VI.
Genome sequence of the “swine flu”
An analysis of the “swine flu” genome sequence by Alexander S Jones indicates that 5% of both these influenza A RNA sequences share no known homology in any public databases (in addition to the avian/swine hybrid nature of both these critical genes), and so a laboratory origin for this virus must be seriously considered.
“Influenza A virus (A/Texas/04/2009(H1N1)) segment 8 nuclear export protein (NEP) and nonstructural protein 1 (NS1) genes, complete cds. http://www.ncbi.nlm.nih.gov/nuccore/FJ981620
HA ("hemaglutinin") protein BLAST sequence homology
Accession
Description
Max score
Total score
Query coverage
E value
Max ident
Links
FJ981615.1
Influenza A virus (A/Texas/04/2009(H1N1)) segment 4 hemagglutinin (HA) gene, complete cds 3142 3142 100% 0.0 100% FJ981612.1 Influenza A virus (A/Texas/04/2009(H1N1)) segment 4 hemagglutinin (HA) gene, complete cds
3142 3142 100% 0.0 100%
FJ966982.1
Influenza A virus (A/Texas/04/2009(H1N1)) segment 4 hemagglutinin (HA) gene, complete cds
3142 3142 100% 0.0 100%
FJ966959.1
Influenza A virus (A/Texas/05/2009(H1N1)) segment 4 hemagglutinin (HA) gene, complete cds
3142 3142 100% 0.0 100%
CY039527.1
Influenza A virus (A/Netherlands/602/2009(H1N1)) segment 4 sequence 3125 3125 99% 0.0 99% FJ969511.1 Influenza A virus (A/California/10/2009(H1N1)) segment 4 hemagglutinin (HA) gene, complete cds
3125 3125 100% 0.0 99%
FJ966952.1
Influenza A virus (A/California/05/2009(H1N1)) segment 4 hemagglutinin (HA) gene, complete cds 3125 3125 100% 0.0 99% FJ969509.1 Influenza A virus (A/New York/19/2009(H1N1)) segment 4 hemagglutinin (HA) gene, complete cds
3120 3120 100% 0.0 99%
FJ966960.1
Influenza A virus (A/California/06/2009(H1N1)) segment 4 hemagglutinin (HA) gene, complete cds 3120 3120 100% 0.0 99%
FJ981613.1
Influenza A virus (A/California/07/2009(H1N1)) segment 4 hemagglutinin (HA) gene, complete cds
3114 3114 100% 0.0 99%
FJ971076.1
Influenza A virus (A/California/08/2009(H1N1)) segment 4 hemagglutinin (HA) gene, complete cds
3114 3114 100% 0.0 99%
FJ966974.1
Influenza A virus (A/California/07/2009(H1N1)) segment 4 hemagglutinin (HA) gene, complete cds
3114 3114 100% 0.0 99%
FJ966082.1
Influenza A virus (A/California/04/2009(H1N1)) segment 4 hemagglutinin (HA) gene, complete cds
3109 3109 100% 0.0 99%
FJ969540.1
Influenza A virus (A/California/07/2009(H1N1)) segment 4 hemagglutinin (HA) gene, complete cds
3107 3107 100% 0.0 99%
FJ973557.1
Influenza A virus (A/Auckland/1/2009(H1N1)) segment 4 hemagglutinin (HA) gene, partial cds
2894 2894 92% 0.0 99%
AF455680.1
Influenza A virus (A/Swine/Indiana/P12439/00 (H1N2)) hemagglutinin (HA) gene, complete cds
2710 2710 100% 0.0 95%
AF250124.1
Influenza A virus (A/Swine/Indiana/9K035/99 (H1N2)) segment 4 hemagglutinin (HA) gene, complete cds
2699 2699 100% 0.0 95%
AY038014.1
Influenza A virus (A/Turkey/MO/24093/99(H1N2)) hemagglutinin (H1) gene, complete cds
2682 2682 100% 0.0 95%
EU139828.1
Influenza A virus (A/swine/Minnesota/1192/2001(H1N2)) hemagglutinin (HA) gene, complete cds
2676 2676 100% 0.0 95%
EF556201.1 Influenza A virus (A/swine/Guangxi/17/2005(H1N2)) hemagglutinin (HA) gene, complete cds
2665 2665 100% 0.0 94%
AF455675.1
Influenza A virus (A/Swine/Ohio/891/01(H1N2)) hemagglutinin (HA) gene, complete cds
2660 2660 100% 0.0 94%
FJ974021.1
Influenza A virus (A/Regensburg/Germany/01/2009(H1N1)) segment 4 hemagglutinin (HA) gene, partial cds
2656 2656 84% 0.0 99%
AY060047.1
Influenza A virus (A/SW/MN/23124-T/01(H1N2)) hemagglutinin (HA) gene, complete cds
2654 2654 100% 0.0 94%
AY060050.1
Influenza A virus (A/SW/MN/16419/01(H1N2)) hemagglutinin (HA) gene, complete cds
2643 2643 100% 0.0 94%
AY060048.1
Influenza A virus (A/SW/MN/23124-S/01(H1N2)) hemagglutinin (HA) gene, complete cds
2643 2643 100% 0.0 94%
AF455681.1
Influenza A virus (A/Swine/Illinois/100085A/01 (H1N2)) hemagglutinin (HA) gene, complete cds
2638 2638 100% 0.0 94%
EF556199.1
Influenza A virus (A/swine/Guangxi/13/2006(H1N2)) hemagglutinin (HA) gene, complete cds
2621 2621 100% 0.0 94%
AF455682.1
Influenza A virus (A/Swine/Illinois/100084/01 (H1N2)) hemagglutinin (HA) gene, complete cds
2621 2621 100% 0.0 94%
EU139830.1
Influenza A virus (A/swine/Minnesota/00194/2003(H1N2)) hemagglutinin (HA) gene, complete cds
2604 2604 100% 0.0 94%
EU139831.1
Influenza A virus (A/swine/Kansas/00246/2004(H1N2)) hemagglutinin (HA) gene, complete cds
2560 2560 100% 0.0 93%
EU604689.1
Influenza A virus (A/swine/OH/511445/2007(H1N1)) segment 4 hemagglutinin (HA) gene, complete cds
2555 2555 100% 0.0 93%
AF455677.1
Influenza A virus (A/Swine/North Carolina/93523/01 (H1N2)) 28 hemagglutinin (HA) gene, complete cds
2534 2534 100% 0.0 93%
DQ666933.1
Influenza A virus (A/swine/Korea/S11/2005(H1N2)) segment 4 hemagglutinin gene, complete cds
2518 2518 99% 0.0 93%
EU798780.1
Influenza A virus (A/swine/Korea/Hong song2/2004(H1N2)) segment 4 hemagglutinin (HA) gene, complete cds
2488 2488 99% 0.0 93%
EU798781.1
Influenza A virus (A/swine/Korea/JL01/2005(H1N2)) segment 4 hemagglutinin (HA) gene, complete cds
