Pope Criminalizes the Reporting of Sex Crimes
VATICAN CITY — Few eyebrows were raised last week when Pope Francis brought the Vatican’s legal system up to date by criminalizing leaks of official information and formalizing laws against sex crimes. But now that the laws have been made public, a closer look revealed that the pope has made it illegal to report sex crimes against children.–According to the new laws, revealing or receiving confidential Vatican information is now punishable by up to two years in prison, while newly defined sex crimes against children carry a sentence of up to twelve years. Because all sex crimes are kept confidential, there is no longer a legal way for Vatican officials to report sex crimes.— “We didn’t mean for this to happen, obviously,” lamented Vatican foreign minister Monsignor Dominique Mamberti. “It’s quite the papal pickle that His Holiness has placed upon our heads. Sex crimes are more illegal than ever, but technically it’s illegal to report them.” Mamberti said that the simultaneous passing of each law is merely a coincidence and insisted that the Church is not trying to protect itself against further embarrassment, but critics outside the Vatican are skeptical.— “We didn’t mean for this to happen, obviously,” lamented Vatican foreign minister Monsignor Dominique Mamberti. “It’s quite the papal pickle that His Holiness has placed upon our heads. Sex crimes are more illegal than ever, but technically it’s illegal to report them.” Mamberti said that the simultaneous passing of each law is merely a coincidence and insisted that the Church is not trying to protect itself against further embarrassment, but critics outside the Vatican are skeptical. “They know exactly what they’re doing,” claims Fabrizio Perona of Italy’s La Repubblica newspaper. “They just thought nobody would notice. The Church wants to impress the world by getting tough on sex crimes, but they criminalized leaks, which is the only way anybody would ever discover their crimes. It’s genius, if you stop and think about it.” Mamberti says plans are already being made to eliminate the loophole, but change often comes slowly to antiquated Vatican law, which is based on the 1889 Italian code. “We’re not going to let a dangerous law like this stand, but people need to understand that this is the Vatican, and there is a process here. Voting, incense, prayer. We ask the minors at risk to please be patient with us.” Fortunately, only clergy and lay people who live and work in Vatican City are subject to the new legislation, which differs from the canon law governing the universal Catholic Church. Fortunately, only clergy and lay people who live and work in Vatican City are subject to the new legislation, which differs from the canon law governing the universal Catholic Church As the Holy See moves to clarify the law, Mamberti has warned would-be offenders within Vatican walls that they “are still subject to the most watchful eye of all: the eye of God. His judgment is greater than—oh, who am I kidding? For now, there is nothing we can do.” – See more at: http://www.newslo.com/pope-criminalizes-the-reporting-of-sex-crimes/#sthash.yuwK7BRC.dpuf
Other common name(s): Kelley’s treatment, Gonzalez treatment, Issels whole body therapy, Gerson therapy
Scientific/medical name(s): none
Metabolic therapy uses a combination of special diets, enzymes, nutritional supplements, and other measures in an attempt to remove “toxins” from the body and strengthen the body’s defenses against disease.
There is no convincing scientific evidence that metabolic therapy is effective in treating cancer. However there are many different practices that make up metabolic therapy. Some of these practices may be harmful.
How is it promoted for use?
Metabolic therapy is based on the belief that toxic substances in food and the environment build up in the body and create chemical imbalances that lead to diseases such as cancer, arthritis, and multiple sclerosis. Some proponents of this approach say that metabolic therapy rids the body of these toxins and strengthens its resistance to disease. Some claim that a special diet can cure serious illnesses, including cancer. Others claim that they can evaluate a patient’s metabolism and diagnose cancer before symptoms appear and that they can locate tumors and learn the tumor’s size and growth rate.
What does it involve?
Metabolic therapies vary a great deal depending on the practitioner, but all are based on special diets and detoxification. This usually involves natural, whole foods such as fresh fruits and vegetables, as well as vitamins and mineral supplements. Other measures may include colonic irrigation with coffee or hydrogen peroxide enemas, juicing, enzyme supplements, visualization, and stress-reduction exercises. At least one metabolic therapy system also includes the drug laetrile (see Colon Therapy, Enzyme Therapy, Imagery, Juicing, and Laetrile).
Among the better known types of metabolic therapy are Kelley’s treatment, the Gonzalez treatment, Issels whole body therapy, and Gerson therapy (see Gerson Therapy,).
Kelley’s treatment includes dietary supplements (such as enzymes and large doses of vitamins, minerals, and amino acids), detoxification (such as fasting, exercising, and using laxatives and coffee enemas), a restricted diet, chiropractic adjustments, and prayer. Practitioners classify people into different metabolic types that form the basis for individual dietary and supplement recommendations.
The Gonzalez treatment is similar to Kelley’s treatment and includes extracts or concentrates from animal organs such as thymus and liver (taken from beef or lamb) and digestive enzymes as part of the plan (see Cell Therapy).
Another form of metabolic therapy is Issels whole body therapy. Patients are asked to remove teeth that contain mercury dental fillings, follow a strict diet, and eliminate the use of tobacco, coffee, tea, and other substances that are considered harmful. Some patients are encouraged to undergo psychotherapy to relieve stress and deal with anger and emotional distress (see Psychotherapy).
