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The Problem with Conventional Healthcare, by Karl Robinson, MD January 30, 2010

Problems with our healthcare system. What homeopathy can offer.

Filed under Medical Issues, Principles & Practice of Homeopathy

Thanks Karl for this brilliant discussion of the problems with conventional medical care. Readers, if you think this only applies to human medicine, you are sadly mistaken. The very same thing is happening in veterinary medicine.  If you haven’t seen the introduction to homeopathy videos by Dr. Karl Robinson, available on this site under the homeopathy tag, take a moment to watch and learn.

It is universally agreed: our healthcare system costs too much and does not work well. As a conventionally trained M.D., who opted years ago to practice homeopathy, I would like to offer my observations on both the conventional and the homeopathic way of approaching illness.

The current gargantuan and enormously complex healthcare system needs to be reduced by a full one half. It is bloated beyond good sense and beyond affordability. And the fault lies only partially with the insurance companies and Big Pharma. I believe the very way conventional medicine is practiced is at fault.

Consider this typical scenario: you go to your Family Doctor complaining of fatigue, weight gain, arthritic pains, disordered digestion with gut pain and constipation. Your doctor runs tests and finds you have low thyroid and sends you to an endocrinologist who runs more tests and prescribes a medicine which you will be expected to take for the rest of your life. Score one for Big Pharma. Your family doc also discovers high blood pressure and, when one drug does not bring it down, prescribes two—for life. Later, you get sent to a gastroenterologist and later still, a rheumatologist. Along the way more tests, and more prescriptions. You already go to a psychiatrist and take an antidepressant. You now have five doctors in play, none of whom talk to each other. A really good Family Doc could manage all your problems with few or no referrals. Fifty or sixty years ago he was known as a “GP” or “General Practitioner” and did just that. But nowadays he or she is practicing “defensive medicine” and doesn’t want to be sued so it’s a kind of insurance to refer out and over test. Little wonder our healthcare is so ruinously expensive. And it is ruining us with healthcare costs going up at roughly twice the rate of the overall Consumer Price Index.

No new healthcare law is going to fix this bloated system. It is inherent in the very structure of modern, technologically oriented medicine. Realize that we have this system because 1) doctors believe in it (we created it) and 2) the public believes in it. People when ill or when they worry they are ill, want all the tests, want to be seen by all the specialists. But realize that all these tests and referrals and prescriptions cost someone whether it be you or your insurance company or Medicare or Medicaid.

Now, if the patient stops any or all of his medicines, the illnesses return. These illnesses are being managed not cured. Not to mention the all too frequent problem of adverse drug effects.

Contrast the above model with the homeopathic. A woman in her late forties comes to me because of debilitating migraines occurring twice a week. They are so severe she cannot function despite two powerful analgesics. I do a one and a half hour interview in which I explore all aspects of her complaints and how she relates to her environment (food, weather, job, relationships, hobbies, fears, anxieties).

I learn she also has hypertension, arthritic pains, poor digestion and constipation. She has five medical problems and is taking six pharmaceuticals.

Then I learn that five years ago her son was killed in Iraq. As she speaks, tears roll down her face and she says, “I’m sorry. I promised myself I wouldn’t do this.” I pause and then, as gently as possible, ask when the migraines began. Four to five years ago—following the tragic loss of her son. I now know more. She is still grieving, and the headaches appeared shortly after her son’s death. So, in truth, I have uncovered a sixth problem—grief.

For a homeopath, how a patient reacts to her problem is as or more important than the problem itself. This woman has unresolved grief which had triggered her pathology. Also, she is hot-natured, can not bear the sun, loves salt, and her face is oily. She is introverted and rejects consolation. These symptoms lead me to select the medicine, Natrum muriaticum, and I give her a single dose.

Within a month her headaches are fewer, her mood brighter, and her bowels are functioning normally. Within three months all problems have resolved. She begins to discontinue her drugs. She now admits she was probably depressed and hadn’t realized it until she came out of it. All this with infrequent doses of Natrum muriaticum!

As a homeopath, I gave one homeopathic medicine unlike the conventional doctor who prescribed six pharmaceuticals. And, that one medicine covered all the pathologies.

This patient is on the road to a radical improvement in which all aspects of her physical and mental well-being have been addressed with a single medicine. This methodology is quite different from the conventional system which strives only to control or manage the problems. And it was accomplished with one medicine given infrequently and one that produced no adverse effects! The positive results this patient achieved are not exceptional with homeopathic medicine. In fact, diseases far more complex and difficult than migraines can be greatly helped with homeopathy.

Does this mean that everyone who is treated with homeopathy always has an excellent outcome? Of course not. Nothing is one hundred percent. But, by taking into account all aspects of the patient, not only the main complaints but her disposition and how she lives in, and reacts to, her total environment we stand a better chance of a good outcome.

Homeopathic medicine is a serious discipline and is effective when administered by a trained homeopathic physician. And it is extraordinarily cost effective.

As a homeopath, I rarely prescribe pharmaceuticals. I write only five to ten prescriptions a year and these simply to tide patients over until they no longer need the drugs. Yes, I aim to get people well enough so they can stop taking their medicines. I try to order as few tests as possible because, as a homeopath, I do not prescribe on laboratory data. I refer to specialists infrequently. If someone has a rectal bleed, sure, I want the gastroenterologist to scope them. If they are having a heart attack they need to be hospitalized swiftly.  When surgery is indicated, it is life saving. But, by and large, I don’t refer much.

