Monday, April 30, 2012

Only 90 ailments scientifically linked to vaccines, so far!


Only 90 ailments scientifically linked to vaccines, so far!

1. Adverse Events including Deaths
2. Neurodevelopmental Disorders
3. Allergies & Related Respiratory Problems
4. Vaccine induced Thrombocytopenia
5. Sudden Infant Death Syndrome
6. High Infant Mortality Rates
7. Autism Prevalence
8. Serious Neurological Disorders
9. Autoimmune Neurological Disorder called Transverse Myelitis
10. Hemolytic Anaemia
11. Acute Necrotizing Encephalopathy
12. Autoimmunity leading to Autism
13. Birth Defects in children born to vaccinated mothers
14. Multiple Sclerosis
15. Chronic Fatigue Syndrome
16. Febrile Convulsions
17. Congenital Malformation in pregnant mothers given the rubella vaccine
18. Elevated CRP levels in vaccinated children
19. Increased morbidity and poor growth
20. Recurrent Seizures
21. Preeclempsia/Premature Birth in vaccinated pregnant women
22. Evidence of increased mercury exposure
23. Autoimmune demyelinating complications
24. Hepatitis/Gastrointestinal disease/liver function test abnormalities
25. Increased risk of liver problems
26. Uveitis
27. Hepatitis C
28. Abortions in vaccinated pregnant women
29. Guillain Barre Syndrome
30. Herpes Zoster
31. Increased risk of cardiovascular events
32. Vasculitis
33. Various injection site reactions
34. Shedding of the injected virus putting unvaccinated population at risk
35. Ulcerative Colitis
36. Immune Thrombocytopenia Purpura
37. Predisposition for encephalopathy
38. Hypotonic/Hyporesponsive Episodes
39. Serious adverse respiratory and non respiratory events
40. Intestinal blockage/intussusception
41. Gastroenteritis
42. Iatrogenic vaccinia
43. Autoimmune neuropathies
44. Symptomatic Gulf War Syndrome
45. Pediatric parapneumonic empyema
46. Atopy
47. Juvenile idiopathic arthritis
48. Erythema multiforme
49. Lupus erythematosus
50. Acute/Subacute post vaccination fiber neuropathy
51. Leukemia Cutis
52. Autoimmune haemolytic anaemia
53. Deep morphia
54. Delayed focal lipoatrophy
55. Fulminate Type 1 Diabetes with thrombocytopenia
56. Anaphylactic shock & death
57. Dermatomyositis
58. Immune mediated myelitis
59. Glyphosate induced Parkinsonism
60. Optic neuritis
61. Systemic Lupus Erythematosus
62. Incontinentia pigmenti reactivation
63. Adjuvant induced arthritis
64. Chronic arthritis
65. Motor neuron death
66. Vaccine induced pyrexia
67. Altered expression of 144 genes in mouse liver, 7 of which related to inflammation and metabolism
68. Cell death in liver cells
69. Excitotoxic brain injuries
70. Neurodevelopmental delays
71. OPV induced IgA nephropathy
72. Immunosuprression & autoimmune effects in mice
73. Adjuvant induced chronic inflammation
74. Chronic Fatigue & Prostrate Cancer
75. Hydranencephaly
78. Adverse changes of cerebellum in mice
79. Lasting neuropathological changes in rat brain
80. DNA vaccines and anti-fertility
81. Vaccine induced scrapie
82. B-cell activation and autoimmunity
83. Macrophagic Myofascitits
84. Urinary Tract Disease
85. Injection site associated sarcomas (cancers)
86. HIV-1/AIDS
87. Exposure to intended and unintended animal viruses
88. Transmissable spongiform encephalopathies
89. Atherogenesis (Heart Disease)
90. Autism like symptoms

http://www.greenmedinfo.com/disease/vaccine-induced-toxicity

The many benefits of sesame seeds.


