Category Archives: toxins

SIDS and the DPT vaccine

SUDDEN INFANT DEATH SYNDROME (SIDS)

written by Dr. Mendelson

The dreadful possibility that they may awaken some morning to find their baby dead in his crib is a fear that lurks in the mind of many parents. Medical science has yet to pinpoint the cause of SIDS, but the most popular explanation among researchers appears to be that the central nervous system is affected so that the involuntary act of breathing is suppressed.14537_lores

That is a logical explanation, but it leaves unanswered the question: What caused the malfunction in the central nervous system? My suspicion, which is shared by others in my profession, is that the nearly 10,000 SIDS deaths that occur in the United States each year are related to one or more of the vaccines that are routinely given children. The pertussis vaccine is the most likely villain, but it could also be one or more of the others.

Dr. William Torch, of the University of Nevada School of Medicine at Reno, has issued a report suggesting that the DPT shot may be responsible for SIDS cases. He found that two-thirds of 103 children who died of SIDS had been immunized with DPT vaccine in the three weeks before their deaths, many dying within a day after getting the shot. He asserts that this was not mere coincidence, concluding that a “causal relationship is suggested” in at least some cases of DIPT vaccine and crib death. Also on record are the Tennessee deaths, referred to earlier. In that case the manufacturers of the vaccine, following intervention by the U.S. surgeon general, recalled all unused doses of this batch of vaccine.

Expectant mothers who are concerned about SIDS should bear in mind the importance of breastfeeding to avoid this and other serious ailments. There is evidence that breastfed babies are less susceptible to allergies, respiratory disease, gastroenteritis, hypocalcaemia, obesity, multiple sclerosis, and SIDS. One study of the scientific literature about SIDS concluded that “Breast-feeding can be seen as a common block to the myriad pathways to SIDS.”image4


Important list of Vaccination ingredients your doctor wont share with you

Vaccine Ingredients;image
In the first 6 years of life your child receives the following:
• 17,500 mcg 2-phenoxyethanol (antifreeze)
• 5,700 mcg aluminum (a known neurotoxin)
• Unknown amounts of fetal bovine serum (aborted cow blood)
• 801.6 mcg formaldehyde (carcinogen, embalming agent)
• 23,250 mcg gelatin (ground up animal carcasses)
• 500 mcg human albumin (human blood)
• 760 mcg of monosodium L-glutamate (causes obesity & diabetis)
• Unknown amounts of MRC-5 cells (aborted human babies)
• Over 10 mcg neomycin (antibiotic)
• Over 0.075 mcg polymyxin B (antibiotic)
• Over 560 mcg polysorbate 80 (carcinogen)
• 116 mcg potassium chloride (used in lethal injection to shut down the heart and stop breathing)
• 188 mcg potassium phosphate (liquid fertilizer agent)
• 260 mcg sodium bicarbonate (baking soda)
• 70 mcg sodium borate (Borax, used for cockroach control)
• 54,100 mcg of sodium chloride (table salt)
• Unknown amounts of sodium citrate (food additive)
• Unknown amounts of sodium hydroxide (Danger! Corrosive)
• 2,800 mcg sodium phosphate (toxic to any organism)
• Unknown amounts of sodium phosphate monobasic monohydrate (toxic to any organism)
• 32,000 mcg sorbitol (Not to be injected)
• 0.6 mcg streptomycin (antibiotic)
• Over 40,000 mcg sucrose (cane sugar)
• 35,000 mcg yeast protein (fungus)
• 5,000 mcg urea (metabolic waste from human urine) —

MERCURY- know toxinSyringe vacc


Gardasil HPV vaccine =infertility

Does the HPV Vaccine LITERALLY Mean “One Less”?

Marketing geniuses are known to play on words and create slogans with quirky double meanings, and if you’ve been tracking the concerns raised about the potential hazards of Gardasil and Cervarix, the potential for these HPV vaccines to cause infertility – whether purposely or inadvertently – is being heard with ever increasing frequency.

The federal government’s Vaccine Adverse Events Reporting System (VAERS) has received over 9,000 reports of problems since the vaccine’s introduction in 2006, which include at least 28 spontaneous abortions, and 27 deaths. 14537_lores

Is it possible that Gardasil’s cry to fame, ‘One Less’, is turning out to be nothing but a sick, ironic play on words?

Anti-Fertility Vaccines

The World Health Organization (WHO) and its subsidiaries have been actively researching and funding the development of contraceptive / anti-fertility vaccines that prevent full-term pregnancies to take place, for over 20 years. There’s even a Task Force on Birth Control Vaccines of the WHO!

However, no anti-fertility vaccine has ever been placed on the market and promoted as such as of yet.

Instead, as described in a 1993 journal paper published in The British Medical Bulletin, anti-fertility vaccines were being engineered “incorporating tetanus or diphtheria toxoid linked to a variety of hCG-based peptides.”

The authors of this article state,

“The fundamental principle behind this approach to contraceptive vaccine development is to prevent the maternal recognition of pregnancy by inducing a state of immunity against hGC, the hormone that signals the presence of the embryo to the maternal endocrine system.”

Free tetanus vaccines that were offered to young women of childbearing age for years in countries such as Tanzania, Nigeria, Mexico, and the Philippines, were found to contain human Chorionic Gonadotropin (hCG), which causes spontaneous abortions if the woman becomes pregnant.

While the woman is not technically sterilized, once injected with hCG, she may never be able to carry a child full term thereafter.

HCG-containing anti-fertility vaccines have also been pursued for more than two decades by the Indian National Institute of Immunology, and The Population Council of the Rockefeller University, among others.

In fact, there are no less than 50 research papers detailing research on “contraceptive vaccines” in the PubMed database.

One disturbing paper published in the FASEB Journal in 1993 states:

“… we initiated studies relating to possible mechanisms of action and potential side effects of this vaccine, which should be relevant to world-wide regulation of population growth.”

So again, why the frantic push for the HPV vaccine, created for young, fertile women, when there’s NO solid, rational basis for its use?

Massive Brazilian Vaccination Program Raises Suspicions of Covert Sterilization Plans

A much more recent case of illogical mass vaccinations against a minor health problem is that of the massive, mandatory vaccination program in Brazil, which has raised suspicions among international pro-life activists, who note that the program is similar to other vaccination programs in recent years that have included a hidden sterilizing agent in the vaccines.

