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QUESTIONS ON NOTICE

Questions are currently being updated, please check back soon for previous questions.

204. Studies have shown that the weight of the protein produced by the mRNA vary by as much as 50% – surely this is evidence that the mRNA is not being produced in a consistent manner by the ribosomes? Is the TGA tracking the product being produced by the ribosomes? 221. Why is TGA/Pfizer calling it mRNA when it isn’t mRNA – the use of Methylpseudouridine means it’s a different substance does it not? 267. Which part of the mRNA code directs it to be processed on the ribosomes bound to the endoplasmic reticulum – could the TGA please state the name of the amino acid and what position the amino acid sits on the mRNA strand? 289. Is pseudouridine impervious to the mRNAse, the enzyme that breaks down mRNA?

21/11/2022

184. Can the TGA provide a breakout of its revenue stream by organisation? 205. Leaked emails from the EMA show they lodged a Major objection with Pfizer, namely that the possibility of translated proteins other than the translated protein resulting from truncated or modified mRNA should be addressed. Were these concerns addressed? The European Medicines Agency’s COVID-19 Vaccine Leaks: Hacks, Regulatory Pressures And Manufacturing Concerns – Health Policy Watch (healthpolicy-watch.news)

21/11/2022

96. There is no evidence that the blood lung barrier will allow IgG antibodies which weight around 150,000 Daltons to cross from the blood into the alveolar space of the lungs where Covid is infecting the epithelial cells. Given this is the case why do authorities claim the Covid vaccine can fight Covid which is present in the lungs? 97. I note that the TGA non-clinical report on the Pfizer vaccine showed there was very little difference in lung inflammation after 8 days in between vaccinated an unvaccinated monkeys. Given they weight 10kgs and got three times the dose of humans on what basis did this trial proof the vaccine was effective noting there was an IgG response for only 35 days. I note the weight to dose ratio for the monkeys was 20 times higher than humans so on that basis there may have been an IgG response for two days (35/20) or a lower IgG response.

21/11/2022

89. In the TGA non-clinical report it states “the S protein is synthesised and processed within the ER for surface expression or secretion.” Why is the vaccine stimulating the human body to export the spike protein from the cell – shouldn’t it be sterilising the virus rather than reproducing it? 90. What impact does the secretion of spike proteins have on the endothelium and other sensitive body organs? 91. Has the TGA done any research on the secretion of proteins from the cell as a result of the vaccine? If not, why not? 92. What evidence does the TGA have to prove that proteins secreted from the cells don’t cause clots and damage to body organs? 93. How does the TGA know that the ribosome translates the mRNA code 100% accurately and no mutations occur if no mutagenic studies have been done? 94. Has the TGA done any distribution and degradation studies to determine the potential toxicity of the secreted spike protein. If not, why not?

21/11/2022

63. Is it possible that the extreme length of the poly-A tail is contributing to longevity. The Roltgen cell paper (https://www.sciencedirect.com/science/article/pii/S0092867422000769) shows mRNA at 60 days post injection still producing spike antigen. Won’t this lead to t-cell exhaustion, as well as risking p53-dependent carcinogenesis risk? Immune imprinting, breadth of variant recognition, and germinal center response in human SARS-CoV-2 infection and vaccination (cell.com) 64. Doesn’t the pathway used by the mRNA vaccine to instruct the body cell’s to produce a toxic spike protein increase the risk of harm to the body? Isn’t the name of the game to kill the pathogen rather than reproduce it on an unknown time basis? 65. Does the vaccine induce an autoimmune response – either by T-cells attaching your own cells or white blood cells attacking protein (whatever its form) created by the vaccine and exported from the cell?

21/11/2022

66. Studies carried out on the lipid in rat trials showed it entered most body organs. Given that lipid concentrations were still increasing in most body organs, most notably the ovaries where it doubled from day 1 to day 2, why did the TGA not request more testing from Pfizer to determine just how long the lipids stay in the body before approving their vaccine? 67. How can the TGA guarantee that lipids that have entered body organs won’t damage those organs without longitudinal testing? 68. Why were biodistribution studies stopped after 9 days when it has been shown that mRNA, Lipids and spike proteins had been found in the body up to 60 days after the second vaccination? How can the TGA say with any confidence what the lifespan of the spike protein if they never tested it? Why didn’t the sponsor continue the trials given concentrations were increasing? 69. Why were no biodistribution studies performed with the spike protein? 70. Has the TGA now got comprehensive and exhaustive data that determines how long the lipids stay in the body. If not, then why are they allowing the rollout of the vaccine to continue? 75. Why is the lipid travelling around the body in increasing concentrations when many Health professionals said it would stay at the injection site?