Open Sesame! 10 Amazing Health Benefits Of This Super-Seed
Sesame (Sesamun indicum) is one of the oldest cultivated plants in the world, prized as an oilseed for at least 5,000 years.  While it is beginning to regain favor due to its exceptionally high calcium and magnesium content, few realize it is also one of the most potent medicinal foods still commonly consumed today.
In fact, its history as a medicine goes back 3600 years to Egyptian times where it was listed in the scrolls of the Ebers as a favored medicine.  Also, women in ancient Babylon were believed to use a mixture of honey and sesame seeds (havla) to prolong youth and beauty, and Roman soldiers ate the mixture for strength and energy.
In the past twenty years, a glut of scientific information has poured in demonstrating that sesame seed, and its components, have over three dozen documented therapeutic properties [see sesame research page].  Given these new revelations, it would seem that sesame would be just as at home in a medicine cabinet as it would be a kitchen cupboard.
Here are just 10 evidence-based medicinal properties of this food-medicine:
  1. Diabetes: A study published in 2011 in the Clinical Journal of Nutrition showed thatsesame oil improved the effectiveness of the oral antidiabetic drug glibenclamide in type 2 diabetic patients. [1]  Another study published in 2006 in the Journal of Medicinal Foods showed that the substitution of sesame seed oil as the sole edible oil lowers blood pressure and glucose in hypertensive diabetics. [2]
  1. High Blood Pressure:  A study published in 2006 in the Yale Journal of Biological Medicine showed that sesame seed oil has a beneficial effect in hypertensive patients on either diuretics or beta-blockers. Substitution of all dietary oils with sesame oil brought down systolic and dystolic  blood pressure to normal, in addition to decreasing lipid peroxidation (bodily rancidity) and antioxidant status. [3] One of the compounds identified behind sesame seed’s antihypertensive effects are peptides that act as angiotensin I-converting enzyme inhibitors.[4]
  1. Gingivitis/Dental Plaque: Sesame seed oil has been used for oral health for thousands of years in the traditional Indian medical tradition known as Ayurveda in a process known as "oil pulling." It involves swishing sesame seed oil in the mouth for prolonged durations and has been said to prevent teeth decay, halitosis, bleeding gums, dry throat, and for strengthening the teeth, gums and jaw. Clinical research now confirms that it compares favorably to chemical mouthwash (chlorhexidine) in improving plaque-induced gingivitis,[5] and that it is capable of reducing Streptococcus mutans growth associated with oral plaque formation. [6]
  1. Infant Health/Massage Oil:  A study published in the Indian Journal of Medical Research in 2000 showed that massaging infants with sesame oil improved both their growth and post-massage sleep, in comparison to control oils such as mineral oil.[7]
  1. Multiple Sclerosis (MS): In the animal model of MS, also known as experimental autoimmune encephalomyelitis, sesame seed oil protects mice from developing the disease by reducing IFN-gamma secretion, a key factor in initiating autoimmune inflammation and injury in the nervous system.[8] It has also been research for its potential beneficial role in another neurodegenerative condition, Huntington’s disease[9]
  1. Antibiotic-Induced Kidney Damage: Sesame seed oil protects against gentamicin-induced kidney damage in rats by reducing oxidative damage caused by the antibiotic.[10]
  1. Atherosclerosis: Sesame seed oil prevents the formation of atherosclerotic lesions in mice fed an atherogenic diet.[11]  The antioxidant and anti-inflammatory lignan found within sesame seeds known as sesamol has been identified to be partially responsible for its anti-atherogenic properties. In fact, sesamol has been shown to possess over two dozen beneficial pharmacologically active properties, many of which may contribute to improving cardiovascular health.
  1. Depression: The sesame lignin sesamol was shown to exert an antidepressant-like effect in behavioral despair in chronically stressed mice, specifically by modulatingoxidative-nitrosative stress and inflammation.[12]
  1. Radiation-Induced DNA Damage: Sesamol has been shown to protect against gamma radiation-induced DNA damage, likely through its antioxidant properties. [13] It is capable of reducing mortality in radiation treated mice, in part through preventing intestinal and spleen damage.[14]   When compared to another powerful antioxidant, melatonin, it was found 20 times more effective as a free radical scavenger.[15]
  1. Cancer: Sesame contains a fat-soluble lignin with phytoestrogenic properties known as sesamin, and which has been studied for inhibiting the proliferation of a wide range of cancer cells, including:
  • Leukemia
  • Multiple Myleoma
  • Colon Cancer
  • Prostate Cancer
  • Breast Cancer
  • Lung Cancer
  • Pancreatic Cancer
  • Lung Cancer
Sesamin’s anticancer effects have been linked to the NF-kappaB signaling.[16]
Sesame deserves to be recognized, along with garlic, honey, turmeric and a select few other substances,  as an easily accessible and affordable food-medicine that, if consumed regularly, could quite possibly save lives.


