Dietrich Klinghardt Autism Conference in August
By Bryan Rosner on Jul 7, 2008 in Conferences & Events
Dr. Dietrich Klinghardt will be hosting an autism conference in August! This conference is sure to be very exciting and informative. Don’t miss it! To learn more, read the details of this post.
Autism 2008
August 8-10, 2008
The increase in new cases of children on the autistic spectrum is increasing at a staggering rate. Dr. Klinghardt has pioneered and developed many methods in the treatment of ASD which have found acceptance worldwide: the focus on heavy metal and chemical toxicity, simple and effective solutions to the vaccine issue, the dramatic improvements often observed after a single session of systematic family work (offered in group sessions) and others. The latest focus of Dr. Klinghardt’s work has been on the importance of recognizing and treating the devastating influence of pathogenic electromagnetic radiation during the intrauterine development of the fetus on the genes of the methylation cycle and other areas of the genome. Following the science published by the Institute of Building Biology in Germany, Dr. Klinghardt has developed a simple approach to diagnose ongoing exposure of the autistic child to illness producing “information-carrying radio waves” and household electromagnetic fields. By correcting influences at home and minimizing exposure of the child miracles are often possible. This workshop is practical and focuses on the immediate needs of the parents and children. It is equally recommended for affected parents and practitioners who want to achieve a level of excellence in this work.
Cost: $600
(Parents receive a 50% discount of $300)
On Aug 3, 2008, Kevin C. said:
Bryan,
I believe mycoplasma is the cause of autism. I believe mycoplasma reeks havoc on the immune system and causes all the other problems we see with children with autism, including the accumulation of heavy metals.
I would like someone to ask Dr. Klinghardt if he would be willing to examine an MMR vaccine with a Somatoscope to detect for the presence of mycoplasma.
I would like someone to ask Dr. Klinghardt that if the MMR vaccine does in fact contain mycoplasma, then can’t children with low PH levels be susceptible to autism and ask him if maybe all this genetic research looking for a genetic cause for autism is a big distraction to what is really a very simple issue?
My theory is that; Vaccines contain mycoplasma. Children with low PH are more susceptible to be affected by mycolasma.
Normal body PH is 7.4 and that is just above the acid range that many disease causing, acid loving, oxygen hating, bacteria love to thrive in.
Some kids that receive biomedical treatments recover, some don’t. Maybe the children with good PH recover and children with bad PH continue to suffer?
Maybe the very poor diets of fast food, processed food, and genetically altered foods that have become the main staples in children’s diets over the last 10 years have driven down their PH levels and low PH levels make them more susceptible to diseases or bullshit syndromes like autism?
On Oct 11, 2008, L. Lopez said:
Hi! I was just checking out a different website on autism and also came to the theory that mycoplasma might be the cause of infection for autism. Then I read this other person’s article, which came to the same idea.
I am currently under treatment for mycoplasma pneumonia. My levels are about three times as much as normal. My son - who is now 18 years old - has many autistic tendencies. Although not severe now, he had many years of difficulties when he was younger. Because he is not showing any respiratory problems now, the doctor has not tested him for mycoplasma.
I hope the doctor will soon decide that it is important for him and my husband to both be tested, as mycoplasma pneumonia is a contagious illness.
Please let me know what you think.
On Oct 11, 2008, Bryan Rosner said:
I would talk to Tami Duncan, http://www.liafoundation.org
Bryan
On Oct 27, 2008, Mike said:
Michael J. Goldberg, M.D., F.A.A.P.
5620 WILBUR AVENUE, SUITE 318
TARZANA, CALIFORNIA 91356
TELEPHONE (818) 343 - 1010
FAX (818) 343 - 6585
Email – office@neuroimmunedr.com
On the web: http://www.neuroimmunedr.com
Picture won’t paste see website
“What If THIS Isn’t Autism?”
Presently, we are in the midst of a major epidemic of children diagnosed with Autism (1 in 133 to 1 in 150).
“One picture is worth 1000 words”. The gray parts of a child’s brain below are normal. The bluish-green areas and some of the scattered small red areas are a vasculitis affected by a virus or the neuro-immune system itself, until proven otherwise. No ongoing toxic exposure of any kind to date shows this activity. It appears to be immune and / or viral mediated.
