I lost an uncle within 48 hours of his first jab too. Accountability can only be forced by revolution, or to take over the running of the country. Those with gene mutations that make them inefficient detoxers like mthfr, make up over 50% of the population. They are the most harmed and discriminated against in allopathic medicine. If we could mobilise them all, we would have a political party with support from over 50% of the population. We could then create a health system (which I’ve already designed over 20 years) that actually helps them and will also help the rest of the public even more, because currently we have no healthcare system. We could create a healthcare system that investigated cause, seeks to cure, and protects the susceptible of society. No more vaccines for inefficient detoxers. This would wipe out adverse events to vaccines and hypersensitivity to the environment( allergies)
"Interestingly, the NZ health authorities have just instructed drs in public health that they are no longer allowed to order genetic testing for any patients. "
Do you have source documentation for this or is it hearsay?
I would like to find out if Australian doctors have been similarly directed. I have tried to have blood tests done that indicate downstream effects of MTHFR variants, and one has been refused - the one that lets me know I've got it right, but so far, the other pathology requests have been fulfilled, so I am at least able to keep an eye on how my MTHFR management strategies are working.
I think in the long run, the genetic tests the doctors order are just for MTHFR and MTHFR variants alone are not enough to know what is going on in your body. Genes work in cycles and there is a cycle of genes that mess up the methylation process of which MTHFR is only one, so you really need the lot - which you won't get from a doctor.
I am working from an old Ancestry DNA test, which does include all the critical methylation genes (although often misses more obscure genes that might be important to me.) I will eventually get a more expensive test done that does the lot, but I am getting enough information to work with for now.
It is fairly pointless getting the test done by a doctor anyway (except for cost) as the doctors have no idea what to do with the information when the get it.
For those who have no idea what we are talking about, this article might help.
My dr told me but my dr is one of the freedom drs and us working in the private system, so as long as she doesn’t order testing through the state, and orders through private providers she can order them. It’s just the drs that accept money from the government that aren’t allowed to order them. My blood has been sent away and will come back with recommendations from their specialists and we will take it from there
Same system as here. So far I have been able to get everything free, except my original Ancestry test that I had done years back, as long as I skirt around the edges. But I fear doors will be closed once "the system" learns that we have caught on.
Fortunately, what we learn we learn, and that can't be taken away from us.
There are clearly two different tiers of medicine, one for "them" that costs big money to pay for and can be used to enhance their health, and one for us that the government pays for, and that is used to slowly but surely, and very profitably, destroy out health .
Doctors over here are treated no different to patients if they have an adverse event or neurotoxic injury, so they try hide adverse events if they happen to them as they know what happens to patients who claim an adverse event to a pharmaceutical product. Two radiologists suffered a neurotoxic event a few months back. But there was no investigation to test for the cause as the hospital isn’t allowed to investigate the cause of neurotoxic events. They just put them in hospital beds and treated symptoms in the hope they’d recover. But no tests to implicate any industry. It was neurotoxic fumes from something builders were using close by coming through the window.
Was there something you referred to that had the info of doctors being told they cannot do genetic testing? It would be nice to have an official document. Thank you for sharing all this. The memorial video was really nicely done.
I'm interested in the same for Aus. I have searched the Medicare website and got down to the pathology testing allowed and whether free or what it costs, but could find nothing on MTHFR or methylation. Tests paid for seem to be related to the risk of congenital deformities rather than epigenetics . This is the site for what it is worth.
No I don’t. My GP is one of the nzdsos drs. They have a private practice that accepts no money off the govt so they have more academic freedom. She told me on the 16th December that the advisory was sent to GPs in the public system. She is still able to order them, but not through the public health system. She has to go to a private company that does this testing.
New Zealanders are known for being quite apathetic. I doubt many would even react as they don’t want to admit they made a mistake and got the genocide jab. And many would also have coerced their family and friends so many of the vaccinated are in denial. They don’t want to admit they shortened their friends life so they ignore reality.
That's well said Mark but I would suggest that the apathy and inability to admit they participated in killing and injuring relatives is pretty common. People are people. I'm in Canada and our behaviour here is exactly the same as you described.
Thanks for reporting the Jab's effects via genetics. I vaguely recall some early 'China-Lab-Leak' extrapolation and discussion of the research of early 2020 - and the abstruse genomics that could steer human response to pathogens - by Race - which is ... BINGO! ... the 'Race Card' ... and still prohibited to discuss.
Your statement may be horrendously prophetic: "The adverse events target the susceptible based on their genetics. This will be beneficial to big pharma as it will wipe out those who have adverse events to their products."
