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Showing posts with label children. Show all posts
Showing posts with label children. Show all posts

Saturday, December 15, 2012

Psychiatrist and children

Don't let your child see a psychiatrist. Ever
(NaturalNews) If you have a child, don't let him/her see a psychiatrist. Ever.

Read Mike Adams' new article about psychiatry. It's one of the best I've ever read, and I've been researching this pseudoscience for 20 years.

http://www.naturalnews.com

Then read this one, too. It's also excellent. I wrote it.

http://jonrappoport.wordpress.com/2012/02/27/the-liars-liar/




Yes, I know, I'm bragging, which is a sign of a mental disorder: Self-Inflation at the Expense of Sacred Psychiatry Disorder. The preferred treatment is electroshock therapy and MKULTRA re-programming. I'm opting for a walk in the park coupled with two doses of outrage at these fake doctors who poison brains and believe they're healers.

Here is a clue. The government gives psychiatry its fake legitimacy. That's how the game works. The government blesses the medical licensing boards that award psychiatrists permission to drug your children, alter their brains, poison them, and of course make all the fake diagnoses in the first place.

Without the government, these fakes would sink into the waves and be gone forever. Nobody in his right mind or wrong mind would ever step into a psychiatrist's office. It would be like volunteering to stumble out on to a mine field seeded with explosives.

Media, naturally, go along with the psychiatric hoax. Thousands of articles keep coming out of the hopper to support the authoritative pronouncements of these deranged monsters with medical degrees and "training" in diagnosing mental illnesses.

There are no mental illnesses or disorders. There never have been.

There are people with problems, there are people who suffer, there are people who are in desperate circumstances, there are people who have severe nutritional deficiencies, there are people who have been poisoned by various chemicals, there are people who have been abused and ignored, there are people who have been told there is something wrong with them, there are people who are different and can't deal with the conforming androids in their midst, but there are no mental disorders.

None.

It's fiction. It's a billion-dollar fiction. It's a gigantic steaming pile of bullshit. Always has been.

There is not a single diagnostic test for any so-called mental disorder. Never has been. No blood test, no urine test, no saliva test, no brain scan, no genetic test. No science.

http://jonrappoport.wordpress.com

So why hasn't psychiatry been destroyed and outlawed? Because there is money in it. Big money. Pharmaceutical money. And because the public is in a trance. Mothers and fathers are quite willing to take their children to these brain poisoners...lambs to the slaughter.

The silence of the lambs.

People are entranced by so-called professionals with fancy degrees who speak technical babble. It all seems real. Because if it weren't real, then...what? People would be forced to admit they are living in a fantasy. And people don't want to admit that. They would rather die than admit that.

But that's what psychiatry is. An elaborate fantasy. If every psychiatrist in the world vanished tomorrow, the world would immediately become a far healthier place.

If every celebrity who outrageously whores for psychiatry would stop on a dime, the world would be a far healthier place right away.

You think Dr. Phil is a fake? He's nothing compared to psychiatrists with their prescription pads. He's a saint by comparison. The drugs are brain poisons. If you really want to know the truth about the drugs, go to breggin.com and read everything Dr. Peter Breggin has ever written about the drugs. He covers the whole slimy waterfront.

There is some horrendous handwriting on wall. Believe me. You can see it all around you if you look. The shrinks are treating younger and younger children with the brain poisons, every day. They're diagnosing children who are practically toddlers and they're drugging them. They're ripping their brains. It's happening. You may not want to know about it, but it's there. It's a crime on the order of murder.

And the bastards at the FDA and the bastards who train doctors in medical schools are going along with it. They're accomplices to the ongoing crime. They have blood on their hands.

Here is a story Dr. Breggin told in his classic book, Toxic Psychiatry. It says it all:

"Roberta was a college student, getting good grades, mostly A's, when she first became depressed and sought psychiatric help at the recommendation of her university health service. She was eighteen at the time, bright and well motivated, and a very good candidate for psychotherapy. She was going through a sophomore-year identity crisis about dating men, succeeding in school, and planning a future. She could have thrived with a sensitive therapist who had an awareness of women's issues.

