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James Sloane
Just posted this on another board where a lady is dealing with her husband who has an aggressive, non-operable stage 4 brain tumor:
I have been researching cancer for over 44 years and I have yet to find anything as safe and effective as ozone therapy for cancer. when used properly. Ozone selectively kills cancer cells through a peroxide overload in a chain reaction, destroys cancer pathogens (viruses, bacteria, etc), destroys many carcinogens through oxidation and increases anticancer cytokines and superoxide dismutase. Ozone also increases the antioxidant enzymes catalase and peroxidases in healthy cells, which is why it will not harm healthy cells when used properly. A study did in Germany followed almost 6 million doses of ozone given in therapy and out of that nearly 6 million there were only just over 30 adverse reactions. Most of these mild such as pain at the injection site or mild rash.
Another advantage of ozone therapy is that it readily enters in to all parts of the body including the brain and cerebral spinal fluid where most drugs and other compounds cannot reach since few things cross the blood brain barrier.
Ozone therapy can be easily done at home by the person themself. With brain tumors though, it is important to go slow as the dead cancer cells form uric acid that irritates the tissues and leads to swelling. Not a god thing if the brain swells in the skull as this can crush the brain. Therefore, when doing ozone for brain tumors, which can be non-invasively through ear insufflation, the treatment is done much slower than for cancers elsewhere in the body.
Hate to say it, but study after study has proven that radiation and chemotherapy rarely ever succeed in completely eliminating cancer. The main reason is that radiation therapy and most chemo drugs, which ironically are carcinogens (cancer causing agents) work on a free radical principle. More specifically an oxygen radical to kill cancer cells. In order to do this, there must first be sufficient oxygen present. As malignant tumors grow though, they form a very irregular vasculature, which leaves some parts of the tumor well oxygenated, but other areas hypoxic. The radiation and most chemotherapy drugs therefore work well in the well oxygenated areas, but do nothing in the hypoxic regions. So, these hypoxic regions survive and will grow back creating more resistant hypoxic regions in the process. This is how radiation and chemo resistant tumors form. Again, this is extremely well documented in the medical journals. Therefore, the radiation and most chemotherapies simply knock back the tumors to undetectable levels, which is known as remission, not cured, as the tumors almost always grow back.
The second issue is that radiation therapy and most chemotherapy drugs do not address the cause of the cancer, which in about 95% of cancers are cancer viruses. To a lesser extent bacteria, mycotoxins, radiation and in extremely rare cases parasites. No cancer has ever been proven to be hereditary and in fact, every oncogene every discovered has been viral. No human oncogene has ever been discovered.
People, including doctors and researchers, often confuse genetic with hereditary. These ARE NOT the same thing. All cancers are genetic as they involve alterations in the genes. To be hereditary though, the person must have inherited the defective gene from one or both parents, which means they have the defective gene and thus the disease/disorder from birth. Not 40, 50, 60..... years down the line. Again, no human oncogene has ever been discovered. The medical establishment still tries to confuse and mislead people by saying ridiculously stupid things such as a person tested positive for the BRCA gene, which has led to many prophylactic mastectomies and prostectomies of non-cancerous tissue. EVERYONE has BRCA genes, these are TUMOR SUPPRESSOR genes, not oncogenes (genes that cause cancer). The BRCA1 and BRCA2 gene mutations are viral mutations where the virus has inserted its own genetic code in to our genes altering the way these genes function. In this case, the viral insertion in to the BRCA genes turns off their tumor suppressor functions.
Brain tumors are also almost always viral in origin. The viruses known to cause brain tumors in humans are simian vacuole virus type 40 (SV40), BK virus, cytomegalovirus (human herpes virus type 5) and the JC virus. To a much lesser extent, brain tumors can occur from bacteria known as mycoplasmas (cell wall deficient bacteria), and is super rare cases the parasite Toxoplasma gondii.
