.

Interview with Peter Breggin, MD,
a psychiatrist denouncing the psychiatric profession and
psychotropics, articulating the futility of DNA and
amino tests etc. Dr Breggin is one of many neuropharmacologists,
psychologists, psychiatrists exposing this fraud.







Part I




Part II




Part III




Health Last Updated: Aug 26th, 2010 - 00:35:19

America’s mental illness epidemic: It turns out that the drugs are the problem
By Gary G. Kohls, MD
Online Journal Contributing Writer

http://www.blogger.com/post-edit.g?blogID=4946057639976740841&postID=868173407396183409







Aug 26, 2010, 00:19

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Tens of millions of innocent, unsuspecting Americans, who are mired deeply in the mental “health” system, have actually been made crazy by the use of or the withdrawal from commonly-prescribed, brain-altering, brain-disabling, indeed brain-damaging psychiatric drugs that have been, for many decades, cavalierly handed out like candy -- often in untested and therefore unapproved combinations of drugs -- to trusting and unaware patients by equally unaware but well-intentioned physicians who have been under the mesmerizing influence of slick and obscenely profitable psychopharmaceutical drug companies, a.k.a. BigPharma.

That is the conclusion of two books by investigative journalist and health science writer Robert Whitaker. His first book, entitled Mad in America: Bad Science, Bad Medicine and the Enduring Mistreatment of the Mentally Ill noted that there has been a 600 percent increase (since Thorazine was introduced in the US in the mid-1950s) in the total and permanent disabilities of millions of psychiatric drug-takers. This uniquely First World mental ill health epidemic has resulted in the life-long taxpayer-supported disabilities of rapidly increasing numbers of psychiatric patients who are now unable to be happy, productive, taxpaying members of society. Whitaker has done a powerful, albeit unwelcome job of presenting previously hidden, but very convincing evidence to support his thesis, that it is the drugs and not the diagnosis that is causing the epidemic of mental illness disability. Many open-minded physicians and many aware psychiatric patients are now motivated to be wary of any and all synthetic chemicals that can cross the blood/brain barrier because all of them are capable of altering the brain in ways totally unknown to medical science, especially when the patients are taking the drugs long-term. .

In Whitaker’s second book Anatomy of an Epidemic: Magic Bullets, Psychiatric Drugs, and the Astonishing Rise of Mental Illness in America, he goes much further in advancing this sobering reality. He documents the history of the powerful forces behind the relatively new field of psychopharmacology and its major shaper and beneficiary, BigPharma. Psychiatric drugs, whose developers, marketers and salespersons are all in the employ of the giant drug companies, are far more dangerous than the drug and psychiatric industries are willing to admit: These drugs, it turns our, are fully capable of disabling -- often permanently -- body, brain and spirit.

More evidence to support Whitaker’s well-documented claims are laid out in two important new books written by psychiatrist and scholar Grace Jackson. Jackson did a beautiful job of researching and documenting, from the voluminous basic neuroscience research (which is uniformly ignored by the clinical sciences) the unintended and often disastrous consequences of the chronic ingestion of any of the five major classes of psychiatric drugs. Her second and most powerful book: Drug-Induced Dementia: A Perfect Crime, proves beyond a shadow of a doubt, that any of the five classes of drugs that are commonly used in psychiatric patients (antidepressants, antipsychotics, psychostimulants, tranquilizers and anti-seizure/”mood-stabilizer” drugs) have shown microscopic, macroscopic, biochemical, clinical and/or radiological evidence of brain shrinkage and other signs of brain damage, which can result in clinically-diagnosable, permanent dementia, premature death and a variety of other related brain disorders that can mimic mental illnesses. Jackson’s first book, Rethinking Psychiatric Drugs: A Guide for Informed Consent was an equally sobering book warning about the many hidden dangers of psychiatric drugs.

This sad truth is that the seemingly knee-jerk prescribing (without very much information being given to patients about the long list of serious long-term adverse effects) of potent and often addicting/dependency-inducing psychiatric drugs has become the standard of care in American psychiatry since the introduction of the so-called anti-schizophrenic “miracle” drug Thorazine in the mid-1950s. (Thorazine was the offending drug that all of Jack Nicholson’s fellow patients were coerced into taking at “medication time” in the Academy Award-winning movie “One Flew Over the Cuckoo’s Nest.”) Thorazine and all the other “me-too” early antipsychotic drugs are now universally known to have been an iatrogenic (= doctor or other treatment-caused) disaster because of their serious long-term, initially unsuspected, brain-damaging effects that resulted in a number of incurable neurological disorders such as tardive dyskinesia and Parkinson’s disease.

Thorazine and all the other knock-off drugs like Prolixin, Mellaril, Navane, etc., are synthetic “tricyclic” chemical compounds similar in molecular structure to the tricyclic “antidepressants” like imipramine and the similarly toxic, obesity-inducing, diabetogenic, “atypical” anti-schizophrenic drugs like Clozaril, Zyprexa and Seroquel.

Thorazine, incidentally, was originally developed in Europe as an industrial dye. That doesn’t sound so good although it may not be so unusual in the closely related fields of psychopharmcology and the chemical industry, especially when one considers that Depakote, a popular drug marketed initially as an anti-epilepsy drug but now is being heavily used as a so-called “mood stabilizer.” Depakote, known to be a hepatotoxin and renal toxin, was originally developed as an industrial solvent capable of dissolving fat -- including, presumably, the fatty tissue in human livers and brains.

Some sympathy and understanding needs to be generated for the various victims of BigPharma’s compulsive drive to expand market share and ”shareholder value” (share price, dividends and the next quarter’s financial report) by whatever means necessary. Both the prescribers and the swallowers of BigPharma’s drugs have succumbed to BigPharma’s cunning marketing campaigns, the prescribers having been seduced by attractive drug company representatives and their “pens, pizzas and post-it note” freebies in the office, and the patients being brain-washed by the inane and unbelievable (if one has intact critical thinking skills) commercials on TV that quickly gloss over the lethal adverse effects in the fine print while urging the watcher to “ask your doctor” about the latest unaffordable wannabe blockbuster drug. .

For a quick overview of these issues, I recommend that everybody with an open mind read a long essay written by Whitaker that persuasively identifies the source of America’s epidemic of mental illness disability (a phenomenon that doesn’t exist in Third World nations because costly psych drugs are not prescribed so cavalierly as in the US).

Whitaker and Jackson (among a number of other ground-breaking and whistle-blowing authors who have been essentially black-listed by the mainstream media and mainstream medical journals) have proven to most critically-thinking scientists, alternative practitioners and assorted “psychiatric survivors” that it is the drugs -- and not the so-called “disorders” -- that are causing our nation’s epidemic of mental illness disability. The Whitaker essay, plus other pertinent information about his books can be accessed at Mad In America. A recent interview on Wisconsin Public Radio can be accessed at www.wpr.org (at their radio archives link) and a long interview with Dr.Joseph Mercola can be heard here.

After reading and studying all these inconvenient truths, mental health practitioners must consider the medicolegal implications for them, especially if the information is ignored or if the information is dismissed out of hand by practitioners who might be tempted to not take the time to study this new information. Those people who are hearing about this for the first time need to pass the word on to others, especially their prescribing healthcare practitioners who should be equally concerned. This is important because the opinion leaders in the highly influential (for good or ill) psychiatric and medical industries have been marketed into submission without hearing the all the facts (which may have been intentionally hidden from them. If that is the case, they cannot be automatically blamed for. proceeding in a practice that some day might represent malpractice. It shouldn’t have to be pointed out that is the solemn duty of ethical practitioners who are in positions of authority to fully examine potential malpractice issues and then warn others, especially their patients, of the dangers.

Sadly, it must be admitted that most of the over-worked, double-booked care-givers in medical clinics have not yet heard the news that most if not all of the brain-altering synthetic chemicals known as psychotropic drugs (which are treated as hazardous waste unless they are packaged in a swallowable capsule!) have been marketed as safe and effective -- but only for short-term use. The captains of the drug industry know that the psychotropic drugs that they present for the FDA-approval have only been tested in animal trials for days and in clinical trials for 6 weeks. They also know -- indeed they hope -- that patients will be taking their drugs for years (despite no long-term trials proving safety and efficacy) as the only “treatment” for mental ill health. They know that their brain-altering drugs are also dependency-inducing (aka addicting, causing withdrawal symptoms when stopped), neurotoxic and increasingly ineffective (a la “Prozac Poop-out”) as time goes by.

The truth is that the people diagnosed as “mentally ill” for life are often simply those unfortunates who find themselves in acute or chronic states of crisis or “overwhelm” due to any number of preventable, curable and treatable (without the use of drugs) bad luck accidents such as poverty, abuse, violence, torture, homelessness, discrimination, underemployment, brain malnutrition, addictions/withdrawal, brain damage from electroshock “therapy” and/or exposure to neurotoxic chemicals in their food, air, water or prescription bottles.

