Thursday, November 12, 2020

vaccines don not take nano tech it will screw your dna up

https://www.nature.com/articles/s41565-020-0737-y






Abstract

The COVID-19 pandemic has infected millions of people with no clear signs of abatement owing to the high prevalence, long incubation period and lack of established treatments or vaccines. Vaccines are the most promising solution to mitigate new viral strains. The genome sequence and protein structure of the 2019-novel coronavirus (nCoV or SARS-CoV-2) were made available in record time, allowing the development of inactivated or attenuated viral vaccines along with subunit vaccines for prophylaxis and treatment. Nanotechnology benefits modern vaccine design since nanomaterials are ideal for antigen delivery, as adjuvants, and as mimics of viral structures. In fact, the first vaccine candidate launched into clinical trials is an mRNA vaccine delivered via lipid nanoparticles. To eradicate pandemics, present and future, a successful vaccine platform must enable rapid discovery, scalable manufacturing and global distribution. Here, we review current approaches to COVID-19 vaccine development and highlight the role of nanotechnology and advanced manufacturing.

Main

In December 2019, a novel coronavirus (nCoV or SARS-CoV-2) belonging to the betacoronavirus family emerged1,2. All human betacoronaviruses are unique from one another, however, they do share a certain degree of genetic and structural homology. SARS-CoV-2 genome sequence homology with SARS-CoV and MERS-CoV is 77% and 50%, respectively3. In contrast to the relatively smaller outbreaks of SARS-CoV in 2002 and MERS-CoV in 2012, SARS-CoV-2 is exhibiting an unprecedented scale of infection, resulting in a global pandemic declaration of Coronavirus Infectious Disease (COVID-19) on 11 March 2020 by the World Health Organization (WHO). On 1 June 2020, the World Health Organization reported >6 million confirmed cases and 371 thousand deaths globally. Of note, during the 1918 influenza pandemic, more death was observed in the second phase of outbreak4. Similar to influenza, COVID-19 harbours the potential to become a seasonal disease5. The high infection rate, long incubation period, along with mild-to-moderate symptoms experienced by many, make COVID-19 a troubling disease. A vaccine is crucial, in particular because data indicate asymptomatic transmission of COVID-196,7,8. More than 10 years ago, scientists predicted the pandemic potential of the coronaviruses9. And for the past 30 years, a once-per-decade novel coronavirus has pushed our public health system to the limit, with SARS-CoV-2 being the most severe. Despite the repeated warnings and discussion, the world was not prepared for this pandemic. The rapid development, distribution and administration of a vaccine to the global population is the most effective approach to quell this pandemic and the only one that will lead to a complete lifting of restrictions. Challenges include the vaccine design itself, but also its manufacture and global distribution; cold chain requirements present logistical and fiscal barriers to the availability of important, life-saving vaccines in resource-poor areas of the world. Innovating vaccine delivery platforms and devices to break cold chain limitations are therefore an efficient solution to safeguard potent vaccination for both wealthy and lower-income countries.

The vaccine strategies

When designing a vaccine, principally, one needs to define the antigen, the adjuvant, the manufacturing system and the delivery strategy (Box 1). The rapid development of vaccines is possible because the genome and structural information of SARS-CoV-2 was made available in record time10,11,12,13,14. These data, along with expedited communication of bioinformatic predictions and epitope mapping15,16,17,18, has provided crucial knowledge enabling vaccine design beyond development of live-attenuated and inactivated vaccines19,20,21,22,23. Also, information available from prior development of SARS/MERS vaccine candidates aids in the development of SARS-CoV-2 vaccine candidates24,25. Nanotechnology platforms offer great utility in modern vaccine design and have helped catalyse novel candidate vaccines toward clinical testing at unprecedented speed. Along with inactivated vaccines, emerging nanotechnologies such as mRNA vaccines delivered by lipid nanoparticles and viral vector vaccines have already reached Phase II and III clinical trials (Fig. 1 and Table 1).


https://pubs.acs.org/doi/10.1021/acsnano.0c07197


Abstract

Humanity is experiencing a catastrophic pandemic. SARS-CoV-2 has spread globally to cause significant morbidity and mortality, and there still remain unknowns about the biology and pathology of the virus. Even with testing, tracing, and social distancing, many countries are struggling to contain SARS-CoV-2. COVID-19 will only be suppressible when herd immunity develops, either because of an effective vaccine or if the population has been infected and is resistant to reinfection. There is virtually no chance of a return to pre-COVID-19 societal behavior until there is an effective vaccine. Concerted efforts by physicians, academic laboratories, and companies around the world have improved detection and treatment and made promising early steps, developing many vaccine candidates at a pace that has been unmatched for prior diseases. As of August 11, 2020, 28 of these companies have advanced into clinical trials with Moderna, CanSino, the University of Oxford, BioNTech, Sinovac, Sinopharm, Anhui Zhifei Longcom, Inovio, Novavax, Vaxine, Zydus Cadila, Institute of Medical Biology, and the Gamaleya Research Institute having moved beyond their initial safety and immunogenicity studies. This review analyzes these frontrunners in the vaccine development space and delves into their posted results while highlighting the role of the nanotechnologies applied by all the vaccine developers.