The whole idea of being a doctor “is to restore the sick to health, to cure as it is termed.” That quote comes from Samuel Hahnemann, the founder of homeopathy. That’s aim one, aim two and aim three.

I would encourage you all to look into this extraordinary, gentle, healing art.


 

Polo Horse Deaths: pharmacy error! April 24, 2009

 

 The needless deaths of a string of  prized polo horses in South Florida has been determined to be the result of pharmacy error! Looking at the stats below for human pharmaceutical errors should we be surprised that a miscalculation by a compounding pharmacist would result in the death of animals given the “tainted” formula? This is one of the biggest problems with drug based therapies. How can you be sure the drug you were prescribed is the one that you are actually given?

One other consideration is the dependence of the  sport horse community on “performance enhancers”. Just like the human sports world, talent doesn’t seem to be enough.  Every trainer has their special blends of drugs and supplements supposed to make the horse a better athalete. What really happpens is the horses are injured younger and they have much shorter careers than in times past. We are breeding and training “flash in the pan” horses without the stamina and long term health to perform into their middle age, or even much beyond puberty.

My friend and trainer Ginny Padgett and I still have a dream of raising a healthy horse  to run naturally and win. I think this goal is  very obtainable.  We just need to find a horse owner willing to “buck” the current system.

 

 

 

 

 

 

 

 

 

 

Medication Error Statistics

 

 

 

 

Medication errors are a

common occurrence and

continue to be a problem in

the health care industry. It

is estimated that the annual

cost of drug-related morbidity

and mortality is nearly

$177 billion in the United

 

 

 

 

States.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

1

Approximately 7,000

 

 

 

deaths occur each year and

medication errors occur in just

about 1 of every 5 doses given

 

 

 

 

in hospitals.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

2

The FDA states

 

 

 

that there is at least one death

per day and 1.3 million people

are injured each year due to

 

 

 

 

medication errors.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

3

 

 

 

 

The National Coordinating

Council for Medication

Error (NCCMERP) defi nes a

medication error as being “any

preventable event that may

cause or lead to inappropriate

medication use or patient

harm, while the medication

is in the control of the health

care professional, patient or consumer.” Such events may be related to professional

practice, health care products, procedures and systems including: prescribing; order

communication; product labeling, packaging and nomenclature; compounding; dispensing;

 

 

 

 

distribution; administration; education monitoring; and use.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

2

 

 

 

 

Common causes of medication errors include incorrect diagnosis, prescribing errors,

drug-drug related reactions, dose miscalculations, incorrect drug administration and lack of

patient education. Other factors that can contribute are job-related stress, improper training

 

 

 

 

or education and sound-alike look-alike packaging of medications.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

3

did aal etPhillips J.

 

 

 

retrospective analysis of medication errors between 1993 – 1998 and found that the most

common types of errors were from administering improper dose (40.9%; 36.4% being

overdose), wrong drug (19%), and wrong route of administration (9.5%). The investigators

also found that the most common causes of errors were performance and knowledge

 

 

 

 

defi cits (44%) and communication errors (15.8%).

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

4

 

 

 

 

 

By Steven Morgan, Pharm.D. Pharmacy Practice Resident

 

 

 

 

 

 

 

 

 

ftjhthtdddscription

 

 

 

 

The

 

 

 

 

A Joint Publication from the University Health System Pharmacy Department, Risk Management and Ambulatory Services

Editor: Brandi Kelly, Pharm. D

 

 

 

 

 

Big Pharm and Misleading Ads April 5, 2009

Filed under: big pharm,Uncategorized — Gulf Coast Well Pets @ 11:22 am
Tags: , ,

Do you ever use Google or other search engines to look up information? Most of us do. It seems 14 major pharmaceutical companies have been using misleading ads.

The Food and Drug Administration has told these pharmaceutical companies to stop using what the FDA calls “misleading” ads on the Internet search engines. The FDA finds the ads misleading due to lack of complete information in the brief ads. The information most likely to be left out is the risk information.

The ads in question are the brief or “sponsored links” in the side bar that link to the companies Web site. Pharmaceutical companies and other interest groups pay search engine operators like Google to post these links after someone types in a related search term.

Many of the “sponsored link” ads are for drugs that carry black box warnings. None of the risks are mentioned in the brief ads. An example is the ad for Tysabri (Biogen Idec Inc.) which says “A Multiple Sclerosis Treatment That’s Different from the Others” or “Satisfied with your MS Medication or Looking for Something Different?” Tysabri carries a black box warning due to its link with a serious brain infection in several patients.

The companies receiving letters were Bayer, Biogen Idec, Boehringer Ingelheim, Cephalon, Eli Lilly, Forest Laboratories, Genentech, GlaxoSmithKline, Johnson & Johnson, Merck, Novartis, Pfizer, Roche and Sanofi-Aventis.

Read:

Do you know what a black box warning is?  It is the warning located on the package insert, generally outlined in a black box. These warnings are associated ONLY with the most severe reactions or adverse events. Is it any wonder that the drug companies would engage in misleading and deceptive advertising?