Those labeled as the “mentally ill” are just like us “normals” who have not yet decompensated because of some yet-to-happen, crisis-inducing, overwhelming (however temporary) life situation. And thus we have not yet been given a billable code number (accompanied by the seemingly obligatory -- and unaffordable -- drug prescription or two signifying we are now chronically mentally ill. Unlabeled, we are likely to remain off prescription drugs but with a label and in “the system,” it is hard to “just say no to drugs.”

The victims of hopelessness-generating situations like simple bad luck, bad circumstances, bad company, bad choices, bad government, big business, and a competitive society that generates a few winners but mostly losers. America tolerates, indeed celebrates, punitive and thus fear-inducing social systems resembling in many ways the infamous police state realities of 20th century European totalitarianism, where people who were different or just dissidents were thought to be abnormal and therefore “disappeared” into insane asylums, jails or concentration camps without just cause or competent legal defense. And many of them were and are drugged with disabling psychoactive chemicals against their will.

The truth is that most, if not all, of BigPharma’s psychotropic drugs are lethal at some dosage level (the LD50, the lethal dose that kills 50 percent of lab animals, is calculated before efficacy testing is done), and therefore the drugs must be regarded as dangerous. The chronic use of these drugs is a major cause of cognitive disorders, brain damage, loss of creativity, loss of spirituality, loss of empathy, loss of energy, loss of strength, fatigue and tiredness, permanent disability and a multitude of metabolic adverse effects that can readily sicken the body, brain and soul by causing insomnia or somnolence, increased depression or anxiety, delusions, psychoses, paranoia, mania, etc. So before filling the prescription, it is advisable to read the product insert labeling under WARNINGS, PRECAUTIONS, ADVERSE EFFECTS, CONTRAINDICATIONS, TOXICOLOGY, OVERDOSAGE and the ever-present BLACK BOX WARNINGS ABOUT SUICIDALITY.

Long-term, high dosage or combination psychotropic drug usage could be regarded as a chemically traumatic brain injury (TBI) or, as drugs like Thorazine were known in the 1950s and 60s, a “chemical lobotomy.” That is a useful way to conceptualize this serious issue, because such chemically brain-altered patients are often indistinguishable from those who have suffered a physically traumatic brain injuries or been subjected to ice-pick lobotomies which were popular in the 1940s and 50s -- before the drugs came on the market.

America has a mental ill health epidemic on its hands that is grossly misunderstood because it is worsening, not by the supposed disease progression, but because of the neurotoxic, non-curative drugs that are somehow regarded as first-line “treatment.”

For more information of these extremely serious topics check out these websites: www.mindfreedom.org, www.breggin.com, www.icspp.org, www.cchr.org, www.drugawareness.org, www.psychrights.org, www.benzo.org.uk, www.quitpaxil, org, www.wildscolts.com, www.endofshock.com, www.mercola.com and www.madinamerica.com and follow the links.

Dr. Kohls is a family physician who, until his retirement in 2008, practiced holistic mental health care. His patients came to see him asking for help in getting off the psychotropic drugs that they knew were sickening and disabling them. He was successful in helping significant majorities of his patients get off their drugs using a thorough and therefore time-consuming program that was based on psychoeducational psychotherapy, brain nutrient therapy, a drastic change away from the malnourishing and often toxic Standard American Diet (SAD) plus a program of gradual, closely monitored drug withdrawal. Dr. Kohls warns against the abrupt discontinuation of any psychiatric drug because of the common, often serious withdrawal symptoms that can occur with the chronic use of any dependency-inducing psychoactive drug, whether illicit or legal. Close consultation with an aware, informed physician who is hopefully familiar with dealing with drug withdrawal syndromes (starting with the original prescribing physician), who will read and study the above books and become aware of the previously unknown dangers of these drugs and the nutritional needs of the drug-toxified and nutritionally-depleted brain.
Dr. Kohls is a member of MindFreedom International and the International Center for the Study of Psychiatry and Psychology. He is the editor of the occasional Preventive Psychiatry E-Newsletter.


Vids on Fox News and ABC News about the futility and addiction of so called anti-depressants and pain killers.

http://wn.com/Dangers_Of_Antidepressants_Suppressed_Fox_News

More info about the ESEA prod

It is interesting, but it also tells that these scientists
were able to use water and salt and stabilitze some molecules
which have never been achieved before.

I read some of Emoto's theory about altering
the molecules of water, by using a vortex device.
Some have reported various sensations when trying doing
this clockwise, anti clockwise, and repeating the process altering
the direction.

The shady part here for me is the corporate style of marketing
this prod. Would it not be an irony if some of these men are fat
cats from Big Pharma? selling us snake oil, lol

watch this vid, very interesting:


http://www.youtube.com/watch?v=smJKRKo5n6U&feature=related

Dr Jerry Tennant discusses
Body voltage, cells, pH balance and
tips concerning balancing body voltage,
hypthyroidism, adrenals,stomach acids, and more.

There were some contradictions, but overall
well worth watching!!

Part I vid:

http://www.globalpreneurs.com/playback.php?t=MzYzMjc1MjM2MjU2ODc5NjI4MzM0NA==

Part II vid:

http://www.globalpreneurs.com/playback.php?pl=YjRkMWQ2ZGQzODg5YzgzNWY1MGZlNWFjM2MyNTk4MDM2Mjg0MT&crmid=1&uid=6809

I am starting a new blog focusing on disease state and symptoms resulting from adverse reactions to medications/iatrogenic/toxicity/vaccines/environmental and other.

It will be accessible to co-authors, guest scientists worldwide,(anti-establishment) and contributing members only. We will co-ordinate and liaise information from various sources with the outcome to greater understanding how to /prevent/reverse/halt the Dis-Ease process regardless of its manifestation.

Meanwhile, this blog will continue to operate, on a smaller scale.

Regardless of the symptoms and manifestation of the ensuing illness/symptoms, the mechanism caused by oxidization of the endothelial cells will result in various disease state, no matter the affects.

Inflammation, will cause varied disease state in individuals. All systems are connected, regardless. The focus will be on mitochondria, methylation, oxidization, ROS (free radicals) metabolism, inflammation, and other cellular and biochemical processes and more.

Healing involves knowledge and intuition. There are forces and energies which are non formulaic.

Equally, there are healing compounds which works both in allopathic medicine (side effects will occur in most) and other healing practices which are not explained. Often, scientific formulas hinder healing process, burdened with academic conflicts and pharmaceutical interests at the forefront of allopathic medicine.

Will blog about empirical and theoretical, whilst discussing various healing approaches.

Science uses the hypothetico-deductive method. The hypothesis itself derived from non logical thinking, observable, intuitive thought pattern to which logic was applied using formulas. The scientific process has to be ampliative in order to evolve.

Watch this vid: http://video.google.com/videoplay?docid=-2502546838698762400#


Still wanna reach for your little candies?



MEDICAL JOURNALS PIMP FOR BIG PHARMA
By Jon Christian Ryter
June 19, 2010 NewsWithViews. com
http://www.newswithviews.com/Ryter/jon321.htm


PLoS Medicine a peer review journal for the Public Library of Science claimed in an article that the most respected medical journals have become much too dependent on revenue from the pharmaceutical industry from two sources. First, advertising revenue which, according to PLoS, is the least corrupting form of revenue since the pharmaceutical industry should have the right to reach their potential customers in the periodicals their customers-doctors- read. What is the bigger problem, and what corrupts the integrity of the advertising process in about 25 different medical journals according to PLoS in an article published by the Public Library of Science five years ago (but never read by the general public which does not generally subscribe to it) is the second source of "advertising" revenue. The PR firms hired by the pharmaceutical giants pay fees to the journals to print well-edited capsulated synopsis of the drug trials.


The PR firms know that when the drug trials are published in any medical journal, the drug and the test tacitly carry that journal's stamp of approval simply by appearing in it. According to PLoS, a favorable review in a periodical like the Journal of American Medicine and the British Medical Journal and Lancet which have global distribution is worth thousands of pages of advertising. The PR companies will sometimes pay upwards of a million dollars for reprints of the articles to send to drug distributors, pharmaceutical wholesalers and medical professionals. While the PR firms admit the recipients of the reprints seldom read them, what they rely on is the name of the prestigious journal printing the review of giving a new drug credibility in the marketplace it has not earned from evidence of their curative abilities. The more important the medical journal, the more credibility the drug receives in the eyes of the physicians who receive the reprints.

Many times the whole content of the written clinical tests are not all that favorable to the drug but that, of course, is not reflected in the capsulated, controlled synopsis that appears in the medical journals. In 1994, Dr. Paula Rochon, adjunct scientist for the Kunin-Lunefeld Applied Research Unit and several of her colleagues wrote a paper examining the impact of journals which were paid to publish controlled excerpts of clinical studies had on the medical community's acceptance of the drugs compared to actual medicinal value of the drugs examined. The study focused on one class of drugs only: nonsteroidal anti-inflammatory drugs designed to combat arthritis. They found 56 trials. Not one of the published reports on the clinical studies presented any facts that were detrimental to the drugs tested.


