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Monday, September 15, 2014

No Child Left Unmedicated: the Dumbing Down of America (and Canada)

Do you remember when "childhood" was..... childhood?  Do you  remember playing with toys, running through the neighborhood with your friends, climbing trees, using your imagination to create wonderful worlds to play in, laughing and singing and telling silly rhymes and jokes?  

Children are noisy, creative, imaginative, energetic, fun loving, little people.  THAT IS CHILDHOOD.

ADHD?  Children = fun,  "hyper"= energetic, "attention deficit" = is the fact that childrens minds are mobile, creative, imaginative, active.    







No Child Left Unmedicated


The pharmaceutical industry has completely taken over the treatment of medical and psychiatric treat,emt. Everything, and I am mean everything is geared towards getting every American on medication and keeping them on medication for the rest of their lives. There is no more vulnerable population, to this medical tyranny, than our children.
teen-screen-have-you-drugged-your-kid-todayThere is no greater example of this medical tyranny than the latest craze in unscientific psychiatric diagnostics than the brand new condition now being referred to as “Sluggish Cognitive Tempo” (SLT). I As a former mental health therapist, I can barely hold back my laughter at this thinly veiled attempt to separate parents from their hard earned money by making them think that the their perfectly normal child is mentally ill.

Sluggish Cognitive Tempo (lol)

This is a remarkably ridiculous name for an even more ludicrous diagnosis. The main characteristics of SLT  are vaguely described but include some combination of daydreaming, lethargy and slow mental processing, you know, like we do when we watch television.
The advocates of this diagnosis contend that SCT afflicts about two million children. And that great pharmaceutical whore, Eli Lilly, is waiting in the wings preparing to medicate the developing and highly vulnerable brains of these two million children with the latest in dangerous and mind-destroying psychotropic medications which will leave the user with a brain damaged future and a medical treatment history which will render many of these children with an uninsurable medical insurance future.
The Journal of Abnormal Child Psychology has sold its professional soul and its professional ethics to Big Pharma as it is seriously promoting this voodoo form of diagnostics. The latest issue of their publication donates a record 136 pages to the topic of SLT. And where do we find children with SLT? Probably standing next to the adults who have Restless Leg Syndrome.

The Diagnostic and Statistical Manual (DSM)-Edition IV & V

DSM is the Bible of mental illnesses. The book serves a training guide for graduate and the PhD students as well as serving as a professional guide for treatment intervention amongst mental health practitioners.
By the time a child is 21 years of age, under DSM -IV guidelines, 80% of all young adults  qualify to be diagnosed as mentally ill and, as such, are subject to being medicated.
The newest version of DSM has made this problem far worse. Normal temper tantrums have been turned into a diagnosable and pharmacologically treatable illness called ‘Disruptive Mood Dysregulation Disorder”. Normal adolescent rebellion is now being labeled as “Oppositional Defiant Disorder”. Normal childhood restlessness is now diagnosed as “ADHD” in children as early as two years of age.  Childhood Autism and childhood Bipolar Disorder are pharmaceutical goldmines and have increased forty fold in the last 20 years

The ADHD Scam

More than 10,000 American toddlers 2 or 3 years old are being medicated for attention deficit hyperactivity disorder outside established pediatric guidelines and professional medical practices, according to data recently presented by the Centers for Disease Control and Prevention.
According to the CDC, 11% of the country’s children are diagnosed with ADHD. This is ludicrous and is just not possible. These children have ADHD according to whom? The answer to this question consists of two parts. First, Big Pharma is using its influence to “push” the diagnostic criteria in the direction of many more positive diagnoses. More diagnoses means more profit-making pill pushing. Second, there is no illness, with these kinds of unsustainable rates of diagnosis that could impact the population to this degree. If there really were an 11% rate of autism in this country, we would be forced to change what is considered to be normal behavior since most mental illness models are loosely based upon a bell curve distribution. Therefore, just based on the surface evidence, these diagnostic rates cannot justified.
If these medications are dangerous for children, we would not know because very few scientific studies have examined the use of ADHD stimulant medications in young children. A widely referenced 2006 study found that the ADHD medication, methylphenidate, could “somewhat” mitigate ADHD like symptoms in preschoolers. However, the study’s conclusions were based on researched derived from insufficiently sized researched groups. Only about a dozen 3-year-olds were included in the study, and there were no 2-year-olds, yet we continue to medicate these young vulnerable minds. Most researchers on that study, sponsored by the National Institute of Mental Health, have significant financial ties to pharmaceutical companies that made ADHD medications.
A multitude of studies indicates that children who are prescribed psychotropic drugs are much more likely to become drug addicts as adults.

