To whom it may concern,
I am watching with terrible sorrow and trepidation the developments in Israel regarding the immunization of the population with the H1N1 vaccines.
This morning I spoke at great length with officials at the Ministry of Health: with the ICDC, with the AGAF LESHEAT CHERUM, with Prof. Dan Engelhard, and with Dr. Alex Leventhal. In addition I called Meuchedet, Clalit, and Maccabi, to get information on procedures and decisions in different parts of the country.
When I called the ICDC, the first person I spoke to was an ARAB, a Dr. Ahmed Kabha, who told me he was in charge. I almost fainted. But afterwards, while speaking with a Dr. Michal Bloomberg there, she explained to me that the ICDC, the equivalent of the CDC in the US ( Center for Disease Control), is only in charge of INFORMING the public, not making decisions as to who gets what.
Nevertheless, one of the officials with whom I spoke, ( unfortunately I did not get her name), had the gall to ask me, after I identified myself as a physician:
"Why do you want to know these things? WHY DO YOU THINK YOU HAVE THE RIGHT TO ASK THESE QUESTIONS?"
And after she gave me the telephone numbers of Professor Engelhard and Dr. Alex Leventhal, she said; " You deceived me, I thought you were working for one of the Kupot Cholim, I should not have given you these numbers."
Obviously there is a certain amount of SECRECY involved, even as regards PHYSICIANS. They want to keep the information IN HOUSE, so to speak. You will understand why as you read further.
Here is how it works.
The new Director of the Ministry of Health , Dr. Eitan CHAI AM, is ultimately the one who makes decisions re: the H1N1 vaccine. He makes his decisions based on the recommendations of a group of about 30 physicians, specialists in their own fields, the head of whom is Professor Engelhard, professor of pediatrics - infectious diseases - at Hadassah Hospital, Jerusalem.
Dr. Alex Leventhal is the doctor in charge of LIAISON with the W.H.O. and the European countries.
The Agaf Lesheat Cherum follows the directives of Dr. Chai Am, and gives the orders as to what to give to whom.
The various Kupot Cholim order their own vaccines as needed.
First of all, from my discussion with Dr. Alex Leventhal, whom I had met a while ago regarding another topic, (at which time his response had been: "WE CANNOT GO AGAINST WHAT THEY DO IN EUROPE, WE CANNOT GO AGAINST THE W.H.O.!"), this is what I gathered;
Israel , like ALL OTHER COUNTRIES IN THE WORLD, he told me - WHICH IS INACCURATE, HE FAILED TO MENTION THAT THE VATICAN IS NOT OBLIGATED TO DO THE W.H.O.'s bidding - for the past 60 years -( but then he mentioned the year 1929, which would make it 80 years, and incidentally 1929 is both the year the VATICAN WAS FOUNDED AS A COUNTRY AND BECAME A POLITICAL POWER, and the year TARPAT MASSACRES TOOK PLACE, before the creation of the state of Israel, so maybe it was either the British Mandate or the Jewish Agency he is talking about, I don't know, -)
so, for the past 60 - or 80 - years, Israel has had an agreement with the W.H.O., according to which it must follow the directives of the WHO. But it is understood that every country has to act according to the individual needs of that specific country.
So I asked him: If W.H.O. says white, and Israel says black, will it be black?
NO, he said, it will be somewhere in between. With other words, the decisions by the Ministry of Health are ALWAYS tainted by the RECOMMENDATIONS OF THE W.H.O.; NO TOTAL INDEPENDENCE HERE; but there is a certain amount of wiggling room available.
This tells me that we COULD make a change here, if we tried hard enough. How much of a change remains too be seen.
Next, Professor Engelhard ADMITTED that he knows all about the squalene, the polysorbate 80 etc. in the vaccines, but that the group of doctors decided , based on statistics from the WHOLE world, on death and dying from the H1N1 virus, that the balance is in favor of giving the H1N1 vaccine anyway.