The group came back a decade later, in 2003, and did a follow-up study on the 56 trial drugs to see if the drugs were living up to their clinical claims. The article was published by Richard Smith, the CEO of UnitedHealth Europe. Smith was Editor-in-Chief of the British Medical Journal for 13 years and held that job when the aforementioned study on the new arthritis drug was done. In many cases the reality of the drugs did not match the printed rhetoric of the promises of the clinical study conducted a decade earlier.


The question raised by the Public Library of Science a decade later was: how do pharmaceutical companies get the results they want once the drug is approved and recommended by physicians to their clients. When we go to our HMO or PPO physicians and they prescribe medication, we assume-and have every right and expectation to assume-that the prescription our physician prescribes will relieve or cure whatever the prescription is taken for. According to Smith, the pharmaceutical companies and their PR firms get the results they want not by fudging the facts but by asking the right questions and providing the right answers. This comes from hiring the right PR top guns who know how to stay a step ahead of the peer review groups. They do this by isolating positive parts of the clinical studies and forcing the dialogue into those positive aspects while ignoring negative ones. Or they combine the results from different centers in multiple combinations to obfuscate negative results in some facet or facets of the clinical study.


These strategies, Smith noted, have been exposed in the cases of risperidone and odansetron. However, with the 56 clinical studies the PLoS were attempting to evaluate, there was an impossible amount of work to examine in order to ascertain how many of the trials were truly independent and not biased on behalf of the fees paid by the pharmaceutical company. Clearly, what the Big Pharma wants is their drugs approved and used, and the PR firms they hire are paid to get positive "reviews" from the medical journals and paid advertising and advertorial (paid editorial copy) in the form of capsulated clinical studies.


What it comes down to, if the world's most prestigious medical journals-which medical professionals read as the Bible of the industry-have sold their souls for money, it is no more factually believable than magazines like The Onion or Mad magazine, the satirical comic book most Americans of read as teenagers back in the 1950s and 1960s. Smith further noted that "...Journal editors are becoming increasingly aware of how they are being manipulated and are fighting back. But, I must confess it took me almost a quarter of a century editing for the BMJ to wake up to what was happening... [E]ditors ask for other related data [related to] the studies submitted to them...But editors do not know what other unpublished studies exist."


Editors generally do not know if they are doing an honest peer review on one product or on a gigantic clever marketing jigsaw. More than likely one or more editors have commented that the material they get, regardless if it's a precise document or a jigsaw puzzle will always be of high technical quality.


The question raised by Smith and investigators like Dr. Rochon is how do we prevent the most prestigious medical journals in the world from selling their editorial souls for money? How do we prevent them from becoming no more credible than Mad Magazine or The Onion? How do we prevent them from becoming an extension of the marketing arm of the pharmaceutical industry? Smith thinks the editors can demand the right to review the protocols, and insist that all trials be registered; and most of all, demand that all clinical studies are completely transparent.


That won't happen because the journal publishers and shareholders know those clinical studies are worth millions of dollars in revenue, and bring additional millions in print advertising dollars from the pharmaceutical industry to reward them for publishing the clinical studies. Meaning, of course, that the medical journals are not going to risk that revenue. So, if you're a doctor who generally reads the New England Journal of Medicine, the Annals of Internal Medicine, JAMA or BMJ or Lancet in England, Canada or Australia for the latest life saving drugs, you might as well read something that will give you a chuckle.


Mad magazine was my magazine of choice as a kid. Give it a try. You have to say one thing about Mad. If you're older than 8 or 10 years of age, you'll always know when Mad's story line is an out-and-out lie or is colouring the truth. According to Smith and the editors of several other medical journals, you can't tell that from clinical studies published in the medical journals until you read the histories of the drugs about a decade later. By then, for some, it's too late. I guess that's why class action lawsuits are still in vogue.

Pyschotropics DO NOT WORK

Sorry about the rant here, but I have seen what those drugs have done to my dearest and closest .... :-@! I have the full report in PDF format for those who want it, just send me a PM.

Psychiatric drugs & suicide in Sweden 2007
A report based on data from the
National Board of Health and Welfare
By Janne Larsson

The purpose of this investigation has been to find data about the preceding psychopharmacological treatment for all persons who committed suicide in Sweden 2007.

The conclusion is that a large percentage of the persons who committed suicide in Sweden in 2007 had received extensive treatment with psychiatric drugs within a year of and close to the suicide.

This is a report about suicides committed in Sweden (with around 9 million citizens) in 2007 and the psychiatric drug treatment that preceded these suicides.

The report has three main parts:

• It gives unique data about all suicides committed in 2007 and the psychiatric
drugs that the persons received within a year of the suicide.

• It compares these data with autopsy reports about psychiatric drugs found in
the blood (of 98%) of all the persons who committed suicide in 2007.

• It gives extensive information about the psychiatric drug treatment given
within a year to the subgroup of persons who committed suicide in 2007 and
then were reported to the National Board of Health and Welfare by reason of
law 3 - one third of all suicides committed that year.

The data presented on these pages should have been published by the responsible national authorities.

A large percentage of the persons who committed suicide in Sweden in 2007 had received extensive treatment with psychiatric drugs within a year of their suicide.

The idea that persons who are depressed are suffering from “chemical imbalances” and are deficient in the substance serotonin has been marketed by the pharmaceutical companies selling antidepressants (in the class SSRI, such as Prozac, Paxil/Seroxat, Zoloft) for more than a decade.

The intensive marketing has led persons to believe that their low mood is a deficiency disease – and that it is vital to supply the substance that corrects this deficiency – the antidepressant drug.

But there is no scientific evidence that a low mood is caused by a ”chemical imbalance” in the brain 10 11. The hypothesis has been rejected with the following words by one of the most well known names in the field: “The serotonin theory of depression is comparable to the masturbatory theory of insanity.” 12 (The old theory that masturbation caused insanity.)

The Swedish medical agencies and their psychiatric consultants have used old data from forensic toxicological screenings to mislead the public and to heavily increase the use of antidepressants and other psychiatric drugs.

The most important information in this area is the patients’ medical history, the treatment history. Antidepressants, neuroleptics and other psychiatric drugs may cause harmful changes in the brain and these brain dysfunctions do not vanish when the drugs are discontinued – in many cases they cause chronic dysfunction to the brain, exemplified by the known neurological harm caused by neuroleptics. Many patients also get serious withdrawal reactions; reactions that can be so severe that they can lead to suicide.

Better sources of information are the unpublished clinical trials of psychiatric drugs done by pharmaceutical companies, and the important studies done by independent researchers.

A number of these studies show that antidepressants and neuroleptics increase the risk of suicidal behaviour and directly cause effects that lead to suicide.

Considering the results presented in this report, it is no longer possible to say that ”more” of the same sort is the solution to the problem. It’s not “more psychiatry” – more psychiatric drugs – that is the solution. Politicians, trying to surpass each other in demanding more funds for a psychiatric industry that only means more “treatment” with psychiatric drugs, should know that they directly contribute to harming people and to the creation of more “results” of the sort presented in this report.

Subservient nodding and voting when psychiatric opinion leaders require changes in law, so that people can be drugged with force in their homes, and so that “drug treatment without exceptions” can be given for people with mental problems, only lead to an increase in the psychiatric results described earlier. This report clearly shows one thing: A large majority of persons committed suicide after having had “adequate drug treatment” – in the meaning used in psychiatry; the very treatment that should prevent suicide. There is no reason to believe that the reporting system for adverse drug events work better in other countries. The catastrophic state of these “surveillance systems” makes it possible to keep destructive drugs on the market year after year.


All it takesis for pharmaceutical companies to show that many persons have been exposed to these drugs, and that almost no adverse event reports have been submitted; the drugs must be “safe and effective”.

This example from Sweden shows that in 338 cases persons committed suicide after having been prescribed psychiatric drugs – and none of these cases were reported to the registry for adverse drug events. Instead of Eli Lilly claiming that the drug Zyprexa was involved in 0 cases of suicide in Sweden 2007, the fact was that the drug was involved in 52 cases in this subgroup of 338 persons. Instead of Wyeth claiming the same for Effexor, the fact was that the drug was involved in 41 cases in
this group.

The reporting system must be completely reformed right away. It must be made mandatory for health care professionals to directly report all suspected serious adverse drug effects, and persons not reporting must be disciplined. Patients must be fully informed about the actual harmful effects of the drugs and given the right to report these effects to the adverse events registry, with the promise of effective follow-up.

The reformed system must not give room for the now ruling psychiatric concealment ideology, where obvious harmful effects of psychiatric drugs are treated as “symptoms” requiring more drugs. Instead all these effects must be reported as suspected harmful effects from the drugs.