Gerson therapy involves a strict dietary program, coffee enemas, and various mineral or chemical supplements.
What is the history behind it?
Gerson therapy was introduced by Max Gerson, MD, a German-born physician who immigrated to the United States in 1936. Gerson initially used the therapy for treating migraine headaches and tuberculosis and began using it for cancer in 1928. Kelley’s treatment was developed in the 1960s by American orthodontist William Donald Kelley, DDS, MS. Nicholas Gonzalez, MD, became interested in metabolic therapy as a medical student in 1981 when he was asked to review Dr. Kelley’s work.
In the 1970s and 1980s, Harold Manner, PhD, a biology professor, was also a major proponent of metabolic therapy. He claimed to have cured cancer in mice with injections of laetrile, enzymes, and vitamin A. In his version of metabolic cancer therapy, patients often received another unproven alternative substance, a chemical compound called dimethyl sulfoxide (see DMSO). In the early 1980s, Dr. Manner moved to Tijuana, Mexico, to treat patients (see Questionable Cancer Practices in Mexico). His clinic there is still open despite his death in 1988.
What is the evidence?
There is general agreement among scientists that there are differences in the metabolism of certain cells in people with cancer compared to people without cancer. There is also general agreement regarding the importance of attention to optimal nutrition as a component of conventional oncology care. Otherwise, there is no convincing clinical evidence that supports the claims made for metabolic therapy or any of its components. Some aspects of metabolic therapy may in fact be harmful.
An article on metabolic therapies on the Memorial Sloan-Kettering Cancer Center Web site concludes that “…retrospective reviews of the Gerson, Kelley, and Contreras metabolic therapies show no evidence of efficacy.” And a review article in the Journal of Clinical Gastroenterology, “Colonic Irrigation and the Theory of Autointoxication,” concludes that
“[c]offee enemas are a hazardous derivative of colon therapy…. Its proponents claim that caffeine is absorbed in the colon and leads to a vasodilatation in the liver, which in turn enhances the process of elimination of toxins. None of this is proved, nor is there any evidence of the clinical efficacy of coffee enemas. Coffee enemas are associated with severe adverse reactions.”
In a 1990 report from the Congressional Office of Technology Assessment, 3 oncologists reviewed the “best cases” collected by Dr. Gonzalez. In the vast majority of these cases, they found claims of benefit from metabolic therapy to be unconvincing. In addition, they found a few cases to be “unusual” at best, meaning that these patients lived longer than typical people with the same type and stage of cancer but concluded that this difference was probably due to statistical variation that occurs when “best cases” are selected from a large group of patients. A group of physicians who practiced alternative medicine (none of whom were cancer specialists) concluded that the alternative regimen was beneficial in some cases.
A small study of patients with pancreatic cancer — conducted by Dr. Gonzalez and published in Nutrition and Cancer in 1999 — found that patients treated with pancreatic enzymes survived longer than typical patients with pancreatic cancer. In a recent review of alternative cancer cures, an expert in integrative oncology research methods noted that, “The study was small and obviously prone to several biases. Not only is the comparison with national averages unadjusted for confounders (other factors that can affect outcome), but the principal results are based on patient selection; twelve patients who did not comply with treatment were excluded from analysis.” A randomized clinical trial has been sponsored by the National Cancer Institute to evaluate the Gonzalez regimen for treating pancreatic cancer, but no results of this trial have yet been published in any available peer-reviewed medical journal.
Are there any possible problems or complications?
These substances may have not been thoroughly tested to find out how they interact with medicines, foods, or dietary supplements. Even though some reports of interactions and harmful effects may be published, full studies of interactions and effects are not often available. Because of these limitations, any information on ill effects and interactions below should be considered incomplete.
Some aspects of metabolic therapy are considered dangerous. There are reports of complications related to liver cell injections, as well as nutritional deficiencies due to restricted diets. Several deaths have been directly linked to injecting live cells from animals (a practice called cell therapy). The drug laetrile may cause nausea, vomiting, headache, dizziness, and even cyanide poisoning, which can be fatal. Care should be taken to make sure that any diet containing raw meat or raw meat juice is free from contamination, given the increasing number of diseases that are known to be transmitted from animals to people.
Reports of illness and even deaths linked to colonic irrigation have been published in several medical journals. (See Colon Therapy for more information.) People with diverticulitis, ulcerative colitis, Crohn’s disease, severe hemorrhoids, or rectal or colon tumors, or who are recovering from bowel surgery, may be at higher risk of bowel injury when using enemas. People with kidney or heart failure may be more likely to experience fluid overload or electrolyte imbalances. Enemas can also cause discomfort and cramps.
Women who are pregnant or breast-feeding should not use this method. Relying on this type of treatment alone and avoiding or delaying conventional medical care for cancer may have serious health consequences.