2486 2486 99% 0.0 93%
EU798784.1
Influenza A virus (A/swine/Korea/Asan04/2006(H1N2)) segment 4 hemagglutinin (HA) gene, complete cds
2481 2481 99% 0.0 93% NS1
("non-structural") protein BLAST sequence homology
Sequences producing significant alignments: Accession Description Max score Total score Query coverage E value Max ident Links
FJ981620.1
Influenza A virus (A/Texas/04/2009(H1N1)) segment 8 nuclear export protein (NEP) and nonstructural protein 1 (NS1) genes, complete cds
1594 1594 100% 0.0 100%
FJ981611.1
Influenza A virus (A/Texas/05/2009(H1N1)) segment 8 nuclear export protein (NEP) and nonstructural protein 1 (NS1) genes, complete cds
1594 1594 100% 0.0 100%
FJ969538.1
Influenza A virus (A/California/07/2009(H1N1)) segment 8 nuclear export protein (NEP) and nonstructural protein 1 (NS1) genes, complete cds
1589 1589 100% 0.0 99%
FJ969533.1
Influenza A virus (A/California/08/2009(H1N1)) segment 8 nuclear export protein (NEP) and nonstructural protein 1 (NS1) genes, complete cds
1589 1589 100% 0.0 99%
FJ969528.1
Influenza A virus (A/California/07/2009(H1N1)) segment 8 nuclear export protein (NEP) and nonstructural protein 1 (NS1) genes, complete cds
1589 1589 100% 0.0 99%
FJ969519.1
Influenza A virus (A/California/08/2009(H1N1)) segment 8 nuclear export protein (NEP) and nonstructural protein 1 (NS1) genes, complete cds
1589 1589 100% 0.0 99%
FJ969514.1
Influenza A virus (A/California/04/2009(H1N1)) segment 8 nuclear export protein (NEP) and nonstructural protein 1 (NS1) genes, complete cds
1589 1589 100% 0.0 99%
FJ971074.1
Influenza A virus (A/California/06/2009(H1N1)) segment 8 nuclear export protein (NEP) and nonstructural protein 1 (NS1) genes, complete cds
1583 1583 100% 0.0 99%
FJ966966.1
Influenza A virus (A/Texas/05/2009(H1N1)) segment 8 nuclear export protein (NEP) and nonstructural protein 1 (NS1) genes, complete cds
1559 1559 97% 0.0 100%
FJ966086.1
Influenza A virus (A/California/04/2009(H1N1)) segment 8 nuclear export protein (NEP) and nonstructural protein 1 (NS1) genes, complete cds
1543 1543 97% 0.0 99%
EU735822.1
Influenza A virus (A/turkey/OH/313053/2004(H3N2)) nonstructural protein 2 (NS2) and nonstructural protein 1 (NS1) genes, complete cds
1395 1395 100% 0.0 95%
EF551057.1
Influenza A virus (A/swine/North Carolina/2003(H3N2)) nonstructural protein 2 (NS2) and nonstructural protein 1 (NS1) genes, complete cds
1389 1389 100% 0.0 95%
EF551049.1
Influenza A virus (A/turkey/Illinois/2004(H3N2)) nonstructural protein 2 (NS2) and nonstructural protein 1 (NS1) genes, complete cds
1389 1389 100% 0.0 95%
DQ150437.1
Influenza A virus (A/swine/IN/PU542/04 (H3N1)) nonstructural protein (NS1) gene, complete cds
1389 1389 100% 0.0 95%
AF153262.1
Influenza A virus (A/Swine/Minnesota/9088-2/98 (H3N2)) segment 8 NS1 and NS2 genes, complete
cds 1386 1386 97% 0.0 96%
AF153261.1 Influenza A virus (A/Swine/Texas/4199-2/98 (H3N2)) segment 8 NS1 and NS2 genes, complete cds
1386 1386 97% 0.0 96%
AF342817.1
Influenza A virus (A/Wisconsin/10/98 (H1N1)) nonstructural protein 1 30 and nonstructural protein 2 genes, complete cds
1384 1384 100% 0.0 95%
DQ335775.1
Influenza A virus (A/turkey/Ohio/313053/04(H3N2)) nonstructural protein (NS) gene, complete cds
1384 1384 100% 0.0 95%
AF153263.1
Influenza A virus (A/Swine/Iowa/8548-1/98) segment 8 NS1 and NS2 genes, complete cds
1380 1380 97% 0.0 96%
EU697208.1 Influenza A virus (A/turkey/Minnesota/366767/2005(H3N2)) nonstructural protein 2 (NS2) and nonstructural protein 1 (NS1) genes, complete cds 1378 1378 100% 0.0 95%
EU735830.1
Influenza A virus (A/turkey/NC/353568/2005(H3N2)) nonstructural protein 2 (NS2) and nonstructural protein 1 (NS1) genes, complete cds
1378 1378 100% 0.0 95%
DQ150429.1
Influenza A virus (A/swine/MI/PU243/04 (H3N1)) nonstructural protein (NS1) gene, complete cds
1378 1378 100% 0.0 95%
EU697213.1
Influenza A virus (A/turkey/North Carolina/353568/2005(H3N2)) nonstructural protein 2 (NS2) and nonstructural protein 1 (NS1) genes, complete cds
1373 1373 100% 0.0 95%
AF250128.1
Influenza A virus (A/Swine/Indiana/9K035/99 (H1N2)) NS1 and NS2 genes, complete cds
1369 1369 97% 0.0 96%
AY038021.1
Influenza A virus (A/Turkey/MO/24093/99(H1N2)) nonstructural protein (NS) gene, complete cds, alternatively spliced
1363 1363 98% 0.0 95%
EU798872.1
Influenza A virus (A/swine/Korea/CAS09/2006(H3N2)) segment 8 nonstructural protein 2 (NS2) and nonstructural protein 1 (NS1) genes, complete cds
1360 1360 97% 0.0 95%
AY060136.1
Influenza A virus (A/SW/IN/14810-S/01(H1N2)) nonstructural protein (NS) gene, complete cds
1360 1360 97% 0.0 95%
AY060135.1
Influenza A virus (A/SW/IN/14810-T/01(H1N2)) nonstructural protein (NS) gene, complete cds
1360 1360 97% 0.0 95%
AY060129.1
Influenza A virus (A/SW/MN/3327/00(H1N2)) nonstructural protein (NS) gene, complete cds
1360 1360 97% 0.0 95%
AF455710.1
Influenza A virus (A/Swine/Minnesota/5“
Alexander S Jones concluded “we must seriously consider a laboratory origin for this virus” because 5% of both these influenza A RNA sequences share no known homology in any public databases.