[1] Sesame oil exhibits synergistic effect with anti-diabetic medication in patients with type 2 diabetes mellitus. Clin Nutr. 2011 Jun ;30(3):351-8. Epub 2010 Dec 16. PMID: 21163558
[2] A pilot study of open label sesame oil in hypertensive diabetics. J Med Food. 2006 Fall;9(3):408-12. PMID: 17004907
[3] Effect of sesame oil on diuretics or Beta-blockers in the modulation of blood pressure, anthropometry, lipid profile, and redox status. Yale J Biol Med. 2006 Mar;79(1):19-26. PMID:17876372
[4] Antihypertensive effect of angiotensin I-converting enzyme inhibitory peptides from a sesame protein hydrolysate in spontaneously hypertensive rats. Biosci Biotechnol Biochem. 2006 May;70(5):1118-26. PMID: 16717411
[5] Effect of oil pulling on plaque induced gingivitis: a randomized, controlled, triple-blind study. Indian J Dent Res. 2009 Jan-Mar;20(1):47-51. PMID: 19336860
[6] Effect of oil pulling on Streptococcus mutans count in plaque and saliva using Dentocult SM Strip mutans test: a randomized, controlled, triple-blind study. J Indian Soc Pedod Prev Dent. 2008 Mar;26(1):12-7. PMID: 18408265
[7] Effects of massage&use of oil on growth, blood flow&sleep pattern in infants. Indian J Med Res. 2000 Dec;112:212-7. PMID: 11247199
[8] The Mechanism of Sesame Oil in Ameliorating Experimental Autoimmune Encephalomyelitis in C57BL/6 Mice. Phytother Res. 2011 Apr 28. Epub 2011 Apr 28. PMID: 21538630
[9]Sesamol attenuate 3-nitropropionic acid-induced Huntington-like behavioral, biochemical, and cellular alterations in rats. J Asian Nat Prod Res. 2009 ;11(5):439-50. PMID: 19504387
[10] Protective effect of daily sesame oil supplement on gentamicin-induced renal injury in rats. Biol Pharm Bull. 2001 Feb;24(2):181-7. PMID: 19487986
[11] Inhibition of atherosclerosis in low-density lipoprotein receptor-negative mice by sesame oil. J Med Food. 2006 Winter;9(4) PMID: 17201634
[12] Neuropsychopharmacological effect of sesamol in unpredictable chronic mild stress model of depression: behavioral and biochemical evidences. Psychopharmacology (Berl). 2011 Apr ;214(4):819-28. Epub 2010 Nov 20. PMID: 21103863
[13] Antioxidant potential of sesamol and its role on radiation-induced DNA damage in whole-body irradiated Swiss albino mice. Environ Toxicol Pharmacol. 2009 Sep ;28(2):192-7. Epub 2009 Apr 11. PMID: 21784002
[14] Effect of sesamol on radiation-induced cytotoxicity in Swiss albino mice. Mutat Res. 2006 Dec 10 ;611(1-2):9-16. Epub 2006 Oct 11. PMID: 17045515
[15] Sesamol as a Potential Radioprotective Agent: In Vitro Studies. Radiat Res. 2011 Sep 7. Epub 2011 Sep 7. PMID: 21899433
[16] Sesamin manifests chemopreventive effects through the suppression of NF-kappa B-regulated cell survival, proliferation, invasion, and angiogenic gene products. Mol Cancer Res. 2010 May;8(5):751-61. Epub 2010 May 11. PMID: 20460401

Vaccine Failure Ignored Over the Years.



