豬流感真的可怕嗎? (轉貼) 必讀

The Swine Flu Pandemic – Fact or Fiction?

引言：

傷風感冒是全美國人看醫生和導致最多病假的原因，全美每年約有10億人次患上感冒，平均每個美國人每年患上兩至四次的感冒。

本港豬流感第二波高峰期將至，首批 50萬劑疫苗已抵港，政府將為五類高危人士接種人類豬流感疫苗，包括醫護人員、長期病患者及孕婦、6個月至未滿 6歲的兒童、65歲及以上長者，以及從事養豬或屠宰豬隻行業人士，合資格注射的醫護估計有 15萬人。十五間學生健康服務中心昨起開始派籌，接受六個月至不足六歲的幼童登記人類豬流感接種計畫。本港目前有超過三萬三千宗豬流感個案，當中六個月至不足六歲的幼童有五千三百多宗，佔總數六分一。

衞生防護中心總監曾浩輝說：新疫苗副作用與季節性流感疫苗相若，只會在針口出現疼痛、腫脹徵狀，及小部分人士會引致發燒等，一般會於廿四至四十八小時內消失。他又指，現時未有證據指疫苗會引致死亡，而出現嚴重過敏反應的比率亦非常低，只有百萬分之一。

港大微生物學系系主任袁國勇卻說，各地正研製人類豬流感疫苗，但新疫苗引起的副作用難以預知。根據30多年前美國的經驗推算，每一百萬注射過疫苗的人，會有大約10人出現癱瘓等嚴重副作用。

What’s Swine Flu

正常地只有type-A influenza影響豬隻，現在變種為影響人類的A(H1N1) ，這種類以前沒有於人類和豬隻上出現過。evolutionary biologist Paul Ewald說，必需有相對擁擠的環境來傳播，和特別的條件下才能變種成為可攻擊人類的病毒，並不是Random而來的，正如禽流感般，並不是容易形成瘟疫的。

人感染豬流感後的早期症狀與普通人流感相似，包括發熱、咳嗽、喉痛、身體疼痛、頭痛、發冷和疲勞等，有些還會出現腹瀉或嘔吐、肌肉痛或疲倦、眼睛發紅等。部分患者病情可迅速進展，來勢兇猛、突然高熱、體溫超過39℃，甚至繼發嚴重肺炎、急性呼吸窘迫綜合征、肺出血、胸腔積液、全血細胞減少、腎功能衰竭、敗血症、休克及Reye綜合征、呼吸衰竭及多器官損傷，導致死亡。

打豬流感針要簽生死狀？

衞生署更要求員工注射疫苗前，先簽署一份類似生死狀的同意書，注射者一旦出現嚴重副作用，政府也未必需要負責任。前線人員多年季節性流感針，從來都係口頭講打唔打，今次突然間要簽同意書，係咪暗示呢支新針有好多我哋唔知嘅副作用，衞生署怕出事要負責任？前線醫生聯盟主席謝耀昌相信，逾半醫護人員不會接種豬流感疫苗，「我哋又唔係老弱殘疾，唔算高危。好多同事擔心打咗有嚴重副作用，搵條命嚟博。」他批評簽署同意書的安排非常奇怪，更令醫護人員卻步，「係咪此地無銀？點解打季節性流感疫苗唔使簽，豬流感就要？係咪諗呢樣嘢嗰個人都驚風險大，先至要我哋簽紙，日後就冇得追究？」

立法會衞生服務界議員李國麟建議醫護人員簽署同意書時，仔細閱讀條款衡量風險，「係自願性質，如果擔心，就唔好簽。」萬一有醫護人員接種後有副作用，當局理應承擔醫療責任。

豬流感疫苗比流感傷死更多人！

因豬流感曾於世界各地殺死了幾百萬人，固美國於1976年大力推行注射豬型流行性感冒，最後這流感疫潮並沒有發生，卻使四百多人患了一種叫做Barre Guillain Syndrome的腦神經病，因此癱瘓或死亡。到1993年為止，政府賠償了超過9,300多萬美元。

研究發現，引起1976年 流感和今年甲型流感的病毒“類似”，都是由豬攜帶並傳播給人類的。很多人因此擔心，今年這些同樣針對豬流感的疫苗是否會仍然帶來“非同尋常”的結果。美國 研究人員承認，截至目前，誰也不敢斷言民眾接種的流感疫苗不會造成任何副作用。

葛蘭素史克公司(GSK)的甲型H1N1流感疫苗在加拿大接種期間，已造成6人出現嚴重的過敏性休克反應，由於此類副作用發生率遠遠超過預期，因此同一批次的疫苗全部被緊急召回。

