Dr Ros Jones - 6th May 2024: Part 3 - What was the emergency for children?

In this part, Dr Jones talks about the intent to replace the old vaccines with the new mRNA therapies, the need for a robust regulator of the pharmaceutical industry, not an enabler, and the idea investigating a product AFTER marketing would be good for innovation.
Dr Ros Jones is a retired Consultant Paediatrician. She came out of retirement at the start of the Covid pandemic scare, but soon realised that things were not as advertised, and went on to work with Us for Them, the group campaigning to keep schools open. She also was part of the group of UK doctors, scientists, economists, psychologists and other academic experts who came together towards the end of 2020 to found HART, the Health Advisory and Recovery Team. HART was founded because of concerns over the response to Covid and the lack of proper scientific debate regarding it, and the censorship of those questioning the narrative.

“The Declaration of Geneva of the WMA binds the physician with the words, “The health of my patient will be my first consideration,” and the International Code of Medical Ethics declares that, “A physician shall act in the patient’s best interest when providing medical care.””
WMA DECLARATION OF HELSINKI – ETHICAL PRINCIPLES FOR MEDICAL RESEARCH INVOLVING HUMAN SUBJECTS
https://www.wma.net/policies-post/wma-declaration-of-helsinki-ethical-principles-for-medical-research-involving-human-subjects/

“The debate on the future of the declaration raises several fundamental questions about the essential purpose of the declaration, its structure (basic principles or procedural rules), its status (static or dynamic), the extent to which it can influence understanding and practice, and the nature and limits of universality in ethics.”
The Declaration of Helsinki
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1995496/

“The MHRA now has more than enough evidence on the Yellow Card system to declare the COVID-19 vaccines unsafe for use in humans.”
https://ukfreedomproject.org/resources/open-letter-to-dr-june-raine-chief-executive-mhra/
“...what I would like to do in taking you into the world I live in, the regulators world, is to talk about how that world is changing, enabling as a regulator rather than being a watchdog or a policeman or some of these more traditional ideas ...”
Making science work for health | Dr Dame June Raine on how regulators are supporting innovation
https://www.youtube.com/watch?v=4FUhWLEF8i0

8 March 2023
“Regulators will need to concentrate on domains where truly novel and transformative therapies are emerging, interacting with innovators from a very early stage to define a route to approval, and ensure that regulators play an enabling role throughout the journey to approval.”
https://www.gov.uk/government/publications/pro-innovation-regulation-of-technologies-review-life-sciences-interim-report/letter-from-sir-patrick-vallance-to-the-chancellor

Patrick Vallance on regulating AI and medical devices based on AI:
“A regulatory sandbox is a live testing environment, with a well-defined relaxation of rules, to allow innovators and entrepreneurs to experiment with new products or services under enhanced regulatory supervision without the risk of fines or liability. They are typically operated by a regulator for a limited time period and seek to inform rule making.”
…
“A sandbox could initially focus on areas where regulatory uncertainty exists, such as generative AI, medical devices based on AI, and could link closely with the ICO sandbox on personal data applications.”
https://assets.publishing.service.gov.uk/media/64118f0f8fa8f555779ab001/Pro-innovation_Regulation_of_Technologies_Review_-_Digital_Technologies_report.pdf

mRNA and the human genome:
“Furthermore, a recent study showed that SARS-CoV-2 RNA can be reverse-transcribed and integrated into the genome of human cells.”
https://www.researchgate.net/publication/359084279_Intracellular_Reverse_Transcription_of_Pfizer_BioNTech_COVID-19_mRNA_Vaccine_BNT162b2_In_Vitro_in_Human_Liver_Cell_Line

Titled “Intracellular Reverse Transcription of Pfizer BioNTech COVID-19 mRNA Vaccine BNT162b2 In Vitro in Human Liver Cell Line,” the study found that the exogenous genetic material coding for the dangerous Spike protein is reverse-transcribed (from RNA to DNA) into the human genome by LINE-1 proteins of the cells.
https://techstartups.com/2022/02/26/new-swedish-study-shows-pfizer-vaccine-becomes-dna-liver-cells-fast-6-hours-vitro/

The DES Daughters:
“In 1971, researchers linked prenatal (while in the womb, or in utero) DES exposure to a type of cancer of the cervix and vagina called clear cell adenocarcinoma in a small group of women. Soon after, the Food and Drug Administration (FDA) notified health care providers throughout the country that DES should not be prescribed to pregnant women. The drug continued to be prescribed to pregnant women in Europe until 1978”
https://www.cancer.gov/about-cancer/causes-prevention/risk/hormones/des-fact-sheet

The HART group:
https://www.hartgroup.org/

The link to the Perseus report can be found on their website here:
MHRA – Is it safe and effective?
https://perseus.org.uk/

"HIGH IMPACT STRATEGIC CAMPAIGNING FOR CHILDREN AND THEIR FUTURES"
https://usforthem.co.uk/