Vaccines have been based on medical fraud for over a hundred years

Sunday, April 29, 2012 by: PF Louis

http://www.naturalnews.com/035715_vaccines_history_fraud.html

Learn more:http://www.naturalnews.com/035715_vaccines_history_fraud.html#ixzz1tVjxRAt0
(NaturalNews) The concept of vaccinating to immunize began in 1796, when British apothecary (pharmacist) Edward Jenner inserted cowpox pus under the skin of an eight year old boy. Jenner based his experiment on an unsubstantiated rumor that anyone who had experienced cowpox would be immune to smallpox.

Over the next couple of years, Jenner vaccinated others with cowpox to immunize them against smallpox. Without any actual proof of efficacy and safety, Jenner impressed King George III enough with a bogus immunization guarantee that he was awarded the equivalent of today's $500,000.

Thus, Jenner was the first medical professional to administer diseased matter as medication to a healthy person and receive a substantial financial award. He was also the first to constantly denounce vaccination detractors successfully. He was protecting both his ego and large public purse.

Many health professionals throughout the 19th Century knew that there had been several cases of smallpox among those with cowpox histories.Jenner's premise was flawed.

This was actually the beginning of a tradition that is carried on by today's vaccinators. Come up with a bogus solution to prevent a disease, make a bundle of cash, and shut down reasonable arguments from those who know immunization by vaccination doesn't work safely or effectively.

England's incidents of smallpox after vaccination rose steadily from five percent in the beginning to 95% by 1895. There was even a serious epidemic around 1872, one year after smallpox vaccinations were decreed mandatory in the UK. The mortality rate among smallpox victims also shot up five fold around that time.

Despite intelligent protests with obvious facts and figures disproving efficacy, and proving harm from toxic materials and viruses contained in vaccines that endanger natural immunity, the inoculation for immunization premise has been maintained.

Protecting the industry against truth by attacking reasonable dissenters viciously has resulted in vaccine industry revenue of $17 billion annually today. This doesn't include revenue from doctors' visits for vaccinations and resulting ill health from them.

The vaccinators' tactics of suppressing scientific data from concerned professionals has become more mafia like. Sincere medical professionals who register health concerns over vaccines are severely punished and slandered by the medical mafia owned mainstream media.

The truth about vaccines and disease outbreaks -allhidden from public view

A 2012 study led by Dr. David Witt, an infectious disease specialist at the San Rafael, CaliforniaKaiser Permanente Medical Centerconcluded thatwhooping cough occurs more among vaccinated children than children not vaccinated.

In 2010, a mumps outbreak occurred among 1000 children in upper New Jersey and lower New York. Almost 80% of them had been vaccinated with the MMR (measles, mumps & rubella) vaccine.

Throughout the 1980s, official agencies reported several outbreaks of measles occurring among childrenwho had been vaccinatedin various locations including an Illinois junior high and high school, a Massachusetts high school, a region in France, and a rural area near Helisinki, Finland.

Both USA schools had well over 90% vaccinated against measles. The vaccinators claim a 90% vaccination rate among any specific populationguarantees herd immunity for that population. This bogus claim serves to create more revenue while blaming non-vaccinators for endangering humanity.

Meanwhile, despite the fact that only five percent of vaccine adverse events get reported to the "voluntary" FDA's vaccine adverse event reporting system (VAERS), there are manyserious adverse eventsrecorded and many more that seep through the cracks to vaccine concerned internet sites.

Thank goodness for the few MDs and others who dare speak out despite the danger it potentially puts them in. It's up to us to learn from them and just say no to vaccinations.

Sources for this article include:

http://www.vaccinationcouncil.org

http://www.naturalnews.com/033399_vaccines_measles.html

http://www.naturalnews.com/028142_mumps_vaccines.html

http://www.naturalnews.com

http://www.naturalnews.com/023080.html

http://www.naturalnews.com/022400.html

Learn more:http://www.naturalnews.com/035715_vaccines_history_fraud.html#ixzz1tVjryRtc

More Proof: Vaccinated Monkeys Display Autistic Symptoms


Monkeys Get Autism-like Reactions to MMR & Other Vaccines In University of Pittsburgh Vaccine Study

