Posted on 02/25/2004 11:31:26 AM PST by Coleus
CDC Vaccine Data Leads Scientists to Shocking Discovery
Monday February 9, 9:20 am ET
The findings are not only disturbing to government officials like U.S. Rep. Dave Weldon, M.D. (R-FL), who is also scheduled to speak before the IOM panel, they suggest autism via TCVs has a higher relative risk than that between lung cancer and smoking, which according to the American Cancer Society is only 22 for men and 11 for women. "This absolutely confirms what parents have been saying for years," says Jo Pike, President, National Autism Association. Like Pike, thousands of parents have reported sharp regressions in their children following a TCV and many of those children have gone on to receive a label of autism. An easy mistake to make since the symptoms of autism and mercury poisoning are almost identical.
Dr. Mark Geier is the lead investigator in the discovery. A medical doctor with a Ph.D. in genetics, he, along with fellow researcher, David Geier, will discuss their findings of the CDC data in front of an IOM panel. Among a host of other physicians and researchers presenting will be Dr. Jeff Bradstreet. He will discuss the results from his peer-reviewed study which concluded that urinary mercury concentrations were six times higher in children with autism vs. normal-age/vaccine-matched controls.
The presentations will begin at 8:00 AM at The National Academy of Sciences, Auditorium 2100 C Street NW. Dr. Mark Geier and David Geier are scheduled to present their findings at 12:15 PM. Weldon speaks at 8:00. Bradstreet at 4:00. For an agenda, go to: http://www.iom.edu/event.asp?id=17047. For information about the National Autism Association, go to www.nationalautism.org.
Like this....
Table A:
Summary Comparison of Characteristics
of Autism & Mercury Poisoning
Mercury Poisoning |
Autism |
|
Psychiatric | Social deficits, shyness, social withdrawal | Social deficits, social withdrawal, shyness |
Disturbances | Depression, mood swings; mask face | Depressive traits, mood swings; flat affect |
Anxiety | Anxiety | |
Schizoid tendencies, OCD traits | Schizophrenic & OCD traits; repetitiveness | |
Lacks eye contact, hesitant to engage others | Lack of eye contact, avoids conversation | |
Irrational fears | Irrational fears | |
Irritability, aggression, temper tantrums | Irritability, aggression, temper tantrums | |
Impaired face recognition | Impaired face recognition | |
Speech, | Loss of speech, failure to develop speech | Delayed language, failure to develop speech |
Language & | Dysarthria; articulation problems | Dysarthria; articulation problems |
Hearing | Speech comprehension deficits | Speech comprehension deficits |
Deficits | Verbalizing & word retrieval problems | Echolalia; word use & pragmatic errors |
Sound sensitivity | Sound sensitivity | |
Hearing loss; deafness in very high doses | Mild to profound hearing loss | |
Poor performance on language IQ tests | Poor performance on verbal IQ tests | |
Sensory | Abnormal sensation in mouth & extremities | Abnormal sensation in mouth & extremities |
Abnormalities | Sound sensitivity | Sound sensitivity |
Abnormal touch sensations; touch aversion | Abnormal touch sensations; touch aversion | |
Vestibular abnormalities | Vestibular abnormalities | |
Motor Disorders | Involuntary jerking movements arm flapping, ankle jerks, myoclonal jerks, choreiform movements, circling, rocking | Stereotyped movements - arm flapping, jumping, circling, spinning, rocking; myoclonal jerks; choreiform movements |
Deficits in eye-hand coordination; limb apraxia; intention tremors | Poor eye-hand coordination; limb apraxia; problems with intentional movements | |
Gait impairment; ataxia from incoordination & clumsiness to inability to walk, stand, or sit; loss of motor control | Abnormal gait and posture, clumsiness and incoordination; difficulties sitting, lying, crawling, and walking | |
Difficulty in chewing or swallowing | Difficulty chewing or swallowing | |
Unusual postures; toe walking | Unusual postures; toe walking | |
Cognitive Impairments | Borderline intelligence, mental retardation - some cases reversible | Borderline intelligence, mental retardation - sometimes "recovered" |
Poor concentration, attention, response inhibition | Poor concentration, attention, shifting attention | |
Uneven performance on IQ subtests | Uneven performance on IQ subtests | |
Verbal IQ higher than performance IQ | Verbal IQ higher than performance IQ | |
Poor short term, verbal, & auditory memory | Poor short term, auditory & verbal memory | |
Poor visual and perceptual motor skills, impairment in simple reaction time | Poor visual and perceptual motor skills, lower performance on timed tests | |
Difficulty carrying out complex commands | Difficulty carrying out multiple commands | |
Word-comprehension difficulties | Word-comprehension difficulties | |
Deficits in understanding abstract ideas & symbolism; degeneration of higher mental powers | Deficits in abstract thinking & symbolism, understanding others mental states, sequencing, planning & organizing |
(iv)
Unusual |
Stereotyped sniffing (rats) | Stereotyped, repetitive behaviors |
Behaviors | ADHD traits | ADHD traits |
Agitation, unprovoked crying, grimacing, staring spells | Agitation, unprovoked crying, grimacing, staring spells | |
Sleep difficulties | Sleep difficulties | |
Eating disorders, feeding problems | Eating disorders, feeding problems | |
Self injurious behavior, e.g. head banging | Self injurious behavior, e.g. head banging | |