And, most importantly, the data presented in this report must lead to basic changes in the ways in which persons with mental problems are being cared for.

http://www.theoneclickgroup.co.uk/news.php?start=3660&end=3680&view=yes&id=4926#newspost

Censored and not revealed in the press, many who are seriously ill with brain tumors, cancers, heart disease, and more, are being forced to go to work.

New welfare rules and regulations in the UK means that it is almost impossible to get disability unless paralyzed from head to toe!!!!

It is equivalent to a MASS CULLING, and this is not being reported in the Press!!

Instead the$150 billion assigned to US company Atos for a period of 7 years (banned from practicing in California for fraud) unfairly dismissing those who are chronically ill. Forcing them to choose between work or face the prospects of loosing your benefits.

Staff members are under pressure to put someone to work, because their salary is linked to how many people they sign fit for work. Atos doctors are given bonuses for signing "fit to work" and yes, you can guess what is going.

We are being vilified by politicians (and the press) as scroungers, cheats, and lazy!! I know of several instances of some on chemo being told they are fit to work by their encologists, despite being very poorly.

I know of one who collapsed at work suffering from a brain tumor, two women who collapsed and died and a man who was left alone in a wheelchair being refused social care. He died of dehydration and organ failure, unable to feed himself for several days.

UK members, those of you are reliant on disability, sign the petition:

http://www.gopetition.com/petitions/sack-atos-healthcare/sign.html

Doctors are being trained to say how well you look even when you look as if you are near death's door, unable to stand up. They are being trained to look at legal loopholes concerning tests and investigations. As we know, tests and investigations are ONLY SUPPORTIVE of a diagnosis which is based on symptoms and medical history.

There are several internet activists groups exposing this MASS SLAUGHTER & GENOCIDE.

It is not about saving money here, since, they are using this money to create dummy jobs within the DWP itself, but not to help the sick and vulnerable, instead, to PERSECUTE.

UK members who are interested in finding out more, send me a PM. Protect yourselves by keeping informed.

This is inhumane. Many are asking for a little to go to sleep, rather than facing worsening of health through destitution and dying of a slow death ....

Not worried, you should be ..

* BIG thanks to the great filmmakers who have made these amazing films! May I be Frank, One Hour Fantasy Girl, Family Divided, Awareness GMW++ 1 day ago

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Legend

Regent Showcase Theater: 614 N. La Brea Ave., Los Angeles, CA 90036 (directions)
Heaven on Earth: 7122 Beverly Blvd. (Upstairs), Los Angeles, CA 90036 (directions)
Marco Polo Loft: 716 Taft St. (Corner of Lincoln and Colorado), Santa Monica, CA 90404 (directions)
Opening & Closing Galas

Certain Adverse Events
When Sunday, May 23, 2010, 1 – 2pm
Where 1 PM (50 MIN)
Event type Fair/Festival
Ticket Web Link store.healoneworld.com…
Note

Heaven On Earth

For more Info: http://awarenessfestival.healoneworld.com/calendar.html?trumbaEmbed=view%3devent%26eventid%3d89412923

This post,and others to follow, will complement research on CYPs, TPRV receptors and Vanilloid Receptors as well as "Altering Brain Chemistry" & "Electromagnetic" threads. It is all linked, all of it, what we eat, what we drink, what we inhale, ingest, meds, environmental, exposure to radio frequencies (RF), etc. All affect cell permeability.

On going research shows some success with calcium, manganese with SOD, Pantethine taurine. Manganese & SOD help with tendinitis too.

Before taking taking anything, check it out yourselves. It is not that simple.

For instance, ethnicity and diet is important here. Apparently, those who are of Mexican descent, seem to have higher content of SOD/Manganese (lucky guys). It binds to minerals. Vit K is supposed to help with tendinitis too, read that it stops calcifications, specially in soft tissues, microvessels. Look this up.

It's all connected. Because I excited the TRPVs with RAW tumeric, I have painful tendinitis, and some recurrence of neurological symptoms. Hence, the impetus and motivation for research.

Professor Yiannis Samaras and Dr Effimia Eriotou found Thyme Essential Oil, (as in herb thyme) and Cinnamon Essential Oil are effective against MRSA!! It was suggested that these could be used as food preservatives instead of toxic chems. Known for thousands of years, validated in 2010!! http://tinyurl.com/ydopvre

Yummy.


See also the post on Black Seed Oil, which is under Glutathione Label

Now for cheerier news, hard to find, but here goes:

For those who are skeptical as to why many develop cascade of symptoms and mulitiple disease processes post adverse drug/vaccine reaction, it is simple and complex.

Considering that many will develop mitochondrial dysfunction, inflammatory process, organ damage, autoimmune illnesses, and other, caused by injury to endolethial cells, leading to oxidization, high level of free radicals, and metabolic syndromes for which there are no labels, no diagnostic tests, over a period of years, we are often labelled as suffering from CFS.

Previous referenced posts have shown that antibiotics can activate dormant infectious pathogens, caused L-Carnitine dysfunction, mitochondrial dysfunction etc..

The XMRV virus has been linked to vaccine and is also transmissible through body fluids, and patients suffering horrific symptoms over many years, are also given the label of CFS/ME. XMRV is a retrovirus, similar to the HIV virus and prostate cancer.

I am not making a direct link between XMRV and ADRs - neverthelss, it deserves a mention
and could be applicable to some.

Considering that little is known about pathogenis of the virus, except that it plays a role in dysfunction of the immune system, undetectable at this time due to the limitations of immunology!!

The good news is that Canada, is the first country to have put a ban on ME/CFS sufferers donating blood.

Is it not curious that the Medical Research Council (MRC) in the UK refuses to release documents dating from 1988 to present in regards to ME/CFS? These documents are unobtainable even through the Freedom of Information Act 2000. These documents are under lock and key until 2071.

Meanwhile Canada is the first country to ban ME/CFS sufferers from donating blood.

Study below about compounds in Triphala, at the end of the
Foreword.

When I started taking Ayurvedic compounds, a year ago, I had little faith , no understanding of how it worked, and was not interested in diet, and meditation even though, I had done meditation
a few years earlier, found it beneficial - SIGNIFICANTLY so!! to the point of being able to control my heart rhythm.

I still have no understanding of Ayurvedic Medicine. But, I can report that the healing experience brought on by prescribed compounds, is supported by blood tests and investigations (but then again those tests are very limited). This is not placebo, or coincidence. I have been ill from multiple ADRs for over ten years, mostly homebound/bedridden, and a stint in a wheelchair.

The healing process resulted in a total change in consciousness, brought on by experiencing the therapeutic effects of those compounds, whilst seeking to understand how Ayurvedic Medicine works, by reading about it in depth, and trying desperately to alter my diet accordingly.

The shift in consciousness, brought me closer to understanding what HEALING means, on cellular level, and that it takes TIME, and motivation to assist in your own HEALING. AVOIDING at all costs, DNA damage from meds, MRIs, Xrays, scans, RF from EMF etc.... I am at last physically feeling the effect of cells rebuilding.

Lastly, the Ayurvedic way, reinforced my convictions concerning allopathic medicine. IT DOES NOT WORK, is solely profit based, little science and no substance.

Even if I had not "discovered" Ayurveda, I had read enough "research" about allopathic medicine from medical and science journals, to feel utter contempt at the arrogance and skewed research and so much conjecture based on a mechanical way, materialistic of how physiology & biochemistry works.

It takes literally decades for the medical establishment to alter wrong assumptions, and moreover, oppose any other view points to protect their own interests and industry, rather than the patients.

A good example of this - Dr Hulda Clark and before her,other scientists, at the beginning of the last Century, showed, that many cancers originated from bacteria and viruses. They were cast aside, ridiculed whilst the establishment went on a witch hunt of such scientists, destroying their careers in the process, leaving them with no credibility.

Similar is happening with scientists showing evidence of how toxicity affects mitochondria, methylation, free radicals increase etc... for over 30 years!!! So many illnesses could have been erased, and so many patients could have benefited. Instead, more illness, more disability, unnecessary more deaths, and more money for Big Pharma.

There is no doubt that in life and death situation, some type of surgery may be life saving, but even then, there will be consequences, even, if not immediate, somewhere along the line, from meds, anesthetics, etc...

Although it is not necessary to meditate, it will assist in healing, there is little doubt of that. It oxygenates cells, brings down BP, promotes release of good hormones, whilst reducing toxic hormones and its effects, reduces CNS, realigns alpha, beta and other brain waves etc... I started again, today, and will try to keep this up.

Below is a study, amongst many concerning compounds from two fruits used in Triphala, which I have been taking daily for a year, except for a few weeks breaks. It even cleared the toxins from my eyes, I no longer need to wear reading glasses!! All my posts have been consistent concerning Triphala and my experience with Ayurvedic Medicine, I wish I started years ago, when first floxed!!

No matter how much analysis or research is done in the West about compounds in fruits and vegetables, there are limitations as to healing compounds. Far too much importance and credits are atributed to those tests, when Triphala has stood the test of time, for over 4000 years.....