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A University of Pittsburgh study showed vaccines altered the behavior in monkeys.
Someone did perform safety studies the U.S. Centers for Disease Control and Prevention (CDC) and the U.S. Food and Drug Administration (FDA) should have mandated be performed and vetted BEFORE numerous vaccines were released into the public sector for mass vaccinations.
Lead investigator Laura Hewitson, PhD, probably dropped a bombshell when she and her colleagues completed a macaque monkey (primates) study of the very same vaccines given to children during 1994-1999, i.e., the Measles-Mumps-Rubella (MMR) vaccine and several Thimerosal mercury-containing vaccines injected into children during that time frame when the autism spectrum disorder skyrocketed.
The results of that pilot study were published as a Research Paper in Acta Neurobiological Experimentals in 2010 and titled “Influence of pediatric vaccines on amydgala growth and opioid ligand binding in rhesus macaque infants: A pilot study.” [1] Even though there was alleged controversy revolving around Hewitson’s monkey studies, e.g., charges of conflicts of interest since she filed a claim with the vaccine court on behalf of her child, [2] the information generated needs to be revisited and duplicate studies need to be undertaken. Why haven’t they?  Is there too much influence from vaccine makers not to do them? Parents need to make demands on the U.S. Congress to require such safety studies on monkeys be duplicated immediately, plus suspend all mandates on vaccinations until the study results are in.  Did Dr Hewitson become another professional persona non-gratabecause she may have been on the right track?
Congress needs to consider seriously the Hewitson, et al. report that stated:
“Vaccine-exposed and saline-injected control infants [monkeys] underwent MRI and PET imaging at approximately 4 and 6 months of age, representing two specific timeframes within the vaccination schedule. …
 “These results suggest that maturational changes in amygdala volume and the binding capacity of [11C]DPN in the amygdala was significantly altered in infant macaques receiving the vaccine schedule.”[1]
That alone should be the explicit reason for duplicating the monkey study with independent non-pharmaceutical industry conflict of interest scientists. 
In this author’s opinion, no one has bigger conflicts of interest in study outcomes than the pharmaceutical makers who routinely perform them.  Those are the very studies that should be subject to the same criticism as Dr Hewitson’s.  Why aren’t they?  Good question?
For those keeping track data, ASD went from 1 in 5,000 in the 1990s to the recently acknowledged [March 2012] figures of 1 in 88 along with 1 in 6 children in the USA having developmental disabilities.  These stats were generated for data in the years 2006 to 2008. [3] There’s a 4 to 6 year lag time.  Could ASD be 1 in 50 by now at the rate it is escalating?, especially since there’s a heavier push on mandates for vaccinations.
According to the Hewitson, et al. research study, biological changes and altered behaviors did occur in vaccinated monkeys, which resembled and were similar to those observed in ASD diagnosed children.  However, there were no such symptoms showing or present in unvaccinated monkeys.  Don’t you just gotta love those little monkeys! Guess what else the ASD monkeys came up with, and Dr Wakefield is gonna like this one: Gastrointestinal problems manifested in vaccinated macaques such as “many significant differences in the GI tissue gene expression profiles between vaccinated and unvaccinated animals.” [3] It’s been a deeply debated topic within medicine that vaccinated children who contract ASD also have GI tract issues.  Personally, I gotta wonder how theBritish Medical Journal is going to deal with encrusted dried egg on its face when duplicate studies confirm the Hewitson monkey results.  Perhaps the infamous BMJ retraction of the Wakefield article and Doctor’s professional evisceration, commonly referred to as the “Wakefield Syndrome,” euphemistically speaking is medicine protecting its vested interests.
Those little monkeys, however, came up with some other significant information that led former National Institutes of Health director Dr Bernadine Healy to voice some bon mots like:
“I think public health officials have been too quick to dismiss the hypothesis as ‘irrational,’ without sufficient studies of causation…without studying the population that got sick.”
“I have not seen major studies that focus on 300 kids who got autistic symptoms within a period of a few weeks of the vaccines.” [4]
Perhaps the most on-point quote regarding the monkey study came from Scott Bono, the National Autism Association chairman, i.e., something those who are accused of being against vaccinations have been questioning and demanding:
 “To date, the CDC has conducted no safety testing on the possible harmful effects of simultaneously administering multiple vaccines to infants, and has steadfastly refused to state a preference for mercury-free vaccines to be given to children and pregnant women.  It’s time for HHS and Congress to step in and take vaccine safety away from the CDC.”  [4]
This author’s retort to Mr. Bono’s remark is that vaccine safety should be taken away from the Food and Drug Administration too!  I’d like to remind readers that Congress is more at fault than anyone in this vaccine debacle. Congress has oversight and it has dropped the ball big time, probably due to all the lobbyists from Big Pharma who prowl the halls of Congress with deep pockets and nice expensive luncheon dates. 
One of the issues I feel Congress has been remiss about is that it has not demanded safety studies and interaction of multiple vaccines studies BEFORE being placed into the marketplace.  According to common and accepted knowledge, no such safety research or studies have been done on the current childhood vaccination regimen, except until the Hewitson ‘monkey business’ that was funded by independent, private money, for which everyone, I think, should be eternally grateful. However, the study had to be shot down since it was not favorable to vaccine makers.  Why isn’t someone else duplicating the monkey studies?  Are they afraid of becoming another victim of science?  Why, when isn’t that what medical science should be all about: investigating problems and theories, publishing results, and interacting with other sciences, NOT excommunication as if they were breaking some religious dogma.  Or, do they, in some vested interests minds?

