Health Supreme by Sepp Hasslberger

Networking For A Better Future - News and perspectives you may not find in the media

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September 24, 2010

Doctor 'fires' patient over bicarbonate cure - Health Supreme NewsGrabs Friday, 24 September 2010

Video: Doctor 'fires' patient for using bicarbonate cancer therapy
(removed from YouTube)
Investigative journalist Frances Oman was diagnosed with cancer in February 2007 - an aggressive soft-tissue sarcoma had developed inside her thigh. Refusing conventional treatment, Frances ended up with the Gerson nutritional regimen, which arrested tumor growth and slowly shrank the mass and eventually she consulted Dr Simoncini in Rome. Her tumor was surgically removed and - after local treatment of the surgery site with a sterile sodium bicarbonate solution - the lady finds herself cured and getting better ... without chemo or radiation therapy and without any metastases. Coming back to the US and telling her oncologist and GP what she had done, she was told to look for a new doctor. In effect, her doctors had 'fired' her.

Vitamin C rapidly improves emotional state of acutely hospitalized patients
Treatment with vitamin C rapidly improves the emotional state of acutely hospitalized patients, according to a study carried out by researchers at Montreal’s Jewish General Hospital and the affiliated Lady Davis Institute for Medical Research.

“Earlier studies, both in our hospital and in other centers, demonstrated that the majority of acutely hospitalized patients have subnormal levels of vitamins C and D in their blood,” said Dr. L. John Hoffer, MD, PhD, an investigator at the Lady Davis Institute for Medical Research.

“About one in five acute-care patients in our hospital have vitamin C levels so low as to be compatible with scurvy,” added Hoffer, also a Senior Physician in the Divisions of Internal Medicine and Endocrinology, and a professor of medicine at McGill University. “But patients are rarely given vitamin supplements. Most physicians are simply unaware of the problem.

EC committee acknowledges hazardous nature of water fluoridation
The European Commission has claimed for years now that its justification limiting public access to natural health products is its extreme concerns over protection of consumer health. Now, with one of its committees acknowledging the crude and hazardous nature of water fluoridation, what is it going to do? Will it continue to do what it appears to have been doing all along, which is to bend in whatever directions big corporate interests are pushing them? Or will it do the right thing by consumers and force the Irish and UK Governments to ban its nonsensical mass fluoridation progammes of the public water supply?

What hidden dangers lie in toothpastes?
Botswana Sunday Standard
Makers of dental hygiene products, including mouthwash, pride themselves in their products containing fluoride, which, according to experts, is an active ingredient that prevents cavities.

“The introduction of fluoride toothpaste dates back to 1955 and different improved formulations have since followed over the years. Fluoride is used for its topical anti-caries properties,” Dr Kalane says.

Though offered as being protective against tooth cavities, fluoride is not considered to be a dietary essential and has effects on the formation of dental enamel and bones.

There are claims that it also acts as an active ingredient in rat and cockroach poison as well as in anaesthetic, hypnotic and psychiatric drugs.

In fact, in the US, fluoride was surprisingly shown not to be that effective in reducing cavities.

Salt Fluoridation: The Big Lie Continued
The website Parents of Fluoride Poisoned Children has a section devoted to salt fluoridation which presents some really disturbing information. As noted the average fluoride dose in areas where salt fluoridation has been adopted is equivalent to those in commercially water fluoridated areas. However, the numbers of people exposed to fluoride through salt fluoridation greatly exceeds those exposed through the water supply. Most of Western Europe and parts of Eastern Europe now use mainly fluoridated salt.

Fluoride is not a nutrient or in any way essential or beneficial to human health, it does make a heck of a rat poison though. Like the elements lead or aluminum one cannot avoid all exposure but it is worthwhile to take reasonable steps to minimize exposure and certainly a public policy of deliberately increasing fluoride exposure is detrimental to health...

The Complex Ethics of Genetic Engineering
While most people believe that GE is too complicated for them to understand, the ethical and social issues that come up in a democratic society have little to do with the technical stuff; the basis of these issues can be easily understood. However, the technological elite hasn't felt any obligation to present materials in a way that invites public participation, and regulatory agencies have often been opposed to transparency or are captives of the industries they are supposedly overseeing...