Comparative study of the antioxidant and reactive oxygen species scavenging properties in the extracts of the fruits of Terminalia chebula, Terminalia belerica and Emblica officinalis

Bibhabasu Hazra email, Rhitajit Sarkar email, Santanu Biswas email and Nripendranath Mandal email

BMC Complementary and Alternative Medicine 2010, 10:20doi:10.1186/1472-6882-10-20
Published: 13 May 2010
Abstract (provisional)

Background

Cellular damage caused by reactive oxygen species (ROS) has been implicated in several diseases, and hence natural antioxidants have significant importance in human health. The present study was carried out to evaluate the in vitro antioxidant and reactive oxygen species scavenging activities of Terminalia chebula, Terminalia belerica and Emblica officinalis fruit extracts.
Methods

The 70% methanol extracts were studied for in vitro total antioxidant activity along with phenolic and flavonoid contents and reducing power. Scavenging ability of the extracts for radicals like DPPH, hydroxyl, superoxide, nitric oxide, hydrogen peroxide, peroxynitrite, singlet oxygen, hypochlorous acid were also performed to determine the potential of the extracts.
Results

The ability of the extracts of the fruits in exhibiting their antioxative properties follow the order T. chebula > E. officinalis > T. belerica. The same order is followed in their flavonoid content, whereas in case of phenolic content it becomes E. officinalis > T. belerica > T. chebula. In the studies of free radicals' scavenging, where the activities of the fruit extracts were inversely proportional to their IC50 values, T. chebula and E. officinalis were found to be taking leading role with the orders of T. chebula > E. officinalis > T. belerica for superoxide and nitric oxide, and E. officinalis > T. belerica > T. chebula for DPPH and peroxynitrite radicals.

Miscellaneous results were observed in the scavenging of other radicals by the fruit extracts, viz., T. chebula > T. belerica > E. officinalis for hydroxyl, T. belerica > T. chebula > E. officinalis for singlet oxygen and T. belerica > E. officinalis > T. chebula for hypochlorous acid. In a whole, the studied fruit extracts showed quite good efficacy in their antioxidant and radical scavenging abilities, compared to the standards.


Conclusions

The evidences as can be concluded from the study of the 70% methanol extract of the fruits of Terminalia chebula, Terminalia belerica and Emblica officinalis, imposes the fact that they might be useful as potent sources of natural antioxidant.

Good Detox recipe using various oils and a smoothie.

Watch out for spinach, some amines can exacerbate CNS, as well as tomatoes, chicken skin and other foods already mentioned here on this thread.

Coconut derivatives has salycylates compounds. Apparently, I read, it can interfere with oxygen transport if " they exceed a threshold concentration. They also occur in honey and prawns etc so certain combinations can lead to higher doses."

Aghhhh - such hard work to remain well, and prevent more symptoms!

Permission requested to copy and pasted:

Phospholipid exchange
From DoctorMyhill

* 1 The Recipe from Beverley Gibson
* 2 Using Other Oils

Phospholipid exchange is a technique for supplying the correct proportion of fats and oils in a bioavailable form to replenish cell membranes and membranes within cells.

This technique has been pioneered by Dr Patricia Kane, who has seen remarkable clinical results. She uses intravenous therapy, but good results are also possible with oral therapy. Together with sufferers I am experimenting with techniques to get the best results. The underlying principles are:

1. The basic membrane structure is made up of phosphatidylcholine . The best source of this is lecithin (available as egg, soya or sunflower lecithin). The trouble with lecithin is that it gets digested in the gut instead of being absorbed as phophatidylcholine. We are experimenting with juicing mixes to see if this will reduce the lecithin to tiny micelles, which will allow it to be absorbed as whole molecules.
2. Membranes then need the right proportion of omega 6 to 3 oils, i.e. 4:1. Hemp oil is very close to this ratio at 3.8:1. (Hemp oil is not the same as linseed oil!) So, add in a small amount of sunflower oil, say 5%. This is the equivalent of Patricia Kane's Body Bio-oil as in the recipe below.
3. Small amount of Eskimo oil (not necessaery if you already take VegEPA)
4. The perfect fuel for brain cells is coconut oil, which is rich in medium chain triglycerides.
5. Furthermore providing an abundance of clean oils helps to displace the toxic oils which have accumulated in the brain as a result of polluting heavy metals, pesticides, volatile organic compounds etc. That is to say these fats will also help detoxification.

The Recipe from Beverley Gibson

Here is the juice that I make 3 times daily - it takes around 5 mins. I use a Juice master available from http://www.juicemas ter.com/product. php?id=3

Juice the following:- (I buy organic and get it delivered to my door from Sainsburys)

* 1/2 lime
* 1/4 medium cucumber
* 1 stick of celery
* Handful of spinach
* 1/2 inch of broccoli stem and/or a few broccoli florets.

* Place all above into a blender and add:-

* 1/4 avocado
* Coconut oil 1 dessert spoon (10ml) (Coconut Oil must have been kept in the fridge in order to blend well)
* Lecithin 1 dessert spoon (10ml)
* Hemp oil 1 dessert spoon (10ml)
* Sunflower oil 1/4 teaspoon (1ml)
* 2-4 Ice cubes

Blend everything until smooth, pour and enjoy.
Using Other Oils

The proportion of omega 6 to 3 in other oils are as follows:

1. Peanut oil - very high!
2. Safflower oil - 152
3. Sunflower oil - 68
4. Corn oil - 54
5. Olive oil - 10
6. Palm oil - 10
7. Soybean oil - 7.7
8. Hemp oil 3.8
9. Canola oil - 2
10. Rapeseed oil - 2
11. Linseed oil - 0.3

You should aim for 4:1 ratio, so if you cannot access hemp oil or there is an allergy problem, make up another mix. So, for example 80% olive oil with 20% linseed oil would also give a 4:1 ratio.

Professor Yiannis Samaras and Dr Effimia Eriotou found Thyme Essential Oil, (as in herb thyme) and Cinnamon Essential Oil are effective against MRSA!! It was suggested that these could be used as food preservatives instead of toxic chems. Known for thousands of years, validated in 2010!! http://tinyurl.com/ydopvre

Yummy.

Watch this Vid

Those who tell the unpalatable truths are often ridiculed, or thought of as eccentrics or conspiratory theorists.

For the most part, factual, a good watch.

DSM-5 REVISION, FLOXIES BEWARE

Floxies and others suffering from ADRs, often develop horrific symptoms, for which there are (conveniently) no tests. The American Psychiatric Association (APA) revising Diagnostic and Statistical Manual for Mental Disorders (DSM-5), proposes to psychologize behaviors such as being justifiably show "concern" "and seeking help and understanding." It will be classified under somatic disorders!!!

Medical doctors and scientists are ignorant, deaf and blind, to symptoms/sufferings arising from ADRs... Most of those symptoms are functional occurring at cellular level. Rather than admit their ignorance and fear of repercussions, they opt for slapping a psychiatric label on to floxies and others.

On a personal level, I remember the days of inexplicable frightening symptoms being reported to doctors, met with deafening silence. Yet, when strong enough to research those symptoms, it was found that those receiving chemo, were suffering the same. There is a biochemical process manifesting itself for which there is limited rational explanation for most of those syptoms, that is TOXICITY from meds and vaccines. Rarely, if iatrogenic illnesses are acknowledged.

Keep in mind that Big Pharma will not allow development of tests linking toxicity from their medicines and vaccines.

Protect yourselves, do your research, use it to "justify" your symptoms, avoid being labeled as "mentally ill." it will be used against you for the rest of your life. Keep yourselves INFORMED.

CFS & Autonomic Dysfunction


Here we are, suffering from autonomic dysfunction for years, and telling doctors that whenever we exert ourselves with minimal physical activities, we feel ill and CRASH,(see previous post on Oxidative Stress) - another published article showing biomedical supportive evidence of this. Are politicians death and blind? Instead, they continue to implement psychological bias!!!


Abstract:
 

Jones DEJ, Hollingsworth KG, Taylor R, Blamire AM, Newton JL (From the Institute of Cellular Medicine, Newcastle Magnetic Resonance Centre, and Institute for Ageing and Health, Newcastle University, UK). Abnormalities in pH handling by peripheral muscle and potential regulation by the autonomic nervous system in chronic fatigue syndrome. J Intern Med 2010; 267: 394-401. Objectives. 

To examine muscle acid handling following exercise in chronic fatigue syndrome (CFS/ME) and the relationship with autonomic dysfunction. Design. 

Observational study. Setting. 

Regional fatigue service. Subjects & interventions. 

Chronic fatigue syndrome (n = 16) and age and sex matched normal controls (n =  8) underwent phosphorus magnetic resonance spectroscopy (MRS) to evaluate pH handling during exercise. Subjects performed plantar flexion at fixed 35% load maximum voluntary contraction. Heart rate variability was performed during 10 min supine rest using digital photophlethysmography as a measure of autonomic function. Results. 