It is impossible to imagine any QUALITY OF LIFE in reality for any of these children, if we do not start addressing immediately this disease process with the tools we ALREADY have. This disease process is not a static encephalopathy or an untreatable developmental disorder.
While we are still researching and studying “Autism” as a developmental disorder, probably genetic disorder, in reality we can only be looking at a complex disease process occurring. We were all told back in Basic Science 101: “you cannot have an epidemic of a developmental or genetic disorder.” It is a hard fact of indisputable science. That means that while we may have genetic pre-dispositions, even new ideas of gene “inductions,” these are going to be medically within the emerging concept of “complex neuro-immune” and / or “complex viral”, not the OLD idea of fixed genetic or developmental disorder.
When Leo Kanner first described autism in 1943 he said “Briefly, the characteristic features consist of profound withdrawal from contact with people, an obsessive desire for the preservation of sameness, a skillful relation to objects, the retention of an intelligent and pensive physiognomy, and either mutism or the kind of language that does not seem intended to serve the purpose of interpersonal communication”. Since a hallmark of the disorder per Kanner is lack of social recognition, most characteristically expressed in the recurrent report of the child to assume an anticipatory posture upon being picked up, and of failure to adjust the body to that of the person holding him(like a sack of potato’s). So If your child was ever affectionate or hugged you or made eye contact that is not AUTISM. So what can it be then?
Most experts agree that the incidence of pediatric neurological dysfunctions (e.g., autism, ADD/ADHD, CFIDS) has increased at least four to five times in the last decade, an unsettling trend that deserves national attention. At this point, the vast majority of promising evidence connects many of these dysfunctions to the emerging inter-relationship of the neurological and immune systems. However, most of the existing efforts to date have focused on identifying the specific etiology of these dysfunctions prior to developing treatment options. While the ultimate etiology is a critical aspect of any search for a treatment, it is also critical that effective therapies be pursued at the same time to maximize the potential of the currently affected populations. History tells us that the pursuit of further clarification of etiology may take at least another seven to ten years or longer to derive new answers… especially sadly when many experts may be coming from the wrong concepts and directions of “etiology.”
During the early 1950s, more than 20,000 new cases of a disease were reported every year and in 1952 a record 57,628 cases were reported. These statistic amounts to 1 in every 1500 to 2000 child being diagnosed. That disease was Polio! Leaving 1.4 million survivors afflicted in this country. This was the largest fear of parents, the largest epidemic this country had every seen. Parents were literally afraid to go to sleep in fear of what they might wake-up too. What does that say when children can present at a ten time fold occurrence to that of Polio and NOBODY realizes this has to be a disease?
The researcher’s I work with and many others now believe that the “normal” timeline for change, will likely minimize the chances for this generation of children to ever rejoin mainstream society (a concern not expressed by those believing things like that are not going to happen, a potentially very mistaken concept). Pre-adolescent children with this disorder cannot wait seven to ten years for a treatment hypothesis to be formulated based upon research related to etiology, while as noted, still looking at the idea of etiology with unfortunately a 50 year plus, misdirection (developmental disorder). I am happy to say, I am involved in new efforts by which we hope to accelerate further clarification of pathologies and related treatment options and hope to make them available to this generation of children. We have decided to take this aggressive research approach because we believe that children with these disorders can fully recover with the appropriate interventions. The fundamental premise of the clinical hypothesis is that children with these disorders have dysfunctional, not permanently damaged, neurological systems.
The goal must be to expedite research and treatments in order to save thousands of children from a lower than necessary quality of life. The medical treatments must be complemented with suitable rehabilitative and educational interventions, as many of these children have missed years of development based upon their neurological dysfunction. To have any chance of this truly happening, parents must begin to join together, focus on the fact this is now more common than polio OR measles was in the 40s and 50s, and demand the same crisis, the same medical effort, the same research effort those children received. IF this is NOT Autism, we can not come to these answers by studying “Autism !”
On Feb 19, 2009, Dr Dietrich Klinghardt said:
Really Good work from Dr Dietrich Klinghardt.