Saturday, December 17, 2011

Flame Retardant Chemical Banned in Europe and Japan Used in U.S. Soda for Decades

Source

sodagreen1 210x131 Flame Retardant Chemical Banned in Europe and Japan Used in U.S. Soda for DecadesWhy has a flame retardant chemical banned in Europe and Japan been used as an ingredient in North American sodas for decades? If you live in the United States and drink citrus-flavored sodas such as Mountain Dew, you may be ingesting this substance that has health professionals up in arms. A synthetic chemical known as brominated vegetable oil (BVO) — first patented by chemical companies as a flame retardant — is increasingly being identified as a threat to your health, but soda companies still have yet to remove BVO as an ingredient.

Added to about 10% of sodas in North America for decades, BVO has reportedly led to soda-drinkers experiencing skin lesions, memory loss, and nerve disorders. Interestingly, these are all the symptoms of overexposure to bromine. What is most concerning is the fact that studies have found that BVO can actually build up in human tissue, accumulating in large quantities over long periods of soda consumption.

Industry Reports Set “Safety Limit” on BVO

Is it any surprise that reports from a group within the industry wereinstrumental in establishing limits on what the FDA considers a “safe limit” for BVO in sodas? Scientists have disputed the supposed safety level, stating that not only is the data frail, but the research is several decades old and needs to be re-examined. Meanwhile, soda drinkers are being exposed to this toxic flame retardant chemical on a daily basis. It is not uncommon for some Americans to drink upwards of 5-6 sodas per day, and Mountain Dew is a popular choice against soda lovers.

“Aside from these reports, the scientific data is scarce,” said Walter Vetter, a food chemist at Germany’s University of Hohenheim and author of a recent, but unpublished, study on BVO in European soda imports.

Imagine the amount of BVO that has accumulated in the tissue of a lifelong soda drinker.

How can you tell which sodas contain BVO? Well, Mountain Dew, Squirt, Fanta Orange, Sunkist Pineapple, Gatorade Thirst Quencher Orange, and Powerade Strawberry Lemonade or Fresca Original Citrus all contain BVO. This is a not a complete list, however, and it is important to check the ingredient list. Sodas should be avoided regardless of BVO content, as BVO is not the only ingredient you need to worry about. Many sodas contain mercury-filled high-fructose corn syrup, or the carcinogenic artificial sweetener aspartame.

You can even hold a bottle of Mountain Dew up to a light and see the presence of BVO. BVO creates the cloudy look of the beverage by keeping the ‘fruity flavor’ mixed into the drink. Without the presence of BVO, the flavoring would float to the surface and separate.

Thursday, December 8, 2011

Hepatitis B Vaccine Causes Lupus

Source

US Government Concedes Hep B Vaccine Causes Systemic Lupus Erythematosus

Here we present the US Federal Court’s decision and order in full below.

The claimant in this case was dead when the damages were awarded. Tambra Harris died on November 9, 2009. Tambra’s mother and Administratix of her estate, Louvonia Deniece Harris, was substituted as petitioner, and an amended petition was filed on October 15, 2010.

Hepatitis B vaccine is given to US infants at birth for a disease which they are not at risk of.

Why? At risk groups are intravenous “recreational” drug abusers and those who practice unsafe sex – which rules out new born babies.

Whilst the risk factors for babies have changed little, there is now impressive evidence that for a preventive measure, hepatitis B vaccine is remarkable for the frequency, variety and severity of complications from its use. The toxicity of this vaccine is so unusual that, even if crucial data are regrettably concealed or covered by Court order, scientific evidence is already far higher than normally needed to justify severe restrictive measures.

Quote from French expert Dr. Marc Girard. See CHS article below for full details: UK Government Caught Lying On Baby Hep B Vax Safety. Whilst other evidence is embargoed by the French Courts, Dr Girard has been able to publish a scientific review of the unembargoed evidence from the French Courts of the vaccine’s hazards (Autoimmun Rev 2005; 4: 96-100). Dr Girard shows that French health authorities suppress studies demonstrating serious risks. Hepatitis B vaccine has been shown in many peer reviewed research papers [including from Harvard University - detailed references at end] to be associated with numerous infant deaths in the USA and Europe, multiple sclerosis and numerous chronic auto-immune disorders [see below for more details].

In the United States Court of Federal Claims
OFFICE OF SPECIAL MASTERS
No. 01-499V
(E-Filed: March 23, 2011)

TO BE PUBLISHED - Stipulated Damages; Hepatitis B Vaccine; Alleged Injuries Include Systemic Lupus Erythematosus (SLE)

_______________________________________
LOUONIA DENIECE HARRIS,
Administratrix of the Estate of TAMBRA
HARRIS,

Petitioner,

v.

SECRETARY OF THE DEPARTMENT OF
HEALTH AND HUMAN SERVICES,

Respondent.
______________________________________

STIPULATED DAMAGES DECISION1

On August 29, 2001, Tambra Harris (“petitioner”), filed a petition for compensation alleging that she suffered certain injuries as a result of receiving a vaccination. 2

Among the injuries petitioner alleged that she had suffered as a result of receiving a hepatitis B vaccination was systemic lupus erythematosus (SLE). She sought an award under the National Vaccine Injury Compensation Program 3

On March 22, 2011, counsel for both parties filed a stipulation, stating that a decision should be entered awarding compensation. The parties stipulated that petitioner shall receive the following compensation:

A lump sum of $ 475,000.00 in the form of a check payable to petitioner as Administratrix of the Estate of Tambra Harris. This amount represents compensation for all damages that would be available under 42 U.S.C. §300aa-15(a);

and

A lump sum payment of $ 9,914.00 in the form of a check jointly payable to petitioner and the State of Mississippi Division of Medicaid, Attn: Ms. Carolyn Hall Williams, Third Party Liability Unit, 550 High Street, Walter Sillers Building, Suite 1000, Jackson MS 39201, for reimbursement of Mississippi’s Medicaid expenses related to Tambra’s care.

Stipulation ¶ 8(a) and ¶ 8(b).

The undersigned approves the requested amount for petitioner’s compensation. Accordingly, an award should be made in the form of a check payable to petitioner as Administratrix of the Estate of Tambra Harris in the amount of $ 475,000.00. In addition, an additional award should be made in the form of a check payable jointly to petitioner and the State of Mississippi Division of Medicaid in the amount of $ 9,914.00. In the absence of a motion for review filed pursuant to RCFC Appendix B, the clerk of the court SHALL ENTER JUDGMENT in accordance with the terms of the parties’ stipulation. 4

IT IS SO ORDERED.
s/Patricia E. Campbell-Smith
Patricia E. Campbell-Smith
Special Master.

1 Because this decision contains a reasoned explanation for the undersigned’s action in this case, the undersigned intends to post this decision on the United States Court of Federal Claims’ website, in accordance with the E-Government Act of 2002, Pub. L. No. 107-347, 116 Stat. 2899, 2913 (Dec. 17, 2002). As provided by Vaccine Rule 18(b), each party has 14 days within which to request redaction “of any information furnished by that party: (1) that is a trade secret or commercial or financial in substance and is privileged or confidential; or (2) that includes medical files or similar files, the disclosure of which would constitute a clearly unwarranted invasion of privacy.” Vaccine Rule 18(b). Otherwise, “the entire” decision will be available to the public. Id. (the Act or the National Childhood Vaccine Injury Act of 1986, Pub. L. No. 99-660, 100 Stat. 3755, codified as amended, 42 U.S.C. §§ 300aa-1 to -34 (2006) (Vaccine Act or the Act). All citations in this decision to individual sections of the Vaccine Act are to 42 U.S.C. § 300aa.

2 Tambra Harris died on November 9, 2009. Tambra’s mother and Administratix of her estate, Louvonia Deniece Harris, was substituted as petitioner, and an amended petition was filed on October 15, 2010.

3 The National Vaccine Injury Compensation Program is set forth in Part 2 of the Program). 42 U.S.C. §§ 300aa-1 to -34 (2006).

4 Pursuant to Vaccine Rule 11(a), entry of judgment is expedited by the parties’ joint filing of notice renouncing the right to seek review.

___________________________________________________________________

UK Government Caught Lying On Baby Hep B Vax Safety

Posted on April 13, 2009

The British Government has been caught lying this week in news reports in two British Sunday newspapers about a proposal to give 8 week old British babies Hepatitis B vaccinations.

A Department of Health spokesman was quoted claiming:-

The safety of children is always paramount whenever decisions are taken regarding what vaccines are included as part of the child vaccination programme.: New vaccination fears over plan to give hepatitis jabs at eight weeks old Mail on Sunday 12th April 2009, Vaccination fears over plan for Hepatitis B jabs for babies : Sunday Telegraph 12 Apr 2009.

Only cost and not safety is legally permitted to be an objection under the UK New Labour Government’s new law in effect from April 1 this year [full details below]. Whilst 8 week old babies are not at risk from Hepatitis B, they are from the vaccine [full details below]. And six five EU Hepatitis B vaccines have lost their marketing authorisations since 2000, the latest being last week – GlaxoSmithKline’s Hepatitis B Energix B vaccine [full details below].

Hepatitis B vaccine has been shown in many peer reviewed research papers [including from Harvard University - detailed references at end] to be associated with numerous infant deaths in the USA and Europe, multiple sclerosis and numerous chronic auto-immune disorders. These latter include Guillain-Barre syndrome, lupus, rheumatism, blood disorders and chronic fatigue. The only potential claimed infant risk group is alleged to be babies born in the UK to mothers from countries with claimed-to-have high rates of infection. Around 2000 British born infants are already being vaccinated annually in the UK. At risk groups are intravenous “recreational” drug abusers and those who practice unsafe sex – which rules out 8 week old babies.

There has been a criminal judicial investigation in France into the adverse effects of this vaccine. France was the first country to introduce universal Hepatitis B vaccination and saw effects which included the first ever seen and harrowing cases of childhood multiple sclerosis in France.

Research also shows that the prevalence of Hepatitis B is low in the UK, consistent with previous estimates and suggesting that many infections were acquired outside the UK. This all suggests Government should concentrate its efforts on effective treatment rather than vaccination of infants against a disease which does not affect them. Proponents of the vaccination claim rates of Hepatitis B infection are “spiralling” but based on “estimates”. Regrettably “estimates” can be “pulled” in one direction or another depending on which direction those responsible for the “estimates” are more interested in seeing them move. And in these circumstances, they can never be justification for vaccinating all babies to protect adult drug abusers and practitioners of unsafe sex.

Additionally, UK and EU authorities have withdrawn marketing licences for6 5 Hepatitis vaccines claiming a lack of efficacy in some cases, voluntary withdrawal by the applicant in others and denying in one case [Hexavac] any association with 6 infant deaths in Germany. The deaths were reported in a 2005 research paper as possibly caused by the vaccine:Unexplained cases of sudden infant death shortly after hexavalent vaccination.” Zinka B, Rauch E, Buettner A, Rueff F, Penning R. – Vaccine. 2005 May 18.

The most recent vaccine to lose its authorisation was last Last week the UK Medicines and Healthcare Products regulatory Agency withdrewrequired recall of a batch of GlaxoSmithKline’s Hepatitis B Engerix Bvaccine marketing authorisation with Professor Kent Woods, chief executive of the MHRA stating:-

The safety of the vaccine is not in question, but it is suspected to be ineffective.” MHRA recalls GSK’s Hepatitis B vaccine - 07 Apr 2009 - Regulatory Affairs – Hays Pharma News

The other most recent vaccine to lose its European marketing authorisation was Quintanrix [also from GSK] in August last year. The other vaccines are: Infanrix [GSK], Hepacare [Celltech] and Primavax [Aventis Pasteur].

So if ‘The safety of children is always paramount’ why the British Department of Health is even contemplating such a vaccine for 8 week old babies is beyond comprehension.”

And do vaccines cause autistic conditions? If you read nothing else we strongly recommend you read this: PDF Download – Text of May 5th 2008 email from US HRSA to Sharyl Attkisson of CBS News]. In it the US Health Resources Services Administration [HRSA] state to CBS News reporter Sharyl Attkisson

We have compensated cases in which children exhibited an encephalopathy, or general brain disease. Encephalopathy may be accompanied by a medical progression of an array of symptoms including autistic behavior, autism, or seizures.

After the Hannah Poling story broke in the USA in February 2008 [see CHS article here] under the media spotlight numerous US health officials and agencies conceded on broadcast US nationwide TV news from CBS and CNN. Full details with links to the original sources can be found in this CHS article: Vaccination Causes Autism – Say US Government & Merck’s Director of Vaccines. Hannah developed an autistic condition after 9 vaccines administered the same day.

But there is worse to come and it shows the UK’s New Labour Government has been irresponsible handing recently from 1st April 2009 legal power to dictate vaccination policy exclusively to the Joint Committee on Vaccination and Immunisation: UK Government Hands Drug Industry Control of Childhood Vaccination. The JCVI regrettably has a demonstrable track-record of recklessness on safety up to and including the present day, as shown in FOI documents: British Government’s Reckless Disregard for Child Health Safety and UK Government Hands Drug Industry Control of Childhood Vaccination.

The DoH statement published in The Mail on Sunday is also untrue because:-

  • Under the new law The Health Protection (Vaccination) Regulations 2009 which came into effect on 1st April for England only, the Secretary of State has no power on the grounds of safety to refuse to implement or reverse any Joint Committe on Vaccination and Immunisation recommendation
  • the JCVI expressly has no remit to take safety into account in its decision-making
    • [that role is supposedly the MHRA's but regrettably they seem to rubber stamp a great deal of what the drug industry come up with - as has been shown time and again and not just with vaccines, but drugs like Seroxat - the "anti-depressant" shown not to work compared to placebo in some trials and which causes adolescents to be 3 times more likely to commit suicide in others.]
  • the only consideration the Secretary of State can take into account in rejecting JCVI recommendations is cost-effectiveness – not safety
  • contrary to the UK Department of Health claims, no childhood vaccines used on British children have ever been tested according to the gold standard of evidence – randomised placebo controlled clinical trials.
  • health officials refuse to ensure large scale studies of total health outcomes between vaccinated and unvaccinated individuals are carried out. These should show differences in overall health between these groups and some medical professionals believe this is because the studies would reveal the unvaccinated are healthier overall and high levels of chronic diseases in vaccinated individuals.
  • there is no clinical benefit to infants from Hepatitis B vaccine but infants are put at risk of the known and unknown adverse effects
  • this also means doctors and nurses are being expected to behave unethically and possibly criminally – because no caring parent will consent to a vaccine administered to an 8 week old baby on being told there are risks but no benefits

The main reason for the new drive to more and more vaccines – and this is well published in the trade press – is that the drug industry has been changing its business model. The financial markets have known for many years the old model would fail – that of patented “blockbuster” drugs:-

  • the drug industry have made vaccines the new growth area because they are highly lucrative
    • they are drugs everyone gets – it is the same business model of Bill Gates’ Microsoft – pretty much everyone has to have Windows software – pretty much everyone gets vax’d
    • and the drug industry has been working hard behind-the-scenes to pursuade everyone – especially legislators – that they are vital when they are not and lobbying for changes in law just like this new law – which was introduced without Parliamentary debate and appears to be unlawful per se: UK Government Hands Drug Industry Control of Childhood Vaccination

Dr Marc Girard, a specialist in the side effects of drugs and commissioned as a medical expert by French courts in the French criminal investigation into the introduction of universal Hepatitis B vaccination in France,suggests that even in high-endemic countries, the risk/benefit ratio of what he describes as “this unusually toxic vaccine” must be carefully re-assessed.

