TRAILER:
CURE: www.LymePhotos.com
In a cooperative agreement starting January 1995, prior to the FDA’s licensure of the varicella vaccine on March 17, the Centers for Disease Control and Prevention (CDC) funded the Los Angeles Department of Health Services’ Antelope Valley Varicella Active Surveillance Project (AV-VASP). Since only varicella case reports were gathered, baseline incidence data for herpes zoster (HZ) or shingles was lacking.
Goldman VaricellaAntelopeValley
VLA COMMENT: The near eradication of the early childhood Chicken Pox has resulted in people who have had natural wild chickenpox as children are not getting their”subtle” exongenous boosters from the subsequent generation of our children or our grandchildren who unfortunately are prevented from getting wild chicken pox, They are getting vaccinated with a different strain that can’t boost us. So, in essence, the CDC has simply brought another chicken pox strain into existence. Now we have two. However, the wild typeis not prevelant enough to give us the necessary booster so we don’t get shingles.
The only reason that “children who get the chickenpox vaccine APPEAR to have a much lower risk of shingles” is that the live vaccine has provided these children with a recent boost to their immunity. However, the vaccine-strain of varicella zoster virus (VZV)–also known as the Oka strain–is genetically different from the wild-type U.S. strain. When a vaccinated child is exposed to an adult with shingles or a child with wild-type varicella, if the strains are sufficiently heterologous, the vaccinated child will break out in chickenpox. It is also possible for the weakened vaccine-strain to revert to a more virulent strain that manifests wild-type pathology. This means when children are exposed to the wild-type strain, even though they may not have a breakthrough infection with chickenpox, they now harbor two heterologous (genetically different) strains of VZV–both of which are at a later time subject to reactivation as shingles. Thus, as they age, they will be even more likely to reactivate with shingles (unless periodically administered booster vaccine doses for life in order to maintain the immunity)–especially if they do not receive exogenous (outside) boosts to their cell-mediated immunity which, in the pre-vaccine era, came from expostures to other children infected with wild-type varicella which provided the adult with a subclinical boost that helped to suppress or postpone reactivattion of shingles.
I would also like to clear up the point that shingles has always been increasing–even prior to the licensing of the varicella vaccine. This statement is true; however, the increases were on the order of 2 to 4% per year (which were likely due to an aging population, or greater access to healthcare). Once a community had widespread distribution of varicella vaccine, increases in herpes zoster were on the order of 20% per year. For example, this source [Yih WK, Brooks DR, Lett SM, et al. The incidence of varicella and herpes zoster in Massachusetts as measured by the Behavioral Risk Factor Surveillance System (BRFSS) during a period of increasing varicella vaccine coverage, 1998-2003. BMC Public Health 2005; 5:68.
32. Schmid DS, Jumaan AO. Impact of varicella vaccine on varicella-zoster virus dynamics. Clin Microbiol Rev 2010; 23(1):202–217] found a 90% increase in shingles over 5 years (1999-2003).
The only reason that “children who get the chickenpox vaccine APPEAR to have a much lower risk of shingles” is that the live vaccine has provided these children with a recent boost to their immunity. However, the vaccine-strain of varicella zoster virus (VZV)–also known as the Oka strain–is genetically different from the wild-type U.S. strain. When a vaccinated child is exposed to an adult with shingles or a child with wild-type varicella, if the strains are sufficiently heterologous, the vaccinated child will break out in chickenpox. It is also possible for the weakened vaccine-strain to revert to a more virulent strain that manifests wild-type pathology. This means when children are exposed to the wild-type strain, even though they may not have a breakthrough infection with chickenpox, they now harbor two heterologous (genetically different) strains of VZV–both of which are at a later time subject to reactivation as shingles. Thus, as they age, they will be even more likely to reactivate with shingles (unless periodically administered booster vaccine doses for life in order to maintain the immunity)–especially if they do not receive exogenous (outside) boosts to their cell-mediated immunity which, in the pre-vaccine era, came from expostures to other children infected with wild-type varicella which provided the adult with a subclinical boost that helped to suppress or postpone reactivattion of shingles.
I would also like to clear up the point that shingles has always been increasing–even prior to the licensing of the varicella vaccine. This statement is true; however, the increases were on the order of 2 to 4% per year (which were likely due to an aging population, or greater access to healthcare). Once a community had widespread distribution of varicella vaccine, increases in herpes zoster were on the order of 20% per year. For example, this source [Yih WK, Brooks DR, Lett SM, et al. The incidence of varicella and herpes zoster in Massachusetts as measured by the Behavioral Risk Factor Surveillance System (BRFSS) during a period of increasing varicella vaccine coverage, 1998-2003. BMC Public Health 2005; 5:68.
