Mycoplasma, AIDS, Degenerative Diseases: What You Don't Know Can Kill You.

John D. Rockefeller  Sr.'s merger with pharmaceutical and chemical giant, I.G. Farben (Auschwitz was a 100% subsidiary of IG Farben) in 1928 "created the largest and most powerful cartel the world has ever known. Not only has that cartel survived through the years, it has grown and prospered. Today it plays a major role in both the science and politics of cancer therapy."

It's important to know Big Pharma's "crimes against humanity" history, because that history fostered the chemical-based drug treatment basis for our "orthodox" healthcare system today. The industry claims that their aim is finding medical truth, and that may be true; nevertheless, publicizing that truth, once found, if that truth entails inexpensive solutions or remedies, will not happen for obvious reasons. There is nothing Big Pharma likes more than chronic illness, for which they can produce chronic palliative costly treatments that make the patient chronically dependent on them.

Which brings me to the seldom, if ever, publicized human pathogen: mycoplasmas. They are the smallest free-living bacteria that can assume multiple shapes including round, pear shaped and even filamentous forms because they lack a cell wall. This makes it possible for them to pass through  filters used to remove bacteria; and hide inside the cell from our immune system, as well as from common antibiotics, all the while interfering with the cell machinery. Because mycoplasmas have lost most of their genetic material; a strict dependence on the host for nutrients and refuge determines its ability to survive and grow.

Mycoplasma is the co-factor that alters the human immune system and opens the door for the autoimmune degenerative diseases such as AIDS, malignant transformation, chromosomal aberrations, Chronic Fatigue Syndrome, Gulf War Syndrome (military vaccine), Amyotrophic lateral sclerosis (ALS), often referred to as Lou Gehrig\'s Disease (every single patient shows mycoplasmal infection), Alzheimer’s, Crohns Disease, Parkinson’s, Huntington’s, Lupus, Lyme disease, Fibromyalgia, Rheumatoid Arthritis, Multiple Sclerosis, Type One Diabetes, Autistic Spectrum Disorder, and cancer.  Yet, these pathogenic organisms show up in vaccines.

“Because certain species of the mycoplasma have an absolute growth requirement for the up-take of pre-formed sterols, including cholesterol they can cause the ‘spontaneous degeneration’ of the cells that they invade. If they do not cause sufficient damage to kill the cell, they at least compromise its capacity to defend itself from other disease agents, such as those which present as Kaposi’s sarcoma, pneumoniae carinii pneumonia, lymphadenopathy, and so on.” Donald W. Scott and William L.C. Scott,

“From its inception, the biowarfare program was characterized by continuing in-depth review and participation by the most eminent scientists, medical consultants, industrial experts and government officials, and it was classified Top Secret. The US Public Health Service also closely followed the progress of biological warfare research and development from the very start of the program, and the Centers for Disease Control (CDC) and the National Institutes of Health (NIH) in the United States were working with the military in weaponising these diseases. These are diseases that have existed for thousands of years, but they have been weaponized—which means they’ve been made more contagious and more effective. And they are spreading.” Donald W. Scott

Currently, Dr. Alan Cantwell is one of the most well-known popular proponents of the link between cancer and bacteria. He has written numerous articles and books on the subject after he isolated and reported cell wall deficient bacteria in breast cancer, Kaposi’s sarcoma and Hodgkin’s disease. He states,

”If a disease like cancer is indeed caused by microscopic bacteria, it would indicate physicians have been unable to see what was quite plain for some nineteenth and twentieth century scientists to observe using simple light microscopy."

Eventually, constantly under intense criticism, Cantwell was ostracized by many in the medical profession.

Females are four times more likely to be infected with Mycoplasmas than males. The same ratio of males to females applies to Rheumatoid Arthritis, Fibromyalgia, Chronic Fatigue and other related auto-immune disorders. Men, pound for pound, have 25% more blood; hence, hemoglobin - the protein molecule in red blood cells that carries oxygen from the lungs to the body's tissues - than females.

AIDS and Mycoplasma: The Crime Beyond Belief

Donald W. Scott, editor of The Journal of Degenerative Diseases (pictured above) and co-founder of the Common Cause Medical Research Foundation, reveals the true and hidden story of weaponized mycoplasma and the protracted creation of AIDS by governments and private corporations. part 1 of a series drawn from the 90 min. talk given at the 9th annual conference, Sudbury, Ontario (Aug 29-31, 2008).  JODD (Journal of Degenerative Disease); Box 133 Station B; Sudbury Ontario; Canada P3E4N5  $25/year





Links:

Fluid Mosaic Model Membrane

The Linking Pathogen in Neurosystemic Diseases

Mycoplasmas Stealth Pathogens

Campaign for Truth in Medicine

Mycoplasma Protocol

Institute for Molecular Medicine

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Rat Genes in Lettuce and Moth Genes in Apples...These Are a Few of My Favorite Things.

In May, 2002, National Geographic magazine reported on the "brave new world of genetic engineering." In the article, plant biochemist, Dean DellaPenna, envisioned fruits and vegetables delivering vaccines and "vegetable so loaded with therapeutic ingredients that doctors 'prescribe' them for patients". At the time of this article, scientists were working on an "apple that could vaccinate children against a virus that is the leading cause of childhood pneumonia". And, another group of scientists were inserting "genes into cows and sheep so that the animals will produce pharmaceuticals in their milk".

