Injuries & deaths from pertussis-containing vaccines are the most compensated claims; brain is most susceptible to oxidative degradation

According to a global report on birth defects which was conducted in 2006, 21 out of 22 countries most affected by birth defects per 1000 live births are Muslim majority countries and the following countries are the ones most affect by birth defects per 1000 live births:
1. Sudan 82.0/1000
2. Saudi Arabia 81.3/1000
3. Benin 77.9/1009
4. Burkina Faso 77.0/1000
5. Palestinian territories 76.6/1000
6. United Arab Emirates 75.9/1000
7. Tajikistan 75.2/1000
8. Iraq 74.9/1000
9. Kuwait 74.9/1000
10. Afghanistan 74.8/1000
11. Oman 74.8/1000
12. Syria 74.3/1000
13. Pakistan 73.5/1000
14. Nigeria 73.5/1000
15. Kyrgyzstan 73.4/1000
16. Qatar 73.4/1000
17. Bahrain 73.3/1000
18. Jordan 73.1/1000
19. Libya 73.0/1000
20. Tunisia 72.7/1000
21. Morocco 72.3/1000
22. Yemen 72.1/1000

Source

Inbreeding which involves marriage between cousins is an islamically valid and approved practise.  Inbreeding is a major cause of birth defects in children so its very likely that the whole cousin marriage thing has a huge role to play in recorded high rates of birth defects in Muslim countries.    http://www.nairaland.com/1448664/muslim-countries-found-highest-rates

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2-26-16    In late 2014, the Ministry of Health of Brazil announced the introduction of the Tdap (Tetanus, diphtheria, and acellular pertussis) vaccine for all pregnant women in that country as part of its routine vaccination program…. Injuries and deaths from pertussis-containing vaccines are the most compensated claims in the federal Vaccine Injury Compensation Program (VICP) and influenza vaccine injuries and deaths are the second most compensated claim.      http://yournewswire.com/is-zika-virus-or-the-dtap-vaccine-causing-birth-defects-in-brazil/

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-Dr. H. Buttram, with C. Frompovich, wrote:

Of all the organs of the body, the brain is the most susceptible to oxidative degradation, commonly referred to “lipid peroxidation.”  Although an infant’s brain receives 15 percent of normal cardiac output, it utilizes nearly 25 percent of the body’s oxygenation. [13] As elevated oxygen levels in the environment bring increased risk of explosions or fire, comparable physiological risks exist in the brain.  In addition to being a highly oxygenated organ, the human brain has heightened vulnerability to harmful peroxidation because the brain has by far the highest fat content of any organ of the body with membrane lipids constituting 60 percent of the solid matter. [14]  In addition, both brain and retina contain a relatively high percentage of the omega-3 polyunsaturated fatty acid, docosahexaenoic acid (DHA) [10-20] and arachidonic acid (ARA) that serve as a primary building block of the membranes of these structures.  DHA and ARA are high in energetics, but they are far more unstable and vulnerable to pro-inflammatory peroxidation (oxidative lipid degradation) than saturated fats. [13-22]

In essence, the brain might be compared with highly inflammable dry grass or brush enclosed in an area with elevated oxygen levels, needing only a spark to set off a conflagration of inflammatory lipid peroxidation. In all likelihood, vaccine adjuvants provide this spark far more often than generally realized….

During the Congressional Hearings on Vaccine Safety (1999-Dec. 2004) an FDA panel was repeatedly asked, “Where are your (safety) studies?”  The panel could only reply with unsatisfactory answers such as, “They would be very expensive.”  However, it was not until January 14, 2009 that it became evident that the avoidance of meaningful vaccine safety studies has long been an established policy by the National Institute of Health, the primary federal agency responsible for funding health research in the United States, as reported by the autistic support group, Age of Autism:

January 17, 2009
National Autism Association on IACC Removal of
Vaccine Safety Research, A Press Release from
The National Autism Association:

“Washington, DC – In an unprecedented move on Wednesday, Jan. 14th, the Interagency Autism Coordinating Committee (IACC) removed previously approved vaccine safety research from the Strategic Plan for Autism Research objectives.”

http://www.vaccinationcouncil.org/2011/06/01/vaccines-and-brain-inflammation/

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“Almost any vaccination can lead to noninfectious inflammatory reaction involving the nervous system.  The common denominator consists of vasculopathy (disease of the blood vessels) that is often associated with demyelination (permeation of the critical “electrical” insulator of the brain cells).”   -Charles M. Poser, Harvard Medical School Department of Neurology, 1947

‘In a model of aluminum-mediated intoxication imposed to mice during pregnancy and early development, a 72% higher content of lipid peroxidation products was found in brain myelin.’   -Department of Biological Chemistry, University of Buenos Aires, Argentina, 08/15/1997

Note: Lipid peroxidation is associated with cellular damage resulting from oxidative stress (or Ischemia), which inhibits the capacity of cellular antioxidants, vital to natural immunity, by the unleashing of free radicals.   – Scientific verification of demyelination linked to mitochondrial breakdown, caused by the intervention of aluminum on early childhood development in the brain.

Two primary factors here, in determining the extent of vaccine derived neurological & corresponding neuro-developmental damage (including the host of typical auto-immune failure responses) which are often overlooked in Medical circles?  Timing & synergy.