To be noted here is that the published CDC statistics are false: about 97% of their alleged deaths from H1N1 were actually related to other, overwhelming health conditions of the patients who died from so -called H1N1, and/or in most cases, H1N1 was not proven to be the infectious agent at all. Overall, in reality, the 2009 H1N1 " pandemic"' has been quite mild as compared to other major viral pandemics.
"Funny how when someone dies of swine flu with a pre-existing condition they died from swine flu - no question. And if someone dies from the vaccine with a pre-existing condition they died from the pre-existing condition - no question."
Now please pay attention to this item:
Germany's newspaper Tagesspiegel analyses the thesis of Wolf-Dieter Ludwig, head doctor of the Helios Klinikim Berlin-Buch, that the "swine flu" pandemic is just "a piece of theatre with which the pharma companies want to earn money", - and comes to the conclusion that
1) there are almost no medical experts left in government or universities who are independent of big pharma;
2) researchers and managers are following the same goal, namely, to get their products used, "if necessary without a real emergency".
Tagesspiegel looks into the "questionable" alliance between big pharma and government.
Twelve of the 16 members of the "vaccine commission" at the Robert Koch Institute have links to big pharma, notes the report.
Robert Haas, who coordinates Germany's pandemic planning at the Robert Koch Institute, is also an advisor of the„European Scientific Working Group on Influenza“, which is financed by GlaxoSmithKline (GSK), Novartis, Baxter und Sanofi and lobbies for their drugs.
„President“ of the lobby group is the Dutch virologist Albert Ostherhaus, who is also the member of a working group established by WHO to develop the swine flu jab.
The head of the WHO expert group for vaccines is David Salisbury, the head of the vaccine department of the UK Health Ministry, who is reported to have lobbied for pharma companies to get immunity.
Salisbury also had a key role in WHO's recommendation to implement mass global vaccination with the "swine flu" jab this July even though the safety of the jab is unpreoven.
Epidemiologist Klaus Stöhr, the head of a WHO-flu programme, has been pushing the idea that a pandemic is inevitable and will cost millions of lives.
Stöhr started working for Novartis in 2007.
The report says that big pharma companies finance almost all medical research today and so have acquired undue influence on it and government health policy.
This is the report in German:
The two vaccines that have arrived in Israel and are already being distributed are PANDEMRIX, FROM GLAXO SMITH KLINE and FOCETRIA, FROM NOVARTIS. Sanofi-Pasteur's vaccine will follow.
Pandemrix will be given in two doses to children from ages 3 to 10, while Focetria will be given to adults. Pregnant women will receive the unadjuvanted vaccine from Sanofi-Pasteur.
To be noted that Israel - according to the Ministry of Health - follows THE EUROPEAN MODEL . Focetria and Pandemrix were approved by the EMEA on September 25, 2009, for all 27 countries of Europe. Israel is joining that group. Both Pandemrix and Focetria were approved only for exceptional circumstances.
Now, for your information, they contain very toxic ingredients. READ THE ADDENDUM BELOW FOR ALL DETAILS.
NOTE THAT THE ADJUVANT SQUALENE IS BANNED IN THE US AT THIS TIME, although they will find ways around it, as there is tremendous pressure coming from the W.H.O. to use it worldwide.
1.FOCETRIA: MF 59, The adjuvant MF59C.1 contains 9.75 mg squalene, 1.175 mg polysorbate 80, and 1.175 mg sorbitan trioleate
Focetria in multidose also contains Thimerosal, a form of mercury, which has been shown to cause autism and other neurological disorders in children who received it in vaccines.
Squalene has been proven to cause severe auto-immune disease in rats, as well as death.It is a very dangerous ingredient.
It was implicated in the Gulf War Syndrome in the US, where hundreds of thousands of US soldiers got very ill and died after receiving the anthrax immunization that contains squalene( other factors were also involved in that particular episode).
In 1976, many of the people who ended with permanent Guillain- Barre Syndrome, a neurological disease similar to polio, had received unapproved material, most likely adjuvant, in their vaccine.
Adjuvant is neurotoxic and causes severe auto-immune disease.