32. Schmid DS, Jumaan AO. Impact of varicella vaccine on varicella-zoster virus dynamics. Clin Microbiol Rev 2010; 23(1):202–217] found a 90% increase in shingles over 5 years (1999-2003).
Many women are experiencing severe and long-lasting side effects after getting a LEEP. So why isn’t the medical community listening
Sarah also experienced a loss of sensation in her labia and overall vagina, which culminated in her loss of feeling during an orgasm, which she believes is a direct result of the surgery.
“It was like something had been removed surgically from my body. It was so frightening. I can’t even begin to say how it affected me sexually,” she explained, adding that her ability to experience an orgasm was also greatly diminished following the LEEP. “I had lost my entire sense of sexual identity and connection to my body. I was in a really terrible place. I couldn’t even cry. I was so numb.”
After my surgery and during my research, a doctor explained to me that the “cervix brain connection is severed [during a LEEP], and that results in the inability to transfer critical sensory afferent information from the cervix to the critical brain areas.”
The route of exposure for natural influenza infection is the respiratory tract, not subcutaneous (SC) or intramuscular (IM) injection. Influenza vaccines artificially changed the route of initial viral protein exposure to SC or IM injection thus making it similar to the route of exposure for dengue. The result is an IgE response to influenza proteins, similar to the response for dengue. It should therefore not come as a surprise that we are modifying the course of influenza infection such that it is acquiring characteristics of a dengue infection (hives and shock).
READ MORE…
Chronic Fatigue Syndrome and Non-HIV AIDS
Allied NATO Government is hiding millions of infectious NON HIV AIDS cases under the “Chronic Fatigue Syndrome (CFS)” ICD-code.
* Cptn. Joyce Riley’s military show THE POWER HOUR: “…HIV-Negative AIDS cases falsely reported and treated as CFS cases may be one of the biggest cover-ups we’ve ever seen…”
* In 1992 (i.e., after Gulf War 1) “…NEWSWEEK made an even more shocking announcement: …CFS patients who had the same immune system deficiencies as the NON-HIV AIDS cases…”
* Neenyah Ostrom’s book “America’s Biggest Cover-up: 50 More Things…CFS & Its Link To AIDS” cites: “Some CFS Patients May Be Non-HIV AIDS Cases.
My case goes up through the NIH, CDC, White House, WHO, to the UN. I hope that you will spread-the-news too (e.g., post on Facebook, Twitter, add to eNews).
“How much more radiation penetrates your body today compared to ten years ago? Is it twice as much, three times as much? No it is a quintillion times more – that is a one with 18 zeros.” Olle Johansson, PhD
Today we encounter a hundred thousand times the level of radiation from wireless technologies than we did decades ago. Yet the safety standards set by federal regulatory agencies are outdated. GENERATION ZAPPED investigates the potential dangers of prolonged exposure to Radio Frequencies (RF) from wireless technology,
its effects on our health and well-being, as well as the health and development of our children. So how can we uncover the facts and reduce our exposure to limit the associated health risks during this technological revolution? GENERATION ZAPPED attempts to do just that.
Many propagandists claim that fetal cells are derrived from one cell line, one fetus, decades ago. Here is Sayerji from Green Meds research on the currency of fetal cell lines. “BIOTECH’S DARK PROMISE!
SNOPES: Although Snopes dances around whether there are fetal cells in Pepsi…they confirm that Pepsi has a deal with Senomyx producers and that Senomyx indeed uses a technology that is derived from fetal cells.
Aborted cells are used in the development of artificial flavor enhancers by biotech company Senomyx, with which PepsiCo signed a four-year, $30 million agreement in 2010 for research and development. No Pepsi products containing Senonymx flavor enhancers should be expected until 2013.
The tongue of a foetus was used solel to develop a technology that could “taste” how sweet, sour, salty etc. To my understanding now, it is not in the products, but a potentially dangerous compound is.
Nestles, Kraft, Pepsi, etc invested in the development of a profound compound whose patent papers show the size of the compound being like half of a copy paper. The consideration we are having is that were there any long term studies? How senomyx (unlabeled) works is that this compound in the product affects the taste buds.
So instead of sugar, this compound is put in the product and fools your tongue to think their is sugar in the product but there is not…so no sugar calories. However, who is to say that this compound won’t destroy the taste buds with its repeated, unnnatural assault and leave our tastebuds damaged. We enjoy food and drink…we really enjoy taste so much that we overeat because though our stomach is full our mouths want some delight. What would the world seems like if we lost our tastebuds due to this ubiquitous unnatural assault? I have put in a FOIA request for a copy of their long term test that should have been done for FDA approval.
