Just how does my mention of the influence of the Illuminati change anything? The world has been under the thumb of a small class of people for hundreds of years now. Dwight Eisenhower made an error in his exit speech from the Presidency. He said: "Beware of the Military/Industrial complex." He should have said: "Beware of the Military/Industrial/pharmaceutical complex."
Bayer Corporation, a subsidiary of the now defunct conglomerate I. G. Farben operated the death camp Buchenwald/Auschwitz where humans were subjected to vaccine experimentation. They were perfecting the nostrums that are given to our children today. The intent being to induce disease later in life from the treatment of which they can profit while eliminating the victim after their productive role in society has ended i.e., retirement. Today they push the flu nostrums so as to hasten their demise. The fact that biological cooties are involved isn't the point. As I have said and will say again, it is impossible for vaccines to work at all once you understand the disease processes. Doctors today are ignorant of that but 100 years ago, it was the basis of sane medical practice. Diseases that today we are told are incurable were routinely dealt with quite successfully way back then when men of medicine had integrity.
Today it's all about the money. Oncologists, for example, know very well that the treatments they dispense don't work. They don't care that the patient suffers excruciating agony while every dime is squeezed out of their body fluids. IMHO oncologists are nothing but sociopathic dungeon masters. Caveat Emptor! Carmi Hazen
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Ebolagate
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Irene de Villiers
- Posts: 3237
- Joined: Sat Aug 02, 2014 10:00 pm
Re: Ebolagate
Dear Soroush,
It is true that viral hemorrhagic fevers (VHF) in general, have been around for a long time. I think there is one recorded in Mexico as far back as the mid-15 th century. Local communities pass on memoriers of illnesses in their area for generations, they do not slip by unnoticed.
Yellow fever killed huge numbers in the 18th century..
However that does not mean they all go back a long way. That would be opposite of what is expected with the way viruses mutate and evolve.
There is always a trigger mechanism for a VHF to cause illness in a specific species. Close crowding of two species will tend to cause it to jump species by adapting, and for exampe that is how we got the 1918 flu.
Similarly the AIDS virus has jumped species from cat to monkey then from monkey to human. You do not find all three kinds present in remains of individuals an equal number of years back. The human one only started mid-last ventury. No human remains earlier than that show it. But similan rmains show it a lot further back, and cats still further.
Each virus has a different length of history, and came into being to take advantage of a specific circumstance.
It's not that they can read the circumstance and take advantage. They can not. It is simpler than that. Viruses mutate all the time randomly into ones with specific new genes. The great majority of those new mutations are "nonsense" mutations for things that can not be used at the time. They have no fertile ground to use the new mutation. But there are only so many genes that can be made, and sooner or later every possible mutation WILL be made, and if there is a way to use it - well then they use it. No brains involved - just cirucmstances.
SO - A virus will adapt and mutate to a new form, and take advantage of any change in its environment. For example:
The fact that humans are so overvaccinated that they have practically no thmus finction left, means that they are ripe for attack by viruses using the immune system cells such as monocytes and macrophages. Any virus can randomly mutate to use that weakness we have. Many new viruses have mutated since vaccines became general use thymus poison, to take advantage of that involuted thymus now called "normal" by the medical profession.
ALL those viruses did not exist before vaccines as there was no fertile substrate for them before that. A mutation to use that apprach would have been killed by Thq1 cytokines triggering neutrophils to engulf the virus and macrophage to remove the rsult from the body - BEFORE it coud infect by entering a monocyte or macrophage or T-cell or whatever.
The VHFs have developed over time according to what family they belong to, as each has specific mechanisms it uses, which had to have fertile environment to take advantage of before the new virus could mutate into existence and survive due to favorable environment. Mutations normally do not survive.
There are at least five separate virus families from which viral hemorrhagic fevers (VHFs) occur, with the (by definition) commonality of "tendency to bleed" plus "fever". Other symptoms vary widely. The ones from long ago do not use mechaniusms related to thymus health, wich humans now destroy on a regular basis, causing LOTS of new viruses to make successful use of the resultant weakkness and survive.