[F1]If no full disclosure then would be suspect of what they are saying has any real credibility—someone here is being mislead with any credibility by hiding there secret—may see something else in them like aborted baby fetus extract—not beyond the realm of possibility
[F2]Organics is a farce and they may grow something but like the rice in the previous comment these to will have sevcre cross contamination—should not use at all—the only beer you should drink is what you make yourself
[F3]If such a thing actually exist—with cross gee tech in plants and the different levels of chemtrail activity —again the raw materials to be bough and make at home would be the best answer to drinking beer ir even wine
Script of the Show August 24 2013
The Liquid Part of Tattoo Ink
Comprehensive List Of Companies That Uses Aborted Fetal Cells As Flavor
Evolution On the Inside Track: How Viruses in Gut Bacteria Change Over Time
Sudden Decline in Testosterone May Cause Parkinson’s Disease Symptoms in Men
To remove pesticides from fruits and Veggies and esp for the purpose of cleaning berries which even if organic are the highest sources of super bacterias that are very powerful (never mind the pesticides if got the inorganic ones)… all you need to do it put the veggies/fruits/berries into a container and fill with water and put in one tbl of 35% Hydrogen Peroxide or ½ cup of regular hydrogen peroxide you buy at any store… —http://www.dfwx.com/h2o2.htm for the 35% food grade hydrogen peroxide… this stuff is a pain in the butt and will bleach your hands quick, so handle with care, I put this stuff into a dropper bottle I put in fridge and take for use with any protocol or heavy metals of lead and/or arsenic I’m trying to remove… my protocol for this is 3 drops 3x/day in 2 to 3 cups of water, for 3 weeks, is usually enough, but Barry Carter mentioned on the call that he does this protocol only once a day like so – 1 drop first day, 2 drops next day, adding one drop each day til at 20 drops, always mix with plenty of water, like 3 cups and do for 3 weeks – til at 20 drops and that’s usually the end of lead and arsenic poisoning…. ( or could just do the mini beet protocol for a couple months, but this is faster, though the mini beet protocol is much more pervasive and will catch all lead and arsenic in all cells and bone no matter how long ago they were deposited there!) –Why 35% – b/c it is purer form of H2O2 than store bought 3%… —
2007 The best de-pesticider in the world is a 99.9% pesticide and herbicide and insecticide remover… it’s $1000 but after this many years it might only be $750 if we’re lucky so I will definitely go thru my files, look it up again.———2011 Luckily an American company came along and spent $10million on FDA and EPA passes and got the USA version of this type device in, will kill all parasites and all filth on outside and thru body of the fruit & veggies (if you wash the wax off first), makes them last longer too, great for removal of pesticides etc… $250 plus shipping, whewww, lot better than $550 that the Japanese one is going for and wow is this 10x better looking but exact same theory… let me know if you would like one…. Robert von 1-940-233-0484 Dallas TX USA—Directions more exact… for say a container of about 3 inches high, 7 inches wide, and 1 foot long… filled with water I put in a couple of sprays of fruit and veggie or a alcohol or Essential Oil to wash (not to de-pesticide but for removal of wax that would hinder de-pesticiding, and start with hot water adding to container then veggies, so that the hot water and the fruit wash will wash the veggies/fruits while filling with water thus melting and removing waxing… then I put in ¼ cup of 3% H2O2, and wait 20 mins and you are done… for half a sink I would put in ½ a cup worth and for full sink worth of veggies and water I would put in full cup of 3%…
One more note: this is a great way to de-pesticide but you are NOT getting rid of the chemical exposure that has transformed your veggies and fruits… so for those fortunate enough to buy nothing but organic, that is awesome and that is the best, and for those not so fortunate enough to buy organic only, then this is a way to help yourself out, b/c I do this wash when I cannot find organic, and the second I’m home with groceries, if any with pesticides, I fill up sink and go at it… then let them all dry – put everything into the fridge… and I’m good to go. (note… anything I de-pesticide that has an easily removeable skin, esp. an apple or say even a squash, I will peel it anyway just for overkill b/4 I eat or cook it, respectively) Again this is not as effective at 99.9% removal as the machine I mentioned, but it is a great and amazingly cheap alternative
For those with a little more knowledge and background, I will put in another note: yes, chemicals etc in the fruits/veggies that are not organic force a chemical change in structure of the foods you eat even if remove 100% of all the pesticides afterwards, there is still the messed up “nature” of these inorganics to take into consideration, but for those on limited budget these inorganics will NOT stop you from being healed of your diseases etc…for those that have the money, buy 100% organic.
35% – for those that get themselves bleached in the process of pouring 35% H2O2, b/c did not use gloves… no problem, just put on some olive oil immediately and then wash hands with soap and water 3 times then put on more olive oil… even if hands are white they will no longer burn, or will stop burning within few mins, no worries…you will find the whiteness will continue for a while, no problem, but the burning has totally stopped and within the hour or within a few hours all whiteness is completely gone… if Barry has better alternatives for those who get a little 35% H2O2 on themselves, please let me know as well, thanx so sooo much!
I also use this as a healthy alternative to bleach when need to bleach clothing instead of using Clorox or etc… so 35% makes for excellent and superior bleach alternative…also good if wash clothes with vinegar and 35% H2O2…
Manufacturers are not required to reveal their ingredients or conduct trials, and recipes may be proprietary. Professional inks may be made from iron oxides (rust), metal salts, plastics. Homemade or traditional tattoo inks may be made from pen ink, soot, dirt, blood, or other ingredients.
