Impossible Cure Newsletter -- February 2017 |
Lots of New Research to Report!Our trusty informant on homeopathic research, Dana Ullman, has let his followers know that a leading medical journal has reported the success of homeopathic/potentized estrogen in treating endometriosis. The European Journal of Obstetrics and Gynecology and Reproductive Biology just published this randomized double-blind and placebo controlled study. Dana also reports that homeopathic Arnica has been found to have specific effects on genes (in the lab) known for wound healing. So much for the placebo effect! This was published in PLOS ONE. Speaking of in vitro studies (and therefore not subject to the placebo effect), another recent study has shown that the remedy Belladonna as well as the nosode of MRSA have shown an inhibiting effect on MRSA bacteria. This information is important, given the development of antibiotic resistant diseases, like MRSA. Homeopath Dr. Peter Fisher, director of research at the Royal London Hospital for Integrated Medicine comments further on the important role of homeopathic remedies in dealing with the growing threat of antibiotic resistant disease in this YouTube.. A long term study in Lucca, Italy has shown the short-term and long-term success of homeopathic treatment of atopic diseases (like eczema and its often successor, asthma) in children. |
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Another Excerpt from Richard Moskowitz's New Book on VaccinationBoston homeopath and family medicine doctor, Richard Moskowitz, MD, has always been an important writer in the area of health, homeopathy, and vaccination. He has written a new book that will appear in 2017, and has been sharing a series of book excerpts with the homeopathic community. I have asked and been granted his permission to share them with you too. Enjoy! From Chapter 1: Immunity, True and False. "The natural immunity acquired by coming down with and recovering from acute febrile diseases like the measles, resulting in expulsion of the offending organism from the body, are the formative experiences by which a healthy immune system is developed and maintained throughout life. This basic truth is reinforced by a large volume of epidemiological research to the effect that contracting and recovering from acute febrile illnesses in childhood provide significant protection against cancer and many other chronic diseases later in life. Whatever good vaccines may accomplish inevitably falls far short of these goals. Without the acute illness, there is no priming of the immune system as a whole, no improvement in the general health, and no reliable mechanism for expelling the invading organism from the blood. Indeed, where that organism actually goes, how it persuades the immune system to continue producing antibodies against it for years or even decades, and what price we have to pay for the partial, counterfeit immunity that they represent, are questions that it seems we are not supposed to ask, and can expect anything from haughty contempt to righteous indignation when we do. What haunts me is the probability that the production of specific antibodies throughout life entails the ongoing physical presence of these vaccines, or the highly antigenic substances produced by or from them, remaining deep inside the body on a chronic and indeed permanent basis, which seems to me a perfect recipe for eliciting autoimmune phenomena routinely and repeatedly in every recipient, whether or not they actually fall ill or develop clinical signs and symptoms at the time. With the live-virus vaccines, it is simple to imagine how such a carrier state might be achieved, by simply attaching themselves to the DNA or RNA of their host cells. As for the other so-called "non-living" vaccines, we know that they cannot survive as antigens for long periods of time without the presence of various chemical adsorbents, fixatives, preservatives, sterilizing agents, and "adjuvants," almost all of them highly toxic, and indeed that enabling such long-term survival is the only reason for their use; but precisely how these chronic phenomena are achieved has been allowed to remain a well-guarded trade secret, if indeed it is known at all. It is dangerously misleading, if not the exact opposite of the truth, to claim that vaccines protect us from acute infection if they merely drive the organism deeper into our bodies and cause us to harbor them chronically instead, rendering us incapable of responding acutely, not only to them, but very probably to other antigens as well. In short, my fear is, and indeed my experience has been, that whereas acute infectious diseases produce genuine immunity through vigorous, acute responses, vaccine-mediated immunity is achieved by creating the equivalent of a chronic infection in its place." |
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Enjoy the Quiet of Winter |
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