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The Shaken Baby Syndrome Myth
renamed "Abusive Head Trauma" or "Non-Accidental Injury"

WAS

SBS: EVERTHING IS BROKEN

* SBS began as an unproven theory and medical opinions, now discredited by biomechanical engineering studies
* No DIFFERENTIAL DIAGNOSIS done to eliminate other causes, abuse assumed without evidence
* Shaken Baby diagnostic symptoms not caused by shaking
* Child protective agencies snatch children, destroy families based on medical accusations without proof of wrong-doing
*Poor or deceptive police investigations, falsified reports, perjured testimony threaten legal rights, due process
* Prosecutors seek "victory", over justice; defense attorneys guilty of ineffective counsel, ignorance, lack of effort
* Care-takers threatened, manipulated, in order to force plea bargains, false confessions
* A fractured criminal justice system--a big piece for the rich, a small piece for the poor, and none for alleged SBS cases.

1. SBS "MYTH" WEBSITE SUMMARY 
2. ARTICLE ABOUT PEDIATRIC ACADEMY SBS FRAUD

3. SUMMARIZED HISTORY OF THE SHAKEN BABY SYNDROME THEORY
4. POLICE ASSAULT: PROTESTING FOR A POLYGRAPH --DJT


Related websites/ important people and projects ShakenBabySyndrome/Vaccines/YurkoProject
CHRISTINA ENGLAND: BOOK
"Shaken Baby Syndrome or Vaccine Induced Encephalitis-- Are Parents Being Falsely Accused?" by Dr Harold Buttram, with Christina England (WEBSITE)
Evidence Based Medicine and Social Investigation:
EBMSI conferences, resources and information Articles and Reports
VacTruth: Jeffry Aufderheide; The SBS conection and other dangerous or deadly side effects of vaccination 

Vaccinefraud.com/The true, suppressed history of the smallpox vaccine fraud and other books:
Patrick Jordan
On SBS:
Sue Luttner, must-read articles and information on Shaken Baby Syndrome: her resources link
The Amanda Truth Project: Amanda's mother speaks out at symposium
Tonya Sadowsky


SUBJECT: SHAKEN BABY SYNDROME: DR. JOHN CAFFEY'S FIRST ARTICLE IN 1972, ACCUSING CARETAKERS OF VIOLENT SHAKING WITH MANY LEVELS OF INJURY
  1. Radiologist Dr. John Caffey's first article in 1972 linking certain injuries or conditions to suspected shaking abuse, particularly unexplained fractures with no external signs of trauma
  2. 1974:John Caffey, Radiologist: Whiplash-shaken Baby Syndrome  #caffey74
  3. Caffey Revisited: A critical look at Dr. Caffey's findings and lack of differential diagnosis to eliminate other causes before making a conclusion of child abuse by internationally-known Dr. C.A.B. Clemetson, MD

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2.) 1974 Article:John Caffey, Radiologist: Whiplash-shaken Baby Syndrome  #caffey74


3.)

Caffey Revisited: A Commentary on the Origin of
“Shaken Baby Syndrome”

Clemetson on Caffey

C. Alan B. Clemetson, M.D.
Journal of American Physicians and Surgeons Volume 11 Number 1 Spring 2006

ABSTRACT

Caffey is often cited as the source of the diagnosis of “shaken baby syndrome” (SBS). Once the “classic” findings attributed to SBS are identified, it is rare for a differential diagnosis to be considered.

Caffey focused on radiologic findings, but while he was aware of the possible diagnosis of scurvy, the radiologic signs of infantile scurvy may not have had sufficient time to develop. Other findings in his cases were compatible with scurvy due to toxic histaminemia, which can cause capillary fragility, retinal petechiae, and subdural hematoma. Although dietary vitamin C deficiency is very rare today in our country, both vitamin C deficiency and toxic histaminemia can accompany systemic infection. Toxic histaminemia may also occur following immunizations.

Skeletal Findings in Caffey's Cases

In 1946, John Caffey, a radiologist, described multiple fractures in the long bones of infants suffering from chronic subdural hematoma. None of the parents reported any knowledge of falls or physical injury, but Caffey suspected child abuse to explain the injuries.

Following this retrospective, radiological study by Caffey, the diagnosis of “shaken baby syndrome” (SBS—including retinal petechiae, multiple fractures of the long bones, and subdural hematomas) evolved and has resulted in many men and women being convicted of child abuse, all without any meaningful consideration of a differential diagnosis.

Although Caffey mentioned the word scurvy in the differential diagnosis of each of the six cases, he stated that none of the infants showed the typical radiological changes of scurvy: many of the fractures were in the shafts of the long bones, instead of at the junctions between the epiphyses and the diaphyses. 

