Home  
Shop Subscribe Contact us About us
---- News Categories -----        

LATEST NEWS
Chemicals
Children's health
Climate change
Diet
Energy sources

Fertility
Food Industry
GM crops
Illnesses
Lifestyle

Transport
Vaccination
Women's health
Workplace health
TOP TWENTY
Subscribe/Renew

TOP TWENTY

Power lines double
risk of leukaemia

Death by chocolate

Killer bras

Cancer on the lawn

Cordless phones
also fry


Bugs drop out
of the air


Children's bones
fizzed away


Organic milk just
oozes health

Animals give GM
the thumbs down


Out of the frying pan
- Teflon 'flu


More trees no answer to
global warming


Fluoride dumbs
down children


Ultrasound
- just looking can hurt


Short mobile calls affect
children's brains
for 50 minutes

Mum's fillings - why there
are four times more
autistic boys


Pot plants hoover
up pollution


Am I a girl or a boy?

Margarine brings fourfold
risk of blindness

Leave the sunscreen at home

Elderberry knocks out 'flu

 
The mercury in mum's mouth
Mercury expert Professor Boyd Haley is concerned that the huge increase in autism may be due to exposure to mercury from mothers’ amalgam fillings while in the womb. He also believes that an interaction between the mercury-based vaccine preservative thimerosal and the male hormone testosterone may play a part. His testimony before the US House Government Reform Committee (14.11.02) included the following:
  • Mercury in the mouth and intestines can mutate into more toxic organic mercury compounds like methyl-mercury, facilitating its uptake by babies in the womb [1,2,3]

  • Methylthiol, one of the major neurotoxins produced during gum diseases, reacts immediately with the mercury ion Hg2+, creating extremely dangerous organic mercury-thiol compounds. Like methyl-mercury, these can easily penetrate the blood/bowel and blood-brain barriers of adults,children and foetuses. This latter might explain why gum disease in the mother is the main risk factor for pre-term low birth weight babies

  • Raised mercury levels in mothers' fluids have been linked with even higher levels present in the cord blood and in the meconium (faeces) passed by the baby during the first days after birth [4]

  • Levels of mercury in the ‘birth hair’ of autistic children are usually lower than in normal children, whilst their blood levels of mercury are higher. In normal children, the level of mercury in ‘birth hair’ increases in line with the number of amalgam fillings in the mother’s mouth. In autistic children there is very little excretion of mercury into the ‘birth hair’ no matter how many amalgam fillings their mother has. When children with autism are exposed to mercury in tests, they retain higher amounts in the body than normal children. This all suggests that the bodies of children with autism are less effective at excreting mercury [5]

  • The mercury-based vaccine preservative thimerosal kills neurons, particularly when inorganic mercury, aluminium, lead or cadmium are present

  • Whereas the female hormone oestrogen decreases thimerosal’s toxic effects, the male hormone testosterone greatly increases its toxicity. Exposing neurons to even a tiny concentration of either thimerosal or testosterone alone killed 5% in three hours. Three hours exposure to the same concentration of thimerosal with just one nanomolar of testosterone added killed all 100%. This may explain the four-to-one ratio of boys to girls that become autistic and the fact that boys represent the vast majority of the severe cases of autism

  • Some children are born autistic. Others develop autism, possibly due to exposure to mercury in early childhood from vaccines, food or pollution. In a normal child, it is quite plausible that protective compounds in the body such as glutathione and metallothionine (which bind with mercury and other heavy metals), would prevent neurological damage. However, when a foetus is exposed to mercury its stores of these compounds are reduced

  • These compounds also decrease in the body with age, disease, other toxic exposures, oxidative stress and genetic susceptibility, possibly explaining why Parkinson’s and Alzheimer’s have, until recently, been primarily diseases of older people

N.B. It is the mercury retained in the body’s cells that causes damage, not the mercury which has been excreted in the urine, hair and faeces.

MMR - a hypothesis
Our studies found that the MMR triple jab (which does not contain thimerosal) was far less neurotoxic than any thimerosal-containing vaccines. If, however, it was given to a child whose blood/bowel or blood/brain barrier had already been damaged by exposure to, say, mercury from the mother’s amalgam fillings or an earlier jab containing thimerosal, the live measles virus in particular could easily penetrate the gut or brain where it could trigger substantial damage.

Ed.- (i) Recently published research found that children with autism had significantly lower levels of glutathione, homocysteine and other amino acids essential for protecting the body against heavy metals like mercury. [6]

(ii) A copy of the US International Academy of Oral Medicine and Toxicology’s list of ‘amalgam-free’ dentists may be obtained from the Green Health Watch office. Please send a large stamped addressed envelope. It can also be downloaded from website: www.amalgam.ukgo.com/ukdent.htm

[1] Kingman et al. Journal of Dental Research 1998;V77(3):461
[2] Mackert,JR & Bergland,A. Critical Revues in Oral Biology and Medicine 1997;8(4):410-36 (states it would take 450-530 amalgam surfaces to produce 30 micrograms mercury/g creatinine of urine mercury per day (roughly estimated as 0.067 to 0.057 mg/day/surface)
[3] Holmes,A et al. International Journal of Toxicology 2003;V22:4
[4] Ramirez,GB et al. Pediatrics 2000;V106(4):774-81
[5] see e.g., Razagui,IB et al. Biological Trace Element Research 2001;81(1):1-19
Drasch,G et al. European Journal of Pediatrics 1995;154(7):585-86
Lorscheider,FL et al. Neuroreport 2001;12(4):733-37
[6] Saxe et al. Journal of American Dental Association 1999;V130:191
[7] Frustaci et al.
Journal of the American College of Cardiology 1999;v33(6):1578-83
[8] see e.g., Lorscheider,FL et al. FASEB Journal 1995;9:504-08
[9] see e.g., Kingman,A et al.
Journal of Dental Research 1998;77(3):461-71
[10] Chew,CL et al. Clinical Preventive Dentistry 1991;13(3):5-7
[11] see e.g., Reinhardt,JW.
Advances in Dental Research 1992;6;110-113
[12] see e.g., Nylander,M et al.
Journal of Swedish Dentistry 1987;11:179-187 and 1989;13:235-43
Zander,D et al.
Zentralblatt fur Hygiene und Umweltmedizin 1992;192(5):447-54
[13] Haley,B. Nordisk Tidsskrift for Biologisk Medisin 2003
[14] see e.g., Opitz,H. Clinical Neuropathology 1996;15(3):130-44
[15] see e.g. Echeverria,D et al. FASEB Journal 1998;12(11):971-80
Aschner,M & Aschner,JL.
Neuroscience and Biobehavioral Reviews 1990;14(23):169-76
[16] see e.g. Hua,MS et al. Brain Injury 1996;10(5):377-84
Siblerud,RL. Psychological Reports 1992;70(3 Pt 2);1139-51
[17] see e.g. Heintze,U et al.
Scandinavian Journal of Dental Research 1983;9(2):150-52
[18] Heintze et al.
Scandinavian Journal of Dental Research 1983;V91:150
[19]
Rowland et al. Experientia 1975;V31:1064
[20] Leistevuo,J et al. Caries Research 2001;V35(3):163
[21] see e.g. Siblerud,RL.
The Science of the Total Environment 1990;99(1-2):23-25
Zentralblatt fur Hygiene und Umweltmedizin 1996 Nov: 199)1): 69-75

(10890) Jenny Spinner. GreenHealthWatch