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Komplotan Roma (The Club of Rome)

antimurtad — Wed, 30 Dec 2009 09:56:37 +0000

Aurelio Pecci. Dialah industriawan Italia pendiri Klub Roma pada tahun 1968. Klub Roma adalah salah satu organisasi rahasia terbesar di dunia. Keberadaannya memunculkan banyak kegelisahan. Ada yang menyebut Klub Roma sebagai kanal pengalir isu global berbasis di Hamburg. Ada yang menyebutnya komplatan elit rahasia yang sangat ambisius menguasai dunia. Mereka selalu berinovasi memanipulasi politik serta perekonamian internasional. Untuk menjalankan misi, mereka bertameng “kerja sama” yang didukung oleh kalangan elit penguasa dunia, Bank Dunia dan Dana Moneter lnternasianal.

Di situs internet (www.clubofrome), Klub Roma memaparkan misi katalisator global dan independen. Slogannya adalah memajukan dunia. Mereka laksanakan rencana setelah menyusunnya dengan cermat. Kecuali anggota elit; pecatur politik tingkat i:nternasional yang berada di balik layar, nama-nama dan alamat ratusan anggotanya terpajang di situs Klub Roma. Seluruh rincian hasil rapat- rapat yang telah dilakukan dan bermacam hasil riset juga bisa disaksikan disitu.

Mereka bernafsu menebar masalah paling rumit dan krusial bagi umat manusia. Jebakan mereka adalah tawaran penyelesaian masalah masyarakat di seluruh dunia (Negara¬negara berkembang) yang tertatih-tatih akibat tarikan arus globalisasi. Seolah mereka satu-satunya pemilik riset hingga mematenkan solusi alternatif masa depan yang wajib ditaati masyarakat dunia. Sejak awal, mereka menjala para pemimpin dunia yang menentukan kebijakan umum rakyatnya masing-masing. Bahkan seringkali dengan para pemimpin itu mereka berkolaborasi membuat skenario agar dunia diguncang “badai masalah”. Setelah masyarakat terjebak kepanikan, baru kemudian mereka menyodorkan solusinya.

Tahun 1972, Klub Roma menerbitkan buku berjudul The Limits to Growth. Buku ini memaparkan hasil riset bahwa sumber daya alam di bumi ini semakin menipis. Perkara ini kemudian mereka asumsikan sebagai akibat negatif dari pesatnya pertumbuhan penduduk dunia. Buku ini best-seller dalam waktu sekejap dan telah diterjemahkan ke dalam 30 bahasa serta terjual lebih dari 30 juta copy.

Publikasi buku Klub Roma itu memastikan perdebatan serius para pakar teori konspirasi. Apa yang terjadi? Celaka! Pakar-pakar itu menegaskan bahwa Klub Roma nyata mencipta “senjata” pemusnah massal. Penegasan ini tidak asing. Sudah menjadi rahasia umum. Mereka menyebar virus AIDS. Pendapat ini dikuatkan oleh beberapa sumber informasi bahwa AIDS adalah virus buatan manusia yang sengaja dikembangbiakkan oleh Klub Roma melalui para penguasa elit dunia, yaitu CIA dan jaringan Bilderbergers.

Sasaran pemusnahan penduduk melalui AIDS ini adalah kelompok masyarakat yang dianggap “tidak layak hidup” hingga harus dilenyapkan. Termasuk di antaranya ras kulit hitam, kaum Hispanik dan kaum homoseksual. William Cooper menyebutkan bahwa sejumlah penduduk terbunuh pada 5 November 2001 atas dasar penegakan hukum. Proyek pengembangbiakan AIDS diberi nama MK-NAOMI. Benua Afrika terinfeksi virus AIDS melalui vaksin cacar tahun 1977, penduduk Amerika Serikat terinfeksi tahun 1978 melalui vaksin Hepatitis B di Pusat Kontrol Penyakit dan Bank Darah New York.” (lihat www. thewatcherfiles.coml cooper laids.htm).

Pemusnahan penduduk secara massal itu bukan tragedi kemanusiaan yang pertama kali mereka lakukan dengan dalih mengendalikan jumlah penduduk dunia. Tahun 1948, George W. McKennan dari Departemen Luar Negeri AS mengeluarkan Foreign Policy Statement-21 (FPS-21 [Surat Pernyataan Kebijakan Luar Negeri 21]). Isi pernyataan itu menekankan pentingnya AS menyusun rencana pengurangan jumlah penduduk dunia yang membengkak.

Tanggal16 Maret 1970, Presiden Richard Nixon diduga kuat menandatangani undang-undang PL91-213. Surat itu adalah pengesahan untuk “stabilisasi” penduduk Gurun Sahara, Afrika. Dengan kata lain mengesahkan pemusnahan
penduduk di sana. Untuk misi itu dia menunjuk John D. Rockefeller III sebagai “pelaksana proyek” biadab ini.

Demikian juga proyek MK-NAOMI. Program riset ini bukan yang pertama kali dirancang CIA untuk memproduksi dan menguji-coba obat-obatan dan senjata biologis. Tahun 1953, proyek 10 tahunan yang disebut MK¬ULTRA, para ahli psikologi dan perilaku melaksanakan program yang bertujuan mengarahkan pikiran dan budaya manusia. Setelah dinyatakan berhasil, proyek tersebut dilanjutkan dengan misi MK-SEARCH dan MK-OFTEN.

Sebagai program lanjutan, tahun 1960, Dr. Robert MacMahan dari Departemen Pertahanan AS meminta $10 juta kepada Kongres AS sebagai dana awal untuk pengembangan senjata biologis yang merusak sistem pertahanan tubuh manusia. Tujuan mereka agar orang¬orang yang “dikehendaki mati” perlahan, mejalani hidup dengan kehilangan daya tahan tubuh alaminya. Proyek ini dijalankan selama kurun waktu sekitar 5-10 tahun. Permintaan ini dikabulkan oleh penyandang dana proyek. Mereka mendapat kucuran dana pada tahun 1970 di bawah H.R. 15090. Dana tersebut dialirkan untuk melicinkan proyek MK-NAOMI tersebut.

Cara yang mereka lakukan sangat rapi dan super canggih. Nyaris tak diketahui bahwa petaka yang timbul di tengah masyarakat adalah hasil dari desain mereka. MK-NAOMI menggunakan teknik-teknik biologi sub¬molekuler sebagai penghasil virus penghancur kekebalan tubuh manusia semisal retro virus AIDS. Bersama dengan itu, CIA meriset dan menebar senjata biologis “pemusnah etnis” yang mampu bekerja sendiri untuk memilih calon korbannya. Setelah ditentukan sasarannya, saat ditebarkan, senjata biologis ini mampu mandiri mengidentifikasi suatu etnis yang menjadi target sasaran berdasarkan genetika dan variasi DNA-nya. Eksperimen-eksperimen untuk menguji senjata biologis itu dilakukan oleh Divisi Operasi Khusus AS di Fort Detrick, Maryland, Amerika Serikat.

Bukti penting yang ditemukan orang-orang yang meneliti bahwa AIDS adalah virus yang sengaja diciptakan adalah berkas catatan hasil penelitian; Progress Report AIDS tahun 1971. Indikasi ini mengabarkan langkah terkoordinir melalui lebih dari 20.000 dokumen paper saintifik dan penelitian yang dilakukan selama 15 tahun oleh Program Federal untuk mengembangbiakkan virus yang identik dengan epidemologi AIDS.

Dokumentasi yang dipublikasikan oleh Freedom of Information Act (Arus Informasi Terbuka) menunjukkan fakta-fakta biadab bahwa masyarakat yang “tidak dikehendaki” hidup dijadikan “kelinci percobaan” oleh Amerika Serikat selama lebih dari 70 tahun.

Tahun 1930-an, serdadu-serdadu Amerika Serikat dan pasien-pasien di rumah sakit sipil dijadikan kelinci percobaan untuk serangkaian program yang membutuhkan eksperimen itu. Masih di tahun 1930-an, Studi Siphilis Tuskegee mendapati 200 orang kulit hitam mengidap penyakit siphilis dibiarkan semarak tanpa pernah diberitahu efek penyakit itu dan tidak mendapat pengobatan. Akibatnya dengan cepat penyakit itu mewabah dalam waktu yang lama.

Komisi Senat Ameika Serikat melakukan investigasi setelah praktek-praktek MK-ULTRA mereka laksanakan. Kesimpulan Komisi Senat AS adalah: Sejak dimulai pada awal tahun1950-an hingga diberhentikan pada tahun 1963, pelaksanaan program LSD yang dilakukan sembunyi¬sembunyi agar tidak diketahui orang-orang yang tanpa sadar hingga hanya bisa menerima dirinya dijadikan obyek penelitian, menunjukkan bahwa kepemimpinan CIA gagal dan hanya efektif membimbing para agen CIA. Kemudian diketahui bahwa uji coba tersebut berbahaya, yaitu mempermainkan dan mengabaikan nyawa manusia yang dijadikan “kelinci percobaan” tersebut. Meski melanggar hukum Amerika Serikat, uji coba tersebut tetap berlanjut. Contoh sebagian kecil orang-orang yang dijadikan kelinci percobaan adalah para pelaku Perang Teluk. Para tentara AS yang diberangkatkan ke medan perang diberi minuman cocktail bercampur obat. Mereka menjadi eksperimen. Obat ini menyebabkan ribuan tentara menderita sindrom Perang Teluk.

Tanggal 3 Oktober 1995, Presiden AS, Bill Clnton akhirnya mengakui bahwa eksperimen radiasi pernah dilakukan Amerika Serikat, karena itu pemerintah AS memberi kompensasi kepada para korban eksperimen tersebut.

Perkembangan AIDS di Barat masih bisa dikendalikan. Tapi tidak demikian dengan Benua Afrika. Fakta menunjukkan virus ganas ini mewabah dan berkembang pesat melintasi Benua Afrika. Seorang pengurus Klub Roma berapologi bahwa buku The Limits to Growth dipahami keliru sebagai sebuah dokumen curang dengan menggunakan rekayasa analisa komputer menyesatkan. Setelah kebusukannya diketahui, dia berkilah bahwa jutaan manusia telah mati akibat virus AIDS selama 25 tahun terakhir dan lebih 70 persen korbannya berasal dari Benua Afrika, tempat epidemi AIDS berkembang pesat. Pernyataan ini justru menjadi bumerang baginya.

Meski asal-usul AIDS dicitrakan masih diselimuti misteri. Namun satu hal yang pasti dan tidak dapat dipungkiri, apapun dalih mereka setelah mencipta kepanikan dan kesengsaraan, bahwa “rekomendasi paksa” rancangan Klub Roma nyata dilaksanakan secara brutal, biadab dan licik serta menyengsarakan masyarakat dunia.

Sumber: Secret Societies – 21 Organisasi Perusak Dunia – Oleh: Michael Nradley hal. 48-55 (akhir zmn)

Daftar Makanan Anak Indonesia Biang Kanker

antimurtad — Fri, 29 May 2009 04:21:13 +0000

Si Manis Peracun Anak

Nyaris 1 juta dolar AS uang riset digelontorkan, sementara lebih dari 1.900 ekor tikus dilibatkan. European Ramazzini Foundation on Oncology and Enviromental, lembaga riset terkemuka di Italia itu, ingin membuktikan, apakah betul Aspartam sejenis pemanis buatan itu berbahaya bagi kesehatan.

Ramazzini tidak keliru. Bahkan, fakta yang mereka kantongi jauh lebih lebih mengerikan ratusan tikus telah siap menunggu ajal. Aspartam, pemanis nonkalori yang memiliki tingkat kemanisan 200 kali gula itu, membikin tikus-tikus tadi langsung dihajar kanker mematikan.

Riset yang digelar pertengahan 2005 lalu itu membuat Uni Eropa kian yakin dengan keputusan mereka melarang penggunaan pemanis buatan pada produk makanan. Jajanan anak-anak, terutama. Jepang, Malaysia, Brunei, Vietnam, langsung mengekor langkah Uni Eropa. Mereka haramkan pula Siklamat, jenis pemanis buatan yang diduga dapat memicu kanker. Bagaimana Indonesia?

Alih-alih dilarang beredar, produk-produk ini sejak lama menjadi kawan akrab anak-anak SD. Mudah ditemui di warung-warung, bahkan dijajakan secara besar-besaran di supermarket. Survei Lembaga Konsumen Jakarta (LKJ) sepanjang Juni hingga Juli di sejumlah titik di DKI Jakarta membuktikan hal itu.

”Dari 49 sampel yang kami ambil, lebih dari separuhnya mengandung pemanis buatan dalam konsentrasi tinggi,” kata Lies Permana Sari. Anggota tim peneliti LKJ itu, kemarin (9/8), membeberkan temuan mereka yang telah dikonfirmasi laboratorium Sucofindo.

Disebut berkonsentrasi tinggi, sebab produk ini memuat kadar gula berlipat-lipat. Selain mengandung gula murni, produk tadi juga ditambahi pemanis. Padahal Badan Pengawas Obat dan Makanan (BPOM) jelas-jelas mengatakan, pemanis buatan hanya digunakan pada pangan rendah kalori dan pangan tanpa penambahan gula. Adapun sampel-sampel yang disisir LKJ meliputi produk jelly, permen, dan minuman. Ini produk jajanan anak-anak. ”Kami sengaja memilih jenis itu,” dia menambahkan. Ada 25 merek jelly, 16 merek minuman serbuk, dan delapan merek permen. Kelebihan zat pemanis ditemukan bukan hanya pada merek-merek tak terkenal, tetapi juga brand-brand yang sering nongol di layar televisi.

Bukan cuma mengandung konsentrasi pemanis tinggi, produk itu juga seperti berupaya menyembunyikan sesuatu. Beberapa produk, seperti Okky Jelly Drink, Okky Bolo Drink, Happydent White, Yulie Jelly, Donna Jelly, Lotte Juicy Fresh, Vidoran Freshdrink, Naturade Gold, dan Mariteh Instant, tidak mencantumkan batas maksimum penggunaan pemanis buatan Aspartam.

Ini, menurut Lies, menyangkut perkara cukup penting. Riset European Ramazzini Foundation tahun silam membuktikan bahwa pemanis buatan Aspartam berisiko memicu kanker dan leukimia pada tikus percobaan bahkan pada dosis pemberian Aspartam hanya 20mg/kg BB.

”Secara anatomis tikus mirip dengan manusia. Apa yang terjadi tikus amat mungkin terjadi pula pada manusia,” kata dr Nurhasan, anggota tim riset LKJ. Karena itu pencantuman komposisi pemanis pada produk amat penting, sebab ada acceptable daily intake (ADI) atau batas jumlah pemanis yang boleh dikonsumsi seseorang sepanjang hidup.

Bahkan, kata dia, jauh-jauh hari riset BPOM pada November-Desember 2002 sudah menunjukkan bahwa konsumsi Siklamat sudah mencapai 240 persen ADI, sementara Sakarin pemanis buatan pemicu kanker kemih sebanyak 12,2 persen nilai ADI. Tak pelak, kata Lies, anak-anak merupakan konsumen yang paling rentan terhadap dampak negatif dari pemanis buatan. ”Otak mereka masih berkembang,” terang dia. Beragam riset menunjukkan bahwa pemanis buatan, terutama Aspartam, berpotensi memicu keterbelakangan mental akibat penumpukan Fenilalanin menjadi Tirosin pada jaringan syaraf.

Berbeda dengan tikus, efek dari pemanis buatan pada manusia memang tak mewujud seketika. Ia terus berakumulasi dan akan dipanen setelah si anak beranjak dewasa. ”Karena itu, ini boleh dibilang silent disease,” tutur Lies seraya mengutip riset di Italia yang menunjukkan bahwa sudah ada bukti serangan kanker akibat konsumsi pemanis buatan.

Apa alasan produsen menaburi pemanis makanan? Sulit dipungkiri, terang Lies, ini terkait dengan upaya mereduksi ongkos produksi. ”Kalau dengan sedikit pemanis saja sudah bisa menggantikan konsentarasi gula, kenapa tidak dipakai?,” kata Lies seraya mengatakan bahwa Aspartam, Sakarin, dan Siklamat memiliki tingkat kemanisan dari 30 hingga 300 kali gula.

Menurut tim LKJ, As’ad Nugroho, BPOM hingga saat ini berkeras pemanis buatan masih aman dikonsumsi umum asalkan memenuhi komposisi. Apalagi ada 50 negara yang masih memperbolehkan meski soal aman tidaknya pemanis buatan masih diperdebatkan hingga detik ini. Pada kenyataannya, terang dia,soal komposisi aman ini banyak produsen yang membandel.