The radiologic signs of scurvy, however, are variable. The most consistent finding used to be elevation and calcification of the periosteum of the long bones due to subperiosteal hemorrhage, above and below the fracture sites. In reviewing Caffey’s six original cases, this finding was present in most of the cases. And, although osteopenia and contrasting white lines of healing are said to be characteristic radiological features of classical scurvy, absence of these findings on radiographs does not rule out a scorbutic state.The precise time course of  increased susceptibility to fractures and the development of osteopenia and white lines of healing seen on radiographs is not known. Bones may be vulnerable to fracture because of proline and lysine hydroxylase deficiencies affecting chondroblasts and osteoblasts before these classic radiological signs appear, especially if scurvy develops rapidly at an early age.

Additional Findings in Caffey’s Case Studies

In addition to the long-bone fractures and subdural hematomas, other clinical signs consistent with infantile scurvy were evident in most of Caffey’s six cases:

Case 1. A purulent discharge from the right ear began at age 5 months and persisted for 2 months; a convulsion due to subdural hemorrhage  occurred at 7months. Spontaneous fracture of the right radius occurred after nine days in the hospital.

Case 2. Convulsions began at age 1 month. At 7 months, the infant developed soft, spongy, bleeding gums typical of scurvy, and retinal petechiae indicative of increased capillary fragility. At age 8 months, he developed signs of subdural hematoma.

Case 3. Multiple fresh hemorrhages were present in both ocular fundi. Petechiae were also scattered on the abdominal wall, and a large ecchymosis was seen on the left side of the face.

Case 4. Radiographs showed evidence of epiphyseal separation at the proximal end of the right humerus, suggestive of scurvy.

Case 5. Subdural hematoma and bone fractures associated with otitis media were present; black-and-blue spots on the fore head and face could be interpreted as either traumatic or scorbutic.

Case 6. There was bilateral proptosis due to retrobulbar hemorrhages consistent with scurvy—akin to the unilateral proptosis seen in vitaminC-deficient18th century sailors.

Even with adequate dietary vitamin C intake, infections can rapidly deplete ascorbic acid stores and increase the blood histamine level. In cases 1 and 5 above, it is noted that subdural hemorrhages occurred in the context of on-going otitis media infections.

Many factors affect vitamin C metabolism, but the most important is systemic infection. Hess, in his Cutter Lecture at Harvard Medical School, recognized that infection and vitamin C deficiency were both related to the development of infantile scurvy. It was a number of years, however, before he realized that each affected the other—vitamin C deficiency predisposes to infection, and infection predisposes to vitamin C deficiency. Blood levels of vitamin C are also inversely related to blood histamine levels.

Onset of Infantile Scurvy

Infantile scurvy used to occur most commonly after age 7 months, when swollen, bleeding gums were evident, as the lower incisor teeth had erupted and bacteria could enter the scorbutic gingival sulcus. In contrast, an earlier onset variant of infantile scurvy now occurs at 8 to12 weeks of age. Bleeding gums are rarely ever seen before the eruption of the lower incisor teeth at 7 months, so the diagnosis of scurvy  may not be obvious.

The hypothesis that subdural hemorrhages, retinal petechiae, and spontaneous fractures of the ribs and long bones can occur as an early variant of scurvy at about 8 to 10 weeks of age has not been adequately studied, and, therefore, has not been disproven. Unless and until vitamin C and histamine levels are actually measured in these infants, who are automatically classified as victims of SBS, we will not know the truth about causation. Unfortunately, even if the diagnosis of infantile scurvy is considered, most hospitals do not have the ability to measure either vitamin C or histamine levels.

Gardner has observed that the age of onset of the diagnosis of so-called “shaken baby syndrome” is significantly later in Japan (peaking at 7 to 9 months) than in the United States (peaking at 2 to
4 months). Is this because Japanese infants are abused at a later age than American infants, or is there another explanation? Gardner noted that these ages correspond to the standard ages when vaccinations have been given in the two countries, respectively.

A Multi factorial Cause?

Infants with the findings attributed to SBS may be affected by a combination of factors causing generalized capillary fragility, which in turn affects the capillaries of the bridging veins between the brain and the dura mater—predisposing to subdural hematoma—due to inadequate ascorbic acid intake and/or depletion by infections or multiple immunizations.

The defective formation of fibrous tissue, bone, and dentin that is known to occur in scurvy results from proline and lysine hydroxylase deficiencies that affect fibroblasts, chondroblasts, osteoblasts, and ameloblasts. However, the increased capillary and venular fragility causing the bleeding associated with scurvy is due to a many-fold increase in the blood histamine level, as shown by Clemetson.  

The total blood histamine increases exponentially as the plasma ascorbic acid falls. Majno and Palade have shown that toxic levels of histamine in the blood cause openings in the tight junctions between the vascular endothelial cells, leading to extravasation of blood. Leakage of blood into the tissue slowly leads to local hemolysis, as evidenced by the yellow color characteristic of the fluid of old subdural hematomas. Hemolysis also leads to local ascorbate depletion.

Chatterjee et al. reported increased blood histamine levels following vaccinations in guinea pigs. This effect would likely be heightened when six vaccinations are given at the same time at 8 weeks of age, such as is now the custom in most English-speaking countries. If vitamin C levels are low at the time of vaccination, a resulting toxic histaminemia may cause further clinical problems.