The only cancer therapies with a relatively high success rate, around 80% long term remission to cure, are the drugs derived from herbs or based on their chemistry. Vincristine and Vinblastine from the herb Madagascar periwinkle, and the podophyllumtoxin derivatives (PDs). The PDs were originally derived from the herb mandrake, then from the Savin juniper herb. It was reported in the Journal of the American Medical Association an the Journal of the American Cancer Society back in the early 1950s to be HIGHLY EFFECTIVE for 6 forms of cancer it was tested on, including breast cancer. The compound was not patentable though, and so it went nowhere for over 50 years while people were dying from these curable cancers. Finally, the University of North Carolina synthesized the PDs over 50 years later and sold the patent to a California drug company who finally got approval on the drug over another decade later. The reason Vincristine, Vinblastine and the PDs have such a high efficacy rate for cancer is that these herbal based compounds are powerful antiviral agents and thus actually address the cause of most cancers.
Really quick, the SV40 virus as mentioned is a cause of brain cancers, and has been a major cause of brain cancers, bone cancers and mesothelioma. Multiple studies have found that mesothelioma is not caused from asbestos, but rather SV40, where the asbestos is simply a co-factor, such as an activator like estrogen and progesterone are for many cancer viruses. SV40 is actually a primate virus, so this confuses people as to how humans are getting this cancer causing primate virus. The virus was introduced in to humans in the 50s and 60s from the polio vaccines we were given as children. The vaccines were cultured on green monkey kidneys, which led to contamination of the vaccines with SV40 that over 90 million Americans alone were given. The virus is a lentivirus (slow virus) and thus takes many decades to show symptom such as cancer. This is why there was such as large surge in normally rare cancers such as brain cancers decades after the polio vaccines had been discontinued.
Back to why radiation therapy and most chemotherapy drugs tend to fail. So, part of the answer is lack of efficacy in hypoxic regions, being themselves carcinogenic and failure to address cancer pathogens.
Another factor is metastasized cells. Cancer cells can naturally metastasize, or they can metastasize from procedures such as biopsies or surgeries where the cancer cells can be knocked loose and float through the vascular or lymphatic system to distant parts of the body where they take up residence. There are two very important things to keep in mind here. First is that cancer cells are very efficient in evading immune detection. They have several mechanisms for doing this including using human chorionic gonadotropin as a shield to hide from the immune system just like a human fetus. In fact, cancer cells share a lot of characteristics with human fetuses and can often be picked up by a pregnancy test. Second thing to keep in mind is that malignant tumors also follow the rule of survival of the fittest. The tumor needs a food supply (glucose, fructose, ketones, lactate, fatty acids and some amino acids), as well as oxygen to survive and thrive. The more oxygen available, the faster the cancer can grow. When the tumor first starts to develop it has no vasculature. Therefore, it relies on diffusion to get its oxygen. This is a very limited process though, and once the tumor reaches a size of 2-3mm the tumor can no longer receive sufficient oxygen through diffusion, and the center of the tumor dies from a lack of oxygen. This in turn stimulates the production of vascular growth factors such as vascular endothelial growth factor (VEGF) that stimulates angiogenesis (blood vessel formation) to increase fuel and especially oxygen levels to the tumor allowing it grow more effectively. Same reason malignant tumors in low blood supply and thus {low} oxygen areas, such as the breast, tend to grow extremely slow, whereas highly oxygenated areas such as the liver and pancreas form very rapidly growing malignant tumors. This brings us to the survival of the fittest part. The primary tumor is not only producing angiogenesis promoters, such as VEGF, but the tumor also at the same time produces small amounts of angiogenesis inhibitors (AIs). This may sound counter intuitive at first, but there is a reason for this. The AIs float through the bloodstream reaching the metastasized cancer cells slowing or stopping their growth so there is a greater fuel and oxygen supply going to the primary tumor. When the primary tumor is removed though, the source of AIs is also now gone and the metastasized cells are now free to grow unimpeded.
The medical establishment though is deceptive and often counts this, or any original tumor that grows back after the 5 year term considered a "cure" as a new tumor as to make the original therapy appear as a success even though they are the {original} cancer cells. This is one of the ways they manipulate the cancer therapy statistics to make the therapies appear way more effective than they actually are.