CHeavy metals used for colors includeC mercury (red); C lead (yellow, green, white); Ccadmium (red, orange, yellow); Cnickel (black); zinc (yellow, white); chromium (green); cobalt (blue); C aluminium (green, violet); Ctitanium (white); copper (blue, green); iron (brown, red, black); and Cbarium (white). Metal oxides used includeC ferrocyanide andC ferricyanide (yellow, red, green, blue). Organic chemicals used include azo-chemicals (orange, brown, yellow, green, violet) and naptha-derived chemicals (red). Carbon (soot or ash) is also used for black. Other compounds used as pigments include antimony, Carsenic, Cberyllium, calcium, Clithium, selenium, and sulphur.–Tattoo ink manufacturers typically blend the heavy metal pigments and/or use lightening agents (such as lead or titanium) to reduce production costs
Traditional monochrome tattoos are still very popular, making black one of the most common colors of tattoo ink. Black pigment typically consists of magnetite crystals, carbon, powdered jet, bone black, wustite or logwood extract. These ingredients cover the range of typical pigment sources, including metal salts, traditional minerals, vegetable dyes and modern organics and plastics. However, according to a study published in the Journal of Cosmetic Dermatology in 2009, few cases of adverse reactions to tattoo ink, including allergic responses, have been linked to black pigments.
Health Canada has advised against the use of “black henna” temporary tattoo ink which containsC para-phenylenediamine (PPD), an ingredient in hair dyes. Black henna is normally applied externally in temporary Mehandi applications, rather than being inserted beneath the skin in a permanent tattoo.–Allergic reactions to PPD include rashes, contact dermatitis, itching, blisters, open sores, scarring and other potentially harmful effects.
Brown or Flesh Tone Pigments
Brown and flesh tone tattoo inks derive their pigments from ochre, or ferric oxides that are sometimes mixed with clay. Although naturally yellow in color, ochre develops a reddish hue when heated and dried.
Red, Orange and Yellow Pigments
While the “warm” colors of red, yellow and orange are similar in hue, they derive from a wide variety of ingredients. Red pigment can consist of cinnabar (mercury sulfide) and cadmium red (both known to be toxic), iron oxide (otherwise known as common “rust”) or napthol, which has a lower incidence of adverse reactions. Orange pigment is made from disazopyrazolone, disazodiarylide or cadmium seleno-sulfide, which are fairly stable organic substance. Yellow pigment is made from curcuma (found in ginger plants such as tumeric), cadmium yellow, ochres, disazodiarylide or chrome yellow.
Green, Blue and Violet Pigments
The “cool” colors of green, blue and violet also derive from a variety of sources. Green pigments are generally metallic or mineral in nature and are sometimes formed by mixing yellow and blue pigments. Sources of green pigments can include chromium oxide, ferro- and ferricyanides, lead chromate, malachite, monoazo pigment and phthalocyanines. Blue pigments include azure and cobalt blue, cobalt aluminate and copper phtalocyanine, which the FDA considers safe enough for use in infant products and contact lenses. Violet pigments include manganese ammonium pyrophosphate, dioxazine/carbazole, quinacridone and aluminum salts. Note that some violet pigments may tend to fade and shift in hue after long exposure to sunlight.
White pigments can be used in isolation to create white tattoo ink, or they can lighten the shade of another color. White pigments are often based on lead carbonate, barium sulfate, titanium dioxide or zinc oxide
The Liquid Part of Tattoo Ink
Tattoo ink consists of pigment and a carrier. The carrier may be a single substance or a mixture. The purpose of the carrier is to keep the pigment evenly distributed in a fluid matrix, to inhibit the growth of pathogens, to prevent clumping of pigment, and to aid in application to the skin. Among the safest and most common ingredients used to make the liquid are:
ethyl alcohol (ethanol)
However, many other substances have been and may be used, including:
denatured alcohols (are toxic and can burn the skin)
other alcohols (methyl alcohol or methanol and isopropyl alcohol or rubbing alcohol are commonly used, although they are toxic)
ethylene glycol (antifreeze, which is toxic)
aldehydes, such as formaldehyde and gluteraldehyde (highly toxic)
various surfactants or detergents
There are many other substances that could be found in an ink. A tattooist has the choice of mixing his or her own ink (mixing dry dispersed pigment and a carrier solution) or purchasing what are called predispersed pigments. Many predispersed pigments are as safe or safer than inks mixed by the tattooist. However, the ingredient list need not be disclosed, so any chemical could be present in the ink. The best advice is to make sure the ink supplier and the particular ink has a long history of safety. Although I have applied the word ‘toxic’ to many substances listed on the pigment and carrier list, that is an oversimplification. Some of these chemicals are mutagens, carcinogens, teratogens, toxins, or participate in other reactions in the body, some of which may not show up for decades.
Another interesting factoid concerning alcohol is that it is known as a ‘promoter’. In biomedical parlance, this means alcohol works synergistically with mutagens, teratogens, and carcinogens to make them more likely to cause harm than they would by themselves. If any hazardous substances are present in the ink, alcohol helps them into the body and then increases the chance that they may cause mutation or disease, not just at the site of the tattoo, but throughout the body
Compostion of Tattoo Pigments
Iron Oxide (Fe3O4)
Iron Oxide (FeO)
Natural black pigment is made from magnetite crystals, powdered jet, wustite, bone black,and amorphous carbon from combustion (soot). Black pigment is commonly made into India ink.