21/11/2022

155. There are almost 20,000 serious injuries to date out of 20 million recipients in a 12- month period since the rollout began. This is an injury rate of 1 in 1000 people who have received the vaccine. This higher than the 1 in 3000 Prof Skerrit mentioned in regard to multi-inflammatory disease and also the few in a million side effects he quoted with John Laws. Given the rate of serious injury from the Covid-19 vaccine shouldn’t they be withdrawn? 156. What is the source of Prof Skerritt’s claim that Covid-19 causes multi-inflammatory disease in 1 in 3000 children? Can the source please be provided? 192. According to Moderna serious adverse events were recorded at one in 200 for six months to five years yet the TGA still approved this jab. Why did they do that knowing that the risk of the jab was 15 times greater than multi-inflammatory disease? I note factcheckers are claiming some of the trial participants already had underlying issues and that only one was an adverse event. This is still one in 1760 which is higher than one in 3000. https://www.nejm.org/doi/full/10.1056/NEJMoa2209367

21/11/2022

233. Can the TGA or Pfizer show studies that all of the mRNA gets taken up by the cells? 234. What happens to the lipid nanoparticles that don’t get taken up by the cells? 235. How long will a spike protein produced by the mRNA vaccine stay in the body? 236. For the mRNA/Lipid Nanoparticles that doesn’t get taken up by cells is there a risk they mutate and become toxic in the body? 237. If the genetic Covid-19 vaccine is damaged in handling or storage how does Pfizer/TGA know that the mRNA won’t produce mutations of the spike protein rather than the protein itself? 238. After the Covid vaccine is given how quickly will the body start to produce spike proteins and how quickly after that will the body start to produce antibodies? 246. What cells or organs is the mRNA code meant to go into – just muscle cells or other organ cells as well – has this been tested – how can the TGA guarantee that Lipid nanoparticles or spike proteins won’t go into other organs?

24/02/2022

204. Prior mRNA vaccine studies in rats resulted in the rats producing super numerary ribs. These are a sign of maternal distress are they not? 205. Given that animals studies indicated maternal distress from the mRNA vaccines why didn’t Pfizer perform more comprehensive studies on pregnant and breastfeeding women before rolling it out to the general population? Furthermore, why didn’t the TGA ask that Pfizer be more thorough in its investigations before approving for pregnant and breast feeding women in Australia?

24/02/2022

70. Two adverse events 703379, a 6 year old girl and 703334, a 7 year old boy have no details. In order to ensure full transparency around adverse events from children vaccines, can ATAGI ask the TGA to disclose what these injuries are? 71. Given the large number of adverse events in children already, will ATAGI revise its decision to allow the rollout of the vaccine given case numbers have dropped significantly and models have overestimated the infection rate in the community? 72. I note that ATAGI is relying on passive surveillance of vaccinated in children in the USA rather than active surveillance. How does ATAGI know that every adverse reaction experienced amongst the 6 million children in the USA has been detected, if the FDA/Pfizer is not actively monitoring every child?

24/02/2022

114. There is now a published case report of two adolescent deaths following vaccination due to toxic cardiomyopathy. https://pubmed.ncbi.nlm.nih.gov/35157759/ and one article reporting on cardiac arrest after covid 19 vaccination. https://www.cureus.com/articles/83238-cardiopulmonary-arrest-after-covid-19-vaccination-a-case-report. Will the TGA halt the rollout of the vaccine for children and teenagers given that cardiomyopathy was initially identified as the reported side effect by Pfizer for teenagers? 174. Why did the TGA dismiss the reported and suspected death of a 14 year old girl from the Moderna vaccine as not being vaccine related? 175. If State governments can shut down the country over cases of Covid why wasn’t the vaccine rollout for teenagers halted while the reported death of the 14 year old girl was being investigated? 245. According to FOI 3586 there has been 8 reported teenage deaths to date from the Covid-19 vaccines. Why hasn’t the rollout of vaccines for teenagers and children been suspended in light of these reports?