YOU WILL NEVER FIND A BLACK BOX WARNING ON A HOMEOPATHIC REMEDY

 

Are Drugs Safe? March 26, 2009

“Properly prescribed and administered” drugs caused death in 106,000 hospital patients making adverse drug reactions the 4th leading cause of death. Journal American Medical Assoc, 4-15-1998.

This is an older study, but I doubt things have improved much. The American public has been totally deceived by the drug companies and their multi-million dollar ad campaigns.  DRUGS DON’T MAKE PEOPLE OR ANIMALS HEALTHY, THEY MAY ALLAY SYMPTOMS BUT THEY RARELY LEAD  TO A LONG TERM INCREASE IN HEALTH AND WELL BEING.

When I went to vet school (a long time ago) the word CURE was still being mentioned.  Rarely do you hear that term used anymore. The new term is manage. We MANAGE disease, especially the chronic ones, we rarely if ever are able to cure using conventional drug based therapies. This is what sends most of us in the alternative world looking for answers outside the pharmaceutical industry. We want to cure our patients. Cure: the alleviation of symptoms and a return to health without the need for ongoing treatment.

Homeopathy is the only method of treatment that I have found that can CURE chronic disease. Once again visit www.beyondflatearth.com  and spend some time reading this fascinating book, change the way you think about health and healing. You won’t be disappointed.

 

Tail Chasing Linked to High Cholesterol! March 26, 2009

Wow, this one threw me for a loop. Who knew that obscessive compulsive behavior such as tail chasing could be linked to high cholesterol?  Probably the the makers of cholesterol medications! 

Stay tuned as we watch for veterinarians to start pushing cholesterol lowering medications to their  patients.  The statin drugs have been linked to a host of complications such as liver disease and muscle aches and weakness in humans, therefor many humans are opting out of taking these medications. A new market must be found, and  profits must be made; so therefor we find a need for lower cholesterol in our animal companions.

I am waiting with baited breath for the new lipitor commercial featuring a tail chasing dog.

 

Gardasil Dangers March 16, 2009

As the parent of young children, I stay current on the new vaccines that are being pushed by the conventional medical community. The most frightening is the “cervical cancer” vaccine. The manufacturer of the vaccine has been lobbying hard for this vaccine to be made manditory for both boys and girls, even though it has been shown to be a problematic vaccine as far as reactions are concerned and has yet to be proven effective in preventing cervical cancer.

VACCINE SAFETY GROUP RELEASES GARDASIL REACTION REPORT
Calls on FDA and CDC to Warn Doctors and Parents to Report to VAERS

 

Washington, D.C. – The National Vaccine Information Center (NVIC) today released a new analysis of the federal Vaccine Adverse Event Reporting System (VAERS) reports of serious health problems following HPV vaccination (Merck’s GARDASIL) during the last six months of 2006. Out of the 385 individual GARDASIL adverse event reports made to VAERS, two-thirds required additional medical care and about one-third of all reports were for children 16-years-old and under, with nearly 25 percent of those children having received simultaneously one or more of the 18 vaccines that Merck did not study in combination with GARDASIL. NVIC is calling on the FDA and CDC to warn parents and doctors that GARDASIL should not be combined with other vaccines and that young girls should be monitored for at least 24 hours for syncopal (collapse/fainting) episodes that can be accompanied by seizure activity, as well as symptoms of tingling, numbness and loss of sensation in the fingers and limbs, all of which should be reported to VAERS immediately.
 

“Because Merck only studied GARDASIL in fewer than 1200 girls under age 16 in pre-licensure trials, it is critical that doctors and parents be made aware of the nature of the initial adverse event reports coming into VAERS and that they report serious health problems after vaccination when they occur,” said NVIC President Barbara Loe Fisher. “There are twice as many children collapsing and four times as many children experiencing tingling, numbness and loss of sensation after getting a GARDASIL vaccination compared to those getting a Tdap (tetanus-diphtheria-acellular pertussis) vaccination. There have been reports of facial paralysis and Guillain-Barre Syndrome. And doctors who give GARDASIL in combination with other vaccines are basically conducting an experiment on their young patients because Merck has not published any safety data for simultaneous vaccination with any vaccine except hepatitis B vaccine.”

According to NVIC’s report, a majority of GARDASIL adverse event reports to VAERS involved those who suffered fever, nausea, headache or pain; 14 percent were for syncopal episodes with or without neurological signs; and 8 percent experienced tingling, numbness and loss of sensation, facial paralysis or Guillain-Barre Syndrome.
Although adverse event reports to VAERS do not prove causation, they can provide an early warning sign that a new vaccine may be causing health problems that could be important. For example, reports to VAERS of bowel blockage (intussusception) in babies following receipt of Merck’s Rota Teq (rotavirus) vaccine prompted the FDA to issue a public warning to doctors and consumers on Feb. 13. [
1]

“About 4 reports per day were filed with VAERS in December 2006 for the HPV vaccine,” said NVIC Health Policy Analyst Vicky Debold, RN, Ph.D. “Some of these girls are being injured when they collapse after getting the vaccine and others are complaining of neurological symptoms that should not be ignored. Doctors and nurses should take note of the patient safety issues related to giving this vaccine. Giving GARDASIL simultaneously with any of the 18 vaccines Merck did not study in combination is not an evidence-based guideline and should involve informed consent and a signed patient release. To avoid unnecessary injuries, teenage girls should be vaccinated laying down, not be left unattended and probably should not walk or drive themselves home from the doctor’s office after they get vaccinated.”