Logwood is a heartwood extract from Haematoxylon campechisnum, found in Central America and the West Indies.
Ochre is composed of iron (ferric) oxides mixed with clay. Raw ochre is yellowish. When dehydrated through heating, ochre changes to a reddish color.
Cadmium Red (CdSe)
Iron Oxide (Fe2O3)
Iron oxide is also known as common rust. Cinnabar and cadmium pigments are highly toxic. Napthol reds are synthesized from Naptha. Fewer reactions have been reported with naphthol red than the other pigments, but all reds carry risks of allergic or other reactions.
disazodiarylide and/or disazopyrazolone
The organics are formed from the condensation of 2 monoazo pigment molecules. They are large molecules with good thermal stability and colorfastness.
Ochres (iron oxides mixed with clay)
Cadmium Yellow (CdS, CdZnS)
Chrome Yellow (PbCrO4, often mixed with PbS)
Curcuma is derived from plants of the ginger family; aka tumeric or curcurmin. Reactions are commonly associated with yellow pigments, in part because more pigment is needed to achieve a bright color.
Chromium Oxide (Cr2O3), called Casalis Green or Anadomis Green
Ferrocyanides and Ferricyanides
The greens often include admixtures, such as potassium ferrocyanide (yellow or red) and ferric ferrocyanide (Prussian Blue)
Blue pigments from minerals include copper (II) carbonate (azurite), sodium aluminum silicate (lapis lazuli), calcium copper silicate (Egyptian Blue), other cobalt aluminum oxides and chromium oxides. The safest blues and greens are copper salts, such as copper pthalocyanine. Copper pthalocyanine pigments have FDA approval for use in infant furniture and toys and contact lenses. The copper-based pigments are considerably safer or more stable than cobalt or ultramarine pigments.
Manganese Violet (manganese ammonium pyrophosphate)
Various aluminum salts
Some of the purples, especially the bright magentas, are photoreactive and lose their color after prolonged exposure to light. Dioxazine and carbazole result in the most stable purple pigments.
Lead White (Lead Carbonate)
Titanium dioxide (TiO2)
Barium Sulfate (BaSO4)
Some white pigments are derived from anatase or rutile. White pigment may be used alone or to dilute the intensity of other pigments. Titanium oxides are one of the least reactive white pigme
Comprehensive List Of Companies That Uses Aborted Fetal Cells As Flavor
(KipNews) Children of God for Life is calling on the public to boycott products of major food companies that are partnering with Senomyx, a biotech company that produces artificial flavor enhancers, unless the company stops using aborted fetal cell lines to test their products.
In 2010, the pro-life organization wrote to Senomyx CEO Kent Snyder, pointing out that moral options for testing their food additives could and should be used.
But when Senomyx ignored their letter, they wrote to the companies Senomyx listed on their website as “collaborators” warning them of public backlash and threatened boycott. Food giants Pepsico, Kraft Foods, Campbell Soup, Solae and Nestlé are the primary targets of the boycott, though Senomyx boasts other international partners on their website.
Senomyx website states that “The company’s key flavor programs focus on the discovery and development of savory, sweet and salt flavor ingredients that are intended to allow for the reduction of MSG, sugar and salt in food and beverage products.…Using isolated human taste receptors, we created proprietary taste receptor-based assay systems that provide a biochemical or electronic readout when a flavor ingredient interacts with the receptor.”
Senomyx notes their collaborators provide them research and development funding plus royalties on sales of products using their flavor ingredients.
“What they do not tell the public is that they are using HEK 293 – human embryonic kidney cells taken from an electively aborted baby to produce those receptors”, stated Debi Vinnedge, Executive Director for Children of God for Life, a pro-life watch dog group that has been monitoring the use of aborted fetal material in medical products and cosmetics for years.
“They could have easily chosen COS (monkey) cells, Chinese Hamster Ovary cells, insect cells or other morally obtained human cells expressing the G protein for taste receptors”, Vinnedge added.
In writing to their collaborators, it took three letters before Nestlé finally admitted the truth about their relationship with Senomyx, noting the cell line was “well established in scientific research”.
After hearing Ms Vinnedge speak publicly on the problem, angry consumers began writing the companies. Both Pepsico and Campbell Soup immediately responded.
Shockingly, Pepsico wrote: “We hope you are reassured to learn that our collaboration with Senomyx is strictly limited to creating lower-calorie, great-tasting beverages for consumers. This will help us achieve our commitment to reduce added sugar per serving by 25% in key brands in key markets over the next decade and ultimately help people live healthier lives.”—Campbell Soup was more concerned in their response: “Every effort is made to use the finest ingredients and develop the greatest selection of products, all at a great value. With this in mind, it must be said that the trust we have cultivated and developed over the years with our consumers is not worth compromising to cut costs or increase profit margins.”–While Campbell did not state they would change their methods, still their response, gave Vinnedge hope. “If enough people voice their outrage and intent to boycott these consumer products, it can be highly effective in convincing Senomyx to change their methods”, she noted.
Click here to read the response letters from Pepsico, Campbell Soup and Nestlé letters (Letter 1, 2, 3)
Need proof of Senomyx use of aborted fetal cell lines?