The campaign to “annihilate rubella” began in early August this year, mandating rubella vaccinations for all women ages 12 to 49, and 12 to 39 for men; a total of 70 million people, despite the fact that only 17 Brazilian children per year suffer birth defects from the disease.

Adolfo Castañeda of Human Life International notes that just two years ago, researchers found that the rubella vaccine used in a similar campaign in Argentina was laced with human Chorionic Gonadotropin (hCG).

“The suspicion that brought about the investigation [into the rubella vaccine] was caused by the fact that there were very few cases of the disease in Argentina, which didn’t merit a large-scale campaign,” Castañeda said, adding, “The ages for women are the same as those who received the vaccines in Nicaragua, where they included a hormone that sterilizes the woman who receives it, and similar to the age of those who received another sterilizing hormone in the Philippines.”

Polysorbate-80 – One Less Mouse, Researchers Found

Now, let me state clearly that there’s no proof of hCG being present in any of the current HPV vaccines.

I am merely playing devil’s advocate as I examine the similarities between these other irrational vaccination programs in other countries for relatively minor public health concerns — that turn out to have far more sinister agendas than mere greed – compared to the fervent, irrational push behind the HPV vaccine here in the U.S.

However, Gardasil does contain Polysorbate-80 – a surfactant used in pharmacology to deliver certain drugs or chemical agents across the blood-brain barrier — which has been linked to infertility in mice.

Researchers Gajdova et.al. found that administration of Polysorbate-80 decreased the weight of the uterus and ovaries, and caused chronic estrogenic stimulation. The ovaries of the mice were also without corpora lutea (a mass of progesterone-secreting endocrine tissue that forms immediately after ovulation) and had degenerative follicles.

So what might the estrogenic effects of Polysorbate-80 be on pre-adolescent girls and pregnant women?

Anti-Fertility Vaccine Ingredient Also Has Clinical Application in Cancer Vaccines…

A potential coincidence I find most disturbing is some of the more recent research detailing the use of hCG, and other molecules, in vaccines against hCG-producing cancers, such as – certain cervical cancers.

One 2005 paper titled, Recent advances in contraceptive vaccine development: a mini-review published in the journal Human Reproduction concludes:

“At the present time, studies are focused on increasing the immunogenicity and efficacy of the birth control vaccine, and examining its clinical applications in various HCG-producing cancers.”

But research published just a few months ago in the journal Molecular Cancer states that the free ?-subunit of hCG (hCG?) – which was originally considered biologically non-functional — has recently been shown to stimulate tumor growth, and lead to more aggressive tumors that are more resistant to therapy.

Again, I’m mentioning all of this because it just goes to show that pharmaceutical companies have little or no clue of the extent of harm these vaccines might cause, especially long-term. Something believed to be completely non-functional or harmless can turn out to be a MAJOR cause for concern after more thorough investigation.

For example, Gardasil also contains L-histadine, and histamines have been found to increase clot production five-fold when combined with, guess what? Surfactants! (L-histidine can also pass through your placental wall to your fetus.)

Granted, this laboratory investigative report titled Surfactants Attenuate Gas Embolism-induced Thrombin Production used surfactants like Perftoran, not Polysorbate-80, in their trials, but could Polysorbate-80 have a similar effect?

Could this explain why death from blood clots within hours or days is the MOST COMMON form of death after receiving Gardasil?

The HPV vaccine clearly has a lot of questions left to be answered. And those questions should be answered BEFORE pushing Gardasil on an unsuspecting public at the rate that it’s being done.

Be One Less to Get Gardasil

I think this would be a more appropriate message to send out to young women: There is absolutely no reason to risk the serious side effects of this vaccine to prevent an infection that goes away on its own 90 percent of the time. And there’s no guarantee that you’ll be protected anyway, since you can still get HPV once you’ve had the vaccine. It’s really a no-win situation for those who receive it.

Of course, you can radically reduce your risk of getting HPV in the first place if you follow safe-sex practices, or wait to have sex until you’re in a committed relationship. Then, keep your immune system in tip-top shape, and it will be more than able to shake any HPV virus that comes its way.


Infant Vitamin K shots important warnings

Vitamin K given to infants-what you may not know…..

PHYTONDIONE VITAMIN K INJECTION14537_lores

Aqueous solution containing fat-soluble vitamin K

An aqueous solution containing fat-soluble vitamin K is prepared by adding vegetable oil(s), gycerol fatty acid ester(s) or sorbitan fatty acid ester(s) in an amount of 0.004 to 5% by weight, based on the whole aqueous solution, to an aqueous solution containing menatetrenone (vitamin K2) or phytonadione (vitamin K1) and hydrogenated lecithin.

http://www.freepatentsonline.com/5021570.html

 

MULTTVITAMIN PREPARATION AND METHOD
US Pat. 2980588 – Filed Jul 18, 1957 – Les Labora
120; 100 mg. vitamin BI, 100 mg. of acetylated vitamin K This is brought up
to exactly 100 cc. by the addition of gelled peanut oil.

 

STABILIZATION OF FAT-SOLUBLE VITAMIN
US Pat. 2973266 – Filed Feb 5, 1958 –
vitamin E in an edible oil solvent, and vitamin K in an edible Limpid
peanut oil 94 Hydrogenated cottonseed oil Hydrogenated soybean oil 35 43 70 68

Aqueous solution containing fat-soluble vitamin K
US Pat. 5021570 – Filed Jul 7, 1989 – Eisai Co., Ltd.
ing fat-soluble vitamin K, which solution contains speci- The term “residual
peanut and corn oils, thin is used together with an adjuvant (cf.

Oxidative stabilization of omega-3 fatty acids in low linoleic acid …
US Pat. 7344747 – Filed Apr 29, 2004 – GFA Brands, Inc.
19 20 Percentage Flax Oil Added to Peanut Butter 10 The blend of 8 percent flax
oil and vitamin K, and a carotenoid that is a carotene or a xanthophyll.

METHOD OF MAKING SAME
US Pat. 2937091 – Filed Jul 2, 1953 –
vitamin E in an 10 15 oe- 40 70 edible oil solvent, and vitamin K in an
edible .oil vehicle or in crystalline form. Hydrogenated peanut oil 45 55.

