Showing posts with label John D. Rockefeller. Show all posts
Showing posts with label John D. Rockefeller. Show all posts

Monday, December 31, 2012

Forced Sterilization in Mexico

By Ahni Jul 2, 2008

Authorities in Guerrero, Mexico "have agreed to pay 490,000 pesos (US$48,000) in compensation to 14 indigenous men coerced into having vasectomies," reports Bill Weinberg of the WW4Report.

The men will each be paid 35,000 pesos (US$3,400) and given water storage tanks and cement to build homes, said state health secretary Luis Barrera Rios. The men agreed to the deal, despite initial demands of 200,000 pesos (US$19,000) each.

The men, represented by the Tlachinollan Center for Human Rights, say that state health workers showed up in the village of El Camalote in 1998 and demanded that men with more than four children have vasectomies. The plaintiffs said they were promised a clinic, medicine, clothes, scholarships for their children and new homes for submitting to the procedure—while those who refused were threatened with removal from government aid programs. The claims were investigated by the National Human Rights Commission (CNDH).

The government earlier refused to pay compensation, saying the men signed consent forms and denying that they had been offered any benefits. After an investigation, the CNDH called on the Guerrero government to compensate the men, finding that health officials made no effort to counsel them on the implications of vasectomies or on alternative birth control methods. (AP, June 26)

Last October, a regional court in the Czech Republic made a similar ruling for a Romani woman. Bill Weinberg also reported on this story.

On Oct. 12, the Regional Court in Ostrava, Czech Republic, awarded compensation of CZK500,000 (US$260,000) to a Romani woman, Iveta Cervenakova, 30, for having been sterilized against her will. Ostrava City Hospital is to pay the damages. According to Kumar Vishwanathan of the Vzajemne Souziti (Life Together) civic association, this is the Czech Republic's first case of compensation for coerced sterilization. Holubová was sterilized 10 years ago. "She was not sufficiently informed and did not even learn she had had such surgery until seven years later," Vishwanathan said. The hospital claims it has Cervenakova's written consent on file and is considering appealing. (Romea.cz, Oct. 12)

Both Mexico and the Czech Republic are among a group of more than a dozen states that have actively sterilized men and women without their knowledge or consent. Other states include China, Canada, America, Peru, Australia, Colombia, Bolivia, Norway, India, Panama, Finland, Estonia, Slovakia, Switzerland, Iceland and Sweden. Few if any of these states have apologized or given reparations to the victims or their families.

John Ahniwanika Schertow is an indigenous rights activist of Mohawk (Kanienkehaka) and mixed-European descent. For the past 8 years, he has served as the editor and publisher of Intercontinental Cry. He is also a correspondent for the Public Good Project.



UNFPA Supports Forced Sterilization in Mexico

January 6, 2003
Volume 5/ Number 1


Dear Colleague:
A growing number of governments are questioning the wisdom of supporting the U.N. Population Fund (UNFPA). As the UNFPA continues to distort the U.S. State Department’s findings that it supports forced abortion in China, new evidence has surfaced showing that UNFPA supports involuntary sterilization in Mexico.
Steven W. Mosher
President

UNFPA Supports Forced Sterilization in Mexico

On the heels of reports of massive financial and programmatic mismanagement within the United Nations Population Fund (UNFPA),1 an independent investigation has found that UNFPA also supports involuntary sterilization and coercive family planning in Mexico.
An official body of the Mexican government, the National Human Rights Commission (NHRC), recently denounced coercion in family planning programs throughout Mexico.
According to the NHRC, “Public health servants have imposed methods of family planning on the native population without their consent and without informing them of the risks.”2 The NHRC has also found that family planning officials “threaten men and women who do not accept a method of family planning,” and that family planning officials deprive men and women of other “medical services” in order to force them to prevent births.3
The NHRC report follows an in-depth investigation of coercive population control programs in Mexico which reveals that UNFPA supports covert abortion, coercive family planning, and involuntary sterilization through the National Population Council of Mexico (CONAPO).
Under the guise of principles of voluntarism, articulated in the Program of Action of the International Conference on Population and Development (ICPD), UNFPA works in Mexico with CONAPO to achieve “population and development objectives”4 through programs that target the poor and victimize women.
UNFPA’s “population objectives” in Mexico include reducing births and lowering Mexico’s overall population by 2015. Through CONAPO, located in Mexico City, (which UNFPA supports with financial, strategic, technical and medical support), national quotas for family planning users are established then assigned to regional hospitals to be fulfilled by teams of local family planning workers.5 Should doctors or health workers fail to achieve assigned quotas, threats and punishments such as loss of pay or employment are imposed on them. Over 40 case studies of victims were obtained in Mexico this summer, including testimonies which note the following abuses:




  • Covert abortion, in the name of "normalization of menstruation," forced on women without informed consent; • Clandestine placement of IUDs; • Forced signing of "informed consent" documents in order to sterilize victim;

  • In one alarming case, a woman testified that, while undergoing a caesarian delivery, her fallopian tubes were ligated (tied) without her foreknowledge or consent.6
    UNFPA conceals its support of coercion behind a variety of masks, including ICPD "voluntarism." According to UNFPA, UNFPA and CONAPO provide "intervention models" aimed at "vulnerable groups" of Mexico's population. In practice, however, such "intervention" may include using the pangs of childbirth to extort signatures from "vulnerable" women on sterilization consent forms.7
    The UNFPA/CONAPO program is based on the wrongheaded notion that reducing the fertility of the poor will somehow jumpstart economic development, a theory with no empirical support.  But it is in pursuit of this chimera that the UNFPA/CONAPO program works vigorously to develop what it calls "innovative" models for expanding "reproductive health services to urban and rural populations living in poverty."8
    Consistent with these findings, the NHRC notes such innovative techniques of coercion as bribing poor men and women with "material goods" and "economic resources" to get them to use contraception.9 Such methods violate established norms of informed consent.
    In its recommendations to the Mexican Ministry of Health (MOH), the NHRC demands that human rights and freedoms be restored to the people of Mexico, and that coercive family planning be ended. To date, however, the MOH has not responded to this recommendation.
    UNFPA also refuses to denounce or even acknowledge the existence of coercive family planning in Mexico. Instead, UNFPA plans to continue funding coercive family planning. UNFPA has funded Mexico’s family planning program since 1972. In 1997, UNFPA provided $15.5 million to the Government of Mexico and CONAPO. Currently in its fourth cycle of assistance with CONAPO, UNFPA is scheduled to provide $12 million for population control over the next five years.10
    As for the U.S. contribution to coercive population control in Mexico, the U.S. Agency for International Development (USAID) has provided over $5 million dollars to “family planning” programs organized by Mexico’s Ministry of Health since 1997. Recently, however, USAID officials report that population funding for Mexico has ended. Instead, USAID is providing funds to the Mexican MOH for basic health and HIV/AIDS programs.
    PRI calls on the Fox administration to end coercive population control programs aimed at Mexico’s most vulnerable citizens.

    Endnotes
    1. Catholic Family and Human Rights Institute (C-FAM), Friday Fax, “Internal UN documents show financial mismanagement at UNFPA, January 3, 2002.
    2. ACI, “Birth Control Imposed on Native Mexicans,” 29 December, 2002.
    3. Ibid.
    4. UNFPA, “UNFPA Proposed Projects and Programs: Recommendation by the Executive Director; Assistance to the Government of Mexico,” 28 January-8 February, 2002, New York.
    5. PRI, “How Mexico Treats Its Poor Women,” PRI Review, September-October 2002, p. 3.
    6. Ibid.
    7. Ibid.
    8. UNFPA.
    9. ACI.
    10. UNFPA.