Visual | Poor eye contact, impaired visual fixation | Poor eye contact, problems in joint attention |
Impairments | "Visual impairments," blindness, near-sightedness, decreased visual acuity | "Visual impairments"; inaccurate/slow saccades; decreased rod functioning |
Light sensitivity, photophobia | Over-sensitivity to light | |
Blurred or hazy vision | Blurred vision | |
Constricted visual fields | Not described | |
Physical Disturbances | Increase in cerebral palsy; hyper- or hypo-tonia; abnormal reflexes; decreased muscle strength, especially upper body; incontinence; problems chewing, swallowing, salivating | Increase in cerebral palsy; hyper- or hypotonia; decreased muscle strength, especially upper body; incontinence; problems chewing and swallowing |
Rashes, dermatitis/dry skin, itching; burning | Rashes, dermatitis, eczema, itching | |
Autonomic disturbance: excessive sweating, poor circulation, elevated heart rate | Autonomic disturbance: unusual sweating, poor circulation, elevated heart rate | |
Gastro-intestinal | Gastroenteritis, diarrhea; abdominal pain, constipation, "colitis" | Diarrhea, constipation, gaseousness, abdominal discomfort, colitis |
Disturbances | Anorexia, weight loss, nausea, poor appetite | Anorexia; feeding problems/vomiting |
Lesions of ileum & colon; increased gut permeability | Leaky gut syndrome | |
Inhibits dipeptidyl peptidase IV, which cleaves casomorphin | Inadequate endopeptidase enzymes needed for breakdown of casein & gluten | |
Abnormal Biochemistry | Binds -SH groups; blocks sulfate transporter in intestines, kidneys | Low sulfate levels |
Has special affinity for purines & pyrimidines | Purine & pyrimidine metabolism errors lead to autistic features | |
Reduces availability of glutathione, needed in neurons, cells & liver to detoxify heavy metals | Low levels of glutathione; decreased ability of liver to detoxify heavy metals | |
Causes significant reduction in glutathione peroxidase and glutathione reductase | Abnormal glutathione peroxidase activities in erythrocytes | |
Disrupts mitochondrial activities, especially in brain | Mitochondrial dysfunction, especially in brain | |
Immune Dysfunction | Sensitivity due to allergic or autoimmune reactions; sensitive individuals more likely to have allergies, asthma, autoimmune-like symptoms, especially rheumatoid-like ones | More likely to have allergies and asthma; familial presence of autoimmune diseases, especially rheumatoid arthritis; IgA deficiencies |
Can produce an immune response in CNS | On-going immune response in CNS | |
Causes brain/MBP autoantibodies | Brain/MBP autoantibodies present | |
Causes overproduction of Th2 subset; kills/inhibits lymphocytes, T-cells, and monocytes; decreases NK T-cell activity; induces or suppresses IFNg & IL-2 | Skewed immune-cell subset in the Th2 direction; decreased responses to T-cell mitogens; reduced NK T-cell function; increased IFNg & IL-12 |
(v)
CNS Structural Pathology | Selectively targets brain areas unable to detoxify or reduce Hg-induced oxidative stress | Specific areas of brain pathology; many functions spared |
Damage to Purkinje and granular cells | Damage to Purkinje and granular cells | |
Accummulates in amygdala and hippocampus | Pathology in amygdala and hippocampus | |
Causes abnormal neuronal cytoarchitecture; disrupts neuronal migration & cell division; reduces NCAMs | Neuronal disorganization; increased neuronal cell replication, increased glial cells; depressed expression of NCAMs | |
Progressive microcephaly | Progressive microcephaly and macrocephaly | |
Brain stem defects in some cases | Brain stem defects in some cases | |
Abnormalities in Neuro-chemistry | Prevents presynaptic serotonin release & inhibits serotonin transport; causes calcium disruptions | Decreased serotonin synthesis in children; abnormal calcium metabolism |
Alters dopamine systems; peroxidine deficiency in rats resembles mercurialism in humans | Possibly high or low dopamine levels; positive response to peroxidine (lowers dopamine levels) | |
Elevates epinephrine & norepinephrine levels by blocking enzyme that degrades epinephrine | Elevated norepinephrine and epinephrine | |
Elevates glutamate | Elevated glutamate and aspartate | |
Leads to cortical acetylcholine deficiency; increases muscarinic receptor density in hippocampus & cerebellum | Cortical acetylcholine deficiency; reduced muscarinic receptor binding in hippocampus | |
Causes demyelinating neuropathy | Demyelination in brain | |
EEG | Causes abnormal EEGs, epileptiform activity | Abnormal EEGs, epileptiform activity |
Abnormalities/ | Causes seizures, convulsions | Seizures; epilepsy |
Epilepsy | Causes subtle, low amplitude seizure activity | Subtle, low amplitude seizure activities |
Population | Effects more males than females | Male:female ratio estimated at 4:1 |
Charact-eristics | At low doses, only affects those geneticially susceptible | High heritability - concordance for MZ twins is 90% |
First added to childhood vaccines in 1930s | First "discovered" among children born in 1930s | |
Exposure levels steadily increased since 1930s with rate of vaccination, number of vaccines | Prevalence of autism has steadily increased from 1 in 2000 (pre1970) to 1 in 500 (early 1990s), higher in 2000. | |
Exposure occurs at 0 - 15 months; clinical silent stage means symptom emergence delayed; symptoms emerge gradually, starting with movement & sensation | Symptoms emerge from 4 months to 2 years old; symptoms emerge gradually, starting with movement & sensation |
Actually, there IS scientific evidence that refutes the link between autism and MMR vaccine/mercury.