“BLAST sequence homology of 'swine flu' indicates both the Hemagglutinin
(HA) surface protein as well as the Non-structural (NS1) interferon
Inhibition proteins are novel recombinants previously unidentified in nature.
Both these influenza proteins, based on the genetic sequences released Friday May 1st by the U.S. Centers of Disease Control (CDC), share their closest genetic identity with turkey (avian) and pig (swine) strains from multiple continents including North America as well as Asia. Even the closest matches indicate 5% previously unidentified genetic material.
I submit this evidence, coupled with the lack of the presence of this virus at the pig farm near the proposed CDC's "patient zero" (a 5 year old from La Gloria, 80km away from the pig farm in Perote, Mexico), shows that the origin of the flu outbreak remains unidentified at this time, and cannot be ascribed to Mexican or North American swine.
Furthermore, I submit that since 5% of both these influenza A RNA sequences share no known homology in any public databases (in addition to the avian/swine hybrid nature of both these critical genes), that we must seriously consider a laboratory origin for this virus.
Future research that may be promising includes identifying critical SNPs, especially in the PB2 and the NS1 coding regions which may be markers for evolution of pathogen virulence, and should be closely monitored. The hemagglutinin protein should also be monitored for acquisition of a poly-basic amino acid site which would give the virus pantropic properties as in the 1918 pandemic. “(Alexander S Jones)
VII.
Evidence as to the role of Baxter and WHO in producing and releasing pandemic virus material in Austria.
Baxter Pharmaceutical http://www.baxter.com/ has been chosen by the WHO to lead the efforts in finding a vaccine cure for the swine flu H1N1 virus.
Baxter AG, headquartered in Vienna, and the Austrian subsidiary of the pharmaceutical company Baxter International, headquartered in Deerfield, IL, USA, sent vaccine material contaminated with deadly live H5N1 bird flu virus to 16 laboratories in four countries in winter 2009 before a technician caught the mistake.
The deadly mixture of live bird flu virus and human flu virus were mixed in a biosecurity level 3 facility, where basic protocol and procedures would make it impossible to ever mix a live virus bioweapon with vaccine material by accident. In the first place, the strain of bird flu that is lethal to humans has no place in the the Baxter facility in Austria. So what was it doing in the facility designed for research into normal flu viruses and vaccines and their production to begin with?
The material released was a combination H3N2 seasonal flu viruses and live, unlabeled H5N1 viruses. If both strains were to incubate and recombine in a human host, a virulent airborne weapon that would cause a pandemic would be released, potentially killing billions.
The Baxter facility did not radiate the material before they sent it out, leaving the deadly virus alive.
To sum up, Baxter International, a global pharmaceutical corporation that has secured lucrative contracts to supply bird flu vaccines in pandemic, mixed live bird flu with human flu vaccine material in a Biosecurity level -3 facility, fail to radiate it and sent it under a false label to 16 labs as vaccine material.
About eight weeks later, a artificial, genetic worldwide interspecies flu pandemic breaks out in Mexico City, close to another Baxter facility, and the same company is given government and WHO contracts to produce vaccines for the outbreak.
According to Austrian Health Minister Alois Stöger , 72 kilograms of vaccine material was contaminated with the live bird flu virus which WHO supplied.
http://www.parlament.gv.at/PG/DE/XXIV/AB/AB_01457/fnameorig_158854.html Parliamentary answers 1457/AB (XXIV. GP) May 20th, 2009,
Fragen 14 und 15:
Das für Forschungszwecke bestimmtes Material -72 kg waren als kontaminiert anzusehen - wurde in die Firma zurück geholt und kontrolliert vernichtet.“
It is still not clear how 72 kilograms of the world’s deadliest bioweapon can be sent by accident from a high biosecurity facilities, not irradiated and under a false label.
However, we know from Baxter itself that it produced the 72 kilograms contaminated material using a wild type live bird flu virus obtained from the WHO reference center.
A statement on behalf of Baxter
---------------
I would like to provide the following update to a posting on ProMED dated 25 Feb 2009 (Avian influenza, accidental distribution - Czech Rep. ex Austria: RFI).
The H5N1 strain was the A/Vietnam/1203/2004 strain, received from a WHO reference centre. All information concerning this incident has been provided to the involved national authorities and appropriate international bodies such as ECDC and WHO.
-- Christopher Bona Director,
Global BioScience Communications
Corporate Communications
Baxter International Inc.
One Baxter Parkway
Deerfield, IL 60015
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=190510&rendertype=abst...
states that kidney cells of green monkeys can be used as hosts to cultivate influenza viruses.
http://www.ippl.org/Jasmine.htm
states that monkeys can carry diseases that can make humans sick or, at worse, can kill them. Monkeys can catch most human diseases.
http://www.sfbr.org/pages/news_release_detail.php?id=47
concerns work by Jonathan Allan to determine the link between African green monkeys and AIDS. Over 50% of the monkeys carry SIV – the simian version of HIV – yet never develop the disease.
If contaminated material were added to the 1,200 liter bioreactors, it would replicate and infect the entire batch of vaccine material in the 1,200 liter tank turning a vaccine into a bioweapon.
Contaminated material could be distributed among sections of the population using false labels and secretly marked batches and so infect millions of people in a way as to delay the reaction or over two doses.
Such vaccine material would kill thousands if not hundreds of thousands of people under the cover of a prophylactic measure against a pandemic created by, and spread, by Baxter.
Imagine the potential for disaster if even one batch was infected and distributed to thousands, if not hundreds of thousands of people, who would not only become ill themselves but also act as incubators of a new more lethal virus.