Background

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In December 2019, the World Health Organization (WHO) Country Office in China was first alerted to an unknown outbreak of contagious and often severe lower respiratory illnesses originating from the city of Wuhan, the biggest city in and capital of China’s Hubei province.(1) The cause of the respiratory illness is a virus of the betacoronavirus class now termed coronavirus infectious disease-19 (COVID-19). The virus was named SARS-CoV-2 due to its genetic and structural similarity with SARS-CoV.(1,2) On March 11, 2020, the WHO officially identified SARS-CoV-2 as a pandemic due to its quick global spread.(1) As of August 11, 2020, there are 19,936,210 confirmed cases worldwide and 732,499 deaths due to SARS-CoV-2.(3) The continued rise of both cases and deaths necessitates the rapid development of an effective SARS-CoV-2 vaccine. The second wave happening in some countries that have reopened their economies further accentuates this need.(4,5) While masking, social distancing, and contact tracing can slow the spread of this virus, it appears too infectious to be eliminated by these strategies, and a vaccine is essential to enable a return to normal human social interaction.
Fortunately, in the relatively few months since SARS CoV-2 was identified as the cause of COVID-19, over two hundred academic laboratories and companies have undertaken vaccine development, and many are making record time in advancing to clinical trials (Table S1).(6,7) Moderna reached clinical trials 63 days after their sequence selection.(8) It is striking that an unestablished nanotechnology formulation reached clinical testing almost a full month before established approaches (i.e., inactivated and live-attenuated vaccines) entered clinical trials.(9,10) This highlights the opportunity for less developed technology platforms in vaccine development and, if proven successful, may enable a more rapid response to future emergent infectious diseases. It is also of note that in previous severe coronavirus outbreaks of SARS-CoV and MERS-CoV clinical trials were not reached until 25 and 22 months after the outbreaks began.(11) Older severe infectious disease outbreaks such as Dengue and Chikungunya did not reach clinical trials until 52 and 19 years after the outbreak.(11) The improved speed into clinical trials is hopeful, but despite the rapid progress, there are still reasons for concern.
Vaccine development takes time as the vaccines must not only be protective but also safe. Unlike other drugs that are delivered into sick patients, vaccines are administered into healthy patients and require very high safety margins.(12) Therefore, the population should be carefully monitored if vaccine candidates are widely administered based on Emergency Use Authorization. This is especially vital as for past respiratory diseases such as SARS-CoV, MERS-CoV, respiratory syncytial virus, and measles it had been shown that antibodies can exacerbate disease severity through antibody-dependent enhancement.(13) Many of the vaccines that are frontrunners are preclinical nanotechnologies and have not been proven in clinical settings. For instance, mRNA vaccines have been in development and clinical testing for the past 30 years, but the technology has not been previously approved.(14) The platform technology offers speed and adaptability, so these vaccine candidates can be rapidly developed by repurposing previously developed nanostructures as shown by Moderna.(15) Likewise, Novavax’s vaccine is also modeled off of their previous vaccine against influenza.(16) Even so, the vaccines must be rigorously tested for safety before widespread vaccination can occur, which Moderna and Novavax have accomplished through their Phase I studies.(17,18) Beyond Moderna and Novavax, several other companies have moved beyond their safety and immunogenicity Phase I and II clinical studies and have released pertinent data corresponding to these trials.(17,19−23) This review analyzes these posted results and highlights the nanotechnological aspects of the vaccines from these leading companies as well as summarizes the potential of other rapidly developed vaccines in clinical trials.