”Saat minta izin BPOM, mereka memberikan produk yang komposisinya tepat. Ke pasar, mereka meluncurkan produk yang lain,” kata dia.

Daftar Makanan Anak Indonesia Biang Kanker

1. Okky Jelly Drink
2. Okky Bolo Drink
3. Inaco Jelly
4. Happydent White
5. Alloy Jelly
6. Donna Jelly
7. Lotte Juicy Fresh
8. Hore
9. Jas Jus
10. Disney SegarSari
11. Nutrisari Hangat
12. Segar Dingin
13. Frutilo Magic
14. Fortiplus
15. Vidoran Freshdrink
16. Hemaviton Jreng 17. Pop Ice
18. Ice Milk Juus
19. Naturade Gold
20. MariMas
21. Finto
22. Buah Sari
23. MariTeh Instan
24. Teh Sisri
25. Marimas degan
26. Kola-Kola
27. Sparta
28. Pop Drink

Sumber: http://bundaathira.multiply.com/journal/item/19

Apa Yang Akan Terjadi Bila Kita Menghentikan Vaksinasi

antimurtad — Fri, 29 May 2009 04:05:24 +0000

Apa Yang Akan Terjadi Bila Kita Menghentikan Vaksinasi Akankah Terjadi Kematian, Menyelamatkan Kehidupan atau Tidak Terjadi Perubahan

In 1975, when Japan stopped vaccinating children under the age of 2 years dramatic improvements in their infant mortality occurred.

Japan’s place in the world scale of infant mortality went from 17, a poor position, to number 1, the best performance. It is quite clear that the shift of the lower vaccination limit to 2 years resulted in a dramatic decrease in SIDS going quickly from a very high to the lowest rate of infant deaths in the world. Between 1970 and 1974, 37 infant deaths occurred after DPT vaccination in Japan and because of this the doctors in one prefecture boycotted the vaccination. Consequently, the Japanese Government stopped DPT vaccination for 2 months in 1975, and, when vaccination was resumed, the vaccination age was lifted to 2 years.

With this change in government policy the entity of sudden death almost disappeared from vaccine injury compensation claims (only 2 deaths were subject of vaccine injury compensation claims in the 2-year olds compared with 37 in younger children). In the late ‘80s, Japanese parents were given the choice to start vaccinating at earlier ages again and most, ignorant of what had gone on before, chose starting at 3 months of age. The rate of SIDS in Japan has since returned to high levels.

Professor Hiroshi Nishida of Tokyo Women’s Medical College said that the SIDS rate among babies aged less than 1 year has sharply increased to 0.33 % in 1992 when compared with 0.07 % in 1980. Dr. Raymond Obomsawin also reported that the “Delay of DPT immunization until 2 years of age in Japan has resulted in a dramatic decline in adverse side effects. In the period of 1970-1974, when DPT vaccination was begun at 3 to 5 months of age, the Japanese national compensation system paid out claims for 57 permanent severe damage vaccine cases, and 37 deaths. During the ensuing six year period 1975-1980, when DPT injections were delayed to 24 months of age, severe reactions from the vaccine were reduced to a total of eight with three deaths. This represents an 85 to 90 percent reduction in severe cases of damage and death.”

SIDS has become a catch-all that conveniently offers the medical profession a loop-hole whereby they can place the blame on the parent.

Sudden infant death syndrome has been reported following administration of vaccines containing Diphtheria, tetanus toxoids, and pertussis vaccine yet in the United States most vaccine-induced deaths are listed as SIDS and thus are not included in vaccine adverse reaction data, even if a child dies only a few hours after receiving inoculation. Some researchers have found that babies die at a rate eight times greater than normal within three days after getting a DPT shot. It is important to note that a highly disproportionate amount of SIDS deaths clustered at 2, 4, and 6 months, which are the very times infants are vaccinated. The three primary doses of DPT are given at two months, four months, and six months. About 85 percent of SIDS cases occur at one through six months, with the peak incidence at age two to four months.

If vaccines had nothing to do with these sudden deaths of “no known cause” there should not be such pronounced clusters. Instead the numbers should be randomly spread throughout the first 6 months of life but they are not. It has been reported that 1 in 175 children who completed the full DPT series suffered “severe reactions,” and some report that as many as 1 in 300 DPT immunizations resulted in seizures. It seems like one of the central mechanisms in which health and even life itself is threatened is the effect the DTP and other vaccines have on breathing. Episodes of apnea (cessation of breathing) and hypopnea (abnormally shallow breathing) were measured before and after DPT vaccinations by some researchers and it has been found that vaccinations have caused an unusual increase in episodes where breathing either nearly ceased or stopped completely. Much more research is needed in this area but there is so much doubt about the safety of vaccines already one need not wait to decide not to vaccinate ones child.

The pediatrician whom I so respected and adored broke down and cried when I gave her the news that my daughter had died. She went back and forth defending the vaccine that she was told was safe, but blamed it for killing my child. She then told me that she also had another patient, an infant boy, die after this same vaccination. Christine Colebeck

In England, after the media in 1975 reported brain damage linked to vaccination, parents stopped vaccinating: the compliance fell down to 30% or even 10% in some areas. A. McFarlane reported in 1982 (Lancet) that the overall infant mortality rate plummeted. There is evidence around the world that low vaccination compliance is linked to low death rate and vice versa.

The vaccination compliance was lowest in 1975-76 when parents were frightened but started climbing up in 1977-78, simply because people have short memories and new parents did not know about the publicity surrounding vaccination as the cause of serious side effects. It is generally known that young couples become interested in these issues only after they have their first children.

For the first 13 days of his life, Nicholas was no different than any other baby. He ate well. When he slept, he slept well. He acted just like my first son acted when he came home from the hospital.”

Nicholas was given a hepatitis B shot at his regular check up at the pediatrician’s office on the 13th day of his life. That night when I got home from work, I noticed that Nicholas was crying a lot more than usual. In fact, he was screaming some of the time. He was acting differently, but because we had just taken him to the doctor for a checkup and they told us he was a big healthy boy, we thought everything was OK. When he was just acting fussy, like babies sometimes do, we didn’t know anything about vaccines or that they can cause problems for some babies. Nicholas cried on and off for most of the night. When I got up and went to work the next day, he was still crying on and off. He continued during most of the day and into the evening. The next morning, his mother found him dead in his crib. From the way he looked, he had been dead for several hours.”

Eventually a clinical professor of pathology reviewed Nicholas’ medical records, autopsy and slides, and then stated in writing that Nicholas did not die of SIDS but died a cardiac death, caused by passive congestive changes with pulmonary edema and hemorrhage caused by the active immunization

with hepatitis B vaccine. The pathologist stated, “I do not believe this was a sudden infant death syndrome death. Sudden infant death syndrome is the most abused diagnosis in pediatric pathology. In this particular case, the infant was two weeks old. Sudden infant death at two weeks old is so rare as to be virtually unheard of.”

The increase in autoimmune and neurological disorders in the past three decades in industrialized countries coincides with the addition of new vaccines to the childhood vaccination schedule as well as rapidly increasing vaccination rates.

original source: http://curezone.com/forums/fm.asp?i=62205

sumber: akhirzaman

Vaksin Mafia Atau Vaksin CIA?

antimurtad — Fri, 29 May 2009 03:49:29 +0000

The Vaccine Mafia Or The Vaccine CIA

Among epidemiologists, it is often half-jokingly referred to as the “medical CIA.” Founded in 1951 by public health professor Alexander Langmuir, the Epidemic Intelligence Service (EIS) was first designed to act as an elite biological-warfare countermeasures unit of the Center for Disease Control (CDC).

Langmuir was hired because he also served as one of the select advisors to the Defense Department’s chemical and biological warfare program.

The Vaccine Mafia Or The Vaccine CIAThe first Epidemic Intelligence Service (EIS) class of 21 recent medical or biological graduates underwent several weeks of intense training at the Center for Disease Control’s Atlanta headquarters, before being dispatched on their two-year assignments on loan to various state or local health departments around the country. They acted as the eyes and ears of the CDC, carefully monitoring for any possible outbreak of war-induced disease.

While on their tours of duty, each EIS officer could be sent elsewhere in the country on a 24 hour-a-day basis. In case of war, the EIS would operate under any emergency powers granted the CDC – potentially including quarantines, mass immunizations, or other drastic measures.

In an article written for the American journal of Public Health (March, 1952), Langmuir made clear that membership in the EIS did not end with the two year assignment, but was permanent. He wrote that “… as a result of their experience, many of these officers may well remain in full-time epidemiology or other public health pursuits at federal, state, or local levels. Some, no doubt, will return to civilian, academic, or clinical practice, but in the event of war they could be returned to active duty with the Public Health Service and assigned to strategic areas to fulfill the functions for which they were trained.”

Every year since 1951 has seen a new crop of EIS recruits, some classes over one hundred members in size. The nearly 2,000 alumni have gone on to high positions in society, though rarely advertising their affiliation. Indeed, the CDC has now made the EIS more secretive than ever, having suppressed the public availability of the membership directory since last year.

EIS MEMBERS PLACED IN KEY POSITIONS

Members can be found in the Surgeons General’s office and elsewhere in the Federal government, as well as in the World Health Organization, state and local health departments, universities, pharmaceutical companies, tax-exempt foundations, hospitals, and even as staff writers, editors, or news anchormen for major newspapers, scientific journals, and television news departments. In these positions, EIS alumni act not only as the CDC’s surveillance arm and emergency reserve, but also as seemingly “independent” advocates for CDC policies.

EIS AND POPULATION “CONTROL”

In time, the fear of artificial disease epidemics faded. But Langmuir and other top CDC officials had always held bigger plans for the EIS. Langmuir, for example, an apostle of Planned Parenthood founder Margaret Sanger, involved the EIS in the population control movement by the 1960s. The CDC has gained most, however, from EIS activities in natural disease epidemics, to which its “disease detectives” have turned their attention.

THE FLU JAB SCAM

The flu, being truly an infectious disease, often proved itself most valuable to the CDC. Although the winter following the end of World War I was the last time a flu epidemic caused widespread death, the CDC has pushed annual flu vaccinations up to the present day. At times, the agency has even rung the alarm over an impending flu crisis, hoping to use memories of the 1918 epidemic to gain emergency powers and impose mass vaccinations. By using such tactics in 1957 over the Asian flu, the CDC managed to wrangle extra money out of Congress to expand the EIS and crash-produce a vaccine. But the flu season was already winding down by the time the vaccine was ready, and the flu itself turned out to have been as mild as in any other year.

By 1976, CDC director David Sencer wanted to try again, though on a grander scale. After one soldier in Pennsylvania died of a flu-related pneumonia in January, Sencer predicted that a pig-borne human virus nicknamed the “swine flu,” would soon devastate the United States.

Panicked with visions of impending doom, Congress moved to authorize the CDC’s immunization plan for every man, woman, and child in the country. Unexpectedly, the legislation suddenly stalled when the insurance companies underwriting the vaccine discovered that it had seriously toxic side effects.

THE “LEGIONAIRES DISEASE” SCAM

Sencer had to do something fast. He immediately set up a “War Room” in Auditorium A at the CDC headquarters, and put the EIS network on full alert to search for any disease outbreak that might resemble the flu. Within weeks, the War Room received word of a pneumonia cluster among men just returning home from the Philadelphia convention of the American Legion. Several Philadelphia-based EIS officers and alumni had detected the outbreak, and acted as a fifth column that not only helped arrange an invitation for the CDC to come in, but also took their orders from the arriving team of CDC and EIS Officers. Even the New York Times staff writer sent to cover the story, Lawrence Altman, was himself an EIS alumnus.

The CDC team allowed media rumors to circulate that this Legionnaires’ disease was the beginning of the swine flu. Within days, Congress decided to pass the vaccine bill. Only later did the CDC admit that the legionnaires had not been infected by the flu virus, too late to stop the immunization program. Some 50 million Americans received the vaccine, leading to more than a thousand cases of nerve damage and paralysis, dozens of deaths, and lawsuits awarding almost $100 million in damages. In the ultimate irony, no swine flu epidemic ever materialized; the only destruction left behind by the phantom swine flu resulted from the CDC’s vaccine.

The agency later blamed Legionnaires’ disease on a common soil bacterium, one that clearly fails Koch’s postulates for causing the disease and is therefore actually harmless. The legionnaires’ deaths are not so hard to understand, since the pneumonias struck elderly men, many of whom had undergone kidney transplant operations, and who had become particularly drunk during the Bicentennial celebration – the classic risks for pneumonia. Thus Legionnaires’ disease” is not an infectious condition, but merely a new name for old pneumonias…

Karin Schumacher
Vaccine Information and Awareness
12799 La Tortola
San Diego, CA 92129
619-339-5498 (voicemail)
619-484-1187 (fax)
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We Must Have The Freedom To Choose & Respect Everyone’s Choice

Original source: http://www.access1.net/via

Oleh: Bryan J. Ellison

sumber:akhirzaman

Tegakah Menyuntik Anak-anak Anda Dengan Bahan Yang Berasal Dari Janin Aborsi?

antimurtad — Fri, 29 May 2009 03:37:00 +0000

Injecting Aborted Fetus Material Into Children?

Doctors have been administering the vaccines for years. Yet, how many of them have ever checked into the ingredients? This has always been right at their fingertips. What would happen if they did? They would read that the vaccine contains “MRC-5″, “WI-38″ (or both) “human diploid cell lines”.

Most parents are not aware that the particular abortions which contribute the fetal tissue parts for vaccine manufacturing, were actually intended for vaccine manufacturing.

One if the most highly misunderstood notions among moral theologians and ethicists is that the abortions involved were not done with the intention of creating vaccines. In fact, in response to President Bush’s decision on federal funding for embryonic stem cell research (ESCR), the USCCB highlights this point as follows:

“In the present case, human lives were taken in order to provide cells for research and, in some cases, precisely to qualify for federal grants; in the case of vaccines, tissues were taken following abortions performed for unrelated reasons.” -(The NCCB Secretariat for Pro-Life Activities, Vol. 12, No. 4 Aug-Sept 2001, The Human Embryo as Research Commodity Special Edition)

It was the intent of the abortionist and the researcher to destroy these babies specifically for vaccine manufacturing. But first, the abortions had to be pre-arranged so the researchers were available to immediately preserve the tissues.

“In order to sustain 96% of the cells, the live tissue would need to be preserved within 5 minutes of the abortion”-Dr. C. Ward Kischer

…”Within one the cells would continue to deteriorate, rendering the specimens useless.”

-[Dr. C. Ward Kischer, Embryologist and Emeritus Professor of Anatomy; Specialist in Human Embryology,
University of Arizona College of Medicine (Tucson, Arizona) Personal interview 7-02, ALL Conference]

1961 Leonard Hayflick, employed by the Wistar Institute, research facility of University of Pennsylvania, started working with aborted fetal cell lines (WI-I through WI-25). Cell strains were derived from the lung, skin, muscle, kidney, heart, thyroid, thymus and liver of 19 separate abortions. The entire research was was for the development of viral vaccine cultivation.

“The isolation of characterization of human diploid cell strains from fetal tissue make this type of cell available as a substrate for the production of live virus vaccines. Other than the economic advantages, such strains in contrast to heteropoloid cells lines exhibit those characteristics usually reserved for normal or primary cells and therefore make the consideration of their use in the production of human virus vaccines a distinct possibility”-(L. Hayflick and P.S.Moorhead, The Serial Cultivation of Human Diploid Cell Strains, Experimental Cell Research, 1961, 25, pg 618)

1964 Hayflick isolates and gives name to the WI-38 cell line derived from the lungs of a baby girl 3 months gestation.

“This fetus was chosen by Dr. Sven Gard, specifically for this purpose. Both parents are known, and unfortunately, for the story, they are married to each other, still alive and well, and living in Stockholm, presumably. The abortion was done because they felt they had too many children. There were no familial diseases in the history of either parents, and no history of cancer specifically in the families.”

-G. Sven, S. Plotkin, K. McCarthy, Gamma Globulin Prophylaxis; Inactivated Rubella Virus; Production and Biological Control of Live Attenuated Rubella Virus Vaccines; Amer J Dis Child Vol 118 Aug 1969

“One of my duties as a young student in the laboratory in, Stockholm was to dissect human fetuses from legal abortions and send organs to the Wistar Institute. Such material was the source of many important studies of cell lines of the Institute, such as Leonard Hayflick’s study of WI-38″

– Norrby, Erling “Listen to the Music: The Life of Hilary Koprowski (review)”, Perspectives in Biology and Medicine – Volume 44, Number 2, Spring 2001, pp. 304-306

Preying on the fear that 20%-25% of pregnant women infected with Rubella pass it to their unborn children, possibly causing defects, doctors encouraged pregnant women to have their unborn children aborted during the 1964 epidemic. The first 26 aborted babies were unaffected. The live rubella virus was found in the 27th killed unborn baby.