A relevant finding by Archie Kalokerinos is that the increased death rate following vaccination of Aboriginal infants in Australia was arrested by administering vitamin C at the time of vaccination—because ascorbic acid “detoxifies” histamine. Indeed, Chatterjee et al. demonstrated that ascorbic acid is essential for the detoxification of histamine (in guinea pigs), by converting it to hydantoin-5-acetic acid, and on to aspartic acid in vivo. Illustrations of the physiology and pathology of ascorbic acid and blood histamine have been presented previously.

Other factors that are not given sufficient weight in evaluations for SBS are the presence of chronic subdural hematomas, often occurring during or shortly after birth, and the fact that chronic subdurals are susceptible to rebleeding. Subdural hematomas have been found using fetal ultrasound in utero, before labor, as reported by Gunn, and also following normal, spontaneous delivery, as reported by Chamnavanakietal. The tendency to rebleed could be exacerbated by toxic histaminemia through the mechanisms explained above.

More Research Needed

The effects of various vaccinations, given alone or together, on whole blood histamine levels and plasma ascorbic acid levels, should be further studied. Concerted research may increase our understanding of the toxicity of different vaccines and the effects of giving single versus multiple, simultaneously administered vaccines. Their impact on vitamin C, histamine, and clinical
manifestations of deficiency/toxemia  must be assessed. It should be helpful to reduce the number of vaccines given simultaneously or in rapid succession.

A better understanding of these factors may help prevent adverse reactions following vaccinations. Dr. Kalokerinos has shown a clear benefit by providing supplemental vitamin C at the time of vaccination in some children. Vitamin C is an extremely safe substance—the only ill effects tend to occur in older children and adults who suffer from hemosiderosis due to sickle cell disease or Mediterranean  anemia. Iron storage depletes ascorbic acid stores via oxidation and hydrolysis, and the dehydroascorbic acid so formed can be harmful. Even then, the toxic effect of vitamin C may only be mild and temporary in young infants.

Conclusions

The so-called “classic” findings of subdural hematoma and retinal hemorrhages in infants, without any evidence of major trauma, do not always automatically equate to a diagnosis of SBS. As in all other areas of medicine, it is prudent to do a differential diagnosis.

The findings in the cases that initially established SBS as a diagnosis were compatible with and even suggestive of infantile scurvy or toxic histaminemia.

C. Alan B. Clemetson, M.D., was Professor Emeritus, Tulane University school of Medicine, New Orleans, La. His people may be contacted by e-mail at megcc2000@yahoo.com (Dr. Clemetson passed away in 2006, but someone is still receiving his emails and responding.)

REFERENCES

  1. Caffey J. Multiple fractures in the long bones of infants suffering from chronic subdural hematoma. 1946;56:163-173. Am J Roentgen Rad Ther
  2. Hess AF. Nutritional disorders in the light of recent investigations.1922;207:101-108. Boston Med Surg J
  3. Gardner HB. Retinal and subdural haemorrhages: Aoki revisited 2004;87:919-920.Brit J Ophthalmol
  4. Gardner HB. Immunizations, retinal and subdural hemorrhages: are they related?
    2005;64:663-664. Med Hypotheses
  5. Clemetson CAB. Histamine and ascorbic acid in human blood.1980;110:662-668.J Nutr
  6. Majno G, Palade GE. Studies on inflammation. 1. The effect of histamine and serotonin on vascular permeability. An electron microscopic study 1961;11:571-605. J Biophys Biochem Cytol
  7. Clemetson CAB. Hemolysis. In: vol 1. Boca Raton Fla.: CRC Press; 1989:181-192.Vitamin C
  8. Chatterjee IB, Majumder AK, Nandi BK, Subramanian N. Synthesis and some major functions of vitamin C in animals 1975;258:24-47. Ann NY Acad Sci
  9. Kalokerinos A. Sydney, Australia: Thomas Nelson; 1974. Every Second Child
  10. Clemetson CAB. Was it “shaken baby” or a variant of Barlow’s disease? 2004;9:78-80. J Am Phys Surg
  11. Gunn TR. Subdural hemorrhage in utero. 1985;76:605-610. Pediatrics
  12. Chamnanvanaki S, Rollins N, Perlman JM. Subdural hematoma in term infants. 2002; 26:301-304. Pediat Neurol
  13. Clemetson CAB. Heavy metals, water supplies: copper, iron, manganese, mercury, and cobalt. In: vol 1. Boca Raton Fla.: CRC Press; 1989:89-100.Vitamin C Journal of American Physicians and Surgeons Volume 11 Number 1 Spring 2006

Dianne Jacobs Thompson  Est. 2007
Also http://truthquest2.com (alternative medicine featuring drugless cancer treatments)
Author publication: NEXUS MAGAZINE "Seawater--A Safe Blood Plasma Substitute?"