Vaccination Immunology

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To gain a better understanding of the clinical data, it is important to understand concepts in vaccine immunology. There is no “one size fits all” protective antiviral immune response. Every virus is different with different routes of infection, different range of infectable cell types, and different associated pathology. Accordingly, the immune response best suited for protection against each virus will also be variable.(24) Other factors such as sex, age, pregnancy, and route of infection can also influence the immune response.(24,25) It is widely reported that some people become heavily infected with SARS-CoV-2, but remain asymptomatic, and that some become critically ill and succumb to the disease. This extreme variability in response to infection underscores the variability of individual immune responses to this virus, suggesting that there may not be a single perfect strategy that will achieve uniform long-lasting immunity in everyone. The specific immune responses that elicit the most rapid and dependable viral clearance need to be understood and replicated by the vaccines. Major unanswered questions are whether humoral and/or cellular cytotoxic responses are required, what types of helper T cells are most effective (e.g., Th1 vs Th2 vs Th17) as well as what isotype of antibody response (e.g. IgG vs IgA) most effectively protects against this virus.(26−28) Most of these questions are being answered through laboratory studies as well as through analysis of serum and circulating cells from recovered patients.
Given the variability of host immune responses, there is unfortunately no guarantee that a vaccine, even if it has progressed into advanced clinical trials, will protect against SARS-CoV-2. While a single vaccination can confer lifelong protection against small pox(29) or poliovirus,(30) HIV continues to evade protection by vaccination despite a major worldwide effort to develop an effective HIV vaccine.(31) Additionally, there are indications that respiratory viruses are especially difficult to protect against with vaccines. The respiratory syncytial virus is a prime example in which there are no approved vaccines, despite considerable efforts to develop one.(32)
One reason for vaccine failure against respiratory viruses is that the respiratory tract, including the lungs, is an external mucosal surface that is protected by the generation of secreted IgA antibodies; yet, the antibodies measured to determine whether an experimental subject has “responded” to a vaccine often focus on IgG, IgM, or total immunoglobulin in the blood.(33,34) Most vaccines are delivered intramuscularly, and mucosal immunity and IgA secretion is thereby minimal.(35) Furthermore, eliciting IgA production from conventional vaccines is difficult, and vaccines may lack the immunogenicity required to elicit necessary IgA protection.(36) Regardless, there are efforts and reports on development of SARS-CoV-2 vaccine candidates that can elicit IgA responses (see Table S1). For instance, Altimmune, an adenovirus (Ad)-based nonreplicating viral vector vaccine administered intranasally, showed 29-fold IgA induction in mice.(37) Other companies such as Stabilitech Biopharma Limited and Quadram Institute Biosciences are also developing mucosal vaccines.(38,39) The value of IgA or other immunoglobulin isotypes in protection against SARS-CoV-2 has not been fully elucidated, but it is believed that IgA can prevent SARS-CoV-2 binding to the airway epithelium thereby helping to block both initial infection and subsequent transmission.(34,37) It is important to note that it is not known what role, if any, IgA plays in protection against SARS-CoV-2 and that many of the current vaccines are not specifically looking to activate IgA responses. Of course, it is possible that IgA production will not be important for an effective vaccine, or may even be harmful, as IgA production was negatively correlated to increased severity in COVID-19 patients.(40)
SARS-CoV-2 is unusual for a respiratory virus in that it binds to a receptor, angiotensin converting enzyme 2 (ACE2), expressed in virtually all organs,(40) but especially in the lungs,(41) brain,(42) and gut.(43) Therefore, unlike most respiratory viruses, SARS-CoV-2 has broader biodistribution and can cause considerable damage outside the respiratory system. It adversely affects the digestive, urogenital, central nervous, and circulatory systems, and the pervasiveness of the ACE2 receptor is why symptoms are highly variable and can range among dyspnea, diarrhea, headache, high blood pressure, venous thromboembolism, and more.(40) Therefore, since much of the pathology is outside the airway due to systemic viral infection, a vaccine that elicits IgG antibodies could protect patients from systemic circulation of the virus. IgG antibodies opsonize the targeted antigens presenting the opsonized products to phagocytes while also activating the complement system.(44)
Another hallmark of vaccine development is T-cell involvement, and differences in T-cell responses can influence generation of high affinity and neutralizing antibodies (NAbs) as well as elimination of infected cells.(45) Immune memory and generation of high affinity class-switched antibodies are highly dependent on T-cells and normally do not develop without proper T-cell involvement.(46,47) Immune memory is the main driver of long-term immunoprotection, and studies have shown that immune titers from patients infected with the first SARS-CoV can have significant antibody levels for up to 3 years postinfection.(48) Such antibody maintenance would be extremely beneficial in the fight against SARS-CoV-2, and this prolonged immune memory could potentially confer long-term protection by a vaccine. However, it is likely that periodic booster vaccination will be necessary in areas of rebounding cases as is done for other infectious diseases.
It is currently unclear whether any of the tested vaccines will confer protection against SARS-CoV-2. Fortunately, as noted below, there are encouraging early results from multiple vaccines that are safe and immunogenic in limited patients. This early success warrants the progression into Phase III clinical trials, and expectations are that 20,000–40,000 subjects would be involved. There is a daunting task left in the effort to develop effective vaccine(s) against SARS-CoV-2, and no guarantee of success, but we are encouraged by the early testing success and rapid development of so many candidate vaccines.