Regarding the health situation in the UK Dr Girard says the conclusion not to vaccinate is obvious. France was the first country to implement universal hepatitis B vaccination in 1994.

Whilst other evidence is embargoed by the French Courts, Dr. Marc Girard has also been able to publish a scientific review of the unembargoed evidence of the vaccine’s hazards (Autoimmun Rev 2005; 4: 96-100). Dr Girard shows that French health authorities suppress studies demonstrating serious risks.

Dr Girard has previously said:

Whilst the risk factors for babies have changed little, there is now impressive evidence that for a preventive measure, hepatitis B vaccine is remarkable for the frequency, variety and severity of complications from its use. The toxicity of this vaccine is so unusual that, even if crucial data are regrettably concealed or covered by Court order, scientific evidence is already far higher than normally needed to justify severe restrictive measures.

______________________________________

REFERENCES

UK & EU MARKETING AUTHORISATION WITHDRAWALS

  • MHRA recalls GSK’s Hepatitis B vaccine - 07 Apr 2009 - Regulatory Affairs – Hays Pharma News
  • Public Statement on Quintanrix (Common name: diphtheria, tetanus, pertussis, hepatitis B, Haemophilus influenzae type b conjugate vaccine) Withdrawal of the Marketing Authorisation in the European Union – 29/08/08 –EMEA/424484/08
  • EMEA announces recommendation for suspension of the marketing authorisation for HexavacEMEA/297369/2005
  • EMEA Withdrawal of the Marketing Authorisation for the Medicinal Product Hepacare (Triple hepatitis B recombinant vaccine)EMEA/32933/02- 20/12/02
    • Public Statement on Hepacare (Triple hepatitis B recombinant vaccine)17/12/02 – EMEA/32933/02
  • Withdrawal of the Marketing Authorisation for the Medicinal ProductPrimavax (Diptheria, Tetanus, and Hepatitis B vaccine) – 04/12/00 – EMEA/H/2681/00

______________________________________

DEATHS, MULTIPLE SCLEROSIS AND OTHER ADVERSE EFFECTS

  • “Unexplained cases of sudden infant death shortly after hexavalent vaccination.” Zinka B, Rauch E, Buettner A, Rueff F, Penning R. – Vaccine. 2005 May 18

Vaccinations are considered to be the most effective and safe method preventing infectious diseases. Although hexavalent vaccines like Hexavac((R)) and Infanrix Hexa((R)) are assumed to be well tolerated and safe regarding the rate of immunity [Liese JG, Stojanov S, Berut F, Minini P, Harzer E, Jow S, et al. Large scale safety study of a liquid hexavalent vaccine (D-T-acP-IPV-PRP-T-HBs) administered at 2, 4, 6 and 12-14 months of age. Vaccine 2002;20:448-54; Mallet E, Fabre P, Pines E, Salomon H, Staub T, Schodel F, et al. Immunogenicity and safety of a new liquid hexavalent combines vaccine compared with separate administration of reference licensed vaccines in infants. Pediatr Infect Dis J 2000;19:1119-27], it was noticed that several cases of death occurred shortly after the vaccination. We report six cases of sudden infant death that occurred within 48h after hexavalent vaccination. At post-mortal examination, those cases showed unusual findings, especially in the brain and in laboratory tests. Crude calculations of local epidemiology are compatible with an association between hexavalent vaccination and unusual cases of sudden infant death. If confirmed in systematic studies, our findings would have potentially serious clinical implications.

Neonatal Deaths After Hepatitis B Vaccine – The Vaccine Adverse Event Reporting System, 1991-1998 – Arch Pediatr Adolesc Med. 1999;153:1279-1282

Results: Of 1771 neonatal reports, there were 18 deaths in 8 boys and 9 girls (1 patient unclassified). The mean age at vaccination for these 18 cases was 12 days(range, 1-27 days); median time from vaccination to onset of symptoms was 2 days (range, 0-20 days); and median time from symptoms to death was 0 days (range, 0-15 days). The mean birth weight of the neonates (n = 15) was 3034 g (range, 1828-4678 g). The causes of death for the 17 autopsied cases were sudden infant death syndrome for 12, infection for 3, and 1 case each of intracerebral hemorrhage, accidental suffocation, and congenital heart disease. Conclusion: Few neonatal deaths following HepB vaccination have been reported, despite the use of at least 86 million doses of pediatric vaccine given in the United States since 1991. While the limitations of passive surveillance systems do not permit definitive inference, these data suggest that HepB immunization is not causing a clear increase in neonatal deaths.

Recombinant hepatitis B vaccine and the risk of multiple sclerosis

NEUROLOGY 2004;63:838-842

A prospective study

Miguel A. Hernán, MD, DrPH, Susan S. Jick, DSc, Michael J. Olek, DO and Hershel Jick, MD

From the Department of Epidemiology (Dr. Hernán), Harvard School of Public Health, Boston; Boston Collaborative Drug Surveillance Program (Drs. Susan S. Jick and Hershel Jick), Boston University, Lexington, MA; and Department of Neurology (Dr. Olek), College of Medicine, University of California, Irvine.

Background: A potential link between the recombinant hepatitisB vaccine and an increased risk of multiple sclerosis (MS) hasbeen evaluated in several studies, but some of them have substantialmethodologic limitations.

Methods: The authors conducted a nested case-control study withinthe General Practice Research Database (GPRD) in the UnitedKingdom. The authors identified patients who had a first MSdiagnosis recorded in the GPRD between January 1993 and December2000. Cases were patients with a diagnosis of MS confirmed throughexamination of medical records, and with at least 3 years ofcontinuous recording in the GPRD before their date of firstsymptoms (index date). Up to 10 controls per case were randomlyselected, matched on age, sex, practice, and date of joiningthe practice. Information on receipt of immunizations was obtainedfrom the computer records.

Results: The analyses include 163 cases of MS and 1,604 controls.The OR of MS for vaccination within 3 years before the indexdate compared to no vaccination was 3.1 (95% CI 1.5, 6.3). Noincreased risk of MS was associated with tetanus and influenzavaccinations.

Conclusions: These findings are consistent with the hypothesisthat immunization with the recombinant hepatitis B vaccine isassociated with an increased risk of MS, and challenge the ideathat the relation between hepatitis B vaccination and risk ofMS is well understood.

Received March 31, 2004. Accepted in final form May 8, 2004.

“Multiple sclerosis and hepatitis B vaccination: Adding the credibility of molecular biology to an unusual level of clinical and epidemiological evidence” Comenge Y; Girard M (Med Hypotheses, doi 10.1016/j.mehy.2005.08.012)

“Autoimmune hazards of hepatitis B vaccine” Girard M (Autoimmun Rev 2005; 4:96-100) (Text available in electronic form on request.)

______________________________________

Low Prevalence in The UK of Hepatitis B and Infections acquired abroad

The prevalence of hepatitis B infection in adults in England and Wales – Epidemiology and Infection (1999), 122:133-138 Cambridge University Press

Cost effectiveness analyses of alternative hepatitis B vaccination programmes in England and Wales require a robust estimate of the lifetime risk of carriage. To this end, we report the prevalence of infection in 3781 anonymized individuals aged 15–44 years whose sera were submitted in 1996 to 16 microbiology laboratories in England and Wales. One hundred and forty-six individuals (3·9%) were confirmed as anti HBc positive, including 14 chronic carriers (0·37%). The prevalence of infection and carriage was higher in samples collected in London and increased with age. No increased risk of infection was seen in sera from genito-urinary (GUM) clinics. Only 15 sera positive for hepatitis B were also positive for hepatitis C. Our results confirm the low prevalence of hepatitis B in England and Wales, are consistent with previous estimates of carriage and suggest that many infections were acquired while resident outside the UK. Future prevalence studies should determine the country of birth and other risk factors for each individual in order to confirm these findings. (Accepted September 14 1998)

ALL the Vaccines Are Contaminated - Every Last One of Them

Source

"The chief, if not the sole, cause of the monstrous increase in cancer has been vaccination" - Dr. Robert Bell, once Vice President International Society for Cancer Research at the British Cancer Hospital

Vaccines
Experts say families need to take a critical look at vaccines.

(WASHINGTON, D.C.) - Have you been rushing out to get a yearly flu vaccine or diligently taking your children for the 40 or so mandated childhood vaccines?

That's really a shame because you have unwittingly been trading a run-of-the-mill flu or just the measles, for loading up your or your children's bodies with cancer and other deadly viruses, a destructive bacteria, a chemical selected to damage fertility, and with synthetic DNA that threatens to damage your own DNA - the biologic code for your existence.

Who is saying the vaccines are contaminated?

None other than the (now deceased) head of vaccines at Merck, Dr. Maurice Hillerman, who on camera admitted that Merck's Hepatitis B vaccines, contaminated with a virus, caused the AIDS epidemic in the US. He went on to say that all of Merck's vaccines are contaminated with cancer and other viruses. (The US government has conceded the HEB B vaccine causes Lupus. That vaccine is mandated for every infant in the US on the day of birth, and is associated with MS as well.)

That vaccine is mandated for every infant in the US on the day of birth, and is associated with MS as well.)

For Jews who have almost religiously believed in medical authorities about vaccines and poo-pooed those worried about the safety of vaccines, they might want to notice that Hillerman was Jewish.

Or they might recognize that so is Dr. Larry Palevsky, a board certified NY pediatrician, who for ten years routinely gave vaccines to his patients until he noticed them losing eye contact and then began looking into the vaccines he had blindly trusted. He found that they are ALL contaminated with viruses that are so small they can never be removed. He no longer gives any vaccines. He now treats his young patients for autism and other neurologic injuries from vaccines.

Donald W. Scott, the editor of The Journal of Degenerative Diseases and the co-founder of the Common Cause Medical Research Foundation, links vaccines to AIDS (as did Hillerman) and to US bio-weapons research, and says they are contaminated with mycoplasma, a primitive bacteria that takes apart cell walls.

Perhaps the highest scientific authority saying vaccines are contaminated is Garth Nicolson. He is a cell biologist and editor of the Journal of Clinical and Experimental Metastasis, and the Journal of Cellular Biochemistry. He is one of the most cited scientists in the world, having published over 600 medical and scientific peer-reviewed papers, edited over 14 books, and served on the editorial boards of 28 medical and scientific journals. He is not just saying that vaccines are contaminated with mycoplasma but is warning the US that they are. Nicolson goes further and says that we are all being damaged by them and contracting chronic degenerative diseases that.

That damage translates into lifelong patients (and thus life-long profit) for the pharmaceutical industry making the vaccines and he says doesn't appear to be accidental.


According To CIA Statistics: As Shots Increase, U.S. Lifespan Is DECREASING

1980: 9 vaccines, autism is rare
2009: 36 vaccine$ before age 5
2010: 55 vaccine$ before age 6

Vaccines vs. Autism, 2009Vaccinations before age 5Deaths per 1000 under 5 yrs old

Autism Rate

Lifespan Ranking
United States (c)367.81 in 9134
Norway134.41 in 2,000 ab5
Denmark125.81 in 2,200 ab18 d
Japan114.21 in 475 a4
Sweden114.01 in 862 a2
Iceland113.91 in 1,1000 ab1



All the vaccines mandated to children and many other vaccines as well, including the seasonal flu vaccines being mandated to health care workers, are contaminated with polysorbate 80, the central ingredient in a pharmaceutical industry patent to damage fertility. The pharmaceutical industry has a long history of of seeking a vaccine that would covertly sterilize whole populations So, in addition to being contaminated with cancer and other viruses, and with the bacteria mycoplasma, vaccines are intentionally "contaminated" with a chemical as well, which is, given the patent, a "patently" sought-after sterilizing agen

Beyond containing polysorbate 80 and cancer and other viruses, and likely mycoplasma, the Gardasil vaccines are contaminated in an additional way. It and all the new vaccines are contaminated with genetically engineered DNA. It can contaminate people's DNA, just a genetically engineered crops can contaminate normal crops. Gardasil itself is contaminated with a man-made version of the HPV DNA, the very virus it was supposed to protect against, which now it threatens not only altering kids' healthy DNA with synthetic DNA (!) but with a diseased version.

Gardasil was suspended in India after 4 girls died but the killing has gone on in the US despite the confirmed deaths of 100 girls. and now the CDC, with special ties to Merck, its maker, wants all boys to take it, too.

Informed consent is the core of the Nuremberg Code that was created by the Nuremberg Tribunal to keep the pharmaceutical industry from ever again committing the hideous "medical" abuses it did during the Holocaust. In California, Jerry Brown is dismantling informed consent in order to get these deadly vaccines associated with infertility, into all school children. And it was during the Holocaust that the pharmaceutical experimented on Jewish women prisoners at Auschwitz to develop a vaccine that sterilized covertly. Henry Kissinger recommended the development of covertly sterilizing vaccines in a major report to the US government and as late as 2009 a Finnish Health Minister said he was behind the H1N1 vaccine that was meant to lower population.

Jerry Brown has just signed into law a bill that will allow children as young as 12 to decide whether to take a vaccine for sexually transmitted disease. Parental consent is not needed and parents will not even be allowed knowledge as to whether the child has taken the vaccine. Merck's Hepatitis B vaccine is one that is included, as is another Merck vaccine, Gardasil, allegedly for ovarian cancer. A Gardasil researcher says there is no evidence it works. "This raises questions about the CDC's recommendation that the series of shots be given to girls as young as 11-years old. 'If we vaccinate 11 year olds and the protection doesn't last... we've put them at harm from side effects, small but real, for no benefit,' says Dr. Harper. 'The benefit to public health is nothing, there is no reduction in cervical cancers … ' "


Current Data for Gardasil up to AUG 12, 2011


Disabled 763
Deaths 103
Did Not Recover 4777
Abnorm. Pap Smear 430
Cervical Dysplasia 157
Cervical Cancer 41
Life Threatening 444
Emergency Rm. Visit 9115

Hospitalized 2307
Extended Hosp. Stay 201
Serious 3111
Adverse Events 23388


But these figures are based on statistics from medical professionals who do not wish to be sued. In reality, "less than 10% of deaths, seizures, paralysis, etc., are being reported as caused by the vaccinations that doctors gave in their office.

The following real-world estimates are based on reports from a law firm:

840 young girls and 2 boys have died after receiving the Gardasil HPV Vaccine 201,010 young girls have suffered debilitating events such as fatigue, seizures, paralysis, etc. after receiving the Gardasil HPV Vaccine.