2.PANDEMRIX contains AS03, their adjuvant:
AS03 adjuvant composed of squalene (10.69 mg), DL-α-tocopherol (11.86 mg) and polysorbate 80 (4.86 mg).
That one also contains squalene, polysorbate 80, thimerosal, and other toxic ingredients.THE QUANTITY OF SQUALENE IN PANDEMRIX IS BETWEEN HALF A MILLION TO A MILLION TIMES GREATER THAN THE QUANTITY FOUND IN THE ANTHRAX VACCINE OF THE GULF WAR SOLDIERS - WHO GOT SO SICK FROM THE CONCOCTION.
To be noted is that the combination of squalene and polysorbate 80, in a buffered solution, is an ideal anti-fertility drug, which was developed by W.H.O. scientists charged with developing anti-fertility vaccines, as part of the W.H.O.'s intensive campaign to reduce world population drastically , from the current 7 billion to half a billion - termed "culling"of the population.
In addition, it has to be noted that Pandemrix was NOT approved for use in children below the age of 18 in Switzerland, as there are almost NO DATA AS TO ITS SAFETY IN CHILDREN. SWITZERLAND HAS NOT ONLY DELAYED STARTING THEIR IMMUNIZATIONS BY ONE MONTH, BUT THEY HAVE ALSO BANNED PANDEMRIX FOR CHILDREN .
ISRAEL WIL BE USING PANDEMRIX IN ITS CHILDREN, IN EFFECT TURNING JEWISH CHILDREN, ONCE MORE, INTO GUINEA PIGS FOR THE REST OF THE WORLD, in particular for pharmaceutical criminal companies. Remember Auschwitz and Dr. Mengele, etc., remember the Yemenite children, and remember our 716 soldiers on whom illegal anthrax vaccine experiments were performed.
In addition, even though Focetria was approved by the EMEA, it was approved under very suspect circumstances. Switzerland as well, it has been found out, only approved Focetria last week because the minister of Health of Switzerland received a personal phone call from Vasella, the CEO of Novartis. It was a good-ole-boy's club decision, and not based on science at all.
In addition, at the Israeli Ministry of Health, when I asked questions about Focetria, one of the experts I spoke to admitted that only the UK has tried it so far in Europe - I couldn't even find any record to that assertion. Not only that, but the actual marketed formulation of Focetria was tested, all in all, in a total of 132 subjects, no more! (http://www.emea.europa.eu/influenza/vaccines/focetria/focetria.html)
WHICH MEANS, ONCE MORE, IN ESSENCE, THAT JEWS WILL BE THE GUINEA PIGS IN EUROPE FOR THE USE OF BOTH FOCETRIA IN ADULTS, AND PANDEMRIX IN CHILDREN.
IS THIS WHAT YOU WANT FOR YOUR CHILDREN AND FAMILY, KNOWING THE DANGERS ASSOCIATED WITH THESE DEADLY VACCINES?
Sweden, which has administered Pandemrix to its medical personnel and a million people, has had hundreds of very ill patients, as well as 5 deaths, plus other new, undocumented deaths, miscarriages, and similar disasters.
Pandemrix is very toxic, and we still don't know all the long-term effects of this poison on people, and know nothing about its effect on children.
There is another, very serious issue: the issue of contamination with live virus.
Just in the past few days, reports are coming in of a very deadly new epidemic, with H1N1 Kalifornia - essentially the same virus as H1N1,- in the Ukraine.
The Israeli scientist Moshe Bar Yosef, an insider, just two months ago warned people that BAXTER is making deadly bio weapons in its facilities in the Ukraine, using H1N1 vaccine as a COVER. He stated that the poisonous ingredients were live H1N1 virus RNA, as well as squalene.
Baxter has also been implicated in another deadly live virus episode, in a seasonal influenza vaccine, 72 kilos of which found their way to Europe and were about to be distributed, when Czech scientists found out it killed all the ferrets they tested the vaccine on.
In addition to that, Baxter was involved in other similar, suspicious occurrences.