I can certainly sympathise with this. However, it is incredibly easy to phony up statistical cases that sound plausible but really don't prove anything. Research on these subjects is ongoing and will eventuall reveal the truth. I already know that there is a net benefit for immunizations; the unknown factor is how much the risks can be reduced.
I said some time ago that I wanted to bow out of this discussion, and now I will reveal why. My father was a state health officer for thiry years and back in the fifties was offered the directorship of CDC. He turned it down because he didn't want to move the family to Atlanta. I might add that at that time the post was not quite as well known or prestigeous as it is now.
But I grew up hearing statistics at breakfast and dinner. There was a time when I could recite the number of cases of a dozen diseases, along with their trend lines. I'm sorry if I offend anyone, but I simply have no respect for folks who question the motivation of medical researchers. I've known these people all my life.
So by your own post you admit some mercury is still in some vaccines. ALL IS AN ABSOLUTE. TRACE AMOUNTS are an AMOUNT. by your own post Jim you refute your position:"All routinely recommended licensed vaccines that are currently being manufactured for children in the U.S. (except influenza) contain no thimerosal or only trace amounts." "Except....trace amounts". Seems like ALL does not apply to these preservatives.
The FR is getting annoying with people parsing the truth like Clinton on almost any subject.
I have not been part of the crowd that is blaming this preservative for everything from acne to liberalism. Lets face it, give something to a million people and you will have no reaction to X percentage, a positive reaction to Y percentage, a negative reaction to Z percent. In a million other people those same reactions, albeit more than likely not in the same percentage, will occur due to genes or other environmental conditions. Researchers simply try to look for a deviation from the norm.
I prefer to look at the benefit to damage ratio of most things. IE: Asbestos has saved more lives then it killed. Fortunately we have discovered better methods but at the time it was the best we had. (I'm sure that will get parsed).
This "yahoo article", as you refer to it, is a PRESS RELEASE. As for the "scientific conference", what exactly is that? Just because someone has a "scientific conference", does that automatically validate as true the material being presented? I can have a "scientific conference" at my house this weekend, give it a fancy name such as The Institute for Lunar Studies and announce that the moon is really made of green cheese. That doesn't mean that it's true, but it sure makes it sound legitimate.
As for you doubting the existence of legitimate scientific research refuting the MMR/Mercury/Autism link, here is a specific study that refutes the link. Note that since removing the mercury-based preservative from the vaccine, the Autism occurance has INCREASED, not decreased. Sign up for an account at www.medscape.com (I'm fairly sure it's still free) and search both Medscape and Medline; there's plenty of research abstracts available on the subject.
Thimerosal and the occurrence of autism: negative ecological evidence from Danish population-based data.