Nanotechnology Offers Opportunities in Vaccine Design

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Nanoparticles and viruses operate at the same size scale; therefore, nanoparticles have an ability to enter cells to enable expression of antigens from delivered nucleic acids (mRNA and DNA vaccines) and/or directly target immune cells for delivery of antigens (subunit vaccines). Many vaccine technologies employ these direct benefits by encapsulating genomic material or protein/peptide antigens in nanoparticles such as lipid nanoparticles (LNPs) or other viruses such as Ads. BioNTech/Pfizer and Moderna encapsulate their mRNA vaccines within LNPs while the University of Oxford/Astrazeneca (from here on out referred to as Oxford/Astrazeneca) and CanSino incorporate antigen-encoding sequences within the DNA carried by Ads.(17,19,22,23) Novavax decorates recombinant S proteins of SARS-CoV-2 onto their proprietary virus like particle (VLP) nanoparticles.(49) The nanoparticles are described in further detail in the discussion below.
Beyond antigen delivery, nanoparticles can codeliver adjuvants to help prime the desired immune responses. Adjuvants are immunostimulatory molecules administered together with the vaccine to help boost immune responses mainly by activating additional molecular receptors that predominantly recognize pathogens or danger signals. These pathways function primarily within the innate immune system, and each adjuvant generally has a different range of stimulation of these pathogen or danger receptors. While the vaccine goal is to stimulate recognition and response by lymphocytes, not innate cells, the activation of the innate immune cells is required to activate the lymphocytes to obtain both B and T-cell responses.(50,51) Encapsulation and/or conjugation of both the adjuvant and antigen within the same nanoparticle enables targeted, synchronous delivery to the same antigen presenting cell (APC). Many adjuvants have previously failed in the clinic due to toxicity issues, and this codelivery can help to direct antigen and adjuvant activity only in APCs that have taken up the antigen thereby reducing off-target side effects.(52) Targeted delivery of appropriate adjuvants can also reduce the necessary antigen dose for immune protection thereby producing a dose-sparing effect.(52) This effect would be abundantly helpful practically and financially in the current pandemic due to the enormous number of doses needed for global vaccination. Furthermore, when adjuvants and antigens are not codelivered they may dissociate quickly within the body, which may lead to off-target effects and/or rapid degradation of the adjuvant reducing the potency of the vaccine.(53) Both Moderna and BioNTech encapsulate their mRNA vaccines within LNPs to protect the mRNA from nuclease degradation.(17,19) Loss of temporal synchronization, i.e., uptake of the antigen and adjuvant by APCs at separate times, can also lead to autoimmunity against host proteins, as the adjuvant can activate APCs that are not primed against the antigen but rather primed against self-antigens.(52) Therefore, nanotechnology offers an opportunity in vaccine design, and there are several strategies that enable codelivery of SARS-CoV-2 antigens and adjuvants. The three main methods are (i) codelivery through encapsulation within or conjugation onto a nanoparticle, (ii) direct antigen-adjuvant conjugation, and (iii) utilizing the delivery vehicle as an adjuvant.(53,54) Another benefit that nanoparticles can confer is multivalent antigen presentation and orientation of subunit antigens in their native form.(55) For example, BioNTech/Pfizer, one of the frontrunner companies producing a SARS-CoV-2 vaccine, formulates their receptor binding domain (RBD) antigens onto a T4 fibritin-derived “foldon” trimerization base to better resemble the trimeric form of the spike (S) protein of SARS-CoV-2.(19,56) Furthermore, display of different RBD epitopes of influenza A on multivalent ferritin nanoparticles can increase production of cross-reactive B-cells against influenza A, and produce a more diverse and effective antibody response than ferritin nanoparticles with homotypic RBD display.(57) The study also found that the multivalent, heterotypic nanoparticles induced a broadly NAb response, which makes the generation of an all-encompassing, universal influenza A vaccine possible.
Lastly, due to the “nano” scale of nanomaterials as well as their composition, they can traffic in vivo differently from other materials. The lymphatic system is critical in initiating immune responses as APCs, and other lymphocytes travel from peripheral organs to nearby lymph nodes using the lymphatic system.(58) Accessing the lymphatic system can be challenging, but nanomaterials can traverse the interstitial spaces and access nearby lymph nodes. For instance, inhaled radiolabeled solid lipid nanoparticles were shown to traffic from the alveoli into nearby lymph nodes via the lymphatic system, while the free radiotracers trafficked via the systemic circulation.(59) Lymphatic drainage especially into lymph nodes near the lungs could be extremely beneficial in the fight against respiratory diseases such as SARS-CoV-2. Companies such as etheRNA and Intravacc are developing intranasally delivered vaccines delivered into the respiratory system that may target such nearby lymph nodes.(60,61)
For further reading on the opportunities of nanotechnology in SARS-CoV-2 vaccine design, we would like to refer the reader to the following review.(62) This review also discusses challenges and opportunities of the manufacturing processes and delivery platforms that are necessary for global vaccination.