“Explant cultures were made of the dissected organs of a particular fetus aborted because of rubella, the 27th in our series of fetuses aborted. This fetus was from a 25-year-old mother exposed to rubella 8 days after her last menstrual period. 16 days later she developed rubella. The fetus was surgically aborted 17 days after maternal illness and dissected immediately. Explants from several organs were cultured and successful cell growth was achieved from lung, skin, and kidney. It was then grown on WI-38,. The new vaccine was tested on orphans in Philadelphia”

-American Journal Diseases of Children; Virus Production and Biological Control of Live Attenuated Rubella Virus Vaccines, Vol. 118 Aug 1969; Attenuation Of RA273 Rubella Virus; Studies of Immunization With Living Rubella Virus; Arch J Dis Child vol 110 Oct 1965

Rubella is clinically named: RA273 (R=Rubella, A=Abortus, 27=27th fetus, 3=3rd tissue explant) cultivated on WI-38 cell line.

Thus, at least 47 separate abortions involved in the research for production of present day rubella vaccine.

Aborted Fetal Cell Line Vaccines And The Catholic Family

Brutal Murder and dissection of the unborn:

“The Fetus As Transplant Donor the Scientific, Social, and Ethical Perspectives,” written by Peter McCullough, who is an immunologist at the University of Western Australia. It’s published by the John Wiley Company in New York.

Here’s McCullough. The Australian International University in Canberra. This is the face page of the book, and he probably knows more about the subject of using fetal tissue than anybody in the world. Incidentally, he is pro-life, and it’s remarkable that his book delineates some of the technologies which have formerly been used to get fetal brain tissue. For example, he talks about how in Sweden they have been puncturing the sac of a pregnant woman at let us say 14 to 16 weeks, and then they put a clamp on the head of the baby, pull the head down into the neck of the womb, drill a hole into the baby’s head, and then put a suction machine into the brain and suck out the brain cells.

And this is directly from his book. Healthy human fetuses from 7 to 21 weeks from legal abortions were used. This is in Sweden. The conceptional age was estimated from crown rump length and so on. Fetal liver and kidney were rapidly removed and weighed. Now at 21 weeks, what they were doing, or 18 weeks, or 16 weeks, was what are called prostaglandin abortions. They would inject a substance into the womb. The woman would then go into mini-labor and pass this baby. 50% of the time, the baby would be born alive, but that didn’t stop them. They would just simply open up the abdomen of the baby with no anesthesia, and take out the liver and kidneys.

Debi Vinnedge, Director of Children of God For Life (www.cogforlife.org) is politically active. Please visit the organization’s site to keep up to date and find out your President’s stand on the issue, along with her correspondence with the manufacturing companies.

U.S. Vaccines Derived from Abortion
Diseases	Vaccine	Manufacturer	Cell line (human fetal)

Polio	Poliovax	Aventis-Pasteur	MRC-5
Measles, Mumps, Rubella	MMR II	Merck & Co.	RA273 and WI-38
Measles-Rubella	Biavax II	Merck & Co.	RA 273 and WI-38
Rubella only	MR-VAX	Merck & Co.	RA 273 and WI-38
Rabies	Imovax	Vantis-Pasteur	MRC-5
Hepatitis A	Hivrax Vaqta	AlaxoSmithKline Merck & Co.	MRC-5 MRC-5
Hepatitis A-B combo	Twinrix	GlaxoSmithKline	MRC-5
Chickenpox	Varixax	Merck & Co.	WI-38 and MRC-5
Smallpox	Acambix 1000	Acambis	MRC-5
Ebola	Unknown (still waiting for trial)	Crucell & N.I.H.	PER C6
HIV	Unknown (still waiting for trial)	Merck & Co.	PER C6
Sepsis	Xigris	Eli Lilley	HEK 293

Read What Focus On The Family has to say of this

About Xigris…

[Published 28 August 2002 Source Espicom Business Intelligence]

Xigris received approval from the FDA on 21st November 2001 for the reduction of mortality in adult patients with severe sepsis who have a high risk of death. Xigris has also been approved in Puerto Rico, Israel, Australia, Argentina, Peru, Romania, Columbia, Mexico, Switzerland, India, Singapore and South Africa.

Xigris is a genetically-engineered version of the human activated protein C molecule, a naturally-occurring protein in the body that helps to balance many of the forces behind sepsis, including coagulation and suppression of fibrinolysis. Additionally, patients with severe sepsis treated with Xigris had a more rapid decline in interleukin-6 levels, consistent with a reduction in the inflammatory response. The drug is administered to patients as a 1-time, 96-hour infusion within an ICU setting.

The precise dosage depends on the weight of the patient. In the PROWESS trial, bleeding was the most common adverse reaction associated with Xigris therapy. Serious bleeding events, including intracranial haemorrhage (0.2 per cent in Xigris-treated patients and 0.1 per cent in placebo-treated patients), were observed during the 28-day study period in 3.5 per cent of Xigris-treated patients and 2.0 per cent of placebo-treated patients. The difference in serious bleeding occurred
primarily during infusion.

A human cell line is used in the production of Xigris, as noted under FDA document, PC 3420 AMP, in the first paragraph, which states:

“Xigris is a recombinant form of human activated protein C. An established human cell line possessing the complementary DNA for the inactive human protein C zymogen secretes the protein into the fermentation medium.”

HEK 293 are cells taken from the kidney of an aborted baby. (If you find this NIH page no longer available, click here)

Abaout the 293 Cell Line …

The protein C is produced in the HEK 293 aborted fetal cell line. 293 cells are available from the American Type Culture Collection. There are variants of the cell line that derive from the parent.

ATCC Number: CRL-1573          Price: $167.00
Designation: 293    Depositors: F.L. Graham
Biosafety Level: 2    Shipped: frozen
Organism: Homo sapiens (human)    Morphology: epithelial
Tissue: kidney; transformed with adenovirus 5 DNA

The 293 cell line is a permanent line of primary human embryonal kidney transformed by sheared human adenovirus type 5 (Ad 5)DNA. [RF32725]

The cells express the transforming gene of adenovirus 5. Although an earlier report suggested that the cells contained Adenovirus 5 DNA from both the right and left ends of the viral genome [RF32764], it is now clear that only left end sequences are present. [RF50113]

The cells express an unusual cell surface receptor for vitronectin composed of the integrin beta-1 subunit and the vitronectin receptor alpha-v subunit. [RF33793] Purified DNA from this line is available as ATCC 45504 (25 micrograms) and ATCC 45505 (100 micrograms).

The Ad5 insert was cloned and sequenced, and it was determined that a colinear seqment from nts 1 to 4344 is integrated into chromosome 19 (19q13.2). [RF50113]

United States Patent 5,681,932
Grinnell October 28, 1997
Inventors: Grinnell; Brian W. (Indianapolis, IN)
Assignee: Eli Lilly and Company (Indianapolis, IN)
Application No.: 458372 Filed: June 2, 1995

1. The recombinant human protein C molecule produced by inserting a vector comprising the DNA encoding human protein C into an adenovirus-transformed host cell then culturing said host cell under growth conditions suitable for production of said recombinant human protein C.

2. The recombinant human protein C molecule of claim 1 wherein the adenovirus-transformed host cell is selected from the group consisting of AV12 cells and human embryonic kidney 293 cells.

3. The recombinant human protein C molecule of claim 2 wherein the adenovirus-transformed host cell is an AV12 cell.

4. The recombinant human protein C molecule of claim 2 wherein the adenovirus transformed host cell is a human embryonic kidney 293 cell.

About the 293 Abortion…

In the FDA report found at http://www.fda.gov/ohrms/dockets/ac/01/transcripts/3750t1_01.pdf

Key statement…Page 81 lines 14-22 “So the Kidney material, the fetal kidney material was as follows. The kidney of the fetus was, with an unknown family history, was obtained in 1972 probably. The precise date is not known anymore.

The fetus, as far as I can remember was completely normal. Nothing was wrong. The reasons for the abortion were unknown to me. I probably knew it at the time, but it got lost, all this information.”

About the PER C6 Abortion and cell lines….

http://www.fda.gov/ohrms/dockets/ac/01/transcripts/3750t1_01.pdf

Key excerpts from the above document: Dr. Van Der Eb, Crucel NV is speaking… “So I isolated retina from a fetus, from a healthy fetus as far as could be seen, of 18 weeks old. There was nothing special with a family history or the pregnancy was completely normal up to the 18 weeks, and it turned out to be a socially indicated abortus – abortus provocatus, and that was simply because the woman wanted to get rid of the fetus.”

“The father was not known not to the hospital anymore, what was written down was unknown father, and that was, in fact, the reason why the abortion was requested.”

“There was permission, et cetera, and that was, however, was in 1985, ten years before this. This shows that the cells were isolated in October 1985, Laeiden University in my lab. At that time already ‘85, I should say the cells were frozen, stored in liquid nitrogen, and in 1995 one of these was thawed for the generation of the PER.C6 cells.

“And this is the final slide just showing you some comparisons between 293 and PER.C6. Again, I remind you that both cell lines were made in my lab for different reasons. The objective, as I indicated, is for 293–was basic research, and we have done many different transformation studies after that, not transformation studies, but gene expressions studies with human embryonic kidney cells in the years following that up to now, I would say.

” PER C6 was made JUST FOR PHARMACEUTICAL MANUFACTURING OF ADENOVIRUS VECTORS As to RCA free, PER.C6 are RCA Free. The history documentation of the cell line has been carried out completely for PER. C6 and was not done at that time for 293.

“And then pharmaceutical industry standards… I realize that this sounds a bit commercial, but PER C6 were made for that particular purpose.”

If you find this document no longer available, click here

About the Cell Lines and Adenovirus (AD5) Safety issues…

http://www.fda.gov/ohrms/dockets/ac/01/briefing/3750b1_01.htm

Background

In 1954, during discussions surrounding the development of adenovirus vaccines for use in the military, the U.S. Armed Forces Epidemiology Board (AFEB) recommended the use of “normal cells” as the substrate for vaccine production rather than cell lines established from human tumors. This decision was based on concerns about the possibility that human tumor cells might be contaminated with occult oncogenic agents that might be transferred to vaccine recipients, an event which might in turn increase the risk of cancer and other neoplastic diseases in vaccinees. As evidenced by current regulatory guidelines and activities of control authorities worldwide, the precedent set in 1954 by the AFEB remains an important factor in the acceptance of all substrates for vaccine manufacture. Currently, the only cultured animal cells that have been used as substrates in U.S. licensed viral vaccines have been primary cells (e.g., derived from monkey, chick, mouse), diploid cell lines (e.g., WI38, MRC-5, FRhL-2), or immortalized (continuous), non-tumorigenic cell lines (e.g., VERO).

Over the past 47 years, two important factors have emerged that warrant serious consideration of the use of immortalized tumorigenic cell lines for viral vaccine production. The first of these factors is that certain novel virus vectors that are presently under development for high-priority target diseases, most notably AIDS, cannot feasibly be propagated in traditionally acceptable cell substrates.

The second factor is that scientific understanding of neoplastic processes and viral-induced carcinogenesis has rapidly advanced, as has the ability to detect and identify infectious, oncogenic agents and other types of adventitious agents that may potentially contaminate cell substrates. These factors underscore the need for developing a regulatory framework in which the relative benefits and risks in using tumorigenic cell lines for vaccine production can be carefully and cautiously revisited.

FDA would like the VRBPAC to consider the potential risks in using two novel cell substrates, 293 cells and PER.C6 cells. These cell lines were developed by transforming human embryonic kidney cells (293) and human embryonic retinal cells (PER.C6) with the transforming early region 1 (E1) of adenovirus type 5 (Ad5). Since cell lines such as 293 and PER.C6 express the Ad5 E1 region, they are able to complement the growth of defective Ad5 vectors which have been “crippled” by deletion of E1. Defective Ad5 vectors have been engineered to express foreign genes such as those from human immunodeficiency virus (HIV), the causative agent of AIDS, and vectors of this type are thought to have significant potential for vaccine development because of their demonstrated ability to generate cell-mediated immune responses to HIV. However, a feature of regulatory importance associated with Ad5-transformed cells is their capacity to form tumors in immunodeficient animals such as nude mice.

In considering potential risks associated with the use of these so-called Designer Cell Substrates – i.e., neoplastic cells derived from normal human cells transformed by defined viral or cellular oncogenes or by immortalizing cellular genes (e.g., telomerase) – OVRR/CBER is considering the approach outlined below within the framework of a “defined-risks” assessment (see enclosed reference Lewis et al., “A defined-risks approach to the regulatory assessment of the use of neoplastic cells as substrates for viral vaccine manufacture”, In Evolving Scientific and Regulatory Perspectives on Cell Substrates for Vaccine Development. Brown, Lewis, Peden, Krause (eds.) Develop. Biol. Stand. [in press]). This framework is intended to examine, and wherever possible, to quantify the potential risk of “transmitting” the tumorigenic components of the cell substrate used for vaccine production, and determine whether that “transmission” might pose a risk, particularly an oncogenic risk, to vaccinees. Factors that could influence the risk associated with the use of Designer Cell Substrates include (1) the known mechanism of cell transformation leading to the development of tumorigenic cells; (2) residual cell substrate DNA; and (3) the presence of adventitious agents, especially oncogenic viruses. These three factors are discussed in more detail below.

Tumorigenicity of Adenovirus 5-Transformed Designer Cell Substrates

The purpose of tumorigenicity testing as applied to cell substrates used for viral vaccine manufacture is to discriminate between cells that have the capacity to form tumors and cells that do not form tumors. The potential risk of oncogenic activity is thought to be higher for cell substrates that have the capacity to form tumors, whereas the potential risk is thought to be low for cell substrates that are unable to form tumors. In considering the risk of tumorigenicity of Ad5-transformed Designer Cell Substrates, it is important to consider the molecular processes that determine the ability of the cells to form tumors.

Adenovirus 5 does not produce tumors when injected into rodents, but it does transform rodent cells in tissue culture. Like adenovirus 5 virions, adenovirus 5-transformed cells do not produce tumors when injected into immunocompetent adult rodents, but these cells can form tumors when injected into immunodeficient rodents such as nude mice. The tumor-forming capacity of Designer Cell Substrates that are produced by transforming normal human cells with adenovirus 5 can be evaluated by comparing them with adenovirus 5-transformed rodent cells.

The adenovirus 5 early region 1 (E1) is composed of the transcription units E1A and E1B, which transform normal cells to neoplastic cells through a multi-step process. The E1A transcription unit immortalizes the cells and establishes those characteristics of the transformed cells that permit them to be eliminated by the antitumor defenses of immunocompetent rodents.

During the transformation process, E1A sensitizes cells to apoptosis (programmed cell death) and increases their susceptibility to killing by natural killer cells, macrophages, and cytotoxic lymphocytes, as well as cytokines such as tumor necrosis factor (see Routes et al., 2000a, 2000b). The adenovirus E1B region alone is unable to immortalize cells, but its function during neoplastic transformation ensures cell survival by inhibiting virus-induced cell killing.

Thus, the E1A region immortalizes cells and determines their limited capacity to form tumors in immunodeficient rodents, whose antitumor immune defenses are compromised. The complexity of these tumor-host processes and their action through nontransferable, immune mechanisms of the host implies that the capacity of adenovirus 5 E1-transformed mammalian cells to form tumors in immunodeficient rodents does not represent a risk factor for the manufacture of viral vaccines provided the cells can be shown to be devoid of adventitious agents (see additional discussion on adventitious agents below).

Several approaches can be considered in evaluating tumorigenicity of adenovirus 5-transformed human cell substrates. These approaches include demonstration that the tumor-forming capacity of the cells in rodents is adenovirus 5-like, and that the cells in the master cell bank are devoid of known and occult adventitious agents. Potential Risks of DNA in Vaccines Residual DNA in vaccines derived from tumorigenic cells, including those transformed by Ad5, can pose potential risks to the vaccine recipient in two respects: oncogenicity and infectivity.

Each of these biological properties must be considered and evaluated for each cell substrate. The oncogenic risk of cell substrate DNA has been considered to be due to several mechanisms.

First, the residual DNA could have dominant activated oncogenes that could exert their effect following expression in recipient cells. In the case of Ad5-transformed cells, the dominant oncogenes would include the E1A and E1B genes.