Parents Are the First Line of Defense


Continue reading HERE



Parents: Get the Facts—Know Your Rights

In the U.S. alone, nearly 9 million children are currently being prescribed psychiatric drugs—more than 1 million are under the age of five. Click image for complete breakdown
About ‘ADHD’ & Child Mental Disorders:
“Virtually anyone at any given time can meet the criteria for bipolar disorder or ADHD.  Anyone.  And the problem is everyone diagnosed with even one of these ‘illnesses’ triggers the pill dispenser.” — Dr. Stefan Kruszewski, Psychiatrist
Parents are quite simply not being given accurate information about psychiatric labels (mental disorders) or the drugs being prescribed to ‘treat’ their children. In the U.S.  alone, 10 million children are currently being prescribed psychiatric drugs—more than 1 million are  under the age of five (source: IMS health). :
These are the actual figures taken from IMS (to see breakdown on whatdrugs these children were prescribed click here.
Children on psychiatric drugs in the United States
0-1 Years                274,804
2-3 Years                370,778
4-5 Years                500,948
6-12 Years               4,130,340
13-17 Years             3,617,593
This is fact: There are no medical tests in existence that can prove ADHD or any other  mental disorder these children are being diagnosed and drugged for is a physical abnormality, brain dysfunction, chemical imbalance or genetic abnormality. Period.  Even the National Institute of Health Consensus (NIH) issued a statement admitting, “We do not have an independent, valid test for ADHD, and there is no data to indicate that ADHD is due to a brain malfunction.”......
....ABOUT PSYCHIATRIC DRUGS
Click image for more drug information
Common Psychiatric Drugs Being Given to Children Are Documented by International Drug Regulatory Agencies to Cause Heart Attack, Stroke, Diabetes, Hallucinations, Violence, Mania, Homicide, Aggression, Depression, Suicide and Death
This is not opinion. This is documented fact by international drug regulatory agencies. Parents are quite simply not given the documented facts about the psychiatric drugs prescribed for their children, yet it is their right to have full information about any drugs being prescribed their child. ADHD drugsAntidepressantsAntipsychoticsand Anti-Anxiety Drugs given to children, have been documented by hundreds of drug regulatory agencies to have severe and life-threatening side effects. Children are commonly prescribed drugs such as RitalinAdderall,ConcertaPaxilProzacCelexaZoloftLuvoxRisperdalSeroquel and parents are not given any warning on the known dangers of these drugs. It is for this reason that CCHR created a simple, easy to understand search engine on psychiatric drugs which provides documented side effects, drug warnings, studies and adverse reaction reports filed with the FDA in a simplified format.
ABOUT PSYCHIATRIC DISORDERS
Contrary to Popular Belief—The Doctor Doesn’t Always Know Best
The child drugging epidemic that has resulted in infants, toddlers, foster children, and a total of 20 million children on psychiatric drugs rests on one fraudulent premise; that mental disorders are biological “diseases” therefore justifying the administration of mind-altering drugs. The falsity of this premise is easily established by the fact that there is not one medical or scientific test that can prove any child has a mental disorder. Not one. Behaviors are not diseases and drugs are notmedication. This isn’t to say that children don’t have emotional or behavioral problems, it is saying that without evidence of disease—a physical disease—children are simply being drugged to change their behavior. Psychiatrists know this—they admit this, their own literature admits as much. But they like to keep these facts to themselves. For more information on psychiatric diagnosis, click here.

Continue reading HERE

Saturday, September 13, 2014

Independent Lab ‘Confirms Viral DNA in Merck Vaccine’




Independent Lab ‘Confirms Viral DNA in Merck Vaccine’

Christina Sarich
by 
September 6th, 2014
Updated 09/06/2014 at 10:25 pm

vaccine girl dna 263x164 Independent Lab Confirms Viral DNA in Merck Vaccine

Independent Lab Confirms Viral DNA in Merck VaccineMerck can say that Gardasil contains ‘no viral DNA’ all they want, but Dr. Sin Hang Lee had reported to the FDA just over two years ago that the vaccine contains fragments of DNA that shouldn’t be in something we give young women – so why is Gardasil still on the market?

After conducting extensive research, Dr. Lee found that in 100% of lab samples tested, fragments of HPV-11, HPV-16, and HPV-18 L1 DNA firmly attached to Merck’s proprietary aluminum adjuvant.