 

Vitamin K –Is this really safe and necessary?  Bronwyn Hancock October 2003

…The vitamin K injections administered by hospitals and manufactured by Merck and Roche and Abbott contain benzyl alcohol as a preservative. … Roche’s vitamin K product KONAKION contains ingredients such as phenol (carbolic acid-a poisonous substance distilled from coal tar), propylene glycol (derived from petroleum and used as an antifreeze and in hydraulic brake fluid) and acetic acid (an astringent antimicrobial agent that may drastically reduce the amount of natural vitamin K that would have otherwise been produced in the digestive tract). As reported in the PDR and as published in the IM vitamin K packet inserts for Merck, Roche and Abbott, “Studies of carcinogenicity, mutagenesis or impairment of fertility have not been conducted with Vitamin K1 Injection (Phytonadione Injection, USP).” · The Vitamin K injection can be in a base of polyethoxylated castor oil. · Vitamin K injections also contain hydrochloric acid and lecithin. Effects of Vitamin K administration · The manufacturers warn on the product insert: “Severe reactions, including fatalities, have occurred during and immediately after intravenous injection of phytonadione even when precautions have been taken to dilute the vitamin and avoid rapid infusion..” …· According to the product insert, adverse reactions include hemolysis (or hemolysis – American spelling) (meaning breakdown of red blood cells), hemolytic anemia (a disorder characterized by chronic premature destruction of red blood cells), hyperbilirubinemia (too much bilirubin in blood) and jaundice (yellow skin and eyes resulting from hyperbilirubinemia), and allergic reactions include face flushing, gastrointestinal upset, rash, redness, pain or swelling at injection site and itching skin. ...

As early as April 17, 1977, an article in one of the world’s most esteemed medical journals, the Lancet, discredited the policy of routine vitamin K injections. “We conclude that healthy babies, contrary to current beliefs, are not likely to have a vitamin K deficiency.. the administration of vitamin K is not supported by our findings..” Van Doorm et al stated in the Lancet article. VKR cited 21 peer-reviewed reports that had been published in prominent medical journals. All of them concur that policies that mandate the universal injection of newborn babies are not based on sound science. There has been much peer-reviewed evidence generated which questions the efficacy of routine vitamin K injections as sound public health policy. ·

http://www.vaccination.inoz.com/VitaminK.html

From the July 1999 Idaho Observer: National standard mandates newborn vitamin K injection

Ignorance becomes tacit consent for the questionable neonatal procedure by Don Harkins In cooperation with a “national standard,” most, if not all states have mandated that U.S. hospitals routinely administer to all newborns a synthetic, fat-soluble vitamin K injection (generic name phytonadione) that exceeds an infant’s recommended daily dietary intake of the vitamin by 100 times…

Five post partem nurses from hospitals in Idaho, Washington and Oregon stated that they “routinely administer vitamin K injections to newborns,” as if all of them were reading from the same script. According to a seasoned Sacred Heart Medical Center (Spokane, WA) Birthplace nurse named Terri, “Routine vitamin K injections are in cooperation with the federal standard.” She also said that Washington hospitals are mandated by state code to provide the injections to all newborns. Terri acknowledged that parents who wish to refuse the shot must present the refusal to the hospital in writing before the baby is born.

…Babies who have been identified as being at risk for vitamin K deficiency include those born to mothers who took drugs or antibiotics during pregnancy, premature babies and babies who are born cesarean. Mothers who had maternity diets low in high vitamin K foods or had diets that were low in fat have also been identified as being more likely to bear vitamin K deficient babies.

…Commonsensically, VKR poses the question, “…how could God (or nature) have erred so badly as to give all newborn babies only an infinitesimal fraction of their required vitamin K? Surely the human race could not have survived to this point if all newborns were born with this deficiency and none being administered at birth until very recently.”

…The body less readily utilizes synthetic vitamins and minerals. The vitamin K administered by hospitals to newborns is the synthetic phytonadione.

…The purpose of this article is to alert expectant parents that their ignorance of federally-suggested, state mandated hospital policy is enough assent to authorize health care professionals to administer what may be a lethal or damaging overdose of a synthetic substance that comes with the following warning from the manufacturers: “Severe reactions, including fatalities, have occurred during and immediately after INTRAVENOUS injection of phytonadione even when precautions have been taken to dilute the vitamin and avoid rapid infusion…” Please pass the preceeding information onto anybody you know who is expecting a baby. Afterall, we have the right to know what substances are being injected into our babies within the first hour of their lives. If we feel that a substance may be injurious to our baby, we have the right to refuse it.

 http://proliberty.com/observer//19990710.htm

Phytonadione Therapy in a Multiple-Drug Overdose: Adverse Effects of Vitamin K Severe adverse effects are associated with intravenous phytonadione, such as cardiac irregularities, chest pain, cyanosis, decreased level of consciousness, circulatory collapse, rapid weak pulse, hypotension, and cardiac or respiratory arrest.[13] It is not known if these reactions are due to the drug or the injection vehicle.[13] Earlier reactions to vitamin K were thought to be due to polyoxyethylated castor oil (cremophor).[29-32] The literature contains numerous cases of anaphylactic reactions[29, 30, 32-38] as well as fatalities[34, 35] with parenteral phytonadione. The recommended infusion rate of vitamin K is no faster than 1 mg/minute[13]; however, anaphylactic reactions have occurred with slower infusion rates[33, 37] as well as with repeated exposure to intravenous vitamin K.[30, 33, 34, 37] Dermatologic reactions were reported after intravenous, subcutaneous, and intramuscular administration of vitamin K.[39] Two distinct types of local cutaneous reactions have been described. The more common one is a pruritic, erythematous, eczematoid, indurated plaque measuring 6-20 cm around the site of injection.[39-52] The acute reaction may resolve in 2-4 weeks with treatment with high-potency corticosteroids (e.g., fluocinonide, betamethasone dipropionate). The second type appears as a scleroderma or morphea-like reaction.[53-56] The onset can be weeks to months, and the skin change may last for years.[39] Dose does not appear to bear a relationship to the onset of these reactions. Liver disease was associated with most reports of vitamin K cutaneous hypersensitivity,[39, 41] but the pathophysiology is unclear.