Second, the incoming DNA could integrate into the host genome in certain genes, such as the p53 gene or the retinoblastoma susceptibility (RB) gene, termed tumor suppressor genes, which are involved in cell cycle control among other cellular processes. Loss of function of tumor suppressor genes has been associated with certain human tumors.

Third, integration of residual cell-substrate DNA could result in the activation of cellular regulatory genes by promoter/enhancer insertion, and this could result in the development of a neoplastic phenotype; this mechanism for tumor development was initially described in chickens for leukemia formation by avian leukosis viruses.

Another result of integration that has been described is an increased methylation of adjacent DNA sequences as well as sequences on other chromosomes, although the consequences of such changes in methylation patterns to a cell are unknown. The second biological activity of DNA that should be considered is its potential infectivity. If a genome of a DNA virus or the provirus of a retrovirus is present in the cell substrate used for vaccine manufacture, then the residual DNA has the potential, upon inoculation into the vaccine recipient, to produce infectious virus from this DNA and thus establish a productive infection.

The assessment of the risk of DNA — both the oncogenic risk and the infectious risk — needs to be considered both in terms of (1) the amount of residual DNA inoculated; and (2) the concentration of oncogene or infectious genome present in this DNA. One assumption is that the biological activity of any DNA administered is directly proportional to the amount of that DNA, and if the active component (oncogene or infectious genome) is carried as part of the cell-substrate DNA, the amounts of the oncogene or infectious genome will be present at a level of 10-5 to 10-6. This is because the haploid mammalian genome is 3 x 109 base pairs, whereas an average gene is between 3 x 103 and 104 base pairs.

Thus, if the residual DNA is present at 10 ng, an oncogene in that DNA would be present at between 0.00001 and 0.0001 ng. Currently there are no data indicating that purified isolated oncogenes or any other DNA are biologically active at these levels. It is also important to note that an additional safety margin for oncogenic activity is provided by the multi-step nature of cancer. This is because if more than one gene or event is required, the risk is diminished and is given by the product of the risk for each event. Thus, if the risk of a neoplastic event being induced by one oncogene is 1 in 106, then if two oncogenes are required, the risk is reduced to 1 in 1012. Strategies that can be considered in evaluating residual DNA for vaccine products manufactured in adenovirus 5-transformed cell substrates include restricting the level of residual DNA to 10 ng or less. If these levels of residual DNA are not feasible, other methods can be considered to demonstrate the safety of higher levels of DNA, such as the inoculation of cell-substrate DNA into neonatal rodents. In the future, more sensitive animal models and in vitro assays may be developed to assess the oncogenic activity of DNA.

The experience in the early 1960s with SV40 contamination of poliovirus and adenovirus vaccines and the continuing questions regarding whether SV40 could be responsible for some human neoplasms underscore the importance of keeping viral vaccines free of adventitious agents. This is particularly important when there is a theoretical potential for contamination of a vaccine with viruses that might be associated with neoplasia. It is unclear whether neoplastic cells have a greater or lower adventitious agent risk than other types of cells.

Because they can be grown for long periods in tissue culture, there may be greater opportunities for any adventitious agents to be detected. Because neoplastic cells survive indefinitely, it is easier to qualify and bank cells that have passed all tests, especially as compared with primary cells (which are derived repeatedly from live tissue and must be re-qualified with each use).

Moreover, many neoplastic cells can be grown in serum-free medium, potentially reducing the likelihood of contamination with bovine adventitious agents. However, if their growth in tissue culture is not well controlled, there may exist additional opportunities for contamination of cells with a longer lifespan. In cases of neoplastic cells for which the transforming event is unknown, there is also a theoretical possibility that transformation occurred as a result of a previous viral infection.

Because some mammalian tumors and some cells transformed by viruses contain infectious virus, cells transformed by an unknown mechanism have a theoretical risk of containing a transforming virus. Cells for which specific knowledge of the transforming event exists (and can be shown not to be a virus that persists in the cells) may be more easily characterized than cells for which there is no specific knowledge of the transforming event (which could theoretically have been due to an infection with a known or an unknown virus).

Extensive adventitious agent testing is required for all cells that are proposed for use in vaccine production. This includes testing in various tissue culture systems, inoculation of animals followed by observation or detection of pathogen-specific antibodies, observation by electron microscopy, and molecular tests as is appropriate based on the history and type of cell to be tested.

Specific polymerase chain reaction assays are used to rule out the presence of many different viruses. PCR-based reverse transcriptase assays are used to rule out the presence of retroviruses. The most sensitive of these assays include amplification steps, either as a result of viral growth in culture or in an organism, or molecular amplification such as in PCR.

Although Ad5-transformed cells are thought to be transformed by a known mechanism, the consequences of overlooking an occult oncogenic agent are significant. As these are the first cells in their class to be considered for vaccine production, evaluating them for the presence of occult oncogenic agents could enhance confidence in their use.

One relevant animal assay that could be used for such an evaluation is the inoculation of cell-free lysates into susceptible newborn rodents, followed by observation for 5-6 months. This assay would detect most known tumor viruses, as well as potentially detect unknown tumor viruses. Several promising areas of research suggest that experimental assays to detect unknown adventitious agents could soon become more generally available.

As such assays become available, they could be considered for use in qualifying novel cell substrates, including neoplastic cell substrates. Risk of Transmissible Spongiform Encephalopathy (TSE) In addition to assessing the possibility of contamination of cell substrates with infectious virus, it is important to consider other agents such as the agent of TSE.

There are several mechanisms by which vaccine cell substrates, including neoplastic cells, could theoretically become infected with a TSE agent. First, viral vaccines are developed and manufactured in cell substrates that may be derived from humans, and all human cells represent a finite possibility of being derived from individuals with a propensity to develop sporadic or familial Creutzfeld-Jakob disease (CJD).

Although the mechanism by which such individuals develop CJD is not understood, CJD has in the past been transmitted to humans by biological products derived from CJD patients, such as human growth hormone and dura mater grafts. Second, vaccine cell substrates are usually exposed to products derived from cattle during tissue culture.

Bovine spongiform encephalopathy (BSE) has been transmitted to humans in Europe in the form of variant CJD, possibly due to ingestion of infected beef. Under certain circumstances, cells in tissue culture can support the replication of certain TSE agents, although it is not known whether human cells in tissue culture can sustain the replication of the BSE agent.

Assays to detect TSE/BSE agent contamination exist, but they may not be sensitive enough to exclude low levels of contamination. Until more is known about the replication of TSE/BSE agents in tissue culture and until more sensitive assays to detect these agents become available, the concern over the possible contamination of viral vaccines with TSE/BSE agents will be at least a theoretical consideration in vaccine development.

The use of immortalized, neoplastic human cells as substrates to develop recombinant viral vectors as vaccines also raises theoretical concerns with regard to possible contamination with TSE/BSE agents. These concerns include:

(1) the implications of the possible presence of a prion protein (PrP)-encoding gene (PRNP) that is abnormal in the individual from whom the cells were derived;

(2) the possibility that the genomic instability attendant with neoplastic processes could produce pathogenic alterations in the normal PRNP gene;

(3) the possible exposure to agents of BSE present in bovine serum used in the propagation of the cells;

(4) the possibility that an increased level of expression of either a normal or abnormal PRNP gene or other unknown factors in neoplastic cells might, upon exposure, sustain the replication of abnormal PrP proteins or otherwise contribute to the development of TSE in humans; and

(5) the possibility that differences in the levels of expression of PRNP genes among clonal/subclonal populations of neoplastic cells may make evaluation of these potential risks more difficult.

Since the lifetime risk of sporadic TSE in the population is about one case per ten thousand people (see Brown, P. et al., [1985], Potential epidemic of Creutzfeldt-Jakob disease from human growth hormone therapy. N Engl J Med. 1985, 313:728-731), there is a finite risk that random tissue samples used for the development of neoplastic cell lines could contain abnormalities that might be associated with TSE transmission. Several strategies can be considered for evaluation of neoplastic human cells for possible contamination with TSE/BSE agents.

These strategies include a determination of the origin of the cells with respect to the possible family history and medical history of the donor regarding TSE risk factors and the identification and documentation of possible exposure of the cell line to bovine-derived materials, such as fetal bovine serum from countries with BSE. Further, two validated methods that could be used to evaluate the potential risk from the TSE agent include sequencing of the PRNP gene from neoplastic cell substrates and evaluating all such cell substrates by Western blot for the presence of protease resistant PrP.

Additional studies may become feasible in the near future and may include evaluation of PRNP expression levels, determination of the ability of a cell substrate to support replication of the BSE agent, and evaluation of for the presence of infectious TSE agents by animal inoculation. As new assays for the detection and evaluation of TSE agents become available, they should be introduced as appropriate for cell substrate screening.

OVRR/CBER plans to present these issues to the FDA TSE Advisory Committee for a comprehensive discussion in the near future. In the interim, for cell substrates for which the presence of TSE could be a risk, sponsors should evaluate this issue by a combination of strategies, as may be technically feasible. Nevertheless, OVRR/CBER would like this Committee to be aware of and consider those issues related to the possible presence or exposure of cell substrates used for the development of viral vaccines to agents associated with TSE/BSE.

SUMMARY Recent animal experiments have demonstrated the utility of Ad5 vaccine vectors as means of stimulating cell-mediated immunity against HIV-1. Based on the review of available data, OVRR/CBER believes that there is an extremely low probability that residual DNA from the adenovirus 5-transformed human cells could transfer traits that could induce neoplastic development in vaccinees. OVRR/CBER also believes that such cells may be considered for the development of HIV vaccines, provided that the phenotype of the cells can be documented to be of an adenovirus 5 E1 type, and that appropriate testing rules out the presence of adventitious agents within the limits of state-of-the-art technology.

For further details visit http://www.cogforlife.org/

Abortion is MURDER!

Vaccinations – The Hidden Facts

The Killer Vaccines

Doctors Are Third Leading Cause of Death

Vaccines – Five Baffling Vaccination FACTS

When Legal Drugs Kill

Vaccines Are Being Made From Aborted Fetuses

Vaccinations Can Kill Your Baby

Ask Your Pediatrician

$20,000 Offer

Adverse Reactions

Vaccines and SIDS

Medical Fascism -FORCED Drugging and Vaccination of Children

Vaccines, by Dr. Len Horowitz (a frightening 121 Minute MP3 audio presentation, 37.3 MB. Did you know that public schools receive government money for vaccinating your child? …Potentially deadly vaccines that parents are NEVER made aware of or given the option to refuse. You can LEGALLY refuse vaccinations and Dr. Horowitz tells you how in this presentation. Dr. Horowitz’ own child was forcibly taken by the state government, you’ll be shocked why. He advises people how not to make the same mistake. If you’re a parent, you need to hear Dr. Len Horowitz!)

Emerging Viruses, by Dr. Len Horowitz (a frightening 204 minute MP3 audio presentation, 114 MB. Dr. Horowitz exposes the evil conspiracy behind AIDS, Ebola, and other emerging manmade viruses. Learn how your own government has conspired against you. AIDS didn’t just happen!)

sumber: akhir zaman

Bahan-bahan Dasar Vaksin – Formaldehyde, Aspartame, Mercury, dll

antimurtad — Fri, 29 May 2009 02:46:08 +0000

Acel-Immune DTaP – Diphtheria-Tetanus-Pertussis Wyeth-Ayerst 800.934.5556

* diphtheria dan tetanus toxoids dan acellular pertussis adsorbsi, formaldehyde, aluminum hydroxide, aluminum phosphate, thimerosal, dan polysorbate 80 (Tween-80) gelatin Act HIB

Haemophilus – Influenza B Connaught Laboratories 800.822.2463

* Haemophilus influenza Tipe B, polyribosylribitol phosphate ammonium sulfate, formalin, dan sucrose

Attenuvax – Measles Merck & Co. , Inc. 800-672-6372

* virus penyakit campak neomycin sorbitol hydrolized gelatin, janin anak ayam.

Biavax – Rubella Merck & Co. , Inc. 800-672-6372

* virus penyakit rubella neomycin sorbitol hydrolized gelatin, jaringan sel diploid ketuban janin bayi aborsi .

BioThrax – Anthrax Adsorbed BioPort Corporation 517.327.1500

* nonencapsulated strain dari Bacillus anthracis aluminum hydroxide, benzethonium chloride, dan formaldehyde

DPT – Diphtheria-Tetanus-Pertussis GlaxoSmithKline 800.366.8900 x5231

*penyakit tenggorokan dan tetanus toxoid dan adsorbsi sel-sel pertussis, formaldehyde, aluminum phosphate, ammonium sulfate, dan thimerosal, washed sheep RBCs

Dryvax – Smallpox (not licensed d/t expiration) Wyeth-Ayerst 800.934.5556

* virus vaccinia, dengan “beberapa kontaminan mikroba”, menurut the Working Group on Civilian Biodefense polymyxcin B sulfate, treptomycin sulfate, chlortetracycline hydrochloride, dan neomycin sulfate glycerin, dan phenol – suatu persenyawaan dihasilkan dari penyulingan cairan gelembung tar kulit anak sapi Engerix-B

Recombinant Hepatitis B GlaxoSmithKline 800.366.8900 x5231

* susunan genetik virus hepatitis B yang dikodekan untuk menampilkan antigen (HbSAg), dikloning menjadi ragi GMO , aluminum hydroxide, dan thimerosal.

Fluvirin Medeva Pharmaceuticals 888.MEDEVA 716.274.5300

* virus influenza , neomycin, polymyxin, beta-propiolactone, cairan janin anak ayam.

FluShield Wyeth-Ayerst 800.934.5556

* virus influenza bervalensi tiga, dari jenis A&B gentamicin sulphate formadehyde, thimerosal, dan polysorbate 80 (Tween-80) cairan janin anak ayam.

Havrix – Hepatitis A GlaxoSmithKline 800.366.8900 x5231

* virus hepatitis, formalin, aluminum hydroxide, 2-phenoxyethanol, dan polysorbate 20 residu MRC5 protein sel diploid manusia dari jaringan ketuban janin bayi aborsi.

HiB Titer – Haemophilus Influenza B Wyeth-Ayerst 800.934.5556

* haemophilus influenza B, polyribosylribitol phosphate, ragi, ammonium sulfate, thimerosal, dan bahan dasar kimia dengan ragi medium.

Imovax Connaught Laboratories 800.822.2463

* adsorbsi virus rabies, neomycin sulfate, phenol, indikator merah albumin manusia, jaringan sel diploid ketuban janin bayi aborsi .

IPOL Connaught Laboratories 800.822.2463

* 3 jenis virus polio neomycin, streptomycin, dan polymyxin B formaldehyde, dan 2-phenoxyethenol lapisan malar ginjal monyet.

JE-VAX – Japanese Ancephalitis Aventis Pasteur USA 800.VACCINE

* strain Nakayama-NIH dari virus encephalitis Jepang, formaldehyde tidak aktif, polysorbate 80 (Tween-80), dan thimerosal serum protein tikus, dan gelatin

LYMErix – Lyme GlaxoSmithKline 888-825-5249

*protein rekombinan (OspA) dari kulit luar spirochete Borrelia burgdorferi kanamycin aluminum hydroxide, 2- phenoxyethenol, phosphate buffered saline – phosphate buffered saline.

MMR – Measles-Mumps-Rubella Merck & Co. , Inc. 800.672.6372

*virus penyakit campak, gondok dan rubella, neomycin sorbitol, hydrolized gelatin, cairan janin anak ayam dan sel diploid jaringan ketuban janin bayi abosrsi.

M-R-Vax – Measles-Rubella Merck & Co. , Inc. 800.672.6372

* virus penyakit campak , rubella neomycin sorbitol hydrolized gelatin, cairan janin anak ayam dan sel diploid jaringan ketuban janin bayi abosrsi.

Menomune – Meningococcal Connaught Laboratories 800.822.2463

*beku-padat polysaccharide antigens dari bakteri Neisseria meningitidis , thimerosal, dan lactose

Meruvax I – Mumps Merck & Co. , Inc. 800.672.6372

* virus penyakit gondok neomycin sorbitol hydrolized gelatin

NYVAC – (new smallpox batch, not licensed) Aventis Pasteur USA 800.VACCINE

*highly-attenuated virus vaccinia, polymyxcin B, sulfate, streptomycin sulfate, chlortetracycline hydrochloride, dan neomycin sulfate glycerin, dan phenol suatu persenyawaan yang dihasilkan dari penyulingan cairan gelembung tar dari kulit anak sapi .