At the same time, the media – controlled by the organised crime syndicate – would so explain the story as to suggest that the deaths came from a naturally occurring virulent virus and the deaths happened in spite of the injections.
Vaccinations are needed to upgrade the “swine flu” bridge virus to the more lethal “bird flu” virus if the international crime syndicate is to achieve its goal of a drastic reduction in the world population with a parallel consolidation of geopolitical power.
There is evidence the bioweapons programs are 'international' in scope with funding coming from the US government, WHO, the UN and also banks.
There are reasonable grounds for believing there are financial and social connections with the incoming administration as Baxter because its executives are based near Chicago, the political base of President Obama, and Baxter has contributed to political parties.
It is clear that Baxter stands to benefit financially from the outbreak of a pandemic through a contaminated season influenza vaccine in late 2009, and that the shareholders will profit directly from this boost.
It has been reported that President Obama holds shares in Baxter.
Certainly, Baxter is guaranteed substantial direct profits from their triggering a bird flu pandemic from their contract sealed in 2006 with the Austrian Health Ministry, led by then Health Minister Maria Rauch-Kallat, to supply 16 million vaccine shots in the event of a bird flu pandemic being declared in Austria alone.
Baxter also has the contract to supply the swine flu vaccine for the Austrian government in spite of its role in releasing pandemic material this winter.
Baxter has contracts with WHO to supply huge quantities of vaccines.
However, upfront profits from sales of vaccines are just one part of the profit that the organised corporate crime syndicate, comprised also of banks, will obtain as mentioned.
If millions, if not billions, of people were to die as a result of a pandemic virus and/or contaminated inoculations, then their assets, their savings, their houses, apartments, farms and companies would be easy to acquire by a crime syndicate that has infiltrated and annexed key government offices.
Baxter Officers
Baxter officers in Austria:
Two Baxter officers associated with Baxter's Austria location where the 72 kilos of pandemic bird flu was released, are Noel Barrett and Hartmut Ehrlich. Barrett and Erlich were part of the Baxter H5N1 Pandemic Influenza Vaccine Clinical Study Team that published A Clinical Trial of a Whole-Virus H5N1 Vaccine Derived Cell Culture. The vaccine was called Celvapan.
Dr. Noel Barrett
Vice President, Global R&D Vaccines
Baxter AG
Dr. Barrett is Vice-President R&D, Vaccines in the Bioscience Division of Baxter Healthcare. He received his Ph.D. in Virology at Trinity College, Dublin in 1979 and subsequently held a postdoctoral fellowship for four years at the University of Würzburg in Germany. He is presently responsible for overseeing the development of a range of viral and bacterial vaccines.
Here is an audio interview with Noel Barrett about "The vaccine-making industry's efforts to combat the bird flu around the world." Of course, Barrett, Baxter and the rest of the vaccine industry would love nothing more than for a bird flu outbreak to occur. Alan Watt points out that the current flu scare is just another example of how we truly live in an age of crisis creation. It's not just to control the public via problem-reaction-solution. Crisis creation is also a great way to make huge profits. Fear has always been a fantastic sales mechanism for the elite. The current flu hype and panic means fantastic business for Baxter, and they're already cashing in on millions and millions of taxpayer dollars.
Barrett is a member of the World Vaccine Council and spoke at the council's 2006 conference in Lyon, France, which took place from October 9-11, 2006. What is it about the dates 9 and 11 and this globalist cabal? It's like an Illuminati gang sign they can't stop flashing down through history. I guess its also just a coincidence that the 'swine' flu outbreak of 2009 occurred 91 years after the 1918 pandemic?
Part of the program for the conference at Lyon included the topic of "Avian flu and influenza: the real situation" and Dr. Barrett gave a presentation on the topic of "The development of a vero cell derived candidate H5N1 vaccine." Vero-cell technology allows Baxter to produce vaccines much faster than the traditional egg based process which uses putrid chicken eggs to grow the viral culture. With vero-cell technology, viruses are placed in in large fermenting tanks with chemicals, heavy metals ("accelerants"), and pulverized monkey kidneys. By not relying on the old system of using millions of eggs to make flu vaccines, Baxter claims it can cut vaccine production time in half, to as little as 12 weeks. It's also interesting to note that the WHO countered Dr. Gibbs' claim that the flu probably came from a laboratory by disputing that there is enough evidence of the traditional egg based laboratory process. News flash for the WHO: Baxter's Vero-cell technology doesn't require any eggs.
Dr Hartmut Ehrlich
Vice President for Global Clinical Research and Development
Baxter scientist since 1995
Hartmuch Ehrlich is a hemophilia specialist who began at Baxter in 1995. In 1996, Bayer AG and Baxter were discovered to have knowingly shipped out millions of ampules of HIV contaminated Factor VIII--a hemophiliac drug--which resulted in the infections and deaths of many thousands of people.
Ehrlich completed his Doctorate at the Clinical Research Unit for Blood Coagulation and Thrombosis of the Max Planck Foundation, and conducted research at the Kerckhoff-Clinic of the Max Planck Foundation. It's worth noting that what is known today as the Max Planck Foundation actually began as the The Kaiser Wilhelm Institute. Founded in 1911, The Kaiser Wilhelm Institute was funded by the Rockefeller Foundation and was the headquarters for Nazi research into eugenics, euthanasia, population control, genetic engineering, and biological warfare. Max Planck (1898-1947)
Known primarily as the German physicist who originated quantum theory, Max Planck was made president of the Kaiser Wilhelm Institute in 1930. At the end of WW II, the Institute was moved and renamed the Max Planck Institute in order to cover up its unsavory past. Einstein never forgave Planck for not being more critical of the Nazis.
After finishing his studies at the Max Planck Institute, Ehrlich joined Baxter in 1995 as Medical Director for its Biotech business, and held several positions of increasing responsibility until September 2003 when he was named Vice President, Global Clinical R&D for the BioScience Division. In September of 2006, he was promoted to his current position, leading all R&D efforts for BioScience. Ehrlich, along with Barrett, helped develop Baxter's bird flu vaccine Celvapan, and helped secure an agreement with the WHO and EMEA to use the viral concoction if a pandemic is declared.