"Instead of moral support and insight, her doctor gave her Haldol. Over the next four years, six different physicians watched her deteriorate neurologically without warning her or her family about tardive dyskinesia [motor brain damage] and without making the [tardive dyskinesia] diagnosis, even when she was overtly twitching in her arms and legs. Instead they switched her from one neuroleptic to another, including Navane, Stelazine, and Thorazine. Eventually a rehabilitation therapist became concerned enough to send her to a general physician, who made the diagnosis [of medical drug damage]. By then she was permanently physically disabled, with a loss of 30 percent of her IQ.

"...my medical evaluation described her condition: Roberta is a grossly disfigured and severely disabled human being who can no longer control her body. She suffers from extreme writhing movements and spasms involving the face, head, neck, shoulders, limbs, extremities, torso, and back-nearly the entire body. She had difficulty standing, sitting, or lying down, and the difficulties worsen as she attempts to carry out voluntary actions. At one point she could not prevent her head from banging against nearby furniture. She could hold a cup to her lip only with great difficulty. Even her respiratory movements are seriously afflicted so that her speech comes out in grunts and gasps amid spasms of her respiratory muscles...Roberta may improve somewhat after several months off the neuroleptic drugs, but she will never again have anything remotely resembling a normal life."

If the smug scum who run the NY Times put THAT story on the front page right under a huge headline, we might see something good happen in this country.

Chronic whiners want to claim the government has to protect everybody all the time, as if that were possible, as if that were really the government's aim. These whiners are busy-bodies, meddlers, and self-made victims. They sometimes pose as scientists. They love psychiatry. They equate psychiatry with government. You know, "share and care."

They assert that government knows best. At bottom, they're vicious little idiots.

But they're very useful idiots, because the government welcomes their help in keeping the populace in line.

And psychiatry is a cardinal strategy in that regard.

Chemical straitjackets for the lambs.

The silence of the lambs.

Jon Rappoport
The author of an explosive collection, THE MATRIX REVEALED, Jon was a candidate for a US Congressional seat in the 29th District of California. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free emails at www.nomorefakenews.com


About the author:
The author of an explosive new collection, THE MATRIX REVEALED, Jon
was a candidate for a US Congressional seat in the 29th District of
California. Nominated for a Pulitzer Prize, he has worked as an
investigative reporter for 30 years, writing articles on politics,
medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine,
Stern, and other newspapers and magazines in the US and Europe. Jon
has delivered lectures and seminars on global politics, health, logic,
and creative power to audiences around the world.
www.nomorefakenews.com

Learn more: http://www.naturalnews.com/038348_psychiatry_quackery_medical_hoax.html#ixzz2F7lwB3V7

Monday, September 3, 2012

Autistic children


Do autistic children have 'starving brains?'


(NaturalNews) McCandless' position in her book, "Children with Starving Brains: A Medical Treatment Guide for Autism Spectrum Disorder," is that ASD is a complex syndrome based on physiological and biochemical disorders that have as a common end-point the cognitive and emotional impairment that we generally associate with autism. In other words, aside from rare genetic cases such as an autism derived from Fragile X syndrome, it has become evident that these are physically ill children who can be greatly helped medically, behaviorally, and cognitively by proper diagnosis and treatment of their underlying medical conditions. This is a vital breakthrough in understanding and one that many practitioners have had a hard time grasping. In the past, autism and other conditions in the autism spectrum were considered "psychiatric" or behavior disorders, with only psychiatric or behavioral approaches considered as appropriate treatments. Consequently, since they are physically ill, affected children require an all-encompassing, natural intervention to maximize their healing potential.