Orimune – Oral Polio Wyeth-Ayerst 800.934.5556

* 3 jenis virus polio, neomycin attenuated neomycin, streptomycin sorbitol – sel ginjal monyet dan serum anak sapi .

Pneumovax – Streptococcus Pneumoniae Merck & Co. , Inc. 800.672.6372

* capsular polysaccharides dari polyvalent (23 types), pneumococcal bacteria, phenol,

Prevnar Pneumococcal – 7-Valent Conjugate Vaccine Wyeth Lederle 800.934.5556

* saccharides dari butiran Streptococcus pneumoniae antigens (7 serotypes) secara individu menghubungkan kepada penyakit tenggorokan diphtheria CRM 197 protein aluminum phosphate, ammonium sulfate, protein kecap, ragi.

RabAvert – Rabies Chiron Behring GmbH & Company 510.655.8729

*strain fixed-virus, Flury LEP neomycin, chlortetracycline, dan amphotericin B, potassium glutamate, dan albumin sukrose manusia, bovine gelatin dan serum “dari negara asal diketahui bebas dari bovine spongioform encephalopathy,” dan protein ayam.

Rabies Vaccine Adsorbed GlaxoSmithKline 800.366.8900 x5231

* adsorbsi virus rabies, beta-propiolactone, aluminum phosphate, thimerosal, dan phenol, rhesus merah sel paru-paru monyet.

Recombivax – Recombinant Hepatitis B Merck & Co. , Inc. 800.672.6372

* susunan genetik virus hepatitis B virus yang dikodekan untuk permukaan antigen (HbSAg), dikloning menjadi ragi GMO, aluminum hydroxide, dan thimerosal.

RotaShield – Oral Tetravalent Rotavirus (recalled) Wyeth-Ayerst 800.934.5556

* 1 rhesus monyet rotavirus, 3 rhesus-manusia reassortant virus neomycin sulfate, amphotericin B potassium monophosphate, potassium diphosphate, sucrose, dan monosodium glutamate (MSG) rhesus sel-sel diploid janin monyet, dan serum janin bovine penyakit cacar (tidak diberikan lisensi karena sudah kadaluwarsa)

40-yr old stuff “found” in Swiftwater , PA freezer Aventis Pasteur USA 800.VACCINE

* virus vaccinia, dengan beberapa kontaminan mikroba ” menurut the Working Group on Civilian Biodefense polymyxcin B sulfate, streptomycin sulfate, chlortetracycline hydrochloride, dan neomycin sulfate glycerin, dan phenol suatu persenyawaan yang dihasilkan dari penyulingan cairan gelembung tar dari kulit anak sapi .

Smallpox (new, not licensed) Acambis, Inc. 617.494.1339 in partnership with Baxter BioScience

* highly-attenuated vaccinia virus, polymyxcin B sulfate, streptomycin sulfate, chlortetracycline hydrochloride, dan neomycin sulfate glycerin, dan phenol – suatu persenyawaan yang dihasilkan dari penyulingan cairan gelembung tar dari kulit anak sapi.

TheraCys BCG (intravesicle -not licensed in US for tuberculosis) Aventis Pasteur USA 800.VACCINE

* live attenuated strain Mycobacterium bovis monosodium glutamate (MSG), dan polysorbate 80 (Tween-80)

Tripedia – Diphtheria-Tetanus-Pertussis Aventis Pasteur USA 800.VACCINE

*Corynebacterium diphtheriae dan Clostridium tetani toxoids dan a cellular Bordetella pertussis adsorbsi aluminum potassium sulfate, formaldehyde, thimerosal, dan polysorbate 80 (Tween-80) gelatin, ekstrak bovine.

US-sourced Typhim Vi – Typhoid Aventis Pasteur USA SA 800.VACCINE

* permukaan sel Vi polysaccharide dari Salmonella typhi Ty2 strain, aspartame, phenol, dan polydimethylsiloxane (silikon)

Varivax – Chickenpox Merck & Co. , Inc. 800.672.6372

* virus varicella neomycin phosphate, sucrose, dan monosodium glutamate (MSG) gelatin yang diproses, serum janin bovine, sel-sel binatang percobaan, albumin darah manusia, dan sel diploid jaringan janin bayi aborsi.

YF-VAX – Yellow Fever Aventis Pasteur USA 800.VACCINE

* 17D virus strain demam kuning sorbitol janin anak ayam, dan gelatin.

http://www.informedchoice.info/cocktail.html

Vaccine Liberation Information: http://www.vaclib.org/pdf/exemption.htm

original source: http://www.rense.com/general59/vvac.htm

sumber: akhirzaman

Mengapa Gempa Berkekuatan 8,7 SR Tidak Menyebabkan Tsunam

antimurtad — Fri, 29 May 2009 02:29:06 +0000

When the Eurasian tectonic plate tilted upwards during the 90 second earthquake on 28 March 2005, it created a brand new island offshore Sumatra. We can use this new island to prove that the March quake was real, and also to prove that the fake quake of December 26, 2004, was a nuclear war crime on an unprecedented scale.

In the center frame, Sumatran citizens sit on an undamaged road surface after the faint 13-second “Richter 8.5″ nuclear tremor on 26 December 2004. Now compare this frame with those on the left and right, both of which were taken immediately after the 90-second Richter 8.7 earthquake on 28 March 2005. Complete shock, awesome property damage, and, as we shall see later, a brand-new island offshore Sumatra.

When the earth roared for 90 seconds late in the evening of March 28, two events follows swiftly on its heels. The first was easily the most obvious, with thousands of buildings destroyed on the Island of Nias and on West Sumatra. Much further east, building collapsed as far away as Medan, and several large concrete structures cracked in Malaysia and Thailand.

The second was that as a direct result of media brainwashing in December 2004, national governments including Thailand and Sri Lanka swiftly sent out makeshift ‘tsunami warnings’ to all of their coastal towns. This second action caused at least four deaths through panic that could easily have been avoided, because an earthquake at a convergence fault like the Sumatran Trench, cannot create a tsunami under any circumstances.

This curious reality was discussed at some length in my earlier tsumani reports, but as a brief refresher, a convergence fault is where one tectonic plate slides under the other. There is no giant collision, but instead, the shattering roar of one huge plate grinding along the underside of the next. Both plates are underwater, so although one might rise slightly, the other will drop by exactly the same amount, each displacing (taking up) the same quantity of water. As a result, excess water displacement, essential for any tsunami, is zero.

All of a sudden, at the end of March, western scientists were faced with the impossible task of explaining why the December ‘earthquake’ (originally declared by NOAA as 8.5 on the Richter Scale), had produced a deadly tsunami, but the more powerful 8.7 real earthquake at the same epicenter in March, had not. Faced with mission impossible, the scientists followed the established media lead, and invented lies they thought sounded plausible. As the London Independent newspaper noted on March 30:

“Scientists are still grappling with the mystery of why such a large earthquake under the ocean did not produce a sizeable tsunami. One thing is certain, however, the Earth did not move as it did on Boxing Day when 10m-high waves killed up to 300,000 people around the Indian Ocean.

“Brian Baptie of the British Geological Survey in Edinburgh said that it would take some days before seismologists can work out precisely what happened on Monday when northern Sumatra was rocked by an earthquake that measured 8.7 on the Richter scale. ‘It is very difficult at the moment to understand why there was not a tsunami following an earthquake this size. One possibility is that its epicentre may have been deeper.’ “

Because the shock effects at the surface were fully 8.7 in nature, and measured as such by both Indonesian and Indian seismic stations, Baptie was either lying or perhaps merely ignorant. But others followed his lead, and the NOAA and media then arbitrarily upped the December nuclear event to a ridiculous 9.3 on the Richter Scale, hoping that the bigger number might help to fool television viewers.

In order to confuse things still further, the BBC showed a graphic in which it moved the December epicenter further north, and the March epicenter further south and east, thus creating the television illusion that the two events were 200 miles apart, and were absolutely NOT connected to each other. Complete rubbish of course. As the chart below reflects, both the Indonesian and Indian seismic stations show the same epicenter for both events.

In the immediate aftermath of the December thermonuclear explosion in the Sumatran Trench, the media was groping around for a parallel event, especially after the Indian Government pointed out harshly that “We don’t have tsunamis in the Indian Ocean”. Clearly the Indians had to be put down swiftly, before the western public has time to become justifiable suspicious. How to do this? Easy, the media invented a fraudulent ‘giant tsunami’ precedent dating back to 1833. Believe me, only the mighty New York Times is allowed to rewrite history in this manner.

At the time of the 1833 earthquake, the locals were more than capable of being able to read, write, and keep accurate journals of events. So were the Dutch colonials authorities in Batavia (now Jakarta, Indonesia), who back then were much admired for their meticulous book keeping. There are copious written records of property damage caused by the earthquake itself, but not a single word about any tsunami at all. So either the Dutch Colonial authorities were lying in 1833, or the New York Times is lying in 2004/2005. You choose whichever one you think is the most likely culprit.

During the undisputed 9.0 earthquake of 1833, a new island was raised out of the sea offshore Sumatra, represented in pink on the chart shown above. This happened simply because the western edge of the Eurasian Plate tilted upwards, as the Indo-Australian Plate slid underneath it, thereby exposing more of the Eurasian Plate seabed. So this new ‘island’ had always been there, with the tilting plate finally exposing it above the old high water mark. A bit like the tide going out, but never coming back in.

One hundred and seventy-one years later, during the March 28 earthquake, another much smaller island was exposed on the Eurasian Plate to the west of Nias island, which is entirely predictable when you think about it. The Eurasion Plate had tilted up slightly again, but not as much as it did in 1833, because this most recent event measured only 8.7 on the Richter Scale. This is a hundred times less powerful than the monster 9.0 earthquake of 1833, so smaller quake = smaller upwards tilt of the Eurasian Plate.

The implications of this simple truth for the conniving liars in the western media are both obvious and disturbing. They have now collectively and fraudulently raised the Richter reading for the December nuclear event from the original 6.4 recorded by both the Indonesian and Indian authorities, through giant creative leaps to a current high of 9.3, which in turn is a hundred times more powerful than the monster earthquake of 1833.

Fine, using basic math (which unlike physics is not theoretical), and knowing the average depth of the continental shelf to the west of Sumatra, we can prove that a “9.3″ earthquake would permanently expose at least 60,000,000 more acres of seabed. In fact, you could now walk all the way from Aceh to Nias Island without getting your feet wet, provided you followed a semi-circular route.

The fact that you cannot make this walk, simply proves conclusively that the media and its tame prostitute ’scientists’ have been lying all the way for the USA. This is probably essential for those who authorized and executed the monstrous Boxing Day war crime, and who don’t want to get caught with their nuclear pants down, having already murdered more than 300,000 Asians with a single thermonuclear weapon. Moreover, bearing in mind the position of the Pacific Trenches relative to Japan and China, these clinically insane madmen may mave more mass murders in mind, using very similar techniques.

The left frame shows the coastline of Nias Island, which is now nearly two feet higher out of the water after the 90-second earthquake on March 28. More convincing is the right frame, which shows the ‘new’ island out to the west of Nias, and thus closer to the extreme western edge of the Eurasian Plate. Before the earthquake on March 28, this structure was a 6″ coral reef, completely submerged at high tide. Now at high tide this reef has been transformed into a new island, with an overall elevation of 4′ 10″. The black band around the base, shows clearly how much of the seabed was permanently lifted out of the water by the March 8.7 magnitude earthquake.

The media is not overwhelmingly clever, but simply exploits the obvious fact that 99% of its viewing and reading public are not specialists in urban warfare, or aviation, nuclear weapons or tectonic plate movements, and so on. This knowledge has served the media’s masters very well, or at least it used to serve them very well, until the Internet started to really blossom out around the world.

Nowadays there are thousands of experts, many of them retired with a lot of time on their hands, who derive considerable pleasure from exposing these media lies and deceptions. It has almost become a sport, in which the establishment media side is steadily losing more and more games to the increasingly professional teams of Internet independents.

With stories like the Sumatran Earthquake, the establishment media does the best it can, hiring two-bit junior scientists and magicians to try and keep you fooled for longer, but in the end they are undermined by real science on the Internet. And the big trick right now (in fact the biggest game in town) is to make you believe that a Richter 6.4 earthquake on December 26, created a massive tidal wave powerful enough to murder 300,000+ people, while the infinitely more powerful Richter 8.7 earthquake on March 28 barely rippled the waters of the Indian Ocean. Hence the fraudulently increased Richter values, and creatively moving the single real epicenter to two different positions, 200 miles apart.

It does not stop there. The public in general keeps asking more and more awkward questions, leading to the media being obliged to elaborate on its basic lies, sometimes in truly hilarious fashion. This was particularly so when one scientist (I use the term ’scientist’ in its loosest sense), did a global piece in which he used graphics to explain how the December 26 ‘earthquake’ managed to cause the giant tsunami that murdered 300,000+ people. Take a look at the two frames below, which I ‘grabbed’ from his television presentation:

The television presentation was a moving graphic, out of which I extracted just a few still frames, but it is essential to remember that it is the motion of the graphic itself which causes deliberate subliminal illusions for your eyes and brain. To understand how and why, you must first record the entire sequence on tape, then single out the most obvious frames for close examination, which I have done for you with the two frames shown above.

The predictably boring ’scientist’ started by telling television viewers that it is “water displacement” which causes all tsunamis. As with most media deceptions, this was part truth and part lie, making it far more difficult for a layman to decode.

Water displacement happens all the time in the deep oceans, for example giant underwater landslides on mid-ocean ridges etc, but these do not and cannot cause tsunamis, because of Archimedes’ Principle, which I explained in detail in the earlier tsunami reports.

To recap briefly, when two large submerged objects change position, they are merely exchanging their water displacements. Because no new rock has been added to the ocean floor (as it would be in the case of a new volcano, for example), there is no EXCESS water displacement to increase the level of the ocean, and lots of excess water is essential for any tsunami. So, no excess water displacement = no tsunami. It really is as simple as that.

Somehow the establishment media had to reverse this truth and make you believe the opposite, which is where the illusory moving graphic shown on television last week comes into the picture. In the left-hand frame, the ’scientist’ was explaining that in the Sumatran (also known as “Suma” and “Sundra”) Trench, the Indo-Australian tectonic plate had slid beneath the Eurasian tectonic plate, which of course is true. But then he said that this action had raised the entire Eurasian tectonic plate so far, that water displacement caused the tsunami. This was a bare faced provable lie, and the point at which the heavy illusion was triggered.

As any advertising executive or psychologist will confirm, the human eye is first drawn to the top-right hand corner of a page, which is why this premier position commands a higher advertising price than (say) the lower left-hand corner. Now take a closer look at the top right-hand corners of the two frames above, which were grabbed by me from the moving film. What do you see, or, more importantly, what does your brain think that it sees?

In the left frame you can see the Indo-Australian plate start to slide diagonally to the right underneath the Eurasian plate, with the Eurasian plate starting to rise (tilt) slightly as a result. The right frame was grabbed about two seconds later, showing the Eurasian plate rising up even further, and apparently squeezing the ocean out of the top of the frame. So the illusory subliminal suggestion at this stage, is that the water above the Eurasian plate is being squeezed out above sea level, and thus causes a tsunami.

In order to drive the first illusion home, this footage was immediately followed by another moving graphic of a huge wave-train, allegedly the ‘tsunami’ resulting from the first illusion. You can laugh as much as you want to, but this is no laughing matter. About 99.9% of the viewing public saw this event only once at 35 frames per second, and it would have been very convincing for all viewers without any real knowledge of Archimedes’ work.

The two still frames above expose the illusion for what it really was. If you study them carefully for a few seconds, your eyes and brain start to see the whole picture, rather than merely catching a glimpse of the preferred top right corners. As the Eurasion plate on the right rises, the Indo-Australian plate on the left sinks downwards exactly the same distance. Because the two plates are in contact with one another, it is impossible for them to do anything else. Have you got that bit?

Fine, now look at the actual area of ocean in each frame very carefully, remembering that both tectonic plate structures are completely submerged under water. As the Eurasian plate rises, the water above it simply moves to the left, in order to fill the exact same void volume space left by the sinking Indo-Australian plate. There is absolutely no excess displacement, and without excess displacement you cannot possibly have a tsunami. Thus we need to look for an alternative way of generating sufficient energy to displace the hundreds of millions of tons of water needed for the December 26 event.