現在於美國暫時已知一6歲和8歲的兒童接受豬流感疫苗後死亡，一名25歲女士殘疾。

　據悉，人類注射豬流感后的嚴重後遺症主要表現為，腿部肌肉麻痺無力，有刺痛感，然後在幾個星期內逐漸向身體其他部位擴散，最終導致半身或者全身癱瘓。造成這種現象的原因是，人體神經外部在注射疫苗後遭到破壞，影響運動信息傳輸。

所有疫苗都含有Thimerosal(水銀) ，因疫苗裡的水銀的傷感愈來愈明確，所以美國的疫苗現在都不含水銀。但Washington's Health Department卻臨時取消對豬流感疫苗這限制，因盛豬流感疫苗的小瓶要載十次的劑量，而水銀可保證針筒於這小瓶抽取十次也不會受細菌所感染，所以除三歲以下的嬰兒，其流感疫苗都含有水銀！

Adjuvants

疫苗添加劑，用來加強免疫反應。Aluminium hydroxide、Aluminium phosphate、Calcium phosphate這三種Adjuvants都被FDA所批准使用，但另外一種Squalene，不被美國FDA所批准使用，卻被歐洲某些藥廠所使用。

流感疫苗效用：

根據美國五間制造疫苗的藥廠之一，CSL's Biotherapies, Inc顯示，18至65歲之人士只有約24%有效，而65歲以上者只有約17%。這麼低，副作用又可能大，值得嗎？

真人白老鼠？

到目前為止，豬流感疫苗並完全沒有於孕婦上作過試驗，美國就曾有20人孕婦懷疑打完豬流感疫苗後流產。孕婦比其他人高達四倍打疫苗後需住院的危機 ( 2.8% vs 0.7% ) 。

現在全球的豬流感疫苗都是草草了事下被批准使用，跟平常的流感疫苗不一樣，有多大效用和多重副作用，沒人知道！

美國現在已經出現抗特感福的反應了！花費了那麼多錢，現在特感福隨時無用！

豬流感有什麼恐怖？

Malaria瘧疾於全球每天殺死最少300人，比豬流感恐怖多幾百倍！好多所謂專家說禽流感會死過百萬人，於2003止，最後全球只死了257人，於2004年一年全球死於被雷電打中的人都不只這麼少，共1170人！

於1918年的Spanish Flu死了2千萬人，14-16世紀的歐洲黑死病死了近1/4的人口，這才是恐怖！

瘧疾每天都死這麼多人，為什麼那麼少人重視？你猜如果豬流感每天都死30人，全世界都發瘋了。發生瘧疾的地方都是貧窮落後的地方，賣這些藥不會賺大錢，這就是最簡單的道理，不然你告訴我為什麼瘧疾天天都死人都沒有人關心？

又是賣藥求榮？

上次禽流感說什麼世紀大災難，最後只死了200多人，但Tamiflu特感福已賣出了3.8億美元了，專家估計未來銷售量會更大增升。又是在虛張聲勢，誇大病情，最後便可大賣特賣！

至2007年，共有1800宗關於Tamifu的不良反應Adverse Report：一般的不良反應：Nausea, Vomiting, Diarrhea, Headache, Dizziness, Fatigue, Cough，還有嚴重的精神錯亂等。但你可知道Tamifu只能減除流感徵狀少一、兩天而已，值得嗎？

豬流感不僅讓研究機構受益，還可以讓製藥工業從中漁利。巴塞爾製藥巨頭羅氏公司抗流感藥達菲在2009年上半年的銷售額已翻3倍達10億瑞郎。美國已花費了15億美元於豬流感疫苗上，還會再多花10億於其它流感，估計全球疫苗的生意超過200億美元，即約1600億港元，嘩！發達了！藥廠。

豬流感是人造的？

人類豬流感這病毒說是最新的變種病毒，是以前所沒有的，第一宗豬流感發生於2009年3月的Mexico，但你可知道，奇怪地，Baxter Healthcare公司卻早於2008年8月時已於其專利申請上Baxter’s patent # US20090060950A1，包括了『influenza A and influenza B in particular ｓ ｅｌｅｃｔed from of one or more of the human H1N1, H2N2, H3N2, H5N1, H7N7, H1N2, H9N2, H7N2, H7N3, H10N7 subtypes, of the pig flu H1N1, H1N2, H3N1 and H3N2 subtypes, of the dog or horse flu H7N7, H3N8 subtypes, or of the avian H5N1, H7N2, H1N7, H7N3, H13N6, H5N9, H11N6, H3N8, H9N2, H5N2, H4N8, H10N7, H2N2, H8N4, H14N5, H6N5, H12N5 subtypes』這些病毒，又說是新的變種病毒？為什一早就有對付這病毒的藥，並申請專利？