“We are very pleased to receive the EMEA’s positive opinion for Celvapan,” said Hartmut Ehrlich, M.D., vice president, BioScience global research and development. “This is another step towards our goal of supplying a safe and effective vaccine to protect the population against a possible influenza pandemic.” This scumbag should definitely be pleased now that the avian/swine flu has been released in Mexico and other locations around the world. If I understand correctly, pharmaceutical corporations are "immune" from liability if their products cause injury or death as long as the distribution is by government mandate during a declared health emergency.
Baxter International Board of Directors
From its inception, Baxter International has had numerous military, medical-industrial complex, and global eugenicist ties. The company was the first and only manufacturer of commercially 40 prepared intravenous solutions for the US Army during WWII. Here is a sample of current Baxter directors to give you some idea of the deep connections.
General Walter E. Boomer
Baxter Director since 1997
USMC Four Star General Over
30 years in the military
"A leader's position is with and in front of the people he is leading."
Walter Boomer - Above & Beyond: Former Marines Conquer the Civilian World (2004)
This is a curious statement from Boomer, who supposedly led all Marines in Operations Desert Shield and Desert Storm. Where was the brave general when his own US Marine troops were under biological attack from their own military command in Iraq? At least one in four U.S. veterans of the 1991 Gulf War suffers from a multi-symptom illness caused by exposure to toxic chemicals during the conflict. How many Marines died from vaccine induced Gulf War illness on Boomer's watch? How many of his men and women still suffer from debilitating symptoms today and can't get medical assistance from their own military? Since the Gulf War, 11 thousand veterans have died from illnesses related to vaccines, DU, and chemical weapons.
I don't see Boomer exactly standing "with and in front of his people" when it comes to biological warfare and cold blooded treason. Should we civilians also entrust our lives to this traitorous bastard, much less believe anything that his cronies at Baxter or the criminals in government tell us about the current flu outbreak or their proposed vaccines? Hell no.
Wayne T. Hockmeyer
Baxter Director since 2007
US Army Special Forces
Entomology degree
Malaria specialist Chair,
Immunology Department, Walter Reed Army Institute of Research (1980-1986)
Founder, President & CEO of MedImmune, a flu vaccine technology company (1988-2000)
Here is an excerpt from the Hockmeyer biography:
"After three months in his first job at Dow Chemical Co. in Michigan, he was commissioned in the Army, and, following airborne and special forces training, was sent to Vietnam in 1968 with the 5th Special Forces Group. The Army assisted with Hockmeyers return to the University of Florida, where he earned his doctorate. He rose to the rank of lieutenant colonel and, during his 20-year military career, authored many research papers with particular emphasis on the development of malaria vaccines."
Hockmeyer served as Chairman of the Immunology Department, Walter Reed Army Institute of Research from 1980 to 1986. Walter Reed houses the largest biomedical research facility administered by the US Defense Department. It was originally founded by US Army Surgeon, General George Steinberg in 1893. Steinberg is known as the father of American bacteriology, and Walter Reed can arguably be said to house some of the world's experts in biological warfare.
Wayne T. Hockmeyer Hall - Structural biology research facility at Purdue University that will contain a BSL-3 laboratory.
Hockmeyer Hall research facility at Purdue University is currently under construction and expected to be completed by Fall of this year. Structural biology focuses on the physical design and functions of viral structures (presumably in order to better manipulate them).
In this video of the dedication for what is essentially a bioweapons research facility, the speaker admits that Hockmeyer Hall will contain a BSL-3 biohazards containment laboratory "specifically designed for the study and growth of pathogenic viruses."
Indeed, the recent research activities of the structural biology department of Purdue indicates a heavy interest in viruses as potential bioweapons:
---They mapped the structure of the Dengue Virus and determined the structure of the immature dengue particle while still within its cellular host, which will obviously help in the virus development process.
---They analyzed the structure of the baseplate of the T-4 Virus helping scientists further understand how viral infection occurs (in other words, how to better cause infection).
---They determined the orientation of the major surface proteins in the viral particle of West Nile Virus. Because these proteins allow the virus to invade a host cell, the research could be a step forward in combating (or spreading) the deadly mosquito-borne disease.
---They genetically modified the Ross River Virus that was then used to alter the liver cells of living mice without killing them. Viruses as agents to alter the very structure of human beings.
---They redesigned the shell of Ebola, "transforming the feared virus into a benevolent workhorse for gene therapy." The new modification is a version of Ebola that can be inhaled. As Alex has mentioned numerous times lately, an airborne, inhalable version of the Ebola virus is the holy grail of bioweapons research for "Dr Death," aka Eric Pianka, the lunatic UT professor who calls for 90% of the world's population be eradicated like vermin. It's unfortunate for the rest of us that Pianka lacks the courage to lead by example and just kill himself, already. Roll up your sleeve, "Dr. Death," Baxter has an injection for you.
Albert Sabin (1906-1993)
In 2005, Hockmeyer received the 2005 Albert Sabin "Humanitarian Award" by the Sabin Vaccine Institute. Oh, that's rich. Sometimes just you have to laugh at the dark humor and doublespeak of the eugenicists. Albert Sabin was a US virologist and developer of the dangerous and deadly oral polio vaccine. During WW II, he devised vaccines for the United States Army. After the war, he developed a live attenuated vaccine against polio, which presumably included monkey kidney tissue that was infected with the notorious cancer causing agent SV-40 (simian virus 40) that resulted in the deaths of millions and an explosion in the number of previously rare cancers. In the 1950s, Sabin persuaded the USSR to use the deadly vaccine on an industrial scale.
Joseph B. Martin
Baxter director since 2002.
Dean, Harvard Medical School, 1997-2007
Founder, Systems Biology Department, Harvard University
By all accounts, Joseph B. Martin is a hardcore eugenicist just like Boomer, Hockmeyer, Pianka, Sabin, and the rest of the whitecoats at Baxter. Over the course of his career, Martin appears to have contributed nothing to the actual curing of diseases or easing of human suffering, but only directed his efforts towards the study of disease etiology and ways to manipulate sickness and spread it on a massive scale. In this evil pursuit he is no different than the rest of his colleagues. Here are some of Martin's contributions to humanity:
"The Role of Pathogenesis of Neurodegenerative Disorders: The Role of Dynamic Mutations." Neuroreport 1996; 8:i-vii.
"The Molecular Basis of the Neurodegenerative Disorders." N Engl J Med 1999, 340:25:1970- 1980.