    Posted by Jim on Marzo 28, 2000
    This very interesting article appeared the other day in the Toronto Star
    Mexico's Indians target of sterilization `sweep'
    Villagers recall threats, gifts by No. 3 Brigade
    By Linda Diebel
    Toronto Star Latin America Bureau

    (Jump to Forum Comments)
    AYUTLA DE LOS LIBRES, Mexico - Jose Toribio, a Mixtec Indian from the Sierra Madre mountains, says he can't walk properly because of pain in his groin and left leg.
    He can't work to support his family.
    He attributes the pain to a vasectomy he had two years ago after visits to his remote village by No. 3 Brigade, a state medical team working in the western Mexican state of Guerrero in 1997 and 1998.
    Toribio now says he had the operation because of threats made to him by No. 3 Brigade.
    His claims are supported by the official Guerrero Human Rights Commission, which carried out a seven-month investigation into allegations of ``forced sterilization'' of 17 Mixtec men and concluded they were improperly sterilized.
    These cases from Guerrero come amid increasing allegations of a pattern of abuse across Mexico. Human rights groups cite evidence that unilingual Indians are being targeted by government sterilization brigades in several states.
    Recent reports include women given tubal ligations without their knowledge following Caesarean sections; women being paid with a kilo of beans or tomatoes for sterilization procedures they don't understand; and a woman who couldn't conceive because an IUD (intrauterine device) had been implanted in her womb without her knowledge and was embedded in her flesh.
    Certainly there is a push to sterilize people in Guerrero, where one-seventh of the state's 3,000,000 people is pure Indian.
    In the past five years, the state sterilized 35,079 people, 95.8 per cent by tubal ligation and 4.8 per cent by vasectomy, according to a government health report released in January.
    The state human rights commission believes the Mixtec men were tricked into the procedure, contravening the most basic principles of global human rights, as well as the laws of the republic of Mexico.
    In a tough report, its legal team describes ``artifice and deceitful measures'' taken by members of No. 3 Brigade to coerce the Indians. It accuses them of preying on people's ``precarious poverty'' by threatening to stop government food, health, and agricultural payments.
    ``Moral pressure was brought to bear, making them fear the loss of those economic means necessary for them to survive,'' it says.
    The report recommends, among other points, an immediate investigation into No. 3 Brigade, with a view to taking legal action ``in accordance with the gravity of the acts committed.''
    It was tabled with the state health ministry in December. Since then, a wall of denial has gone up from both state and federal officials.
    ``In the beginning, I did not want to accept the operation,'' Toribio tells The Star through an interpreter. ``But they told me I had to have it. They said if I didn't, my wife would die the next time she became pregnant.
    ``They warned me they would cut off (government) programs if I didn't agree. They said if I had the operation, they would pay me $1,500 pesos ($250) every two months and give us food, clothing and shoes.''
    `In the beginning, I did not want to accept the operation. But they told me I had to have it. They said if I didn't, my wife would die the next time she became pregnant.' - Jose Toribio
    And so, Toribio, 31, who lives in extreme poverty with his wife and six children, agreed to the procedure. He joined 16 men from three villages who were trucked by state health authorities to the regional hospital here in Ayutla de los Libres to undergo vasectomies.
    The issue is whether they were forced. The Indians believe they were and say the government ``wants to annihilate'' them.
    There has been no concerted federal investigation into these reports of abuse. And even though the state of Guerrero has not completed its investigation of the human rights report, its attitude is clear.
    ``There has been no violation of human rights,'' Daniel Pano Cruz, chief spokesman for Guerrero Governor Rene Juarez Cisneros, told The Star.
    ``There is no evidence the decision-making (abilities) of the sterilized people were in any way abused. These accusations have a political basis. . . . No one can prove this has happened here.''
    On a recent March morning, some 40 Mixtec Indians arrive at a small community centre in Ayutla de los Libres, a three-hour drive into the Sierra Madre mountains from Acapulco. They have come in flatbed trucks and rickety buses, leaving their villages at dawn.
    This meeting with The Star was arranged over two months, through indigenous leaders in Ayutla and surrounding villages who have only sporadic access to phones. One by one, they file in and pull up plastic chairs, waiting for interpreters to translate from Mixtec to Spanish.
    They don't speak Spanish. Most sign with a thumbprint.
    The men wear dusty work pants, open shirts - often with a crucifix around their necks - and shabby sandals. They carry intricately woven bags.
    The women, none over five feet tall, wear brightly coloured skirts and long braids. Their feet are bare. They sit quietly, eyes cast down, hands clasped, and speak only when spoken to.
    These people are from nearby La Fatima and Ocotlan, which were investigated by state human rights officials, along with Ojo de Agua.
    ``I was afraid I wouldn't be able to support my family if they cut off the programs,'' says Toribio, from La Fatima. ``I have never felt well since and I can't support my family.''
    He says No. 3 Brigade specifically threatened to cut off Progresa and Procampo federal aid programs administered by the state. Progresa covers health and family planning. The men say there was no follow-up treatment.
    Martin Garcia, 34, is also from La Fatima.
    ``They said it was an order of the government and that we would lose our programs,'' he says. ``I believed them. But now I think the government is doing this because it wants to annihilate Indians. They are tired of the problems of us poor people.''
    Juan Garcia, 40, was village health president when No. 3 Brigade came to La Fatima.
    ``When the nurses arrived, they already had the names of five people. We don't know how they got the names or why they wanted the information,'' he says. He adds the medical team told people ``they already had enough children.''
    The men talk about how they were told they had a ``sickness'' and how they would be ``cured'' by the procedure.
    The report says it has ``fully proven'' the complainants were not duly informed about sterilization because proper release forms would never use words such as ``sickness'' to refer to a vasectomy. It adds: ``We conclude their decision could not be responsible because it lacked free choice and truly adequate and effective information.''
    Some men say they received a kilo of beans and a kilo of cornmeal for their vasectomies.
    They say the government never kept any promises to pay them money.
    Agapito Cornelio, 57, is an elder from Ocotlan.
    ``This happened because of ignorance, because people can't read and they don't understand Spanish. So the villagers believe what the doctors say,'' he explains. ``It is very bad what has happened.''
    The Star couldn't locate No. 3 brigade members Dr. Ernesto Guzman, nurse Mayra Ramos and organizer, Rafael Almazon.
    State health officials refuse to say whether they are still working in Guerrero.
    However, the three denied in a joint interview with the human rights commission to having duped people. They said they relied on a translator and were ``unaware whether the translator . . . had offered them something in exchange for having the vasectomy.''
    The commission concludes that ``it is illogical that three translators, belonging to different communities . . . would have offered the same conditions for the operation in similar terms (including identical terms in the communities of Ojo de Agua and La Fatima).''
    ``What is most worrisome is that those who were sterilized are in bad health,'' says Filemon Santos, co-founder of the Independent Organization of Mixtec and Tlapaneca Peoples.
    ``The programs are meant to heal people, but on the contrary, they were destructive. It's the reverse of healing. They have changed people's lives for the worse - and the government has washed its hands of the problem.''
    Benito Morales, the indigenous group's other founder, says the villages took their allegations to the health ministry in 1998.
    ``They wouldn't accept the complaints,'' he says. ``They say they have nothing against indigenous peoples, but they haven't delivered on their promises. They think if the people are indigenous, they won't complain.''
    The Mexican constitution protects people's right to decide ``in a free, responsible and informed way'' about the number and spacing of children.
    That right is guaranteed in international conventions signed by Mexico, including accords on indigenous peoples.
    There are global sanctions for abuse. The most prominent is the U.N. Convention on the Prevention and Punishment of the Crime of Genocide, which cites ``imposing measures intended to prevent births within (a) group'' as a definition of genocide.
    In recent months, there has been widespread coverage in the Mexican media of allegations of forced sterilizations, including ground-breaking reports by Gloria Leticia Diaz in Proceso magazine.
    Officials from federal and state governments say claims are political, and that no such activity occurs in Mexico.
    ``We reiterate the policy of the Mexican government: full freedom for women, men and couples to be well-informed whether they . . . want contraceptive measures, but it should never be obligatory,'' federal health minister Jose Antonio Gonzalez told reporters last week.
    ``We have said in reaction to these allegations (in Guerrero) that there is no proof which shows it happened and, if there were, we would want to be the first to know if there had been any crime committed under the law.''
    He declined to be interviewed by The Star. So did Guerrero Gov. Juarez Cisneros and state health minister Carlos de la Pena.
    A spokesman from President Ernesto Zedillo's office failed to get back to The Star, as promised, about allegations of forced sterilizations across the country.
    The international community has a link to these cases.
    The Guerrero vasectomies (which nobody denies took place) were covered under a federal health program, funded by a $465 million loan from the World Bank (which is supported by member nations, including Canada). The loan is slated to improve conditions among 15 million impoverished people in nine states.
    ``It's absolutely false from our point of view,'' says World Bank spokesman Chris Neal from Washington, referring to allegations of ``forced sterilization'' in Guerrero. ``These are informed programs by which individuals or couples decide the method of family planning like everybody else in the free world.
    ``We don't support forced sterilizations. That's ridiculous.''
    Meanwhile, similar reports continue to surface across Mexico, particularly in states where the country's 12 million Indians are concentrated.
    For example:
    Elsewhere in the Guerrero mountains, health officials performed tubal ligations in 1998 on 11 Nahuatl women, without proper consent, according to the Human Rights Centre of Tlachinollan, a non-governmental group.
    Their report describes cases in which women were either told the operation was free and would prevent cervical cancer (and given a litre of oil and a kilo each of tomatoes and green chilies), or operated on without their knowledge after Caesareans and found out much later.
    In the eastern state of Veracruz, community groups have urged a federal investigation into what they say are ``forced sterilizations.''
    In the Sierra Norte mountains of Puebla state, east of Mexico City, there are reports some 200 women have been improperly sterilized since 1994. Some women say the state promised 30,000 pesos ($4,600).
    Dr. Rodolfo Cardenas, former director of four state hospitals, recently told reporters that squads went into isolated areas ``where they improvised places, without proper hygiene or lighting, in which to perform tubal ligations.''
    At the Ayutla meeting, Mixtec women say they, too, were pressured.
    They are not part of the state's human rights report and they don't want to speak. They do so only when this reporter keeps asking through the translators.
    They are so timid, it's easy to understand the clout medical authority figures, sweeping into villages in big trucks, would have had with them.
    Several women from La Fatima say No. 3 Brigade lined them up when the village elders were away and treated them at a clinic. They were not transported to hospital in Ayutla like the men.
    They describe a painful gynecological procedure - but they don't know what it was.
    ``I was very frightened,'' says Toribio's wife, Maria Feliciana Faustino, 31. ``They said I had no choice. They said I would die if I had another child.''
    As the meeting winds down, Vicente Lauro, 25, from Ocotlan, stands up in the back.
    He says he can't sow maize since his vasectomy.
    ``When the people of Canada find out what is happening to us,'' he asks, ``will they make the government keep its promises?''
    Posted by Richard Ferguson on Marzo 28, 2000
    Unfortunately, this report fits in with the general pattern of Indians in Mexico being discriminated against at almost any level that you care to view, whether income, education, etc. It is not a coincidence that the armed revolutionary groups in Mexico (EZLN, EPR, etc.) have a base of indigenous people. Occasionally Mexicans will claim that they do not have racial discrimination in Mexico. Anyone who doubts the race consciousness of Mexican society has only to watch any TV program with a studio audience. The people on stage will invariably be very white, (gueros), while the audience will be obviously mixed race (mestizo). There is no Indian counterpart of Oprah Winfrey in Mexico, unless you want to count a comedienne who plays a dumb Indian for cheap jokes.