NVIC also found that there were several VAERS reports of HPV infection, genital warts and cervical lesions after GARDASIL vaccination. It is unknown if the girls were infected with HPV before being vaccinated or if GARDASIL failed to protect them. One case of HPV infection occurred in a 22-year-old girl who had participated in a Merck GARDASIL trial in 2003 when she had shown “strong conversion to all 4 vaccine types” but “tested positive for high risk HPV” in 2006, according to the VAERS report.

In a May 18, 2006 Background Document for the FDA Vaccines and Related Biological Products Advisory Committee (VRPBAC), the FDA staff stated that Merck clinical trial data indicated there may be “the potential for GARDASIL to enhance cervical disease in subjects who had evidence of persistent infection with vaccine-relevant HPV types prior to vaccination.”  [2] Girls and women now being vaccinated with GARDASIL are not routinely being tested for active HPV infection before vaccination.

The FDA staff also questioned whether the “HPV types not contained in the vaccine might offset the overall clinical effectiveness of the vaccine.” There are more than 15 types of HPV associated with cervical cancer but GARDASIL only contains HPV types 16 and 18. It is unknown whether non-vaccine HPV types will become more dominant in the future. However, there are indications this could occur because some of the seven strains of pneumococcal contained in Wyeth’s PREVNAR vaccine, which was recommended by the CDC for universal use in all babies in 2000, have been replaced by some of the more than 80 other pneumococcal strains not contained in the vaccine. [4] [5] [6]

VAERS is a passive surveillance system and depends upon voluntary reporting of serious health problems following vaccination, even though safety provisions in the National Childhood Vaccine Injury Act of 1986 mandated that health care providers report vaccine adverse events. There have been estimates that fewer than 10 percent, even as low as 1 to 4 percent, of adverse events which occur after prescription drug or vaccine use are ever reported to government adverse event reporting systems. [7] [8] [9] [10]

“If only 1 to 4 percent of all adverse events associated with GARDASIL vaccination are being reported to VAERS, there could have been up to 38,000 health problems after GARDASIL vaccination in 2006 which were never reported,” said Fisher. “How many girls are really having short-term health problems associated with getting this vaccine that could turn into long-term neurological or immune system disorders? And how many will go on to develop fertility problems, cancer or damage to their genes, all of which Merck admits in its product insert that it has not studied at all? We just don’t know enough to be mandating GARDASIL for anyone, much less vulnerable 11 to 12 year old girls entering puberty.”

For a copy of NVIC’s Report on VAERS and GARDASIL, references for this statement and information about how to report a vaccine reaction to VAERS, go to www.nvic.org.

 

[1] Food and Drug Administration, Center for Biologics Evaluation Research. Feb. 13, 2007. FDA Public Health Notification: Information on Rota Teq and Intussusception. 
[2] Food and Drug Administration. May 18, 2006 FDA Background Document for Vaccine and Related Biological Products Advisory Committee. Gardasil HPV Quadrivalent Vaccine. Page 13.
[3] Ibid. Page 25.
[4] Porat N, Barkai G et al. 2004.
New antibiotic resistant clones of Streptococcus pneumoniae unrelated to the pneumococcal conjugate vaccine serotypes causing acute otitis media in Southern Israel.  J Inf Dis 189: 385-392. 
[5] Temine L, Guillemot D et al. 2004. Short and long-term effects of pneumococcal conjugate vaccination of children on penicillin resistance. Antimicrobial Agents and Chemotherapy 48 (6): 2206-2213.
[6] Kyaw MH, Lynfield R et al. 2006.
Effect of introduction of the pneumococcal conjugate vaccine on drug resistant Streptococcus pneumoniae. NEJM 354 (14): 1455-1463. 
[7] Scott HD, Rosenbaum SE et al. Rhode Island physicians’ recognition and reporting of adverse drug reactions. RI Med J 1987; 70:311-316.
[8] Rosenthal S, Chen R.
The reporting sensitivities of two passive surveillance systems for vaccine adverse events. Am J Public Health 1995; 85:1706-9.
[9] Braun M.
Vaccine adverse event reporting system (VAERS): usefulness and limitations. John’s Hopkins Bloomburg School of Public Health. www.vaccinesafety.edu/VAERS.htm
[10] Food and Drug Administration, Center for Drug Evaluaton and Research. The clinical impact of adverse event reporting. MedWatch. October 1996.

 

 

 

Hope for the Future March 12, 2009

 

Could our country finally move away from drug based, big pharm controlled healthcare? Perhaps the future is here!

