返回列表 发帖

[转贴] 乙肝疫苗 VS 男孩罹患智力障碍

乙肝疫苗后面的那一盘烂污账
http://www.wenxuecity.com/blog/201607/41693/1113257.html
闲话少说,先上干货。 根据国家卫生和计生委的官方网站指出,1)我国目前乙肝携带者大约占7.18%。2)接受全程接种乙肝疫苗后,约80~95%的人群可以产生免疫力,保护效果可持续20年以上。 看起来很有成效对吧? 唯一的问题是,根据资料显示,感染乙肝的人群95%是可以自愈完全康复的! 这不是开了个天大的玩笑吗? 即使没有疫苗接种,95%感染乙肝的人都可以自行愈合完全康复。现在全民疫苗接种后,而且还是全程接种(三针),产生的免疫保护竟然只有80~95%之间? 花大力气全民疫苗接种后,难道不应该产生即使没有100%也至少99.99%左右的免疫保护吗? 真的无语了。。。 但是到底这个乙肝有多可怕,以致于出生第一天就要进行疫苗接种呢? 首先,乙肝的传染途径是体液,也就是说血液或者精液之类的。寻常的身体接触,打喷嚏,握握手,亲个嘴,是不会导致感染的。所以,美国的CDC(疾病控制中心)说,乙肝的高风险人群主要是三种,静脉注射的瘾君子,滥交的性工作者(男妓或女妓),还有母亲是乙肝感染者。 所以,高感染风险阶段是20~30岁的时候。也就是这些瘾君子和妓女妓男们的啪啪高峰期。 既然如此,为啥要全体初生婴儿都要陪葬,一起打屁股呢?有哪个母亲会预期自己的孩子长大后变成瘾君子或者男妓女妓,所以必须打这个预防针? 至于母体传染,产前检查必定会发现待产的母亲有没有乙肝,那么其余90%以上的没有乙肝的母亲为啥要一起陪葬呢? 这明显不符合逻辑好不好,受益的除了制药厂的老板外,我不知道还有谁是受益者。 原来当年制定这个政策的官老爷们说,20~30岁年龄段的人比较不听话,很难找到他们来疫苗接种,所以就柿子专挑软的捏,找那些初生婴儿和孕妇下手,一锅端。 那么到底这个乙肝病毒有多危险啊? 原来95%以上的感染者会完全恢复。95%会完全恢复! 剩下的5%倒霉蛋里,一部分人会在20~40年的时间内演变成肝硬化或者肝癌。而据统计,乙肝病毒和肝癌的相关性最大。 1%的感染者里,2成的人属于急性感染,有生命危险。 但是打了这个乙肝疫苗后,又会有啥副作用呢? 2008年美国纽约的Stony Brook 州大医学院发布了一个研究报告,报告对比了2000年以前注射了三针乙肝疫苗的1824个孩子,1~9岁。该研究发现,打了乙肝疫苗的男孩罹患智力障碍(需要特殊教育、自闭症)的几率是没有疫苗接种的男孩的9倍之高。(此处应该和2000年以前乙肝疫苗仍然使用含水银的防腐剂有关)。
这是外星人写的吗?!强烈呼唤亲你来亲身体验一下。先不说卫生证体检证神马的,单是手拿钱再抓食物的外卖我一天就遇到无数!食堂饭店的餐具我也不信任……医院的扶手、饭店的桌椅、浴室的衣箱和旅店的床……对了有次一高中食堂不合格是因为新出锅的馒头贴墙放置,馒头和墙都是雪白但那检测数据真是触目惊心。其实婚检应该强制执行的,对生活经历单纯的人群来说,现在乙肝其实比艾滋还可怕。易中招难治愈传染性强改变染色体遗传后代花费大受罪多,且死的不是时候!统计下认识的逝者,大多是在其子女上大学到就业期间去世。可惜壮年!乙肝和结核对中国的破坏是隐形的,因此就更加可怕。因为有更多的你因为无知而无畏……
1亿的携带者,我不知作者的这篇文章从哪里来的,但是还是应该多看几篇再写比较适合
还自愈?!呵呵
乙肝在现实社会很容易被歧视 被孤立
不要以为乙肝离我们很遥远,口腔溃疡的时候很容易感染的
君且知,我心蒲草情,我心磐石意,蒲草怎可比,磐石岂可拟。
http://healthimpactnews.com/2013 ... ctive-in-new-study/
By Dr. Mercola

By the time your newborn is 12 hours old, federal health officials recommend administering the first dose of hepatitis B vaccine. TWELVE HOURS! If you want to avoid it you must make it VERY clear to all hospital staff well before the delivery and monitor your baby closely until you leave the hospital.

Three hepatitis B shots are part of the standard government-recommended childhood vaccination schedule, with the third dose to be given before 18 months of age.

But hepatitis B is a primarily blood-transmitted adult disease associated with risky lifestyle choices such as unprotected sex with multiple partners and intravenous drug use involving sharing needles — it is NOT primarily a “children’s disease” or one that is a common threat to newborn babies.

In fact, according to the National Vaccine Information Center (NVIC):1


“The primary reason that the CDC recommended hepatitis B vaccination for all newborns in the United States in 1991 is because public health officials and doctors could not persuade adults in high risk groups (primarily IV drug abusers and persons with multiple sexual partners) to get the vaccine.”