    Richard Ferguson
    Posted by Bill on Marzo 29, 2000
    After spending more than 6 years living in Mexico I must admit that I don't feel qualified, or comfortable, taking a stand on something like this with any degree of certainty. There is a great deal of complexity involved, and I really don't know enough of the facts. There is probably nothing that upsets Mexicans more than foreigners commenting on internal matters when those same foreigners may have similar, or more serious, situations that exist, or that existed, in their home countries. That's not to say that those of us who are not Mexican comment. It's just that many of us do so with an attitude of superiority, as if the places we come from are free of such situations.
    The existence of forced sterilization, of men and women, in the United States, is widely known. Recently, I think it was the ABC 20/20 program that told the story of mental patients (who were really not mentally ill at all) that were forced to undergo sterilization against their will. We also know that many poor black women in the South were subject to forced sterilization, until recent times. The victims of these acts were all minorities, in one way or another, either by race or by assumed condition.
    Today, in the United States, we live in one of the most racially segregated countries, yet we are quick to point the finger at other countries without cleaning our own house first. The record of abuse against indigenous peoples by the majority in the United States is hardly in dispute. Our own record is shameful. Yet today, few people raise their voices in defense of the American Indian. My experience has been that discrimination based on race per se is not common in Mexico. Class distinction is present, and there may be discrimination based on economic level, but I don't often hear someone comment negatively about someone's color. The Costa Chica area of Guerrero, where some of these sterilization stories are coming from, is governed by Mexico's first Afro-Mestizo "Black" governor, Rene Cisneros. I have traveled to many places and I'm not certain I've come across a country where just about everyone is accepted for who they are.
    I see no grand plan by the Mexican Government to sterilize the indigenous. The average Mexican is appalled at these stories. And, our Mexican friends need to understand that we are not people living in glass houses who are throwing stones at them. The forced sterilization reports are indeed disturbing. Let's not judge Mexicans and the society in Mexico solely on these reports.





    Dateline Mexico 
    by CarlosMendez

    EIR Volume 17, Number 11, March 9, 1990

    On Feb. 4, President Carlos Salinas de Gortari signed a foreign debt renegotiation pact under the Brady Plan, an event attended by World Bank president Barber Conable, International Monetary Fund (IMF) managing director Michel Camdessus, and United States Treasury Secretary Nicholas Brady. Two days later, in presenting the National Population Program for 1989-94, President Salinas fulfilled an unwritten condition of the debt pact, in declaring that "the level of demographic growth continues very high" in Mexico, and that "therefore it is fundamental to achieve a population growth rate of only 1 % by the year 2000."

    To achieve such a barbaric result will require "a good dose of coercion, as has occurred in China," charged journalist Moises G. Barbosa in the daily Unomasuno Feb. 11.

    President Salinas' statements surprised many, above all in light of the upcoming May visit to Mexico of Pope John Paul II, and because the Catholic Church is a fierce opponent of sterilization and other artificial methods of birth control.

    But increasingly, commentators are suggesting that the emphasis on such a population goal is the result of pressures from the World Bank and IMF, backed by the U.S. government.

    On Feb. 9, columnist JoseE. Perez wrote in the daily Excelsior that "within days of having concluded the foreign debt renegotiation process, the meeting of the National Population Council awakened the idea among various circles that multinational credit
    agencies are pressuring for the imposition of population control policies here. In the circles where this rumor was spreading, the old strategy followed by the World Bank under [Robert Strange] McNamara, through which population control was imposed
    as a condition for economic aid to the developing nations, was cited."

