Mycoplasma Thrives On Cholesterol

http://www.bioelectric.ws/eng/mycoplasma.html

What makes these designer diseases so elusive is that they're genetically engineered only for DNA replication, transcription and translation with no organelle or cell wall. They have lost their genes for amino acid and fatty acid synthesis, forcing them to invade and steal proteins, sugars and sterols (cholesterol) from healthy neighbouring cells to survive.

These cholesterol dependent molecular terrorists immediately take up residency in the individual's genetically pre-disposed weaknesses, (the weak link in the chain of organs or systems), or the path of least resistance. Since Mycoplasma has absolute dependence upon the uptake of preformed sterols (cholesterol structures), they have an affinity toward cell membranes, nerve cells, sex hormone cell factories, glands and the gray matter in brain tissue, where cholesterol sterols are found. Since cholesterol is a co-factor in glandular hormone production, the endocrine balance is drastically altered with cholesterol being pulled out of the cell cycle. That is why pathogenic changes are seen most often during pregnancy, hormone replacement therapy, steroid therapy, menstrual cycles and xenoestrogens from pesticides, herbicides, meat and dairy.

With the disruption of the hormones, comes an open invitation for the RNA directed HIV to replicate. The newly formed HIV RNA makes its way to the host cell surface where it connects and breaks away carrying with it a GP 120 protein envelope that was hijacked from the previous cell's surface. It repeats by countering another cell, adheres to the cell surface and accesses the interior genetic material of its new host where the cascade process is repeated.

Unless Mycoplasma penetrates into tissues and cells they cannot exert their terrorist effects. They will lay dormant, sometimes for a decade, until physical or emotional trauma, severe stress or vaccine contaminants wake up the sleeping giant to invade and feed on the cell's genetic material like an intracellular parasite, taking the cell hostage until it ruptures and dies.

Since the disease pattern of CFS, FMS and GWI affect all major body systems (cardio vascular invasion involving the left ventricle, neurological damage ranging from mild cognitive problems to bi-polar depression or schizophrenia, genitourinary damage presenting incontinence or urethritis, pulmonary symptoms of asthma and the development of fibro masses or nodules in the lungs etc.), this multi-faceted symtomatology is causing a medical merry-go-round in the medical profession starting with a general practitioner who will usually prescribe an anti-inflammatory and a short-term antibiotic regimen for the chronic infection. Since you also exhibit symptoms of neurological disorders and your general practitioner is not versed in neurology, you will be referred to a neurologist. After the examination with a neurologist and a couple scripts later for your anxiety and insomnia, you will be pawned off on an endocrinologist for your hormonal imbalance because the neurologist has limited knowledge in endocrinology. Due to the combined adverse side effects of the antibiotics, anti-inflammatories, analgesics and tranquilizers, you may exhibit signs of gastric disturbances and skin reactions where you will be further drugged by a dermatologist or a gastrologist. Next in line on the "gist" medical treadmill is the cardiologist who will push a beta-blocker or a diuretic on you for your cardiomyopothies. After seeing ten different disease specialists and spending thousands of dollars on MRI's, CT Scans, X-Rays, surgery, pharmaceuticals, etc., without finding a solution to your dilemma, you will be labeled psychosomatic, hypochondriac or suffering from severe depression where you will end up with a psychologist. You're now a walking drug store with more complications than what you started with thanks to the combined adverse reactions of the drugs and the limitations of medical doctors who specialize in only 1/10th of the body. What a racket!!!