The California law even approves in advance, ALL yet-to-be made (and completely untested) vaccines for sexually transmitted diseases, though of the two current Merck vaccines they are pushing on children, one Merck vaccine caused AIDS and causes Lupus and the other Merck vaccine is contaminated in multiple ways and proving highly lethal. Children will be the ones decide whether to take the vaccines, and they will make that decision after being forced to see videos of people dying terrible deaths from cancer. Not only would the vaccine be given without parental consent, but parents are denied knowledge that the vaccine is going to be given or that it was given. If the child has a seizure or dies afterward, parents may not see their own children's medical records.

This is what is left of the "informed consent" meant to provide human rights to protect the world from pharmaceutical industry abuses against mankind.

After World War II, it was Merck which received the flight capital of the pharmaceutical industry indicted for crimes against humanity, human enslavement and mass murder.

In the case of children, rather than their facing childhood diseases of insignificant threat, they are, by legal mandate, being bombarded repeatedly throughout their childhood with viruses that cause diseases (including cancer), a cell-destroying bacteria, a a threat to the very integrity of their DNA, and a chemical specifically chosen to impair fertility. And laws are being written to add to the already long list of vaccines they must take, including two mandated Merck vaccines. One is an old Merck vaccine that caused AIDS and is causing Lupus. The other is a Merck vaccine claiming to prevent cervical cancer though girls have little chance of contracting it in the first place (and boys, none!) and it can easily be detected by pap smear and treated successfully and there is NO evidence the vaccine prevents it. Meanwhile, it is killing children.

Contamination of the polio vaccine and the continuing effects

FACT: Before the Polio Vaccine, there had never been a virus from another species deliberately injected into humans.

FACT: 61% of all human tumors (at autopsy) now contain the SV40 monkey virus, traceable to the Polio vaccine of the 1950s and 60s

FACT: CUTTER vaccine division and WYETH produced a deadly Polio vaccine with a live virus that actually gave the recipient POLIO

FACT: All above information was withheld from the public for years to avoid a public panic and to prevent a loss of faith in vaccines. polio was a very rare infectious disease that presented little risk to the public, but the risk was greatly exaggerated by the Polio Foundation before the introduction of the polio vaccine, the miracle vaccine - contaminated with a monkey virus which has been the cause of soft tissue cancers for decades since.

Though facing no serious health risk, people are paying to have their bodies contaminated by contaminated vaccines. In taking vaccines, they are trading the minimal risk of even contracting common diseases and which themselves are rarely dangerous and can be treated if contracted - for the absolute certainty of loading their bodies with

1. cancer and other infectious viruses,

2. a destructive bacteria, and

3. a fertility impairing chemical.

They are doing this because they are being terrorized by their own government with false information on the risks of various diseases and denied critical information on the scientific risk of the vaccines.

Those vaccines without a doubt threaten their own and their children's fertility, and their very lives.

Friday, November 11, 2011

50 Reasons to Oppose Fluoridation

Source

Updated August, 2011

By Paul Connett, PhD and other members of the Fluoride Action Network (including James Beck, MD, PhD, Michael Connett, JD, Hardy Limeback, DDS, PhD, David McRae and Spedding Micklem, D.Phil.)

Introduction

Fluoridation is the practice of adding a fluoride compound to the public drinking water supply ostensibly for the purpose of fighting tooth decay. The levels used range from 0.6 to 1.2 milligrams of fluoride ion per liter (or parts per million, ppm). The practice began in the U.S. in 1945 and was endorsed by the U.S. Public Health Service (PHS) in 1950. Very few countries have adopted this practice to any significant extent. Only eight countries in the world have more than 50% of their populations drinking artificially fluoridated water (Australia, Colombia, Ireland, Israel, Malaysia, New Zealand, Singapore, and the U.S.). In Europe, only Ireland (with 73% of the population fluoridated), the U.K. (10%) and Spain (10%) fluoridate some of their water supplies. In the U.S., about 70% of the population is drinking fluoridated water – that is approximately 200 million people and about half the number of people drinking artificially fluoridated water worldwide. Some countries have areas with high natural fluoride levels in the water. These include India, China and parts of Africa. In these countries measures are being taken to remove the fluoride because of the health problems that fluoride can cause.

Fluoridation is a bad medical practice

  1. Fluoride is the only chemical added to water for the purpose of medical treatment. The U.S. Food and Drug Administration (FDA) classifies fluoride as a drug when used to prevent or mitigate disease (FDA 2000). As a matter of basic logic, adding fluoride to water for the sole purpose of preventing tooth decay (a non-waterborne disease) is a form of medical treatment. All other water treatment chemicals are added to improve the water's quality or safety, which fluoride does not do.
  2. Fluoridation is unethical. Informed consent is standard practice for all medication, and one of the key reasons why most of Western Europe has ruled against fluoridation. With water fluoridation we are allowing governments to do to whole communities (forcing people to take a medicine irrespective of their consent) what individual doctors cannot do to individual patients. While referenda are preferential to imposed policies from government, it still leaves the problem of individual rights versus majority rule. Put another way: Does a voter have the right to require that their neighbor ingest a certain medication (even if it is against that neighbor's will)?
  3. The dose cannot be controlled. Once fluoride is put in the water it is impossible to control the dose each individual receives because people drink different amounts of water. Being able to control the dose a patient receives is critical. Some people (e.g., manual laborers, athletes, diabetics, and people with kidney disease) drink substantially more water than others.
  4. The fluoride goes to everyone regardless of age, health or vulnerability. According to Dr. Arvid Carlsson, the 2000 Nobel Laureate in Medicine and Physiology and one of the scientists who helped keep fluoridation out of Sweden:
  5. "Water fluoridation goes against leading principles of pharmacotherapy, which is progressing from a stereotyped medication -- of the type 1 tablet 3 times a day -- to a much more individualized therapy as regards both dosage and selection of drugs. The addition of drugs to the drinking water means exactly the opposite of an individualized therapy" (Carlsson 1978).
  6. People now receive fluoride from many other sources besides water. Fluoridated water is not the only way people are exposed to fluoride. Other sources of fluoride include food and beverages processed with fluoridated water (Kiritsy 1996; Heilman 1999), fluoridated dental products (Bentley 1999; Levy 1999), mechanically deboned meat (Fein 2001), tea (Levy 1999), and pesticide residues (e.g., from cryolite) on food (Stannard 1991; Burgstahler 1997). It is now widely acknowledged that exposure to non-water sources of fluoride has significantly increased since the water fluoridation program first began (NRC 2006).
  7. Fluoride is not an essential nutrient (National Research Council [NRC] 1993; Institute of Medicine [IOM] 1997, NRC 2006). No disease has ever been linked to a fluoride deficiency. It has never been shown that ingested fluoride is needed to produce decay-free teeth. Not a single biological process has been shown to require fluoride. On the contrary there is extensive evidence that fluoride can interfere with many important biological processes. Fluoride interferes with numerous enzymes (Waldbott 1978). In combination with aluminum, fluoride interferes with G-proteins (Bigay 1985, 1987). Such interactions give aluminum-fluoride complexes the potential to interfere with signals from growth factors, hormones and neurotransmitters (Strunecka & Patocka 1999; Li 2003). More and more studies are indicating that fluoride can interfere with biochemistry in fundamental ways (Barbier 2010).
  8. The level in mothers' milk is very low. Considering reason #6 it is perhaps not surprising that the level of fluoride in mother's milk is remarkably low (0.004 ppm, NRC, 2006). This means that a bottle-fed baby consuming fluoridated water (0.6 – 1.2 ppm) can get up to 300 times more fluoride than a breast-fed baby. There are no benefits (see reasons #11-19), only risks (see reasons #21-36), for infants ingesting this heightened level of fluoride at such an early age (an age where susceptibility to environmental toxins is particularly high).
  9. Fluoride accumulates in the body. Healthy adult kidneys excrete 50 to 60% of the fluoride they ingest each day (Marier & Rose 1971). The remainder accumulates in the body, largely in calcifying tissues such as the bones and pineal gland (Luke 1997, 2001). Infants and children excrete less fluoride from their kidneys and take up to 80% of ingested fluoride into their bones (Ekstrand 1994). The fluoride concentration in bone steadily increases over a lifetime (NRC 2006).
  10. No health agency in fluoridated countries is monitoring fluoride exposure or side effects. No regular measurements are being made of the levels of fluoride in urine, blood, bones, hair, or nails of either the general population or sensitive subparts of the population (e.g., individuals with kidney disease).
  11. There has never been a single randomized clinical trial to demonstrate fluoridation's effectiveness or safety. Despite the fact that fluoride has been added to community water supplies for over 60 years, "there have been no randomized trials of water fluoridation" (Cheng 2007). Randomized studies are the standard method for determining the safety and effectiveness of any purportedly beneficial medical treatment. In 2000, the British Government's "York Review" could not give a single fluoridation trial a Grade A classification – despite 50 years of research (McDonagh 2000). The U.S. Food and Drug Administration (FDA) continues to classify fluoride as an "unapproved new drug."
  12. Swallowing fluoride provides no (or very little) benefit

  13. Benefit is topical not systemic. The Centers for Disease Control and Prevention (CDC, 1999, 2001) has now acknowledged that the mechanism of fluoride's benefits are mainly topical, not systemic. There is no need whatsoever, therefore, to swallow fluoride to protect teeth. Since the purported benefit of fluoride is topical, and the risks are systemic, it makes more sense to deliver the fluoride directly to the tooth in the form of toothpaste. Since swallowing fluoride is unnecessary, and potentially dangerous, there is no justification for forcing people (against their will) to ingest fluoride through their water supply.
  14. Fluoridation is not necessary. Most western, industrialized countries have rejected water fluoridation, but have nevertheless experienced the same decline in childhood dental decay as fluoridated countries. (See data from World Health Organization presented graphically in Figure 1).

  15. Tooth Decay Trends

  16. Fluoridation's role in the decline of tooth decay is in serious doubt. The largest survey ever conducted in the US (over 39,000 children from 84 communities) by the National Institute of Dental Research showed little difference in tooth decay among children in fluoridated and non-fluoridated communities (Hileman 1989). According to NIDR researchers, the study found an average difference of only 0.6 DMFS (Decayed, Missing, and Filled Surfaces) in the permanent teeth of children aged 5-17 residing their entire lives in either fluoridated or unfluoridated areas (Brunelle & Carlos, 1990). This difference is less than one tooth surface, and less than 1% of the 100+ tooth surfaces available in a child's mouth. Large surveys from three Australian states have found even less of a benefit, with decay reductions ranging from 0 to 0.3 of one permanent tooth surface (Spencer 1996; Armfield & Spencer 2004). None of these studies have allowed for the possible delayed eruption of the teeth that may be caused by exposure to fluoride, for which there is some evidence (Komarek 2005). A one-year delay in eruption of the permanent teeth would eliminate the very small benefit recorded in these modern studies.
  17. NIH-funded study on individual fluoride ingestion and tooth decay failed to find a significant correlation. A multi-million dollar, U.S. National Institutes of Health (NIH) -funded study (Warren 2009) found no relation between tooth decay and the amount of fluoride ingested by children. This is the first time that tooth decay has been investigated as a function of individual exposure as opposed to mere residence in a fluoridated community.
  18. Tooth decay is high in low-income communities that have been fluoridated for years. Despite some claims to the contrary, water fluoridation cannot prevent the oral health crises that result from rampant poverty, inadequate nutrition, and lack of access to dental care. There have been numerous reports of severe dental crises in low-income neighborhoods of US cities that have been fluoridated for over 20 years (e.g., Boston, Cincinnati, New York City, and Pittsburgh). In addition, fluoridation has been repeatedly found to be ineffective at preventing the most serious oral health problem facing poor children, namely "baby bottle tooth decay," otherwise known as early childhood caries (Barnes 1992; Shiboski 2003).
  19. Tooth decay does not go up when fluoridation is stopped. Where fluoridation has been discontinued in communities from Canada, the former East Germany, Cuba and Finland, dental decay has not increased but has generally continued to decrease (Maupomé 2001; Kunzel & Fischer, 1997, 2000; Kunzel 2000; Seppa 2000).
  20. Tooth decay was coming down before fluoridation started. Modern research (e.g., Diesendorf 1986; Colquhoun 1997) shows that decay rates were coming down before fluoridation was introduced in Australia and New Zealand and have continued to decline even after its benefits would have been maximized (see Figure 2). Many other factors influence tooth decay.

  21. Number of Decayed Teeth Per Child

    Figure 2. The number of decayed teeth in 5-year olds in New Zealand, over the period 1930-1990. The percentage of the population drinking fluoridated water and the percentage of the total toothpaste sold containing fluoride are shown on the right hand axis (Colquhoun, 1993).

