Most people are aware of my study into the health
effects of radionuclides (especially as it relates to
BSE, and the findings of Mark Purdey et al. see his
book "Animal Pharm").
I received an email from Dr. Gordon Edwards of
Montreal, which contains an animated
demonstration of where, when and who detonated
atomic bombs around the planet (atmospheric and
underground/water). Over 2000 explosions of
atomic weapons since 1945; only 2 of which were
used as a weapon of war (Nagasaki and Hiroshima
- 1945). The video demonstration is really worth
sitting down and watching, as it give perspective of
the levels of destruction and contamination (1945-
1998).
This video can be watched at:
http://www.zerohedge.com/article/how-world-
nuked-itself-over-2000-times
(scroll down and click on the video, starts slow but
gets moving as the years progress - tracking year,
month at top right hand of screen, country and
number of bombs each, top and bottom screen).
There is, I believe, as strong relationship between
the nuclear industry (as a whole) and the planetary
radionuclide exposure AND health effects like
Alzheimer's Disease (and other neurological
disorders). The following is an example of on-
going research demonstrating the association
between AD plaques and RAD - radon decay
daughters like polonium etc.
Those who smoke also have high levels of these
RAD in their brain plaques, due to the fact that the
fertilizer applied heavily to tobacco contains high
amounts of these radionuclides. The term
'naturally occurring' RAD is confusing, as with each
bomb detonated... the majority of the metal by
weight involved in the building of the nukes is
uranium 238 (a natural element). Uranium mining
puts massive amounts of "tailings" on the surface
which releases radon gas, which in turn floats low
to the ground (heavy air) and contaminates
land/people down-wind. I hope you'll watch the
video some time. My daughter thought it was
pretty cool!
The study here is free and is an excellent read for
those who are dealing with family with Alzheimer's
Disease/dementia. What is of great importance in
the studies by this group, on this subject, is that
the radioactive elements where strongly associated
with proteins and lipids that make up the plaques
found in the brains of AD and Parkinson's Disease
victims.
http://www.ncbi.nlm.nih.gov/pubmed/16965619
Mol Neurodegener. 2006 Sep 11;1:11.
Natural distribution of environmental radon
daughters in the different brain areas of an
Alzheimer disease victim.
Momcilović B, Lykken GI, Cooley M.
Institute for Medical Research and Occupational
Health, PO Box 291, 10001 Zagreb, Croatia.
Abstract
BACKGROUND: Radon is a ubiquitous noble gas in
the environment and a primary source of harmful
radiation exposure for humans; it decays in a
cascade of daughters (RAD) by releasing the cell
damaging high energy alpha particles. RESULTS: We
studied natural distribution of RAD 210Po and
210Bi in the different parts of the postmortem
brain of 86-year-old woman who had suffered
from Alzheimer's disease (AD). A distinct brain map
emerged, since RAD distribution was different
among the analyzed brain areas. The highest RAD
irradiation (mSv x year(-1)) occurred in the
decreasing order of magnitude: amygdala (Amy) >>
hippocampus (Hip) > temporal lobe (Tem)
approximately = frontal lobe (Fro) > occipital lobe
(Occ) approximately = parietal lobe (Par) >
substantia nigra (SN) >> locus ceruleus (LC)
approximately = nucleus basalis (NB); generally
more RAD accumulated in the proteins than lipids
of gray and white (gray > white) brain matter. Amy
and Hip are particularly vulnerable brain structure
targets to significant RAD internal radiation damage
in AD (5.98 and 1.82 mSv x year(-1), respectively).
Next, naturally occurring RAD radiation for Tem and
Fro, then Occ and Par, and SN was an order of
magnitude higher than that in LC and NB; the later
was within RAD we observed previously in the
healthy control brains. CONCLUSION: Naturally
occurring environmental RAD exposure may
dramatically enhance AD deterioration by selectively
targeting brain areas of emotions (Amy) and
memory (Hip).