voter fraud






Saturday, May 30, 2020

PLANDEMIC


IT APPEARS THAT WE HAVE ALLOWED OURSELVES TO FOOLED AGAIN BY ANOTHER FAKE FALSE FLAG. YEA PEOPLE DIED BUT PEOPLE DIED ON 911 TO AND IT WAS A FALSE FLAG ATTACK ON OURSELVES.911 WAS FOR THEM TO TELL US THAT WE GOT TO GIVE UP OUR PRIVACY FOR SECURITY SO THE COULD SPY ON EVERYTHING YOU DO.THEY BUILT A BIG DATA FARM IN UTAH WITH YOUR TAX PAYER MONEY
      NOW THEY HAVE FUCKED UP THE WORLD WITH A FAKE PANDEMIC FOR A FLU LIKE VIRUS AND SHUT DOWN THE WHOLE WORLD TO PUT CHINA BACK ON TOP AND TO URSHER IN THE N W O  WHERE THEY WILL CONTROL AND TRACK YOUR EVERY MOVEMENT EVEN IN THE FUCKING TOILET YOUR HOUSE WHO YOU FUCKING AND SUCKING THEY WILL BE MONITORING ALL OF THIS.AND IF YOU CLAIM YOUR FUCKING RIGHTS THEN YOU GO TO CONCENTRATION CAMP AND TAKE YOUR FREEDOM AND YOU LIVE OFF THEM TILL THEY KILLYA ONE WAY OR ANOTHER.
NOW THIS SHIT IS ALREADY IN PLACE THEY ALREADY THE LITTLE COVI PASS SHIT SETUP .
    NOW SEE WHAT THE PLANDEMIC IS REALLY ALL ABOUT IS THE FINAL BATTLE BETWEEN GOOD AND EVIL AND YOU GET TO PLAY YOUR PART IN IT.  CAUSE THEY ARE YOU USING A WEAK WEAK MILD FLU VIRUS TO SCARE THE SHIT OUT OF YOU AND MAKE YOU SUBMIT TO A FAKE VACCINE THAT MAY HAVE NANO TECH RIFD CHIPPING IN IT. YOU TAKE A SHOT OR VACCINE YOU CHIPPED YOUR ARE A BORG NOW. NOW YOU RIDE THE BEAST MACHINE. CAUSE THE THING ABOUT THE NANO TECH WHEN THEY INJECT IT IN TO YOU IT WILL BECOME A PART OF YOU. FOREVER CHANGING YOUR DNA AND YOUR SOUL WANT BE ABLE TO LIVE WITH THAT.


  DONT TAKE MY WORD FOR THIS SHIT LOOK THIS STUFF UP AND RESEARCH IT SOME OF YALL THINK GOD CONTROLS ALL WEATHER YALL ARE THE ONE WHO REALLY NEED TO WAKE UP CAUSE YOU CAN FIND GOVERNMENT DOCUMENTS THAT DATE BACK 60 YEARS ABOUT WEATHER MODIFICATIONS. WHY YOU THINK HURRICANE KATRINA HARVEY HUGO ANDREW DONE SO MUCH DAMAGE . THESE PEOPLE GOT TECHNOLOGY YOU WANT BELIEVE I WILL TELL YOU A GOOD ONE HOLOGRAMS ARE REAL LIKE YOU SEEN IN THE STAR TREK NEXT GENERATION CALL ON 911 PEOPLE THOUGHT THEY SEEN PLANES FLY INTO BUILDING THAT MELTED RIGHT THE FUCK INTO THEM. NOW YOU KNOW DAM WELL FUCKING PLANES CANT MELT INTO BUILDINGS IMPOSSIBLE. THEY FOOLED THE MASSES  AND MAINSTREAM MEDIA HAD YOU RIDING THAT PONY SHOW JUST LIKE THEY GOT US RIDING THIS PONY SHOW
  I TELL EVERY BODY STOP PARTICIPATING IN A FAKE PANDEMIC DID THE WORLD SHUT DOWN FOR ANY ANY OF THEM PANDEMIC THEY HAD IN AFRICA WHEN THEY WAS DYING BY THE THOUSANDS DID THEY SHUT THE WORLD DOWN FOR THE PANDEMIC IN MADAGASCAR DID THE SHUT DOWN THE WORLD FOR MAD COW SARS EBLOA  SWINE FLU WEST NILE ETC DID THEY SO WHY IN THE HELL DID YOU FALL FOR IT THIS TIME THESE FUCKERS DONT RUN YOUR HOUSEHOLD YOU DO AND UNDER THE CONSTITUTION YOU HAVE A RIGHT AND THEY ARE TAKING YOUR RIGHTS AND FREEDOMS ACCORDING TO THE CONSTITUTION ITS SLICK WAY THEY BRAINWASHING THE MASSES JUST LIKE IN THE MOVIES REMEMBER THE PANDEMIC MOVIES CAUSE THE DEVIL HAS TO TELL YOU WHAT HE GONNA DO TO YOU BEFORE HE DOES IT CAUSE EVEN THE DEVIL KNOWS HE CAN NOT ESCAPE DIVINE JUDGEMENT

