Spread the word far and wide.

The World Health Organization has listed Nipah virus as an emerging pathogen likely to cause major epidemics or even pandemics and stated that “A therapeutic treatment for Nipah virus disease is urgently needed.”

Meanwhile Gilead Sciences, a California based Biotech company is conducting phase 2 trials of Remdesivir in Liberia and Guinea on supposed Ebola victims. They now claim that this same drug is also a good candidate to be used on the Nipah virus.

By injecting some monkeys with the Nipah virus and claiming that the ones who did not have Remdesivir died, now constitutes a new breakthrough?


In 2017,they collaborated with these partners to conduct nonclinical and clinical research advancing the development of investigational agent remdesivir (GS-5734):

National Institute of Allergy and Infectious Diseases (NIAID) We continued an existing collaboration with NIAID in Liberia on testing remdesivir in Ebola survivors. The study expanded to Guinea in early 2018. United States Army Medical Research Institute of Infectious Diseases In collaboration with the United States Department of Defense, we have demonstrated the efficacy of remdesivir in the lethal nonhuman primate model of Marburg infection with similar efficacy as against Ebola. We filed an Investigational New Drug application with the FDA to conduct clinical trials for Marburg virus infection in February 2018. United States Centers for Disease Control In collaboration with the CDC, we have published a full broad-spectrum antiviral profile using in vitro data of remdesivir that includes not only Ebola, but also other pathogenic filoviruses (namely Marburg), coronaviruses (MERS, SARS) and paramyxoviruses (measles, Nipah, Hendra)



This company is no stranger to law suits for false claims involving secret and unapproved ingredients. In which the Federal Govt purchased for $5 Billion. https://www.forbes.com/sites/erikakelton/2017/09/26/revival-of-gilead-whistleblowers-lawsuit-should-stoke-fear-in-big-pharma/

Gilead also had two whistleblowers who spoke out about the ingredients in HIV medications and yet ironically, one of the directors, Richard Whitley, is the chairman for the NIAID HIV vaccine data safety and management board.

Reports that Gilead are having financial problems just months ago https://www.barrons.com/articles/gilead-sciences-stock-is-sinking-after-its-earnings-fell-short-of-expectations-51549383772?refsec=biotech

And who decides who IS an EBOLA victim or who has died from Ebola in these countries?
A point-of-care test developed by OraSure with support from BARDA, and authorised for emergency use by the U.S. Food and Drug Administration (FDA).

These rapid diagnostic tests provide results in minutes, giving responders the information they need to make more effective decisions.

OraQuick® HCV Rapid Antibody Test
OraQuick® HCV Rapid Antibody Test

The OraQuick® Ebola Rapid Antigen Test has been granted an Emergency Use Authorization (EUA) by the U.S. Department of Health and Human Services for the following two uses:

A. For presumptive detection of Ebola Zaire virus in whole blood specimens from individuals with signs and symptoms of Ebola virus infection in conjunction with epidemiological risk factors (including geographical location with high prevalence of Ebola infection)

B. For detection of Ebola Zaire virus in cadaveric oral fluid specimens to aid in diagnosing Ebola Zaire virus as the cause of death in order to make informed decisions on safe and dignified burial procedures to prevent transmission of the Ebola Zaire virus in the community.

The OraQuick rapid Ebola antigen test is the first point-of-care Ebola virus testing device to receive BARDA support.

The contract was awarded under Solicitation Number: BAA-13-100-SOL-00013

So once again, the reported numbers of Ebola victims will be claimed using test equipment that has been funded by BARDA.

Many people in and out of the medical community were shocked to read in an articlepublished in 2015 in the medical journal the BMJ that the U.S. Centers for Disease Control and Prevention (CDC) takes funding from industry.

Both Gilead and Orasure are corporate members of the Viral Hepatitis Action Coalition along with other pharma companies formed with the CDC Foundation which donated $26 Million dollars to the CDC.
CDC’s recommendation that everyone born between 1945 and 1965 be screened for the hepatitis C virus has been challenged because every corporate member produces products to test for or treat hepatitis C infection. https://www.minnpost.com/second-opinion/2015/05/revelations-cdcs-industry-funding-raise-questions-about-some-its-decisions/

These levels of industry funding and influence within agencies that declare pandemics is a total conflict of interest.

The revolving door of pharma executives and Govt agencies is also highly suspect.