Studies have shown that ASD children, compared to controls with neurotypical children, report higher occurrences of the following nutrient levels:

• Increased serum copper
• Magnesium deficiency
• Increased copper/zinc ratios
• Iron deficiency
• Increased glutamate
• Zinc deficiency
• Decreased vitamin B6
• B12 deficiency
• Decreased plasma sulphate
• Calcium deficiency
• Decreased methionine
• Fatty acid deficiencies
• Decreased glutamine
• Inadequate vitamins A, D, and E
• Decreased amino acids tyrosine, carnosine, lysine, hydroxylysine

Many experts have further noted that several common factors are seen in most ASD patients; namely, impaired immunity, GI inflammation, higher infection rate and subsequent increased use of antibiotics, impaired nutritional status, maldigestion/malabsorption, and decreased ability to metabolize toxins like heavy metals and pathogens. The crux of the all-encompassing, natural intervention model; therefore, is to restore proper brain function by balancing the nutrients above. This can be done in a variety of ways; namely nutrition, supplements, chiropractic, acupuncture, etc. This approach, though, has been criticized by the medical model because it apparently takes longer than other modalities and may not be as complete with older children since biochemical abnormalities and toxic conditions have already become a part of their cellular functioning and are therefore harder to change. The "golden window" of opportunity, they contend, has been suggested to be between 18 months and five years of age, though it is never too late to initiate care. Many older children and adults have experienced dramatic results as well.

This criticism from the medical community is false. Research is full of evidence-based, "natural" interventions that have dramatic, rapid results. If you suspect your child has autism, contact your natural health care provider as soon as possible.

Sources for this article include:

McCandless, J. Children with starving brains: a medical treatment guide for autism spectrum disorder 2nd ed. Bramble Books, Putney. 2003.

Guliani K, Rubin D. Improvements in developmental delay, colic, and GERD in a Child Undergoing Chiropractic Care: A Case Report and Review of Literature. J Pediatr Matern & Fam Health Chiropr 2012; 1:online access only (4 pages).

Benach JL, Li E, McGovern MM. A microbial association with autism. MBio. 2012;3(1).
Jyonouchi H, Geng L, Ruby A, Reddy C, Zimmerman-Bier B. Evaluation of an association between gastrointestinal symptoms and cytokine production against common dietary proteins in children with autism spectrum disorders. J Pediatr. 2005;146(5):605-10.

Ibrahim SH, Voigt RG, Katusic SK, Weaver AL, Barbaresi WJ. Incidence of gastrointestinal symptoms in children with autism: a population-based study. Pediatrics. 2009;124(2):680-6.

Scelfo TA, Chelenyak PL. Resolution of autistic symptoms in a child undergoing chiropractic care to correct vertebral subluxations: A case study: case report. J Pediatr Matern & Fam Health Chiropr 2011; 4:106-110.

About the author:
Eric is a peer-reviewed, published researcher. His work on heart disease and autism has been accepted internationally at various scientific conferences through organizations like the American Public Health Association and Australian-based Baker IDI Heart and Diabetes Institute. The mission he shares with his wife, Sabrina, is to help people achieve their God-given potential in what they have coined The 7 Key Areas to Abundant Living: Both Eric and his wife are Life Coaches specializing in helping people overcome cognitive disorders like ADD/ADHD naturally. Visit his blog. Track his work on facebook. Read Eric's other naturalnews.com articles.

Learn more: http://www.naturalnews.com/037046_autistic_children_starving_brains_medical_treatment.html#ixzz25QQEIPnJ

Monday, July 30, 2012

Alternating hemiplegia of childhood (AHC)


Gene Discovery Set to Help With Mysterious Paralysis of Childhood

ScienceDaily (July 29, 2012) — Alternating hemiplegia of childhood (AHC) is a very rare disorder that causes paralysis that freezes one side of the body and then the other in devastating bouts that arise at unpredictable intervals. Seizures, learning disabilities and difficulty walking are common among patients with this diagnosis.