But now new research has shown that by the time a child reaches his or her teenage years – the time when acquiring a hepatitis B infection may be more likely – the protection from the childhood vaccine may have long since waned…

Infant Hepatitis B Vaccination May be Ineffective in Teenagers

The study, which involved nearly 9,000 high school students, found that by the age of 15, about 15 percent of teens who received the full series of hepatitis B shots as infants tested positive for hepatitis B surface antigen (HBsAg), which is an early indicator of infection or a sign that the person is a chronic carrier of the virus.2

This percentage was even higher among teens who had received the hepatitis B vaccine off schedule, or whose mothers were high risk, meaning they tested positive for hepatitis B e antigen (HBeAg).

In other words, it appears that in many this vaccine does NOT provide lasting protection. The researchers noted:


“A significant proportion of complete vaccinees may have lost their immunological memories against HBsAg.”

It’s for this reason that the hepatitis B vaccine for newborns and young children is the least justifiable of any vaccine I can think of and certainly should not be mandated for daycare or school attendance. Remember, the disease is only transmitted via contaminated needles, blood transfusion, or contact with contaminated blood and/or body fluids.

In fact, it is described by the CDC primarily as a sexually-transmitted disease, e.g. vaginal, anal, oral sex transmitted. While babies can contract hepatitis B vertically via their mother at birth, this very rare risk can be identified via prebirth hepatitis screening of mothers, hence making vaccination essentially unnecessary in nearly every case
Hepatitis B Vaccine Linked to SIDS and Other Serious Side Effects

The recommendation to vaccinate newborns against a disease they have little to no risk of catching becomes all the more ludicrous when you consider the serious side effects the vaccine may cause. As NVIC reported:3


“As of March 2012, there was a total of 66,654 hepatitis B vaccine-related adverse events reported to the federal Vaccine Adverse Events Reporting System (VAERS), including reports of headache, irritability, extreme fatigue, brain inflammation, convulsions, rheumatoid arthritis, optic neuritis, multiple sclerosis, lupus, Guillain Barre Syndrome (GBS) and neuropathy.

There have been more than 1,500 hepatitis B vaccine-related deaths reported, including deaths classified as sudden infant death syndrome (SIDS).”

Keep in mind that this is likely an underestimation because only a fraction of the serious health problems, including deaths, following vaccination are ever acknowledged due to a lack of public awareness about how to recognize signs and symptoms of vaccine reactions.

Also, vaccine adverse events are substantially underreported — some estimate only between one and 10 percent of all serious heath problems and deaths that occur after vaccination are ever reported — even though the National Childhood Vaccine Injury Act of 1986 mandated that all doctors and other vaccine providers report serious health problems, including hospitalizations, injuries and deaths following vaccination.

Moreover, often only acute reaction symptoms that occur soon after vaccination are recognized, since chronic inflammation and other subclinical adverse effects may take weeks, months, years or even decades to fully manifest. This makes it very difficult, if not impossible in many cases, to link chronic health problems back to an earlier vaccination or series of vaccinations, especially when doctors fail to inform themselves or their patients about vaccine risks and fail to keep accurate medical records.

The 1986 Act did not include sanctions for failing to inform, record or report potential vaccine reactions, injuries and deaths to the federal Vaccine Adverse Events Reporting System (VAERS). So most vaccine providers, for reasons that are obvious, e.g. their guilt and desire to conveniently write off all vaccine-associated health problems as a “coincidence,” do not file a report when the health of a person recently vaccinated begins to deteriorate.

Truth be told, many vaccine reactions are not even recognized by medical personnel as vaccine-related, in part because many have been mislead into believing that vaccine-induced injuries are exceedingly rare.

For instance, when babies die after hepatitis B vaccinations, most of the time their deaths are automatically attributed to SIDS — without investigation into whether the vaccine caused the baby’s sudden death. When a baby’s death is listed as “SIDS,” rarely does anyone ask about the deceased infant’s vaccination history to find out whether there were symptoms of vaccine reactions before death, even though the biomedical literature has repeatedly signaled this connection.4

60 Diseases and Adverse Reactions are Associated With the Hepatitis B Vaccine

As Dr. Jane Orient of the Association of American Physicians and Surgeons (AAPS) testified to Congress:


“For most children, the risk of a serious vaccine reaction may be 100 times greater than the risk of hepatitis B.”

Indeed, at least 60 diseases or adverse unintended consequences are associated with hepatitis B vaccination.5 Common reactions to the vaccine include fatigue, muscle weakness, fever, headache, irritability and joint pain. A study published in Annals of Epidemiology6 also found that giving hepatitis B vaccine to infant boys more than tripled their risk for an autism spectrum disorder. This was doubly concerning because an earlier study by the same researcher group, using a different database, found the same results. And there have been reports of disabling neurological and immunological disorders that have developed following hepatitis B vaccinations as well, including:



Multiple sclerosis (MS)

Guillain Barre syndrome

Bell’s Palsy



Diabetes

Rheumatoid arthritis

Lupus



Idiopathic Thrombocytopenia purpura

Convulsions and brain disorders such as encephalitis (brain swelling) and brain demyelination

Immune dysfunction



Visual and hearing impairments, including optic neuritis

Pancreatitis

Autism spectrum disorders


The association between hepatitis B vaccine and autism, particularly the 3-fold higher risk in males as reported by parents,7 may be explained by the well-known phenomena of molecular mimicry. Some researchers have proposed that the hepatitis B vaccine induces autoimmune demyelinating disease through the molecular mimicry that exists between the vaccine antigen, Epstein-Barr virus and human myelin. Basically, the vaccine stimulates an antibody response that cross-reacts against neurological self-structures, such as myelin, resulting in neurological damage.8
返回列表