Following is the link to the on-line article for their patent on sweet receptors (they filed several separate patents for each of the different taste receptors): http://www.ncbi.nlm.nih.gov/pmc/articles/PMC123709/
As it is lengthy and technical, we recommend you simply do a search in the document for HEK-293.
HEK CELL (Human Embryonic Kidney 293 cells), also often referred to as HEK 293, 293 cells, or less precisely as HEK cells are a specific cell line originally derived from human embryonic kidney cells grown in tissue culture. HEK 293 cells are very easy to grow and transfect very readily and have been widely-used in cell biology research for many years. They are also used by the biotechnology industry to produce therapeutic proteins and viruses for gene therapy.
Below is a list of products that contain HEK cells.
HEK cell Products; http://www.cogforlife.org/fetalproductsall.pdf
Pepsi Beverages on the Boycott
• All Pepsi soft drinks
• Sierra Mist soft drinks
• Mountain Dew soft drinks
• Mug root beer and other soft drinks
• No Fear beverages
• Ocean Spray beverages
• Seattle’s Best Coffee
• Tazo beverages
• AMP Energy beverages
• Aquafina water
• Aquafina flavored beverages
• DoubleShot energy beverages
• Frappuccino beverages
• Lipton tea and other beverages
• Propel beverages
• SoBe beverages
• Gatorade beverages
• Fiesta Miranda beverages
• Tropicana juices and beverages
Other Senomyx Partner Products
At this time we are formally boycotting PepsiCo products, however many have asked us for lists of the other companies involved with Senomyx and what products are involved.
Unless we know a certain product or brand name specifically, we intend to boycott all of the company’s products.
• All coffee creamers
• Maggi Brand instant soups, bouillon cubes, ketchups, sauces, seasoning, instant noodles
Kraft – Cadbury Adams LLC Products:
• Black Jack chewing gum
• Bubbaloo bubble gum
• Bubblicious bubble gum
• Freshen Up Gum
• Sour Cherry Gum (Limited)
• Sour Apple Gum (Limited)
Cadbury Adams LLC Candies
• Sour Cherry Blasters
• Fruit Mania
• Bassett’s Liquorice All sorts
• Maynards Wine Gum
• Swedish Fish
• Swedish Berries
• Juicy Squirts
• Original Gummies
• Fuzzy Peach
• Sour Chillers
• Sour Patch Kids
• Mini Fruit Gums
Other Cadbury Adams LLC Products
• Certs breath mints
• Halls Cough Drops
Not part of Senomyx – N eocutis 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 Restorative Skin Cream
Vaccines Containing HEK Cells And the Manufacturers:
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)
Pulmozyme (Cystic Fibrosis – Genetech)
Enbrel (Rheumatoid Arthritis – Amgen)
Note: Moral options exist for Rabies, Polio,
Rheumatoid Arthritis. Separate moral options
currently not available for Measles and Mumps.
source; http://birthofanewearth.blogspot.com viahttp://www.cogforlife.org/
Back in January, Oklahoma Senator Ralph Shortey proposed legislation to ban the production of aborted fetal cell-derived flavor chemicals in his home state. If passed, S.B. 1418 would also reportedly ban the sale of any products that contain flavor chemicals derived from human fetal tissue, which includes Pepsi products as well as products produced by Kraft and Nestle (http://www.naturalnews.com)
.Biotech company using cell lines from aborted babies in food enhancement testing http://www.lifesitenews.com/news/biotech-company-using-cell-lines-from-aborted-babies-in-food-enhancement-te
Pro-life groups call for Pepsi boycott over aborted fetal cell lines
Oklahoma lawmaker wants to stop Pepsi from using aborted fetus cells in soda flavoring research (NaturalNews)
To Contact PepsiCo:
Jamie Caulfield, Sr. VP
700 Anderson Hill Road
Purchase, NY 10577
Edmund M. Carpenter, Chair, Corporate Development
1 Campbell Place
Camden, NJ 08103-1701
Pro-life groups joining CGL in the boycott to date are: Life Issues Institute, American Life League, Colorado Right to Life, American Right to Life, Sound Choice Pharmaceutical Institute, ALL Arizona, Central Nebraskans for Life, Pro-Life Waco, Houston Coalition for Life, Mother and Unborn Baby Fox Valley, Womankind, Billboards for Life, Movement for a Better America, Defenders of the Unborn, Focus Pregnancy Help Center, Idaho Chooses Life, EMC Frontline Pregnancy Centers of NY, Four Seasons for Life, CREDO, Life Choices, STOPP Dallas, CA Right To Life, Human Life Alliance, International Right to Life Federation, Operation Rescue, Pro-Life Nation, LifeNews.com, and Mary’s Outreach for Women.
To be clear, the aborted fetal tissue used to make Pepsi’s flavor chemicals does not end up in the final product sold to customers, according to reports — it is used, instead, to evaluate how actual human taste receptors respond to these chemical flavorings. But the fact that Pepsi uses them at all when viable, non-human alternatives are available illustrates the company’s blatant disregard for ethical and moral concerns in the matter.
Origins of HEK 293 Cells
HEK 293 cells were generated in the early 70s by transformation of cultures of normal human embryonic kidney cells with sheared adenovirus 5 DNA in Alex Van der Eb’s laboratory in Leiden, The Netherlands.
