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Health & Freedom

American Medical Revolutions

by Jack Phillips

About 170 years ago our ancestors forced the repeal of licensing laws which had created a monopoly over the practice of medicine for orthodox physicians. Ordinary people, farmers, artisans, tradesmen and others got together and forced politicians to act on their behalf. They were tired of bloodletting, and harsh medications like mercury compounds that ruined their teeth and weakened their bodies. They opted for kinder and gentler alternatives with lower casualty rates, particularly the newly introduced homeopathy. They were impressed that tiny doses of medicine were able to cure cholera much better than the massive doses used by orthodox physicians.

Homeopathy, introduced in America in 1825, was a brand new medical discipline developed by a German physician named Samuel Hanhemann (1744-1843). He was disillusioned with the results of medical practices of his day. He stopped practicing and began to study the effects of medicine on a healthy person, himself. He tried quinine, a very popular medication, first. It caused symptoms of malaria, the disease which it was able to cure. Similarly mercury produced symptoms of syphilis on which it had therapeutic effects. This experimental evidence lead to an assumption: substances which produce symptoms in healthy people can have a curative effect on sick people who experience the same symptoms. Extensive experimentation with his family and friends resulted in collection of the symptomology of 27 medications. With this information he was able to investigate the validity of his hypothesis.

Returning to the practice of medicine he found that clinical experience validated his hypothesis. By this means his hypothesis became a theory in accordance with scientific methodology. Ultimately, confirmed by other investigators, it became the law of similars.

Subsequently experimentation with varying doses disclosed that small amounts of medicines had more effect on the diseases of patients than large amounts. This experimental evidence led him to conclude that his medications were stimulating the inherent healing powers of his patients. They were getting well without the damaging side effects of excessive amounts of medicines.

Many orthodox physicians in Germany, observing Hahnemann’s successes, sought training in the application of the new doctrines and began to practice homeopathy-generating a new school of medicine in the process. It became popular all across Europe. Homeopathic physicians began treating the royalty and nobility of Europe.

Homeopathic physicians didn’t try to find the cause of diseases. They spent a lot of time identifying symptoms in consider-able detail since each patient was considered to be unique. The symptoms defined the disease. Matching the symptoms of the patient with the symptoms associated with medications was not an easy job. Intelligence, training and dedication were required to achieve the full benefits of homeopathic technology. Ultimately some homeopaths limited themselves to the use of low potency medications while the most effective practitioners used the high potency variety, those with the highest dilutions.

Hahnemann did not claim to have discovered the law of similars. The therapeutic systems of empiric physicians in ancient Greece and Paracelsus had included this theory. The important discovery that medicinal substances could be more active at high dilutions was his alone and he was vilified because of it. Those whose incomes depended on the sale of large quantities of drugs found it economically damaging. Orthodox physicians, whose use of excessive amounts of mercury caused their patients to lose teeth and deteriorate physically, hated it as a serious threat to their physical safety as well as their professional reputation. But many physicians trained in the orthodox tradition abandoned it and took up the practice of homeopathy with great success.

Success of homeopathic treatments with camphor, copper sulfate and Veratrum album, recommended by Hahnemann during the Asiatic cholera epidemic in Europe in 1832, firmly established homeopathy in France. When Hahnemann arrived in Paris in 1835 he was granted a license to practice medicine within 6 month. He subsequently cured the Marquess of Anglesea of tic deleureux which French physicians had been trying unsuccessfully to cure for 20 years. After losing prestige and patients to the homeo-paths, member of the French National Academy of Medicine called them knaves, ignoramuses, charlatans and quacks. Nevertheless orthodox physicians adopted camphor, copper sulfate and Veratrum album as remedies for cholera.

American homeopaths were as successful treating cholera in the 1830s as the French homeopaths. They added to their reputation when in 1978 a yellow fever epidemic spread from New Orleans into the Mississippi Valley with alarming death rates: 4,600 of 27,000 cases in New Orleans, 5,000 out of 18,500 cases in Memphis with a total of 15,934 death out of 74,265 cases reported in the Mississippi Valley. Homeopathic physicians in New Orleans had treated 1,945 cases with loss of 110. In the rest of the south they had treated 1,969 cases with loss of 151–7.7%. The overall death rate for reported cases in the south was at least 16%. The French Government awarded a gold medal to a French homeopath for his work during the New Orleans epidemic. Homeopaths were popular!