The Creepy Science Behind Genetically Engineered "Frankenfish"
The company that developed the GE salmon, AquaBounty Technologies, claims the fish grows to market weight in 16 to 18 months instead of the usual 30 required for farmed Atlantic salmon. The fish was created by inserting genetic material of both Chinook (the largest variety of Pacific salmon) and ocean pout (an eel-like fish) into the genome of Atlantic salmon. The commercialized fish will all be females, making them unable to breed. AquaBounty's intellectual property will be further protected because the fish will be sterile, as they will all be triploids (fish with three complete sets of chromosomes instead of the usual two).

Bon appetit!

AquaAdvantage Salmon Ready for Commerce?
In the absence of feeding studies the commercial release of GM salmon is too hazardous to consider - Prof. Joe Cummins
In the case of GM AquAdvantage salmon, it is puzzling to find that FDA describes AquAdvantage salmon as a veterinary drug but does not appear to have required animal feeding studies followed by complete tissue necropsy of the fed animals. It appears as if FDA is prepared to dance in the dark as the public are fed GM salmon. In the absence of feeding studies the commercial release of GM salmon is too hazardous to consider. Also, the many defects of the GM fish and the additional costs needed to raise the fish may well make it commercially undesirable as well as dangerous.

USA: Demand that the FDA Label Genetically Modified Foods!
The FDA has announced a 60-day period of consultation and public hearings over whether to permit a genetically modified strain of salmon, which they have named AquAdvantage (“frankenfish” to its critics) to be eaten by humans. The approval process could take less than a year, and if it gets the green light the fish could be on the market in eighteen months.

There are two sets of hearings. This hearing will determine whether the salmon (if approved) must be labeled as genetically engineered or not. One question the hearing will try to determine is whether and how AquAdvantage salmon is “materially different” from regular Atlantic salmon. In past hearings on GMOs, the FDA has never found that genetic engineering in itself constitutes a material difference, and the FDA cannot require labeling based on differences in the production process if the resulting products are not materially different.

Going to the site linked in the title of this item, you can demand that the FDA, if it approves the application for AquAdvantage salmon, ensure that all such fish are clearly labeled as genetically modified at the point of sale.

Chemtrails: Atmospheric Geoengineering
The Case Orange report cites a number of US patents for the invention of a “Specific contrail generation apparatus for producing a powder contrail having maximum radiation scattering ability for a given weight of material. The seeding material consists of 85 percent metallic particles and 15 percent colloidal silica and silica gel in order to produce a stable contrail that has a residence period of up to 1 to 2 weeks.”

Then in 2009, the publication of a report entitled “Modification of cirrus clouds to reduce global warming” put the case for further geo-engineering strategies [3]. These all had the stated intent of creating a layer of reflective cloud capable of bouncing back the sun's rays to prevent unwanted terrestrial climate heating. The report states that the findings of The Intergovernmental Panel on Climate Change supports the proposition outlined in the Hughes Aircraft Patent 1991 on stratospheric seeding for reduction of global warming. Hughes was later bought by Raytheon, The US government's private defence contractor. This is the same company that acquired the contract to build HAARP (The High Frequency Active Auroral Research Program) in Gakona, Alaska.

Other significant reports include an important paper by Dr Ilya Perlingieri, entitled “The Consequences of Toxic Metals and Chemical Aerosols on Human Health”. She states: “Over the past decade, independent testing of Chemtrails around the country have shown a dangerous, extremely poisonous brew that includes: barium, nano-aluminium coated fibreglass (known as CHAFF), radioactive thorium, cadmium, chromium, nickel, dessicated blood, mould spores, yellow fungal mycotoxins, ethylene dibromide and polymer fibres. Barium can be compared to the toxicity of arsenic and is known to adversely affect the heart. Aluminium has a history of damaging brain function.” I need hardly add that ethylene dibromide is a highly toxic agricultural pesticide.

Internet Domain Name Firm To Screen Fake Meds
eNom, which is the world’s second-biggest seller of web site addresses (otherwise known as domain names), is now going to screen its customers for unapproved drug sales, The Financial Times writes.

"There are roughly 4,000 rogue Internet pharmacies violating the criminal laws specified above that are utilizing eNom’s registration services, more than any other Registrar by a factor of seven. eNom is aware of the illegal nature of these domains. eNom has been notified by the organization that represents pharmacy regulatory authorities about this problem, and has been requested to work with LegitScript, as other US-based Registrars do, and non-US Registrars who do business in the United States, to identify clearly illegal websites and suspend them..."