It's my guess at this stage that the genocide is not so much racially targeted as volume based, and biased by race. I am speculating that the people currently dying are those with variants on the MTHFR gene, which reduces their capacity to detox amongst many other things. Around 50% of the white population and a little less of the black population, about 30% of the Asian and 0% of the Amish, carry these variants - overall around 45% of the global population. Variants on this gene make 21st century living extraordinarily hard - we are designed for a harsh and carnivorous lifestyle but not this one.
We can get fairly cheap genetic testing via the genealogy sites like Ancestry, although they are a bit hit and miss in their coverage. So far I have plenty to learn from my old Ancestry DNA test, but am speculating that I may need to get a Whole Genome Sequencing test at some stage to get into more obscure areas (I am trying to find the genetic source of Fibromyalgia (fibrositis).)
A lot of people who have implant allergy or allergy to metals or metal salts in dental work, often initially get diagnosed with fibromyalgia by allopathic drs. An LTT test or Melisa test will tell you if you are currently suffering any hypersensitivities to metals. Life is very hard for people suffering from metal hypersensitivity, especially when neurotoxic metals are involved. Once you remove the metal causing the problems, you are no longer hypersensitive and suddenly life is easy again.
I can attest to that with aluminium. It is virtually impossible to remove all exposure to aluminium as well, but I have managed to reduce it enough that casual exposure no longer knocks me out. I learned that what I thought was gluten sensitivity was actually aluminium sensitivity, with almost all gluten rich product being treated with, cooked with or cooked in aluminium. I can now consume gluten as long as the food has not been in contact with aluminium.
I wanted to ask you about the silica. I cannot get high silica mineral water, except Fiji which is in terrible low grade plastic, and so was given some of this product to try. I have no idea if it is detoxing aluminium or not. https://grassesoflife.com.au/product/activated-silica-45ml/
I doubt it would work. It has to be orthosilicilic acid in water so it the aluminium can be taken out in your urine. You can make orthosilicilic acid using biochemist Dennis n crouses recipe. That’s what I do and it’s a lot cheaper than buying Fiji water. Dr Robert Yoho from the surviving healthcare Substack interviewed Dennis too. Here’s the link to the recipe.
One of the names listed here was a personal friend and dearly missed. There must be accountability. When? How?
I lost an uncle within 48 hours of his first jab too. Accountability can only be forced by revolution, or to take over the running of the country. Those with gene mutations that make them inefficient detoxers like mthfr, make up over 50% of the population. They are the most harmed and discriminated against in allopathic medicine. If we could mobilise them all, we would have a political party with support from over 50% of the population. We could then create a health system (which I’ve already designed over 20 years) that actually helps them and will also help the rest of the public even more, because currently we have no healthcare system. We could create a healthcare system that investigated cause, seeks to cure, and protects the susceptible of society. No more vaccines for inefficient detoxers. This would wipe out adverse events to vaccines and hypersensitivity to the environment( allergies)
"Interestingly, the NZ health authorities have just instructed drs in public health that they are no longer allowed to order genetic testing for any patients. "
Do you have source documentation for this or is it hearsay?
I would like to find out if Australian doctors have been similarly directed. I have tried to have blood tests done that indicate downstream effects of MTHFR variants, and one has been refused - the one that lets me know I've got it right, but so far, the other pathology requests have been fulfilled, so I am at least able to keep an eye on how my MTHFR management strategies are working.
I think in the long run, the genetic tests the doctors order are just for MTHFR and MTHFR variants alone are not enough to know what is going on in your body. Genes work in cycles and there is a cycle of genes that mess up the methylation process of which MTHFR is only one, so you really need the lot - which you won't get from a doctor.
I am working from an old Ancestry DNA test, which does include all the critical methylation genes (although often misses more obscure genes that might be important to me.) I will eventually get a more expensive test done that does the lot, but I am getting enough information to work with for now.
It is fairly pointless getting the test done by a doctor anyway (except for cost) as the doctors have no idea what to do with the information when the get it.
For those who have no idea what we are talking about, this article might help.
https://curingcoviddiseases.substack.com/p/its-all-about-methylation-everything
My dr told me but my dr is one of the freedom drs and us working in the private system, so as long as she doesn’t order testing through the state, and orders through private providers she can order them. It’s just the drs that accept money from the government that aren’t allowed to order them. My blood has been sent away and will come back with recommendations from their specialists and we will take it from there
Same system as here. So far I have been able to get everything free, except my original Ancestry test that I had done years back, as long as I skirt around the edges. But I fear doors will be closed once "the system" learns that we have caught on.
Fortunately, what we learn we learn, and that can't be taken away from us.
There are clearly two different tiers of medicine, one for "them" that costs big money to pay for and can be used to enhance their health, and one for us that the government pays for, and that is used to slowly but surely, and very profitably, destroy out health .