Insurance companies began offering reduced rates to persons employing homeopathic physicians and homeopathic life insurance companies were being chartered. In 1870 the Homeopathic Life Office of New York reported that it had sold 7,927 policies to followers of homeopathy and 2,258 to other; 84 deaths in the first category and 66 in the second justified the lower premiums charged to the former.

As a result of these successes by 1892, homeopaths in the United Stated controlled about 110 hospitals, 145 dispensaries, 62 orphan asylums and old peoples homes, over 30 nursing homes and sanitaria and 16 insane asylums.

In 1889 the Westborough, Massachusetts insane asylum was run by homeopaths and the Springfield Republican reported that the cost of maintenance is much less and recoveries and general success greater than in allopathic asylums.

Meanwhile competing medical technologies and an oversupply of physicians drastically reduced the income and status of about 110,000 orthodox physicians. An average one earned $750 per year in 1900 and about 40 per year committed suicide because of financial difficulties. But about 15,000 homeopathic physicians prospered and 26 schools of homeopathy flourished at the end of the century. Unsuspecting homeopaths, fully occupied with their lucrative practices, gave grudging support to their own organization not realizing that they were in danger.

Orthodox physicians at the American Medical Association (AMA) plotted their downfall. The first objective was reduction in the number of medical schools and medical students. This had been a cherished goal since 1846 when the founding convention of the AMA occurred.

Politically astute George Simmons, M.D. who graduated from Hahnemann Medical College of Chicago in 1882 and later attended Rush Medical School, was appointed secretary of the AMA and editor of its journal (JAMA) in 1899. Soon thereafter he was appointed secretary of a committee to consider reorganization. In 1901 a reorganized AMA changed from a loose federation of independent professionals into a political powerhouse. The reorganization substantially reduced the influence of individual physicians who had been objecting to unethical drug company advertising.

In 1904 the AMA established a Permanent Council on Medical Education. In 1905 the Council arranged a conference of state medical licensing boards to review the status of medical education and set standards for medical schools. A temporary standard required four years of high school and 4 years of medical school and examination of graduates by state boards before licensing. In 1906, the committee inspected 160 medical schools, grading 82–A, 46–B and 32–C. Fifty schools agreed to require 1 year of college sciences courses for admission.

In 1907 Arthur D. Bevan, M.D., the Council’s chairman, convinced Henry Pritchard, former President of MIT, who now headed the Carnegie Foundation, to sponsor a study of medical education. That Foundation, founded in 1905 with the objective of upgrading the status of college teachers and creating a uniform system of higher education, was a logical ally. In November of that year the trustees approved the proposed study and Pritchard hired Abraham Flexner, an educator who had graduated from Johns Hopkins University, to work on the project.

Flexner headed for his alma mater’s medical school, which he used as his standard of comparison. Accompanied by Nathan Caldwell, M.D., who replaced Bevan as Chairman of AMA’s Council on Medical Education, Flexner made a comprehensive survey of medical schools in 1910. His opinions of most of the schools he visited and evaluated were not flattering. Harvard University was incensed at his opinion of their medical school which had been reorganized by Charles Elliot in 1870.

Flexner was convinced, probably by Dr. Caldwell, that Hahnemann and homeopathy were frauds, since this was the official opinion of the AMA which denied that homeopathy possessed therapeutic efficacy. Flexner also bought the opinion of William Osler, M.D. that “sectarian allopathy and homeopathy” were yielding to the new scientific medicine.

Flexner’s famous report, coauthored by Nathan Caldwell, caused substantial changes. It started a process that empowered the AMA, disorganized the homeopaths and forced the closure of homeopathic medical schools. Even though John D. Rockefeller favored homeopathy and repeatedly insisted that it be sup-ported, all of his money was spent on “scientific medicine”. Frederick Gates who was influential in disbursing Rockefeller’s money wrote that Hahnemann was in-sane. John D., Jr. told his father that the homeopaths were integrating with the allopaths. Letter requests for funds from one homeopathic school were said to have been unanswered.