Compared to normal controls, the CFS/ME group had significant suppression of proton efflux both immediately postexercise (CFS: 1.1 ± 0.5 mmol L−1 min−1 vs. normal: 3.6 ± 1.5 mmol L−1 min−1, P < 0.001) and maximally (CFS: 2.7 ± 3.4 mmol L−1 min−1 vs. control: 3.8 ± 1.6 mmol L−1 min−1, P <  0.05). Furthermore, the time taken to reach maximum proton efflux was significantly prolonged in patients (CFS: 25.6 ± 36.1 s vs. normal: 3.8 ± 5.2 s, P < 0.05). In controls the rate of maximum proton efflux showed a strong inverse correlation with nadir muscle pH following exercise (r2 = 0.6; P < 0.01). In CFS patients, in contrast, this significant normal relationship was lost (r2 = 0.003; P  = ns). In normal individuals, the maximum proton efflux following exercise were closely correlated with total heart rate variability (r2 = 0.7; P = 0.007) this relationship was lost in CFS/ME patients (r2 < 0.001; P = ns). Conclusion. 

Patients with CFS/ME have abnormalities in recovery of intramuscular pH following standardised exercise degree of which is related to autonomic dysfunction. This study identifies a novel biological abnormality in patients with CFS/ME which is potentially open to modification.

Keywords: autonomic dysfunction; chronic fatigue syndrome; magnetic resonance spectroscopy; muscle bioenergetics

Document Type: Research article

DOI: 10.1111/j.1365-2796.2009.02160.x

Affiliations: 1: From the Institute of Cellular Medicine 2: Newcastle Magnetic Resonance Centre

More Health News for the bad ass


Electromagnetic Field Exposure (EMF)and Glutamate Receptors
EMF sufferers are a source of ridicule despite thousands of published article showing the damage caused by exposure.

Glutamate receptors

Those of us who do suffer from EMF, are often told it is psychosomatic. Vested interests plays a major role acknowledging both iatrogenic and environmental Dis-ease.

Professor Morrissey used to work for Motorola as a senior scientist. He developed an interest in how heat and radio frequencies affects cancer cells.

Professor Morrissey resigned to pursue research about the effects of cancer and electromagnetic field.

He started working for Nova Southeastern University, Assistant Professor in the Pharmacology Department.

A few days ago, he was murdered in his house. Two men came in, shot him dead, tied up his wife, and set the house on fire. The wife of Professor Morrissey miraculously escaped with her young son.

Scientists seem to have a shorter lifespan than other professionals, most meeting with violent deaths. Specifically, ethical scientists ..

See below the published article concerning EMF, Reactive Oxygen Species (ROS), and breakages in DNA strands. There are hundreds of articles reporting the same findings. Those who are suffering from CNS symptoms would benefit from minimizing exposure to EMF. It affects glutamate receptors!!


Neurosci Lett. 2010 Mar 31;473(1):52-5. Epub 2010 Feb 13.
Reactive oxygen species levels and DNA fragmentation on astrocytes in primary culture after acute exposure to low intensity microwave electromagnetic field.

Campisi A, Gulino M, Acquaviva R, Bellia P, Raciti G, Grasso R, Musumeci F, Vanella A, Triglia A.

Dipartimento di Chimica Biologica, Chimica Medica e Biologia Molecolare, Università degli Studi di Catania, Viale A. Doria 6, I-95125 Catania, Italy. campisag@unict.it
Abstract

The exposure of primary rat neocortical astroglial cell cultures to acute electromagnetic fields (EMF) in the microwave range was studied. Differentiated astroglial cell cultures at 14 days in vitro were exposed for 5, 10, or 20min to either 900MHz continuous waves or 900MHz waves modulated in amplitude at 50Hz using a sinusoidal waveform and 100% modulation index. The strength of the electric field (rms value) at the sample position was 10V/m. No change in cellular viability evaluated by MTT test and lactate dehydrogenase release was observed. A significant increase in ROS levels and DNA fragmentation was found only after exposure of the astrocytes to modulated EMF for 20min. No evident effects were detected when shorter time intervals or continuous waves were used. The irradiation conditions allowed the exclusion of any possible thermal effect. Our data demonstrate, for the first time, that even acute exposure to low intensity EMF induces ROS production and DNA fragmentation in astrocytes in primary cultures, which also represent the principal target of modulated EMF. Our findings also suggest the hypothesis that the effects could be due to hyperstimulation of the glutamate receptors, which play a crucial role in acute and chronic brain damage. Furthermore, the results show the importance of the amplitude modulation in the interaction between EMF and neocortical astrocytes. Copyright 2010 Elsevier Ireland


A simplified brief few words about Glutamate Receptors
by Beebs Tweet sourced from Neuronal science books
and journals:

Glutamate is found in the body including the brain. It is also responsible for memory and learning. For this purpose, if there is high concentraton of glutamate which is caused by extra cellular activity, either by medication, food, EMF or other toxicity, it will cause over-excitation. This will lead to cellular damage, which turns into an excitotoxin. This will cause agitation or manifest in various ways, if the NMDA receptors are involved, symptoms will differ when in contact with foods, solvents, etc.. I don't know the mechanism by which EMF is involved with glutamate receptors at this point.

PolitiKo/Medico-legal & some good news

Life for independent thinkers, in the UK, is becoming more sinister with governmental interference and infringement on free speech, freedom of expression, persecution of journalists, and other free thinking individuals.

There is now sanctioned bashing of those who are sick, disabled, elderly and other maginalized and vulnerable population.

Dr Myhill, a GP with an excellent record, is being
hounded by the General Medical Council (GMC).
WHY? She uses vitamins and supplement mostly!!
see her site: http://www.drmyhill.co.uk/

She has been threatened several times with having
her license revoked. To date, Dr Myhill has not caused
harm to her patients, but help many improve.

Her patients supporters will campaign and testify on her behalf. Dr Myhill is once more under attacked from the GMC, who have decided to revoke her medical license despite having no grounds. Tried, judged and found guilty. This is not legal. Read more on her website, scroll down the page to categories and click on "My GMC Hearing." She needs our support, having valliantly supported us over the years, putting her own career at risk. http://www.drmyhill.co.uk/

In contrast, a doctor who KILLED 12 patients to keep them quiet, at a nursing home,
continues to practice:

Dr Jane Barton gave patients drugs to 'keep them quiet'

Dr Barton was overdosing her elderly and sick patients with opiates to keep them quiet. 12 patients died as a result. Read the whole article here:
http://www.portsmouth.co.uk/newshome/Dr-Jane-Barton-gave-patients.5347802.jp

http://tinyurl.com/ybrfj77

Although conditional, Dr Barton continues to practice, no more than a slap on the wrist from the General Medical Council (GMC). http://news.bbc.co.uk/1/hi/england/hampshire/8486936.stm

Do you really believe medical and governmental health institutions have your best interest at heart? Do ya???

Well, think again ...

Mmm, still want your flu shot? Following the so called swine flu pandemic, frantic puppet scientist rushing around to publish their findings concerning flu shot vaccines, linked to boosting the risk of H1N1 infection.

Hey presto,
government officials are now squeaky clean,

OINK OINK





Read on:

H1N1 Spread Linked to Seasonal Flu Shots

The four new studies conducted by Canadian researchers conclude that the traditional seasonal flu vaccine seems to have boosted the risk of infection with pandemic H1N1 swine flu by almost double.

In one study, the researchers revealed to use ongoing sentinel monitoring system in order to assess the frequency of prior vaccination with the seasonal flu vaccine in people suffering from H1N1 swine flu in 2009 compared to people without swine flu.

The study discovered that seasonal flu vaccination was linked with a 68 percent boosted risk of falling in prey to swine flu.

"I do think that they did the best they could with the data they had", said Dr. Mark Loeb, an infectious diseases expert at McMaster University in Hamilton who was not part of the study and who seems to be sceptical about the study’s conclusion. http://topnews.us/content/215882-h1n1-spread-linked-seasonal-flu-shots

Canada is the first country to ban CFS/ME sufferers from giving blood.

How comforting!!

Canada bans blood donations from people with chronic fatigue

Read more: http://www.montrealgazette.com/health/Canada+bans+blood+donations+from+people+with+chronic+fatigue/2775203/story.html#ixzz0kdRxvp74

More good news from the UK

A Labor candidate was fired from his job for his shocking Tweets.