 http://www.medscape.com/viewarticle/409632_7

Anaphylactoid Reactions to Vitamin K

Louis D. Fiore1, Michael A. Scola1, Colleen E. Cantillon1 and Mary T. Brophy1 (1) Massachusetts Veterans Epidemiology Research and Information Center (MAVERIC), VA Boston Healthcare System, 150 South Huntington Avenue, Boston, MA, 02130

Abstract

Anaphylactoid reactions in patients receiving intravenously administered vitamin K have been reported in the literature. To summarize the known data on anaphylactoid reactions from administration of vitamin K, we reviewed all published and unpublished reports of this adverse reaction. Published reports were obtained through medline (1966–1999) and EMBASE (1971–1999) searches of the English language literature and review of references from identified case reports. Unpublished reports were obtained using the Spontaneous Reporting System Adverse Reaction database of the United States Food and Drug Administration (FDA) between August 1968 and September 1997. All adverse drug reactions to vitamin K were categorized by route of drug administration, dose and standard adverse reaction code. In the FDA reports, we defined anaphylactoid reactions as any adverse drug reaction coded as either anaphylaxis, allergic reaction, apnea, dyspnea, death, heart arrest, hypotension, shock or vasodilatation. Additionally, all fatal and life-threatening FDA reported reactions were reviewed to determine if they could represent an anaphylactoid reaction missed by the above definition. The literature review uncovered a total of 23 cases (3 fatal) of anaphylactoid reactions from intravenous vitamin K. The FDA database contained a total of 2236 adverse drug reactions reported in 1019 patients receiving vitamin K by all routes of administration. Of the 192 patients with reactions reported for intravenous vitamin K, 132 patients (69%%) had a reaction defined as anaphylactoid, with 24 fatalities (18%%) attributed to the vitamin K reaction. There were 21 patients with anaphylactoid reactions and 4 fatalities reported with doses of intravenous vitamin K of less than 5[emsp4 ]mgs. For the 217 patients with reactions reported due to vitamin K via a non-intravenous route of administration, 38 patients had reactions meeting the definition of anaphylactoid (18%%), with 1 fatality (3%%) attributed to the drug. The absolute risk of an anaphylactoid reaction to intravenous vitamin K cannot be determined by this study, but the relatively small number of documented cases despite widespread use of this drug suggest that the reaction is rare. Anaphylactic reactions and case fatality reports were found even when intravenous vitamin K was given at low doses by slow dilute infusion. The pathogenesis of this reaction is unknown and may be multifactorial with etiologies including vasodilation induced by the solubilizing vehicle or immune-mediated processes. We conclude that use of intravenous vitamin K should be limited to patients with serious hemorrhage due to a coagulopathy that is secondary to a relative or absolute deficiency of vitamin K.

 http://www.springerlink.com/content/v16l551682716431/

Neurosurgeon, Dr. Russell Blaylock, shares the science on how particular vaccine ingredients lead to convulsions, seizures, ADD, ADHD, autism…etc.

Vitamin K and Hepatitis B are mandated in most states to be given to newborns before they go home with mom. This has been proven to be a dangerous procedure at best. Potentially lethal.

Vitamin K

The marketed purpose of the Vitamin K injection is that newborns have very little to begin with. Vitamin K is essential for the ability of blood clotting should any injury occur. Another marketed purpose is the prevention of hemorrhagic diseases of the newborn (HDN). HDN is a bleeding disorder associated with low levels of vitamin K in newborn babies. It was first defined in 1894 by Townsend as spontaneous external or internal bleeding occurring in newborn infants. Diagnosis was based solely on the opinion of the attendant medical personnel because there was no criteria in determining the cause of hemorrhaging. Townsend did not label hemophilia as a cause of HDN. The vaccine is also marketed to be essential prior to surgery. Thus, supposedly prevents excessive bleeding. Vitamin K is naturally stored and metabolized by the liver. The cell division that rapidly continues after birth depends on precise amounts of vitamin K to proceed at the proper rate. Introduction of levels that are 20,000 times the newborn level, the amount usually injected, can have devastating consequences. Nursing naturally raises the infant’s vitamin K levels very gradually after birth so that no disregulation occurs that would encourage leukemia development. This is the way the Creator designed it to be. The clotting system of the healthy newborn is well planned, and healthy breastfed infants do not suffer bleeding complications, even without any supplementation. While nursing infants demonstrate lower blood levels of vitamin K than the “recommended” amount, they show no signs of vitamin K deficiency. This can only lead to the question of how and where the “recommended” amount was brought about….

The only known reported cases of vitamin K toxicity result from having used the synthetic inoculated form. Vitam K inoculations can cause possibly fatal allergic reactions even during injection. The risks of injecting vitamin K into a newborn baby are nerve or muscle damage because it is injected deeply into the muscle, not subcutaneously under the skin. wpe49F.jpg (16360 bytes)

On the product insert, some reactions are listed:

You may notice pain, swelling and tenderness at the injection site for a few days. Notify your doctor if you experience any of the following while taking this drug: chest pain, flushing, strange movements, rapid pulse, tightness of the chest, cramps. In the unlikely event you have an allergic reaction to this drug, seek medical attention immediately. nerve and muscle damage as the Vitamin K injection must be given deeply into the muscle. However, should a newborn experience any of these, it is incredibly difficult for them to “notify” anyone, difficult for the parents to see or understand the reason behind a newborns cries, and difficult for physicians to see these signs in infants. Majority of physicians are not educated or trained to fully examine an infant in discomfort for vaccine related symptoms. Instead, they are most likely to dismiss any vaccination link.