After the December 26 thermonuclear weapon was detonated in the Sumatra Trench, Australian authorities knocked back all requests for seismic traces of the event, using stupid excuses like “our equipment wasn’t switched on”, “Australian seismographs cannot record above 8.0 on the Richter Scale”, and “You must ask the American authorities about that”. In other words, Australian officials were ordered to lie to the Australian public. This was all forgotten on March 28 this year, when Australian government geophysicists excitedly displayed the seismic trace of the Sumatran 8.7 earthquake, thus proving their equipment could read any magnitude, and furthermore proving they blatantly lied back in December. Put bluntly, New York has Australia’s officials by the balls.

Because the required energy is so huge, only one other device known to man could have caused the rapid blast expansion needed to temporarily displace this huge volume of water and send it surging across the ocean towards India’s two advanced (Russian) nuclear reactors on its Tamil Nadu coastline, and towards India’s advanced (Russian) Sukhoi 30 fighters allocated to the Nicobar Islands in the Bay of Bengal. The device in question is of course the thermonuclear weapon, otherwise known as the “Hydrogen Bomb”. Minimum size required for this event would be 5+ megatons equivalent TNT, with a more likely practical yield of 8 -10 megatons

Only two nations on earth have ever developed and tested weapons of this size – America and Russia. Therefore, in order to find the culprit we must examine possible motives, and any activity before detonation which indicated that either America or Russia was moving into the area prematurely, in order to take military or economic advantage of the monstrous aftermath of death and destruction caused by the artificial tsunami.

After careful analysis, Russia comes up with a completely clean bill of health. Not only has India been a key ally and economic partner for more than forty years, India is also crucial to Moscow as a leading player in the new Russia-China-India-Brazil Coalition. So for Russia to attack India at this point in history would be as stupid as Russia attacking Russia. Rest assured that President Vladimir Putin is not stupid.

As explained in detail in my two tsunami reports, America managed to get two large battle groups into position in record-breaking time from Hong Kong and Guam during the festive season. Each battle group was carrying more than twice the normal complement of Marines, and had recently exercised for a gargantuan (though unspecified) “Humanitarian Relief Operation”.

My personal assessment of the situation is that taking into account sea tracks, navigable channels and possible sailing speeds, neither fleet could have arrived in the eastern Indian Ocean when it did, unless every ship was literally waiting for the starter’s gun, fully manned and with steam up.

New York and Washington also had a strong motive, though it is a little obscure. By forming the Russia-China-India-Brazil coalition, Putin has completely blocked “Fortress Americas”, a Zionist fall-back plan to isolate the Western Hemisphere if things got too rough in the Eastern Hemisphere, and overrun South America and Canada for their mineral resources. If the tsunami had been slightly more powerful it would have caused a second (and possible third) nuclear Chernobyl in southern India, thus breaking a critical link in the new coalition’s chain of command.

The fact that this did not eventuate might have more to do with luck than science, because it seems the criminals who designed the December 26 event, genuinely believed that the weapon would be powerful enough to cause a subduction slip of the stressed Indo-Australian plate under the Eurasian plate, at the time of detonation.

If this had actually happened, it would have been virtually impossible to expose the covert action, because the sharp compression wave caused by the thermonuclear weapon detonating, would have been mixed up with the 90-second jumble of transverse shear waves on the seismograph, exactly the same as those shown above for the March 28 quake.

Fortunately, it seems likely that ‘God’ has left the side of these homicidal ‘Christian’ crusaders, and although placed under enormous nuclear stress, the two mammoth tectonic plates managed to stay in their correct positions, though unquestionably weakened. During January and February more than 100 significant events further north towards Chittagong proved that the integrity of the Sumatran Trench had been seriously compromised, and then on March 28, the deep portion of the trench where the nuclear weapon was detonated finally gave way, with the Indo-Australian plate sliding several yards under the Eurasian plate.

And here you have the final proof. If there really had been a ‘Richter 9.3′ earthquake on December 26, the enormous pressure between the Indo-Australian plate and the Eurasian plate would have been relieved completely by the quake, leaving the Sumatran Trench stable for another 50 years or so. Minor aftershocks of course, as the zillions of tons of tectonic plates ‘bedded in’ again, but absolutely no major events like March 28.

The Declaration of Independence makes it abundantly clear what is expected and demanded of all American citizens when an elected Government moves to quash their unalienable rights, or acts illegally in any other way including war crimes:

“when a long train of abuses and usurpations, pursuing invariably the same Object evinces a design to reduce them under absolute Despotism, it is their right, it is their duty, to throw off such Government, and to provide new Guards for their future security.”

Understandably perhaps, the authors of the Declaration could scarcely have envisioned the day when an elected Government would become completely subservient to a bunch of Wall Street bankers instead of the ‘governed’, which would then invent fictional terrorist organizations in order to remove the unalienable rights of the ‘governed’, and finally order the brutal murder of more than 300,000 people in South and South-East Asia with a single nuclear weapon. Back in 1776, such blatantly obvious abuses of power would have seemed ridiculous.

Though there are no hard and fast rules on exactly how the governed are expected to carry out their duty in respect of the above-noted high political crimes and treason, it does seem unreasonable to ask the American public to go to the trouble of building several wooden gallows on Capitol Hill, when an abundant number of mobile cranes are readily available today at low hire rates. The center picture above shows five Iranian drug pushers after sentence was passed and carried out.

Back in 1978 the Shah of Iran was the biggest global drug pusher of all, and like most American politicians today, would have scoffed at the prospect of he or his fellow criminals ever being brought to justice by ‘ordinary’ Iranian people. Though the Shah managed to escape the country in 1979, most of his murderous cohorts and collaborators wound up hanging from cranes less than five days after the Revolution started. These abusive Iranian officials were deluded into believing they had absolute power over the people, but slowly choking to death at the end of manila hemp ropes proved they did not. History is full of such examples.

American politicians and officials must be executed with the same attention to detail as any other common criminal, so the ‘governed’ should make sure that correct protocol is followed. The traditional American hangman’s noose has from five to thirteen coils, which slide down the rope delivering a heavy blow to the side of the neck. The modern American coiled noose is prepared in accordance with a procedure laid down in a US army manual, from 30 feet of 3/4″ – 1″ diameter manila hemp rope, boiled to take out stretch and any tendency to coil. It is formed into six coils and then waxed, soaped or greased to assure that the knot slides easily.

It seems unlikely that the American public in general will be sufficiently motivated to take action for at least another year (or when crude oil prices exceed $100 per barrel), but this does not mean that you personally cannot prepare yourself for the day when New York and Washington’s murderous master criminals are brought to justice. If you have time on your hands and a little spare cash, why not drive down to the hardware store and buy a 30′ length of manila hemp rope? Pick up a can of axle grease from the gas station on your way home, and then use the twilight hours to grease your rope, and learn how to fashion a really good hangman’s noose.

It pays to be ready, and try to remember that this is not a joke, or even simple vengeance for being abused and suppressed by these out-of-control fanatics. Removing these criminals from power, and punishing them for their crimes, is your solemn duty under the Declaration of Independence.

original source: http://www.bibliotecapleyades.net/oleh : Joe Vialls 5 April 2005

sumber: akhirzaman

Terbukti Tsunami Asia Merupakan Kejahatan Perang

antimurtad — Fri, 29 May 2009 02:24:49 +0000

The total footage in this film was derived from four different amateur cameras in Banda Aceh, and is thus not the intellectual property of the BBC. The British editors have cleverly strung the four individual clips together to create the misleading illusion that the “earthquake” and “tsunami” were in reality a single traumatic event lasting more than two minutes, with buildings crumbling everywhere while the ocean crushes the poor Indonesians.

Not only this, but the editors have also slipped later frames into the earlier part of the footage, thereby subliminally suggesting that the buildings were wrecked by the ‘earthquake’ BEFORE the tidal wave overwhelmed the town. These frames can be easily identified by perceptive viewers who care to pinpoint water under and around the wreckage. These frames were shot after the first wave hit Banda Aceh, but before the second much larger wave.

This is entirely deceitful. The “Richter 9.3 Earthquake” (NOAA) in actuality only shook Banda Aceh for a total of 13 seconds, with no aftershocks at all during the following 22 minutes, until the giant tidal wave appeared out of nowhere, killing everyone in sight. As the real 13-second sequence on the main page shows, the alleged ‘earthquake’ killed no one and caused no property damage, apart from a power cut which disabled the elevators in the Kuala Tripa Hotel.

By direct comparison, the San Francisco Earthquake of April 18, 1906 was a ‘mere’ 7.9 on the Richter Scale, but nonetheless caused severe vibrations for a total of 67 seconds (48 +11 + 8), because it was a real earthquake generating transverse shear waves. As thousands of old photographs will attest, these violent Californian transverse shear waves in 1906 caused structural damage and death as far away as Oregon.

The Sumatran event captured by the Indonesian Padang seismic station (shown below), is a very good example of the massive single compression wave recorded after an underground nuclear blast. The sole remaining question is which New York Nutcase ordered the operation, and the deaths of nearly half a million innocent people – mostly Muslims of course…

original source: http://www.bibliotecapleyades.net/ciencia/esp_ciencia_tsunami14e.htm

sumber: akhirzaman

Nuklir Tsunami, Akhirnya Terungkap, Sebagai Senjata Pemusnah Massal

antimurtad — Fri, 29 May 2009 02:17:17 +0000

Please help us throw ink at the devil by printing and distributing this article!!

Sebelum ditemukannya senjata nuklir, Tsunami terakhir terjadi pada tahun 1883. Tsunami yang terjadi disebabkan oleh sebuah LETUSAN VULKANIS di pulau KRAKATAU, Indonesia!!

“Seperti Sebuah Medan Perang”…. Sebagian dari kerusakan sebagai akibat Nuklir Tsunami yang menghantam Indonwsia pada tanggal 26 Desember 2004 yang membunuh hampir 300.000 orang.

Bisa saja KEBETULAN tetapi tsunami berikutnya terjadi di lepas pantai Alaska pada tahun 1946.

Pada tanggal 1 April, 1946, sebuah “gempa bumi” besar dan tsunami menerjang Kepulauan Aleutian di lepas pantai Alaska.

Pentagon menghantam lagi . . . Iran . . ..dengan senjata nuklir lain, yaitu “gempa bumi” . . . .Special report from the BBC

Lihat U.S. Geological survey setiap hari untuk melihat aktivitas nuklir Pentagon

Pentagon memiliki lebih dari 10,000 buah Nuklir yang mematikan di dalam gudang persenjataannya.

Pentagon memiliki lebih dari 10,000 buah Nuklir di dalam gudang persenjataannya yang mematikan. Setiap bom hydrogen adalah 50 kali lebih kuat daripada bom atom yang dijatuhkan di Hiroshima, Jepamg pada tahun 1945.

Sebuah bom hidrogen bila ditempatkan secara strategis dapat menghancurkan sebuah negara sebesar Inggris. Hitler memiliki Bom-H pada tahun dan Pentagon membawa bom=-H Hitler ke Amerika Serikat dan diuji coba di Alaska pada bulan April 1946.


	Secara teoritis, Pentagon 9 megaton W-53 hulu-ledak termonuklir (kiri atas), bisa dengan mudah dikemas dalam sebuah tempat kecil ‘menyerupai’ saturasi untuk menyelam (kanan atas), supaya terlindung dari tekanan 10,000 pound dari setiap inci persegi di dasar laut Sumatra Trench. Keseluruhan kemas yang dilapisi baja beratnya kurang dari lima ton, bisa diselipkan di buritan kapal penyuplai anjungan minyak, yang di Asia sendiri terdapat lebih dari 300 buah. Siapa yang akan memperhatikan?

	Bom hidrogen yang mematikan adalah nuklir di dalam nuklir.!

Hidrogen atau bom thermonuklir adalah nuklir di dalam nuklir. Dengan kata lain, ia menggunakan fisi (pembelahan sel) dan milyaran derajat dalam sebuah bom atom konvensional (primary) untuk memicu sebuah reaksi berantai (fusion) dalam bom lain (secondary) dalam rangka menciptakan ledakan nuklir. Tahap ketiga atau tertiary dapat ditambahkan hingga hasilnya mencapai 20 juta ton TNT!!

Dr. Edward Teller mengatakan bahwa limit monster ini adalah 100 juta ton TNT!!

Bom-H pertama diproduksi oleh Nazi Jerman dengan bentuk yang sangat besar dan memerlukan pendingin khusus (cryogenics) untuk menjaga agar cairan deuterium tetap berada di bawah 400 derajat Fahrenheit

Pada waktu itu kapal selam merupakan cara yang ideal untuk mengantarkannya, namun akan meletus juga sewaktu terjadi ledakan.

Uji coba Bom Atom pertama bertempat di Port Chicago pada tanggal 17 Juli 1944!!

Ledakan atom pertama di dunia terjadi di Port Chicago di sebelah utara San Francisco pada tanggal 17 Juli, 1944. Ledakan atom ini merupakan uji coba senjata yang dirakit dengan bom uranium yang kemudian dijatuhkan di Hiroshima, Jepang pada tanggal 6 Juli, 1945.

Uji coba atom dilakukan dengan pura-pura menggunakan bahan peledak konvensional. Ratusan pelaut memuat perlengkapan senjata ke atas kapal di pelabuhan untuk persiapan Perang Pasifik. Ledakan terjadi dan menghancurkan segalanya dalam jarak 1/2 mil dan menyebabkan gelombang air laut besar. Pentagon mengatakan bahwa perlengkapan senjata di atas kapal terbakar api yang menyebabkan ledakan. Ini merupakan kebohongan murni karena tidak ada api sebelum terjadinya ledakan.

Prinsip-prinsip bom Hidrogen sudah diketahui pada tahun 1944!!

Prinsip-prinsip bom hidrogen sudah diketahui sejak tahun 1944 …. Kekuatan penghancur sebuah bom hidrogen dibandingkan dengan sebuah bom atom biasa adalah seperti sebuah MAINAN …. Hitler tidak main-main dan para ilmuwannya memfokuskan dalam membuat dan mengirim Bom-H.

Menurut Dr. James B. Conant, Presiden Universitas Harvard dan penasehat ilmiah untuk Jenderal Groves, Super Bom Amerika Serikat dengan seksama dikembangan pada tahun 1944.

Dr. James B. Conant (1893-1978). President of Harvard University and scientific adviser to General Groves.

“Dengan menggunakan berbagai macam metoda, nampak sangat mungkin untuk mengembangkannya dalam jangka waktu enam bulan setelah bom pertama disempurnakan, dan harus memungkinkan untuk dapat ditingkatkan efisiensinya … dalam kasus ini sejumlah materi yang sama akan menghasilkan sama dengan kira-kira 24,000 ton TNT. Pengembangan lebih lanjut sepanjang alur kebijakan ini memungkinan untuk diproduksinya sebuah bom tunggal dengan jumlah materi dan efisiensinya untuk mengejar jumlah yang sama dengan beberapa ratus ribu ton TNT, atau bahkan sebanding dengan satu juta ton TNT… Semua kemungkinan-kemungkinan ini hanya terdapat dalam menyempurnakan efisiensi penggunaan unsur-unsur “25″[U235] dan “49″[Pu239]. Dengan demikian Anda akan melihat bahwa sebuah bom “super” yang patut dipertimbangkan adalah dalam penggunaannya di tengah-tengah laut tidak lagi terlepas dari reaksi nuklir lain.”( Bush-Conant Letter on the Super Bomb, National Archives).

Surat ini ditulis oleh Dr. Conant kepada Vannevar Bush pada tanggal 20 Oktober 1944!!

“Gempa bumi” pertama dan Tsunami dalam abad ke-20 terjadi di Alaska pada tanggal 1 April 1946!!

Pada tanggal 1 April 1946, sebuah “gempa bumi” yang sangat besar dan Tsunami menerjang kepulauan Aleutian tepi pantai Alaska:

“Salah satu Tsunami luas yang paling desktruktif di Pasifik adalah yang disebabkan oleh gempa bumi berkekuatan 7.8 di dekat kepulauan Unimak di Alaska, di rangkaian kepulauan Aleutian. Sebuah gelombang sangat besar 35 meter menghancurkan seluruh bangunan mercusuar U.S. Coast Guard’s Scotch Cap di Unimak dan membunuh semua orang petugasnya yang berjumlah lima orang. Bahan struktur mercusuar terbuat dari baja-yang diperkuat beton, berdiri tegak sekitar 30 meter di atas permukaan laut. Tanpa peringatan, gelombang Tsunami yang menghancurkan mencapai kepulauan Hawai , lima jam kemudian, menyebabkan kerusakan parah dan merengut nyawa manusia. Gelombang Tsunami menghancurkan pelabuhan Hilo di pulau Hawaii, membunuh 159 orang. Jumlah korban semuanya 165 orang, termasuk anak-anak yang sedang belajar di sekolah Hawaii Laupahoehoe Point, dimana gelombang laut mencapai 8 m, juga menghancurkan sebuah rumah sakit. Kerusakan diperkirakan sebesar US $26 juta (nilai dolar tahun 1946). Pada tahun 1948, dan sebagai akibat Tsunami ini, kemudian Amerika Serikat mendirikan sebuah “Pacific Tsunami Warning Center di Hawaii.”( Intl. Tsunami Info. Center) .