24/02/2022

204. Studies have shown that the weight of the protein produced by the mRNA vary by as much as 50% – surely this is evidence that the mRNA is not being produced in a consistent manner by the ribosomes? Is the TGA tracking the product being produced by the ribosomes? 221. Why is TGA/Pfizer calling it mRNA when it isn’t mRNA – the use of Methylpseudouridine means it’s a different substance does it not? 267. Which part of the mRNA code directs it to be processed on the ribosomes bound to the endoplasmic reticulum – could the TGA please state the name of the amino acid and what position the amino acid sits on the mRNA strand? 289. Is pseudouridine impervious to the mRNAse, the enzyme that breaks down mRNA?

21/11/2022

184. Can the TGA provide a breakout of its revenue stream by organisation? 205. Leaked emails from the EMA show they lodged a Major objection with Pfizer, namely that the possibility of translated proteins other than the translated protein resulting from truncated or modified mRNA should be addressed. Were these concerns addressed? The European Medicines Agency’s COVID-19 Vaccine Leaks: Hacks, Regulatory Pressures And Manufacturing Concerns – Health Policy Watch (healthpolicy-watch.news)

21/11/2022

96. There is no evidence that the blood lung barrier will allow IgG antibodies which weight around 150,000 Daltons to cross from the blood into the alveolar space of the lungs where Covid is infecting the epithelial cells. Given this is the case why do authorities claim the Covid vaccine can fight Covid which is present in the lungs? 97. I note that the TGA non-clinical report on the Pfizer vaccine showed there was very little difference in lung inflammation after 8 days in between vaccinated an unvaccinated monkeys. Given they weight 10kgs and got three times the dose of humans on what basis did this trial proof the vaccine was effective noting there was an IgG response for only 35 days. I note the weight to dose ratio for the monkeys was 20 times higher than humans so on that basis there may have been an IgG response for two days (35/20) or a lower IgG response.

21/11/2022

89. In the TGA non-clinical report it states “the S protein is synthesised and processed within the ER for surface expression or secretion.” Why is the vaccine stimulating the human body to export the spike protein from the cell – shouldn’t it be sterilising the virus rather than reproducing it? 90. What impact does the secretion of spike proteins have on the endothelium and other sensitive body organs? 91. Has the TGA done any research on the secretion of proteins from the cell as a result of the vaccine? If not, why not? 92. What evidence does the TGA have to prove that proteins secreted from the cells don’t cause clots and damage to body organs? 93. How does the TGA know that the ribosome translates the mRNA code 100% accurately and no mutations occur if no mutagenic studies have been done? 94. Has the TGA done any distribution and degradation studies to determine the potential toxicity of the secreted spike protein. If not, why not?

21/11/2022

63. Is it possible that the extreme length of the poly-A tail is contributing to longevity. The Roltgen cell paper (https://www.sciencedirect.com/science/article/pii/S0092867422000769) shows mRNA at 60 days post injection still producing spike antigen. Won’t this lead to t-cell exhaustion, as well as risking p53-dependent carcinogenesis risk? Immune imprinting, breadth of variant recognition, and germinal center response in human SARS-CoV-2 infection and vaccination (cell.com) 64. Doesn’t the pathway used by the mRNA vaccine to instruct the body cell’s to produce a toxic spike protein increase the risk of harm to the body? Isn’t the name of the game to kill the pathogen rather than reproduce it on an unknown time basis? 65. Does the vaccine induce an autoimmune response – either by T-cells attaching your own cells or white blood cells attacking protein (whatever its form) created by the vaccine and exported from the cell?

21/11/2022

66. Studies carried out on the lipid in rat trials showed it entered most body organs. Given that lipid concentrations were still increasing in most body organs, most notably the ovaries where it doubled from day 1 to day 2, why did the TGA not request more testing from Pfizer to determine just how long the lipids stay in the body before approving their vaccine? 67. How can the TGA guarantee that lipids that have entered body organs won’t damage those organs without longitudinal testing? 68. Why were biodistribution studies stopped after 9 days when it has been shown that mRNA, Lipids and spike proteins had been found in the body up to 60 days after the second vaccination? How can the TGA say with any confidence what the lifespan of the spike protein if they never tested it? Why didn’t the sponsor continue the trials given concentrations were increasing? 69. Why were no biodistribution studies performed with the spike protein? 70. Has the TGA now got comprehensive and exhaustive data that determines how long the lipids stay in the body. If not, then why are they allowing the rollout of the vaccine to continue? 75. Why is the lipid travelling around the body in increasing concentrations when many Health professionals said it would stay at the injection site?