VLA Comment: Apparently, Cog for Life has done “extensive research” on the issue and is assured that there is no fetal DNA or cloned human DNA in the final products as the technology using fetal cells were just to identify the taste receptors in order to make “chemical compounds” to alter and fool our tastebuds. Although, apparently, except for using fetal cells of healthy but aborted babies to discover the mechanism of taste receptors, the final aim was to develope chemical compounds to alter our tastebuds. My question is how good is that for our species that we can no longer can trust our God given senses? And moreover, are these chemical compounds poisonous, carcinogenic or ultimately destructive to the organic tastebud receptors?
Not part of Senomyx – Neocutis Products:
This company produces anti wrinkle creams that contain cells from a 14 week gestation aborted malebaby. Following is the list of the creams, but we recommend a full boycott of all Neocutis Products.
• Bio-Gel Prevedem Journee
• Bio-Serum Lumiere
• Bio Restorative Skin Cream
Vaccines do contain HEK Cells:
MMR II (Merck)
ProQuad (MMR + Chickenpox – Merck)
Varivax (Chickenpox – Merck)
Pentacel (Polio + DTaP + HiB – Sanofi Pasteur)
Vaqta (Hepatitis-A – Merck)
Havrix (Hepatitis-A – Glaxo SmithKline)
Twinrix (Hepatitis-A and B combo – Glaxo)
Zostavax (Shingles – Merck)
Imovax (Rabies – Sanofi Pasteur)
Other medicines:
Pulmozyme (Cystic Fibrosis – Genetech)
Enbrel (Rheumatoid Arthritis – Amgen)
Note:
Moral options exist for Rabies, Polio,Rheumatoid Arthritis. Separate moral optionscurrently not available for Measles and Mumps.
VLA COMMENT: It must be over 10 years ago that VLA tried to influence the FDA regarding Senomyx when it was just getting off the ground. We did the same with GMO technology…but much of the corporate establishment knows no bounds when it comes to greed. There is more to know.
San Diego-based Senomyx has created novel flavors such as cold and creamy based on a rethinking of how taste buds perceive flavor. Using nanoscale assays, researchers have identified which individual cells on a given taste bud perceive a flavor. Each cell would recognize just one of the five main flavors — bitter, salty, sweet, sour and umami. Working within this conceptualization, the company has developed a library of flavors, incluing compounds called bitter blockers. These specialized molecules trick the tongue into not tasting the bitterness naturally inherent in foods such as cocoa or soy. These bitter blockers as well as Senomyx’s sweet and salty enhancers have already gotten the nod of approval from food giants such as Nestle and Coca Cola who are responding to consumer desires for packaged foods and beverages formulated with less salt and sugar. READ MORE…
VLA Comment: Quote from Bittermyx (Senomyx) “Our scientists have identified the function of 22 bitter taste receptors responsible for sending the bitter taste signals in many API products used in OTC and prescription drugs. Leveraging this knowledge, Senomyx has developed a comprehensive bitter receptor profile to more effectively screen APIs and to identify the specific bitter receptors associated with bitter taste of a given API”.
You see, they are affecting the receptors on our tongues, basically without our knowledge or permission. http://www.senomyx.com/api-program/
Lawyer Impulsively Jumps In Front of Train: Effexor, like All A/D’s, Can Cause Impulsivness | ||||
Suicide | Med For Depression | 2011-11-11 | England | Physician Kills Himself Shortly After Starting an A/D |
Personality Drained Away/Huge Weight Gain | Med For Depression | 2011-11-10 | England | After Many Years on A/D’s, Man Felt Like His Personaity Was Drained Away & He Became Obese |
Violence | Med For Depression | 2011-11-10 | Canada | Man Strikes an Ax at a Neighbor |
Death | Antidepressant | 2011-11-10 | England | 23 Year Old Woman Dies of Cardio-Respiratory Arrest: High Level of A/D’s in Body: No Alcohol or Drug |
Suicide | Celexa Antidepressant | 2011-11-10 | England | Woman, 73, Kills Herself While on Celexa |
Murder-Suicide | Prozac | 2011-11-09 | California | Man Kills Two Police Officers & Himself |
Heart Disease | Med For Depression | 2011-11-09 | Global | ++Depression Meds Are More Likely to Cause Heart Disease |
Murder Attempt | Med For Depression | 2011-11-08 | Malta/Mediterranean | Man Attempts to Murder Uncle With Hammer: Confused & Agitated |
Bizarre Behavior | Lexapro & Desyrel Antidepressants | 2011-11-08 | California | +Famous Actress Kim Richards Exhibits Bizarre Behavior on TV |
Dulled Mind/Numbed Body | Zoloft | 2011-11-07 | Georgia | Woman Physician Quits Zoloft: Tells How She Recovered From Depression |
Suicide | Med For Depression | 2011-11-07 | Texas | Woman Drives Her Car Into Lake |
Suicide | Antidepressants | 2011-11-05 | Ohio | Soldier, 22, Kills Himself: Black Box Warning on Suicidality for This Age Group |