Even though SaneVax Inc reported their findings to the FDA, the controversial vaccine used to treat cervical cancer is still being sold, and the FDA states that ‘these fragments pose no health risk.’ Once again, the FDA has ignored science which proves that a drug created by a big pharmaceutical company is less than safe.

Dr. Lee also found that the HPV DNA fragments were not only bound to Merck’s proprietary aluminum adjuvant, but they had also adopted a non-B conformation, thereby creating a novel (new) chemical compound of unknown toxicity.

Furthermore, Non-B DNA conformations are known through Dr. Lee’s research to be associated with genetic abnormalities, as well as mutations which cause 70 serious diseases in human beings. Among them:

Follicular lymphomas
Polycystic kidney disease
Spermatogenic failure
Adrenoleukodystrophy
The FDA clearly should have investigated these claims by now, and at last put a temporary moratorium on Gardasil. But instead, the organization ignores the obvious possibility that Gardasil, as many have suspected, cause infertility problems and possibly even forms of cancer -the very disease that Gardasil is supposed to protect women against.

Instead of researching the possibility that the HPV vaccine was harming women, government officials and HPV vaccine supporters have been eager to discredit Dr. Lee’s research.

Fortunately, some industrious and intelligent people have come to Dr. Lee’s aid. Helen Petousis-Harris PhD, the Director of Immunisation Research and Vaccinology Immunisation Advisory Centre at The University of Auckland, gave a a public hearing on HPV vaccine safety in February 2014, in which she outlined the tactics of these agencies (through her own criticism) to discredit scientists that offer opposing facts to the Big Pharma propaganda line.

She argued that:

Dr. Lee’s tests were over-sensitive. (Interesting – if findings go a deeper level than the cursory three-week toxicity trials, they are considered aberrant).
No one else has replicated Dr. Lee’s findings. This is likely untrue, and what is more probable is that no one has been able to bring similar findings to the surface..
But, both of these ‘concerns’ were put to rest via data presented by Laurent Bélec at the 9th International Congress on Autoimmunity on March 26-30, 2014 in Nice, France. They published their findings in a paper titled, “Confirmation of the Creation of a Novel Molecule in Gardasil.”

“. . .Human papillomavirus (HPV) infection causes cervical cancer, a significant portion of anal, genital and oropharyngeal cancers, genital warts and recurrent respiratory papillomatosis. In June 2006, a prophylactic HPV vaccine (Gardasil®; Merck, NJ, USA) was licensed in the USA, with subsequent approval granted in the European Union. Gardasil® is a quadrivalent HPV protein-based vaccine containing genotype-specific L1 capsid proteins of HPV-16, HPV-18, HPV-6 and HPV-11 in the form of virus-like particles as the active ingredient, which are produced by a DNA recombinant technology in yeast.

Recently Lee SH showed that Gardasil® contained fragments of HPV-11 or HPV-18 DNA, evidenced by nested PCR, of unknown significance [J Inorg Biochem. 2012 Dec;117:85-92]. We herein looked by optimized single PCR in different batches of Gardasil® from France for HPV L1 DNA using MY09/MY11 degenerate and nondegenerate primers, for HPV E2 and E6 DNA genes, and for contaminating Saccharomyces cerevisiae DNA.

All amplified amplicons were sequenced and resulting FASTA sequences were analyzed by Genotyping software from NCBI. In-house quantitative single PCR using as external calibrator serial dilutions of HPV-16 DNA extracted from CaSki cell line allowed estimating the load of residual HPV DNA fragments in vaccine ampoules.

Preliminary data showed the presence of contaminating HPV L1 DNA in all tested different batches of Gardasil® vaccine from France. Our observations confirm independently and extend the previous observations by Lee SH, without using conflicting nested PCR detection possibly subjected to contamination. Persistence in muscle tissue of residual HPV DNA

Not only has another independent laboratory confirmed the findings of Dr. Lee in every Gardasil sample tested from France, this lab used a different and less ‘sensitive’ methodology to arrive at the same conclusion regarding Gardasil recombinant (genetically engineered) HPV DNA fragment contamination.

Co-authors

L. Belec1, H. Péré1, C. Fayard1.

1Microbiologie, Université Paris Descartes, Paris, France.”

Dr. Lee and Prof. Bélec and the SaneVax team indicate the need for further investigation for vaccine safety. Without even this minimum standard for vaccines, why should we trust the makers of the drugs or the agencies which allow for their distribution at all?