Virus's and the shots will kill us | |
abeland1 The Art of making Colloidal Silver User ID: 81679411 ![]() 03/13/2022 06:09 PM ![]() Report Abusive Post Report Copyright Violation | [link to theartofmakingcolloidalsilver.com (secure)] HuffPost Antibiotic Resistance Could Take Us Back To The Days Where 40% Of Us Died From Infections. To paint a picture of a post-antibiotic apocalypse, it is necessary to understand the history. We do not need to go back far—just to the beginning of the last century, before the discovery of our miracle drugs, antibiotics, along with preventative vaccines. Before these truly revolutionary medical leaps, life was very different. Infections regularly killed or caused significant disabilities, many of the operations we now consider routine did not exist and the powerful drugs we use to treat cancer were unthinkable. In particular, I want to share one key statistic—in this time before antibiotics and vaccines, around 40% of deaths were due to infections. Now, that number is just 7%. These developments, including Sir Alexander Fleming’s discovery of the first antibiotic—penicillin—have underpinned countless medical advances since. They have allowed us to treat basic infections so surgical procedures like caesarean sections can take place safely and patients can receive chemotherapy. People are now living longer and healthier than ever before. I think it is grossly overlooked how much of our current quality of life is down to these key achievements in medicine. Indeed antibiotics add, on average, twenty years to our lives. But even as Sir Alexander Fleming accepted his Nobel Prize for this discovery, he foresaw a troubling future. In his acceptance speech he flagged that he was already seeing bacteria in the laboratory that developed resistance and therefore survived, and urged people to get ahead of this threat before it occurred more widely. And here we stand, more than 70 years later, having made little progress in addressing this threat. It continues to grow globally—and this inaction seriously risks us returning to the dark ages of medicine. Again, I do not think people fully appreciate just how much our quality of life hinges on antibiotics being effective. We are so familiar with these wonder drugs that we take them for granted. The truth is that we have been abusing antibiotics—as patients, as doctors, as travellers, as farmers and food producers globally, for short term personal gain without thinking about the future. Many people demand them of our doctors when they simply do not need them. Surveys suggest that one in five people expect a prescription for antibiotics incorrectly believing they will treat coughs and colds caused by viruses. Doctors have to make difficult decisions and sometimes prescribe antibiotics when they may not be needed, often because they do not have the tools to diagnose quickly and definitively. Estimates suggest that as many as half of all patients who visit their GP with a cough or cold leave with a prescription for antibiotics. Some countries feed them to animals in huge numbers to promote growth and as a crude form of infection control. In some countries, antibiotics can be bought without prescription or online, and poor quality or fake medicines can exacerbate the problem, as well as causing harm and fatalities. Added to that, there are many countries which we simply do not know how many antibiotics are being used and what bugs are becoming resistant, due to the lack of surveillance. To compound these issues, we have not developed any new classes of antibiotics since the 1980s as both the public and private sector disinvested in this area and the science is challenging. Drug companies say they are too expensive to develop when they sell for such a low price. Because of the growing threat of resistance, we are trying to limit their inappropriate use—making it far less profitable than developing drugs for other therapeutic areas such as cancer. Given the failure rate is high and it can take 10-20 years to bring an antibiotic from discovery to market, developing new antibiotics also becomes too high risk for industry due to the lack of a return on investment. All of these failures to act are collectively driving bugs that cannot be treated by any medicines we have on this earth. Already four in 10 patients with an E.coli bloodstream infection in England cannot be treated with the commonest antibiotic (co-amoxiclav) used in hospitals. In addition, almost one in five of these bacteria were resistant to at least one of five other key antibiotics This truly is the doomsday scenario we fear in medicine. Our apocalypse is a return to these dark ages, where people regularly died in childbirth, from stomach bugs, from simple cuts and abrasions. The risk is worrying enough that the UK Government put this issue on its national risk register—up there with security threats, floods and pandemic flu. And already we are seeing horror cases worthy of this classification. In the United States earlier this year, we saw a tragic case where a woman died after contracting an infection that we simply did not have the medicine to treat. All 14 kinds of antibiotics the hospital had on hand did not work. Even more stark—none of the 26 antibiotics available in the United States would have worked either. All of these failures to act are collectively driving bugs that cannot be treated by any medicines we have on this earth. Already four in 10 patients with an E.coli bloodstream infection in England cannot be treated with the commonest antibiotic (co-amoxiclav) used in hospitals. In addition, almost one in five of these bacteria were resistant to at least one of five other key antibiotics And yet Big Pharma and .Gov have information that simply adding some EIS/CS with an antibiotic multiplies the effectiveness of the antibiotic, ALL antibiotics. Just no new Revenue Stream is developed, meaning no new exorbitant price gouging can be created. Big Pharma is Snake-oil Salesmen. [link to theartofmakingcolloidalsilver.com (secure)] [link to www.ncbi.nlm.nih.gov (secure)] I quote from the “Summary and Conclusions.” “We presented the similarities and differences in the mode of silver action on Gram-positive and Gram-negative bacteria. We noticed a gap in knowledge about the molecular mechanism of bacteria, both Gram-positive and Gram-negative, to silver nanoparticles. If we assume that silver nanoparticles are silver ions source, it is possible that the molecular mechanism of bacterial resistance is analogue to mechanism described for Ag+. If there is another way of antibacterial toxicity of silver nanoparticles, it is likely that different mechanisms of resistance to silver nanoparticle exist, for both Gram-negative and Gram-positive bacteria. The variety of silver nanoforms causes that every product with silver nanoparticles should be considered separately as a compound with different physico-chemical properties, different mode of action and different mechanisms of resistance.” Last Edited by abeland1 on 11/23/2022 09:02 PM |
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