Stuart McLennan, posted outrageous Tweets about "slaves" "chavs" and "coffin dodgers" the latter is very scary considering many of us are terminally ill and for the elderly!! So, yep, we are dodging coffins, whilst doctors are speeding the process with murderous injections of morphine or simply withdrawing IV drips, read here: http://blog.taragana.com/n/british-doctors-complain-of-tick-box-approach-to-care-of-terminally-ill-patients-158753/ A Dutch doctor killed a patient because he needed her bed: http://www.chninternational.com/licenced_to_kill_dutch_euthanasia.htm Note that in Holland doctors are not penalized for killing newborn deformed babies. The approval of politicians leading to those who are unproductive to feel they have a duty to die ... in view of politicians allowing financial collapse, causing recession, there is a tendency, certainly in the UK, to make those who are ill, feel pressurized to work regardless of their condition, unless paralyzed from head to toe. Those who are bedridden because of chronic illnesses such as ME/CFS are denied medical care, investigations (unless there is other pathology), welfare & disability. There is a high suicide rate amongst ME/CFS sufferers in the UK, which essentially, is forced euthanesia.

Read more here about his offensive, foul-mouthed verbal garbage: http://www.thisislondon.co.uk/standard/article-23823138-labour-candidate-sacked-for-tweets-on-chavs-and-coffin-dodgers.do

Now, now, don't fall prey to long term chronic illness .. not safe to be a "coffin dodger" in Holland and the UK!!

The irony is that it is not the first time a UK politician mouths off its population - it will be of no surprise if McLennan resurfaces with a promotion after the general election in May 2010!! Watch this space.

Drug Poisoning, Failing Health & some good news

There seems to be a pattern in regards to deaths associated with drug toxicity published articles. Replicated studies in various countries have shown in-hospital deaths to be 6 out 10 caused by medication. This paper discusses drug poisoning in Sweden, (in/out of hospitals not specified) http://www.ncbi.nlm.nih.gov/pubmed/19397805

Dr Jeffrey H Cohen, will be publishing a paper in May this year. Dr Cohen based at West Viriginia School of Medicine, bases his study over a period of ten years from 1996-2006. The study mentions an increase of 400% poisoning from methadone, and benzos by 39% It would be difficult to establish in those cases if intentional.

My own view here is that we will see an increase of published research warning about "drug toxicities," invasive procedures, and futility of expensive diagnostic tools, and dentisty just as health care costs rise. Some countries with a model of socialized health care system, are now either minimizing patients'symptoms, or openly discouraging patients from having expensive investigative procedures. There is also a tendency towards pushing drugs that are on trial rather than prescribing older safer drugs. http://tinyurl.com/yfj7bw2

More striking news which ties up with the increase of the US population on meds and failing health at a younger age.

This article illustrates the above. Professor Linda Martin, published a study showing significant rise of disabilities and mobility problems amongst a population between the ages of 50-64 years old. http://tinyurl.com/y8dqure Interesting, could it be a associated with the rise in use of pharmaceuticals?

This ties in with expanding palliative care across the USA. There is an increase of 125.8% between the years of 2000-2008. http://tinyurl.com/y9mz7p5

The Dark side of Scans - What your doctors don't tell you!!


CT Scans & other intrusive diagnostic tool, causes cancer & ineffective detection

High tech diagnostic tools are not more useful than taking a patient's medical history, examination, note of present symptoms. For instance, studies show that women who regularly examine their breasts, detect unusual lumps earlier. Some report show an increase of cancer risks by 50% following routine mammograms over a period of six years. There is no doubt that mammograms are to be avoided. Breast tissue is very sensitive to radiation, considering that radiation does cause cell mutation, is it worth the risk? see this thought provoking article: http://tinyurl.com/y9eko3b

Moving on, the article below discusses FDA corruption, suppression of information, self interest, and mentions the dangers of colonscopy.

In a nutshell, an efficient MD should be a good diagnostician without resorting to harmful high tech diagnostics tools unless - there is justifiable cause.


See the article below:

From Medscape Medical News

Experts Debate Extent of FDA Reform in Wake of Whistleblower Testimony

Robert Lowes

April 5, 2010 — Did a former consulting scientist at the US Food and Drug Administration (FDA) lose his position — as he contends — because he blew the whistle about the risk for radiation exposure from computed tomography (CT) scanners used in colon cancer screenings?

Or is the FDA right when it claims that the Department of Health and Human Services (HHS) found no criminal wrongdoing after investigating the charges of Julian Nicholas, MD, who testified March 30 at an agency hearing on preventing unnecessary radiation exposure from medical imaging?

Although all the facts surrounding the case of Dr. Nicholas have yet to be sorted out, some FDA watchers say one thing is clear — the agency is still recovering from the antiregulatory, probusiness climate of the George W. Bush administration in which public health took a back seat.

"The new leadership of the FDA inherited a mess," said Diana Zuckerman, PhD, president of the nonpartisan National Research Center for Women and Families, which specializes in health issues. "You have a change of leadership at the top, but the vast majority of the people in the FDA at the office or center level are exactly the same [as before]."

"People got promoted during the 8 years of the Bush administration for reasons that had to do with ideology. They may be very capable and smart, but they also have a proindustry point of view, not a public-health point of view."

Like Dr. Zuckerman, Steven Nissen, MD, chair of the Department of Cardiovascular Medicine at the Cleveland Clinic, in Ohio, and a long-time FDA critic, thinks that the Nicholas case is a sign of a hangover from the Bush administration.

...............Dr. Nicholas said that his superiors in the agency's Center for Devices and Radiological Health pressured him to change his scientific opinion when he objected to letting a manufacturer — reportedly General Electric — market a CT scanner for "virtual colonoscopies." Nicholas said he warned FDA managers last year that such scans could significantly increase a patient's risk for cancer. His whistleblowing, he said, led the FDA not to renew his contract when it expired last October. http://tinyurl.com/yeyoheg

Marketing of Madness

New Additons to DSM-V are sinister. The group of psychiatrists with strong ties with the psychopharmacology industry continues to "invent" more psychiatric disorders and subtypes, such as "Oppositional Defiant Disorder" (ODD) that's for anyone with a clear, analytical mind, and their own opinion, those who are defiant of authority!!!

"Antisocial Personality Disorder" that is for someone who is difficult, spiteful, mean, manipulative or a prick, yep, that too.

When your kid throws a tantrum, he is not just throwing a tantrum, he is suffering from "Temper Dysregulation Disorder with Dysphoria." There is now a "Pediatric Bipolar Disorder."

If you think about sex too often, you don't have a high healthy libido related to high testosterone, you are suffering from "Hypersexual Disorder."

Essentially, characteristics of personalities are now being turned into psychiatric disorders.

Considering side effects - Lucrative and assured income for the pharmaceutical companies.

The Wall Street Journal reports $10 billion in profits in 2009, for pharmaceutical companies selling psychotropics in the US. At this rate, it will double by end of fiscal year 2010.

Incidentally, the Federal Aviation Association (FAA) lifted the ban on pilots taking psychotropics. Some pilots will be granted waivers whist taking Prozac, Lexapro, Celexa, Zoloft and generics. http://tinyurl.com/ybn6rnc

Hum, Welcome Aboard ....

Incidentally, those who suffer from serious addictions to psychotropics, are no longer suffering from addiction. This has now been altered to a "chemical dependency." Sounds nicer. This is clever marketing ploy, making the lure of psychotropics even more attractive.

Hide your grief, or you will be labelled as being "depressive", don't be shy now, you will be labelled with "Social Anxiety Disorder", apprehension is now "Anxiety" etc..

Not labeled yet, worry not, there is a new label which might suit you, it is called the "Psychosis Risk Syndrome", for those who are strong indviduals, slightly eccentric, strong opinions. This will apply regardless of the fact, that you are NOT psychotic, delusional, or hearing voices. This new label is an extension to "Schizophrenia" mainly to identify those who are at risks of becoming "schizophrenic."

Are we so disconnected that the only way to "connect" and "belong" is by discussing which "mental illness" we suffer from (as if belonging to a special club) and which are the most effective psychotropics, how to dodge inter dosage withdrawal symptoms? It never fails to irritate me when I hear someone who is basically capricious, manipulative, high/low intensities of emotions, lacking in self control and social skills, proudly announce they suffer from "bi-polar" disorder!!! They then perpetuate this behavior by acting out what is conceived as being "bi-polar."

Wake up, Stop being fooled about brain chemical imbalances, there is NO scientific evidence to support this.

Read up and research about psychiatric labels and anti-depressants.

What you will find instead - a strong lobby of psychiatrists, conflict of interest, skewed research, scandals involving drugging of children, disgraced and corrupt psychiatrists linked with politics, coercion, compliance, submission, and greed.

We live in a dysfunctional society, there is no doubt that in order to survive, we all need to be slightly dysfunctional - nothing more ......


http://www.cchr.org/#/home (Watch "Making a Killing Video" psychiatrists tell you that psychotropics and psychiatrics labels HAVE NO SCIENTIFIC BASIS)
http://www.dsm-5diagnosis.com/
http://www.ahrp.org/cms/component/option,com_frontpage/Itemid,1/

Have some fun with the Disease Mongering Engine:
http://www.naturalnews.com/disease-mongering-engine.asp

Black Seed Oil (Nigella Sativa)

An earlier post about Black Seed Oil, with references,
not listed some compounds such as WARNING -

Tried one drop of Black Seed Oil. Had immediate reaction.
Am devastated!!!