21/11/2022

155. There are almost 20,000 serious injuries to date out of 20 million recipients in a 12- month period since the rollout began. This is an injury rate of 1 in 1000 people who have received the vaccine. This higher than the 1 in 3000 Prof Skerrit mentioned in regard to multi-inflammatory disease and also the few in a million side effects he quoted with John Laws. Given the rate of serious injury from the Covid-19 vaccine shouldn’t they be withdrawn? 156. What is the source of Prof Skerritt’s claim that Covid-19 causes multi-inflammatory disease in 1 in 3000 children? Can the source please be provided? 192. According to Moderna serious adverse events were recorded at one in 200 for six months to five years yet the TGA still approved this jab. Why did they do that knowing that the risk of the jab was 15 times greater than multi-inflammatory disease? I note factcheckers are claiming some of the trial participants already had underlying issues and that only one was an adverse event. This is still one in 1760 which is higher than one in 3000. https://www.nejm.org/doi/full/10.1056/NEJMoa2209367

21/11/2022

233. Can the TGA or Pfizer show studies that all of the mRNA gets taken up by the cells? 234. What happens to the lipid nanoparticles that don’t get taken up by the cells? 235. How long will a spike protein produced by the mRNA vaccine stay in the body? 236. For the mRNA/Lipid Nanoparticles that doesn’t get taken up by cells is there a risk they mutate and become toxic in the body? 237. If the genetic Covid-19 vaccine is damaged in handling or storage how does Pfizer/TGA know that the mRNA won’t produce mutations of the spike protein rather than the protein itself? 238. After the Covid vaccine is given how quickly will the body start to produce spike proteins and how quickly after that will the body start to produce antibodies? 246. What cells or organs is the mRNA code meant to go into – just muscle cells or other organ cells as well – has this been tested – how can the TGA guarantee that Lipid nanoparticles or spike proteins won’t go into other organs?

24/02/2022

204. Prior mRNA vaccine studies in rats resulted in the rats producing super numerary ribs. These are a sign of maternal distress are they not? 205. Given that animals studies indicated maternal distress from the mRNA vaccines why didn’t Pfizer perform more comprehensive studies on pregnant and breastfeeding women before rolling it out to the general population? Furthermore, why didn’t the TGA ask that Pfizer be more thorough in its investigations before approving for pregnant and breast feeding women in Australia?

24/02/2022

70. Two adverse events 703379, a 6 year old girl and 703334, a 7 year old boy have no details. In order to ensure full transparency around adverse events from children vaccines, can ATAGI ask the TGA to disclose what these injuries are? 71. Given the large number of adverse events in children already, will ATAGI revise its decision to allow the rollout of the vaccine given case numbers have dropped significantly and models have overestimated the infection rate in the community? 72. I note that ATAGI is relying on passive surveillance of vaccinated in children in the USA rather than active surveillance. How does ATAGI know that every adverse reaction experienced amongst the 6 million children in the USA has been detected, if the FDA/Pfizer is not actively monitoring every child?

24/02/2022

114. There is now a published case report of two adolescent deaths following vaccination due to toxic cardiomyopathy. https://pubmed.ncbi.nlm.nih.gov/35157759/ and one article reporting on cardiac arrest after covid 19 vaccination. https://www.cureus.com/articles/83238-cardiopulmonary-arrest-after-covid-19-vaccination-a-case-report. Will the TGA halt the rollout of the vaccine for children and teenagers given that cardiomyopathy was initially identified as the reported side effect by Pfizer for teenagers? 174. Why did the TGA dismiss the reported and suspected death of a 14 year old girl from the Moderna vaccine as not being vaccine related? 175. If State governments can shut down the country over cases of Covid why wasn’t the vaccine rollout for teenagers halted while the reported death of the 14 year old girl was being investigated? 245. According to FOI 3586 there has been 8 reported teenage deaths to date from the Covid-19 vaccines. Why hasn’t the rollout of vaccines for teenagers and children been suspended in light of these reports?

24/02/2022

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