Note that Baxter's CEO is a Jesuit , Jesuit trained, was DEAN of Chicago's Jesuit Loyola University School of Economics until he joined Baxter in 2004. He also serves on the board of directors of Catholic charities. We therefore see that he is heavily involved with the Vatican via the Jesuits, their most deadly branch, which has historically poisoned countless "undesirable" people, including popes, time and time again.
Note also that Baxter obtained its virus directly from the W.H.O. They all work together like one big, happy family, including Novartis, Glaxo, and all the other vaccine manufacturers.
As for Novartis, it was also found last year doing illegal tests on Polish vagrants, with its H5N1 vaccine , Aflunov - which was resurrected under a different name, Celtura, apparently . In those tests, 21 people died from that vaccine.
Is this only the tip of the iceberg???
The issue of inactivated, genetically engineered H1N1 virus turning deadly because of recombination of its fragments with other viruses in the population is a very serious one, and has been studied by numerous physicians and scientists.
There is also the issue of deadly NANOPARTICLES, present in some H1N1 vaccines, which has been addressed . These questions are ongoing and deserve serious inquiry.
THE W.H.O. HAS DECLARED THAT H1N1 vaccinations ARE MANDATORY WORLDWIDE.
EACH COUNTRY CAN STILL CHOSE TO DO AS THEY WISH. From my questions to the Ministry of Health this morning, I gathered that there would be no serious consequences for going against W.H.O. directives at this time ( although I must say they are probably wrong about that).
WHY SHOULD AM YISRAEL BOW TO THE DICTATES OF ITS DEADLY ENEMY, THE U.N., SPECIALLY WHEN THE ONLY COUNTRY EXEMPT of W.H.O. obligations IS THE VATICAN, and while the link between the Vatican and the W.H.O.'s evil deeds is quite obvious?
AND WHEN WE FIND THAT OTHER SELECT COUNTRIES, SUCH AS CATHOLIC PORTUGAL FIND WAYS TO BYPASS W.H.O. DICTATES?
AND WHEN WE FIND THAT 250,000 GERMAN SOLDIERS WILL NOT BE RECEIVING THE DEADLY INGREDIENTS?
On another note:
There is a pattern of deception here in Israel. First, the secrecy I encountered at the Ministry of Health, the reluctance to share GENUINE information with physicians. This can be explained by the following :
If you can read French, you will discover at http://www.lepoint2.com/sons/pdf/vaccin-H1N1%20medias.pdf that the maker of PandemRix, that is used in Sweden, passed a secret contract, the same in every European country, which specified a "Green List" of what the government MAY communicate (hardly anything!) and the "Red List" of what may absolutely NOT be made public, like intermediary results of the side effects that appear in the studies of the controversial squalene (and thiomersal) adjuvantated PandemRix until they have been sanitized by Glaxo Smith Kline researchers, and published by GSK themselves.
In the German documentary shown on ARTE it was said that GSK was relentless in pushing the identical contract through in each European country that had signed up (in 2006!) for it's "pandemic" vaccine.
SINCE ISRAEL FOLLOWS THE EUROPEAN MODEL, IT FOLLOWS THAT THIS APPLIES HERE TOO, AND EXPLAINS THE COVER-UP.
RED LIST :
The following information concerning the transaction cited in this document are subject to confidentiality :
a) All of the text of this document and its annexes, with the exception of the element listed in the “GREEN LIST, paragraph 1.2.
b) The price per dose.
c) The price per component.
d) The characteristics of the vaccine (as opposed to the standard description “The new adjuvented H1N1 vaccine.”
e) Any detail or reference to the agreements of GSK and a third party.
f) Any detail concerning the development plan, including the intermediary or final results of the clinical trials, before they have been published by Glaxo Smith Kline.
g) Any information concerning the pharmacovigilance (Note from the translator: in this case, we are talking about the reported side effects that are collected after the product has received it’s Emergency Use Authorisation clearance) with the guarantee that this clause does not interfere with the rights and obligations of the local competent authorities in conducting their legal obligations.
h) The principles of production of the vaccine (change of production based on the recommendation of the WHO and the vote of the client countries.