Institute of Medicine’s Historic Summit on Integrative Medicine
By Dana Ullman, MPH

The Institute of Medicine (IOM) is considered America’s preeminent body of physicians, scientists and academians interested in health and medical issues.  It is a part of the United States National Academies, which also includes the National Academy of Sciences.  The Institute of Medicine produces independent recommendations and policy reports by enlisting various experts to address the scientific and technical aspects of some of society’s health problems.
On February 25-27, 2009, the IOM convened a “Summit on Integrative Medicine and the Health of the Public” at its headquarters in Washington, DC.  Approximately 600 people participated in this historic meeting which included a wide variety of experts in integrative medicine as well as people in leading positions in government, industry, and academia.  This Summit was co-sponsored by the Bravewell Collaboration, a foundation composed of leading philanthropists dedicated to transforming the culture and delivery of health care.
The summit content and discussions provided vital information for transforming the U.S. health care system.  Topics included: patient-centered care, the scientific basis of integrative medicine, health care financing reform and value-driven care, and mind-body relationships and health.  Prior to the conference, the IOM commissioned several papers to provide background information on integrative medicine’s performance in prevention and wellness, patient-centered care, research, public education, professional education, and economics and policy.

THE PLAYERS…
The speakers at this Summit included many of the movement’s high profile leaders, including Dean Ornish, Mehmet Oz, and Kenneth Pelletier. Evidence of interest in the broad field of integrative medicine was the inclusion on the program of Thomas Donahue (the CEO of the US Chamber of Commerce), George Halvoson (Chairman and CEO, Kaiser Foundation Health Plan), Senator Tom Harkin (Iowa), Bill Novelli (CEO, AARP), and Reed Tuckson (Chief of Medical Affairs, United Health Group, a major HMO, and former Senior Vice President, AMA).  Other speakers included Mimi Guarneri, (cardiologist and medical director of the Scripps Center for Integrative Medicine), David Katz (internist and founder of Yale’s Prevention Research Center), Victor Sierpina (University of Texas), Victoria Maizes (University of Arizona), Tracy Gaudet (Duke University), and Josephine Briggs (Director, NIH’s National Center for Complementary and Alternative Medicine).  The chairperson of the planning committee for the conference was the eminent Ralph Snyderman, Chancellor Emeritus, Duke University.
Perhaps most impressive of all was the audience itself who consisted of many health and medical experts who often serve as keynoters at health conferences, including: Jeffrey Bland, Jon Kabat-Zinn, Larry Dossey, Woodson Merrill, and Wayne Jonas, as well as dozens of professors of medicines who teach at leading medical schools, naturopathic, nursing, acupuncture and chiropractic colleges. 

THE PRESENTATIONS…
Harvey Feinberg, the President of the IOM, welcomed attendees and acknowledged that integrative medicine is a bit like a Rorschach blot test because it meaning seems so varied.
Ralph Synderman gave the opening address expressing concern about the state of medicine today.  He asserted, “No other industry holds its customers in such high disregard, except perhaps the airline industry.”  He described health care today as uncoordinated, disease-oriented, reactive, physician-directed, not personalized or safe, and extremely expensive.  Synderman expressed his strong appreciation for modern medical science, but he humbly acknowledged that most drugs and technologies have not been proven efficacious and that at best it may only impact around 25% of modern health concerns.
Reed Tuckson, who represents one of the large HMOs, warned attendees that we all may want health care reform, but whatever changes we want must have evidence of benefit.  He urged scientific inquiry as well as evaluation of demonstration projects. However, Tuckson also noted that “the enemy of the good is the perfect,” and we cannot wait until all of the evidence is in or that there is wide consensus before we begin to make serious changes.
Kenneth Pelletier echoed a similar viewpoint by asserting, “Trust in God, but everyone else must present data.”  Pelletier noted that we may not necessarily need new monies in health care but just better allocation of present resources.  Because so many high-tech methods presently used have not yet been proven efficacious, there are great savings to be obtained by no longer providing reimbursement for questionably effective (and expensive) health interventions.
Pelletier has served as a consultant to many major American corporations who have developed various disease prevention and health promotion programs for their employees.  He noted that 62 of 63 studies of cost-effectiveness, cost benefit, and return on investment have shown positive results.  According to his review of this research, a return on investment for health programs usually takes only 3.25 years.  Further, evidence-based return on investment ranges from $3.50 to $4.90 for every $1.00 invested.
Bill George, a professor of Business Management at Harvard Business School, was the CEO, President, and Chairman of the Board at Medtronic, Inc., the largest medical technology company in the world that began by creating heart pacemakers.  His wife, Penny George, was past President of the Bravewell Collaboration, co-sponsor of this Summit, and the George Family Foundation has been a leading supporter of many Bravewell efforts (yes, there does seem to be a bit of social and spiritual justice that profits from high-tech medical endeavors are being used to support various high-touch health strategies).  Bill George spoke about his personal experience at Medtronic during his presentation.  He insisted that it was important for employers to reward good healthy behaviors rather than punish bad ones.  He noted that his company gave employees $50/month ($600/year) for complying with some healthy behaviors.  He also noted that a gym is not a perk of an office but is a necessary component of it.