    This World Bank strategy, of course, continues in force today. On Nov. 7, 1989, bank president Conable declared in Ottawa, Canada that the bank would nearly triple its expenses on population reduction activities.

    Conable, who spoke before the International Planned Parenthood Federation, added that the World Bank will be working with private groups to make "family planning" an accepted practice by "at least one-half of all Third World couples."

    According to the Washington, D.C. correspondent of the Mexican daily EI Financiero,
    "sources maintain that the 'happy conclusion' of the refinancing package between Mexico and the creditor banks is implicitly tied to a reduction of Mexico's population growth to 1 % by the year 2000. The conditions stipulated by the International Monetary Fund rarely contain explicit reference to demographic
    policy, but it appears 'between the lines' of the negotiation process, the
    sources noted."

    It is thus clear that one of the renegotiation conditions was the drastic reduction of population growth. But it is also clear that achieving this will require application of the methods of Communist China, a task which required the oversight of the Red Army in that unhappy country.

    In his Feb. 11 article in Unomasuno, Moises G. Barbosa wrote, ''To achieve a rate of 1 % by the year 2000, one need only avoid a little more than 5 million births by that year," meaning that of the nearly "2.5 million births that occurred in 1988, we must reach approximately 2 million births a year in 1994, avoiding thus the first
    2.5 million. From then on, the efforts will be 'redoubled' even more, so that the number of yearly births would continue to fall, reaching approximately 1.6 million in the year 2000, thereby achieving the proposed reduction.

    The problem emerges when one observes that the existing children and youth, proportionally higher than the adult population, will shortly be entering the group of fertile-age women, and from the 21.1 million that existed in 1988, that number will reach 25.6 million in 1994 and 29.5 million in 2000, independent of the hypothesis we are dealing with, since this corresponds to an already existing population which as can be seen . . . cannot easily be made to disappear."

    Barbosa concluded:
    "One can only hope that the proposed goal, which is only achievable with a good dose of coercion, as happened in China, is not translated into an abrupt rise in the number of sterilizations or in the proliferation of phrases such as those used by many doctors following administration of abortions: 'Little mother, we put in a little thing so you won't be having any more children. ' "

    The warning is not far-fetched.

    The clinics of the Mexican Institute of Social Security and the State Workers'
    Social Security Institute have been sterilizing mothers for years, without consulting them first-that is, following in the fascist footsteps of Communist China.

    Sunday, December 23, 2012

    health paranoia



    Paranoia [ˌpærəˈnɔɪ.ə] (adjective: paranoid [ˈpærə.nɔɪd]) is a thought process believed to be heavily influenced by anxiety or fear, often to the point of irrationality and delusion. Paranoid thinking typically includes persecutory beliefs, or beliefs of conspiracy concerning a perceived threat towards oneself. (e.g. "Everyone is out to get me.") Making false accusations and the general distrust of others also frequently accompany paranoia. For example, an incident most people would view as an accident or coincidence, a paranoid person might believe was intentional. However, just because an individual is paranoid does not necessarily mean his or her suspicions are false, as noted in Catch-22: "Just because you're paranoid doesn't mean they aren't after you."

    Historically, this characterization was used to describe any delusional state. In modern colloquial use, the term "paranoia" is sometimes misused to describe a phobia. The general lack of blame in phobia disorders sharply differentiates the two. In other words, fearing that something bad or harmful might happen does not in itself imply paranoia. Rather, with paranoia there is an irrational fear of malice by others (excepting rare cases of schizophrenia).

    The word paranoia comes from the Greek "παράνοια" (paranoia), "madness"[1] and that from "παρά" (para), "beside, by"[2] + "νόος" (noos), "mind".[3] The term was used to describe a mental illness in which a delusional belief is the sole or most prominent feature. In an original attempt at classifying different forms of mental illness, Kraepelin used the term pure paranoia to describe a condition where a delusion was present, but without any apparent deterioration in intellectual abilities and without any of the other features of dementia praecox, the condition later renamed "schizophrenia". Notably, in his definition, the belief does not have to be persecutory to be classified as paranoid, so any number of delusional beliefs can be classified as paranoia. For example, a person who has the sole delusional belief that he is an important religious figure would be classified by Kraepelin as having 'pure paranoia'. According to Phelan, M. Padraig, W. Stern, J (2000)[4] paranoia and paraphrenia are debated entities that were detached from dementia praecox by Kraepelin, who explained paranoia as a continuous systematized delusion arising much later in life with no presence of either hallucinations or a deteriorating course, paraphrenia as an identical syndrome to paranoia but with hallucinations. Even at the present time, a delusion need not be suspicious or fearful to be classified as paranoid. A person might be diagnosed as a paranoid schizophrenic without delusions of persecution, simply because their delusions refer mainly to themselves.



    Everything Dr. Russel Blaylock is 100% documented. The drinking water is poisoned/a mass medication, with sodium fluoride. Aspartame a neuro-toxin is added to various food products.



    The artificial sweetener aspartame has been the subject of several controversies since its initial approval by the U.S. Food and Drug Administration (FDA) in 1974. The FDA approval of aspartame was highly contested,[1] with critics alleging that the quality of the initial research supporting its safety was inadequate and flawed and that conflicts of interest marred the approval of aspartame.[2][3][4] In 1987, the U.S. Government Accountability Office concluded that the food additive approval process had been followed properly for aspartame.[2][5] In spite of this, critics such as activist Betty Martini[6] have promoted undocumented claims that numerous health risks (such as multiple sclerosis, systemic lupus, methanol toxicity, blindness, spasms, shooting pains, seizures, headaches, depression, anxiety, memory loss, birth defects and death[7]) are associated with the consumption of aspartame in normal doses. These health risk claims have been examined and debunked by numerous scientific research projects, and are also generally dismissed by governments and major health and food safety organizations.[2][8][9]

    Publicity of this controversy has been spread through an elaborate health scare[10] and "Internet smear campaign"[11] involving hoax[10][12][11] e-mails repeating Betty Martini's widely circulated conspiracy theory. Her undocumented claims are still repeated by thousands of self-published Web sites.

    Aspartame has been found to be safe for human consumption by more than ninety countries worldwide,[13][14] with FDA officials describing aspartame as "one of the most thoroughly tested and studied food additives the agency has ever approved" and its safety as "clear cut".[4] The weight of existing scientific evidence indicates that aspartame is safe as a non-nutritive sweetener.

    In 1997, due to public concerns the UK government introduced a new regulation obliging food makers who use sweeteners to state clearly next to the name of their product the phrase "with sweeteners".[33]
    In 2007, the Indonesian government considered banning aspartame.[34] In the Philippines, the small political party Alliance for Rural Concerns introduced House Bill 4747 in 2008 with the aim of having aspartame banned from the food supply.[35] The U.S. state of New Mexico introduced a bill to ban aspartame in 2007,[36][37][38] and Hawaiian legislators signed a 2009 resolution asking the FDA to rescind approval.[39] In March 2009, the California OEHHA identified aspartame as a chemical for consultation by its Carcinogen Identification Committee, in accordance with California state Proposition 65.[40]

    In 2007, the UK supermarket chains Sainsbury's,[41] M&S,[42] and Wal-Mart subsidiary Asda,[43] announced that they would no longer use aspartame in their own label products.[44] In April 2009, Ajinomoto Sweeteners Europe, the makers of Aspartame in Europe, responded to Asda's "no nasties" campaign by filing a complaint of malicious falsehood against Asda in the English courts.[45][46] In July 2009, Asda initially won the legal case after the trial judge construed the "no nasties" labelling to "not mean that aspartame was potentially harmful or unhealthy".[47][48] The decision was reversed in June 2010, upon appeal,[49] and was settled in 2011 with ASDA removing references to aspartame from its packaging.[50]
    In 2009, the South African retailer Woolworths announced it was removing aspartame from its own-brand foods.[51]

    In 2010, the British Food Standards Agency launched an investigation into aspartame amid claims that some people experience side-effects after consuming the substance. A significant proportion of volunteers participating in the study are those who have claimed to experience side-effects.[52]
    In September 2011, the European Food Safety Authority (EFSA), which is due to release the findings of its full re-evaluation of aspartame in September 2012, made all 600 datasets it is using in its full re-evaluation available publicly. This includes previously unpublished scientific data, "including the 112 original studies on aspartame which were submitted to support the request for authorisation of aspartame in Europe in the early 1980s.