(the Flu Case)
Another thing to note is that each Kupat Cholim is responsible for ordering their own vaccines.
Just for curiosity's sake, I called to find out which vaccines the Kupot Cholim in Cesarea, Kochav Yair and Savyon, where the rich and famous live, will use.
Surprise, surprise: WHAT KUPOT? Who said those people even USE KUPOT CHOLIM? PRIVATE PROFESSORS, THAT'S WHOM.
No Meuchedet, no Maccabi, no Clalit in Cesaria, only a Professor of Pediatrics, Prof. Beder;
Kochav Yair has one Maccabi clinic, no Meuchedet, no Clalit,
While Savyon has no Meuchedet, no Maccabi, and no Clalit.
TWO TIER MEDICINE IN ISRAEL? WHAT WILL THE CHILDREN OF THE RICH AND FAMOUS, OF THE WELL- CONNECTED, BE ADVISED TO DO? WILL THEIR CHILDREN ALSO BE USED AS GUINEA PIGS FOR THE PHARMACEUTICAL COMPANIES?
BETTER YET, WILL THE DELIBERATE MAIMING , STERILIZING AND MURDERING OF OUR POPULATION ALSO AFFECT THEM???
AND WHAT IS GOING ON WITH THIS DEADLY NEW EPIDEMIC IN THE UKRAINE, ENGINEERED BY THE W.H.O.? HOW FAR WILL IT SPREAD? IS THAT THE FAMOUS PANDEMIC THEY ARE SO SCARED OF? AFTER ALL, THE CURRENT PANDEMIC IS ONE BIG FRAUD..... ON THE OTHER HAND, if they have advance information of some terrible epidemic being unleashed into the population of the world BY VACCINE, they better tell us, and make sure NONE OF THESE VACCINES AND INFECTIONS REACH OUR SHORES!
We need to act immediately, and stop this horrible development NOW! We cannot afford to have our children, our adults, our mothers, our doctors, our soldiers, hurt and incapacitated by this cruel, greedy, murderous and unconscionable enemy, the UN- WHO- NWO-VATICAN COMPLEX. With proper effort, we should be able to reverse the evil decrees and prevail against the inhumane beasts.
Thank you for your assistance.
Daisy J. Stern, MD
The UK has made provisions to acquire 132 million doses of the GSK vaccine. The following 2 vaccines have been approved by the EMEA
Description: Pandemrix is a suspension and emulsion for injection, meaning fluid from 2 vials must be mixed to form a multidose container that stays usable for 24 hours.
After mixing, 1 dose (0.5 ml) contains: Split influenza virus, inactivated, containing 3.75 µg A/California/7/2009 (H1N1)v-like strain (X-179A) (haemagglutinin ) (propagated in eggs). AS03 adjuvant composed of squalene (10.69 mg), DL-α-tocopherol (11.86 mg) and polysorbate 80 (4.86 mg). The suspension (2.5ml) and emulsion (2.5ml) vials once mixed form a multidose container (10 doses) containing 5 micrograms thiomersal (0.5 µg per dose). There does not seem to be a single dose container planned for Pandemrix at this time.
Indications and Usage: H1N1 Pandemrix is indicated for the active immunisation of individuals 18 years and up against influenza disease caused by pandemic (H1N1) 2009 virus. Adults aged 18-60 years of age, one dose can be given although 2 doses are recommended at an interval of 3 weeks between the first and second doses. Adults >60 years old should receive 2 doses, 3 weeks apart.
Children 6 months to 17 years may receive this vaccine if medically indicated: Children and adolescents aged 10-17 years: If vaccination is considered to be necessary, consideration may be given to dosing in accordance with the recommendations for adults. However, the choice of dose for this age group should take into account the available data on safety and immunogenicity in adults and in children aged from 3-9 years. See sections 4.8 and 5.1.