THE MOST POWERFUL PRESENTATION…
Dean Ornish made what many attendees considered to be the most powerful presentation of the Summit.  He described his and many others research that showed significant changes in the health status of people suffering from many of the leading causes of mortality in the US.  Ornish’s own research has shown that significant changes in dietary and exercise were substantially effective in improving health status in people suffering from cardiovascular disease and prostate cancer.  Further, he noted that the minor dietary and exercise recommendations of the American Heart Association and the National Cancer Society were simply inadequate to create significant positive results, thereby leading to poor compliance due to the small health improvements.
Ornish’s wisdom and experience here seems in sync with President Obama’s desire to make significant changes in various orthodox institutions in order to create real solutions that work.  With America’s present health statistics rank us 37th (!) in the world, suggesting that doing more of the same or making minor changes in health reform will not provide the real improvements that Americans want and need today.
Ornish also made reference to one study in which curcumin (an active ingredient in the herb, tumeric) was found to have 2,000% increase in bioavailability and therefore significant better health benefits when used with a type of pepper used in curries.  Ornish sought to warn attendees to avoid looking at studies that test simply one ingredient.  Many recent studies, for instance, have found little or no results from using vitamin C or E or a single type of multi-vitamin, when, in fact, most nutritional-oriented physicians and practitioners do not limit themselves to such single ingredient treatments.
Ornish also discussed several bodymind treatment programs, including certain meditative, visualization, and yoga practices, to improve health status and quality of life for people suffering from a host of serious ailments.  He also noted their importance for soldiers as they return from combat operations, usually suffering from PTSD.

Many speakers made reference to the challenge in health care today in which physicians and other primary care clinicians do not have the time or expertise to be their patients’ “health coach.”  There seems to be a real need for a person on the health care team who works personally with the patient to help enact behavioral changes that are health enriching.  Some attendees thought that psychologists might fill this role, others thought nurses may be best, and others wondered if a new type of health professional was needed.
Further, Ornish reported on genetic research on telomeres, a gene associated with long life.  Ornish’s research published in Lancet Oncology (November 2008) discovered that significant dietary changes had direct effects on telomeres, thereby verifying that our genetic heritage can be influenced and changed.  While our genes may indeed have powerful effects upon our health and life, such influences are not in stone but can be transformed.
Ornish’s expansive message also included reference to the provocative notion that a vegetarian diet is not only healthier for people but also for our planet.  He noted that livestock production leads to more global warming effects than all transportation sources combined.

A VIEW TO AND FROM THE HILL…
Two days before the conference began, the Senate Sub-committee on Health, Education, Labor, and Pensions held a hearing on integrative medicine.  Chaired by Maryland Senator Barbara Mikulski, testimony from Wayne Jonas, James Gordon, Sister Charlotte Kerr, Mary Jo Kreitzer, and Cathy Baase, corporate medical director for Dow Chemical Company was presented to the sub-committee and for the public record.  Then, in the middle of the Summit, Senator Harkin held another hearing on integrative medicine with what some of us referred to as the “integrative health dream team,” including Dean Ornish, Andrew Weil, Mehmet Oz, and Mark Hyman.
The third day of the Summit began with a rousing presentation from Senator Tom Harkin.  Harkin reported on these Senate hearings noting that just that week President Obama had asserted that health reform was a major priority for him and for the American people and that prevention and wellness programs have to have an important place in this health reform.  President Obama has also designated that over $1 billion would be devoted to outcomes evaluation for health and medical treatment programs to begin to be evaluated to determine what really works.
Harkin asserted, “American always do the right thing…after they have tried everything else.”  Indeed.  Harkin has been a long-term advocate for integrative health (although he originally expressed interest and support for “integrative medicine,” an attendee suggested to him what others at this Summit had previously expressed:  “integrative health” is more comprehensive a term than “integrative medicine;” within the remaining time of the Q&A session with Harkin, he referred to integrative health).  Harkin was the primary sponsor that created the Office of Alternative Medicine, as well as the National Center for Complementary and Alternative Medicine.
Harkin noted that the status quo (which he also called the “stagnant quo”) has reimbursement and incentive priorities in the wrong place.  Harkin promised to make certain that these priorities be changed.