Each virus family uses different techniques and has a different shape to accommodate their tecniques.
The EBola may have been in animals for some time, but its transfer to huamns in Africa IS new.
I can so far find no research to show Ebola evolved/mutated before 1976, to affect humans. I have so far not found research to show how long it goes back in animals, but that has to be a lot longer, as at least three species can get ill from it (chimpanzees, monkeys and duikers) and that suggests at least three opportunistic mutations before the one to humans.
The virus group to which Ebola affecting humans belongs, is not an old one however. There is no evidence of filoviruses a long time ago, though there is plenty of evidence for many other VHFs.
Ebola and Marburg alone, as VHFs, belong to the Filovirus family. ALL other VHFs beloing to the other four or five virus families and use completely different mechanisms:
Arenviridae eg Lasso, Lujo, Venezuelan etc VHFs
Bunyviridae eg Hanta, Rift Valley, etc VHFs
Flaviviridae eg Dengue, Yellow Fever VHFs, etc
Rhadboviridae eg Bas-Congo VHF
Ebola and Marburg belong to Filoviridae.
Filovirus is using a thymus/immune system involution weakness for its mechanism - typical of the NEW virus mutations since thymus damage became the western medical standard of operation even in babies, in mid-20th century. It is since then, that we have seen the most disastrous virus mutations, all of them taking advantage of damaged thymus.
We see Ebola where vaccines have been dished out - and it matters not what vaccine is dished out - they ALL cause thymus involution - as do any serioiusly toxic drugs - eg AIDS drugs - also handed out in Africa.
Drs and drug companies KNOW this thymus damage occurs - they just keep silent about it.
(Just this week my new Dr invited me to have a flu vaccine and a pneumonia one. I declined saying No thanks, I value my thymus health. The Dr had no response as there is none.)
It is the normal function of the thymus to ensure that all foreign invaders are engulferd and removed BEFORE they can infect. This new stupidity to induce excessive antibodies at the EXPENSE of the thymus, (skewing the immune system away from TH-1 activity towards excess Th-2 antibody activity) means there is NO first line of defence at all - no macrophage and neutrophil etc activity, to remove invaders BEFORE they cause disease.
Antibodies are useless things, only called into play AFTER an infection is not only established but is out of hand and thus needing "extra" secondary immune system forces.
In addition the new viruses (like Ebola, FIP, etc) have developed a defence against those antibodies anyway, called ADE for Antibody dependent enhancement. LOTS of the new viruses have that mutation to ADE capability. Viruses will take ANY advantage we give them and mutate a way to use it. They set up receptors on those vulnerable macrophages, to use up any antibodies trying to come to the rescue, and turn the macrophages into easy entry cells instead, to enhance or speed up the virus attack - the opposite of what vaccines are supposed to help do in theory. (There are now many illness for which a antibody-making vaccine has no way to work, becasue of the skewed mechanisms of a particular virus.)
So Ebola is easily seen to have the mutations needed to take advantage of the damaged thymus, and filoviruses are long filaments which wrap themseles all over an immue cell such as a macrophage, with attack projections all over it, so that they force the cell to engulf them inside where thery can take over. The fact that Ebola uses a mechanism for the modern damaged thymus, is proof it is a new virus. There was no vulnerable thymus as standard in an unvaccinated population - and no human Ebola then. (Nor HIV or FIP for that matter. These kinds of viral attack were rare before vaccines. To quote as pecific, FIP was extremely rare before it was first seenin the 1960s, and now kills 10 million cats per year, increasing at the ratye at qhich cats are vaccinated. There is no mystery there, except for those collecting cat vaccine/spay/drug dollars with blinders on.)
We can expect more and more horrendously nasty viruses to mutate to take advantage of our nonexistent first defence and innate chronic defence immune systems via the thymus and TH-1 cytokine side plus their now destroyed mechanisms to engulf invaders before they attack (whether the attack is needed for cancer cells or Ebola viruses or MRSA bacteria or some other chronic condition for which our natural innate defense no longer exists) - now all lost to vaccine skewed systems - thanks to modern medicine.