  22. The studies that launched fluoridation were methodologically flawed. The early trials conducted between 1945 and 1955 in North America that helped to launch fluoridation, have been heavily criticized for their poor methodology and poor choice of control communities (De Stefano 1954; Sutton 1959, 1960, 1996; Ziegelbecker 1970). According to Dr. Hubert Arnold, a statistician from the University of California at Davis, the early fluoridation trials "are especially rich in fallacies, improper design, invalid use of statistical methods, omissions of contrary data, and just plain muddleheadedness and hebetude." Serious questions have also been raised about Trendley Dean's (the father of fluoridation) famous 21-city study from 1942 (Ziegelbecker 1981).
  23. Children are being over-exposed to fluoride

  24. Children are being over-exposed to fluoride. The fluoridation program has massively failed to achieve one of its key objectives, i.e., to lower dental decay rates while limiting the occurrence of dental fluorosis (a discoloring of tooth enamel caused by too much fluoride. The goal of the early promoters of fluoridation was to limit dental fluorosis (in its very mild form) to 10% of children (NRC 1993, pp. 6-7). In 2010, however, the Centers for Disease Control and Prevention (CDC) reported that 41% of American adolescents had dental fluorosis, with 8.6% having mild fluorosis and 3.6% having either moderate or severe dental fluorosis (Beltran-Aguilar 2010). As the 41% prevalence figure is a national average and includes children living in fluoridated and unfluoridated areas, the fluorosis rate in fluoridated communities will obviously be higher. The British Government's York Review estimated that up to 48% of children in fluoridated areas worldwide have dental fluorosis in all forms, with 12.5% having fluorosis of aesthetic concern (McDonagh, 2000).
  25. The highest doses of fluoride are going to bottle-fed babies. Because of their sole reliance on liquids for their food intake, infants consuming formula made with fluoridated water have the highest exposure to fluoride, by bodyweight, in the population. Because infant exposure to fluoridated water has been repeatedly found to be a major risk factor for developing dental fluorosis later in life (Marshall 2004; Hong 2006; Levy 2010), a number of dental researchers have recommended that parents of newborns not use fluoridated water when reconstituting formula (Ekstrand 1996; Pendrys 1998; Fomon 2000; Brothwell 2003; Marshall 2004). Even the American Dental Association (ADA), the most ardent institutional proponent of fluoridation, distributed a November 6, 2006 email alert to its members recommending that parents be advised that formula should be made with "low or no-fluoride water." Unfortunately, the ADA has done little to get this information into the hands of parents. As a result, many parents remain unaware of the fluorosis risk from infant exposure to fluoridated water.
  26. Evidence of harm to other tissues

  27. Dental fluorosis may be an indicator of wider systemic damage. There have been many suggestions as to the possible biochemical mechanisms underlying the development of dental fluorosis (Matsuo 1998; Den Besten 1999; Sharma 2008; Duan 2011; Tye 2011) and they are complicated for a lay reader. While promoters of fluoridation are content to dismiss dental fluorosis (in its milder forms) as merely a cosmetic effect, it is rash to assume that fluoride is not impacting other developing tissues when it is visibly damaging the teeth by some biochemical mechanism (Groth 1973; Colquhoun 1997). Moreover, ingested fluoride can only cause dental fluorosis during the period before the permanent teeth have erupted (6-8 years), other tissues are potentially susceptible to damage throughout life. For example, in areas of naturally high levels of fluoride the first indicator of harm is dental fluorosis in children. In the same communities many older people develop skeletal fluorosis.
  28. Fluoride may damage the brain. According to the National Research Council (2006), "it is apparent that fluorides have the ability to interfere with the functions of the brain." In a review of the literature commissioned by the US Environmental Protection Agency (EPA), fluoride has been listed among about 100 chemicals for which there is "substantial evidence of developmental neurotoxicity." Animal experiments show that fluoride accumulates in the brain and alters mental behavior in a manner consistent with a neurotoxic agent (Mullenix 1995). In total, there have now been over 100 animal experiments showing that fluoride can damage the brain and impact learning and behavior. According to fluoridation proponents, these animal studies can be ignored because high doses were used. However, it is important to note that it takes 5-20 times more fluoride to reach the same plasma levels in rats as reached in humans (Sawan 2010). In fact, one animal experiment found effects at remarkably low doses (Varner 1998). In this study, rats fed for one year with 1 ppm fluoride in their water (the same level used in fluoridation programs), using either sodium fluoride or aluminum fluoride, had morphological changes to their kidneys and brains, an increased uptake of aluminum in the brain, and the formation of beta-amyloid deposits which are associated with Alzheimer's disease. Other animal studies have found effects on the brain at water fluoride levels as low as 5 ppm (Liu 2010).(For a complete listing of these studies.
  29. Fluoride may lower IQ. There have now been 24 studies from China, Iran, India and Mexico that have reported an association between fluoride exposure and reduced IQ. One of these studies (Lin Fa-Fu 1991) indicates that even just moderate levels of fluoride exposure (e.g., 0.9 ppm in the water) can exacerbate the neurological defects of iodine deficiency. In the absence of iodine deficiency, another research team (Xiang 2003a,b) estimated that fluoride may lower IQ at 1.9 ppm, while a recent preliminary study (Ding 2011) found a lowering of IQ in children drinking water at levels ranging from 0.3 to 3 ppm. The authors of this latter study reported that for each increase of 1 ppm fluoride measured in the urine there was a loss of 0.59 IQ points. None of these studies indicates an adequate margin of safety to protect all children drinking artificially fluoridated water from this affect. According to the National Research Council (2006), "the consistency of the results [in fluoride/IQ studies] appears significant enough to warrant additional research on the effects of fluoride on intelligence." Except for an early and small IQ study from New Zealand (Shannon et al., 1986) no fluoridating country has investigated the matter for themselves.
  30. Fluoride may cause non-IQ neurotoxic effects. Reduced IQ is not the only neurotoxic effect that may result from fluoride exposure. At least three human studies have reported an association between fluoride exposure and impaired visual-spatial organization (Calderon 2000; Li 2004; Rocha-Amador 2009); while three other studies have found an association between prenatal fluoride exposure and fetal brain damage (Han 1989; Du 1992; Yu 1996).
  31. Fluoride affects the pineal gland. Studies by Jennifer Luke (2001) show that fluoride accumulates in the human pineal gland to very high levels. In her Ph.D. thesis, Luke has also shown in animal studies that fluoride reduces melatonin production and leads to an earlier onset of puberty (Luke 1997). Consistent with Luke's findings, one of the earliest fluoridation trials in the U.S. (Schlesinger 1956) reported that on average young girls in the fluoridated community reached menstruation 5 months earlier than girls in the non-fluoridated community. Inexplicably, no fluoridating country has attempted to reproduce either Luke's or Schlesinger's findings or examine the issue any further.
  32. Fluoride affects thyroid function. According to the U.S. National Research Council (2006), "several lines of information indicate an effect of fluoride exposure on thyroid function." In the Ukraine, Bachinskii (1985) found a lowering of thyroid function, among otherwise healthy people, at 2.3 ppm fluoride in water. In the middle of the 20th century, fluoride was prescribed by a number of European doctors to reduce the activity of the thyroid gland for those suffering from hyperthyroidism (overactive thyroid) (Stecher 1960; Waldbott 1978). According to a clinical study by Galletti and Joyet (1958), the thyroid function of hyperthyroid patients was effectively reduced at just 2.3 to 4.5 mg/day of fluoride ion. To put this finding in perspective, the Department of Health and Human Services (DHHS, 1991) has estimated that total fluoride exposure in fluoridated communities ranges from 1.6 to 6.6 mg/day. This is a remarkable fact, particularly considering the rampant and increasing problem of hypothyroidism (underactive thyroid) in the United States and other fluoridated countries. Symptoms of hypothyroidism include depression, fatigue, weight gain, muscle and joint pains, increased cholesterol levels, and heart disease. In 2010, the second most prescribed drug of the year was Synthroid (sodium levothyroxine) which is a hormone replacement drug used to treat an underactive thyroid.
  33. Fluoride causes arthritic symptoms. Some of the early symptoms of skeletal fluorosis (a fluoride-induced bone and joint disease that impacts millions of people in India, China, and Africa), mimic the symptoms of arthritis (Singh 1963; Franke 1975; Teotia 1976; Carnow 1981; Czerwinski 1988; DHHS 1991). According to a review on fluoridation published in Chemical & Engineering News, "Because some of the clinical symptoms mimic arthritis, the first two clinical phases of skeletal fluorosis could be easily misdiagnosed" (Hileman 1988). Few, if any, studies have been done to determine the extent of this misdiagnosis, and whether the high prevalence of arthritis in America (1 in 3 Americans have some form of arthritis - CDC, 2002) and other fluoridated countries is related to growing fluoride exposure, which is highly plausible. Even when individuals in the U.S. suffer advanced forms of skeletal fluorosis (from drinking large amounts of tea), it has taken years of misdiagnoses before doctors finally correctly diagnosed the condition as fluorosis.
  34. Fluoride damages bone. An early fluoridation trial (Newburgh-Kingston 1945-55) found a significant two-fold increase in cortical bone defects among children in the fluoridated community (Schlesinger 1956). The cortical bone is the outside layer of the bone and is important to protect against fracture. While this result was not considered important at the time with respect to bone fractures, it did prompt questions about a possible link to osteosarcoma (Caffey, 1955; NAS, 1977). In 2001, Alarcon-Herrera and co-workers reported a linear correlation between the severity of dental fluorosis and the frequency of bone fractures in both children and adults in a high fluoride area in Mexico.
  35. Fluoride may increase hip fractures in the elderly. When high doses of fluoride (average 26 mg per day) were used in trials to treat patients with osteoporosis in an effort to harden their bones and reduce fracture rates, it actually led to a higher number of fractures, particularly hip fractures (Inkovaara 1975; Gerster 1983; Dambacher 1986; O'Duffy 1986; Hedlund 1989; Bayley 1990; Gutteridge 1990. 2002; Orcel 1990; Riggs 1990 and Schnitzler 1990). Hip fracture is a very serious issue for the elderly, often leading to a loss of independence or a shortened life. There have been over a dozen studies published since 1990 that have investigated a possible relationship between hip fractures and long term consumption of artificially fluoridated water or water with high natural levels. The results have been mixed – some have found an association and others have not. Some have even claimed a protective effect. One very important study in China, which examined hip fractures in six Chinese villages, found what appears to be a dose-related increase in hip fracture as the concentration of fluoride rose from 1 ppm to 8 ppm (Li 2001) offering little comfort to those who drink a lot of fluoridated water. Moreover, in the only human epidemiological study to assess bone strength as a function of bone fluoride concentration, researchers from the University of Toronto found that (as with animal studies) the strength of bone declined with increasing fluoride content (Chachra 2010). Finally, a recent study from Iowa (Levy 2009), published data suggesting that low-level fluoride exposure may have a detrimental effect on cortical bone density in girls (an effect that has been repeatedly documented in clinical trials and which has been posited as an important mechanism by which fluoride may increase bone fracture rates).
  36. People with impaired kidney function are particularly vulnerable to bone damage. Because of their inability to effectively excrete fluoride, people with kidney disease are prone to accumulating high levels of fluoride in their bone and blood. As a result of this high fluoride body burden, kidney patients have an elevated risk for developing skeletal fluorosis. In one of the few U.S. studies investigating the matter, crippling skeletal fluorosis was documented among patients with severe kidney disease drinking water with just 1.7 ppm fluoride (Johnson 1979). Since severe skeletal fluorosis in kidney patients has been detected in small case studies, it is likely that larger, systematic studies would detect skeletal fluorosis at even lower fluoride levels.
  37. Fluoride may cause bone cancer (osteosarcoma). A U.S. government-funded animal study found a dose-dependent increase in bone cancer (osteosarcoma) in fluoride-treated, male rats (NTP 1990). Following the results of this study, the National Cancer Institute (NCI) reviewed national cancer data in the U.S. and found a significantly higher rate of osteosarcoma (a bone cancer) in young men in fluoridated versus unfluoridated areas (Hoover et al 1991a). While the NCI concluded (based on an analysis lacking statistical power) that fluoridation was not the cause (Hoover et al 1991b), no explanation was provided to explain the higher rates in the fluoridated areas. A smaller study from New Jersey (Cohn 1992) found osteosarcoma rates to be up to 6 times higher in young men living in fluoridated versus unfluoridated areas. Other epidemiological studies of varying size and quality have failed to find this relationship (a summary of these can be found in Bassin, 2001 and Connett & Neurath, 2005). There are three reasons why a fluoride-osteosarcoma connection is plausible: First, fluoride accumulates to a high level in bone. Second, fluoride stimulates bone growth. And, third, fluoride can interfere with the genetic apparatus of bone cells in several ways; it has been shown to be mutagenic, cause chromosome damage, and interfere with the enzymes involved with DNA repair in both cell and tissue studies (Tsutsui 1984; Caspary 1987; Kishi 1993; Mihashi 1996; Zhang 2009). In addition to cell and tissue studies, a correlation between fluoride exposure and chromosome damage in humans has also been reported (Sheth 1994; Wu 1995; Meng 1997; Joseph 2000).
  38. Proponents have failed to refute the Bassin-Osteosarcoma study. In 2001, Elise Bassin, a dentist, successfully defended her doctoral thesis at Harvard in which she found that young boys had a five-to-seven fold increased risk of getting osteosarcoma by the age of 20 if they drank fluoridated water during their mid-childhood growth spurt (age 6 to 8). The study was published in 2006 (Bassin 2006) but has been largely discounted by fluoridating countries because her thesis adviser Professor Chester Douglass (a promoter of fluoridation and a consultant for Colgate) promised a larger study that he claimed would discount her thesis (Douglass and Joshipura, 2006). Now, after 5 years of waiting the Douglass study has finally been published (Kim 2011) but in no way does this study discount Bassin's findings. The study, which used far fewer controls than Bassin's analysis, did not even attempt to assess the age-specific window of risk that Bassin identified. Indeed, by the authors' own admission, the study had no capacity to assess the risk of osteosarcoma among children and adolescents (the precise population of concern). For a critique of the Douglass study, click here.
  39. Fluoride may cause reproductive problems. Fluoride administered to animals at high doses wreaks havoc on the male reproductive system - it damages sperm and increases the rate of infertility in a number of different species (Kour 1980; Chinoy 1989; Chinoy 1991; Susheela 1991; Chinoy 1994; Kumar 1994; Narayana 1994a,b; Zhao 1995; Elbetieha 2000; Ghosh 2002; Zakrzewska 2002). In addition, an epidemiological study from the US found increased rates of infertility among couples living in areas with 3 ppm or more fluoride in the water (Freni 1994), two studies have found reduced level of circulating testosterone in males living in high fluoride areas (Susheela 1996; Barot 1998), and a study of fluoride-exposed workers reported a "subclinical reproductive effect" (Ortiz-Perez 2003). While animal studies by FDA researchers have failed to find evidence of reproductive toxicity in fluoride-exposed rats (Sprando 1996, 1997, 1998), the National Research Council (2006) has recommended that, "the relationship between fluoride and fertility requires additional study."
  40. Some individuals are highly sensitive to low levels of fluoride as shown by case studies and double blind studies (Shea 1967; Waldbott 1978; Moolenburgh 1987). In one study, which lasted 13 years, Feltman and Kosel (1961) showed that about 1% of patients given 1 mg of fluoride each day developed negative reactions. Many individuals have reported suffering from symptoms such as fatigue, headaches, rashes and stomach and gastro intestinal tract problems, which disappear when they avoid fluoride in their water and diet. Frequently the symptoms reappear when they are unwittingly exposed to fluoride again (Spittle, 2008). No fluoridating government has conducted scientific studies to take this issue beyond these anecdotal reports. Without the willingness of governments to investigate these reports scientifically, should we as a society be forcing these people to ingest fluoride?
  41. Other subsets of population are more vulnerable to fluoride's toxicity. In addition to people suffering from impaired kidney function discussed in reason #30 other subsets of the population are more vulnerable.to fluoride's toxic effects. According to the Agency for Toxic Substances and Disease Registry (ATSDR 1993) these include: infants, the elderly and diabetics. Also vulnerable are those who suffer from malnutrition (e.g., calcium, magnesium, vitamin C, vitamin D and iodine deficiencies and protein-poor diets. See: Massler & Schour 1952; Marier & Rose 1977; Lin Fa-Fu 1991; Chen 1997; Teotia 1998).
  42. No Margin of Safety

  43. There is no margin of safety for several health effects. No one can deny that high natural levels of fluoride damage health. Millions of people in India and China have had their health compromised by fluoride. The real argument is about whether there is an adequate margin of safety between the doses that have been shown to cause harm in published studies and the total dose people receive consuming uncontrolled amounts of fluoridated water and non-water sources of fluoride. This margin of safety has to take into account the wide range of individual sensitivity expected in a large population (a safety factor of 10 is usually applied to the lowest level causing harm). Another safety factor is also needed to take into account the wide range of doses to which people are exposed. There is clearly no margin of safety for dental fluorosis (CDC, 2010) and based on the following studies nowhere near an adequate margin of safety for lowered IQ (Xiang 2003a,b; Ding 2011); lowered thyroid function (Galletti & Joyet 1958; Bachinskii 1985; Lin 1991); bone fractures in children (Alarcon-Herrera 2001) or hip fractures in the elderly (Kurttio 1999; Li 2001). All these harmful effects are discussed in the NRC (2006) review.
  44. Environmental Justice