On the surface, Dr. Martin is a neurology professor who specializes in degenerative diseases like Alzheimer's, Parkinson's, MS, ALS, and Huntington's, many of which are spreading at incredible rates and are now widely believed to be caused by environmental and medical factors and in particular, by vaccines. It's as if Martin and the other Baxter executives could have never conceived that diseases might have iatrogenic causes.
"Dr. Martin's research focuses on the "application of neurochemical and molecular genetics to better understand the causes of neurological and neurodegenerative disease." Remember: vaccines are essentially dual use bioweapons. A better understanding of the causes of disease is just the same as learning how to better cause and spread disease among the human population. The difference is only a matter of intention. In 1980, Dr. Martin established the NIH sponsored "Disease Center Without Walls." A "disease center without walls?" I don't like the sound of that, especially when eugenicists are involved.
In 1984, Martin played a key role in establishing the Massachusetts Alzheimer's Disease Research Center. Let's see, after 60 years, there's still no cure for Alzheimer's, it's spreading at alarming rates, there's no end in sight, and it's believed to be caused by environmental factors. Is Dr. Martin actually trying to cure Alzheimer's? If so, his "disease research center" isn't helping much.
In 2003, Martin founded the Systems Biology department at Harvard. No doubt it was at the behest of his globalist masters.
You only have to read the first two sentences of the Wikipedia definition of Systems Biology to realize it is mere pseudo-science masquerading as genuine holistic scientific inquiry. "Because the scientific method has been used primarily toward reductionism, one of the goals of systems biology is to discover new emergent properties that may arise from the systemic view." In other words, the scientific method need not apply here. Systems Biology is just another academic cover for the eugenicist elite's agenda.
Not surprisingly, eugenicist Andrew Huxley is known as the forefather of Systems Biology. Andew Fielding Huxley was the youngest son of Leonard Huxley and half brother to Julian and Aldous Huxley, all of whom were inbred, parasitic, elite eugenicists. According to Alan Watt, Aldous Huxley, author of Brave New World (1931), the novel that eerily predicts the very sociobiological nightmare we are currently living through, died of cancer of the tongue. Did he say too much? Who might have had the viral expertise to kill Aldous with such a targeted cancer at the time?
Andrew Fielding Huxley (1917-?)
Gail D. Fosler
Baxter Director since 2001
Council on Foreign Relations
Bretton Woods Committee Federal Reserve Bank of New York Advisory Panel
Trustee, The Economic Club of New York
"It is industries, not nations, that compete globally."
-- Gail D. Fosler, Chief Economist, The Conference Board
An unabashed globalist, Gail Fosler is President and Chief Economist for The Conference Board, a key policymaking NGO for globalists and bankers. Prior to joining The Conference Board in 1989, Fosler was Chief Economist and Deputy Staff Director of the US Senate Budget Committee. The Wall Street Journal twice named Fosler America's most accurate economic forecaster. So, although she has absolutely no biology or chemistry background, it would seem that Fosler knows a bit about pseudo-science herself.
Headquartered in New York, The Conference Board is a global organization with offices in Brussels, Hong Kong, India, the Middle East, and Beijing. It began with a 1915 meeting at the Yama Farms Inn in New York which consisted of the presidents of 12 major corporations and six of the foremost industry associations. The gathering included Frank A. Vanderlip, a member of the Jekyll Island group, the notorious group of bankers that wrote the bill that became the Federal Reserve Act.
Frank A. Vanderlip (1864-1937)
Joining Fosler on the Conference Board are two fellow globalist scumbags:
Harry M. J. Kraemer Jr. (Vice Chair), former Baxter Chairman and CEO. Director of SAIC.
Josef Ackermann (Vice Chair), director of Bayer AG, Deutsche Bank AG, Royal Dutch Shell, Siemens. Bilderberg attendee: 2005, 2008
Gail Fosler is also a member of The Council on Foreign Relations and the Bretton Woods Committee, director and a member of the Executive Committee of the National Bureau of Economic Research, and a trustee of The Economic Club of New York. She has served on the Advisory Panel to the Federal Reserve Bank of New York. She is a director of Caterpillar Incorporated, Unisys Corporation, and H.B. Fuller, one of the world's largest polluters. There are a number of Baxter officials that have also worked for H.B. Fuller.
Gail's husband, R. Scott Fosler, is also a globalist public policy hack.
Among his publications are:
The Challenge to New Governance in the Twenty-First Century: Achieving Effective Central Local Relations.
Public Private Partnership in American Cities, and The New Economic Role of American States: Strategies in a Competitive World Economy
Albert P. L. Stroucken (Netherlands)
Baxter Director since 2004
Bayer AG (1969-1998)
HB Fuller (1998-2006)
It was during Stroucken's tenure in 1997 that both Bayer and Baxter agreed to a $670 million settlement after knowingly distributing blood products that infected thousands of hemophiliacs with HIV during the 1980s.
Bayer has a long history of atrocities dating all the way back to WW II. According to a lawsuit, Bayer paid Nazi officials during World War II for access to concentration camp victims and collaborated in Nazi experiments with Joseph Mengele as a form of research and development for their products. A physician identified only as Dr. Koenig was a representative of Bayer and accompanied "Angel of Death" Mengele as he performed his grotesque medical experiments at the Nazi concentration camp at Auschwitz. Bayer provided toxic chemicals to the Nazis, and Mengele used them in the experiments, while Koenig recorded the results and reported the information back to Bayer.
The Angel of Death, Joseph Mengele
James R. Gavin III
Baxter Director since 2003
Lieutenant Commander, US Public Health Service (1971-73)
Senior Science Officer, Howard Hughes Medical Institute (1991-2002)
Trustee, Robert Wood Johnson Foundation
Another not-for-profit NGO helping to usher in the New World Order, the Howard Hughes Medical Institute is really a front for eugenics research and activities. They even proudly issue a publication called "The Genetic Trail."
The Howard Hughes Medical Institute (HHMI) is one of the largest private medical research organizations in the US, second in funding only to fellow eugenics operation, the Bill & Melinda Gates Foundation. Unlike most such organizations, HHMI directly employs the researchers it funds, and the 350+ "investigators," as the institute likes to call them, include a dozen Nobel Prize winners. They concentrate primarily on such areas as cell biology, genetics, immunology, and neuroscience, as well as the formerly discussed eugenics pseudoscience, structural biology. To top it all off, James Baker III is on the board of HHMI. What more needs to be said?