                      IT HAS BEEN SAID THAT GOD TOLD THE DEVIL HE CAN NOT INSLAVE ANOTHER SOUL WITHOUT THEM KNOWING ABOUT IT.SO THE DEVIL HAS BEEN TELLING MAN WHAT HE WAS GONNA DO TO MAN ALL THE TIME ONE WAY OR ANOTHER CAUSE LIKE THE DEVIL KNOWS AND HILLARY CLINTON KNOWS YOU CAN ESCAPE DIVINE JUDGEMENT

SO AT THIS POINT WE CANT SAY WE DIDNT KNOW BUT A  BUNCH FEW MILLION OF US DONT FUCKING PAY ATTENTION AND THINK OUT SIDE THE BOX PEOPLE TAKE IT FOR FACE VALUE. DONT YALL THINK THE EVIL ONE PLAYED HIS HAND IN WRITING THE BIBLE MOST OF THE OLD TESTAMENT IS A STORY WHICH IS ABOUT ANNUNAKI GODS ENSLAVING MAN REALLY HAHA ACCORDING TO SOME ANCIENT TEXT ITS ALL UP TO YOU TO DO YOUR OWN RESEARCH 
     IF YOU KEEP PARTICIPATING IN THIS FAKE PANDEMIC YOU GONNA LOSE RISE UP AND RESIST THIS TYRANNY THAT HAS BEEN IMPOSED UPON THE WORLD JUST TO WATCH YOUR EVERY MOVE INCLUDING SEX

  IN SOME AREAS THEY TRYING TO FORCE YOU TO WHERE A MASK. LIKE THE ONE WHERE THEY RAN THE LADY OUT THE STORE BECAUSE SHE DIDNT HAVE A MASK ON. NOW FUCKING THINK ABOUT IT IF EVERY BODY ELSE IN THE STORE GOT A MASK ON AND YOU DONT HOW IN THE HELL COULD YOU INFECT EACH OTHER ANYWAY THE PEOPLE THAT GOT MASK ON CANT BLOW THERE FREAKING GERMS ON YOU AND THEY GOT A MASK ON AND YOU CANT BLOW YOUR GERMS ON THEM .    DUH DUH DUH
  THIS IS HOW MAIN STREAM MEDIA HAS BRAINED WASHED THE MINDLESS PUBLIC. YOU WOULD THINK THAT AFTER ALL THE LIES MAIN STREAM MEDIA PROJECTED ON THE RUSSIAN COLLUSION AND IT TURNED OUT TO BE ALL LIES AND TWISTED TRUTH  ONE WOULD THINK NEVER TRUST THE MAIN STREAM MEDIA AGAIN BUT HELL NO ALL THESE DEEP STATE ORGANIZATIONS WHO CDC ETC. CAME OUT AND SAID ITS A WORLD WIDE PANDEMIC CAUSE CHINA WAS KILLING PEOPLE AND BURNING BODIES OVER THERE TO STOP THE HONG KONG PROTEST WITH A BIOWEAPON OF CORONA AND THE CABAL THREATEN EVERY LEADER ON THE PLANET THAT IF THEY DONT GET TO HAVE THEIR  NWO  THEY WOULD UNLEASH THE REAL ONE ON THE WORLD.
     MOST OF YALL NEVER WORE A MASK FOR EBOLA SWINE FLU BIRD FLU OR ANY OTHER FLU WHY THE HELL YOU DOING IT NOW CAUSE LYING MAIN STREAM SAID SO IT IS FUCKING BRAIN WASHING AND IF YOU GET OFF YOU ASSES AND DO SUM RESEARCH YOU WILL FIND OUT HOW MUCH YOU BEEN LIED TO AND THEY ARE TRYING TO EXTERMINATE THE HUMAN POPULATION













SO LOOK AT IT THIS ON THE CDC WEB SITE   THEY ARE MIND CONTROLLING YOU










ITS JUST LIKE ALL THE DEATHS THEY HAVE SAID THAT HAVE CAME FROM THIS FAKE PANDEMIC THEY HAVE OVERLY INFLATED THE NUMBERS THE REGULAR SEASONAL FLU HAS KILLED MORE PEOPLE IN ONE YEAR THAN CORONA VIRUS WILL WORLD WIDE THESE DOCTORS HAVE BEEN INSTRUCTED TO LIST ANY BODY WITH CORONA VIRUS OR CORONA VIRUS ANTIBODIES THAT DIES LIST THEM AS DYING OF CORONA VIRUS
       








