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Archive for March, 2006

This Bird flu isn’t Flying

Thursday, March 30th, 2006

Reports this past week from Japan, Holland, and the initial “site” of bird-flu, Vietnam, indicate that, indeed, this H5N1 virus is highly unlikely to become a world-wide pandemic. And physicians at the initial site, Vietnam, agree with what several others in international development have been saying: the amount of attention and resources ($$$) being put into a possible avian flu pandemic is irrational and detracts from other more pressing and real health issues globally.

Dr. Jeremy Farrar has treated about two dozen patients with avian influenza in the past three years at the Hospital for Tropical Diseases in Ho Chi Minh City—and no new cases yet this year. He put the avian flu into perspective in an interview with the International Herald Tribune: “Billions of chickens in Asia have been infected, and millions of people lived with them, yet less than 200 people have gotten infected.”

The disease has been known in Asia nearly ten years, since 1997, and 105 people have died from it according to the latest figures from the World Health Organization. In the outbreak among fowl in eastern Turkey in January, 10 persons were found to have the virus, and two children died. Others carrying the virus had symptoms no more serious than a cold.

Reports in Nature and Science last week told why the virus isn’t spreading as governments would have us believe and why the two boys’ symptoms were no more than that of a cold. Scientists in Japan and Holland published similar findings: the receptors for the avian virus are clustered in the deepest branches of the human respiratory tract, thus the virus cannot be spread by coughs and sneezes.

The avian flu virus would have to undergo at least two major mutations in order to be transmitted between humans. The H5 strain of avian flu has been infecting people since the late 1950s and has not yet mutated into a form transmittable between humans.

So why is there such government frenzy at this time? The birds have been migrating all these decades, long before increased global travel spread viruses such as SARS. Attempts by the pharmaceutical companies to create a vaccine for this virus have killed half as many people as the disease has.

In the meantime the U.S. government’s brilliant advice to prepare for this pandemic: buy an extra can of tuna fish every time you’re shopping and powdered milk so that when there’s a quarantine you’ll have a food supply. Now the tuna has so much mercury in it, more than one can a week isn’t recommended (even by the same government), and the traces of antibiotics and chemicals in milk puts everyone who’s “got milk” at risk. This is your government’s recommended diet for a flu outbreak? One has to question the intelligence of those at the helm.

In case of any flu outbreaks, the homeopathic pharmacies have always developed the safest and only effective remedies. That’s who I’ll be calling on.

The Right & Responsibility to “Practice Medicine”

Wednesday, March 15th, 2006

Nearly everything written for Women’s Medicine Bowl, Inc. is reviewed by our legal counselor to be assured that we’re not “practicing medicine.” And few things raise my ire more than the notion (and laws) that only members of the AMA are legally permitted to “practice medicine.” The underlying principle of WomensMedicineBowl.com is that if you’re alive you have not only the right but the responsibility, of taking care of your health, i.e. of practicing medicine.

Subscribing to the notion that laws regarding “practicing medicine” should be limited to those licensed “to prescribe drugs and/or perform surgery”, I investigated how do the various legal entities—medical societies, state legislatures, the courts– define “practicing medicine.”

The results are dire and depressing. And changes in the state legislatures and, following that, in the courts’ rulings will take a rebellion by the public, much as it did in the early 1800s when the primary treatments of physicians were bloodletting, purgatives, emetics and blistering. (The creation of medical societies to license physicians in the late 1700s had much more to do with protecting the members’ social status and financial turf than protecting the public.)

The severe and deadly treatments of “regular” physicians led to the public’s move to botanical treatments, herbalism, and homeopathy which arrived in America 1825, quickly becoming the preferred medical treatment. Two best-selling books in the 1830s were Homeopathic guidebooks to use with a kit of remedies.

Many “regular” physicians incorporated homeopathy into their practice, and these renegades were ostracized from the medical societies. Indeed, the AMA was formed in 1848 to counter the influence of homeopathic care.

There is no universal definition of what is “practicing medicine”; each state has its own definition—drawn up by the state medical society (singular not plural). So who can practice which healing modalities varies greatly across the country. In 1983, a reflexologist in Illinois was convicted of “practicing medicine”. Midwives in many states are continually battling with the legislatures and courts that pregnancy and childbirth aren’t within the definition of treating “disease, injury, or deformity”. Although by all measures of outcomes, birthing by midwives is healthier than in hospitals, the ancient practice of midwifery is hounded to the edges of the U.S. healthcare system. The court cases involving many healing modalities are numerous.