You might be interested in this article posted today. Flashing red lights. https://www.mendelspod.com/p/ai-and-the-future-of-genetic-testing
Doctors over here are treated no different to patients if they have an adverse event or neurotoxic injury, so they try hide adverse events if they happen to them as they know what happens to patients who claim an adverse event to a pharmaceutical product. Two radiologists suffered a neurotoxic event a few months back. But there was no investigation to test for the cause as the hospital isn’t allowed to investigate the cause of neurotoxic events. They just put them in hospital beds and treated symptoms in the hope they’d recover. But no tests to implicate any industry. It was neurotoxic fumes from something builders were using close by coming through the window.
Was there something you referred to that had the info of doctors being told they cannot do genetic testing? It would be nice to have an official document. Thank you for sharing all this. The memorial video was really nicely done.
I'm interested in the same for Aus. I have searched the Medicare website and got down to the pathology testing allowed and whether free or what it costs, but could find nothing on MTHFR or methylation. Tests paid for seem to be related to the risk of congenital deformities rather than epigenetics . This is the site for what it is worth.
https://www9.health.gov.au/mbs/search.cfm?cat1=147&cat2=156&cat3=&adv=
No I don’t. My GP is one of the nzdsos drs. They have a private practice that accepts no money off the govt so they have more academic freedom. She told me on the 16th December that the advisory was sent to GPs in the public system. She is still able to order them, but not through the public health system. She has to go to a private company that does this testing.
Wow - this is really big. I wonder if the general population has any idea and how they would react if they did?
New Zealanders are known for being quite apathetic. I doubt many would even react as they don’t want to admit they made a mistake and got the genocide jab. And many would also have coerced their family and friends so many of the vaccinated are in denial. They don’t want to admit they shortened their friends life so they ignore reality.
That's well said Mark but I would suggest that the apathy and inability to admit they participated in killing and injuring relatives is pretty common. People are people. I'm in Canada and our behaviour here is exactly the same as you described.
Thanks for reporting the Jab's effects via genetics. I vaguely recall some early 'China-Lab-Leak' extrapolation and discussion of the research of early 2020 - and the abstruse genomics that could steer human response to pathogens - by Race - which is ... BINGO! ... the 'Race Card' ... and still prohibited to discuss.
Your statement may be horrendously prophetic: "The adverse events target the susceptible based on their genetics. This will be beneficial to big pharma as it will wipe out those who have adverse events to their products."
It's my guess at this stage that the genocide is not so much racially targeted as volume based, and biased by race. I am speculating that the people currently dying are those with variants on the MTHFR gene, which reduces their capacity to detox amongst many other things. Around 50% of the white population and a little less of the black population, about 30% of the Asian and 0% of the Amish, carry these variants - overall around 45% of the global population. Variants on this gene make 21st century living extraordinarily hard - we are designed for a harsh and carnivorous lifestyle but not this one.
We can get fairly cheap genetic testing via the genealogy sites like Ancestry, although they are a bit hit and miss in their coverage. So far I have plenty to learn from my old Ancestry DNA test, but am speculating that I may need to get a Whole Genome Sequencing test at some stage to get into more obscure areas (I am trying to find the genetic source of Fibromyalgia (fibrositis).)
A lot of people who have implant allergy or allergy to metals or metal salts in dental work, often initially get diagnosed with fibromyalgia by allopathic drs. An LTT test or Melisa test will tell you if you are currently suffering any hypersensitivities to metals. Life is very hard for people suffering from metal hypersensitivity, especially when neurotoxic metals are involved. Once you remove the metal causing the problems, you are no longer hypersensitive and suddenly life is easy again.
I can attest to that with aluminium. It is virtually impossible to remove all exposure to aluminium as well, but I have managed to reduce it enough that casual exposure no longer knocks me out. I learned that what I thought was gluten sensitivity was actually aluminium sensitivity, with almost all gluten rich product being treated with, cooked with or cooked in aluminium. I can now consume gluten as long as the food has not been in contact with aluminium.
I wanted to ask you about the silica. I cannot get high silica mineral water, except Fiji which is in terrible low grade plastic, and so was given some of this product to try. I have no idea if it is detoxing aluminium or not. https://grassesoflife.com.au/product/activated-silica-45ml/
Here’s the interview with Dennis Crouse
https://open.substack.com/pub/robertyoho/p/death-by-aluminum-part-2-our-automatic?r=1e6k8r&utm_medium=ios
I doubt it would work. It has to be orthosilicilic acid in water so it the aluminium can be taken out in your urine. You can make orthosilicilic acid using biochemist Dennis n crouses recipe. That’s what I do and it’s a lot cheaper than buying Fiji water. Dr Robert Yoho from the surviving healthcare Substack interviewed Dennis too. Here’s the link to the recipe.
https://prevent-alzheimers-autism-stroke.com/silicade/
The biolabs in Ukraine were working on pathogens that target certain genetics