SEE WHAT PEOPLE FAIL TO REALIZE THAT IF CORONA VIRUS IS BEEN AROUND FOR 50YEARS AND ITS BEEN ON THE BACK OF A CAN OF LYSOL FOR DECADES SEE THEY NOT PAYING ATTENTION FAUCI AND GATES KEPT TALKING ABOUT THE ANTI BODIES THAT MAYBE FOUND IN THE BLOOD WHICH REALLY MEAN YOU GOT OVER IT YOU WELL AND PRETTY MUCH IMMUNE TO IT SEE THEY ALREADY KNOW THAT EVRY BODY ON PLANET EARTH IS GOING TO TEST POSITIVE  FOR THE ANTI BODIES
THIS IS THE TRICK THEY ARE GOING TO BRAIN WASH YOUR ASS WITH FOR  THE CONTACT TRACING ON YOUR EVERY MOVE AND IF GOT ANTIBODIES YOU ARE NOT GOING TO INFECT ANYBODY



















PEOPLE PEOPLE PLEASE WAKE UP
#WEDONOTCONSENT







THIS THE VIDEO THAT SHOWS FAUCI IS BEHIND WUHAN














Friday, June 28, 2019

FAKE HOPE

Well i wanna talk about the demon democrat. What i wanna know is why are the democrats fighting so hard and to fight against a president on immigration. Now that should send a lite bulb off in your head right there . did they fight that hard for the American citizens $15 hr min wage did they fight that hard to get rid of the unconstitutional tax on fining you for not having medical insurance ,oh wait it was there plan that fucked the american people out of their money. Ask your self why haven't they fought for us like they do immigrants. You don't count any more to them haven't you been listening to what obama and hillary been saying about letting immigrants in the country in past years. It's a U.N. Agenda 2021--2030 plan to flood america with immigrants to turn it into a third world country full of disease and shit so it can continue bringing about a NWO. Its why they hate russia or putin so bad he was the first to ditch monsanto the bankers the rauthchilds and the NWO.See most people dont even have the slightest clue on the shit that's goin on behind the closed doors. this is why this country is fucked up too many close door deals over 200 years that has screwed the people of this nation and was done using their own tax dollars against them. Now see that's fucked up i take money and destroy myself. Now the democrats wanna take your money and support 600000000 million immigrants by 2030 by then we will be a full third world country cause we are one quarter of the way already into being a third world country with more than 22000000 undocumented aliens in the country. Now asked yourself why your min wage still $7.25 hr but the ceo is getting  a $1000000 plus and why immigrants getting more free stuff than american citizens who need the same dam help. Think about this some of these democrats and republicrats have been in office for 20 plus yrs ain't done jack shit for the people or the country.

REPARATION  why all of a sudden democrats talking about reparation. Here's why they lost so many black votes that they are using this tactic to get black voters black and using the same old uncle toms like sharpton to lead the shit. I'm like the dark skinned guy who testified before a committee hearing on reparation quote   he said if anybody should pay for reparation it should be the democratic party cause they are the ones that did not want to abolish slavery and was partly to blame for the civil war. There was other factors in play to go along with that civil war it really was a mere distraction for the european banker and the rauthchilds was really planning for america. See black people don't be fooled by this reparations crap it is just another smoke screen from the d- evil party of the demoncrats. If they was really serious about it why didn't obama do it. Most of the same dam top people in congress and the senate are still there so why wasn't it done years ago don't fall for the bull shit like the collusion obstruction bull crap. Its just like when trump announced that he was gonna run for office they didn't say nothing. Then it looked liked trump was going to out do the rest of them and did the media just went crazy on how bad and no good he would be. That didn't make sense to me. Cause how in the hell me [being trump] and you [being mainstream] gonna be dam friends for 30 plus yrs in the media and shows and people wanting to be like trump have that trump money and now i run for president im the fucking lowest scum of the earth that shit don't make no sense it don't even add up to make sense i'm totally shocked at how many people bought that bull shit cause the propaganda was feed thru main stream tv shows news entertainment and hollywood , but bought hook line and sinker. I BELIEVE  that some beings are vibrating on a higher level of consciousness and manipulate some people's brain cause the bible quotes
        WE NOT WRESTLE AGAINST FLESH AND BLOOD ONLY BUT BEINGS WHO OPERATE ON A HIGHER LEVEL CONSCIOUSNESS
That means that their are beings here who manipulate the weak minded and the unaware. Now i understand why the bible quotes   "keep the full amour of GOD on at all times" get your tin foils hats and that really is some real shit cause your ass is a frequency and your ass can be manipulated as a frequency. MK ULTRA MIND CONTROL yea its a real thing its been around since the 50s. So maybe this is why so many bought the lie maybe they just really needed something to believe in hell i don't know. But one dam thing is for sho people who rely on or get most of their information from main stream media have been getting lied to or mislead with information for over 60 years. I personally go thru 10 or 20 different independent journalist news sources and my  own dam research to find out what the hell is really goin on. Cause they got a grand illusion goin on and some of the public is hooked on like a junkie on a needle real bad.