  45. Low-income families penalized by fluoridation. Those most likely to suffer from poor nutrition, and thus more likely to be more vulnerable to fluoride's toxic effects, are the poor, who unfortunately, are the very people being targeted by new fluoridation programs. While at heightened risk, poor families are least able to afford avoiding fluoride once it is added to the water supply. No financial support is being offered to these families to help them get alternative water supplies or to help pay the costs of treating unsightly cases of dental fluorosis.
  46. Black and Hispanic children are more vulnerable to fluoride's toxicity. According to the CDC's national survey of dental fluorosis, black and Mexican-American children have significantly higher rates of dental fluorosis than white children (Beltran-Aguilar 2005, Table 23). The recognition that minority children appear to be more vulnerable to toxic effects of fluoride, combined with the fact that low-income families are less able to avoid drinking fluoridated water, has prompted prominent leaders in the environmental-justice movement to oppose mandatory fluoridation in Georgia. In a statement issued in May 2011, the Rev. Andrew Young, a colleague of Martin Luther King, Jr., and former Mayor of Atlanta and former US Ambassador to the United Nations, stated:
  47. "I am most deeply concerned for poor families who have babies: if they cannot afford unfluoridated water for their babies' milk formula, do their babies not count? Of course they do. This is an issue of fairness, civil rights, and compassion. We must find better ways to prevent cavities, such as helping those most at risk for cavities obtain access to the services of a dentist…My father was a dentist. I formerly was a strong believer in the benefits of water fluoridation for preventing cavities. But many things that we began to do 50 or more years ago we now no longer do, because we have learned further information that changes our practices and policies. So it is with fluoridation." (see:http://www2.fluoridealert.org/Alert/United-States/Georgia/Atlanta-Civil-Rights-Leaders-Callfor- Halt-to-Water-Fluoridation)
  48. Minorities are not being warned about their vulnerabilities to fluoride. The CDC is not warning black and Mexican-American children that they have higher rates of dental fluorosis than Caucasian children (see #38). This extra vulnerability may extend to other toxic effects of fluoride. Black Americans have higher rates of lactose intolerance, kidney problems and diabetes, all of which may exacerbate fluoride's toxicity.
  49. Tooth decay reflects low-income not low-fluoride intake. Since dental decay is most concentrated in poor communities, we should be spending our efforts trying to increase the access to dental care for low-income families. The highest rates of tooth decay today can be found in low-income areas that have been fluoridated for many years. The real "Oral Health Crisis" that exists today in the United States, is not a lack of fluoride but poverty and lack of dental insurance. The Surgeon General has estimated that 80% of dentists in the US do not treat children on Medicaid.
  50. The largely untested chemicals used in fluoridation programs

  51. The chemicals used to fluoridate water are not pharmaceutical grade. Instead, they largely come from the wet scrubbing systems of the phosphate fertilizer industry. These chemicals (90% of which are sodium fluorosilicate and fluorosilicic acid), are classified hazardous wastes contaminated with various impurities. Recent testing by the National Sanitation Foundation suggest that the levels of arsenic in these silicon fluorides are relatively high (up to 1.6 ppb after dilution into public water) and of potential concern (NSF 2000 and Wang 2000). Arsenic is a known human carcinogen for which there is no safe level. This one contaminant alone could be increasing cancer rates – and unnecessarily so.
  52. The silicon fluorides have not been tested comprehensively. The chemical usually tested in animal studies is pharmaceutical grade sodium fluoride, not industrial grade fluorosilicic acid. Proponents claim that once the silicon fluorides have been diluted at the public water works they are completely dissociated to free fluoride ions and hydrated silica and thus there is no need to examine the toxicology of these compounds. However, while a study from the University of Michigan (Finney et al., 2006) showed complete dissociation at neutral pH, in acidic conditions (pH 3) there was a stable complex containing five fluoride ions. Thus the possibility arises that such a complex may be regenerated in the stomach where the pH lies between 1 and 2.
  53. The silicon fluorides may increase lead uptake into children's blood. Studies by Masters and Coplan 1999, 2000, 2007 show an association between the use of fluorosilicic acid (and its sodium salt) to fluoridate water and an increased uptake of lead into children's blood. Because of lead's acknowledged ability to damage the developing brain, this is a very serious finding. Nevertheless, it is being largely ignored by fluoridating countries. This association received some strong biochemical support from an animal study by Sawan et al. (2010) who found that exposure of rats to a combination of fluorosilicic acid and lead in their drinking water increased the uptake of lead into blood some threefold over exposure to lead alone.
  54. Fluoride may leach lead from pipes, brass fittings and soldered joints. Maas et al (2007) have shown that fluoridating agents in combination with chlorinating agents such as chloroamine increase the leaching of lead from brass fittings used in plumbing. While proponents may argue about the neurotoxic effects of low levels of fluoride there is no argument that lead at very low levels lowers IQ in children.
  55. Continued promotion of fluoridation is unscientific

  56. Key health studies have not been done. In the January 2008 issue of Scientific American, Professor John Doull, the chairman of the important 2006 National Research Council review, Fluoride in Drinking Water: A Review of EPA's Standards, is quoted as saying:
  57. What the committee found is that we've gone with the status quo regarding fluoride for many years—for too long really—and now we need to take a fresh look . . . In the scientific community people tend to think this is settled. I mean, when the U.S. surgeon general comes out and says this is one of the top 10 greatest achievements of the 20th century, that's a hard hurdle to get over. But when we looked at the studies that have been done, we found that many of these questions are unsettled and we have much less information than we should, considering how long this [fluoridation] has been going on.

    The absence of studies is being used by promoters as meaning the absence of harm. This is an irresponsible position.

  58. Endorsements do not represent scientific evidence. Many of those promoting fluoridation rely heavily on a list of endorsements. However, the U.S. PHS first endorsed fluoridation in 1950, before one single trial had been completed and before any significant health studies had been published (see chapters 9 and 10 in The Case Against Fluoride for the significance of this PHS endorsement for the future promotion of fluoridation). Many other endorsements swiftly followed with little evidence of any scientific rational for doing so. The continued use of these endorsements has more to do with political science than medical science.
  59. Review panels hand-picked to deliver a pro-fluoridation result. Every so often, particularly when their fluoridation program is under threat, governments of fluoridating countries hand-pick panels to deliver reports that provide the necessary re-endorsement of the practice.
  60. In their recent book Fluoride Wars (2009), which is otherwise slanted toward fluoridation, Alan Freeze and Jay Lehr concede this point when they write:

    There is one anti-fluoridationist charge that does have some truth to it. Anti-fluoride forces have always claimed that the many government-sponsored review panels set up over the years to assess the costs and benefits of fluoridation were stacked in favor of fluoridation. A review of the membership of the various panels confirms this charge. The expert committees that put together reports by the American Association for the Advancement of Science in 1941, 1944 and 1954; the National Academy of Sciences in 1951, 1971, 1977 and 1993; the World Health Organization in 1958 and 1970; and the U.S. Public Health Service in 1991 are rife with the names of well-known medical and dental researchers who actively campaigned on behalf of fluoridation or whose research was held in high regard in the pro-fluoridation movement. Membership was interlocking and incestuous.

    The most recent examples of these self-fulfilling prophecies have come from the Irish Fluoridation Forum (2002); the National Health and Medical Research Council (NHMRC, 2007) and Health Canada (2008, 2010). The latter used a panel of six experts to review the health literature. Four of the six were pro-fluoridation dentists and the other two had no demonstrated expertise on fluoride. A notable exception to this trend was the appointment by the U.S. National Research Council of the first balanced panel of experts ever selected to look at fluoride's toxicity in the U.S. This panel of twelve reviewed the US EPA's safe drinking water standards for fluoride. After three and half years the panel concluded in a 507- page report that the safe drinking water standard was not protective of health and a new maximum contaminant level goal (MCLG) should be determined (NRC, 2006). If normal toxicological procedures and appropriate margins of safety were applied to their findings this report should spell an end to water fluoridation. Unfortunately in January of 2011 the US EPA Office of Water made it clear that they would not determine a value for the MCLG that would jeopardize the water fluoridation program (EPA press release, Jan 7, 2011. Once again politics was allowed to trump science.

    More and more independent scientists oppose fluoridation

  61. Many scientists oppose fluoridation. Proponents of fluoridation have maintained for many years— despite the fact that the earliest opponents of fluoridation were biochemists—that the only people opposed to fluoridation are not bona fide scientists. Today, as more and more scientists, doctors, dentists and other professionals, read the primary literature for themselves, rather than relying on self-serving statements from the ADA and the CDC, they are realizing that they and the general public have not been diligently informed by their professional bodies on this subject. As of July 2011, over 3700 professionals have signed a statement calling for an end to water fluoridation worldwide. This statement and a list of signatories can be found on the website of the Fluoride Action Network (see: www.FluorideAlert.org). A glimpse of the caliber of those opposing fluoridation can be gleaned by watching the 28-minute video "Professional Perspectives on Water fluoridation" which can be viewed online at the same FAN site.
  62. Proponents' dubious tactics

  63. Proponents usually refuse to defend fluoridation in open debate. While pro-fluoridation officials continue to promote fluoridation with undiminished fervor, they usually refuse to defend the practice in open public debate – even when challenged to do so by organizations such as the Association for Science in the Public Interest, the American College of Toxicology, or the U.S. EPA (Bryson 2004). According to Dr. Michael Easley, a prominent lobbyist for fluoridation in the US, "Debates give the illusion that a scientific controversy exists when no credible people support the fluorophobics' view" (Easley, 1999). In light of proponents' refusal to debate this issue, Dr. Edward Groth, a Senior Scientist at Consumers Union, observed that, "the political profluoridation stance has evolved into a dogmatic, authoritarian, essentially antiscientific posture, one that discourages open debate of scientific issues" (Martin 1991).
  64. Proponents use very dubious tactics to promote fluoridation. Many scientists, doctors and dentists who have spoken out publicly on this issue have been subjected to censorship and intimidation (Martin 1991). Dr. Phyllis Mullenix was fired from her position as Chair of Toxicology at Forsythe Dental Center for publishing her findings on fluoride and the brain (Mullenix 1995); and Dr. William Marcus was fired from the EPA for questioning the government's handling of the NTP's fluoride-cancer study (Bryson 2004). Many dentists and even doctors tell opponents in private that they are opposed to this practice but dare not speak out in public because of peer pressure and the fear of recriminations. Tactics like this would not be necessary if those promoting fluoridation were on secure scientific and ethical grounds.

Conclusion

When it comes to controversies surrounding toxic chemicals, vested interests traditionally do their very best to discount animal studies and quibble with epidemiological findings. In the past, political pressures have led government agencies to drag their feet on regulating asbestos, benzene, DDT, PCBs, tetraethyl lead, tobacco and dioxins. With fluoridation we have had a sixty-year delay. Unfortunately, because government officials and dental leaders have put so much of their credibility on the line defending fluoridation, and because of the huge liabilities waiting in the wings if they admit that fluoridation has caused an increase in hip fracture, arthritis, bone cancer, brain disorders or thyroid problems, it will be very difficult for them to speak honestly and openly about the issue. But they must, not only to protect millions of people from unnecessary harm, but to protect the notion that, at its core, public health policy must be based on sound science not political expediency. They have a tool with which to do this: it's called the Precautionary Principle. Simply put, this says: if in doubt leave it out. This is what most European countries have done and their children's teeth have not suffered, while their public's trust has been strengthened.

Just how much doubt is needed on just one of the health concerns identified above, to override a benefit, which when quantified in the largest survey ever conducted in the US, amounts to less than one tooth surface (out of 128) in a child's mouth?

While fluoridation may not be the greatest environmental health threat, it is one of the easiest to end. It is as easy as turning off a spigot in the public water works. But to turn off that spigot takes political will and to get that we need masses more people informed and organized. Please get these 50 reasons to all your friends and encourage them to get fluoride out of their community and to help ban this practice worldwide.

Postscript

Further arguments against fluoridation, can be viewed at http://www.fluoridealert.org and in the book The Case Against Fluoridation (Chelsea Green, 2010). Arguments for fluoridation can be found at http://www.ada.org

Publication history of the 50 Reasons

These 50 Reasons were first compiled by Paul Connett and presented in person to the Fluoridation Forum in Ireland in October 2000. The document was refined in 2004 and published in Medical Veritas. See: http://www.fluoridealert.org/50reasons.htm In the introduction to this 2004 version it was explained that after over four years the Irish authorities had not been able to muster a response to the 50 Reasons, despite agreeing to do so in 2000. Eventually, an anonymous, incomplete and superficial response was posted on the Irish Department of Health and Children's website (see this response and addendum at:http://www.dohc.ie/other_health_issues/dental_research/. Paul Connett's comprehensive response to this response can be accessed athttp://www.fluoridealert.org/50reasons.htm We learned on August 7, 2011 that this governmental response was prepared by an external contractor at a cost to the Irish taxpayers' of over 30,000 Euros. See: http://www.independent.ie/national-news/staggering-sums-spent-on-reportscommissioned- by-the-state-2841922.html Since 2004, there have been many major scientific developments including the publication of the U.S. National Research Council report (NRC, 2006); the publication of Bassin's study on Osteosarcoma (Bassin 2006), and many more studies of fluoride's interaction with the brain, that have necessitated a major update of the 50 Reasons. This was compiled in August 2011.

References

Agency for Toxic Substances and Disease Registry (ATSDR) (1993). Toxicological Profile for Fluorides, Hydrogen Fluoride, and Fluorine (F). U.S. Department of Health & Human Services, Public Health Service. ATSDR/TP-91/17.

Alarcon-Herrera MT, et al. (2001). Well Water Fluoride, Dental fluorosis, Bone Fractures in the Guadiana Valley of Mexico. Fluoride. 34(2): 139-149.

Allain P, et al. (1996). Enhancement of aluminum digestive absorption by fluoride in rats. Research Communications in Molecular Pathology and Pharmacology. 91: 225-31.

Armfield JM and Spencer AJ (2004). Consumption of Nonpublic Water: Implications for Children's Caries Experience," Community Dentistry and Oral Epidemiology. 32(4): 283–96

Arnold HA. (1980). Letter to Dr. Ernest Newbrun. May 28, 1980. http://www.fluoridealert.org/uc-davis.htm

Awadia AK, et al. (2002). Caries experience and caries predictors - a study of Tanzanian children consuming drinking water with different fluoride concentrations. Clinical Oral Investigations. (2002) 6:98-103.