3個月後澳洲一記者Jane Burgermeister，搜集了資料指出Baxter釋放禽流感病毒以換取大賣其藥來途利，她指出除了Baxter外，World Health Organization和United Nations都有份參與這恐怖生化活動來危害全球人類健康。信與不信，你們自己研究！她的網址：http://www.theflucase..com/

人造的毒害？

不少專家都相信，跟Ebola、AIDS、禽流感一樣，豬流感都是人類自己造出來的禍：疫苗，所以，不打疫苗，特別是流感疫苗是利人利己的做法。關於這方面的詳細，請參：

Emerging Viruses: AIDS And Ebola : Nature, Accident or Intentional? by Leonard G. Horowitz

Dr. Mary's Monkey: How the Unsolved Murder of a Doctor, a Secret Laboratory in New Orleans and Cancer-Causing Monkey Viruses are Linked to Lee Harvey Oswald, ... Assassination and Emerging Global Epidemics by Edward T. Haslam

AIDS: A Second Opinion  by Gary Null

Infectious AIDS : Have We Been Misled? by Peter Duesberg

The Origin, Persistence and Failings of HIV/AIDS Theory by Henry H. Bauer

Science Sold Out: Does HIV Really Cause AIDS? by Rebecca Culshaw

Inventing the AIDS Virus by Peter H. Duesberg

The Great AIDS Hoax by Terry C. Fry

What If Everything You Thought You Knew About AIDS Was Wrong?  by Christine Maggiore

The Great Bird Flu Hoax: The Truth They Don't Want You to Know About the "Next Big Pandemic" by Dr. Joseph Mercola

Selling Sickness: How the World's Biggest Pharmaceutical Companies Are Turning Us All into Patients by Ray Moynihan

禍是自己弄出來，最後卻又能賺錢，作藥廠和西醫的真好，收人錢放火後，又有人給錢救火！

如何自保？

健康好的生活和飲食習慣，有好的身體才有強的抵抗力，我們只相信細胞致病論Cellular Theory of Disease，絕不相信細菌致病論Germ Theory of Disease，即是身體差才發生病變，身體好所有微生物對我們都只有好處，當然這是從正常的生活上來說，絕不是用特別方法去毒害自己，如直接用人工方法注入大量或非常毒的致病原體於體內。

注重衛生是好的，但我們卻反對用化學的所謂消毒劑來洗手，人體的皮膚有天然的分泌，皮膚表面上的微生物將這些分泌物分解後，便形成天然保護層，用這些化學劑洗手或消毒劑只會破壞這上天給我們最好的保護層，是自己傷自己，最後又是賣這些東西的人在賺錢！

最簡單是可吃幾瓣的生蒜頭，Garlic和Oregano Oil都是Full Spectrum的抗菌劑。較好的可服用一些增強抵抗力和抗病毒的配方，如包括以下類別的有機草本配方：增強抵抗力最強的必定是Echinacea；調理免疫系統的有五味子、女貞子、北耆、側柏葉、冬蟲夏草、靈芝等這些菇類；增強腎上腺的有甘草、人參、紅景天、西伯利亞人參等這些參類；抗病毒的有Pau D Arco、甘草、大蒜、Oregano Oil、金銀花、連翹、北美黃連等；舒緩和抗上呼吸道感染的有側柏葉、Boneset、辛荑花、Thyme、Elderflower、穿心蓮、Marshmallow、Wild Cherry、(北美)半邊蓮、薄荷等；增強血循環的辣椒或花椒等。

http://swineflu.mercola.com/sites/swineflu/home.aspx

以上只是一些點滴，只作參考，自己作思考和研究吧！

關於疫苗和西醫的毒害，請參考網址：http://health4u.hk 

Dr Levite Man

參考資料：水銀的傷處：

Studies CONFIRMING Thimerosal as a Health Hazard

1) Environmental Health Perspectives, August, 2005

Fourteenstudies.org states: “This study demonstrates clearly and unequivocally that ethyl mercury, the kind of mercury found in vaccines, not only ends up in your brain, but leaves double the amount of inorganic mercury as methyl mercury, the kind of mercury found in fish.