Timing is CRITICAL.  A newborn lacks sufficient protection to guard against premature damage to the blood barrier (physiological mechanism that alters the permeability of brain capillaries so that some substances, such as certain drugs, are prevented from entering brain tissue, while other substances are allowed to enter freely) on the brain – so that vital, unfinished area is still completely raw.

A baby’s blood-brain barrier takes no less than 7 months in utero (latter stages of third trimester) to establish its primary protective shielding:

‘It has been established that by week 28 of the intrauterine development the process of the structural and functional establishment of the BBB (blood-brain barrier) had been over as evidenced by the lack of specific alpha-1-globulin in umbilical blood of the neonates of the given gestation age.‘    -Volodin NN, Chekhonin VP, Tabolin VA, Rogatkin SO, Kashparov IA.

The Myelin Sheath is also significantly under-developed at birth. In fact, a baby undergoes continuous Myelin formation well after birth.

‘Myelination appeared to occur earliest in the posterior fossa, with the middle cerebellar peduncle identifiable at only 3 months.  By the age of 1 year, all major white matter tracts including the corpus callosum, subcortical white matter, and the internal capsule were well defined.  However, due to subtle changes in appearance, the refined configuration of the adult brain was not attained until early adolescence.‘   -B A Holland, D K Haas, D Norman, M Brant-Zawadzki and T H Newton

Similarly, the Meninges layering is designed to insulate the brain & spinal cord from injury – notwithstanding the accumulative barrage of synergistic toxicity associated with early childhood vaccines. ”Probably no field in embryology has been less explored than that relating to the meninges.”  -Lewis H. Weed

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8-21-2011       ‘The organs of the central nervous system (brain and spinal cord) are covered by 3 connective tissue layers collectively called the meninges. Consisting of the pia mater (closest to the CNS structures), the arachnoid and the dura mater (farthest from the CNS), the meninges also support blood vessels and contain cerebrospinal fluid. These are the structures involved in meningitis, an inflammation of the meninges, which, if severe, may become encephalitis, an inflammation of the brain.’ -Medline Plus

Early Onset Autism, which occurs anywhere from 12-18 months, coincides precisely with most intense period of standard immunization. By 15 months the average child in most developed countries, has received a minimum of 25 injections. This results in severe heavy metal toxicity interfering with the earliest stage of development, during the first 6 months after birth.

The synergy of vaccine derived heavy metal-virus-mycoplasma-excipient toxicity “sludge” targets 3 primary core “electrical grid” stations encasing the nerve center/brain – kin to throwing water over a main keyboard operating system. In the event the Blood-Brain barrier, Myelin sheath & Meninges are breached, particularly at such a critical stage in early childhood development, neuro-developmental disorders will inevitably follow. It seems a master Electrician knows more about overall functionality of the human body than your average Pediatrician. …

Aluminum is a positively charged bio-conductive element, 64 times more positive than colloidal blood products (ie. anything suspended in your blood) are negative; with the properties of a coagulant. It literally draws in all other metals & toxins in its path. When injected into deep muscle tissue or subcutaneously, this neurotoxin gets redistributed via the bloodstream (consisting of 90% water) to areas of fatty tissue (highly electrical tissues – negatively charged) throughout the body, builds up over time in these delicate centers; primarily in the Brain, Spinal cord, Myelin sheath, Meninges, cardiac cells, breasts & ovaries (in women), prostate (in men), kidneys, liver, gut & bowels.

This “sludging” is activated when Aluminum interacts with Hemoglobin in flow, in the negatively charged environment. This causes the negatively charged blood products to “attract” towards the larger, more massive positively charged Aluminum, causing clumping or “sludging”. This restricts blood flow, and it changes the Zeta Potential to change from -15mv (minus 15 milivolts) towards -10 mv (minus 10 milivolts), or possibly closer to zero. This is an increase in Zeta Potential, from a negatively charge towards neutral. (This is somewhat analogous to a change in state of water as it turns to ice – it’s a change in viscosity, affecting blood flow).

“Your blood has no method of excretion; Heavy metals & live viruses, formaldehyde are redistributed by the blood to areas of fatty tissue (highly conductive/electrical tissues) – found in the gray matter of the brain, the Myelin Sheath, neurons, the meninges/spine, cardiac cells, breasts & ovaries (in women), prostate (in men). Blood is made of water. When you stick aluminum in your blood, anything that’s toxic debris is going to bond to and coagulate and cause a congestive coccidiosis and this stuff gets caught in the tiny highways & byways. So you have the big gushing arteries & veins but they byfricate and branch into streams like a river; and they branch in again to the tiny arterial & capillary bits. That’s where the blockages are occurring, the brain, the spine, (the intestines/bowel) fingers & toes – which turn blue, choking of the micro-vessels from all the sludge that gets caught from all these repetitive hits/vaccinations, over & over. There are 60,000 miles of blood-vessels in one body.They run through every part of your muscle, your bone, your brain. Anywhere you stick an inter-muscular injection it goes into the blood.”   –Dr. Gary Tunsky

According to Dr. Russell Blaylock, world renowned former brain surgeon, the average doctor receives the equivalent of a weekend seminar, in their first year only, on the specific topic of the neurological side-effects & disorders associated with vaccine uptake; approximately seven hours of careful, focused study into the complex strata of auto-immune breakdown type complexities. Without this fundamental bedrock of knowledge a critical component is missing from any doctor’s arsenal, considering the widespread impact neurological side-effects to vaccines have had on the community at large.                http://vaccineresistancemovement.org/?p=8787

 

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