    By 1984, three years after its initial approval for use in tabletop sweeteners and dry food, U.S. consumption of aspartame had already reached 6.9 million pounds per year. This number doubled the following year, and continued to climb well into the 90's.

    According to statistics published by Forbes Magazine [i] based on Tate & Lyle estimates, aspartame had conquered 55 percent of the artificial sweetener market in 2003. One of the driving factors behind aspartame's market success is the fact that since it is now off patent protection, it's far less expensive than other artificial sweeteners like sucralose (Splenda).
    2010-08-03-pie_chart_sweeteners_v2.jpg



    Today, the statistics on the aspartame market are being kept so close to the vest, it has proven to be virtually impossible to find current data on usage, unless you're willing to pay tens of thousands of dollars for a market analysis reports and I felt there were better uses for the money than to purchase the answer to that question.
    However, a 2009 FoodNavigator article[ii]cites the current global market for aspartame as being less than 37.5 million pounds and worth $637 million.

    According to aspartame.org [iii], diet soda accounts for 70 percent of the aspartame consumed. A 12 ounce can of diet soda contains 180 mg of aspartame, and aspartame users ingest an average of 200 mg per day.
    However, it can be quite difficult to calculate just how much you're really ingesting, especially if you consume several types of aspartame-containing foods and beverages. Dosing can vary wildly from product to product. For example, the amount of aspartame will vary from brand to brand, and from flavour to flavour. Some can contain close to twice the amount of aspartame as others, and some contain a combination of aspartame and other artificial sweeteners.

    Interestingly, aspartame consumption now seems to have stalled, and there is some indication it may even be on the decline. Perhaps sufficient numbers of people are finally waking up to the unsavory truth about this chemical sweetener. It is my intention to educate you about the truth of this harmful and toxic ingredient and drive sales down even further. I have no ulterior motives other than to warn you so that you can protect your and your family's health, and I sell no competing products.

    The only alternative sweetener I recommend is natural stevia, especially the flavoured ones which avoid many of the aftertaste objections some people have about using stevia. It is interesting to note that the powerful food industry has made it illegal to sell natural stevia as a sweetener. If I recommended to use stevia as a sweetener and sold it, the government would immediately file criminal charges and confiscate our product.
    On December 17, 2008, the FDA did grant GRAS (Generally Recognized as Safe) status to rebaudioside , which is one component of the whole stevia plant, and this specific purified component of stevia may be used as a food additive and sold as an alternative sweetener. Examples of include Truvia and Purevia. The jury is still out, however, on whether consuming this one component of stevia is as safe as consuming extract from the whole plant, as all the synergistic, protective factors have been removed in these refined products.
    Thankfully there is a loophole that allows vendors to sell extract of whole stevia as a dietary supplement. Since virtually everyone knows it is a sweetener it doesn't have to say it on the label, so you can still bypass this industry initiated censorship.

    Ajinomoto, one of the leading aspartame manufacturers in the world next to NutraSweet, actually rebranded aspartame to AminoSweet [iv] last year, in order to dissociate itself from the negative associations of aspartame.

    It also wanted to "remind the industry that aspartame tastes just like sugar, and that it's made from amino acids -- the building blocks of protein that are abundant in our diet," -- as opposed to a concoction of chemicals never before consumed by man, some ingredients of which are more toxic than others. They will probably deceive some consumers with this newer, more sweetly innocent name that does not bear the same controversial past as the word "aspartame." But I sincerely doubt they'll fool anyone even remotely aware of its dangers.

    Aspartame can already be found in some 6,000 food products and beverages, and the list is about to get even longer, I'm sure, as Ajinomoto announced a global R&D alliance agreement with Kellogg Company [v] earlier this month.

    Researchers Continue to Contest 'the Most Contested' FDA Approval in History

    Concerned scientists and researchers fought and were successful in keeping aspartame out of the food supply for over ten years, ever since it was first considered as a potential food additive, and many of those still alive continue to speak out against it today.

    If we fail to learn from history we are doomed to repeat the mistake we made. Many readers have long forgotten what the 60-Minutes' correspondent Mike Wallace stated in his 1996 report on aspartame - available to view in this 2009 article - that the approval of aspartame was "the most contested in FDA history." And for good reason.

    At the time, independent studies had found it caused brain cancer in lab animals, and the studies submitted by G.D. Searle to the FDA for the approval were quickly suspected of being sloppy at best...
    In that 60-Minutes video, former Senator Howard Metzenbaum states:
    "According to the FDA themselves, Searle, when making their presentation to the FDA, had willfully misrepresented the facts, and withheld some of the facts that they knew would possibly jeopardize the approval."
    Metzenbaum's staff investigated the aspartame approval process. He goes on to explain that:
    "FDA officials were so upset they sent the file to the U.S. Attorney's office in Chicago for the purposes of presenting it to the grand jury as to whether or not there should be indictments. But it wasn't presented. It was delayed."
    Samuel Skinner, the U.S. attorney who led the grand jury probe ended up withdrawing from the case when he entered into job discussions with Searle's Chicago law firm, Sidley & Austin - a job he later accepted. Subsequently, the investigation stalled until the statute of limitation ran out, at which point the investigation against Searle was dropped.

    For more details on the story of how aspartame made it through the FDA approval process despite warning signs of potential health hazards and alleged scientific fraud, please watch the 60-Minutes report, as Wallace does a nice job of summarizing an otherwise long story.
    There are a number of well-written books on the market that detail the twists and turns of this part of history. This Harvard law summary of the legal wrangling [vi] that took place is also a worthwhile read.
    Those who claim that aspartame watch-dogs are somehow engaged in conspiracy theories, perhaps do not understand the word "conspiracy," the simplest definition of which is: "a secret agreement between two or more people to perform an unlawful act." In the case of aspartame, it sure does look as though it was a conspiracy -- by G.D. Searle & Co., to get a tremendously profitable product to market, no matter what the potential cost in terms of human health.