Bachinskii PP, et al. (1985) Action of the body fluorine of healthy persons and thyroidopathy patients on the function of hypophyseal-thyroid the system. Probl Endokrinol (Mosk) 31: 25-9. http://www.fluoridealert.org/epa-sf/appendix-e.pdf

Barbier O. (2010) Molecular mechanisms of fluoride toxicity. Chemico-Biological Interactions. 188: 319–333.

Barnes GP, et al. (1992). Ethnicity, location, age, and fluoridation factors in baby bottle tooth decay and caries prevalence of Head Start children. Public Health Reports. 107: 167-73.

Barot VV. (1998). Occurrence of endemic fluorosis in human population of North Gujarat, India: human health risk. Bulletin of Environmental Contamination and Toxicology. 61: 303-10.

Bassin EB. (2001). "Association Between Fluoride in Drinking Water During Growth and Development and the Incidence of Osteosarcoma for Children and Adolescents," DMSc thesis, Harvard School of Dental Medicine, Boston, Massachusetts.

Bassin EB et al. (2006). Age-specific Fluoride Exposure in Drinking Water and Osteosarcoma (United States). Cancer Causes and Control. 17 (4): 421–28.

Bayley TA, et al. (1990). Fluoride-induced fractures: relation to osteogenic effect. Journal of Bone and Mineral Research.5(Suppl 1):S217-22.

Beltrán-Aguilar ED et al. (2010). Prevalence and severity of dental fluorosis in the United States, 1999-2004. NCHS DataBrief No. 53. U.S. DHHS, CDC, National Center for Health Statistics.

Beltrán-Aguilar ED et al. (2005). Surveillance for dental caries, dental sealants, tooth retention, endentulism, and enamel fluorosis—United States, 1988- 1994 and 1999-2002. CDC, MMWR, Surveillance Summaries, August 26, vol. 54, No SS-3, pp. 1-44. See Table 23.

Bentley EM, et al. (1999). Fluoride ingestion from toothpaste by young children. British Dental Journal. 186: 460-2.

Bhatnagar M, et al. (2002). Neurotoxicity of fluoride: neurodegeneration in hippocampus of female mice. Indian Journalof Experimental Biology. 40: 546-54.

Bigay J, et al. (1987). Fluoride complexes of aluminium or beryllium act on G-proteins as reversibly bound analogues of the gamma phosphate of GTP. EMBO Journal. 6:2907-2913.

Bigay J, et al. (1985). Fluoroaluminates activate transducin-GDP by mimicking the gamma-phosphate of GTP in its binding site. FEBS Letters. 191:181-185.

Brothwell D, Limeback H. (2003). Breastfeeding is protective against dental fluorosis in a nonfluoridated rural area of Ontario, Canada.Journal of Human Lactation 19: 386-90.

Brunelle JA, Carlos JP. (1990). Recent trends in dental caries in U.S. children and the effect of water fluoridation. Journalof Dental Research. 69(Special edition): 723-727.

Bryson C. (2004). The Fluoride Deception. Seven Stories Press, New York.

Burgstahler AW, et al. (1997). Fluoride in California wines and raisins. Fluoride. 30: 142-146.

Caffey J. On Fibrous Defects in Cortical Walls: Their Radiological Appearance, Structure, Prevalence, Natural Course, and Diagnostic Significance in Advances in Pediatrics, ed. S. Z. Levin, (New York: Interscience, 1955).

Calderon J et al. (2000). Influence of fluoride exposure on reaction time and visuospatial organization in children. Epidemiology11(4):S153.

Carlsson A. (1978). Current problems relating to the pharmacology and toxicology of fluorides. Journal of the Swedish Medical Association. 14: 1388-1392.

Carnow BW, Conibear SA. (1981). Industrial fluorosis. Fluoride. 14: 172-181.

Caspary WJ, et al (1987). Mutagenic activity of fluorides in mouse lymphoma cells. Mutation Research. 187:165-80.

Centers for Disease Control and Prevention (CDC). (2002). Prevalence of Self-Reported Arthritis or Chronic Joint Symptoms Among Adults --- United States, 2001. Mortality and Morbidity Weekly Report. 51: 948-950.

Centers for Disease Control and Prevention (CDC). (2001). Recommendations for Using Fluoride to Prevent and Control Dental Caries in the United States. Morbidity and Mortality Weekly Report. 50(RR14): 1-42.

Centers for Disease Control and Prevention (CDC). (1999). Achievements in Public Health, 1900-1999: Fluoridation of Drinking Water to Prevent Dental Caries. Mortality and Morbidity Weekly Report. 48: 933-940.

Chachra et al. (2010) The long-term effects of water fluoridation on the human skeleton. Journal of Dental Research. 89(11): 1219-1223.

Chen J, et al. (2003). Selective decreases of nicotinic acetylcholine receptors in PC12 cells exposed to fluoride. Toxicology. 183: 235-42.

Chen J, et al. (2003). Selective decreases of nicotinic acetylcholine receptors in PC12 cells exposed to fluoride. Toxicology. 183: 235-42.

Chen J, et al. (2002). [Studies on DNA damage and apoptosis in rat brain induced by fluoride] Zhonghua Yu Fang Yi Xue Za Zhi. 36 222-224.

Chen YC, et al. (1997). Nutrition survey in dental fluorosis-afflicted areas. Fluoride. 30(2):77-80.

Chinoy NJ, Narayana MV. (1994). In vitro fluoride toxicity in human spermatozoa. Reproductive Toxicology. 8:155-9.

Chinoy NJ, et al. (1991). Microdose vasal injection of sodium fluoride in the rat. Reproductive Toxicology. 5: 505-12.

Chinoy NJ, Sequeira E. (1989). Effects of fluoride on the histoarchitecture of reproductive organs of the male mouse.Reproductive Toxicology. 3: 261-7.

P. D. Cohn (1992). An Epidemiologic Report on Drinking Water and Fluoridation, New Jersey Department of Health, Environmental Health Service, November 8, 1992. Note: The original title of this report was A Brief Report on the Association of Drinking Water Fluoridation and the Incidence of Osteosarcoma Among Young Males. The word “osteosarcoma” was deleted from the title soon after the report was released; http://fluoridealert.org/cohn-1992.pdf.

Colquhoun J. (1997). Why I changed my mind about Fluoridation. Perspectives in Biology and Medicine 41: 29-44.http://www.fluoride-journal.com/98-31-2/312103.htm

Connett PH, Beck J and Micklem S. The Case Against Fluoride: How Hazardous Waste Ended Up in Our Drinking Water and the Powerful Politics and Bad Science That Keep it There. Chelsea Green, White River Junction, VT, 2010.

Connett,P (2004) 50 Reasons to Oppose Fluoridation (updated April 12, 2004). Reprinted in
Medical Veritas. 1:70–80, http://www.fluoridealert.org/50reasons.htm

Connett M. (2004). Fluoride & Bone Damage: Published Data. Submission to National Research Council (NRC).http://www.fluoridealert.org/bone-data.pdf

Connett, P. (2000). Fluoride: A Statement of Concern. Waste Not #459. January 2000. Waste Not, 82 Judson Street, Canton, NY 13617.http://www.fluoridealert.org/fluoride-statement.htm

Connett P, Neurath C and Connett M. (2005). Revisiting the Fluoride-Osteosarcoma Connection in the Context of Elise Bassin’s Findings: Part II.” Submission to the National Research Council of the National Academies review panel on the Toxicologic Risk of Fluoride in Drinking Water, March 21, 2005 (revised April 8, 2005), http://www.fluoridealert.org/health/cancer/fan-nrc.part2.pdf

Czerwinski E, et al. (1988). Bone and joint pathology in fluoride-exposed workers. Archives of Environmental Health. 43:340-343.

Dambacher MA, et al. (1986). Long-term fluoride therapy of postmenopausal osteoporosis. Bone 7: 199-205.

De Liefde B. (1998). The decline of caries in New Zealand over the past 40 Years. New Zealand Dental Journal. 94: 109-113.

Department of Health & Human Services. (U.S. DHHS) (1991). Review of Fluoride: Benefits and Risks. Report of the Ad Hoc Committee on Fluoride, Committee to Coordinate Environmental Health and Related Programs. Department of Health and Human Services, USA.

DenBesten, P (1999). Biological mechanism of dental fluorosis relevant to the use of fluoride supplements. Community Dentistry and Oral Epidemiology. 27: 41-7.

De Stefano TM. (1954). The fluoridation research studies and the general practitioner. Bulletin of Hudson County Dental Society.February.

Diesendorf M.(1986). The mystery of declining tooth decay. Nature. 322: 125-129.
http://www.fluoridealert.org/diesendorf.htm

Ding Y et al. (2010. The relationships between low levels of urine fluoride on children's intelligence, dental fluorosis in endemic fluorosis areas in Hulunbuir, Inner Mongolia, China. Journal of Hazardous Materials.
doi:10.1016/j.jhazmat.2010.12.097.

Ditkoff BA, Lo Gerfo P. (2000). The Thyroid Guide. Harper-Collins. New York.

Douglass CW and Joshipura K. (2006) “Caution Needed in Fluoride and Osteosarcoma Study” (letter), Cancer Causes & Control. 17 (4): 481–82.

Du L. 1992. The effect of fluorine on the developing human brain. Chinese Journal of Pathology 21(4):218-20 (republished in Fluoride41:327-30). Online at http://fluoridealert.org/scher/du-2008.pdf

Duan X. et al. (2011). Excess Fluoride Interferes with Chloride-channel-dependent Endocytosis in Ameloblasts. J Dent Res. 90(2):175-180.

Easley, M. (1999). Community fluoridation in America: the unprincipled opposition. Dental Watch,http://www.dentalwatch.org/fl/opposition.pdf (accessed March 21, 2010).

Ekambaram P, Paul V. (2001). Calcium preventing locomotor behavioral and dental toxicities of fluoride by decreasing serum fluoride level in rats. Environmental Toxicology and Pharmacology. 9: 141-146.

Ekstrand J, et al. (1981). No evidence of transfer of fluoride from plasma to breast milk. British Medical Journal (Clin Res Ed). 83: 761-2.

Ekstrand J, et al. (1994). Fluoride pharmacokinetics in infancy. Pediatric Research. 35:157–163.

Ekstrand J. (1996). Fluoride Intake. In: Fejerskov O, Ekstrand J, Burt B, Eds. Fluoride in Dentistry, 2nd Edition. Munksgaard, Denmark. Pages 40-52.

Elbetieha A, et al. (2000). Fertility effects of sodium fluoride in male mice. Fluoride. 33: 128-134.

Emsley J, et al (1981). An unexpectedly strong hydrogen bond: ab initio calculations and spectroscopic studies of amidefluoride systems.Journal of the American Chemical Society. 103: 24-28.

Fagin, D. (2008). Second Thoughts on Fluoride. Scientific American 298 (1)(January): 74–81; excerpts athttp://www.fluoridealert.org/sc.am.jan.2008.html

Fein NJ, Cerklewski FL. (2001). Fluoride content of foods made with mechanically separated chicken. Journal of Agricultural Food Chemistry. 49: 4284-6.

Feltman R, Kosel G. (1961). Prenatal and postnatal ingestion of fluorides - Fourteen years of investigation - Final report. Journal of Dental Medicine. 16: 190-99.

Finney WF et al. (2006) Reexamination of Hexafluorosilicate Hydrolysis by Fluoride NMR and pH Measurement. Environmental Science & Technology 40 (8): 2572–77.

Fluoridation Forum (2002). Forum on Fluoridation (Dublin, Ireland: Stationery Office, 2002),http://fluoridealert.org/re/fluoridation.forum.2002.pdf

Fomon SJ, et al. (2000). Fluoride intake and prevalence of dental fluorosis: trends in fluoride intake with special attention to infants.Journal of Public Health Dentistry. 60: 131-9.

Franke J, et al. (1975). Industrial fluorosis. Fluoride. 8: 61-83.

Freni SC. (1994). Exposure to high fluoride concentrations in drinking water is associated with decreased birth rates. Journal of Toxicology and Environmental Health. 42: 109-121.

Freeze RA and Lehr JA. The Fluoride Wars: How a Modest Public Health Measure Became America’s Longest-Running Political Melodrama. (Hoboken, NJ: John Wiley, 2009).

Freni SC, Gaylor DW. (1992). International trends in the incidence of bone cancer are not related to drinking water fluoridation. Cancer.70: 611-8.

Galletti P, Joyet G. (1958). Effect of fluorine on thyroidal iodine metabolism in hyperthyroidism. Journal of Clinical Endocrinology 18: 1102-1110. http://www.fluoridealert.org/galletti.htm

Gerster JC, et al. (1983). Bilateral fractures of femoral neck in patients with moderate renal failure receiving fluoride for spinal osteoporosis. British Medical Journal (Clin Res Ed). 287(6394):723-5.

Ghosh D, et al. (2002). Testicular toxicity in sodium fluoride treated rats: association with oxidative stress. Reproductive Toxicolology.16: 385.

Gray, AS. (1987). Fluoridation: time for a new base line? Journal of the Canadian Dental Association. 53: 763-5.

Grobleri SR, et al. (2001). Dental fluorosis and caries experience in relation to three different drinking water fluoride levels in South Africa.International Journal of Paediatric Dentistry. 11(5):372-9.

Guan ZZ, et al (1998). Influence of chronic fluorosis on membrane lipids in rat brain. Neurotoxicology and Teratology.20: 537-542.

Gutteridge DH, et al. (2002). A randomized trial of sodium fluoride (60 mg) +/- estrogen in postmenopausal osteoporotic vertebral fractures: increased vertebral fractures and peripheral bone loss with sodium fluoride; concurrent estrogen prevents peripheral loss, but not vertebral fractures. Osteoporosis International. 13(2):158-70.

Gutteridge DH, et al. (1990). Spontaneous hip fractures in fluoride-treated patients: potential causative factors. Journal of Bone and Mineral Research. 5 Suppl 1:S205-15.

Han H, Cheng Z, Liu W. 1989. Effects of fluorine on the human fetus. Chinese Journal of Control of Endemic Diseases 4:136-138 (republished in Fluoride 41:321-6). Online at
http://www.fluorideresearch.org/414/files/FJ2008_v41_n4_p321-326.pdf

Hanmer R. (1983). Letter from Rebecca Hanmer, deputy assistant administrator for water, U.S. Environmental Protection Agency, to Leslie A. Russell, D.M.D, March 30, 1983. http://fluoridealert.org/re/hanmer1983.pdf

Hazan S. (2004). Letter from Stan Hazan, General Manager, NSF Drinking Water Additives Certification Program, to Ken Calvert, Chairman, Subcommittee on Energy and the Environment, Committee on Science, US House of Representatives.July 7.http://www.keepersofthewell.org/product_pdfs/NSF_response.pdf

Health Canada (2008). Findings and Recommendations of the Fluoride Expert Panel (January 2007). April 2008,http://fluoridealert.org/re/canada.fluoride.expert.panel.2007.pdf

Health Canada (2010). Guidelines for Canadian Drinking Water Quality: Guideline Technical Document – Fluoride. Health Canada Dated Dec 2010, published June 21, 2011. http://www.hc-sc.gc.ca/ewh-semt/pubs/water-eau/2011-fluoride-fluorure/index-eng.php

Hedlund LR, Gallagher JC. (1989). Increased incidence of hip fracture in osteoporotic women treated with sodium fluoride. Journal of Bone and Mineral Research. 4: 223-5.