CURRENT VACCINE SAFETY ACTIVISM IN CONGRESS

Now here is something every VacTruth reader should consider seriously: Supporting Congressman Dan Burton’s (R-5-IN) request to the House Committee on Oversight and Government Reform Chairman Darrell Issa to hold hearings on the Vaccination Injury Compensation Program. Back on January 12, 2011, this writer filed a Whistleblower’s Complaint on Vaccines with Chairman Issa and has yet to receive an acknowledgement of that filing. 
Isn’t about time to revisit, update, and do more extensive research into the Autism Spectrum Disorder pandemicthat is spreading globally?
April 24, 2012 Congressman Burton posted a letter to The Hill’s Congress Blog titled, “It is time to re-engage on the autism epidemic.”  He also wants to pass legislation to force the President to address the ASD epidemic and its impact on Americans.  Burton is committed to helping millions of children, adults, and families afflicted with ASD.  We need to support Congressman Burton ASAP and here’s how:
  1. Contact the Canary Party to support their Facebook pages to hold Congressional hearings and a White House Conference on Autism.  Contact News@CanaryParty.org.
  2. Contact Congressman Darrell Issa at the Oversight and Government Reform Committee at 2157 Rayburn House Office Bldg., Washington, DC 20515 or preferably telephone your request for Autism Investigation Hearings to 202-225-5074.
For those who want to know about this information, the National Autism Association (www.nationalautism.org) will be holding a rally for toxin-free immunizations in Washington, DC on June 4, 2012, titled “Green Our Vaccines,” which this author thinks is an oxymoron.  How can you green vaccines when every ingredient is toxic?  Just check out the CDC’s PinkBook Vaccine Excipient & Media Summary athttp://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/b/excipient-table-2.pdf.
Before I leave this article, I would like VacTruth readers to know that my colleague who also writes for VacTruth, Laraine C Abbey, RN (retired) and I co-edited a 150 page monograph in January 2011 titled Vaccines & Vaccinations: The Need for Congressional Investigation, which you can read in full on VacTruth athttp://vactruth.com/vaccines-vaccinations-the-need-for-congressional-investigation/.
Apparently others have read it and agree.
Congressman Burton, Nurse Abbey and I congratulate you on taking the stand you have, and we offer you our resources in obtaining a Congressional investigation.
President Obama, Nurse Abbey and I respectfully request a White House conference on Autism, and we offer you our resources to effectuate a non-biased conference.
VacTruth readers, I charge you with spreading this information and article as far and wide as you possibly can so that we can get an investigation that ought to be open, not biased, and the scientific facts—nothing but the facts, like those the monkeys finally had to prove.  It was not monkey business; it’s the real deal.


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