The human embryonic kidney cells were obtained from an aborted fetus and originally cultured by Van der Eb himself; the transformation by adenovirus was performed by Frank Graham who published his findings in the late 1970s after he left Leiden for McMaster University in Canada.
They are called HEK for human embryonic kidney, while the number 293 comes from Graham’s habit of numbering his experiments; the original HEK 293 cell clone was simply the product of his 293rd experiment.
HEK 293 Transfection and Selection Data @ Cell-culture Database
HEK 293 Database
293 Cells (CRL-1573) in the ATCC database
Transcript of FDA meeting, in which, starting page 77, Dr. Alex Van der Eb describes in detail the origin of HEK 293 cell .pdf
Evolution On the Inside Track: How Viruses in Gut Bacteria Change Over Time
Phylogenetic tree of microphages detected in PNAS study and other studies. The four microphage contigs with the highest substitution rates observed in the PNAS study are shown in large black lettering. The scale bar indicates the proportion of amino acid substitutions within the 919 amino acid major coat protein, which was aligned to make the tree. (Credit: Frederick Bushman, PhD, Perelman School of Medicine, University of Pennsylvania; PNAS)
July 26, 2013 — Humans are far more than merely the sum total of all the cells that form the organs and tissues. The digestive tract is also home to a vast colony of bacteria of all varieties, as well as the myriad viruses that prey upon them. Because the types of bacteria carried inside the body vary from person to person, so does this viral population, known as the virome.—By closely following and analyzing the virome of one individual over two-and-a-half years, researchers from the Perelman School of Medicine at the University of Pennsylvania, led by professor of Microbiology Frederic D. Bushman, Ph.D., have uncovered some important new insights on how a viral population can change and evolve — and why the virome of one person can vary so greatly from that of another. The evolution and variety of the virome can affect susceptibility and resistance to disease among individuals, along with variable effectiveness of drugs.–Their work was published in the Proceedings of the National Academy of Sciences.–Most of the virome consists of bacteriophages, viruses that infect bacteria rather than directly attacking their human hosts. However, the changes that bacteriophages wreak upon bacteria can also ultimately affect humans.—“Bacterial viruses are predators on bacteria, so they mold their populations,” says Bushman. “Bacterial viruses also transport genes for toxins, virulence factors that modify the phenotype of their bacterial host.” In this way, an innocent, benign bacterium living inside the body can be transformed by an invading virus into a dangerous threat.—At 16 time points over 884 days, Bushman and his team collected stool samples from a healthy male subject and extracted viral particles using several methods. They then isolated and analyzed DNA contigs (contiguous sequences) using ultra-deep genome sequencing .—“We assembled raw sequence data to yield complete and partial genomes and analyzed how they changed over two and a half years,” Bushman explains. The result was the longest, most extensive picture of the workings of the human virome yet obtained.—The researchers found that while approximately 80 percent of the viral types identified remained mostly unchanged over the course of the study, certain viral species changed so substantially over time that, as Bushman notes, “You could say we observed speciation events.”—This was particularly true in the Microviridae group, which are bacteriophages with single-stranded circular DNA genomes. Several genetic mechanisms drove the changes, including substitution of base chemicals; diversity-generating retroelements, in which reverse transcriptase enzymes introduce mutations into the genome; and CRISPRs (Clustered Regularly Interspaced Short Palindromic Repeats), in which pieces of the DNA sequences of bacteriophages are incorporated as spacers in the genomes of bacteria.—Such rapid evolution of the virome was perhaps the most surprising finding for the research team. Bushman notes that “different people have quite different bacteria in their guts, so the viral predators on those bacteria are also different. However, another reason people are so different from each other in terms of their virome, emphasized in this paper, is that some of the viruses, once inside a person, are changing really fast. So some of the viral community diversifies and becomes unique within each individual.”–Since humans acquire the bacterial population — and its accompanying virome — after birth from food and other environmental factors, it’s logical that the microbial population living within each of us would differ from person to person. But this work, say the researchers, demonstrates that another major explanatory factor is the constant evolution of the virome within the body. That fact has important implications for the ways in which susceptibility and resistance to disease can differ among individuals, as well as the effectiveness of various drugs and other treatments.–The research was supported by Human Microbiome Roadmap Demonstration Project (UH2DK083981) the Penn Genome Frontiers Institute, and the University of Pennsylvania Center for AIDS Research (CFAR; P30 Al 045008).–Samuel Minot, Alexandra Bryson, Christel Chehoud, Gary D. Wu, James D. Lewis, all from Penn, are co-authors.–Story Source-The above story is based on materials provided by Perelman School of Medicine at the University of Pennsylvania. –Journal Reference: S. Minot, A. Bryson, C. Chehoud, G. D. Wu, J. D. Lewis, F. D. Bushman. Rapid evolution of the human gut virome. Proceedings of the National Academy of Sciences, 2013; 110 (30): 12450 DOI: 10.1073/pnas.1300833110
Sudden Decline in Testosterone May Cause Parkinson’s Disease Symptoms in Men