Uji Coba Pertama bom hidrogen bertempat di Alaska pada tanggal 1 April 1946!!

Setelah Perang Dunia II, Alaska dipilih sebagai sebuah tempat favorit oleh Pentagon untuk melakukan uji coba senjata-senjata nuklir. Wilayah tersebut berdekatan dengan wilayah Rusia, dengan demikian jatuhan radio aktif akan mengkontaminasi Siberia dan cukup jauh dari wilayah daratan Amerika Serikat untuk menyembunyikan efek dari “tembakan” atau uji-coba. Koordinator uji-coba nuklir di Alaska adalah Dr. Edward Teller—disebut juga “bapak dari Bom-H:”

Dr. Edward Teller, tengah (1908-2003), dijuluki sebagai “bapak bom-H” sering melakukan kunjungan ke Alaska . Dengan kedok penggunaan nuklir untuk tujuan damai ia melakukan uji-coba beberapa bom-H di Alaska dengan nama sandi Project Chariot .

Teller melakukan uji-coba sebuah bom hidrogen di Alaska pada tanggal 1 April 1946. Media massa dunia yang dikendalikan Pentagon melaporkan kejadian tersebut sebagai sebuah kejadian “gempa bumi” dan Tsunami.

Ledakan bom hidrogen ini dipicu oleh sebuah alat berupa senjata rakitan mirip dengan yang digunakan pada “Little Boy”— bom Hiroshima.

Hitler telah menyempurnakan pembuatan bom-H yang akan digunakan untuk melawan Inggris atau menghancurkan pelabuhan – pelabuhan Amerika Serikat.

Peralatannnya apakah merupakan tiruan dari bom Jerman atau penemuan Teller di Los Alamos.?

Kekuatan penghancur bom-H tidak dapat dibayangkan sebagaimanan diperlihatkan oleh akibat-akibat dari “gempa bumi” dan Tsunami.

Bom hidrogen juga disebut SUPER. Di bawah ini sebuah kutipan pejabat berwenang dari the U.S. Nuclear Weapons: The Secret History, sbb:

“Sebuah pertemuan awal penting setelah masa berakhirnya perang mengulas status bom-H Super telah diadakan di Los Alamos dari tanggal 17 April s/d 23 April 1946. Mengkaji ulang hasil pekerjaan yang telah dicapai sampai saat ini dalam memproses thermonuklir, juga dipresentasikan sebuah model yang khas dari sebuah bom thermonuklir. Konferensi memusatkan perhatian terhadap kelayakan model, yang telah dipilih untuk amenability dalam kaitan teoritis ketimbang praktek-praktek rekayasa maupun efisiensi dengan digunakannya bahan fissile dan tritium. Tujuan daripada konferensi adalah untuk mempelajari kelayakan bom thermonuklir dalam prinsip, namun tidak bermaksud untuk mengusulkan rancangan senjata yang sebenarnya. Serangkaian perhitungan yang ekstensif ENIAC mengenai salah satu pembakaran tritium dan deuterium telah selesai. Tujuan tambahan dari pertemuan adalah untuk membicarakan hasil-hasil perhitungan dan untuk memberikan penilaian ke depan dalam merealisasikannya secara pisik dari sebuah peralatan thermonuklir. Meskipun disederhanakan namun sebenarnya relatif ambisius dalam model, kesepakatan umum dicapai bahwa hasil-hasil awal untuk di dorong (disampaikan apa yang telah diketahui pada waktu itu mengenai faktor-faktor yang menyangkut radiasi pendingin serta dispersi bahan bakar) Beberapa dokumen komprehensif dibuatkan konsepnya sebagai tahapan awal dari pengembangan program thermonuklir yang akan berakhir. (Hansen, U.S. Nuclear Weapons: The Secret History , p. 45). ..”(Intl. Tsunami Info. Center)

Ledakan Kedua Bom Hidrogen Bertempat di Lepas Pantai Rusia pada tahun 1952

Menurut “para ahli” Rusia tidak meledakkan bom hidrogen sampai dengan tahun 1955. Oleh karena itu, “gempa bumi” dan Tsunami mestinya merupakan kerja Pentagon. Pada waktu itu, situasi Perang Korea sedang memburuk untuk Jenderal McArthur. Di bawah ini kutipan lain dari the International Tsunami Info Center:

“Pada tanggal 4 Nopember 1952, sebuah gempa kuat (berkekuatan 8.2) di lepas pantai Semenanjung Kamchatka mendorong terjadinya kerusakan Tsunami Pasifik yang luas. Gelombang Tsunami menerjang Semenanjung Kamchatka, Kepulauan Kuril dan wilayah Timur Jauh Rusia lainnya, menyebabkan kerusakan yang parah dan kematian. Tsunami secara luas diobservasu dan dicatat di Jepang, tetapi tidak terjadi kerusakan maupun kematian. Terdapat kerusakan yang cukup berarti di Kepulauan Hawai dan beberapa kerusakan di Peru dan Chili. Tsunami juga dicatat atau diobservasi di seluruh kepulauan Pasifik. Di Selandia Baru gelombang laut naik setinggi 1 meter. Di Alaska, di Kepulauan Aleutian dan di California gelombang air laut mencapai 1,4 meter yang juga di catat atau diobservasi. Sejauh ini, gelombang air laut terbesar diluar daerah asal Tsunami diobservasi di Kepulauan Hawaii. Beruntung tidak ada manusia yang menjadi korban di Hawai dari terjangan Tsunami, namun kerusakannya parah, diperkirakan kerugian materi berkisar antara US$ 800.000 – US$ 1.000.000 (nilai dolar tahun 1952). Tsunami juga menyebabkan kerusakan di Pulau Midway. Dibeberapa tempat di rangkaian kepulauan Hawai, gelombang pasang air laut merusakkan perahu dan dermaga, memutuskan hubungan telepon, dan menyebabkan erosi pantai yang parah. Di beberapa lokasi, gelombang Tsunami merusak di beberapa lokasi tertentu namun hampir tidak ada catatan. Di pantai sebelah utara Oahu gelombang pasang yang tergadi mencapai ketinggian sampai dengan 4.5 meter. Di pantai sebelah selatan di pulau tersebut, Tsunami cukup kuat menghanyutkan kapal barang bermuatan semen di Pelabuhan Honolulu..”(Intl. Tsunami Info. Center)

Ledakan Ketiga Bom Hidrogen Terjadi di Alaska pada tanggal 9 Maret 1957.

Pentagon meledakkan sebuah thermonuklir a BIG ONE pada tanggal 9 Maret 1957 di Alaska. Mungkin peledakkan ini berkaitan dengan Operation Dropshot—rencana invasi ke Rusia yang ditetapkan tahun 1958:

“Pada tanggal 9 Maret 1957, sebuah gempa berkekuatan 8.3 di selatan Kepulauan Andreanof, di Kepulauan Aleutean, Alaska – di wilayah yang umumnya sama dengan yang terjadi pada tanggal 1 April 1946 – mendorong sebuah Tsunami Pasifik yang luas. Meskipun tidak ada manusia yang menjadi korban, Tsunami menghancurkan harta benda di Kepulauan Hawaii yang kerusakannya ditaksir berjumlah kira-kira US$ 5 Juta (nilai dolar tahun 1957). Gelombang air laut terutama tinggi di pantai sebelah utara di pulau Kauai yang mencapai ketinggian 16 meter, membanjiri jalan raya dan menghancurkan rumah-rumah dan menghanyutkan jembatan. Tsunami ini merupakan dua kali lipat daripada Tsunami yang terjadi pada tahun 1946. Di Hilo, Hawaii, Tsunami menerjang dengan ketinggian 3.9 meter dan merusakkan beberapa bangunan di sepanjang pantai. Di dalam Teluk Hilo, Pulau Coconut tertutup air setebal 1 meter termasuk jembatan yang menghubungkan ke pantai, sebagaimana pada tahun 1952, saat ini pun hancur lagi. (Intl. Tsunami Info. Center) .

Ledakan Keempat Bom Hidrogen Terjadi di Pantai Chili Tahun 1960.

Pada tanggal 22 Mei 1960, sebuah “gempa bumi” yang besar dan Tsunami terjadi di pesisir Chili. Pada waktu itu Pentagon tidak sedang resmi berperang dengan Chili, namun pemerintah Chili mungkin mengancam akan mengusir orangnya Rockefeller yang mengontrol perusahaan-perusahaan minyak. Di bawah ini kutipan dari the International Tsunami Info. Center:

“Gempa bumi terbesar” (berkekuatan 9.5) abad ke-20 terjadi pada tanggal 22 Mei 1960 di pantai Chili dan di sepanjang Laut Pasifik. Tsunami diperkirakan membunuh 2.300 orang di Chili. Terjadi kematian yang luar biasa dan kehilangan harta benda di Kepulauan Hawaii, di Jepang dan disekitar wilayah Pasifik. Gelombang menghancurkan Hilo, Hawaii, menghancurkan pantai dan membunuh 61 orang. Kerugian diakibatkan kerusakan diperkirakan seluruhnya berjumlah lebih dari US$ 500 juta (nilai dolar tahun 1960).” (Intl. Tsunami Info. Center)

Ledakan Kelima Bom Hidrogen Terjadi di Alaska pada tanggal 28 Maret 1964.

Pada tahun 1963, President Kennedy menandatangani Perjanjian Larangan Percobaan Senjata Nukliryang mencegah percobaan nuklir di udara, luar angkasa dan di bawah permukaan air. Pentagon GUSAR – FURIOUS. Kennedy membuat permasalahannya semakin buruk dengan melarang mereka melakukan uji coba di kedalaman tanah di Alaska. Di bawah ini kutipan dari Sekretaris Pers Presiden Kennedy,

President John F. Kennedy
(President from 1961 to ‘63).

“Dari semua pejabat pers yang bekerjasma dalam masalah ini, salah seorang yang paling terkenal adalah Arthur Sylvester. Departemen Pertahanan merupakan sebuah labyrinth – membingungkan yang nyata, dan untuk setiap Sekretaris Presiden atau Menteri Pertahanan agar tetap menjaga selalu terpeliharanya mengenai segala sesuatu yang sedang terjadi disini adalah hampir tidak mungkin. Informasi Sylvester kepada saya mengenai usulan kegiatan dari Departemen Pertahanan membuktikan alasannya yang menjadi tidak bernilai. Sebagai contoh, sekali waktu ia melaporkan kepada saya bahwa sebuah rencana sedang berjalan di Departemen Pertahanan dalam membangun tempat uji coba nuklir untuk Amerika Serikat di Alaska. Ketika dia memberikan informasi ini kepada saya, seketika terpikir di dalam pikiran saya mengenai kemungkinan aksi Uni Sovyet terhadap uji coba nuklir Amerika Serikat yang dekat dengan perbatasannya. “Saya melaporkan masalahnya kepada Presiden, yang tidak pernah mendengar rencana tersebut. Sebuah panggilan Presiden kepada Menteri Pertahanan McNamara untuk menghadap (juga tidak mengetahui rencana tersebut), kemudian menghentikan keseluruhan rencana tersebut. “(Pierre Salinger, With Kennedy , p. 137)

Larangan Presiden Kennedy kepada Pentagon untuk tidak melakukan uji coba nuklir menjadi salah satu alasan bagi mereka untuk membunuhnya.

“Gempa bumi” terbesar di wilayah sebelah utara terjadi pada tanggal 28 Maret 1964 di Alaska. Perjanjian Larangan Uji Coba Nuklir sudah ditandatangani oleh Presiden Kennedy dan berlaku mulai tanggal 11 Oktober 1963. Uci coba ini merupakan pelanggaran terang-terangan terhadap perjanjian tersebut. … Di bawah ini kutipan yang lain dari the International Tsunami Info. Center:

“Gempa bumi terbesar pada abad ke -20 terjadi di belahan bumi bagian utara, dengan kekuatan 8,4 dan wilayah yang terkena di Alaska hampir sepanjang 1600 km dan lebih dari 300 km luasnya – memanjang dari Valdez sampai ke Kepulauan Trinity, sebelah barat daya Pulau Kodiak di Teluk Alaska. Gempa bumi ini menyebabkan tanah di wilayah tertentu terangkat setinggi 15 meter (50 kaki), sementara banyak di wilayah lain tanah permukaannya amblas sangat dalam. Sebagai tambahan pendorong tsunami lokal di daerah Prince William Sound, kerak bergeser secara vertikal rata-rata 18 meter (6 kaki) di atas wilayah yang luasnya kira-kira 300.000 km persegi (115.000 mil persegi) memanjang dari Teluk Alaska celah kontinental, mendorong sebuah Tsunami Pasifik yang melebar. Gelombangnya sangat merusak di wilayah tenggara Alaska, di Pulau Vancouver (British Columbia), dan di negara bagian Washington, California dan Hawaii, Amerika Serikat. Tsunami membunuh lebih dari 120 orang dan menyebabkan kerusakan yang kerugiannya ditaksir sejumlah US$ 106 juta, membuatnya termahal yang pernah terjadi yang menghantam wilayah Barat Amerila Serikat dan Kanada. Lima dari tujuh komunitas Alaska terbesar rusak binasa sebagai akibat kombinasi gempa bumi dan gelombang Tsunami. Industri perikanan Alaska dan sebagian besar fasilitas pelabuhannya rusak berat. Gelombang Tsunami di Pulau Koduak menghanyutkan sejumlah 156 rumah dan bangunan lainnya dua blok ke tepi pantai. Perahu-perahu penangkap ikan terseret ratusan meter dari daratan. Gelombang Tsunami tahun 1964 juga menyebabkan kerusakan besar di Pulau Vancouver (British Columbia), dan di negara bagian Washington, California dan Hawaii, Amerika Serikat. Gelombang merusak keseluruhan pantai California, tetapi menerjang lebih tinggi di kota Crescent sampai ke Monterey berkisar antara 21-63 meter (7-21 kaki). Yang paling keras dihantam adalah kota Crescent, California, dimana gelombang mencapai setinggi 6 meter (20-21 kaki) menghancurkan setengah dari distrik bisnis pantai. Sebelas orang meninggal di sana. Di Santa Cruz Harbor, gelombang Tsunami mencapai setinggi 33 meter (11 kaki) menyebabkan beberapa keruskan. Terdapat kerusakan yang besar di Teluk San Francisco, pelabuhan wisata di Marin County dan Noyo, pelabuhan-pelabuhan di Los Angeles dan Long Beach. Kerugian di California diperkirakan mencapai jumlah US$ 7.414.000.” (Intl. Tsunami Info. Center).

Ledakan Keenam Bom Hidrogen Terjadi Di Indonesia pada Tanggal 26 Desember 2004.

Sehari setelah CHRIST MASS, Pimpinan Jesuit Jenderal di Vatican, Black Pope memerintahkan Pentagon untuk sementara menghentikan kegiatan ekumene dan mengirim sebuah hadiah Christ Mass kepada Muslim di Indonesia. Secara tradisional Satan, maksud Saya Santa, biasanya datang via udara … Kali ini datang melalui laut membawa KEMATIAN – DEATH dan Kehancuran kepada ratusan ribu orang-orang kafir.

Nuklir atau beberapa buah Nuklir ditanam oleh Angkatan Laut Pentagon di Sumatra Trench, di pantai Indonesia.

Waktu – TIMING dari kejadian ini merupakan petunjuk keterlibatan Roma.

Semua inquisi besar dalam sejarah dimulai sekitar waktu CHRIST MASS. Charlemagne, Kaisar Romawi Pendosa naik tahta pada hari CHRIST MASS pada tahun 800, segera setelah itu, teror datang dari laut ke pulau kecil Inggris dalam bentuk kapal panjang Viking.

Semua tahun “suci” Vatican atau Jubilees dimulai pada hari Christ Mass..

Uni Sovyet secara resmi dipecah-belah oleh Jesuit Gorbechev pada hari 19 Christ Mass

Hitler Memiliki Bom Hidrogen Pada Tahun 1945!!

Bom yang dimiliki Hitler menggunakan senjata yang dirakit untuk memicu uranium untuk merangsang reaksi berantai. Setelah Sekutu membom fasilitas air berat di Norwegia, Hitler mendapatkan air berat dari Congo Belgia. Dia membangun sebuah pusat fasilitas senjata nuklir bawah tanah di Sangerhausen di sebelah timur Jerman.