Went to check, it contains quinones ....
Many of us can't tolerate quinones, such as benzoquinones, anthraquinones (as in Aloe Vera), quinazoline, etc.

Collateral Damage

ADRs, ME/CFS, GWVs, Infections, MCS, metabollic syndromes and other "Syndromes"

It is no coincidence that many suffering ADRs are labeled as suffering from ME/CFS.

The mechanism leading to long term illness, stemming from ADRs, vaccines and the aforementioned, triggers glycation, inflammation, oxidative stress, producing too much Nitric Oxide and other free radicals, leading to degeneration over a long period of time, spanning between ten to twenty years.

Dis-Ease state manifests over a period of time, affecting the individual with a myriad of symptoms. Symptoms vary, but the mechanism is the same - TOXICITY. The mechanism begins with oxidization of endothelial cells leading to apoptosis (programmed cell death).

The general consensus amongst progressive medical doctors and scientists is that TOXICITY or nutritional imbalances are main causes of degenerative diseases.

It has already been established that medication causes damage to the mitochondria, leading to progressive degeneration manifesting as diabetes, and other auto-immune illnesses, metabolic syndromes, (http://aac.asm.org/cgi/reprint/AAC.00729-05v1.pdf and http://www.ceri.com/mito.htm) such as depleting L-Carnitine http://www.ncbi.nlm.nih.gov/sites/entrez and http://ods.od.nih.gov/factsheets/carnitine.asp, antibiotics weakening the immune system, activating viruses such as EBV and HHV-6. L-Carnitine deficiency is very difficult to diagnose, can lead to dangerous arrythmia and heart failure!

Furthermore, the principle that drugs only benefit a small percentage of the population as in this article: http://jcp.sagepub.com/cgi/content/abstr....ourcetype=HWCIT and hundreds more published articles, taking medicines is not only redundant, but will cause more harm.

Antibioitics can activate EBV & HHV6: http://tinyurl.com/yetmly3 and C.Difficile: http://tinyurl.com/ykqauw4

Likewise, antimicrobials are no longer effective, mutating pathogens, whilst weakening the immune system whilst causing even more damage to the digestive tract, which is 80% responsible for a healthy immune system!

Reading about oxidative stress, Nitric Oxide Cycle, Free Radicals, Inflammation over a period of two years, leads to the conclusion that preventing escalation of symptoms from ADRs is crucial to maintain good health.

Lastly, it is irrelevant if ME/CFS was triggered by an infection, which could have been triggered by the effects of antibiotics, or toxicity form vaccines, or medications. It will lead to oxidization and inflammation.

See articles below:

Treatment of myalgic encephalomyelitis/ chronic fatigue syndrome (ME/CFS), a multisystem disease, should target the pathophysiological aberrations (inflammatory and oxidative and nitrosative stress pathways), not the psychosocial "barriers" for a new equilibrium.

Maes M, Twisk FN.

Patient Educ Couns. 2010 Mar 17. [Epub ahead of print]
Maes Clinics, Belgium.

In a recent article published by B. van Houdenhove and P. Luyten it is claimed that cognitive behavioral therapy and graded exercise therapy (CBT/GET) are evidence based and are the most adequate treatments to control symptoms and improve quality of life of patients with myalgic encephalomyelitis/ chronic fatigue syndrome (ME/CFS). However, these authors do not disclose that their own treatments at the Belgian CFS Reference Centers with CBT/GET have proven to have no clinical effects. The Belgian minister declared in the parliament that CBT/GET at those centers are no curative therapies. Even more, measured by objective standards the CBT/GET approach has shown to be counterproductive. van Houdenhove and Luyten neglect or deny all scientific findings on the pathophysiology and possible medical treatments of ME/CFS. However, there is now a consensus that inflammatory and oxidative and nitrosative (IO&NS) pathways underpin the pathophysiology of ME/CFS in humans and in animal models as well. Human and animal data show that treatments which target IO&NS pathways are useful in treating ME/CFS. van Houdenhove and Luyten also propose that the time has come to shift treatment research in CFS from efficacy studies to effectiveness studies in 'real life'. In our opinion, future research should use a high throughput screening, made possible by the translational approach, in order to further examine the IO&NS pathways in detail; further delineate novel drug-targets in the IO&NS pathways and develop new drugs to treat this complex and serious medical disorder.

Medication-induced mitochondrial damage and disease.
Neustadt J, Pieczenik SR.
Montana Integrative Medicine, Bozeman, MT 59718, USA. drneustadt@gmail.com

Since the first mitochondrial dysfunction was described in the 1960s, the medicine has advanced in its understanding the role mitochondria play in health and disease. Damage to mitochondria is now understood to play a role in the pathogenesis of a wide range of seemingly unrelated disorders such as schizophrenia, bipolar disease, dementia, Alzheimer's disease, epilepsy, migraine headaches, strokes, neuropathic pain, Parkinson's disease, ataxia, transient ischemic attack, cardiomyopathy, coronary artery disease, chronic fatigue syndrome, fibromyalgia, retinitis pigmentosa, diabetes, hepatitis C, and primary biliary cirrhosis.

Medications have now emerged as a major cause of mitochondrial damage, which may explain many adverse effects. All classes of psychotropic drugs have been documented to damage mitochondria, as have stain medications, analgesics such as acetaminophen, and many others.

While targeted nutrient therapies using antioxidants or their precursors (e. g., N-acetylcysteine) hold promise for improving mitochondrial function, there are large gaps in our knowledge. The most rational approach is to understand the mechanisms underlying mitochondrial damage for specific medications and attempt to counteract their deleterious effects with nutritional therapies.

This article reviews our basic understanding of how mitochondria function and how medications damage mitochondria to create their occasionally fatal adverse effects.

In conclusion, staying from medication and finding the key to restoring health post ADRs is crucial. Doctors who risk their careers to expose this genocide should be taken seriously!!



Toxic Injury

According to toxicologists, varied and multiple toxicity symptoms will manifest from identical mechanism that is oxidization of endothelial cells.

Worth noting, the medical establishment is very quick at making judgments concerning toxicology of herbal remedies, but reluctant, even defiant about known adverse drug reactions (ADRS) and side effects ...

To recapitulate concerning the toxicology of Lariam/Mefloquine or other meds:

In general, pharmacologist accept that approximately, only 10% of meds are effective. Genetic variations, polymorphisms, biochemistry, ethnicity, weight, age, gender, body temperature, weather, etc ... all contribute to pharmacodynamics and pharmacokinetics. To date, it has not been possible to manufacture meds tailored for individuals precisely, because, there are so much that we don't know happening at cellular level.

The question here is why some don't react, rather, than, why we reacted? After all, Lariam/Mefloquine is toxic, as are fluoroquinolones and most meds.

The general consensus is that drug metabolism is unpredictable. http://tinyurl.com/yc6empe

DRUG METABOLISM/TRANSPORT

Nuclear Receptors and the Regulation of Drug-Metabolizing Enzymes and Drug Transporters: Implications for Interindividual Variability in Response to Drugs

Bradley L. Urquhart, PhD, Rommel G. Tirona, PhD and Richard B. Kim, MD

From the Division of Clinical Pharmacology, Department of Medicine (Dr Urquhart, Dr Tirona, Dr Kim), and the Department of Physiology & Pharmacology (Dr Tirona), University of Western Ontario, London, Ontario, Canada.

Division of Clinical Pharmacology, London Health Sciences Centre-University Hospital, Room ALL-152, 339 Windermere Road, London, Ontario N6A 5A5, Canada.

Erratic or unpredictable response to drugs remains a challenge of modern drug therapy. An important determinant of such interindividual differences in drug response is variability in the expression of drug-metabolizing enzymes and/or transporters at sites of absorption and/or tissue distribution. Variable drug-metabolizing enzyme and transporter expression can result in unpredictable exposure and tissue distribution of drugs and may manifest as adverse effects or therapeutic failure. In the past decade, important new insights have been made relating to the regulatory mechanisms governing the expression of drug-metabolizing enzymes and transporters by ligand-activated nuclear receptors. Specifically, there is compelling evidence to demonstrate that PXR, CAR, FXR, LXR, VDR, HNF4alpha, and AhR form a battery of nuclear receptors that regulate the expression of many important drug-metabolizing enzyme and transporters. In this review, the authors focus on clinically important drug-metabolizing enzymes such as CYP3A4, CYP2B6, CYP2C9, CYP2C19, UGT1A1, SULT2A1, and glutathione S-transferases and their regulation by nuclear receptors. They also review the nuclear receptor-mediated regulation of drug transporters such as MDR1, MRP2, MRP4, BSEP, BCRP, NTCP, OATP1B3, and OATP1A2. Finally, they outline how the drug development process has been affected by the current understanding of the involvement of nuclear receptors in the regulation of drug disposition genes.