The following are from the vaccine product insert:

* Clinical Pharmacology: “little is known about the metabolic fate of Vitamin K”. * Contraindication: “Hypersensitivity to any component of this medication”. * Precautions: “Studies of carcinogenicity, mutagenesis, or impairment of fertility have not been conducted with phytonadione.” * Pediatric Use: “Hemolysis, jaundice, and hyperbiliruminemia in newborns, particularly in premature infants, may be related to the dose of phytonadione.” * Adverse reactions: “Deaths have occurred after intravenous administration…The possibility of allergic sensitivity should be kept in mind…Hyperbilirubinemia has been observed in the newborn following administration of phytonadione…” Newborns are not pre-screened for allergic hypersensitivity….

 http://poisonevercure.150m.com/vaccines7.htm

Update, new information. Added 2/16/2015

The rise in life-threatening food anaphylaxis in children coincided with significant changes to the pediatric injection and vaccination schedules of the affected countries: injection of the Vitamin K1 prophylaxis (containing legume oil) became routine in the mid-1980s; the novel conjugate vaccine Hib B that was soon rolled into an unprecedented 5 vaccines in one needle and delivered to babies without benefit of long term study.  The injected adjuvants and toxoids and food proteins designed to provoke the immune system also increased the risk of provoking allergy.  Allergy is an evolved defense against acute toxicity.

 http://www.smartvax.com/index.php?option=com_content&view=article&id=73%3Avaccine-induced-allergies
http://www.smartvax.com/index.php?option=com_content&view=article&id=73%3Avaccine-induced-allergies

 

This information was taken from Merck vaccine manufacturer, who also make this injection.

Ingredients: Phytondione 2 or 10mgs, polyoxyethylated fatty acid 70mgs (the data sheet didn’t say where the fatty acid was derived from, but one type of oral brand has bovine gall bladder fatty acid in it, so I assume similar here), dextrose, benzyl alcohol and water.

Other brands such as the one by Roche Pharmaceuticals, may have varying ingredients. Roche’s also contains hydrochloric acid.

Hospira Inc’s version contains aluminium.

Warnings: This injection should be administered subcutaneously (just under the skin) because severe reactions including fatalities have occurred immediately after intramuscular (deep muscle) and intravenous injection (via a drip). Those reactions include hypersensitivity, anaphylactic shock, and cardiac and respiratory arrest.

Benzyl Alcohol as a preservative as been associated with toxicity in newborns (Writer’s comment: why are they then using it in an injection meant for newborns?)

 

Adverse Reactions: Deaths have occurred after intramuscular and intravenous injection, ‘flushing’ sensations, dizziness, rapid and weak pulse, profuse sweating, hypotension, dyspnea, cyanosis, pain, swelling at the injection site, allergic sensitivity, scleroderma like skin lesions that persist for long periods. Hyperbilirubinemia has occurred in newborns following the administration of vitamin K injection (jaundice).

This drug has not been tested to see if it is carcinogenic (causes cancer),whether it mutates or if it impairs fertility. It is not known whether it can cause fetal harm or whether it is excreted in human milk.

 

Contraindication

 

Hypersensitivity to any of the injection’s ingredients. (Writer’s comment: how would they know, since they give it to newborns with no medical history?).

It is interesting to note that vitamin K injections are given intramuscularly even though some manufacturer’s such as Merck say this is dangerous.

Hospira’s data sheet also says this:

‘Benzyl alcohol has been reported to be associated with a fatal “Gasping Syndrome” in premature infants.

WARNING: This product contains aluminium that may be toxic. Aluminium may reach toxic levels with prolonged parenteral administration if kidney function is impaired. Premature neonates are particularly at risk because their kidneys are immature, and they required large amounts of calcium and phosphate solutions, which contain aluminium.

Research indicates that patients with impaired kidney function, including premature neonates, who receive parenteral levels of aluminium at greater than 4 to 5 mcg/kg/day accumulate aluminium at levels associated with central nervous system and bone toxicity. Tissue loading may occur at even lower rates of administration.’

 

Childhood Leukaemia

 

In 1970, a study was undertaken to see what the risk factors were for childhood cancers. 16,193 babies were studied who had all been born in April 1970. 99 children developed cancer by the age of 10 in the control group and 33 children in the other group. The researchers found that when babies had received vitamin K in the first week of life, their risk of cancer increased three fold. They had not been looking at vitamin K specifically and did not expect to see such an association, so they approached Roche Pharmaceuticals, asking them to do a further trial. They initially refused, until stories about vitamin K and cancer forced them into a corner, and, determined to prove the safety of their product, they began a new study.

588 healthy children and 195 children with cancer were studied. All of these children had been born at one of two hospitals in Bristol. One hospital used oral vitamin K drops and the other used the injection. The researchers found a two fold increase in childhood Leukaemia among those who had received the injection and stated that as many as 980 cases of childhood Leukaemia were caused by the vitamin K injection every year in the UK alone.

Newer studies have been done as recently as 1998 which seem to confirm this. Two studies in the British Medical Journal in that year found that there was a two fold risk of Leukaemia among 1-6 year old’s who had been given the injection at birth, and that there was a ‘significant risk’ of all cancers after the shot.

 

An Alternative View Of Vitamin K Deficiency

 

Some medical professionals question whether newborns are actually deficient in vitamin K or whether in fact this is their normal level. Levels have been described as low due to the comparison with adult levels of the vitamin, but this doesn’t make a lot of sense, since newborns and adults are not compared in other areas. For instance, in weight and nutritional requirements. Drugs are also measured differently with lower amounts given to babies.

All babies have this universally ‘low’ level of vitamin K, so surely that would point to it being normal? Normality is based on what is seen in the majority of cases. Perhaps babies need less vitamin K than we do?

According to Archives of Disease in Childhood, 1997, a baby given a vitamin K injection receives 300 times more vitamin than is recommended for an adult and has a 9000 times higher blood plasma level. This may be why some babies then develop jaundice, as an overdose effect of the drug. Bilirubin is a natural by-product which is formed during the body’s normal break down of red blood cells. It is excreted by the liver. Jaundice happens when there is an excess of bilirubin and the liver is unable to properly cleanse the blood, i.e. liver overload. As babies receive such a huge dose of vitamin K, combined with other toxic ingredients in the shot, this liver overload isn’t surprising.

In turn, jaundice can cause kernicterus (brain damage from high bilirubin levels) and haemolysis (destruction of red blood cells), as reported in journals such as the British Journal of Obstetrics and Gynaecology, 1996.

 

The Truth About Breast Milk

 

Breast milk undoubtedly gets a bad press in the vitamin K deficiency argument, with doctors and drug manufacturer’s both suggesting that breast milk is ‘too low’ in vitamin K. Just as with vaccines, it is another step to undermine the mother, by suggesting that she is not good enough for her baby, and in ensuring reliance on drugs from birth.