So, what's the big deal? Well, for the first time in history, scientists are using irradiation and mutagenic chemicals to transfer genes between species that are not related at all.  For instance, they can - and have - take  a gene from a rat and implant  it into lettuce...or moth genes into apples...or spider genes into goat's milk...or salmon genes into tomatoes...or the genes of moths and bees into potatoes...or silkworms into grapes...These are a few of my favorite things!

Some crops are engineered to make their own insecticide that is said to be lethal to insects, but harmless to humans.  Really? How did they discover that this is the case in such a short period of time?  
The general population is, mostly, unaware that they've been eating genetically modified foods since the mid-1990s. As of 2002, 60% of all processed foods on US supermarket shelves contained ingredients from engineered foods. Nine years later, that percentage is close to 100%!

Fast forward fifteen years, and amidst the strange devastating weather patterns that are beginning to take hold,  strange new diseases are developing, and the number of people diagnosed with established medical conditions, such as diabetes, Multiple Sclerosis, Autism, just to name a few, are exploding.  
In the U.S. alone, 105 million people have Diabetes or prediabetes according to the CDC. By the year 2019,  Morningstar projects the Diabetes market, alone, will grow to over $55 billion! 
E-coli and E-coli 0157

Are scientists genetically modifying natural strains of bacteria into faster growing super-toxic E-coli strains? So, Novartis and Phizer can market new vaccines?

Back in the day, most strains of E-coli, were a harmless part of the normal flora of the gut. In fact, natural E-coli benefits the hosts by producing vitamin K2, and by preventing the establishment of pathogenic bacteria within the intestine. However, it was found that this bacterium is grown so easily, and its genetics so simple and easily manipulated or duplicated through a process of metagenics, that it's one of the most important species used in genetic engineering.

Analysis of the genome sequence of the strain of E. coli responsible for the deadly outbreak in Germany revealed that it is "an entirely new super-toxic E. coli strain."  As e-coli is to biowarfare as peanut butter is to jelly, it's not so farfetched to wonder if this could be a mutated, developed killer bacteria, created in a lab.

Whatever the cause, the outcome is predictable. More laws and regulations. More genetic engineering. More vaccines. More pharmaceuticals. And most of all, more profit for the pharmaceutical and agriculture industry, and the military industrial complex.

Links:

Bowel Cancer's alarming rise in young people

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Bone Cells Affect How Much You Weigh

The skeleton affects energy metabolism.

If your blood glucose is out of whack, the problem may be in your bones. Research in mice shows that bone cells exert a surprising influence on  how the body regulates sugar, energy, and fat. The discovery could lead to new ways to treat type-two diabetes, a disease involving poor regulation of blood glucose. It also means that skeletons act as endocrine organs, which affect other body tissues by releasing hormones into the bloodstream.

The team announcing the finding, led by Gerard Karsenty of Columbia University, had previously found that fat cells secrete a hormone that influences bone-forming cells called osteoblasts. Because hormone regulation between two cell types is often reciprocal, Karsenty and his  team reasoned that osteoblasts might also be emitting hormones that control fat tissue. Osteoblasts make bone throughout a healthy person's lifetime,  while cells called osteoclasts tear down bone processes that constantly remodel the skeleton. Osteocalcin, a somewhat enigmatic protein produced  only by osteoblasts, seemed like a good hormone candidate, Karsenty says.

"[It] has been the flagship molecule of the [bone-research] field for 30 years, but nobody knew what it was doing." -- Gerard Karsenty

Karsenty's team fed a normal diet to mice engineered to lack the gene for osteocalcin. The mice became  obese and had low blood concentrations of insulin, a key hormone for controlling blood glucose. The animals also had poor sensitivity to insulin, a hallmark of people with diabetes. Another group of mice, which had been engineered to have extra osteocalcin, stayed thin despite being fed a high-calorie diet. These animals also maintained higher insulin concentrations and better sensitivity to insulin than the mice lacking osteocalcin did, the team reports in the Aug. 10 Cell. Further tests on mice showed that osteocalcin causes the insulin-making cells in the pancreas to proliferate and ramp up insulin production. The bone protein also causes fat cells to store less fat and to secrete a hormone called adiponectin. In people as well as in mice, this substance improves cells' sensitivity to insulin. Previous research has shown that many people with type 2 diabetes have low blood concentrations of osteocalcin. "Osteocalcin, if everything goes well, could be a treatment for type 2 diabetes. That's where the excitement is," Karsenty says.

"This could also have important ramifications for cardiovascular disease because of the effect on metabolic syndrome," a condition related to diabetes, comments Dana T. Graves of Boston University. "The fact that bone cells regulate energy metabolism, and that they do it through osteocalcin, is a major finding," he saysIt is already known that fat cells secrete a hormone that affect bone cell growth and because the hormone secreting process is often a reciprocal process, Gerard Karsenty of Columbia University assumed that the bone cells may be secreting hormone(s) that affect fat cells or fat tissue and he was right.

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