specific recognition for UG- and TG-rich nucleic acids. Nucleic Acids Research. 2014; 42: 4712-4722.6. Tollervey JR, Curk T, Rogelj B, et al. Characterizing the RNA targets and position-dependent splicing regulation by TDP-43; implications for neurodegenerative diseases. Nat Neurosci. 2011; 14: 452-458.7. Imperatore JA, McAninch DS, Valdez-Sinon AN, et al. FUS recognizes G quadruplex structures within neuronal mRNAs. Frontiers in Molecular Biosciences. 2020; 7: 6.8. Shang J, Ye G, Shi K, et al. Structural basis of receptor recognition by SARS-CoV-2. Nature. 2020; 581: 221-225.9. Garnier C, Devred F, Byrne D, et al. Zinc binding to RNA recognition motif of TDP-43 induces the formation of amyloid-like aggregates. Sci Rep. 2017; 7: 6812.10. Classen JB. COVID-19, MMR vaccine, and bioweapons. Diabetes & its Complications.2020; 4: 1-8.11. Classen JB. Evidence supporting the hypothesis that the 2019 epidemic of E-vaping acute lung injury (EVALI) was caused in part by COVID-19. Diabetes & Complications. 2020; 4: 1-2.12. Pfizer-Biotech: COVID-19 Vaccine (BNT162, PF-07302048), Vaccines and Related Biological Products Advisory Committee Briefing Document. Meeting Date: 10 December 2020.13. Roundtree IA, Evans ME, Pan, et al. Dynamic RNA modifications in gene expression regulation. Cell. 2017; 169: 1187-1200.14. Classen JB. Review of Vaccine Induced Immune Overload and the Resulting Epidemics of Type 1 Diabetes and Metabolic Syndrome, Emphasis on Explaining the Recent accelerations in the Risk of Prediabetes and other Immune Mediated Diseases. J Mol Genet Med. 2014; S1: 025.15. Amiral J. Can COVID-19 Induce an autoimmune disease associated with long- lasting symptoms and delayed complications? Ann Clin Immunol Microbiol. 2020; 2: 1014.16. Wang EY, Mao T, Klein J, et al. Diverse functional autoantibodies in patients with COVID-19. medRxiv preprint. 2020.17. Lyons-Weiler J. Pathogenic priming likely contributes to serious and critical illness and mortality in COVID-19 via autoimmunity. Journal of Translational Autoimmunity. 2020; 3: 100051.18. Tetz G, Tetz V. SARS-CoV-2 prion-like domains in spike proteins enable higher affinity to ACE2. Preprint. 2020.19. Young MJ, O’Hare M, Matiello M, et al. Creutzfeldt-Jakob disease in a man with COVID-19: SARS-CoV-2-accelerated neuro degeneration? Brain, Behavior, and Immunity. 2020; 89: 601-603.© 2021 Classen JB. This article is distributed under the terms of the Creative Commons Attribution 4.0 Internationa
 

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Someone is in a posting frenzy!!!
Can't get over the loss!!!
Nov. orange man lost.

March 4th came and went, orange man not coming back.
One term loser.
 

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This from the clown waiting everyday for some loser to repost batshit crazy delusions from little Ronnie Watkins, aka Qmoron

I'm not waiting for anything.. The loser such as yourself is visiting and waiting for reposts in this thread more than I am.

Go back to your playtime little one.
 
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Imagine that!

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