I firmly believe - due to the strong evidence - that Ebola is one of these new viruses taking advantage of the new thymus damaged environment - and not an old virus that kiulled many but nobody in Africa noticed or mentioned it somehow. It's MECHANISM would not have worked till after vaccines became widespread.
Namaste,
Irene
--
Irene de Villiers, B.Sc AASCA MCSSA D.I.Hom/D.Vet.Hom.
P.O. Box 4703 Spokane WA 99220.
www.angelfire.com/fl/furryboots/clickhere.html (Veterinary Homeopath.)
"Man who say it cannot be done should not interrupt one doing it."
It is true that viral hemorrhagic fevers (VHF) in general, have been around for a long time. I think there is one recorded in Mexico as far back as the mid-15 th century. Local communities pass on memoriers of illnesses in their area for generations, they do not slip by unnoticed.
Yellow fever killed huge numbers in the 18th century..
However that does not mean they all go back a long way. That would be opposite of what is expected with the way viruses mutate and evolve.
There is always a trigger mechanism for a VHF to cause illness in a specific species. Close crowding of two species will tend to cause it to jump species by adapting, and for exampe that is how we got the 1918 flu.
Similarly the AIDS virus has jumped species from cat to monkey then from monkey to human. You do not find all three kinds present in remains of individuals an equal number of years back. The human one only started mid-last ventury. No human remains earlier than that show it. But similan rmains show it a lot further back, and cats still further.
Each virus has a different length of history, and came into being to take advantage of a specific circumstance.
It's not that they can read the circumstance and take advantage. They can not. It is simpler than that. Viruses mutate all the time randomly into ones with specific new genes. The great majority of those new mutations are "nonsense" mutations for things that can not be used at the time. They have no fertile ground to use the new mutation. But there are only so many genes that can be made, and sooner or later every possible mutation WILL be made, and if there is a way to use it - well then they use it. No brains involved - just cirucmstances.
SO - A virus will adapt and mutate to a new form, and take advantage of any change in its environment. For example:
The fact that humans are so overvaccinated that they have practically no thmus finction left, means that they are ripe for attack by viruses using the immune system cells such as monocytes and macrophages. Any virus can randomly mutate to use that weakness we have. Many new viruses have mutated since vaccines became general use thymus poison, to take advantage of that involuted thymus now called "normal" by the medical profession.
ALL those viruses did not exist before vaccines as there was no fertile substrate for them before that. A mutation to use that apprach would have been killed by Thq1 cytokines triggering neutrophils to engulf the virus and macrophage to remove the rsult from the body - BEFORE it coud infect by entering a monocyte or macrophage or T-cell or whatever.
The VHFs have developed over time according to what family they belong to, as each has specific mechanisms it uses, which had to have fertile environment to take advantage of before the new virus could mutate into existence and survive due to favorable environment. Mutations normally do not survive.
There are at least five separate virus families from which viral hemorrhagic fevers (VHFs) occur, with the (by definition) commonality of "tendency to bleed" plus "fever". Other symptoms vary widely. The ones from long ago do not use mechaniusms related to thymus health, wich humans now destroy on a regular basis, causing LOTS of new viruses to make successful use of the resultant weakkness and survive.
Each virus family uses different techniques and has a different shape to accommodate their tecniques.
The EBola may have been in animals for some time, but its transfer to huamns in Africa IS new.
I can so far find no research to show Ebola evolved/mutated before 1976, to affect humans. I have so far not found research to show how long it goes back in animals, but that has to be a lot longer, as at least three species can get ill from it (chimpanzees, monkeys and duikers) and that suggests at least three opportunistic mutations before the one to humans.
The virus group to which Ebola affecting humans belongs, is not an old one however. There is no evidence of filoviruses a long time ago, though there is plenty of evidence for many other VHFs.
