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|    When the Cure Is Worse Than the Disease     |
|    19 Feb 15 21:13:48    |
      From: hound23x@gmail.com              When the Cure Is Worse Than the Disease              by Bill Sardi                            Mary wonders why the new young doctor she visited recently says to nearly       every patient, after examining their throat, that it looks like their       esophagus is being eroded by stomach acid and they need to start taking       acid-blocking pills. He hands        patients free samples provided by pharmaceutical companies. The patients are       oblivious to the fact that if they begin using the drug, they may never be       able to stop taking it without experiencing an excruciatingly painful bout of       rebound heartburn.              One way to build an income in private medical practice is to hook patients on       drugs that continually require re-examination, testing and prescription       renewal.               For example, blood thinners require prothrombin tests to determine how long it       takes the blood to clot. Blood pressure pills require monitoring of blood       pressure. And in the example above, once patients start taking acid-blocking       medications they will        find it is nearly impossible to stop taking them because withdrawal will       provoke rebound acidity with throat-gripping pain.              Since the early 1990s it has been known that acid-blocking (histamine       blocking) drugs commonly prescribed for heartburn create dependency.        Withdrawal from the drug will create rebound hyper-acidity that causes the       patient to reach for the antacid pills        in desperation again. [1] , [2] To make matters worse, acid blockers may       induce more, not less, disease. Stomach acid is a defense against invading       pathogenic bacteria that enter the gut in food (foods are not sterile, but       have low bacteria and mold        counts that stomach acid normally kills). The habitual use of acid blockers       may result in infection and even cancer. [3]               Most drugs don't work, are inappropriate or are designed to make things worse              Critical examination of the effectiveness of prescription drugs reveals that       there is (1) convincing data that most prescription drugs are not only       ineffective but may worsen the condition being treated (yet are approved by       the FDA), that (2) some of        these medications appear to be designed to create life-long dependency upon       the drug (drug withdrawal exacerbates symptoms), and that (3) some       long-standing drugs that are the hallmarks of modern medicine have begun to       lose their biological punch.              There are many examples of this:              It has recently been shown that asthma symptoms worsen upon withdrawal of the       drug Accolate (zafirlukast), with benefits lasting only for the first five       weeks and then symptoms return soon thereafter. The FDA approved this drug       based upon short-term use        data. Benefits are seen for only the first five weeks, after which symptoms       return to their original state within seven weeks. Side effects range from       diarrhea to liver damage. With no long-term benefits, the drug is only       problematic for users. [4]               Other asthma drugs, such as albuterol, ventolin and salbutamol, work in the       short term to relax airways, but over the long term over-sensitize the body       and make the drugs less effective. Then airways become more sensitive to       asthma triggers. [5]               Quetiapine, a drug commonly used in nursing homes to treat agitation and       related symptoms in people with Alzheimer's disease, actually worsens their       condition and speeds the rate of their mental decline. [6]               First-line drugs used to treat Alzheimer's do not stop the progression of the       disease and are largely disappointing, [7] and side effects caused by       second-line treatments (like Quetiapine) for Alzheimer's-related psychosis,       aggression and agitation,        offset any modest advantages of first-line drugs. [8] Drugs like these ensure       your loved ones will never make it out of the Alzheimer's care facility.              Diabetes rates are exploding in America. Millions of Americans are being       placed on anti-diabetic drugs. But nearly all anti-diabetic drugs result in       weight gain and eventual total dependency upon insulin injections. [9] ,       [10] This is another example        of drugs locking patients into inevitably more severe disease.              Disease substitution, not disease treatment              All too frequently, drugs substitute one disease for another. For example,       most anti-psychotic drugs induce weight gain and diabetes. [11] , [12] This       is so typical that many people believe a pudgy body always accompanies mental       disorders.               Another example of disease substitution is the treatment of high blood       pressure with diuretics which can induce a vitamin B1 (thiamine) deficiency       that results in heart failure. One study found a third of patients       hospitalized for heart failure, who are        often treated with diuretics, were vitamin B1 deficient. [13] Vitamin       therapy is uncommon in hospital settings.              Blood pressure drugs: inappropriate treatment              Consider drug therapy for high blood pressure, what doctors call       hypertension. The idea is to lower blood pressure with medications and reduce       the risk for a stroke. But no single blood pressure pill seems to work. More       than one drug is often needed,        and there are few if any studies that prove combination therapies are safe and       effective. [14]               Most blood pressure drugs do not address the cause of the disease, which       commonly are age-related changes in blood sugar or hardening of the arteries,       resulting in inability of the blood vessels to dilate (widen) upon physical or       mental exertion or        stress.               Age-related inability to control blood sugar levels is generally caused by       insulin resistance (inability of insulin to enter cells) which is induced by       iron overload, [15] , [16] , [17] and hardening of the arteries by       calcification which impairs        dilation.              Diabetics experience buildup of underlying calcium in their arteries, which       largely explains diabetic hypertension. [18]               Calcification of the inside wall of arteries induces coronary artery disease       and hypertension, which can be measured by a CT scan. [19] Rats that       spontaneously develop hypertension exhibit calcified aortas (the aorta is the       first blood vessel outside        the heart). [20]                      [continued in next message]              --- SoupGate-Win32 v1.05        * Origin: you cannot sedate... all the things you hate (1:229/2)    |
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