My name is Dr. Michael Yeadon. My original training was first class honors degree in bio chemistry and toxicology, followed by a researched based PHD in respiratory pharmacology and after that I’ve worked my entire life on the research side of the pharmaceutical industry, both Big Pharma and also biotech. My specific focus has been inflammation, immunology, allergy.

In the context of respiratory diseases so the lung but also the skin so I would say I’m kind of a deeply experienced inflammation immunology pulmonology kind of research person.

I am an Allergy & Respiratory Therapeutic Area expert with 23 years in the pharmaceutical industry.

I trained as a biochemist and pharmacologist, obtaining my PhD from the University of Surrey (UK) in 1988. I then worked at the Wellcome Research Labs with Salvador Moncada with a research focus on airway hyper-responsiveness and effects of pollutants including ozone and working in drug discovery of 5-LO, COX, PAF, NO and lung inflammation. With colleagues, he was the first to detect exhaled NO in animals and later to induce NOS in lung via allergic triggers. Joining Pfizer in 1995, I was responsible for the growth and portfolio delivery of the Allergy & Respiratory pipeline within the company. I was responsible for target selection and the progress into humans of new molecules, leading teams of up to 200 staff across all disciplines and won an Achievement Award for productivity in 2008. Under my leadership the research unit invented oral and inhaled NCEs which delivered multiple positive clinical proofs of concept in asthma, allergic rhinitis and COPD. I led productive collaborations such as with Rigel Pharmaceuticals (SYK inhibitors) and was involved in the licensing of Spiriva and acquisition of the Meridica (inhaler device) company. I have published over 40 original research articles and now consult and partner with a number of biotechnology companies.

Before working with Apellis, I was VP and Chief Scientific Officer (Allergy & Respiratory Research) with Pfizer. I left on excellent terms and Pfizer was even a partial investor in my next venture.

1.Senior principle scientist, Wellcome Research (1998-1995)

2. Chief scientific officer, Allergy and Respiratory research, Pfizer R&D (1995-2011)

3. Vice President Allergy and respiratory Head, Research head, Research Pfizer R&D (2005-2008)

4. CSO and Vice President, Allergy and respiratory research Head. Pfizer Global R&D (2006-2011)

5. Consultant (scientific advisory board) Pulmatrix (2011-2016)

6. Consultant Apellis Pharmaceuticals (2011-2016)

7. Co founder of Ziarco (2011-2017)

I have no conflicts of interest and nothing to gain from this testimony. In fact, I have lost decades old friends and been defamed and attacked by mainstream media for speaking my truth based in real science.

It’s a big claim that I’m going to say. I’m afraid I came to the conclusion that literally every single one of the narrative points by that all government tells you about this virus and what you should do, they are all lies.

The injectable products called messenger RNA (mRNA) based vaccines are inherently unsafe.

The mechanism of action is to instruct cells of the recipient to make the protein encoded by the mRNA. When a human cell manufactures a non-self, or foreign protein, our immune system recognises this as dangerous and kills that cell creating an auto immune like disorder. This is basic immunology and it is beyond question that the pharmaceutical companies associated with these products did know that. The design of these products was the result of a series of design decisions.

Each of the decisions made compounded the risk to human health, as we will show. For example, choosing *spike protein as the immunogen meant that recipients cells were instructed to make a toxic product. Additionally, the mRNA was chosen to be formulated in lipid nanoparticles (LNP), which are inherently toxic, accumulates in the ovaries and is able to travel everywhere in the body.

The immune responses to this injected material resulted in predictable and predicted toxicities, ranging from temporary illness all the way to death, as well as damaging fertility in the survivors. 

The only reasonable conclusion is that these preparations are “toxic by design”, with all the implications that follow from this conclusion.