    The FDA itself suspected Searle had unlawfully produced "evidence" to support its claims of safety, and FDA officials were sufficiently disturbed by what they received to launch its first-ever criminal investigation. A section in the Harvard Law School summary on the history of aspartame states:
    "Another study that engendered severe criticism from the Department of Health Education and Welfare was the 46- week toxicity study performed on the hamster.
    Although the data appears to be faulty and incomplete, Searle argues that any falsehood in the study is not material to the appraisal of the safety of aspartame."
    How's that for assurance?
    "...In addition to criticizing the study as a whole, the Department alleges that Searle violated Title 18, Section 1001 by falsifying data. The report alleges that the testing ran into problems and instead of correcting them, Searle covered the problem up."
    FDA toxicologist, M. Jacqueline Verrett, Ph.D., discussed what she knew about some of these concerns in her testimony before Congress on November 3, 1987 (S.hrg;100-567).
    Verrett's individual testimony is reprinted here, in which she states:
    "From 1957-1977 I was employed as a Biochemist/Toxicologist in what is now designated the Center for Food Safety and Applied Nutrition of the Food and Drug Administration. ... In the early l970's, I examined the animal studies submitted by G. D. Searle and Co. on aspartame prior to the initial approval by FDA in l974... these studies raised numerous questions in a number of areas that needed to be resolved before approval of aspartame for any food additive use.
    In 1977 I served as a member of an FDA team... charged with examining three studies... to determine if they were 'authentic'. I wish to emphasize at this point that we were specifically instructed not to be concerned with, or comment upon, the overall validity of the study, this was to be done in a subsequent review carried out at the Bureau level.
    It is apparent that that review, on a point by point basis, discarded or ignored the problems and deficiencies outlined in this Team report, and concluded that, even in toto, these problems were insufficient to render the study invalid. It also appears that the serious departures from acceptable toxicological protocols that were noted in the reevaluation of these studies were also discounted."
    Verrett goes on to point out a number of the "deficiencies and improper procedures encountered" by her investigative team, which included but were not limited to:
    *Animals were not permanently tagged to avoid mix-ups
    *Tumors were removed and the animals returned to the study
    *Animals were recorded as dead, but subsequent records, after varying periods of time, indicated the same animal was still alive (almost certain evidence of mix-ups)
    *Many animal tissues were decomposed before any postmortem examinations were performed

    "Almost any single one of these aberrations would suffice to negate a study designed to assess the safety of a food additive," Verrett said, "and most certainly a combination of many such improper practices would, since the results are bound to be compromised. It is unthinkable that any reputable toxicologist, giving a completely objective evaluation of data resulting from such a study, could conclude anything other than that the study was uninterpretable and worthless,and should be repeated.
    This is especially important for an additive such as aspartame, which is equally vital since DKP is a major breakdown product of aspartame in liquid media.
    Not only is aspartame being used in the absence of basic toxicity information, but there is also no data to assess the toxicity of the interactions of DKP with the excess phenylalanine generated, with any other metabolite of aspartame, and its interactions with other additives, drugs, or other chemicals which may be present simultaneously in persons exposed to high levels of DKP in presweetened liquids such as diet drinks."

    Many critics are using the lack of toxicity data as proof that aspartame is safe, when in fact aspartame appears to have been approved WITHOUT such data - which in my opinion is just another sign of aspartame's inherent LACK of empirical safety record...
    Which brings us to a crucial point.

    If you do not know this fact, you may never be able to extract the truth, because the 200+ studies that form the basis of aspartame's multiple FDA approvals DO exist. Those studies were published, and are quite easy to find as they're cited by every single conventional health agency and every single aspartame peddler across the world. No one is trying to refute the fact that they exist.

    However, they were ALL funded by the aspartame industry.

    And guess what happens when you remove corporate interest and influence from the equation...

    All Industry-Funded Studies Give Aspartame Clean Bill of Health, While Majority of Independent Research Find Indications of Hazards


    A 1996 review of 165 studies [vii] [viii] believed to be relevant to human safety, by Dr. Ralph G. Walton, a professor of Clinical Psychiatry, showed a remarkable discrepancy between study results and their source of funding.

    Of the 165 studies, 74 had industry related funding (such as Searle, Nutrasweet®, Ajinomoto, and the International Life Sciences Institute Nutrition Foundation), and 91 were independently funded.
    Of those:
    *100 percent of the industry funded studies supported aspartame's safety, while
    *92 percent of the independently funded studies identified at least one potential health concern

    However, Dr. Walton also pointed out that of the seven remaining non-industry funded studies, which supported aspartame's safety, six were done by the FDA, and the seventh was a literature review of mostly industry sponsored research.

    Considering the long-standing revolving door between various industries (especially Monsanto, which acquired G.D. Searle in 1985) and the FDA, it's questionable as to whether an FDA study can be considered truly "independent," even though they were counted as independent in Walton's review.

    If you give that concern any merit, you'd more or less be looking at 100% of industry related studies claiming aspartame to be safe, and 100% of independent studies flagging some sort of health concern.

    If this doesn't make you raise an eyebrow, then no need to read any further. You've slipped comfortably into the all-accepting fold of corporate self-interests, created by massively successful propaganda and public relations efforts, backed by powerful political lobbying.

    Only you can decide whether or not you find this discrepancy to be acceptable evidence of rigorous scientific inquiry.

    If it makes you question the validity of aspartame's "100% safe" designation, then read on...

    Your Brain on Aspartame

    In the Sweet Misery video above, Dr. Russell Blaylock, a recently retired board-certified neurosurgeon and author of the book Excitotoxins: The Taste That Kills, says that because aspartame is "a poison that affects protein synthesis; affects how the synapses operate in the brain, and affects DNA, it can affect numerous organs. So you can get many different symptoms that seem unconnected."

    However, "when looking at the list of symptoms submitted to the FDA, most of them are neurological," Dr. Blaylock says.

    He's referring to a Department of Health and Human Services report that categorizes 10,000 adverse reaction reports logged by the FDA (Department of Health and Human Services Quarterly Report on Adverse Reactions Associated with Aspartame Ingestion, DHHS, Washington, DC, October 1, 1986), published here in a 24-page primer on aspartame by Donald Harkins [ix], the former editor and publisher of the Idaho Observer.

    Two years prior to that, a CDC MMWR dated November 2, 1984 [x] , discusses several hundred adverse reaction reports received, and at that time, the majority -- 67 percent - of complainants also reported neurological/behavioral symptoms.

    Some of the most commonly reported neurological symptoms include:
    *Headaches
    *Changes in behavior or mood
    *"Fuzzy" thinking
    *Seizures
    *Depression[xi]

    A 1987 study published in the journal Environmental Health Perspectives [xii] states:
    "If only 1% of the 100,000,000 Americans thought to consume aspartame ever exceed the sweetener's ADI, and if only 1% of this group happen coincidentally to have an underlying disease that makes their brains vulnerable to the effects of an aspartame-induced rise in brain phenylalanine levels, then the number of people who might manifest adverse brain reactions attributable to aspartame would still be about 10,000, a number on the same order as the number of neutrally related consumer complaints already registered with the FDA and other federal agencies."
    [Note: the ADI for aspartame is 50 mg/kg of body weight in the US. ADI in Europe and Canada is 40 mg/kg of body weight. ]
    Published in the European Journal of Clinical Nutrition in 2008 [xiii], a South African study offers further information on the potential workings of aspartame on your brain:
    "Phenylalanine plays an important role in neurotransmitter regulation, whereas aspartic acid is also thought to play a role as an excitatory neurotransmitter in the central nervous system. Glutamate, asparagines and glutamine are formed from their precursor, aspartic acid.
    Methanol, which forms 10 % of the broken down product, is converted in your body to formate, which can either be excreted or can give rise to formaldehyde, diketopiperazine (a carcinogen) and a number of other highly toxic derivatives.
    Previously, it has been reported that consumption of aspartame could cause neurological and behavioral disturbances in sensitive individuals. Headaches, insomnia and seizures are also some of the neurological effects that have been encountered, and these may be accredited to changes in regional brain concentrations of catecholamines, which include norepinephrine, epinephrine and dopamine.
    The aim of this study was to discuss the direct and indirect cellular effects of aspartame on the brain, and we propose that excessive aspartame ingestion might be involved in the pathogenesis of certain mental disorders (DSM-IV-TR 2000) and also in compromised learning and emotional functioning."
    There has been loads of conflicting "science" regarding the metabolism of methanol. The emerging evidence suggests that it may be a toxic poison that is one of the leading contributing factors for MS, and that some of the research is subsidized by the producers of methanol to make it appear less harmful.