Heilman JR et al. (1999). Assessing Fluoride Levels of Carbonated Soft Drinks. Journal of the American Dental Association. 130 (11): 1593–99.

Heller KE, et al (1997). Dental caries and dental fluorosis at varying water fluoride concentrations. Journal of Public Health Dentistry. 57: 136-143.

Hileman B. (1989). New studies cast doubt on fluoridation benefits. Chemical and Engineering News. May 8.http://www.fluoridealert.org/NIDR.htm

Hileman B. (1988). Fluoridation of water: Questions about health risks and benefits remain after more than 40 years. Chemical and Engineering News. August 1: 26-42. http://www.fluoridealert.org/hileman.htm

Hirzy JW. (1999). Why the EPA's Headquarters Union of Scientists Opposes Fluoridation. Press release from National Treasury Employees Union. May 1. http://www.fluoridealert.org/hp-epa.htm

Hong L, et al. (2006). Timing of fluoride intake in relation to development of fluorosis on maxillary central
incisors. Community Dentistry and Oral Epidemiology 34:299-309.

Hoover RN, et al. (1991a). Time trends for bone and joint cancers and osteosarcomas in the Surveillance, Epidemiology and End Results (SEER) Program. National Cancer Institute In: Review of Fluoride: Benefits and Risks Report of the Ad Hoc Committee on Fluoride of the Committee to Coordinate Environmental Health and Related Programs US Public Health Service. Appendix E.

Hoover RN, et al. (1991b). Time trends for bone and joint cancers and osteosarcomas in the Surveillance, Epidemiology and End Results (SEER) Program. National Cancer Institute In: Review of Fluoride: Benefits and Risks Report of the Ad Hoc Committee on Fluoride of the Committee to Coordinate Environmental Health and Related Programs US Public Health Service. Appendix F.

Inkovaara J, et al. (1975). Prophylactic fluoride treatment and aged bones. British Medical Journal. 3: 73-4.

Institute of Medicine. (1997). Dietary Reference Intakes for Calcium, Phosphorus, Magnesium, Vitamin D, and Fluoride. Standing Committee on the Scientific Evaluation of Dietary Reference Intakes, Food and Nutrition Board. National Academy Press.

Johnson WJ, et al. (1979). Fluoridation and bone disease in renal patients. In: Johansen E, Taves DR, Olsen TO, Eds.Continuing Evaluation of the Use of Fluorides. AAAS Selected Symposium. Westview Press, Boulder, Colorado. pp. 275-293.

Joseph S, Gadhia PK. (2000). Sister chromatid exchange frequency and chromosome aberrations in residents of fluoride endemic regions of South Gujarat. Fluoride. 33: 154-158.

Juncos LI, Donadio JV. (1972). Renal failure and fluorosis. Journal of the American Medical Association 222: 783-5.

Kelly JV. (2000). Letter to Senator Robert Smith, Chairman of Environment and Public Works Committee, U.S. Senate, August 14, 2000.http://www.fluoridealert.org/fda.htm

Kilborn LG, et al. (1950). Fluorosis with report of an advanced case. Canadian Medical Association Journal. 62: 135-141.

Kim FM et al. (2011). An Assessment of Bone Fluoride and Osteosarcoma. J. Dent.Res. July 28, 2011 (published online).http://jdr.sagepub.com/content/early/2011/07/23/0022034511418828.full.pdf+html

Kiritsy MC, et al. (1996). Assessing fluoride concentrations of juices and juice-flavored drinks. Journal of the American Dental Association. 127: 895-902.

Kishi K, Ishida T. (1993). Clastogenic activity of sodium fluoride in great ape cells. Mutation Research. 301:183-8.

Komárek AE (2005). A Bayesian Analysis of Multivariate Doubly-Interval-Censored Dental Data,” Biostatistics. 6 (1):145–55.

Kour K, Singh J. (1980). Histological finding of mice testes following fluoride ingestion. Fluoride. 13: 160-162.

Kumar A, Susheela AK. (1994). Ultrastructural studies of spermiogenesis in rabbit exposed to chronic fluoride toxicity. International Journal of Fertility and Menopausal Studies. 39:164-71.

Kumar JV, Green EL. (1998). Recommendations for fluoride use in children. NY State Dental Journal. 64: 40-7.

Kunzel W, Fischer T. (2000). Caries prevalence after cessation of water fluoridation in La Salud, Cuba. Caries Research.34: 20- 5.

Kunzel W, et al. (2000). Decline in caries prevalence after the cessation of water fluoridation in former East Germany. Community Dentistry and Oral Epidemiology. 28: 382-389.

Kunzel W, Fischer T. (1997). Rise and fall of caries prevalence in German towns with different F concentrations in drinking water. Caries Research. 31: 166-73.

Kurttio PN, et al. (1999). Exposure to natural fluoride in well water and hip fracture: A cohort analysis in Finland. American Journal of Epidemiology. 150(8): 817-824.

Lalumandier JA, et al. (1995). The prevalence and risk factors of fluorosis among patients in a pediatric dental practice.Pediatric Dentistry. 17: 19-25.

Levy SM, Guha-Chowdhury N. (1999). Total fluoride intake and implications for dietary fluoride supplementation. Journal of Public Health Dentistry. 59: 211-23.

Levy SM et al. (2009). Associations of fluoride intake with children's bone measures at age 11. Community Dent OralEpidemiol.37(5):416-26.

Levy SM, et al. (2010). Associations Between Fluorosis of Permanent Incisors and Fluoride Intake From Infant Formula, Other Dietary Sources and Dentifrice During Early Childhood. JADA 141:1190-1201.

Li J, Yao L, Shao QL, Wu CY. 2004. Effects of high fluoride level on neonatal neurobehavioural development. Chinese Journal of Endemiology 23:464-465 (republished in Fluoride 41:165-70). Online at
http://fluoridealert.org/scher/li.2008.pdf

Li L. (2003). The biochemistry and physiology of metallic fluoride: action, mechanism, and implications. Critical Reviews of Oral Biology and Medicine. 14: 100-14.

Li XS. (1995). Effect of fluoride exposure on intelligence in children. Fluoride 28: 189-192.

Li Y, et al. (2001). Effect of long-term exposure to fluoride in drinking water on risks of bone fractures. Journal of Bone and Mineral Research 16: 932-9.

Lin FF, et al. (1991). The relationship of a low-iodine and high-fluoride environment to subclinical cretinism in Xinjiang. Iodine Deficiency Disorder Newsletter. Vol. 7. No. 3. http://www.fluoridealert.org/IDD.htm

Locker D. (1999). Benefits and Risks of Water Fluoridation. An Update of the 1996 Federal-Provincial Sub-committee Report. Prepared for Ontario Ministry of Health and Long Term Care.

Long YG, et al. (2002). Chronic fluoride toxicity decreases the number of nicotinic acetylcholine receptors in rat brain. Neurotoxicology and Teratology. 24: 751-7.

Lu XH, et al. (2000). Study of the mechanism of neurone apoptosis in rats from the chronic fluorosis. Chinese Journal of Epidemiology.19: 96-98.

Luke J. (2001). Fluoride deposition in the aged human pineal gland. Caries Research 35: 125-128.

Luke J. (1997). The Effect of Fluoride on the Physiology of the Pineal Gland. Ph.D. Thesis. University of Surrey, Guildord.

Maas RP et al. (2007). Effects of Fluoridation and Disinfection Agent Combinations on Lead Leaching from Leaded-Brass Parts.Neurotoxicology. 28 (5): 1023–31.

Mahaffey KR, Stone CL. (1976). Effect of High Fluorine (F) Intake on Tissue Lead (Pb) Concentrations. Federation Proceedings. 35: 256.

Mahoney MC, et al. (1991). Bone cancer incidence rates in New York State: time trends and fluoridated drinking water. American Journal of Public Health. 81: 475-9.

Mann J, et al. (1990). Fluorosis and dental caries in 6-8-year-old children in a 5 ppm fluoride area. Community Dentistry and Oral Epidemiology. 18: 77-9.

Mann J, et al. (1987). Fluorosis and caries prevalence in a community drinking above-optimal fluoridated water.Community Dentistry and Oral Epidemiology. 15: 293-5. Marcus W. (1990). Memorandum from Dr. William Marcus, to Alan B. Hais, Acting Director Criteria & Standards Division ODW, US EPA. May 1, 1990. http://www.fluoridealert.org/marcus.htm

Marcus W. (1990). Memorandum from Dr. William Marcus, to Alan B. Hais, Acting Director Criteria & Standards Division ODW, US EPA. May 1, 1990. http://www.fluoridealert.org/marcus.htm

Marier J and Rose D. (1977). Environmental Fluoride. National Research Council of Canada. Associate Committee on Scientific Criteria for Environmental Quality. NRCC No. 16081, Ottawa, Canada.

Marshall TA, et al. (2004). Associations between Intakes of Fluoride from Beverages during Infancy and Dental Fluorosis of Primary Teeth. Journal of the American College of Nutrition 23:108-16.Martin B. (1991). Scientific Knowledge in Controversy: The Social Dynamics of the Fluoridation Debate. SUNY Press,Albany NY.

Martin B. (1991). Scientific Knowledge in Controversy: The Social Dynamics of the Fluoridation Debate. SUNY Press, Albany NY.

Massler M, Schour I. (1952). Relation of endemic dental fluorosis to malnutrition. Journal of the American Dental Association. 44: 156-165.

Masters R, et al. (2000). Association of silicofluoride treated water with elevated blood lead. Neurotoxicology. 21: 1091-1099.

Masters RD, Coplan M. (1999). Water treatment with silicofluorides and lead toxicity. International Journal of Environmental Studies. 56: 435-449.

Matsuo S, et al. (1998). Mechanism of toxic action of fluoride in dental fluorosis: whether trimeric G proteins participate in the disturbance of intracellular transport of secretory ameloblast exposed to fluoride. Archives of Toxicology. 72: 798- 806.

Maupome G, et al. (2001). Patterns of dental caries following the cessation of water fluoridation. Community Dentistry and Oral Epidemiology. 29: 37-47.

McClure F. (1970). Water fluoridation, the search and the victory. US Department of Health, Education, and Welfare, Washington DC.

McDonagh M, et al. (2000). A Systematic Review of Public Water Fluoridation. NHS Center for Reviews and Dissemination, University of York, September 2000. http://www.fluoridealert.org/york.htm

Meng Z, Zhang B. (1997). Chromosomal aberrations and micronuclei in lymphocytes of workers at a phosphate fertilizer factory. Mutation Research. 393: 283-288.

Mihashi, M. and Tsutsui,T.(1996). Clastogenic activity of sodium fluoride to rat vertebral body-derived cells in culture.Mutation Research368: 7-13.

Moolenburgh H. (1987). Fluoride: The Freedom Fight. Mainstream Publishing, Edinburgh.

Morgan L, et al. (1998). Investigation of the possible associations between fluorosis, fluoride exposure, and childhood behavior problems.Pediatric Dentistry. 20: 244-252. Mullenix P, et al. (1995). Neurotoxicity of sodium fluoride in rats. Neurotoxicology and Teratology. 17: 169-177.

Mullenix P, et al. (1995). Neurotoxicity of sodium fluoride in rats. Neurotoxicology and Teratology. 17: 169-177.

Narayana MV, et al. (1994). Reversible effects of sodium fluoride ingestion on spermatozoa of the rat. International Journal of Fertility and Menopausal Studies. 39: 337-46.

Narayana MV, Chinoy NJ. (1994). Effect of fluoride on rat testicular steroidogenesis. Fluoride. 27: 7-12.

NHMRC (2007). National Health and Medical Research Council, A Systematic Review of the Efficacy and Safety of Fluoridation,reference no. EH41, Australian Government, December 27, 2007, http://www.nhmrc.gov.au/publications/synopses/eh41syn.htm

National Research Council (1977). Drinking Water and Health, National Academy of Sciences, Washington DC: National Academy Press, 1977, 388–89. National Research Council. (1993). Health Effects of Ingested Fluoride. National Academy Press, Washington DC. National Sanitation Foundation International (NSF). (2000)

National Research Council. (1993). Health Effects of Ingested Fluoride. National Academy Press, Washington DC. National Sanitation Foundation International (NSF). (2000)

National Toxicology Program [NTP] (1990). Toxicology and Carcinogenesis Studies of Sodium Fluoride in F344/N Rats and B6C3f1 Mice. Technical report Series No. 393. NIH Publ. No 91-2848. National Institute of Environmental Health Sciences, Research Triangle Park, N.C. The results of this study are summarized in the Department of Health and Human Services report (DHHS,1991).

NRC (2006). National Research Council of the National Academies, Fluoride in Drinking Water: A Scientific Review of EPA’s Standards. Washington, DC: National Academies Press, http://books.nap.edu/openbook.php?record_id=11571

O'Duffy JD, et al. (1986). Mechanism of acute lower extremity pain syndrome in fluoride-treated osteoporotic patients.American Journal of Medicine. 80: 561-6.

Olsson B. (1979). Dental findings in high-fluoride areas in Ethiopia. Community Dentistry and Oral Epidemiology. 7: 51-6.

Orcel P, et al. (1990). Stress fractures of the lower limbs in osteoporotic patients treated with fluoride. Journal of Bone and Mineral Research. 5(Suppl 1): S191-4.

Ortiz-Perez D, et al. (2003). Fluoride-induced disruption of reproductive hormones in men. Environmental Research 93:20-30.

Paul V, et al. (1998). Effects of sodium fluoride on locomotor behavior and a few biochemical parameters in rats. Environmental Toxicology and Pharmacology. 6: 187–191.

Pendrys DG, Katz RV. (1998). Risk factors for enamel fluorosis in optimally fluoridated children born after the US manufacturers' decision to reduce the fluoride concentration of infant formula. American Journal of Epidemiology 148:967-74.

Pinkham, JR, ed. (1999). Pediatric Dentistry Infancy Through Adolescence. 3rd Edition. WB Saunders Co, Philadelphia.

Public Health Service (PHS). (1993). Toward improving the oral health of Americans: an overview of oral health status, resources, and care delivery. Public Health Reports. 108: 657-72.

Retief DH, et al. (1979). Relationships among fluoride concentration in enamel, degree of fluorosis and caries incidence in a community residing in a high fluoride area. Journal of Oral Pathology. 8: 224-36.

Riggs BL, et al. (1990). Effect of Fluoride treatment on the Fracture Rates in Postmenopausal Women with Osteoporosis. New England Journal of Medicine 322: 802-809.