Ebola and Marburg alone, as VHFs, belong to the Filovirus family. ALL other VHFs beloing to the other four or five virus families and use completely different mechanisms:
Arenviridae eg Lasso, Lujo, Venezuelan etc VHFs
Bunyviridae eg Hanta, Rift Valley, etc VHFs
Flaviviridae eg Dengue, Yellow Fever VHFs, etc
Rhadboviridae eg Bas-Congo VHF
Ebola and Marburg belong to Filoviridae.
Filovirus is using a thymus/immune system involution weakness for its mechanism - typical of the NEW virus mutations since thymus damage became the western medical standard of operation even in babies, in mid-20th century. It is since then, that we have seen the most disastrous virus mutations, all of them taking advantage of damaged thymus.
We see Ebola where vaccines have been dished out - and it matters not what vaccine is dished out - they ALL cause thymus involution - as do any serioiusly toxic drugs - eg AIDS drugs - also handed out in Africa.
Drs and drug companies KNOW this thymus damage occurs - they just keep silent about it.
(Just this week my new Dr invited me to have a flu vaccine and a pneumonia one. I declined saying No thanks, I value my thymus health. The Dr had no response as there is none.)
It is the normal function of the thymus to ensure that all foreign invaders are engulferd and removed BEFORE they can infect. This new stupidity to induce excessive antibodies at the EXPENSE of the thymus, (skewing the immune system away from TH-1 activity towards excess Th-2 antibody activity) means there is NO first line of defence at all - no macrophage and neutrophil etc activity, to remove invaders BEFORE they cause disease.
Antibodies are useless things, only called into play AFTER an infection is not only established but is out of hand and thus needing "extra" secondary immune system forces.
In addition the new viruses (like Ebola, FIP, etc) have developed a defence against those antibodies anyway, called ADE for Antibody dependent enhancement. LOTS of the new viruses have that mutation to ADE capability. Viruses will take ANY advantage we give them and mutate a way to use it. They set up receptors on those vulnerable macrophages, to use up any antibodies trying to come to the rescue, and turn the macrophages into easy entry cells instead, to enhance or speed up the virus attack - the opposite of what vaccines are supposed to help do in theory. (There are now many illness for which a antibody-making vaccine has no way to work, becasue of the skewed mechanisms of a particular virus.)
So Ebola is easily seen to have the mutations needed to take advantage of the damaged thymus, and filoviruses are long filaments which wrap themseles all over an immue cell such as a macrophage, with attack projections all over it, so that they force the cell to engulf them inside where thery can take over. The fact that Ebola uses a mechanism for the modern damaged thymus, is proof it is a new virus. There was no vulnerable thymus as standard in an unvaccinated population - and no human Ebola then. (Nor HIV or FIP for that matter. These kinds of viral attack were rare before vaccines. To quote as pecific, FIP was extremely rare before it was first seenin the 1960s, and now kills 10 million cats per year, increasing at the ratye at qhich cats are vaccinated. There is no mystery there, except for those collecting cat vaccine/spay/drug dollars with blinders on.)
We can expect more and more horrendously nasty viruses to mutate to take advantage of our nonexistent first defence and innate chronic defence immune systems via the thymus and TH-1 cytokine side plus their now destroyed mechanisms to engulf invaders before they attack (whether the attack is needed for cancer cells or Ebola viruses or MRSA bacteria or some other chronic condition for which our natural innate defense no longer exists) - now all lost to vaccine skewed systems - thanks to modern medicine.
I firmly believe - due to the strong evidence - that Ebola is one of these new viruses taking advantage of the new thymus damaged environment - and not an old virus that kiulled many but nobody in Africa noticed or mentioned it somehow. It's MECHANISM would not have worked till after vaccines became widespread.
Namaste,
Irene
--
Irene de Villiers, B.Sc AASCA MCSSA D.I.Hom/D.Vet.Hom.
P.O. Box 4703 Spokane WA 99220.
www.angelfire.com/fl/furryboots/clickhere.html (Veterinary Homeopath.)
"Man who say it cannot be done should not interrupt one doing it."