There are many other factors to consider, such as whether the baby has fed and how often he has breast fed, what his overall condition is like, whether he has been exposed to antibiotics.

 

Studies have shown that:

• Breast fed babies whose mothers ate leafy green vegetables while pregnant, did not get VKDB

• Breast fed babies whose mothers were supplemented with vitamin K tablets while pregnant did not get VKDB

• There are higher levels of vitamin K in colostrum, the baby’s first milk, so it is really important that he gets to drink colostrum as soon as possible. A study in the British Medical Journal in 1992 showed that babies who had unrestricted access to the breast immediately after birth, and who had breast fed before they were 24 hours old, did not get VKDB.

 

Protecting Your Baby From Vitamin K Deficiency Bleeding

 

To summarise:

1. Don’t take medications while pregnant. If you are epileptic and on anti-seizure medication, talk to your doctor to see if it is possible to alter your drugs. Don’t take antibiotics unless there is a life threatening emergency.

2. Don’t drink alcohol during pregnancy.

3. Eat plenty of leafy green vegetables and fresh foods.

4. Avoid junk foods, and in particular, fats and margarine. Margarine contains butylated hydroxytoluene, which is an inhibitor of vitamin K.

5. Opt for a natural birth. Drugs in childbirth can make the baby unwell or drowsy, interfere with breast feeding and increase the risk of VKDB. Say no to a forceps delivery. You don’t have to have them, even in difficulty, there are other ways to help the baby into the world.

6. Delay the cord clamping. Leave your baby attached to his cord until it has stopped pulsing, or longer.

7. Breast feed your baby immediately after he is born. If he won’t feed, keep offering. If he is ill and cannot suckle, ensure he gets breast milk through a tube soon after he is born.

8. If you have a son, DON’T circumcise him! Research has shown that circumcision can cause heavy bleeding and lead to VKDB.

9. If you are considering giving artificial vitamin K supplementation, choose an oral brand rather than the injection. It is less stressful for the baby and it hasn’t been linked to cancer. Check ingredients carefully. Some may contain animal products, phenols or aluminium.

10. Consider having a natural vitamin K supplement in pregnancy and while you are nursing your child, as this won’t have the same risk of side-effects as the ones manufactured by the pharmaceutical industry.

 

Sources used for this article:

Information on VKDB came from source 1.

1. Joint statement and recommendations on

Vitamin K administration to newborn infants to prevent vitamin K deficiency bleeding in infancy.

National Health and Medical Research Council

Paediatric Division of the Royal Australasian College of Physicians

Royal Australian and New Zealand College of Obstetrics and Gynaecology

Royal Australian College of General Practitioners

Australian College of Midwives Inc

 

2. Merck and Co. Manufacturers data sheet for Aquamephyton vitamin K injection, dated February 2002. http://www.fda.gov/medwatch/SAFETY/2003/03Jun_PI/AquaMEPHYTON_PI.pdf

3. Hospira Inc manufacturer’s information http://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?id=1448

4. Roche Phrmaceutical’s Manufacturer’s data sheet, dated July 2006. http://www.betterhealth.vic.gov.au/bhcv2/bhcmed.nsf/pages/rockonmm/$File/rockonmm.pdf

5. Golding J, Paterson M and Kinlen L. Factors associated with childhood cancer in a national cohort study. Brit. J Cancer 1990;62:304-8.

6. Greenwood R. Vitamin K and childhood cancer. MIDIRS 1994;4(3):258-9.

7. Greer F, Marshall S, Cherry J and Suttie J. Vitamin K status of lactating mothers, human milk, and breast-feeding infants. Pediatrics 1991;88(4);751-6.

8. British Medical Journal, 316:189-193, Jan 17, 1998

9. Passmore S, Draper G, Brownbill P, Kroll M. Ecological studies of relation between hospital policies on neonatal vitamin K administration and subsequent occurrence of childhood cancer. BMJ 1998;316:184-9

10. Meyer T and Angus J. The effect of large doses of Synkavit in the newborn. Arch Dis Child 1956;31:212-5 in, Ruby, C. Vitamin K: a historical perspective. MIDIRS 1997;7(3):362-4.

11. New Ethicals Compendium; 3c: 303-304.

12. Hall M. and Pairaudeau P. The routine use of vitamin K in the newborn. Midwifery 1987;3(4):170-7

13. O’Connor M. and Addiego J. Use of oral vitamin K1 to prevent hemorrhagic disease of the newborn infant. J Pediatr 1986;108:616-9.

14. Hathaway W. New insights on Vitamin K. Hematol Oncol Clin North Am 1987;1(3):367-379.

15. Golding J, Greenwood R, Birmingham K. et al. Childhood cancer, intramuscular vitamin K and pethidine given during labour. BMJ 1992;305 (6849):341-6.

16. Henderson-Smart, D. Giving vitamin K to newborn infants: a therapeutic dilemma. MJA 1996;165:414-5.

 

Written by Joanna Karpasea-Jones.


Diet soda= formaldehyde,rat poison see why

FDA Lists 92 Symptoms from Nutrasweet (Aspartame)
(including Death!)photo by ginatyler

Please Note: Nutrasweet is in Diet Coke and Diet Pepsi

Update: Aspartame – NutraSweet – Is now called AminoSweet

Article courtesy of: Mark Gold mgold@tiac.net
(researcher for twenty years on such subjects)
This article originally appeared on http://www.dorway.com

Note: This information required a Freedom Of Information Act request to pry it from the reluctant hands of the FDA.

Nutrasweet (brand name for Aspartame) was not approved until 1981, in dry foods. For over eight years the FDA refused to approve it because of the seizures and brain tumors this drug produced in lab animals. The FDA continued to refuse to approve it until President Reagan took office (a friend of Searle) and fired the FDA Commissioner who wouldn’t approve it. Dr. Arthur Hull Hayes was appointed as commissioner. Even then there was so much opposition to approval that a Board of Inquiry was set up. The Board said: “Do not approve aspartame”. Dr. Hayes OVERRULED his own Board of Inquiry.

Shortly after Commissioner Arthur Hull Hayes, Jr., approved the use of aspartame in carbonated beverages, he left for a position with G.D. Searle’s Public Relations firm.