  So the only thing the demoncrats are really wanting that i have really heard them admit is this right here .
LATE TERM ABORTION what lunatic thinks like this
DECRIMINALIZE ILLEGAL BORDER CROSSING its illegal for a reason
HEALTH CARE AND SOCIAL SECURITY FOR ILLEGALS they not citizens
MEDICARE FOR ALL INCLUDING ILLEGALS                       "     "     "       "
DRIVER LICENSES FOR ILLEGALS                                          "    "     "        "
OPEN BORDERS its why we have them so we know where we are
IMPEACH and INVESTIGATE TRUMP  till the 2020 election
FAKE REPARATION
NO CITIZENSHIP QUESTION ON CENSUS   i mean really you gotta be kidding



Where is anything they wanting to do for america. They gave nato a trillion dollars not one penny for the wall cause the wall mite be to late cause california already needs to be quarantine for the diseases that are floating around from being over ran with immigrants downtown LA look like a third world country immigrants homeless people living everywhere. Most of the businesses have closed down in downtown LA it won't be long before they will be in beverly hills and hollywood they will keep that out of main stream like some of the diseases in cali ain't been seen since the mid evil times and one the gray doctors who had a show even admitted it but they keep that buried now. I ts one dam thing for sho cause its simple math the more free welfare and social security they give illegals the less it will be for you and you my fellow americans yall paid yalls social security in they getting theirs for free and when the money run out where the democrats gonna get the money for yours that you paid in.
 For over a year trump been saying it's a crisis on our southern border now the demoncrats are finally coming around about a crisis at the border cause a kid or two got killed crossing the river and drowned but they invited them to come any way they could so who fault is it. But they wont give trump the money for beds and housing they just want to release some of them diseased people in over here to roam  freely and spread what ever they got and turn your country into a country they left from cause they got paid and brain washed that we are giving away free shit and the democrats are trying to make sure that the illegal immigrants get way more than the american people qualify to get. So how can people support people who really ain't talking about doing a dam thing for you but want you to pay for the shit they wanna give away to get them votes and keep their evil ass in power after it was the d-evil one domain now its ours but we got to fight for it  so we the people are gonna have to kick out the demoncrat party cause they the ones who are hijacking your country away from you cause aint no dam one million people all of a sudden wanna pack up and come to america from every fucking where in the world oh you didn't know their are africans from the ebloa stricken CONGO  arabs from the middle east latinos from way down south isis  etc. THAT'S what's been confirmed on what and who has been identified coming across that southern border but democrats claimed we don't need a wall if it had been there the bigger problem we could face could have been very small all i can say is you better get a mask like them japanese wear a lot .




















Sunday, March 24, 2019

https://www.infowars.com/watch/?video=5c97e83296f802002664dedb

THE EYES OF THE NEW BLACK AMERICA



I FEEL LIKE WE HAVE A NEW BLACK AMERICA. NOT A BLACK AMERICA THATS MADE UP OF ALL SHADES OF BROWN BUT A BLACK AMERICA BORN AND RAISED AND RAISED HERE AND WHO HAS WOKE UP AND REALIZED THAT THE DEMOCRAT PARTY IS ONLY MADE UP OF HOPES AND DREAMS AND NO DELIVERIES. BRAINWASHED BY THE 1964-1965 CIVIL RIGHTS ACT INTO THINKING DEMOCRATS WOULD ALWAYS HAVE THEIR BACK HAVE OPEN THEIR EYES AND REALIZE THAT THEM DEMONCRATS DONT HAVE ANYBODY'S BACK BUT THEIR MASTERS THEY SERVE AND THEIR OWN ASS. 

       ITS LIKE MAIN STREAM MEDIA SOME OF THEM BOUGHT THE RUSSIAGATE HOAX HOOK LINE AND SINKER. BUT IT WAS JUST SOME BLACK PEOPLE BUT A LOT OF OTHER PEOPLE BOUGHT THAT BULL CRAP  TOO. IM PROUD THA BLACK PEOPLE ARE STARTING TO REALIZE THAT YOU DONT HAVE TO BE A HARD PARTY VOTER BUT A VOTER FOR THE BETTER GOOD