This work is groundbreaking because little is known about ethyl mercury, and many health authorities have asserted that the mercury found in vaccines is the "safe kind."

This study also delivers a strong rebuke of the Institute of Medicine's recommendation in 2004 to no longer pursue the mercury-autism connection. Excerpt:

"A recently published IOM review (IOM 2004) appears to have abandoned the earlier recommendation [of studying mercury and autism] as well as back away from the American Academy of Pediatrics goal [of removing mercury from vaccines].

This approach is difficult to understand, given our current limited knowledge of the toxicokinetics and developmental neurotoxicity of thimerosal, a compound that has been (and will continue to be) injected in millions of newborns and infants."

2) Cell Biology and Toxicology April 9, 2009 [Epub Ahead of Print]

Exerpt: “In conclusion, MT-1 and MT-3 mRNAs but not MT-2 mRNA are easily expressed in the cerebellum rather than in the cerebrum by the injection of low-dose thimerosal. It is thought that the cerebellum is a sensitive organ against thimerosal.

As a result of the present findings, in combination with the brain pathology observed in patients diagnosed with autism, the present study helps to support the possible biological plausibility for how low-dose exposure to mercury from thimerosal-containing vaccines may be associated with autism.”

3) Annals of Epidemiology September 2009: 19(9);659

Male infants who received thimerosal-containing hepatitis-B vaccinations had a three-fold risk of developing autism.

4) Neurotoxicology October 1, 2009

The above findings are confirmed in this study wherein infant primates injected with just ONE dose of thimerosal-containing hepatitis B vaccine manifested significant developmental delays.

5) Brain Research September 9, 2009 [Epub Ahead of Print]

Study concluded that injecting thimerosal into suckling infant rats, and adult rats, impairs sensitivity to pain, apparently due to activation the endogenous opioid system.

6) Toxicology & Environmental Chemistry September-October 2008: 90(5);997-1008

Male infants who received thimerosal-containing hepatitis-B vaccinations were nine times as likely to be receiving special education services

7) Generation Rescue Survey of 9,000 boys, aged 4-17, in California and Oregon, found that vaccinated boys had a 155 percent greater chance of having a neurological disorder than unvaccinated boys. Vaccinated boys were 224 percent more likely to have Attention Deficit Hyperactivity Disorder (ADHD), and 61 percent more likely to have autism.

For boys in the 11-17 age bracket, the results were even more pronounced.. Vaccinated boys were 158 percent more likely to have a neurological disorder, 317 percent more likely to have ADHD, and 112 percent more likely to have autism.

8) Report to the Legislature on the Principle Findings from The Epidemiology of Autism in California: A Comprehensive Pilot Study by the MIND Institute, October 2002, concluded that the rise in autism cannot be explained by better diagnosis and expanded diagnostic criteria, but rather is a real event, likely propelled by “environmental exposures to substances such as mercury; viral exposures; autoimmune disorders; and childhood vaccinations."

9) Toxicology and Applied Pharmacology 2006: 214; 99-108

This French study used a new, sophisticated measurement for environmental toxicity by assessing porphyrin levels in autistic children. It provides clear and unequivocal evidence that children with autism spectrum disorders are significantly more toxic than their neurotypical peers.

10) Journal of American Physicians and Surgeon, 2003

Exerpt: "The data from this study, along with emerging epidemiological data showing a link between increasing mercury doses from childhood vaccines and childhood neurodevelopmental disorders, increases the likelihood that mercury is one of the main factors leading to the large increase in the rate of autism and other neurodevelopmental disorders. It is hoped that removing thimerosal from all childhood vaccines will contribute to a decline in the numbers of new cases of autistic spectrum disorders."

11) Journal of Toxicology and Environmental Health 2007: 70; 837-851

This study reviewed the case histories and medical profiles of nine autistic children and concluded that eight of the nine children were mercury toxic and this toxicity manifested itself in a manner consistent with Autism Spectrum Disorders.

12) Neuropediatrics, August 2006

Exerpt: "There was significant difference in blood mercury levels between cases and controls, which persists after adjustment for age, gender and parental occupational status. The geometric mean blood mercury level was also significantly higher in children with inattentive and combined subtypes of ADHD. CONCLUSION: High blood mercury level was associated with ADHD. Whether the relationship is causal requires further studies."

13) International Journal of Toxicology 2003: 22; 277-285

Fourteenstudies.org states: “This recent study demonstrates that the levels of mercury in the birth hair of autistic children were significantly lower than their control peers. While this may at first appear contradictory, it highlights one of the critical insights to understanding mercury poisoning and autistic children: many autistic children are non-excretors of mercury. This means their capacity to excrete mercury is significantly lower than their neurotypical peers and contributes to their condition.”