PERSONAL THOUGHTS…
In 1993, I served as a consultant to the World Health Organization at a special conference they sponsored that sought to inquire what they should and would be doing in the year 2020.  Whenever one attempts to predict the future, it is important, perhaps necessary, to include some heretics because what may be unconventional or even heretical today may be an integral part of the future.  What is equally true about the future is that what is conventional today is tomorrow’s quackery.  These observations are not actually predictions; they are statements of the evolution of social history.
At this WHO meeting, Harvey Feinberg, MD, PhD, who was at the time the dean of Harvard’s School of Public Health, was a fellow consultant.  He was one of a select few who reached out to me to learn more about homeopathy.  He and I shared a private lunch, and his inquiring mind gave me a certain confidence that our paths again would cross.  Indeed, we have.
The very concept of “integrative health” is quite comprehensive, and yet, with respect to getting the biggest bang for the buck, we must honor the Hippocratic tradition that asserts “First, do no harm.”  How this translates into health improvements is that we should explore and exhaust safer methods first before resorting to the big (and expensive) guns of medicine and medical technology.  Also, there is general recognition that we need to move our thinking about health care where the physician is at the center to where the PERSON is at the center.
Several speakers at this Summit expressed the need and the demand for “data.”  During audience participation moments at this Summit, I voiced my concurrence, but I also voiced a warning.  In homeopathic and naturopathic thought and practice, there is a profound respect for the “wisdom of the body.”  If we set up clinical trials that simply evaluate whether a treatment is effective in getting rid of a symptom, we may be discovering that this treatment is effective but only in suppressing a symptom and sometimes creating a more serious chronic ailment rather than enacting a true cure.
We therefore need to have clinical trials, but they must not only evaluate specific symptoms but also overall health status.  They must not ignore side effects because such new symptoms are not side effects at all; they are usually the direct result of a drug’s toxicity or its ability to suppress the disease to deeper and more serious levels.
Further, when we seek ‘evidence,” we should not only evaluate evidence obtained from randomized double-blind trials, but we should also evaluate evidence from outcome studies, cost-effectiveness studies, and when possible and appropriate, basic science trials.
We need to remember that we today accept most surgical practices even though the vast majority of them have not been proven to be effective based on double-blind placebo controlled trials.  Few people consider surgery to be “unscientific” just because it is not viable to conduct placebo-controlled trials.  And yet, many physicians, scientists, and health policy analysts assume certain that some alternative treatment methods are unscientific because they too cannot be evaluated in placebo controlled trials (how does one give a placebo meditation or a placebo yoga posture?).
Likewise, many treatments that “integrative practitioners” use comprise a “package of treatments” that include various dietary changes, vitamin and mineral supplements, herbal remedies, homeopathic medicines, yoga practice, stress management methods, and on and on.  Evaluations of the outcomes of such packages of treatment are truly necessary.
At the Summit, I made reference to two cost-effectiveness studies that were conducted by the French government. In 1991, the totality of costs associated with homeopathic care per physician was approximately one-half of the totality of care provided by conventional primary care physicians.  However, because homeopathic physicians, on average, saw significantly fewer patients due to the more labor-intensive tendency of homeopathic care, the overall cost per patient under homeopathic care was still a significant 15% less.  It is also interesting to note that these savings appear to increase the longer a physician has been using homeopathy.  A follow-up study in 1996 confirmed these results.
This survey also noted that the number of paid sick leave days by patients under the care of conventional physicians (general practitioners) were 3.5 times more than patients under the care of homeopathic physicians.  These figures suggest further benefit and savings to the homeopathic approach to care.
At this Summit, there were several professors of genetics and other basic sciences who discussed the most recent scientific discoveries in their fields.  However, I was a bit surprised at the casual reference to “genetic causes” of illness and to new (and old) infective agents that “cause” this or that disease.  My concern here is that because language is so important, it is necessary that we draw from systems biology and systems thinking to realize that it is more accurate to say that these influences are “co-factors” to diseases, not causes of them.  The concept of causality tends to be linear, when, in fact, cause is rarely so simple.  The susceptibility of the host always influences whether infective agent leads to disease or not, and as Dean Ornish and others have now noted, even genetic status of an individual can be altered.
Finally, we must be more humble in how we all make use of the words and concepts of “scientific medicine.”  An IOM special report, “Informing the Future: Critical Issues in Health” (published in 2007), noted that 1/3 of Americans today take five or more medications.  And yet, even if all of these drugs have been proven “scientifically” to work, each drug was tested individually, not in combination with one or two, let alone five, drugs.  Further, most of the studies conducted have not been on children or the elderly, and yet, the high quantities of drugs are prescribed them.  Still further disconcerting is that most medication is tested for very short periods of time, even though many drugs are used over years or decades.  I certainly realize that such evaluations are complex and difficult, but these issues simply mean that we must remain humble in our sense of which drugs work, when, and for whom.
 

 

Dana Ullman, MPH, is a leading advocate for homeopathic medicine.  He has authored 10 books in the field, including his best-selling Everybody’s Guide to Homeopathic Medicines and his newest book is The Homeopathic Revolution: Why Famous People and Cultural Heroes Choose Homeopathy.  His ebook is the most up-to-date source of information on clinical research in homeopathy (“Homeopathic Family Medicine: Evidence Based Homeopathy” –available at www.homeopathic.com.) Dana can be reached atdana@homeopathic.com.

 

Think Twice about that Next Flu Vaccine March 7, 2009

Filed under: avian flu,big pharm,flu vaccine,Uncategorized,VACCINATION,vaccine danger — Gulf Coast Well Pets @ 12:00 am
Tags: ,

I am not usually one to believe in conspiracy theories, but this article is enough to make me think twice. I frequently joke with my clients that big pharm will kill us all, maybe I am not so far from the truth!