Gavin is also involved with the Robert Wood Johnson Foundation – another NGO eugenics front. 9/11 coverup artist Thomas Kean is is Chairman of the Robert Wood Johnson Foundation .
Appendix: Baxter International Officers
In addition to its board of directors, Baxter officers also indicate deep military, med-industrial complex, and global eugenicist ties. Here's a quick list.
Robert L. Parkinson, Jr.
Baxter Executive Admits Heparin Contamination Appears Deliberate
Wilbur H. Gantz
CEO, PathoGenesis
Military Service: USMC
Princeton
Harvard
Harry M. Jansen Kraemer, Jr.
Director, SAIC (1997-)
Vernon R. Loucks, Jr.
Skull and Bones Society
Military service: USMC
Director, Harvard Business School
National Institutes of Health Special Adviser (1983-86)
Sabin Vaccine Institute Lifetime Achievement Award, 2006.
James R. Tobin
Military service: US Navy (Lt., 1968-72)“
IX.
Evidence Baxter has deliberately contaminated drugs.
That vaccine material has been deliberately contaminated causing death and injury has even been admitted by Baxter’s CEO Robert Parkinson.
Baxter is at the center of a lawsuit alleging that Baxter altered an ingredient in heparin that flowed through heparin syringes to patients, resulting in pain and suffering, and sometimes death, to those affected.
“Baxter International chief executive Robert Parkinson admitted to what looks to be the deliberate contamination of its heparin product which contributed to 81 deaths and prompted a product recall. He said that a contaminating agent that is an altered form of chondroitin sulfate was purposely added to the material before it reached Baxter's supplier in China.“ (Sturgeon, 2009)
“We're alarmed that one of our products was used in what appears to have been a deliberate scheme to adulterate a lifesaving medication,“ Baxter Chief Executive Officer Robert Parkinson told the House Energy and Commerce Committee's investigative subcommittee.
“It seems to us that it's an intentional act upstream in the supply chain“ said David Strunce, the chief executive officer of Waunakee, Wisconsin-based Scientific Protein, during the hearing. “We don't know specifically where.“
The drug's main ingredient was contaminated before reaching the Chinese factory of Baxter's supplier, Scientific Protein Laboratories, executives of both companies testified at a U.S. House hearing today.
The Food and Drug Administration suspects the contamination was deliberate, though there isn't proof, according to the agency.
Baxter recalled heparin, used to prevent blood clots, in January of this year after reports of harmful side effects. Since January 2007, 81 people have died after allergic reactions, the FDA said on April 21. Tainted heparin made by other drugmakers has been found in more than a dozen countries since Baxter's recall, and regulators have said they don't know how it was introduced.
Some samples of Baxter's heparin were found contaminated with a cheaper substance known as over-sulfated chondroitin sulfate, according to the company and the FDA.
In a class-action lawsuit filed filed January 5th 2009 by Joyce Ann Osteen at the St. Clair County Circuit Court for compensation for scores of patients harmed by tainted heparin, the claim is made that Baxter altered the profile of the drug, in an attempt to reduce costs.
The lawsuit accuses Baxter of using a more dangerous and unapproved ingredient, OSCS to dilute, or to substitute for the more costly, natural ingredient in heparin to "reap greater profits as a result of utilizing cheap component parts."
About 3500 pig intestines are required to produce 2.2 pounds of raw heparin. While the suit did not quantify heparin mass relative to value, it was alleged that it costs Baxter $900 to produce heparin the old-fashioned way.
It is alleged, Baxter found a way to make that same amount of heparin for just $9. And the heparin mimic OSCS, according to the lawsuit, was the key.
The lawsuit notes that OSCS is not found in nature, and is not approved in the United States.
"Un-approved APIs significantly increases the likelihood that exposed patients will experience adverse side effects and reactions that can result from the un-approved doses," the suit states. "In other words, an unapproved API enhances the risk and danger."
As of April 8, there have been 103 reported deaths in patients who received tainted heparin since January 1st of 2007, the suit states. Of those deaths, 91 were reported after January 1st of last year.
"On or about July 30th, 2008 the (US Food and Drug Administration) conclusively linked the deaths of patients infused with heparin to specific lots made by Baxter," the suit states. "The specific lots of Baxter product tested positive for OSCS."
Heparin crude lots received in August 2006 are said to have included material from an unacceptable workshop vendor, according to the suit. Raw material inventory records were incomplete, the control of material flow in the processing area was found to be inadequate, and a collection of outer foil bags containing heparin sodium were unlabeled. There was also no report or data to verify that the leachable for certain bags used for heparin sodium had been evaluated, according to the complaint.
Inspectors reported a breakdown in critical processing steps identified for heparin sodium USP process, a lack of an impurity profile established for heparin sodium, and a lack of evaluation for degradents. Manufacturing instructions were found to be incomplete, and there had been no verification performed for the reported USP test methods.
When even the CEO of Baxter has said that the contamination of Baxter’s blood-thinner heparin appears to have been deliberate and he has a “strong sense of personal responsibility“ for this “deliberate scheme“, how much more likely is a deliberate contamination of the “swine flu“ vaccine?
"We're alarmed that one of our products was used, in what appears to have been a deliberate scheme, to adulterate a life-saving medication, and that people have suffered as a result," Baxter Chief Executive Robert Parkinson said.
http://www.reuters.com/article/topNews/idUSWAT00940720080429
"We deeply regret that this has happened, and I feel a strong sense of personal responsibility for these circumstances," he said.
Under the current set of regulations, acts and provisions, it would be possible for a bioterrorist organisation that has access to the production facilities or to the 1,200 liter bioreactors or that could influence the composition of vaccine material to kill all Americans by contaminating the vaccine material and forcing them to take it without adequate checks or face being shot.
Theoretically, the lethal effect of the vaccination could be delayed or triggered by a second substance.
Dr. Marc Girard predicted this Bird Flu disaster.....he was however the one behind the decision of France to stop use of the Hep B vaccine due to autoimmune disease. He has seen however, this coming where the vaccines are not even worth the risk and yet they keep recommending them.
Dr. Marc Girard was commissioned as a medical expert witness by a French judge in a criminal inquiry in France in September 1994 into deaths following a campaign of vaccination against hepatitis B upon the recommendations of the World Health Organization (WHO).