14) Journal of Pediatrics, May 2000: 136; 679-681

This study measured mercury levels in infants before and after the administration of a Hepatitis B vaccine containing thimerosal and found that a "comparison of pre and post-vaccination mercury levels showed a significant increase in both preterm and term infants after vaccination."

15) Neurotoxicology January 2005: 26; 1-8

Study demonstrates that thimerosal lowers or inhibits your body's ability to produce glutathione, an antioxidant and your body's primary cellular-level defense against mercury.

Excerpt: "Thimerosal-induced cytotoxicity was associated with depletion of intracellular Glutathione in both cell lines...The potential effect of Glutathione or N-acetylcysteine against mercury toxicity warrants further research as possible adjunct therapy to individuals still receiving Thimerosal-containing vaccines."

16) Environmental Health Perspectives, July 2006

Study demonstrates that very low-levels of Thimerosal can contribute to immune system disregulation.

17) Molecular Psychiatry July 2004; 1-13

Study demonstrates how thimerosal inhibits methylation, a central driver of cellular communication and development.

Exerpt: "The potent inhibition of this pathway [methylation] by ethanol, lead, mercury, aluminum, and thimerosal suggests it may be an important target of neurodevelopmental toxins."

18) Molecular Psychiatry September 2004; 1-13

Fouteenstudies.org states: “This work by Columbia University Doctors explores whether genes are important in determining if mercury exposures akin to those in childhood immunizations can disrupt brain development and function.

It is the first known scientific study done specifically on ethlymercury administered in a way similar to the vaccine schedule. Dr. Hornig discussed the study before Congress in September 2004.”

Excerpt: "The premise of our research is that if mercury in vaccines ｃ ｒｅａｔｅs risk for neurodevelopmental disorders such as autism, genetic differences are likely to contribute to that risk. Earlier studies, however, did not use the form of mercury present in vaccines, known as thimerosal, and did not consider whether intramuscular, repetitive administration during early postnatal development, when the brain and immune systems are still maturing, might intensify toxicity.

Our predictions were confirmed. Using thimerosal dosages and timing that approximated the childhood immunization schedule, our model of postnatal thimerosal neurotoxicity demonstrated that the genes in mice that predict mercury-related immunotoxicity also predicted nuerodevelopmental damage. Features reminiscent of those observed in autism occurred in the mice of the genetically sensitive strain."

19) Toxicological Sciences 2003: 74

Study demonstrates the potent toxicity of thimerosal on brain cells.

20) Autoimmunity Reviews June 2005: 4(5):270-275

Study demonstrates the clear link between ethylmercury [from thimerosal] and autoimmune responses.

21) Congressional Record - Extensions of Remarks by Congressman Dan Burton (R-IN), Committee on Government Reform, May 21, 2003

Fouteenstudies.org states: “This extensive report was prepared by the staff of the Subcommittee on Human Rights and Wellness and was the result of a three-year investigation. The Committee on Government Reform, chaired by Congressman Dan Burton, initiated the investigation and compiled the testimony of hundreds of researchers and physicians, as well as representatives from the FDA and CDC, who presented to the committee.”

Excerpt: "Mercury is hazardous to humans. Its use in medicinal products is undesirable, unnecessary and should be minimized or eliminated entirely. Manufacturers of vaccines and thimerosal, (an ethlymercury compound used in vaccines), have never conducted adequate testing on the safety of thimerosal. The FDA has never required manufacturers to conduct adequate safety testing on thimerosal and ethlymercury compounds...

Thimerosal used as a preservative in vaccines is likely related to the autism epidemic. This epidemic in all probability may have been prevented or curtailed had the FDA not been asleep at the switch regarding injected thimerosal and the sharp rise of infant exposure to this known neurotoxin. Our public health agencies' failure to act is indicative of institutional malfeasance for self-protection and misplaced protectionism of the pharmaceutical industry."

22) Journal of American Physicians and Surgeons 2006; 11(1); 8-13

Upon analysis of the Vaccine Adverse Events Reporting System (VAERS), researchers reported significantly increased odds ratios for autism, speech disorders, mental retardation and thinking abnormalities following vaccination with thimerosal-containing vaccines (DTP and Hib), compared to children who received a vaccine containing half the amount of thimerosal (DTPH).

The American Academy of Pediatrics decided that this study was flawed because it relied on VAERS data, which as a “passive surveillance system” is no intended to be used for proving hypotheses.