    I hope to an interview in the near future with an expert to review and clarify these details.


    Aspartame and Headaches

    The Sweet Misery documentary also includes Dr. H.J. Roberts M.D., a board-certified internist and author of Aspartame Disease: An Ignored Epidemic, who does a fine job of explaining, in layman's terms, what aspartame is made of, and how patients have, and can, test their vulnerability to this chemical using cessation and rechallenge. (I will also offer further suggestions on how to do this at the end of this article.)

    This type of anecdotal evidence, which critics love to dismiss as silly nonsense, can nonetheless be invaluable to the individual in question, as you can clearly discover whether there's a direct cause and effect on your body from consuming aspartame.

    Dr. H.J. Roberts is one of several expert investigators on aspartame and has testified before congress on the topic of aspartame safety.

    In a document titled, Professional Opinion of H.J. Roberts, M.D., F.A.C.P., F.C.C.P., Concerning Headaches Caused by the Use of Products Containing Aspartame, he states that:
    "People who suffer aspartame-induced headache are likely to encounter denial of this condition by physicians, the FDA and manufacturers. This situation is largely influenced by "negative scientific studies" sponsored by corporate interests.
    I have repeatedly challenged the nature of such studies, especially when the aspartame was administered as capsules or freshly-prepared cool solutions rather than "real world" products, namely soft drinks and other products sold in markets that undergo changes on exposure to high temperature or with storage of more than one or two months."
    One study commonly cited by industry to refute the claim that aspartame causes headaches is the 1987 NEJM study [xiv] which concluded that "aspartame is no more likely to produce headache than placebo."
    However, this study, again, has financial ties to Monsanto (owner of G.D. Searle), and the aspartame was given in capsule form, for one day...

    There are a number of studies that point to concerns related to aspartame's detrimental impact on neurological function.

    Under Sources above, you will find a link to a page on my site where I've created a list of studies, sorted by the health concern they pertain to, and headaches is just one of many potential concerns. That page is evolving, and I will continue to add to it as I find more relevant studies.

    In my follow-up article, I will foray into a couple of the other health problems associated with aspartame.

    Taking the Precautionary Principle into Account

    Any good scientist, and any skeptic worth their own weight, would follow the evidence to its logical conclusion, no matter where it leads. Unfortunately, we have overwhelming evidence showing that it's nearly impossible to be impartial when your paycheck is on the line. Any corporation that pays you to investigate their product wants you to produce favorable results, and we know that powerful corporations can make these desires well understood by those who work for them.

    Likewise, any good doctor or health professional would adhere to the Hippocratic Oath that says, "First, do no harm." Yet here we have a chemical sweetener being added to some 6,000 food products, which, due to its sheer prevalence and fervent backing by the conventional medical industry and health agencies, has the potential to harm a vulnerable section of the population.

    You're told it is perfectly safe. (Unless you have a genetic disease called phenylketonuria (PKU), which prevents you from digesting the amino acid phenylalanine. An estimated 1 out of every 15,000 people are born with PKU. This is why aspartame containing products bear a warning label stating the product contains phenylalanine.)

    But do you know whether or not you have phenylketonuria, or are part of any other "generally vulnerable" group of people?

    Wouldn't you want to know if you might be at risk?

    And if you knew you were vulnerable to its toxic effects, would you still consume high amounts of aspartame?

    If you were not, but you knew that a family member or friend was part of that vulnerable subgroup, would you warn them?

    These are simple questions that tend to get completely lost in the pro- versus anti-aspartame debate.
    Do you think it's acceptable to willfully sacrifice those who are more vulnerable by issuing no warnings whatsoever? And worse -- pulling the wool over their eyes and saying aspartame has no related health hazards whatsoever, even at very high amounts?

    I think not.

    Consider the 1986 review of 231 adverse reactions to aspartame [xv], which found "no clear symptom complex that suggests a widespread public health hazard associated with aspartame use." Yet in the following sentence, the researchers admit that:
    "...in some case reports... the symptoms may be attributable to aspartame in commonly-consumed amounts. The systematic application of pre-defined review criteria, such as those described here, to monitor consumer complaints related to food additives will help identify products that warrant more focused clinical studies."
    Staunch aspartame promoters pay no attention to that part - the part that states a certain number of individuals may indeed suffer health consequences, even from commonly-consumed amounts.
    They also pay no attention to the fact that this review occurred a mere three years after the US became saturated with aspartame-containing beverages. Today we have thousands upon thousands of adverse reaction reports, anecdotal reports, and physician's case histories...

    These people are indeed being sacrificed, without remorse whatsoever, by those hiding behind supremely biased, profit-driven, industry-funded research.

    The conventional medical establishment and our health agencies are frightfully resistant to the possibility that aspartame may have anything to do with health problems - after all, aspartame is FDA approved and has been "safely used" for years!

    I have one word for you - Vioxx.

    Just one of a multitude of FDA-approved products that -- lo and behold - killed tens of thousands of people while the establishment reiterated the industry-funded "scientific evidence" that was the basis for its widespread use.

    Are Your Health Problems Related to Aspartame Consumption?

    You might not realize you're having a reaction to aspartame. In fact, most people don't make the connection, and a tremendous amount of time and money is spent by aspartame "reactors" (people sensitive to the chemical), trying to find out why they are sick.

    To determine if you're a reactor, take the following steps:
    1. Eliminate all artificial sweeteners from your diet two weeks. (Note: If you typically consume aspartame in caffeinated drinks, you'll want to gradually reduce your intake in order to avoid caffeine withdrawal symptoms.)
    2. After two weeks of being artificial sweetener-free, reintroduce aspartame in a significant quantity (about three servings daily) and avoid other artificial sweeteners during this period.
    3. Do this for one to three days and notice how you feel, especially as compared to when you were consuming no artificial sweeteners.
    4. If you don't notice a difference in how you feel after re-introducing aspartame, it's a safe bet you're able to tolerate aspartame acutely, meaning your body doesn't have an immediate, adverse response. However, this doesn't mean your health won't be damaged in the long run by this chemical and its breakdown products.
    I'm not trying to deny anyone the pleasure of life that is generated from consuming sweets. However, to promote aspartame to the population at large, without warning that a certain percentage of people may suffer terribly from its consumption is a reckless, irresponsible ethical breech, and clearly contributes to much unnecessary suffering in exchange for hundreds of millions of dollars of profit..
    In the end it's up to you to decide what you want to put into your body. Just make it an educated decision.



    Rofecoxib (play /ˌrɒfɨˈkɒksɪb/) is a nonsteroidal anti-inflammatory drug (NSAID) that has now been withdrawn over safety concerns. It was marketed by Merck & Co. to treat osteoarthritis, acute pain conditions, and dysmenorrhoea. Rofecoxib was approved by the Food and Drug Administration (FDA) on May 20, 1999, and was marketed under the brand names Vioxx, Ceoxx, and Ceeoxx.

    Rofecoxib gained widespread acceptance among physicians treating patients with arthritis and other conditions causing chronic or acute pain. Worldwide, over 80 million people were prescribed rofecoxib at some time.[1]

    On September 30, 2004, Merck voluntarily withdrew rofecoxib from the market because of concerns about increased risk of heart attack and stroke associated with long-term, high-dosage use. Merck withdrew the drug after disclosures that it withheld information about rofecoxib's risks from doctors and patients for over five years, resulting in between 88,000 and 140,000 cases of serious heart disease.[2] Rofecoxib was one of the most widely used drugs ever to be withdrawn from the market. In the year before withdrawal, Merck had sales revenue of US$2.5 billion from Vioxx.[3]

    Rofecoxib was available on prescription as tablets and as an oral suspension. It was available by injection for hospital use.




