VLA Comment: The United States scientist has been working for years on GAIN OF FUNCTION (This includes Fauci) with the Chinese. Gain of Function is taking a animal virus that does not jump species and manipulate it to infect another species, namely human being.
- Profusa, in partnership with the U.S. Defense Advanced Research Projects Agency (DARPA), has created an injectable biosensor capable of detecting the presence of an infection in your body
- Injectable hydrogel biosensors are not rejected as foreign bodies like earlier implants, instead becoming one with your own tissue
- The technology consists of three components: the implanted sensor, a reader placed on the surface of the skin, and the software that allows the reader to send the collected data via Bluetooth to your phone or tablet, which in turn can be connected to other online sources such as your doctor’s website
- Profusa’s DARPA-backed technology will be able to detect the presence of flu-like infections including SARS-CoV-2 infections in the population before they become symptomatic. As such, the biosensors may become part of future pandemic detection systems
- Mass surveillance of biological data will require massively increased bandwidth in cellphone and Wi-Fi networks, and it’s possible that this is why governments are rushing implementation of 5G networks around the world without giving potentially adverse effects a second thought
- READ MORE
NanoLuc Luciferase – A Multifunctional Tool for High Throughput Antibody Screening (Study)
VLA Comment: Hydrogel and Luciferase (enzyme that is florescent) Another step closer to Transhumanism
Judge Rules Pennsylvania Governor’s Shutdown Orders Unconstitutional
A federal judge has struck down Pennsylvania Gov. Tom Wolf’s CCP virus restrictions that required people to stay at home, put limits on gatherings, and ordered “non-life-sustaining” businesses to stay shut down.
The judge, who was appointed by President Donald Trump, argued that the actions taken by Wolf and Pennsylvania Secretary of Health Rachel Levine, who are both Democrats, “were undertaken with the good intention of addressing a public health emergency,” but that “even in an emergency, the authority of government is not unfettered.”
U.S. District Judge William Stickman IV on Sept. 14 sided with plaintiffs that included drive-in movie theaters, hair salons, farmers markets, and several GOP officials who sued as individuals. Butler, Greene, Fayette, and Washington counties were also listed as plaintiffs.
DID THE FEDERAL AGENCY HHS…through administrative rule take over VACCINES….that authority which belongs to the States
The enactment of The PREP Act (Public Readiness and Emergency Preparedness 2005) was declared by the Secretary of HHS on March 10, 2020.
This allowed our nation to address the COVID “pandemic” by extending legal protections to manufacturers of medical supplies and equipment, plus allowing our federal government to harness the resources necessary to combat this virus.
This also extended to the states for them to enact Emergency Powers that restricted businesses, social gatherings, focusing medical responses to COVID only.
At the same time, the Secretary of HHS forwarded his intentions via a Notice of Proposed Rulemaking (NPRM) to remove shoulder injury (SIRVA) and syncope (fainting) from the NVICP, thus any claims for injuries resulting in shoulder injuries or the result of injured incurred after falling because of fainting. READ MORE…
Consultation document: changes to Human Medicine Regulations to support the rollout of COVID-19 vaccines
A temporary authorization of the supply of an unlicensed vaccine could be given by the UK’s licensing authority under regulation 174 of the Human Medicines Regulations (see below). A COVID-19 vaccine would only be authorized in this way if the UK’s licensing authority was satisfied that there is sufficient evidence to demonstrate the safety, quality and efficacy of the vaccine. ‘Unlicensed’ does not mean ‘untested’: this temporary authorization process exists to address the possibility that, in certain situations of public health need, the licensing authority may consider that the balance of risk and benefit to patients justifies the temporary supply of the relevant vaccine pending the issue of a product licence. Regulation 345 of the Human Medicine Regulations transposes into UK law a requirement of EU law that key actors in the medicines supply chain cannot generally be sued in the civil courts for the consequences resulting from the use of an unlicensed product, or a new use of a licensed product, that a national licensing authority is recommending in order to deal with certain specific health threats. READ More...
VLA Comment: It is a long compilation by UK Goverment changing regulations to accommodate worldwide vaccination of Covid Vaccine…but I don’t see “mandating” vaccines, unless I missed it by their use of more subtle language. 2 things we have to look out for….
1) I believe in the USA the Epidemic Intelligence Service (EIS) will be orchestrating the distribution.We should be alert…alert Trump… to make sure the Military is not going to be used as the usual guinea pigs to get this vaccine, or the result will be after all the money Trump spent on the military…he will have a lot of incoherent and potentially nano-chipped Deep State controlled Military. (same goes for any country that is planning on mandating this vaccine to their military…potentially then there will be AI Global control of all militaries…sounds like science fiction…but don’t dismiss it.
2) In the USA it is the states that control vaccines and “mandating” not the Federal Government. Be far sighted…will the school children be “mandated”. Can we get on a plane without it, etc.