July 26, 2013 — The results of a new study by neurological researchers at Rush University Medical Center show that a sudden decrease of testosterone, the male sex hormone, may cause Parkinson’s like symptoms in male mice. The findings were recently published in the Journal of Biological Chemistry.–One of the major roadblocks for discovering drugs against Parkinson’s disease is the unavailability of a reliable animal model for this disease.–“While scientists use different toxins and a number of complex genetic approaches to model Parkinson’s disease in mice, we have found that the sudden drop in the levels of testosterone following castration is sufficient to cause persistent Parkinson’s like pathology and symptoms in male mice,” said Dr. Kalipada Pahan, lead author of the study and the Floyd A. Davis endowed professor of neurology at Rush. “We found that the supplementation of testosterone in the form of 5-alpha dihydrotestosterone (DHT) pellets reverses Parkinson’s pathology in male mice.”—“In men, testosterone levels are intimately coupled to many disease processes,” said Pahan. Typically, in healthy males, testosterone level is the maximum in the mid-30s, which then drop about one percent each year. However, testosterone levels may dip drastically due to stress or sudden turn of other life events, which may make somebody more vulnerable to Parkinson’s disease.—“Therefore, preservation of testosterone in males may be an important step to become resistant to Parkinson’s disease,” said Pahan.[F1]–Understanding how the disease works is important to developing effective drugs that protect the brain and stop the progression of Parkinson’s disease. Nitric oxide is an important molecule for our brain and the body.–“However, when nitric oxide is produced within the brain in excess by a protein called inducible nitric oxide synthase, neurons start dying,” said Pahan.–“This study has become more fascinating than we thought,” said Pahan. “After castration, levels of inducible nitric oxide synthase (iNOS) and nitric oxide go up in the brain dramatically. Interestingly, castration does not cause Parkinson’s like symptoms in male mice deficient in iNOS gene, indicating that loss of testosterone causes symptoms via increased nitric oxide production.” “Further research must be conducted to see how we could potentially target testosterone levels in human males in order to find a viable treatment,” said Pahan.–Other researchers at Rush involved in this study were Saurabh Khasnavis, PhD, student, Anamitra Ghosh, PhD, student, and Avik Roy, PhD, research assistant professor.–This research was supported by a grant from the National Institutes of Health that received the highest score for its scientific merit in the particular cycle it was reviewed- Parkinson’s is a slowly progressive disease that affects a small area of cells within the mid-brain known as the substantia nigra. Gradual degeneration of these cells causes a reduction in a vital chemical neurotransmitter, dopamine. The decrease in dopamine results in one or more of the classic signs of Parkinson’s disease that includes resting tremor on one side of the body; generalized slowness of movement; stiffness of limbs and gait or balance problems. The cause of the disease is unknown. Both environmental and genetic causes of the disease have been postulated.
Parkinson’s disease affects about 1.2 million patients in the United States and Canada. Although 15 percent of patients are diagnosed before age 50, it is generally considered a disease that targets older adults, affecting one of every 100 persons over the age of 60. This disease appears to be slightly more common in men than women. —Story Source–The above story is based on materials provided by Rush University Medical Center. –Journal Reference–S. Khasnavis, A. Ghosh, A. Roy, K. Pahan. Castration Induces Parkinson Disease Pathologies in Young Male Mice via Inducible Nitric-oxide Synthase. Journal of Biological Chemistry, 2013; 288 (29): 20843 DOI: 10.1074/jbc.M112.443556
[F1]Interesting enough the T levels for males are declining due to the phytoestrogen and xenoestrogen exposure and the encouragement of consuming highly contaminated foods that are estrogenically based
Script of the Show August 31 2013
Effects of nicotine, its metabolites and tobacco extracts on human platelet function in vitro
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Apple pectin for the reduction of niacin-induced flushing.
Effects of nicotine, its metabolites and tobacco extracts on human platelet function in vitro.
Toxicol In Vitro. 2013 Mar;27(2):932-8–Authors: Ljungberg LU, Persson K, Eriksson AC, Green H, Whiss PA
Cigarette smoking is a leading cause of cardiovascular disease. The cardiovascular effects of smoking are probably multifactorial, including effects on platelets. Previous reports investigating the effects of nicotine and tobacco on platelet function are inconsistent. The present study investigated in vitro effects of nicotine, its major metabolites, tobacco extracts and extract of tobacco-free snuff on human platelets. None of the metabolites cotinine, cotinine-N-oxide, nicotine-1′-N-oxide or trans-3′-hydroxycotinine (0.1-10 μM) affected platelet aggregation or P-selectin expression. Nicotine (10 μM) weakly increased platelet aggregation, whereas trans-3′-hydroxycotinine (0.1 μM) and nicotine-1′-N-oxide (1-10 μM) weakly inhibited adhesion to fibrinogen. To elucidate the influence of other tobacco compounds, we investigated the impact of moist tobacco and smoke extracts on platelet function. Filtered extracts of oral snuff, cigarette smoke and tobacco free snuff inhibited platelet adhesion concentration-dependently. The inhibitory effects of tobacco extracts on platelet adhesion were independent of nicotine content and the nitric-oxide-pathway and not mediated through a platelet-nicotine-receptor. Taken together, tobacco extracts inhibit platelet activation during short-term in vitro challenge. As only limited effects of nicotine and nicotine metabolites were seen, the tobacco-induced platelet inhibition are likely induced by other compounds present in tobacco and tobacco free snuff.