http://icare4autism.files.wordpress.com/2008/11/gene_system.jpg?w=71&h=96

Researchers at Duke University Medical Center have now discovered that mutations in one gene cause the disease in the majority of patients with a diagnosis of AHC, and because of the root problem they discovered, a treatment may become possible.
The study was published online on July 29 in Nature Genetics.
AHC is almost always a sporadic disease, which means that typically no one else in the family has the disease, said Erin Heinzen, Ph.D., co-author of the study and Assistant Professor of Medicine in the Section of Medical Genetics. "Knowing that we were looking for genetic mutations in children with this disease that were absent in the healthy parents, we carefully compared the genomes of seven AHC patients and their unaffected parents. When we found new mutations in all seven children in the same gene we knew we had found the cause of this disease."
All of the mutations were found in a gene that encodes ATP1A3, one piece of a key transporter molecule that normally would move sodium and potassium ions across a channel between neurons (nerve cells) to regulate brain activity.
In a remarkably broad international collaborative effort, the authors partnered with three family foundations (USA, Italy and France), including scientists from 13 different countries, to study an additional 95 patients and showed over 75 percent had disease-causing mutations in the gene for ATP1A3.
"This study is an excellent example of how genetic research conducted on a world-wide scale really can make a difference for such a rare disorder as AHC," said Arn van den Maagdenberg, Ph.D., and co-author on the study and geneticist from Leiden University Medical Centre in the Netherlands. "It truly was an effort from many research groups that led to this remarkable discovery."
"This kind of discovery really brings home just what the human genome project and next-generation sequencing have made possible," said David Goldstein, Ph.D., Director of the Duke Center for Human Genome Variation and co-senior author on the study. "For a disease like this one with virtually no large families to study, it would have been very difficult to find the gene before next-generation sequencing.
"Ideally what you want from a study like this is a clear indication of how the mutations change protein function so you know how to screen for drugs that will restore normal function or compensate for the dysfunction," said Goldstein, who is also a Professor in Duke Molecular Genetics and Microbiology. "While there is considerably more work to do, our initial evaluation of the mutations suggests that they may alter the behavior of the transporter pump as opposed to reducing its activity, as do other mutations in the gene that cause a less severe neurological disease."
Co-senior author Mohamad Mikati, M.D., Professor of Pediatrics and of Neurobiology, and Chief of Pediatric Neurology at Duke, said, "Many years ago my work with other collaborators on a family with this disease proved that AHC can be caused by genetic factors, but until now we did not know the underlying gene abnormality.
"The finding that ATP1A3 mutations cause AHC will increase awareness of the disease and the ability to accurately diagnose patients," Mikati said. "While it may take a while for novel drugs to be developed to better treat this disease, we will see an immediate impact through specific testing for mutations in this gene when we suspect a case of AHC. This direct testing will prevent misdiagnoses that too often have caused patients to be treated with inappropriate medications."
Other authors worked at the University of Utah, Salt Lake City; Università Cattolica Sacro Cuore, Rome; UPMC Univ Paris, INSERM, CNRS and Groupe Hospitalier de la Pitié-Salpêtrière, in Paris; Leiden University Medical Centre, Leiden, The Netherlands; University of Melbourne, Melbourne, Australia; University Hospitals of Lyon, France; University of Chicago, Illinois; University of California, San Francisco; Rijnland Hospital, Leiderdorp, The Netherlands; Sydney Children's Hospital, Randwick, and University of Sydney, New South Wales, Australia; Royal Hobart Hospital, Hobart, Australia; Our Lady's Children's Hospital, Crumlin, and the Childrens University Hospital, Dublin, Ireland; Rigshospitalet, University of Copenhagen; CRNL, CNRS INSERM, in Lyon, France; and UCL Institute of Neurology, London.
Story Source:
The above story is reprinted from materials provided byDuke University Medical Center.
Note: Materials may be edited for content and length. For further information, please contact the source cited above.

Journal Reference:
  1. Erin L Heinzen et al. De novo mutations in ATP1A3 cause alternating hemiplegia of childhoodNature Genetics, 2012; DOI: 10.1038/ng.2358