Accidental’ Contamination Of Vaccine With Live Avian Flu Virus Virtually Impossible
Czech Papers Question Whether Contaminated Baxter Vaccine Was ‘Attempt to Provoke Pandemic’
Paul Joseph Watson
Prison Planet.com
Thursday, March 5, 2009
Czech newspapers are questioning if the shocking discovery of vaccines contaminated with the deadly avian flu virus which were distributed to 18 countries by the American company Baxter were part of a conspiracy to provoke a pandemic.
The claim holds weight because, according to the very laboratory protocols that are routine for vaccine makers, mixing a live virus biological weapon with vaccine material by accident is virtually impossible.
“The company that released contaminated flu virus material from a plant in Austria confirmed Friday that the experimental product contained live H5N1 avian flu viruses,” reports the Canadian Press.
Baxter flu vaccines contaminated with H5N1 – otherwise known as the human form of avian flu, one of the most deadly biological weapons on earth with a 60% kill rate – were received by labs in the Czech Republic, Germany, and Slovenia.
Initially, Baxter attempted to stonewall questions by invoking “trade secrets” and refused to reveal how the vaccines were contaminated with H5N1. After increased pressure they then claimed that pure H5N1 batches were sent by accident. This was seemingly an attempt to quickly change the story and hide the fact that the accidental contamination of a vaccine with a deadly biological agent like avian flu is virtually impossible and the only way it could have happened was by wilful gross criminal negligence.
According to a compiled translation from Czech newspaper stories, the media over there is asking tough questions about whether the contamination was part of a deliberate attempt to start a pandemic.
“Was this just a criminal negligence or it was an attempt to provoke pandemia using vaccination against flu to spread the disease – as happened with the anti-B hepatitis vaccination with vaccines containing the HIV virus in US? – and then cash for the vaccines against H5N1 which Baxter develops? How could on Earth a20virus as H5N1 come to the ordinary flu vaccines? Don’t they follow even basic precautions in the american pharma companies?” states the translation.
The fact that Baxter mixed the deadly H5N1 virus with a mix of H3N2 seasonal flu viruses is the smoking gun. The H5N1 virus on its own has killed hundreds of people, but it is less airborne and more restricted in the ease with which it can spread. However, when combined with seasonal flu viruses, which as everyone knows are super-airborne and easily spread, the effect is a potent, super-airbone, super deadly biological weapon.
As the Canadian Press article explains, “While H5N1 doesn’t easily infect people, H3N2 viruses do. If someone exposed to a mixture of the two had been simultaneously infected with both strains, he or she could have served as an incubator for a hybrid virus able to transmit easily to and among people.”
There can be little doubt therefore that this was a deliberate attempt to weaponize the H5N1 virus to its most potent extreme and distribute it via conventional flu vaccines to the population who would then infect others to a devastating degree as the disease went airborne.
The Canadian Press article states, “That mixing process, called20reassortment, is one of two ways pandemic viruses are created,” but then claims that there is no evidence that this is what Baxter were doing, despite there being no clear explanation as to why Baxter has samples of the live avian flu virus on its premises in the first place.
However, to reiterate, the key aspect of this story is that it is virtually impossible for live avian flu virus to find its way into a vaccine by “accident”.
As health expert Mike Adams points out, “The shocking answer is that this couldn’t have been an accident. Why? Because Baxter International adheres to something called BSL3 (Biosafety Level 3) – a set of laboratory safety protocols that prevent the cross-contamination of materials.”
As explained on Wikipedia (http://en.wikipedia.org/wiki/Biosaf…):
“Laboratory personnel have specific training in handling pathogenic and potentially lethal agents, and are supervised by competent scientists who are experienced in working with these agents. This is considered a neutral or warm zone. All procedures involving the manipulation of infectious materials are con ducted within biological safety cabinets or other physical containment devices, or by personnel wearing appropriate personal protective clothing and equipment. The laboratory has special engineering and design features.”

Under the BSL3 code of conduct, it is impossible for live avian flu viruses to contaminate production vaccine materials that are shipped out to vendors around the world.
This leaves only two possibilities that explain these events:
Possibility #1: Baxter isn’t following BSL3 safety guidelines or is so sloppy in following them that it can make monumental mistakes that threaten the safety of the entire human race. And if that’s the case, then why are we injecting our children with vaccines made from Baxter’s materials?
Possibility #2: A rogue employee (or an evil plot from the top management) is present at Baxter, whereby live avian flu viruses were intentionally placed into the vaccine materials in the hope that such materials might be injected into humans and set off a global bird flu pandemic.

Spreading bird flu would create an instantaneous surge of demand for bird flu vaccines. The profits that vaccine companies such as Baxter International could reap out of such a panic are astronomical.
In addition, as we have previously reported, those that have a stake in the Tamiflu vaccine include top globalists and BIlderberg members like George Shultz, Lodewijk J.R. de Vink and former Secretary of Defense Donald Rumsfeld.
Authorities in both Europe and the U.S. have openly detailed plans for martial law, quarantine and internment should a bird flu pandemic occur.
The other motivation, as we have exhaustively documented on this website for years, is the fact that elites throughout history have openly stated that they want to see a world population reduction of around 80 per cent. Shocking stories like this take the plausibility of that narrative out of the realms of conspiracy theory and into the dangerous reality of conspiracy fact.
“Baxter is acting a whole lot like a biological terrorism organization these days, sending deadly viral samples around the world. If you mail an envelope full of anthrax to your Senator, you get arrested as a terrorist. So why is Baxter — which mailed samples of a far more deadly viral strain to labs around the world — getting away with saying, essentially, “Oops?”, Adams concludes.
This is not the first time that v accine companies have been caught distributing vaccines contaminated with deadly viruses.
In 2006 it was revealed that Bayer Corporation had discovered that their injection drug, which was used by hemophiliacs, was contaminated with the HIV virus. Internal documents prove that after they positively knew that the drug was contaminated, they took it off the U.S. market only to dump it on the European, Asian and Latin American markets, knowingly exposing thousands, most of them children, to the live HIV virus. Government officials in France went to prison for allowing the drug to be distributed. The documents show that the FDA colluded with Bayer to cover-up the scandal and allowed the deadly drug to be distributed globally. No Bayer executives ever faced arrest or prosecution in the United States.

visit www.prisonplanet.com to read more

Another great blog talking about the dangers of vaccines and the drug companies:http://chanceforchange.wordpress.com/2009/03/13/who-can-make-the-fda-do-their-job/

 

 
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