Long-Term Damage. It appears to cause slow, silent damage in those unfortunate enough to not have immediate reactions and a reason to avoid it. It may take one year, five years, 10 years, or 40 years, but it seems to cause some reversible and some irreversible changes in health over long-term use.

METHANOL (AKA WOOD ALCOHOL/POISON) (10% OF ASPARTAME) Methanol/wood alcohol is a deadly poison. People may recall that methanol was the poison that has caused some “skid row” alcoholics to end up blind or dead. Methanol is gradually released in the small intestine when the methyl group of aspartame encounter the enzyme chymotrypsin.

The absorption of methanol into the body is sped up considerably when free methanol is ingested. Free methanol is created from aspartame when it is heated to above 86 Fahrenheit (30 Centigrade). This would occur when aspartame-containing product is improperly stored or when it is heated (e.g., as part of a “food” product such as Jello).

Methanol breaks down into formic acid and formaldehyde in the body. Formaldehyde is a deadly neurotoxin. An EPA assessment of methanol states that methanol “is considered a cumulative poison due to the low rate of excretion once it is absorbed. In the body, methanol is oxidized to formaldehyde and formic acid; both of these metabolites are toxic.” The recommend a limit of consumption of 7.8 mg/day. A one-liter (approx. 1 quart) aspartame-sweetened beverage contains about 56 mg of methanol. Heavy users of aspartame-containing products consume as much as 250 mg of methanol daily or 32 times the EPA limit.

The most well known problems from methanol poisoning are vision problems. Formaldehyde is a known carcinogen, causes retinal damage, interferes with DNA replication, and causes birth defects. Due to the lack of a couple of key enzymes, humans are many times more sensitive to the toxic effects of methanol than animals. Therefore, tests of aspartame or methanol on animals do not accurately reflect the danger for humans. As pointed out by Dr Woodrow C. Monte, Director of the Food Science and Nutrition Laboratory at Arizona State University, “There are no human or mammalian studies to evaluate the possible mutagenic, teratogenic, or carcinogenic effects of chronic administration of methyl alcohol.”

It has been pointed out that fruit juices and alcoholic beverages contain small amounts of methanol. It is important to remember, that the methanol in natural products never appears alone. In every case, ethanol is present, usually in much higher amounts. Ethanol is an antidote for methanol toxicity in humans.

The troops of Desert Storm were “treated” to large amounts of aspartame-sweetened beverages which had been heated to over 86 degrees F. in the Saudi Arabian sun. Many of them returned home with numerous disorders similar to what has been seen in persons who have been chemically poisoned by formaldehyde. The free methanol in the beverages may have been a contributing factor in these illnesses. Other breakdown products ofaspartame such as DKP, may also have been a factor.

In a 1993 act that can only be described as “unconscionable”, the FDA approved aspartame as an ingredient in numerous food items that would always be heated to above 86°degrees F (30°Degrees C).

Much worse, on 27 June 1996, without public notice, the FDA removed all restrictions from aspartame allowing it to be used in everything, including all heated and baked goods.

The truth about aspartame’s toxicity is far different than what the NutraSweet Company would have you readers believe. In February of 1994, the U.S. Department of Health and Human Services released the listing of adverse reactions reported to the FDA (DHHS 1994). Aspartame accounted for more than 75% of all adverse reactions reported to the FDA’s Adverse Reaction Monitoring System (ARMS). By the FDA’s own admission fewer then ONE PERCENT of those who have problems with something they consume ever report it to the FDA. This balloons the almost 10,000 complaints they once had to around a million.

However, the FDA has a record keeping problem (they never did respond to the certified letter from the WEBMASTER of this site a major victim!) and they tend to discourage or even misdirect complaints, at least on aspartame. The fact remains, though, that MOST victims don’t have a clue that aspartame may be the cause of their many problems! Many reactions to aspartame were very serious including seizures and death.

Those reactions included:

Abdominal Pain
Anxiety attacks
arthritis
asthma
Asthmatic Reactions
Bloating, Edema (Fluid Retention)
Blood Sugar Control Problems (Hypoglycemia or Hyperglycemia)
Brain Cancer (Pre-approval studies in animals)
Breathing difficulties
burning eyes or throat
Burning Urination
can’t think straight
Chest Pains
chronic cough
Chronic Fatigue
Confusion
Death
Depression
Diarrhea
Dizziness
Excessive Thirst or Hunger
fatigue
feel unreal
flushing of face
Hair Loss (Baldness) or Thinning of Hair
Headaches/Migraines dizziness
Hearing Loss
Heart palpitations
Hives (Urticaria)
Hypertension (High Blood Pressure)
Impotency and Sexual Problems
inability to concentrate
Infection Susceptibility
Insomnia
Irritability
Itching
Joint Pains
laryngitis
“like thinking in a fog”
Marked Personality Changes
Memory loss
Menstrual Problems or Changes
Migraines and Severe Headaches (Trigger or Cause From Chronic Intake)
Muscle spasms
Nausea or Vomiting
Numbness or Tingling of Extremities
Other Allergic-Like Reactions
Panic Attacks
Phobias
poor memory
Rapid Heart Beat
Rashes
Seizures and Convulsions
Slurring of Speech
Swallowing Pain
Tachycardia
Tremors
Tinnitus
Vertigo
Vision Loss
Weight gain
Aspartame Disease Mimics Symptoms or Worsens the Following Diseases

Alzheimer’s Disease
Arthritis
Birth Defects
Chronic Fatigue Syndrome
Diabetes and Diabetic Complications
Epilepsy
Fibromyalgia
Lupus
Lyme Disease
Lymphoma
Multiple Chemical Sensitivities (MCS)
Multiple Sclerosis (MS)
Parkinson’s Disease
How it happens:

Methanol, from aspartame, is released in the small intestine when the methyl group of aspartame encounters the enzyme chymotrypsin (Stegink 1984, page 143). Free methanol begins to form in liquid aspartame-containing products at temperatures above 86 degrees F. also within the human body.

The methanol is then converted to formaldehyde. The formaldehyde converts to formic acid – ant sting poison. Toxic formic acid is used as an activator to strip epoxy and urethane coatings. Imagine what it does to your tissues! (Note from Stephanie Relfe – Even the Australian Cancer Council says that there are NO safe levels of formaldehyde).