What is needed—and it’s coming—is a revolution in thinking. Two hundred years ago it was the physicians’ use of harsh chemicals and severe treatments such as wearing a coat of leeches (bloodletting) that drove a revolt by the public. In addition to being more effective, herbalism and homeopathy were more affordable. Doesn’t this sound familiar? With over 100,000 deaths each year due to pharmaceuticals and over 250,000 deaths due to physicians errors (and the pharmaceuticals), costs of healthcare spiraling (largely due to lawsuits caused by the above), and one in six of the US population without any health insurance coverage—isn’t it time for a revolution? (This sad scenario is limited to the U.S., by the way; every other developed or developing nation has better managed the healthcare of its citizens.)

New paradigms can’t occur without revolution because the debate is framed in terms of the current paradigm. Concerning the “practice of medicine” the current paradigm is: (1) If you are afflicted, see a licensed physician; (2) because the source of all healing is the licensed physician, any non-AMA health practitioner might be a fraud or a quack and is, in any case, unlawfully “practicing medicine”.

The revolutionary (again) new paradigm reframes the scenario as such: (1) If afflicted, you may choose from among a menu of healing modalities; (2) healing isn’t exclusively the province of MDs; other healing methods can exist alongside allopathic medicine.

A comprehensive review of the history of the regular or orthodox medical profession in the US, state regulations of “practicing medicine”, and a route to regulatory reform was published in the Arizona State Law Journal by Michael H. Cohen. See the complete well-written article, including references to over 500 court rulings, at http://www.rosenthal.hs.columbia.edu/legal/fixedstar.contents.html.

Defend Your Right to Choose Natural Hormones Before April 4!

Wednesday, March 1st, 2006

As the first of the Boomers approached the perimenopause stage of life about 10 years ago a number of books were published discussing, very thoughtfully, the pros and cons of Hormone Replacement Therapy (HRT). The premise of having these thoughtful discussions was largely that the numbers of women who were on the cusp of menopause, some 35 million, were huge. The medical community—or these thoughtful authors–was anxious about how this huge pool of women would respond to this change of life.

The correct premise is Individually, each one on her own! It was and is irrelevant that this huge generation is going through “the change”. Five years later I found myself in Virginia, for my daughters’ high school history assignments, wandering through graveyards of the Revolutionary and Civil War eras. I started to do the math. The majority of women in those cemeteries in Manassas and Leesburg had lived into their 80s. They had survived menopause! And they did it without the wonder of pharmaceutical medicines—probably because they didn’t have pharmaceuticals!

The medicines of the majority in the 18th and 19th centuries were herbals. Herbals remain excellent medicines, and new scientific developments such as Human Growth Hormone (HGH) ease this transition in life. But, basically, women’s bodies are designed to adapt to lower estrogen levels after the child-rearing years—which is why the higher testosterone levels give us a little mustache!

The Women’s Health Initiative study, the largest randomized controlled clinical trial of HRT, was abruptly halted in 2002. Researchers concluded after five years that women who were taking the hormones were at increased risk for breast cancer, stroke and clots, and were not protected from heart disease. The women, aged 50 to 79, were at significantly increased risk for heart attacks during the first year of treatment; they benefited from fewer fractures overall and initially appeared to have lower rates of colorectal cancer.

The downsides of treating menopause as if it were a disease were so startling that the study was halted, and women by the millions weaned off the drugs. Nearly four years later many women haven’t found satisfactory alternatives to the synthetic chemical HRT and have returned to Premarin and Prempro, two popular drugs manufactured by Wyeth Pharmaceuticals.

But Wyeth isn’t satisfied with its share of the market, and has filed a petition with the FDA to impose broad restrictions on bioidentical hormones, claiming that these natural alternatives to Wyeth’s drugs are unsafe, etc. A pharmaceutical company claiming a natural compound is UNSAFE! They have evidently overdosed on a drug for ENHANCED GALL!

This wouldn’t have anything to do, of course, with the fact that sales of Wyeth’s Premarin products fell 68% between 2002 and 2004 and profits fell 72% in those years. The FDA received $300 million in drug user fees in 2004 from the pharmaceutical companies that sell the drugs the FDA approves. Compounding pharmacies don’t pay drug user fees because they’re regulated by the states, not the federal government. So, who is the FDA working for? We’ll see…

Bioidentical hormones, derived from estrogen-like plant compounds, are, as the name implies, identical to natural hormones in the body. This certainly isn’t true of synthetic HRT. A compounding pharmacy customizes the medicine according to the doctor’s prescription, which is determined by lab tests. So the level of three types of estrogen and natural progesterone are used with natural hormone replacement therapy. The therapy has been used in the U.S. since1982 with great successes, obviously enough to irritate Big Pharma.

If you have experience using Bioidentical Hormones—or want to have a Choice in the future—file your comments at the link below. And tell your women friends and daughters! The FDA will take comments until April 4, 2006.
Here is the direct link to the FDA

 
 
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