Quackpots: Why the Doctor's Data v Barrett case is important to North America...
Neither Obamacare, nor any other current health care solution on the table, proposed by the "thinkers," is going to help North Americans for one simple reason. The proposed solutions fail, at first, to identify the real problems of North American Health Care - and that problem is that we are on a maintenance of symptom system rather than a cure system. In short, Cancer, Heart Disease, Diabetes, Stroke, Autism, Cerebral Palsy, and more can all be beaten right now with existing science and technology - but all of that science and technology is blocked, and its proponents intentionally smeared in the public's eye.

But then, something happened that could change all that. Someone had enough. That "someone" is a laboratory called Doctor's Data, that, in essence, did one simple thing - they took the leash off their junkyard dogs...

US House of Representatives passes bill to crack down on health care fraud
The House has just passed a bill that would ban corporate execs from doing business with Medicare and Medicaid if their companies were convicted of fraud. The measure also gives the Department of Health & Human Services Office of the Inspector General the ability to exclude parent companies that may be committing fraud through shell companies, which are otherwise known in polite circles as subsidiaries.

The legislation was designed to close a pair of loopholes in existing law. Currently, execs at companies that are convicted of fraud can be excluded from federal health care programs, but if an exec had left the company by the time of conviction, there was no mechanism to enforce a ban.

Sleeping Pills and Anxiety Medications May Increase Mortality Rate
The study, published in the September issue of the Canadian Journal of Psychiatry, analyzed Statistics Canada's National Population Health Survey and tracked the use of sedatives and insomnia medications in more than 14,000 Canadians between the ages of 18 and 102.

Researchers at the Laval University School of Psychology in Quebec discovered a 36 percent increase in mortality rates in participants who used insomnia or anxiety medications at least once a month during the 12-year period.

Did Johnson & Johnson hide birth control patch risks?
MSN Health Today is reporting that Johnson & Johnson may have known years ago about the deadly risks of its birth control patch Ortho Evra.

Data from patient reports between 2002 and 2004 show a 12 percent increased risk for stroke and an 18 percent increased risk for blood clots associated with Ortho Evra, compared with the conventional birth control pill.

The Rise and Fall of Provigil – Part I
The Rise and Fall of Provigil - Part II
On July 22, 2010, the European Medicines Agency recommended restricting the use of modafinil. Doctors and patients should be advised to use the drug only for the treatment of narcolepsy and all other indications should be withdrawn from market authorization. In addition to the brand-name, Provigil, marketed by Cephalon in the US, modafinil is also sold as Alertec, Modalert, Modavigil, Modiodal, Provake, and Vigil.

This is the story of an addictive pharmaceutical drug often prescribed for conditions it was not meant - and not approved - to treat. Evelyn Pringle has done the research and found 'off label' marketing and cynical disregard for both patient safety and the warnings issued by several health agencies... an ordinary story in these times of pharma-dominated healthcare.

FDA Restricts Avandia, Europe Suspends The Drug
In a move that many anticipated, the FDA is leaving the controversial Avandia diabetes pill on the market, but with restrictions for patients who are unable to control their illness by using other meds.

At the same time, though, the European Medicines Agency is suspending use of Avandia, but not revoking approval.

GlaxoSmithKline, which has been criticized for failing to sufficiently disclose clinical trial data about cardiovascular risks, is being required to create a restricted access program under a risk evaluation and mitigation strategy.

- - -

You too can contribute to these newsgrabs...
just tell me about a link to an article or a site you think is particularly interesting.
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More information out there...

There is a lot I cannot cover but other sources for this kind of information exist.

Dr Mercola has a good health blog
Mike Adams publishes Natural News.
In the UK we have the One Click Group.
The Dr Rath Foundation campaigns for a New Healthcare System.
Natural health and nutrition on La Leva di Archimede
Food, Agriculture and more on the Organic Consumers Association site.

"The individual is supreme and finds the way through intuition"


posted by Sepp Hasslberger on Friday September 24 2010
updated on Thursday December 23 2010

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The Individual Is Supreme And Finds Its Way Through Intuition


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