Phenylalanine and aspartic acid, 90% of aspartame, are amino acids normally used in synthesis of protoplasm when supplied by the foods we eat. But when unaccompanied by other amino acids we use [there are 20], they are neurotoxic.

That is why a warning for Phenylketonurics is found on EQUAL and other aspartame products. Phenylketenurics are 2% of the population with extreme sensitivity to this chemical unless it’s present in food. It gets you too, causing brain disorders and birth defects! Finally, the phenyalanine breaks down into DKP, a brain tumor agent.

In other words: Aspartame converts to dangerous by-products that have no natural countermeasures. A dieter’s empty stomach accelerates these conversions and amplifies the damage. Components of aspartame go straight to the brain, damage that causes headaches, mental confusion, seizures and faulty balance. Lab rats and other test animals died of brain tumors.

Despite the claims of Monsanto and bedfellows:

1. Methanol from alcohol and juices does not get converted to formaldehyde to any significant extent. There is very strong evidence to confirm this fact for alcoholic beverages and fairly strong evidence for juices.

2. Formaldehyde obtained from methanol is very toxic in *very small* doses as seen by recent research.

3. Aspartame causes chronic toxicity reactions/damage due to the methanol to formaldehyde and other break down products despite what is claimed otherwise by the very short, industry-funded experiments using a test substance that is chemically different and absorbed differently than what is available to the general public. “Strangely enough”, almost all independent studies show that aspartame can cause health problems.

4. A common ploy from Monsanto is to claim that aspartame is “safe” yet a few select people may have “allergic” reactions to it. This is typical Monsanto nonsense, of course. Their own research shows that it does not cause “allergic” reactions. It is there way of trying to minimize and hide the huge numbers of toxicity reactions and damage that people are experiencing from the long-term use of aspartame.

Summary

Given the following points, it is definitely premature for researchers to discount the role of methanol in aspartame side effects:

1. The amount of methanol ingested from aspartame is unprecedented in human history. Methanol from fruit juice ingestion does not even approach the quantity of methanol ingested from aspartame, especially in persons who ingest one to three liters (or more) of diet beverages every day. Unlike methanol from aspartame, methanol from natural products is probably not absorbed or converted to its toxic metabolites in significant amounts as discussed earlier.

2. Lack of laboratory-detectable changes in plasma formic acid and formaldehyde levels do not preclude damage being caused by these toxic metabolites. Laboratory-detectable changes in formate levels are often not found in short exposures to methanol.

3. Aspartame-containing products often provide little or no nutrients which may protect against chronic methanol poisoning and are often consumed in between meals. Persons who ingest aspartame-containing products are often dieting and more likely to have nutritional deficiencies than persons who take the time to make fresh juices.

4. Persons with certain health conditions or on certain drugs may be much more susceptible to chronic methanol poisoning.

5. Chronic diseases and side effects from slow poisons often build silently over a long period of time. Many chronic diseases which seem to appear suddenly have actually been building in the body over many years.

6. An increasing body of research is showing that many people are highly sensitive to low doses of formaldehyde in the environment. Environmental exposure to formaldehyde and ingestion of methanol (which converts to formaldehyde) from aspartame likely has a cumulative deleterious effect.

7. Formic acid has been shown to slowly accumulate in various parts of the body. Formic acid has been shown to inhibit oxygen metabolism.

8. The are a very large and growing number of persons are experiencing chronic health problems similar to the side effects of chronic methanol poisoning when ingesting aspartame-containing products for a significant length of time. This includes many cases of eye damage similar to the type of eye damage seen in methanol poisoning cases.

Note: It often takes at least sixty days without any aspartame NutraSweet to see a significant improvement. (Note from Stephanie Relfe: Drink plenty of good water. Preferably water filtered by reverse osmosis. If not that, spring water. Not tap, distilled or mineral water).

Check all labels very carefully (including vitamins and pharmaceuticals). Look for the word “aspartame” on the label and avoid it. (Also, it is a good idea to avoid “acesulfame-k” or “sunette.”) Finally, avoid getting nutrition information from junk food industry PR organizations such as IFIC or organizations that accept large sums of money from the junk and chemical food industry such as the American Dietetic Association.

If you are a user of any products with aspartame, and you have physical, visual, mental problems take the 60-day no aspartame test. If, after two months with no aspartame your symptoms are either gone, or are much less severe, please get involved to get this neurotoxin off the market. Write a letter to the FDA, with a copy to Betty Martini (for proof of how the FDA doesn’t keep proper records). Write your congressmen. Return products containing aspartame to the point of purchase… for a FULL refund. Make a big stink if they WON’T give you a full refund! Tell all your friends and family… and if they stop using aspartame and also “wake up well”… get them involved in the same way.

Aspartame is an “approved sweetener” because of a few greedy and dishonest people who place profits above human life and well-being. With the FDA and our Congress culpable, only an INFORMED and ACTIVE public will affects its reclassification from “food additive” to TOXIC DRUG, and removed from the human food chain.

From Stephane Relfe: Note that Michael J. Fox, who was spokesperson for Pepsi, has an old man’s disease (Parkinson’s Disease) at only 30 years old!

Also Note: Aspartame has one use that I know of – it makes an EXCELLENT ant poison. Put a few tablespoons on a nest of fire ants and see how long before they disappear.

Please visit the Home Page for Latest News

For more information:

See What Ants Do to Aspartame!

My wife is not sick anymore – She gave up Aspartame

http://www.aspartamekills.com

List of Foods Containing Aspartame

http://www.holisticmed.com/aspartame

http://www.heall.com/body/askthedoctor/nutrition/artificialsweeteners.html

Addresses:

Commissioner
Food and Drug Administration
5600 Fishers Lane
Rockville, Maryland 20857

Mrs. Betty Martini
Mission Possible International
9270 State Bridge Road Suite 215
Duluth, Georgia 30097
Internet E-mail: bettym19@mindspring.com

NOW… that you are aware of the 92 FDA recognized symptoms (that required a Freedom Of Information Act request to pry from their reluctant hands) and HOW aspartame does its dirty work, change to Dorway’s Official Dogma page.

http://www.dorway.com/offasprt.html

On this page Mark Gold has taken the IFIC “Official” aspartame safety myth and


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