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Pediatrics 2003 Sep;112(3 Pt 1):604-6 (ISSN: 1098-4275)
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Madsen KM; Lauritsen MB; Pedersen CB; Thorsen P; Plesner AM; Andersen PH; Mortensen PB
Danish Epidemiology Science Centre, Department of Epidemiology and Social Medicine, University of Aarhus, Denmark. kmm@dadlnet.dk. |
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OBJECTIVE: It has been suggested that thimerosal, a mercury-containing preservative in vaccines, is a risk factor for the development of autism. We examined whether discontinuing the use of thimerosal-containing vaccines in Denmark led to a decrease in the incidence of autism. DESIGN: Analysis of data from the Danish Psychiatric Central Research Register recording all psychiatric admissions since 1971, and all outpatient contacts in psychiatric departments in Denmark since 1995. PATIENTS: All children between 2 and 10 years old who were diagnosed with autism during the period from 1971-2000. OUTCOME MEASURES: Annual and age-specific incidence for first day of first recorded admission with a diagnosis of autism in children between 2 and 10 years old. RESULTS: A total of 956 children with a male-to-female ratio of 3.5:1 had been diagnosed with autism during the period from 1971-2000. There was no trend toward an increase in the incidence of autism during that period when thimerosal was used in Denmark, up through 1990. From 1991 until 2000 the incidence increased and continued to rise after the removal of thimerosal from vaccines, including increases among children born after the discontinuation of thimerosal. CONCLUSIONS: The discontinuation of thimerosal-containing vaccines in Denmark in 1992 was followed by an increase in the incidence of autism. Our ecological data do not support a correlation between thimerosal-containing vaccines and the incidence of autism.
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Indexing Check Tags: Female; Human; Male; Support, Non-U.S. Gov't
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Language: English
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MEDLINE Indexing Date: 200310
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Publication Type: Owner: NLM
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Publication Type: Journal Article; Multicenter Study
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PreMedline Identifier: 0012949291
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Journal Code: AIM; IM
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AMEN!!!
It is hard to have a rational discussion with people who believe it is all or nothing. Most medications, vaccines have side effects. Some are mild others are devastating. Most will not see any side effect (assuming a properly researched medication).
Depending on what ailment is being treated or possibly prevented, we all need to make that educated decision to take the risk for the possible gains. If it is all or nothing, you cannot make an educated decision
Do I understand that the MMR is a live vaccine? If so, is it true that it would not ever have had the thimerosal preservative in it?
The 2nd MMR shot gave my daughter a very bad reaction (extremely high fever and febrile seizures) but she is fine, 15 years old and doing well in school.
Our second child is an in-family adoption, the child of my late sister. We have noted developmental problems with him ever since we adopted him at age 2 - late talking, coordination, eye contact, etc. He has been under a psychiatrist's care since age 4, and while he is not full blown autistic he exhibits some of the symptoms and is probably Asperger's. But here are my three observations:
1. He is improving. Puberty has been a real benefit for him, he is more socially adept, his schoolwork has improved (he is in a special school for ADD/LD children), and he is just easier to live with all round. Since he's very bright, he should be able to catch up and live an essentially normal life.
2. My sister was a lot more "geeky" than I am - very science and math focussed and looking back I can see in retrospect that she exhibited a lot of autistic/Asperger's type traits. She married a man who really was a poster child for Geeks Anonymous. So if there's a genetic component you would expect it to be concentrated in their child, and that appears to be the case.
3. This is the real kicker -- I found out at my son's yearly checkup in December that he never got his MMR! In all the uproar and confusion leading up to my sister's death he apparently never got taken to the pediatrician. We have heard the stories and followed the discussion here on FR with respect to the vaccine, and had been wondering all these years if somehow the vaccine was responsible for some of my son's troubles. Apparently not.
As for the Hep B vaccine's safety, I've personally administered hundreds of Hep B vaccines to children, and have yet to see ANY adverse reaction from it, so it's probably a very safe vaccine (which is also supported by research on the vaccine).
I can only imagine what it is like to have a child with autism, and I can understand your hesitancy regarding vaccines. For what it's worth, I'm an RN in a large outpatient pediatric clinic at a medical center/teaching hospital. One of the doctors I have worked with is a Neurodevelopmental Pediatrician (neurodevelopmental peds is a specialty dealing with disorders such as autism, learning disorders, ADHD, pervasive developmental disorder, etc.). Needless to say, a large part of his practice involves autistic children (up until recently, there haven't been many specialists for autism). I have discussed with him at length the vaccine/autism "link", and he contends there is no link whatsoever based on current scientific evidence. Unfortunately, the cause of autism is unknown.
As for vaccines in general, current vaccines are safe and effective. Does that mean that 100%? No. There will always be that 1 in a million person who may have a serious reaction to a vaccine. But the risk of the vaccines are still much lower than the risk of the diseases they are preventing. I have personally seen a child with Tetanus early in my career, and it's not pretty (imagine the pain of labor only multiply that 10 fold; he ended up on a ventilator for several days on chemical paralysis and sedation; he did eventually get better). I've also taken care of numerous children with Hib meningitis (this was common prior to Hib vaccine). Many of these kids developed complications such as seizure disorders, hearing loss, and even mental retardation due to the meningitis. Had the vaccine been available at the time, they wouldn't have gotten meningitis (it's rare to see Hib meningitis these days). As for these diseases still being present, they are. We still have whole populations in this country who don't get vaccinated (the Amish), so the organisms and people who develop the diseases are still out there. My point in all of this is so that you keep an open mind, make informed decisions, and try to do what's best for your children.
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