PMID: 16965619 [PubMed]PMCID: PMC1579210
Free PMC Article
effects of radionuclides (especially as it relates to
BSE, and the findings of Mark Purdey et al. see his
book "Animal Pharm").
I received an email from Dr. Gordon Edwards of
Montreal, which contains an animated
demonstration of where, when and who detonated
atomic bombs around the planet (atmospheric and
underground/water). Over 2000 explosions of
atomic weapons since 1945; only 2 of which were
used as a weapon of war (Nagasaki and Hiroshima
- 1945). The video demonstration is really worth
sitting down and watching, as it give perspective of
the levels of destruction and contamination (1945-
1998).
This video can be watched at:
http://www.zerohedge.com/article/how-world-
nuked-itself-over-2000-times
(scroll down and click on the video, starts slow but
gets moving as the years progress - tracking year,
month at top right hand of screen, country and
number of bombs each, top and bottom screen).
There is, I believe, as strong relationship between
the nuclear industry (as a whole) and the planetary
radionuclide exposure AND health effects like
Alzheimer's Disease (and other neurological
disorders). The following is an example of on-
going research demonstrating the association
between AD plaques and RAD - radon decay
daughters like polonium etc.
Those who smoke also have high levels of these
RAD in their brain plaques, due to the fact that the
fertilizer applied heavily to tobacco contains high
amounts of these radionuclides. The term
'naturally occurring' RAD is confusing, as with each
bomb detonated... the majority of the metal by
weight involved in the building of the nukes is
uranium 238 (a natural element). Uranium mining
puts massive amounts of "tailings" on the surface
which releases radon gas, which in turn floats low
to the ground (heavy air) and contaminates
land/people down-wind. I hope you'll watch the
video some time. My daughter thought it was
pretty cool!
The study here is free and is an excellent read for
those who are dealing with family with Alzheimer's
Disease/dementia. What is of great importance in
the studies by this group, on this subject, is that
the radioactive elements where strongly associated
with proteins and lipids that make up the plaques
found in the brains of AD and Parkinson's Disease
victims.
http://www.ncbi.nlm.nih.gov/pubmed/16965619
Mol Neurodegener. 2006 Sep 11;1:11.
Natural distribution of environmental radon
daughters in the different brain areas of an
Alzheimer disease victim.
Momcilović B, Lykken GI, Cooley M.
Institute for Medical Research and Occupational
Health, PO Box 291, 10001 Zagreb, Croatia.
Abstract
BACKGROUND: Radon is a ubiquitous noble gas in
the environment and a primary source of harmful
radiation exposure for humans; it decays in a
cascade of daughters (RAD) by releasing the cell
damaging high energy alpha particles. RESULTS: We
studied natural distribution of RAD 210Po and
210Bi in the different parts of the postmortem
brain of 86-year-old woman who had suffered
from Alzheimer's disease (AD). A distinct brain map
emerged, since RAD distribution was different
among the analyzed brain areas. The highest RAD
irradiation (mSv x year(-1)) occurred in the
decreasing order of magnitude: amygdala (Amy) >>
hippocampus (Hip) > temporal lobe (Tem)
approximately = frontal lobe (Fro) > occipital lobe
(Occ) approximately = parietal lobe (Par) >
substantia nigra (SN) >> locus ceruleus (LC)
approximately = nucleus basalis (NB); generally
more RAD accumulated in the proteins than lipids
of gray and white (gray > white) brain matter. Amy
and Hip are particularly vulnerable brain structure
targets to significant RAD internal radiation damage
in AD (5.98 and 1.82 mSv x year(-1), respectively).
Next, naturally occurring RAD radiation for Tem and
Fro, then Occ and Par, and SN was an order of
magnitude higher than that in LC and NB; the later
was within RAD we observed previously in the
healthy control brains. CONCLUSION: Naturally
occurring environmental RAD exposure may
dramatically enhance AD deterioration by selectively
targeting brain areas of emotions (Amy) and
memory (Hip).
PMID: 16965619 [PubMed]PMCID: PMC1579210
Free PMC Article
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