Rocha-Amador D et al. (2009). Use of the Rey-Osterrieth Complex Figure Test for neurotoxicity evaluation of mixtures in children.Neurotoxicology 30(6):1149-54.

Rozier RG. (1999). The prevalence and severity of enamel fluorosis in North American children. Journal of Public Health Dentistry. 59: 239-46.

Sawan RMM et al. (2010) Fluoride Increases Lead Concentrations in Whole Blood and in Calcified Tissues from Lead-Exposed Rats.Toxicology. 271 1–2: 21–26.

Schlesinger ER et al. (1956) Newburgh-Kingston Caries-Fluorine Study. XIII. Pediatric Findings After Ten Years,” Journal of the American Dental Association. 52 (3):296–306.

Schnitzler CM, et al. (1990). Bone fragility of the peripheral skeleton during fluoride therapy for osteoporosis. Clinical Orthopaedics.(261): 268-75.

Seholle RH. (1984). Preserving the perfect tooth (editorial). Journal of the American Dental Association. 108: 448.

Seppa L, et al. (2000). Caries trends 1992-98 in two low-fluoride Finnish towns formerly with and without fluoride. Caries Research. 34: 462-8.

Shannon, FT et al. (1986). Exposure to Fluoridated Water Supplies and Child Behaviour. New Zealand Medical Journal.99, (803): 416–18

Shao Q, et al. (2000). Influence of free radical inducer on the level of oxidative stress in brain of rats with fluorosis.Zhonghua Yu Fang Yi Xue Za Zhi. 34(6):330-2.

Sharma R et al. (2008). Fluoride Induces Endoplasmic Reticulum Stress and Inhibits Protein Synthesis and Secretion. Environ Health Perspect. 116:1142–1146.

Shashi A. (2003). Histopathological investigation of fluoride-induced neurotoxicity in rabbits. Fluoride. 36: 95-105.

Shea JJ, et al. (1967). Allergy to fluoride. Annals of Allergy. 25:388-91.

Sheth FJ, et al. (1994). Sister chromatid exchanges: A study in fluorotic individuals of North Gujurat. Fluoride. 27: 215-219.

Shiboski CH, et al. (2003). The association of early childhood caries and race/ethnicity among California preschool children. Journal of Public Health Dentistry. 63:38-46.

Shivarajashankara YM , et al. (2002). Brain lipid peroxidation and antioxidant systems of young rats in chronic fluoride intoxication.Fluoride. 35: 197-203.

Shivarajashankara YM , et al. (2002). Histological changes in the brain of young fluoride-intoxicated rats. Fluoride. 35:12-21.

Singh A, Jolly SS. (1970). Fluorides and Human Health. World Health Organization. pp 239-240.

Singh A, et al. (1963). Endemic fluorosis: epidemiological, clinical and biochemical study of chronic fluoride intoxication in Punjab.Medicine. 42: 229-246.

Spencer AJ et al. (1996).Water Fluoridation in Australia. Community Dental Health. 13 (suppl. 2):27–37.
Spittle B. Fluoride Fatigue: Is Fluoride in Your Drinking Water—and from Other Sources— Making You Sick? (Dunedin, New Zealand: Paua Press, 2008), http://www.pauapress.com/fluoride/files/1418.pdf

Sprando RL, et al. (1998). Testing the potential of sodium fluoride to affect spermatogenesis: a morphometric study. Food and Chemical Toxicology. 36: 1117-24.

Sprando RL, et al. (1997). Testing the potential of sodium fluoride to affect spermatogenesis in the rat. Food and Chemical Toxicology.35: 881-90.

Sprando RL, et al. (1996). Effect of intratesticular injection of sodium fluoride on spermatogenesis. Food and ChemicalToxicology. 34: 377-84.

Stannard JG, et al. (1991). Fluoride Levels and Fluoride Contamination of Fruit Juices. Journal of Clinical Pediatric Dentistry. 16: 38-40.

Stecher P, et al. (1960). The Merck Index of Chemicals and Drugs. Merck & Co., Inc, Rathway NJ. p. 952

Strunecka A, Patocka J. (1999). Pharmacological and toxicological effects of aluminofluoride complexes. Fluoride 32:230-242.

Sun ZR, et al. (2000). Effects of high fluoride drinking water on the cerebral functions of mice. Chinese Journal of Epidemiology. 19: 262-263.

Susheela AK. (1993). Prevalence of endemic fluorosis with gastrointestinal manifestations in people living in some North-Indian villages.Fluoride. 26: 97-104.

Susheela AK and Jethanandani P (1996). Circulating testosterone levels in Skeletal Fluorosis patients. Clinical Toxicology.34 (2): 1-7.

Susheela AK, Kumar A. (1991). A study of the effect of high concentrations of fluoride on the reproductive organs of malerabbits, using light and scanning electron microscopy. Journal of Reproductive Fertility. 92: 353-60.

Sutton P. (1996). The Greatest Fraud: Fluoridation. Lorne, Australia: Kurunda Pty, Ltd.

Sutton P. (1960). Fluoridation: Errors and Omissions in Experimental Trials. Melbourne University Press. Second Edition.

Sutton, P. (1959). Fluoridation: Errors and Omissions in Experimental Trials. Melbourne University Press. First Edition.

Teotia M, et al. (1998). Endemic chronic fluoride toxicity and dietary calcium deficiency interaction syndromes of metabolic bone disease and deformities in India: year 2000. Indian Journal of Pediatrics. 65: 371-81.

Teotia SPS, et al. (1976). Symposium on the non-skeletal phase of chronic fluorosis: The Joints. Fluoride. 9: 19-24.

Tsutsui T, Suzuki N, Ohmori M, Maizumi H. (1984). Cytotoxicity, chromosome aberrations and unscheduled DNA synthesis in cultured human diploid fibroblasts induced by sodium fluoride. Mutation Research. 139:193-8.

Tye CE et al. (2011). Fluoride Does not Inhibit Enamel Protease Activity. J Dent Res. 90(4): 489-494.

U.S. EPA (2011). EPA and HHS Announce New Scientific Assessments and Actions on Fluoride / Agencies working together to maintain benefits of preventing tooth decay while preventing excessive exposure. Joint press release with DHHS, Jan 7, 2011http://www2.fluoridealert.org/Alert/United-States/National/HHS-and-EPA-announce-new-scientificassessments- and-actions-on-fluoride

Varner JA et al. (1998). Chronic Administration of Aluminum-Fluoride or Sodium-Fluoride to Rats in Drinking Water:Alterations in Neuronal and Cerebrovascular Integrity. Brain Research. 78 (1–2): 284–98.

Waldbott GL, et al. (1978). Fluoridation: The Great Dilemma. Coronado Press, Inc., Lawrence, Kansas.

Waldbott GL. (1965). A Struggle with Titans. Carlton Press, NY.

Wang C, et al. (2000). Treatment Chemicals contribute to Arsenic Levels. Opflow. (Journal of the American Water Works Association. October 2000.

Wang Y, et al. (1997). Changes of coenzyme Q content in brain tissues of rats with fluorosis. Zhonghua Yu Fang Yi Xue Za Zhi. 31: 330-3.

Warren JJ et al. (2009). Considerations on Optimal Fluoride Intake Using Dental Fluorosis and Dental Caries Outcomes - A Longitudinal Study. Journal of Public Health Dentistry. 69 (2): 111–15.

WHO (Online). WHO Oral Health Country/Area Profile Programme. Department of Noncommunicable Diseases Surveillance/Oral Health. WHO Collaborating Centre, Malmö University, Sweden.

Williams JE, et al. (1990). Community water fluoride levels, preschool dietary patterns, and the occurrence of fluoride enamel opacities.Journal of Public Health Dentistry. 50: 276-81.

Wu DQ, Wu Y. (1995). Micronucleus and sister chromatid exchange frequency in endemic fluorosis. Fluoride. 28: 125-127.

Xiang Q, et al. (2003a). Effect of fluoride in drinking water on children's intelligence. Fluoride. 36: 84-94.

Xiang Q. (2003b). Blood lead of children in Wamiao-Xinhuai intelligence study. Fluoride. 36: 138.

Yu Y et al. (1996) Neurotransmitter and receptor changes in the brains of fetuses from areas of endemic fluorosis. ChineseJ Endemiology 15: 257-259 (republished in Fluoride 41(2):134-8).

Zakrzewska H, et al. (2002). In vitro influence of sodium fluoride on ram semen quality and enzyme activities. Fluoride.35: 153-160.

Zhang, R., et al. (2009). A stable and sensitive testing system for potential carcinogens based on DNA damage-induced gene expression in human HepG2 cell. Toxicology in Vitro. 23:158-165.

Zhang Z, et al. (2001). [Effects of selenium on the damage of learning-memory ability of mice induced by fluoride]. Wei Sheng Yan Jiu.30: 144-6.

Zhang Z, et al. (1999). [Effect of fluoride exposure on synaptic structure of brain areas related to learning-memory in mice] [Article in Chinese]. Wei Sheng Yan Jiu. 28:210-2.

Zhao ZL, et al. (1995). The influence of fluoride on the content of testosterone and cholesterol in rat. Fluoride. 28: 128-130.

Ziegelbecker R. (1970). A critical review on the fluorine caries problem. Fluoride. 3: 71-79.

Ziegelbecker R. (1981). Fluoridated Water and Teeth. Fluoride. 14 (3): 123–28,
http://fluoridealert.org/re/ziegelbecker-1981.pdf.

Zhai JX, et al. (2003). Studies on fluoride concentration and cholinesterase activity in rat hippocampus. Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 21: 102-4.

Zhao XL, Wu JH. (1998). Actions of sodium fluoride on acetylcholinesterase activities in rats. Biomedical and Environmental Sciences.11: 1-6

Zhao LB, et al (1996). Effect of high-fluoride water supply on children's intelligence. Fluoride. 29: 190-192.

Popular Posts

Total Pageviews

Men Who Wanted To Be Left Alone

The most terrifying force of death, comes from the hands of “Men who wanted to be left Alone”.

They try, so very hard, to mind their own business and provide for themselves and those they love.

They resist every impulse to fight back, knowing the forced and permanent change of life that will come from it.

They know, that the moment they fight back, their lives as they have lived them, are over.

The moment the “Men who wanted to be left Alone” are forced to fight back, it is a form of suicide.

They are literally killing off who they used to be.

Which is why, when forced to take up violence, these “Men who wanted to be left Alone”, fight with unholy vengeance against those who murdered their former lives.

They fight with raw hate, and a drive that cannot be fathomed by those who are merely play-acting at politics and terror.

TRUE TERROR will arrive at these people’s door, and they will cry, scream, and beg for mercy… but it will fall upon the deaf ears of the “Men who just wanted to be left alone.”

Author Unkown

Labels

ADE (1) Africa (1) Agent Orange (1) AIDS (4) Alzheimer’s Disease (4) amalgam fillings (1) Antibacterial Soap (1) Antibody Dependent Enhancement (2) Aspartame (1) Australia (1) autism (10) Baxter (2) Bayer (1) BCG (1) Big Pharma (1) Bill Gates (2) Biological Weapon (2) Bisphenol (1) BMJ (4) bowel disease (1) Bret Weinstein (1) Brianne Dressen (1) British Medical Journal (3) BVO (1) cancer (5) CDC (4) CDC Fudging numbers (1) Cell Phones (1) Children Mass Vaccination (1) China (1) Clade X (1) Clinical Trials (1) Corrupt Links (1) Court case (2) COVID (2) COVID Death (3) COVID Origins (1) COVID Vaccine (22) cure (1) Death to Vaccination (1) Definitions (1) diabetes (3) DNA (1) Dr Andrew Moulden (2) Dr Anne McCloskey (1) Dr Anthony Fauci (3) Dr Brian Tyson (1) Dr Bryan Bridle (3) Dr Charles Hoff (2) Dr Christian Perrone (2) Dr Dan Stack (2) Dr David Ayoub (1) Dr Geert Vanden Bossche (4) Dr Heather Gessling (1) Dr john Littell (1) Dr Joseph Ladapo (1) Dr Joseph Varon (1) Dr Karladine Graves (1) Dr Kazuhiro Nagao (1) Dr Larry Palevsky (1) Dr Lee Merritt (1) Dr Luc Montagnier (2) Dr Mark McDonald (1) Dr Michael Yeadon (1) Dr Peter Doshi (1) Dr Peter McCullough (7) Dr Pierre Kory (4) Dr Richard Amerling (1) Dr Richard Fleming (2) Dr Richard Urso (3) Dr Rick Kelly (1) Dr Robert E Willner (1) Dr Robert Malone (7) Dr Ryan Cole (6) Dr Sherri Tenpenny (1) Dr Sucharit Bhakdi (2) Dr Sucharit Bhakti (1) Dr Vladimir Zelenko (4) Dr. Carrie Madej (1) Dr. Maurice Hilleman (2) Dr.Rebecca Carley (1) Epilepsy (1) ER Swamped (1) European Parliament (1) FDA (6) FLCCC (1) flouride (11) flu vaccines (5) Food Colouring (1) Food poison (1) Fort Detrick (1) Gadrasil (2) GMO (4) GMO Mosquitoes (1) Graphene Oxide (2) Green Passport (1) H1N1 Vaccine (7) Heather Heying (1) Heavy Metals (2) Hepatitis B Vaccine (1) Hexavalent (1) hiding evidence (1) high fructose corn syrup (2) HIV (3) HIV Vaccine (1) Israel (1) Ivermectin (5) J&J (1) Japan (1) Joe Rogan (2) John O'Looney (1) Joseph Moshe (2) Lewisite (1) LSD (1) Lupus (1) Maddie De Garay (1) Makeup (1) Manufactured Flu Virus (1) Menactra (1) meningococcal vaccine (1) Merck (2) Mercury (6) mercury poisoning (2) metabolic syndrome (1) Mike Adams (1) Mirror Project (1) MKUltra (1) Moderna (2) MRNA Vaccine (2) MRR (1) Music (1) Mustard Gas (1) narcolepsy (1) Nurses (1) Off Label Use (1) Pandemrix (1) Pfizer (12) Plandemic (3) Plutonium (1) Polio Vaccine (4) Prescription Drugs (1) Professor William Campbell (1) Project veritas (2) Radiation (1) Remdesivir (1) Ritalin (1) Robert F Kennedy (1) Robert Wood Foundation (1) Roundup (2) Russell Blaylock (2) Sen Ron Johnson (2) STD (1) Steve Kirsch (1) sugar (1) Swine Flu Vaccine (13) Syngenta (1) Syphilis (1) Tamiflu (3) Tdap Vaccine (1) thimerosal (3) Transplanting Cancer (1) Trial Results (1) TSA Scans (1) Ukraine (2) Vaccinated Blood (1) vaccine adverse effect (1) vaccine deaths (3) vaccine indemnity (1) Vaccine Nanoparticles (1) Vaccine Superspread Hypothesis (1) Vaccines (23) Variants (2) Vivisection (1) Whooping Cough (1) Zika Virus (1)