    Is it safe to mix fluoridated tap water with infant formula? 

    I've heard that too much fluoride can harm a baby's teeth.

    Answer

    from Jay L. Hoecker, M.D.
    It's considered safe to use fluoridated tap water to prepare infant formula.

    Exposure to fluoride during infancy helps prevent tooth decay. However, regularly mixing powdered or liquid infant formula concentrate with fluoridated water may increase your child's risk of developing faint white markings or streaks on the teeth — a sign of mild enamel fluorosis. Fluorosis is a cosmetic issue that affects both baby teeth and permanent teeth while they're forming under the gums. In children younger than age 8, combined fluoride exposure from all sources — water, food, toothpaste and other products — contributes to fluorosis.

    If you're concerned about fluorosis, you can minimize your baby's exposure to fluoride by using ready-to-feed formula. You can also alternate using tap water and nonfluoridated water for formula preparation, or mix powdered or liquid infant formula concentrate with low-fluoride water most or all of the time. However, if you use only nonfluoridated water — such as purified, demineralized, deionized or distilled bottled water — to prepare your baby's formula, your baby's doctor may recommend fluoride supplements beginning at age 6 months.



    Q. Can I use warm or hot water from the tap to make my baby's formula? Cassie, Dallas, Texas
    A. Since few babies like cold baby formula and you do usually have that extra step of warming the formula after you make it, using warm or hot water to start with from the tap does seem like it could save an extra step. You shouldn't do it though.

    Instead, follow the directions on your baby's formula package and if using tap water, start with cold tap water. According to the U.S. Environmental Protection Agency, you should "never cook or mix infant formula using hot water from the tap."

    What's wrong with hot tap water? Many homes have plumbing with lead or lead solder and hot water can concentrate the lead. Running the water for 15 to 30 seconds and only using cold water can help reduce your baby's exposure to lead from tap water.

    Boiling the water doesn't get rid of the lead either. Many home water filters, including pitcher and faucet filters, do remove lead from drinking water though.

    Boiling Water???

    Another common question about preparing baby formula is whether or not you have to boil the water first. While most brands of baby formula once recommended boiling as a part of their instructions, they now often recommend "asking your baby's doctor or "local health department" instead.
    The American Academy of Pediatrics doesn't offer any formal advice on the subject either. The latest book on newborns that they published, Heading Home with Your Newborn: From Birth to Reality, does say that "you may want to use boiled or purified (bottled or filtered) water, at least in the first month or two."
    The main problem with that statement is that purified, bottled, or filtered water, even the brand Nursery Purified Water, isn't sterile, so isn't necessarily any safer than tap water that hasn't been boiled first. Bottled and filtered water should have fewer impurities and contaminants, including lead, but could still have harmful bacteria, which was the whole reason you were supposed to boil tap water when making baby formula in the first place.

    And there is no research which states that doing anything special to the water that you use for your baby's formula "in the first month or two" is helpful or does anything at all. That advice is likely based on the fact that younger babies are simply supposed to have weaker immune systems.
    If you do decide to boil the water when preparing your baby's formula, the FDA recommends that you "bring it to a very bubbly boil. Keep boiling it for a minute or two, then let it cool." Once it has cooled, you will be ready to add it to your baby's formula.

    WHO Guidelines for Preparing Formula

    The World Health Organization issued guidelines on the safe preparation, storage and handling of powdered infant formula after experts recognized that powdered formula was not sterile and was sometimes putting babies at risk for serious bacterial infections.
    To reduce this risk, the WHO recommends cleaning and sterilizing feeding and preparation equipment and then making a fresh bottle of powdered infant formula for each feed by:
    • cleaning and disinfecting all surfaces you will be using and washing your hands properly
    • boiling water, even if it is bottled water
    • let the water cool (not more than 30 minutes though, so it doesn't get below 70 degrees) and pour it into a cleaned and sterilized bottle
    • add the exact amount of powdered formula to the water
    • assemble the bottle and mix the powdered formula thoroughly
    • quickly cool the bottle by holding it under running tap water or by placing it in a container of cold water or iced water
    • dry the bottle with a clean cloth
    • check the temperature of the formula so that it doesn't burn your baby's mouth
    • feed your baby if the formula is at an appropriate temperature
    The WHO also offers detailed advice on storing extra formula and traveling with prepared formula.

    Baby Formula Safety

    After you prepare your baby's formula, you should follow some simple rules to keep your baby safe.
    • Unless you refrigerated the prepared formula, feed it to your baby within two hours (hold time).
    • If you do put the prepared formula in the refrigerator, be sure to use it within 24 hours.
    • Once your baby starts feeding from a bottle, be sure he finishes the formula within one to two hours (hang time) and don't put the bottle back in the refrigerator. Unused formula should not be saved for later. Instead, simply prepare less formula next time so that you don't have so much lefted over.
    • Don't warm baby formula bottles in the microwave. Instead, use a baby bottle warmer or place the bottles in a container of warm water.
    • Follow the baby formula mixing instructions carefully and don't dilute or concentrate the baby formula unless your pediatrician tells you to.

    Fluoride and Preparing Baby Formula

    Experts often recommend that children should get fluoridated water to help prevent cavities. Surprisingly, infants who are fed powdered or concentrated liquid formula which is mixed with fluoridated water can get too much fluoride.
    Getting too much fluoride when your child's teeth are still forming can lead to enamel fluorosis, which can cause tooth staining. This staining can appear as faint while markings on a child's baby teeth, and even more importantly, their permanent teeth.

    Fortunately, fluorosis is usually very mild when it is caused by fluoridated water and baby formula and the staining is barely noticeable. To reduce your baby's chance of developing even mild fluorosis, it can help to use low-fluoride water (less than 0.7 mg/L) when you prepare your baby's formula, including some types of tap water, and water that has been purified, deionized, demineralized, distilled, or filtered by reverse osmosis.

    You don't have to be concerned about fluorosis if you are exclusively or mostly breastfeeding your baby or using a ready-to-feed baby formula.

    What You Need To Know

    • Talk to your pediatrician to see if you need to boil your water, especially if you are using well water that hasn't been recently tested, or if you aren't convinced that the tap water where you live is safe and healthy for a baby. Your pediatrician can also recommend water -- tap, filtered tap, or bottled water -- that is best for mixing your baby's formula.

    • Powdered baby formula is not sterile and there have been cases of Salmonella and Cronobacter sakazakii infections linked to powdered infant formula.

    • Boiling water when preparing baby formula is very important in many parts of the world, especially developing countries that do not have safe water supplies.

    • Sterile liquid baby formula is recommended for infants in high risk situations, if the babies aren't breastfeeding, especially for premature babies in the NICU.



    Sources:
    U.S. EPA. Is There Lead in my Drinking Water?
    American Academy Of Pediatrics. Heading Home with Your Newborn: From Birth to Reality (Paperback). by Laura A. Jana, Jennifer Shu
    Brouard C. Two consecutive large outbreaks of Salmonella enterica serotype Agona infections in infants linked to the consumption of powdered infant formula. Pediatr Infect Dis J - 01-FEB-2007; 26(2): 148-52
    Mimouni FB. Bacterial contamination during routine formula preparation. - Am J Infect Control - 01-FEB-2002; 30(1): 44-5
    U.S. Food and Drug Administration. Feeding Your Baby with Breast Milk or Formula
    CDC. Community Water Fluoridation. Background: Infant Formula and the Risk for Enamel Fluorosis
    WHO. Guidelines for the safe preparation, storage and handling of powdered infant formula. http://www.who.int/foodsafety/publications/micro/pif2007/en/ Accessed Dec. 2011.