The chief patent officer of Gilead serves on the US Govt Industry Trade Advisory committee and other advisory boards.

Another director, George Shultz is an ex US Secretary of State whilst John F Cogan holds positions in US Govt as Assistant Secretary for policy in the US and deputy director in the US office of management.

This was the headline in an Indian newspaper today. 5-6-19

Kerala confirms 1st Nipah infection in India this year. A 23 yr old student reported to have tested positive, 5 more are suspected to have Nipah due to being in contact with him including nurses whilst 311 people have been identified as being indexed to have had contact. (Yes, they do love their numbers!)

Read more at:

I have pointed out in research at the beginning of the year that 2019 would be the year of another fake pandemic and also the links to the Nipah virus encoded into the London marathon.

Expect to hear a lot more from the new kid on the block called ‘Nipah’.

The vaccination programme in the very state that Gilead operate in, California, has now made vaccines mandatory with fines and jail sentences.


There is an organisation called Gavi: Global Alliance for vaccines and immunizations that was founded by Bill Gates, So countries and organisations pledge millions to GAVI to roll out vaccinations programs worldwide.

The UK govt pledged about one and a half million from about 2000 to 2015, for 2016 to 2020 they have pledged a billion pounds! Yet after that from 2021 to to 2032 there are no pledges. Other countries have quadrupled pledges in that same period, and some countries like China, Saudi,Italy and Qatar, have all pledged money for that period only, 2016 to 2020.

The JCVI : Joint committee on vaccines and immunisations advises the UK govt and in 2009 they passed a new law to say that the govt HAD to act on any proposals that this group pushes, and of course they are linked to big pharma.

Of course we all know that viruses are manufactured -genetically modified to create sickness in the body which is why Jane Bergermeister went to court and blew the whistle on Baxter International who had contaminated swine flu vaccines with the swine flu.

A man called Dr Joseph Kim, who teamed up with his university lecturer called Professor Wiener, who is the leading DNA technology inventor, created a few companies one was called Inovio, in which the Professor was the chairman.

Dr Kim was funded by Merck for his education, he produced something called PCV2 which is Porcine Circovirus, they were working on a veterinary drug that would help pigs escape a wasting disease.

So this was evaluated by the Dept of Homeland Security and Plum Island animal research, this DNA plasma for pigs had approval in 2005, in the same year, the swine flu vaccines were filing for a patent.
In 2009 Dr Kim’s company was filing with FDA to start trials on humans for the swine flu.

What is crazy is that his partner Prof Wiener is not only the worlds DNA technology expert but he is also a special employee and adviser to the FDA.

A couple of years after they were given the patent for this pig DNA vaccine using PCV2 that same ingredient was found to be in Merck’s Rotarix vaccine for diarrhoea and GSK vaccine rotateq for diarrhoea.
Now how does pig virus magically turn up in a vaccine for diarrhoea?It doesn’t! It gets put there. And what is unbelievable is that even though both vaccines were suspended and it transpired that all the vaccines for 2 years had been contaminated , the FDA suspended them for a few months then let them carry on.

The Information about the two drugs being suspended was found on the
Med worm website and the article was written by Dr Kim.

So we can see how geneticists using scientists are tampering with the building blocks of our existence and what is disturbing is that Prof Wiener is a HIV pioneer and we know that soon after the Polio vaccines were given to millions in Africa that HIV emerged.

They have perfected the art of injecting animal or bird DNA into human chromosomes which alters our DNA and causes things like haemorrhaging, fever, cancers and even death.
With Polio, genetic analysis has shown that mutated viruses from the vaccines has caused 7 separate outbreaks of polio in Nigeria, when polio could be wiped out easily by cleaning and removing sewage from water and the environment. The Polio vaccines paralysed the kids in Africa.

The Spanish Flu of 1918 was the after affect of the massive nationwide vaccine campaign. It suddenly struck just after WW1 ended.

It is clear that Govt agencies, pharma companies and so called scientists and doctors are creating the conditions for the next pandemic called Nipah and it is best that we NIP that in the bud!


  1. remdesivir is an ‘anti-viral’ drug. The same crap developed to ‘treat’ AIDS (AZT). Anti-‘virals’ are in fact dangerously strong antibiotics and were originally developed as ‘chemo’ for cancer but killed patients too quickly. They are desperately looking for new markets for this crap which is pure POISON!! To sell it they have to sell the disease as DEADLY.

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