Children aged 3-9 years: If vaccination is considered to be necessary, the available data suggest that administration of 0.25 ml of vaccine (i.e. half of the adult dose) at an elected date and a second dose administered at least three weeks later may be sufficient.
There are very limited safety and immunogenicity data available on the administration of AS03-adjuvanted vaccine containing 3.75 μg HA derived from A/Vietnam/1194/2004 (H5N1) and on administration of half a dose of the same vaccine (i.e. 1.875 μg HA and half the amount of AS03 adjuvant in 0.25 ml ) at 0 and 21 days in this age group.
See sections 4.8 and 5.1.
Children aged from 6 months to 3 years: If vaccination is considered to be necessary, consideration may be given to dosing in accordance with the recommendation in children aged 3-9 years.
Contraindications: History of an anaphylactic (i.e. life-threatening) reaction to any of the constituents or trace residues (egg and chicken protein, ovalbumin, formaldehyde, gentamicin sulphate and sodium deoxycholate) of this vaccine. If vaccination is considered to be necessary, facilities for resuscitation should be immediately available in case of need. Please consult the full package insert for other warnings and precautions.
Clinical Trials: There are numerous phase II and III trials listed here although it is unclear the antigen concentrations and adjuvanted or non-adjuvanted vaccines used.
Safety and Efficacy: Clinical data from trials are not yet available.
Description: Focetria comes as a suspension for injection in pre-filled syringes. It is an H1N1 pandemic influenza vaccine (surface antigen, inactivated, adjuvanted) containing (per 0.5ml dose) haemagglutinin and neuraminidase 7.5 µg (expressed in µg haemagglutinin) from A/California/7/2009 (H1N1)v like strain (X-179A) virus propagated in eggs. The adjuvant MF59C.1 contains 9.75 mg squalene, 1.175 mg polysorbate 80, and 1.175 mg sorbitan trioleate. Other excipients include: sodium chloride, potassium chloride, potassium dihydrogen phosphate, disodium phosphate dihydrate, magnesium chloride hexahydrate, calcium chloride dihydrate, sodium citrate, citric acid and water. The single dose vial comes in a thimerosal free formulations of pre-filled syringes.
Indications and Usage: Novartis H1N1 monovalent vaccine is indicated for adults 18 years and older with 2 doses given at a ≥ 3 week interval. Children between the ages of 6 months and 17 years can also receive this vaccine with 2 doses given at a ≥ 3 week interval.
Contraindications: History of an anaphylactic (i.e. life-threatening) reaction to any of the constituents or trace residues (egg and chicken proteins, ovalbumin, kanamycin and neomycin sulphate, formaldehyde and cetyltrimethylammonium bromide (CTAB)) of this vaccine. If vaccination is considered to be necessary, facilities for resuscitation should be immediately available in case of need. Please consult the full package insert for other warnings and precautions.
Clinical Trials: Safety and immungenicity and dose response in healthy adults (18-50 years old) was a randomised study to examine the efficacy of 2 different antigen concentration doses administered at different intervals and MF59 adjuvanted versus non-adjuvanted. This study has been completed and the results published. Safety and Immunogenicity of A/H1N1-SOIV (Swine Flu) Vaccine With and Without Adjuvant in Children (3 to less than 9 years old) is a randomized, single blind, dose comparison, single group assignment, safety/efficacy study. The anticipated primary outcome date is November, 2009. Immunogenicity, safety and tolerability of 2 doses of adjuvanted and non-adjuvanted swine origin A/H1N1 Monovalent Influenza Vaccine (egg-derived) in healthy subjects from 6 months to 17 years of age is a randomized, single blind, uncontrolled, parallel assignment, safety/efficacy study. The anticipated study completion date is April, 2011, but the primary outcome data will be completed in November, 2009. More trials can be found here.
Safety and Efficacy: Titers of the hemagglutination-inhibition antibody exceeded 1:32 in 88% of subjects who had received one vaccine dose by this time and in 92 to 100% of subjects who had received both doses (Figure 2A). All subjects had microneutralization antibody at a titer exceeding 1:40 by day 21 (Figure 2B).