In an open letter to the then WHO Director- General, he indicates that WHO is guilty of criminal misconduct.
http://www.impfkritik.de/forum/showthread.php?t=534
While much information concerning World Health Organization (WHO) recommendations on vaccines, particularly against hepatitis B, remains secret, there is sufficient evidence in the open literature to suggest scientific incompetence, misconduct, or even criminal malfeasance. The benefits are overstated and toxicity greatly understated. Influenza vaccine recommendations falsely imply that the available vaccines could help prevent avian influenza,“ he writes.
French judges investigate vaccine manufacturer for manslaughter
March 19th, 2008
In what was called a “thunderclap in the vaccine industry,” French authorities have opened a formal investigation concerning a hepatitis B vaccination campaign by GlaxoSmithKline and Sanofi Pasteur in the 1990s. It is alleged that the companies failed to fully disclose neurologic side effects. Another investigation opened by Judge Marie-Odile Bertella-Geffroy concerns the death (“manslaughter”) of a 28-year-old woman from multiple sclerosis, allegedly connected to the vaccine (Le Figaro 1/31/08).
>From 1994 to 1998, almost two-thirds of the French population and almost all newborn babies were vaccinated against hepatitis B, but the campaign was temporarily suspended because of concerns about side effects.
Some 30 plaintiffs, including the families of five patients who died after the vaccination, have launched civil actions (Reuters 1/1/08).
A British case-controlled analysis showed an odds ratio of 3.1 (95% CI 1.5-6.3) for first symptoms of multiple sclerosis in recipients of recombinant hepatitis B vaccine compared to controls. Two previous French studies had shown a RR of about 1.5. Other studies showed a nonsignificant increase or null findings, especially when date of diagnosis rather than date of first symptoms was used (Neurology 2004;63:838-842).
According to attorney Clifford Miller, “British doctors administering hepatitis B vaccine to infants could face criminal prosecution if fully informed consent is not obtained. Civil prosecution for damages is possible over 21 years later if the injured survive as adults” (UK Press Association Newswire/Romeike, September 2005).
The hepatitis B vaccine has been considered “one of the safest vaccines ever produced” (Neurology, op. cit.). On the other hand, French medical expert Marc Girard has said that “for a preventive measure, hepatitis B is remarkable for the frequency, variety and severity of complications from its use” (Romeike, op.cit.)
http://www.jpands.org/vol11no1/girard.pdf
He gives evidence that WHO systematically manipulates scientific data to exaggerate the benefits of vaccines and playdown the risks.
Meanwhile, WHO or its “experts” go on publishing reassuring statements based upon an explicit reference to a safety study that, according a public communiqué of February 2000, even the French agency decided to “discard.”An unfortunate misprint in Table 2 of this study—uncorrected to my knowledge—allows the authors to halve the clear increase of multiple sclerosis in vaccinated teenagers and young adults. Such an error would normally lead one to suspect fraud.
Girard calls WHO „merely a screen for the commercial promotion“ of vaccines.
He says notes that apparently neutral government boards are packed with vaccine company employees.
"In the promotion of the hepatitis B vaccination, WHO has evidently served merely as a screen for commercial promotion, in particular via the Viral Hepatitis Prevention Board (VHPB), which was created, sponsored, and infiltrated by the manufacturers. In September 1998, after the serious hazards of the campaign had been given their first media coverage in France, the VHPB organized a panel of “experts,” whose reassuring conclusions were extensive media coverage as reflecting WHO’s position. Yet some of the participants in this panel had no expertise beyond being employees of the manufacturers, and the vested interests of the rest did not receive any attention.“
World Health Organization Vaccine Recommendations: Scientific Flaws, or Criminal Misconduct?
Journal of American Physicians and Surgeons Volume 11 Number 1 Spring 2006
World Health Organisation accused of improper soliciting of funds from the pharmaceutical industry
Posted on 19 February 2007
It seems that not a week goes by without some information leaking out about the sometimes too cosy relationship that can exist between the pharmaceutical industry and organisations we rely on for giving us impartial health information and advice. This particular week’s story concerns accusations that a representative of the World Health Organisation (WHO) attempted to solicit funds from the pharmaceutical company GlaxoSmithKline, and then siphon them through an organisation to obscure the source of the those funds.
The individual at the centre of this controversy is Dr Benedetto Saraceno, director of the WHO’s department of mental health and substance abuse. It is alleged that he was seeking £5000 ($10,000; 7000 euros) to pay for the preparation for a report on neurological diseases including Parkinson’s disease. The WHO has a strict policy that forbids it from taking funds from the pharmaceutical industry, and quite right so.
However, in an email that has been passed to the British Medical Journal, Dr Saraceno appears to suggest that to get around this, money from GSK should be paid to an organisation known as the European Parkinson’s Disease Association (EPDA). In an email to the EPDA, Dr Saraceno writes “WHO cannot receive funds from the pharmaceutical industry,” and goes on to add “I suggest that this money should be given to EPDA and eventually EPDA can send the funds to WHO which will give and invoice (and acknowledgment contribution) to EPDA but not to GSK.”
It is alleged that GSK promptly withdrew its offer once it became clear they would not be officially recognised as the source of this funding.
Since the somewhat—damning correspondence came to light, it seems that Dr Saraceno has attempted to do some major backtracking. He claims that his original email to EPDA was “clumsily worded” and that he denied ever suggesting that funds from GSK be siphoned through the EPDA. Personally, I find it hard to imagine what it is about the wording of Dr Saraceno’s email to the EPDA that is in any way clumsy. And neither does Mary Baker - the person at the EPDA to whom Dr Saraceno was writing. She is quoted as saying “There is absolutely no doubt in my mind that Dr Saraceno knew the $10,000 was coming from GSK and that he was intending to take it and disguise its origins by getting EPDA to accept it first before passing it on.”
When the BMJ put its concerns about this rather distasteful episode to the WHO, a spokesman apparently replied “It’s astonishing that the BMJ thinks there’s a story here. Dr Saraceno sent a second email saying he had not meant to ask for the money. So I don’t think there’s anything to answer.” Does the WHO really believe that just because one of its employees denies impropriety, even when presented with evidence that appears to suggest otherwise, that there is no case to answer? I have a feeling that many who learn of this sorry state of affairs would beg to differ.
References:
1. Day M. Who’s funding WHO? British Medical Journal 2007;334:338-340
next
Evidence Novartis is using vaccines as bioweapons.
source
https://www.bibliotecapleyades.net/archivos_pdf/evidence-use-pandemic-flu.pdf
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