Norsk Hydro di Norwegia menyuplai Nazi Jerman dengan air berat untuk bom Hidrogen sampai di bom Inggris tahun 1943.

Hitler memperoleh uranium murni (U-235) dari agen-agen rahasianya di Oak Ridge, Tennessee, dan isotop air berat deuterium dari Congo Belgia.

Tambang uranium Congo Belgia diserang Inggris tetapi sebuah dam hidroelektrik di Sungai Congo digunakan oleh Nazi untuk memproduksi air berat untuk bom hidrogen.

Dalam bulan Januari tahun 1945, Hitler telah siap untuk menghantam Inggris dengan Bom-H menggunakan kapal selam ke pelabuhan Liverpool, Inggris.

Sebuah bom-H dapat meluluh-lantakkan hampir seluruh wilayah Inggris.

Air Berat Tidak Diperlukan Untuk Membuat Bom Atom … Tetapi Benar-benar Penting Untuk Membuat Bom Hidrogen.

Beberapa reaktor dewasa ini menggunakan air berat sebagai moderator untuk melambatkan reaksi berantai, tetapi di Amerika Serikat, Enrico Fermi menggunakan graphite pile – baterai grafit … bukan air berat … untuk memperlambat reaksi.

Reaktor nuklir ini secara umum dikenal sebagai reaktor graphite pile -baterai grafit. Selama penelitian Fermi membombardir nukles atom dengan netron. Selama masa bombardir ini, nukles atom terbelah dan terjadi reaksi fisi nuklir. Fermi menggunakan grafit dalam reaktor untuk memperlambat netron cukup untuk bereaksi dengan reaksi nukles. Di bawah ini sebuah kutipan dari Critical Assembly:

“Teller menunjukkan bahwa deuterium akan jauh lebih murah dibanding dengan U-235 atau Pu-239 dan daya ledaknya dapat dibuat besar dengan meningkatkan jumlah deutrium yang ditempatkan di dekat fisi bom. Dari maksud tersebut, meskipun Oppenheimer mencoba untuk membawa kembali diskusi kepada fisi bom, Bethe dan yang lainnya banyak menghabiskan waktunya dalam pertemuan berargumentasi dengan Teller mengenai ide SUPER. Bethe menyebut Teller terlalu asyik dengan SUPER dalam satu titik, dalam sebuah diskusi mengenai Jerman yang menghendaki air berat (sebagai seorang moderator dalam reaktor nuklir), Teller seperti biasanya melompat jauh 30 tahun ke masa depan dengan mengatakan, ‘Tentu saja mereka menginginkan air berat untuk membuat SUPER..” (Hoddeson , Critical Assembly , p. 45).

Dimana Pentagon Akan Menyerang Lagi Dengan “Gempa Bumi” dan Tsunami?

Kami tidak mengetahui berapa banyak bom yang telah diledakkan Pentagon di bawah permukaan air laut, namun pasti mereka telah banyak melakukannya. Dimana berikutnya Pentagon akan menyerang dengan senjata penghancur massalnya? Tidak seorangpun akan selamat dari senjata-senjata mematikan Fatima Crusaders.

Vital Links

Joevialls.co.uk …. how the Pentagon orchestrated the Asian “earthquake” and tsunami !!

Pentagon “earthquake” strikes Iran on Dec 26, 2003

First atomic test at Port Chicago in 1944

Assassination of President Kennedy

Editor’s Notes

Dr. Edward Teller belajar di Jerman di bawah seorang ahli fisika Jerman, Dr. Werner Heisenberg—bapak Bom-H yang sebenarnya” Teller datang ke Amerika Serikat pada tahun 1935 di bawah sponsor scholarship Yayasan Rockefeller:

“Masih didukung oleh bantuan Rockefeller Foundation, Teller ke Inggris selama satu tahun di University of London, mempelajari dan bekerja di bawah Dr. F. G. Donnan, seorang ahli biokimia terkenal. Kemudian menjadi terkenal dalam lingkungan ilmiah melalui karyanya dalam Rockefeller Foundation, Teller menarik perhatian dua buah universitas. Princeton menawarkan kepada Teller beasiswa; George Washington (di Washington D.C.) menawarkan juga kepadanya jabatan guru besar. Teller menerima tawaran yang terakhir, dan dalam tahun 1935, pindah ke Amerika Serikat, dimana dia tinggal sampai akhir hayatnya. (Shepley, The Hydrogen Bomb , pp. 43-44).

The Rockefeller Foundation juga mendirikan the Kaiser Wilhelm Institute for Physics di Berlin dalam bulan Januari 1938. Dimana disana penelitian Bom-H Jerman dilakukan … Dalam hal Hitler kalah dalam Perang Dunia II, Rockefeller telah mendapatkan dukungan Pentagon terhadap rencananya sebagai seorang Fatima Crusade yang fanatik untuk menyerang Rusia

Dalam bulan Desember 1938, dua orang ahli ilmu fisika Hahn dan Strassman mengumumkan penemuannya dalam fisi uranium. Dalam bulan Maret 1939, Jerman menyerbu Cekoslovakia dalam ranga mengendalikan tambang uranium di negara tersebut. Dalam bulan September 1939, Perang Dunia II secara resmi dimulai dengan diserangnya Polandia.

Mengapa Hitler memulai sebuah Perang Dunia dengan melakukan kontrol atas uranium dan kemudian tidak melakukan usaha yang maksimal untuk mengembangkan senjata mematikan – Bom-H?.

Referensi

Conant, James B. My Several Lives: Memoirs of a Social Inventor . Harper & Row, New York, 1970.

Hershberg James. James B. Conant. Harvard to Hiroshima and the Making of the Nuclear Age . Alfred A. Knoph, New York, 1993.

Hansen, Chuck. U.S. Nuclear Weapons: The Secret History. Crown Publishers, New York, 1988.

Hoddeson, Lillian. Critical Assembly: A Technical History of Los Alamos during the Oppenheimer Years, (1943-1945) . Cambridge University Press. New York, 1993.

Kohlhoff, Dean W. Amchitka and the Bomb. Nuclear Testing in Alaska. University of Washington Press, Seattle, 2002.

Morland, Howard. The Secret that Exploded , Random House, New York, 1981.

O’Neill, Dan. The Firecracker Boys . St. Martin’s Press, New York, 1994. (A great exposé of Edward Teller and Alaska nuclear testing called Project Chariot and Operation Plowshares).

Powers, Thomas. Heisenberg’s War: The Secret History of the German Bomb . Alfred A. Knopf, New York, 1993.

Rhodes, Richard. The Making of the Atomic Bomb . Simon & Schuster, New York, 1986.

Rhodes, Richard. Dark Sun: The Making of the Hydrogen Bomb . Simon & Schuster, New York, 1995.

Salinger, Pierre. With Kennedy . Doubleday & Co., Garden City, New York, 1966.

Shambroom, Paul. Face to Face with the Bomb: Nuclear Reality after the Cold War . Johns Hopkins University Press. Baltimore, MD., 2003.

Shepley, James R. The Hydrogen Bomb . David McKay Co., New York, 1954.

Diterjemahkan oleh: akhirzaman.info

original source: http://www.reformation.org/

sumber: akhirzaman

Yahudi Gagal Membunuh Nabi Isa A.s.

antimurtad — Thu, 26 Jun 2008 09:24:31 +0000

Berbeda sekali dengan konsep keimanan seorang Kristen yang meyakini jika Nabi Isa a.s. atau Yesus Kristus meninggal karena disalib untuk menebus dosa umat manusia, maka kitab suci Al-Qur’an yang dijaga Allah SWT kemurnian dan kesuciannya sampai dengan hari akhir menyatakan jika yang disalib bukanlah Nabi Isa a.s., melainkan seseorang yang wajahnya diserupai Isa a.s. Sedangkan Isa a.s. sendiri diselamatkan Allah SWT dengan diangkatnya ke surga (QS. An-Nisaa: 157-158).

Nabi Isa a.s. diturunkan ke tengah-tengah Bani Israil, kaumnya Nabi Musa a.s., untuk mengembalikan mereka ke jalan ketauhidan. Namun kaum Yahudi yang cenderung kepada kejahatan dan kesesatan, bahkan banyak melakukan pembunuhan terhadap para nabi Allah—Nabi Zakaria a.s. dibelah badannya, Nabi Yahya a.s. dipenggal kepalanya, dan sebagainya seperti yang dimuat dalam eramuslim digest edisi 6 “Genesis of Zionism: Jejak Berdarah Kaum Yahudi Sepanjang Masa (Bagian 1)”—malah menganggap Nabi Isa a.s. sebagai orang yang harus dibunuh karena telah menggoyahkan kedudukan istimewa mereka di tengah masyarakat yang telah berhasil ditipunya.

Para pendeta Yahudi yang tergabung dalam Dewan Pendeta Sanhendrin membujuk Raja Herodes untuk melakukan pengejaran terhadap Isa a.s. dan menangkapnya. Isa a.s. berhasil ditangkap dan hendak disalibkan. Namun Allah menolong Isa a.s. dan mengangkatnya ke surga. Dari hadist Nabi Muhammad SAW kita akan mengetahui jika menjelang akhir zaman, Isa a.s. akan kembali turun ke bumi di Menara Putih sebuah masjid di Damaskus, Syiria. Hal pertama yang dilakukan Isa a.s. ketika turun kembali ke bumi adalah sholat.

“Tidak ada seorang nabi pun antara aku dan Isa dan sesungguhnya ia benar-benar akan turun (dari langit), apabila kamu telah melihatnya, maka ketahuilah;bahwa ia adalah seorang laki-laki berperawakan tubuh sedang, berkulit putih kemerah-merahan. Ia akan turun dengan memakai dua lapis pakaian yang dicelup dengan warna merah, kepalanya seakan-akan meneteskan air waulupun ia tidak basah”. (HR Abu Dawud).

“Isa ibn Maryam akan turun di ‘Menara Putih’(Al-Mannaratul Baidha’) di Timur Damsyik”. (HR Thabrani dari Aus bin Aus)

“Sekelompok dari ummatku akan tetap berperang dalam dalam kebenaran secara terang-terangan sampai hari kiamat, sehingga turunlah Isa Ibn Maryam, maka berkatalah pemimpin mereka (Al-Mahdi): “ Kemarilah dan imamilah shalat kami”. Ia menjawab;”Tidak, sesungguhnya sebagian kamu adalah sebagai pemimpin terhadap sebagian yang lain, sebagai suatu kemuliaan yang diberikan Allah kepada ummat ini (ummat Islam)”. (HR Muslim & Ahmad).

“Tiba-tiba Isa sudah berada di antara mereka dan dikumandangkanlah shalat, maka dikatakan kepadanya, majulah kamu (menjadi imam shalat) wahai ruh Allah.” Ia menjawab:”Hendaklah yang maju itu pemimpin kamu dan hendaklah ia yang mengimami shalat kamu”. (HR Muslim & Ahmad).

Hal pertama yang dilakukan Nabi Isa setelah turun dari langit adalah menuaikan shalat sebagaimana yang dijelaskan oleh hadist-hadist di atas. Nabi Isa akan menjadi makmum dalam shalat yang di imami oleh Imam Mahdi. Kedatangan Nabi Isa akan didahului oleh kondisi dunia yang dipenuhi kedzaliman, kesengsaraan dan peperangan besar yang melibatkan seluruh penduduk dunia. Setelah itu kemunculan Imam Mahdi yang akan menyelamatkan kaum muslimin, kemudian kemunculan dajjal yang akan berusaha membunuh Imam Mahdi, setelah dajjal menyebarkan fitnahnya selama 40 hari, maka Nabi Isa akan diturunkan dari langit untuk menumpas dajjal.

Turunnya nabi Isa ke bumi mempunyai misi menyelamatkan manusia dari fitnah Dajjal dan membersihkan segala penyimpangan agama, ia akan bekerjasama dengan Imam Mahdi memberantas semua musuh-musuh Allah.

Dikisahkan setelah Isa as. selesaikan menunaikan shalat, ia berkata, “Keluarlah kamu (pasukan kaum muslimin) semua bersama kami untuk menghadapi musuh Allah, yaitu dajjal.” Lalu mereka pun keluar, kemudian Ia (Isa) dilihat oleh dajjal si laknat yang baru saja mendakwa kepada manusia, bahwa ia adalah raja yang mendapat petunjuk dan pemimpin yang jenius serta bijaksana, bahkan mengaku sebagai Tuhan Yang Maha Tinggi. Begitu ‘Isa dilihat oleh dajjal, dajjal pun meleleh seperti garam yang meleleh di di air. Kemudian dajjal kabur, tetapi ia dihadang oleh Isa di pintu kota Lud di Palestina. Sekiranya Isa membiarkan saja hal ini maka dajjal akan hancur seperti garam dalam air, akan tetapi Isa berkata kepadanya, “Sesungguhnya aku berhak untuk menghajar kamu dengan satu pukulan.” Lalu Isa as. menombak dan membunuhnya, maka Isa as. memperlihatkan kepada semua orang darah dajjal di tombaknya. Maka tahu dan sadarlah para pengikut dajjal dari kalangan Yahudi, bahwa dajjal bukanlah Allah. Jika benar apa yang didakwakan dajjal(dajjal mengaku sebagai tuhan) tentulah dajjal tidak akan dapat dibunuh oleh Nabi ‘Isa.

Ketika itu Nabi Isa a.s. menyeru kepada umat Kristiani untuk mengucapkan kalimat tauhid, kembali kepada jalan yang haq seperti apa yang telah disampaikannya ribuan tahun lalu sebelum agama Nasrani dirusak oleh tangan Yahudi bernama Paulus dari Tarsus.

Menurut suatu riwayat Nabi Isa, setelah turun dari langit akan menetap dibumi sampai wafatnya selama 40 tahun. Ia akan memimpin dengan penuh keadilan, sebagaimana yang diceritakan dalam hadist berikut: “Demi yang diriku berada ditangannya, sesungguhnya Ibn Maryam hampir akan turun di tengah-tengah kamu sebagai pemimpin yang adil, maka ia akan menghancurkan salib, membunuh babi, menolak upeti, melimpahkan harta sehingga tidak seorangpun yang mau menerima pemberian dan sehingga satu kali sujud lebih baik dari dunia dan segala isinya” (HR Bukhari, Muslim, Ahmad, Nasa’I, Ibn Majah dari Abi Hurairah).

Juga dkisahkan bahwa Nabi Isa akan melaksanakan haji: ”Demi Dzat yang diriku berada ditanganya, sesungguhnya Ibn Maryam akan mengucapkan tahlil dengan berjalan kaki untuk melaksanakan haji atau umrah atau kedua-duanya dengan serentak”.(HR Ahmad & Muslim dari Abi Hurairah).

Nabi Isa a.s. akan meninggal setelah membunuh dajjal, menjadi pemimpin yang adil, dan membenarkan risallah yang dibawa Rasulullah Muhammad SAW di akhir zaman. Hanya saja kita tidak mengetahui kapan dan bilamana ini semua akan terjadi, karena Yahudi Talmudian terus-menerus bekerja siang-malam untuk menyesatkan umat manusia dari jalan kebenaran dengan membuat berita-berita palsu.

Majalah eramuslim digest edisi 6 “Genesis of Zionism” (Bagian 1) memuat kisah tentang lahirnya Bani Israil dan kedurhakaan serta kejahatan mereka terhadap para Nabi Allah, hingga peran mereka dalam episode awal Perang Salib. Edisi 6 ini akan berlanjut sebagai satu kesatuan di eramusim digest edisi 7 “Genesis of Zionism” (Bagian 2) yang mengupas kejahatan-kejahatan, jejak berdarah Yahudi sepanjang sejarah, dari masa Perang Salib, penguasaan mereka atas Inggris dan Perancis juga seluruh Eropa, pembentukan gerakan Zionis Internasional, penghancuran khilafah Islam Turki Utsmani, Perang Dunia I dan II, aktor di belakang kekejaman Nazi, sejumlah pembantaian terhadap rakyat Palestina, hingga konspirasi mereka di hari ini. Juga Anda bisa simak keyakinan Yahudi Talmudian tentang hari akhir dan apa saja syarat-syaratnya sebelum mereka akan meruntuhkan Masjidil Aqsha dan mendirikan kembali Haikal Sulaiman ketiga di atas puing-puingnya.

Jangan lewatkan sajian-sajian kami di eramuslim digest, cepatlah berlangganan sebelum kehabisan! (rz/era)