Scientific medicine was designed to be capital intensive. Requirements for teaching it increased costs beyond the capability of students to support the schools with tuition and fees. As a result schools, unable to supplement their income from other sources like grants and bequests, were forced to close or consolidate. In 1910 the number of medical schools was reduced from 166 to 131. Only 63 were left in 1929. In the 1930s and 1940s, 11 homeopathic schools closed. After 1930 even the Hahnemann Medical College of Philadelphia was teaching allopathic medicine except for one or two classes of homeopathy.

New laws gave the AMA the power to control what the schools taught. Curricula were heavy in the sciences, but there was only minimal training in nutrition and pharmacology. Physicians who used to make up their own remedies began to rely on pharmaceutical company formulations and for information on drugs. Production of physicians was substantially reduced. Competing medical sects, whose members had totaled less than 10% of all physicians, were all but emasculated.

Evidently our present unsatisfactory situation came about because the frustrated monopolists of the 1820s found a way to put themselves back in the driver’s seat. They convinced upper and middle class people that they were scientists who could bring the benefits of science to their patients. At least $300 million ($600 million according to Harris Coulter’s The Divided Legacy) contributed by wealthy donors, supplemented by an unknown amount funneled through the JAMA by the pharmaceutical industry and other advertisers, helped them regain control. At a time when one dollar bought a 10-hour day’s work, this was an irresistible flood that carried the orthodox physicians back into power and supported the monopoly for almost a hundred years.

Once in control, efforts to reduce competition and increase income have been unceasing. Physicians who practice alternative medicine, in competition with regular physicians, are subject to harassment. In the state of Washington about 30% of them are being harassed at this time. Those who make substantial advancements in medical science often find the Federal Government moving against them. The FDA and FTC have used taxpayer money to suppress new technology in a number of cases. Even State legislators have cooperated, in cases where other means failed,

The purpose of the new licensing laws was to protect the public but, in fact, monopolized medical care, according to reports, has been killing over 200,000 of us every year and promises to bankrupt the country. These laws are used to prevent free public access to less lethal, more effective and less expensive therapies. As Daniel Haley so eloquently wrote, in Politics in Healing, “we don’t need government protection from things that can’t hurt us”.

Medical science should be a search for the truth and many medical scientists have spent their lives in this search. Unfortunately scientific medicine, as practiced by the medical monopoly during the last century, has rejected the discoveries of a number of medical scientists. Too many promising technologies have been consigned to the dust bin of history. As a result, medical services are much more expensive than they should be and lower in quality than they could be. Less suppression and more competition can make people healthier at lower cost.

One hundred years of suppression of advancements in medical science is enough. Even physicians have been victimized. Their expensive schools don’t teach them about the suppressed science and give them inadequate training in nutrition and therapeutics. We can do without the high prices and poor care. Let’s recover and apply the suppressed technology and reward, rather than discourage, innovations that promise lower costs and better quality care. Replace the medical monopoly with laws guaranteeing freedom of choice in medical care.

Again in 2008, as in the 1830s, orthodox medicine is killing lots of people and creating lots of invalids. The exorbitant price of $2 trillion a year is too much. We owe it to ourselves and our descendants to reintroduce competition into the medical marketplace. Forcing the repeal of the Medical Practices Act will be a good start. The Access to Medical Treatment Act proposed in the 2000 session of Congress might also be resurrected.

– Jack Phillips


JOURNAL OF ORTHOMOLECULAR MEDICINE
Official Journal of the International Society for Orthomolecular Medicine
Volume 23 3rd Quarter 2008 (Download Full Text PDF)

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Featured Articles

Hidden Cause of Weight Gain May Be Poor Liver Function

by: Derrell Jones

(NaturalNews) The issue of weight is a prevalent source of discontent especially in western cultures. It seems that we havewoken upand realized that weight control is about much more than keeping up appearances. Obesity rates have skyrocketed along with the associated adverse health conditions. Each year more and more people choose to eat right and exercise but still struggle with weight issues and chronic degenerative conditions such as high blood pressure, diabetes mellitus, heart disease, etc. A seldom-discussed yet extremely important aspect of weight loss is liver function. Traditional diets see-saw between high fat, nutritionally void foods and weight loss gimmicks and products that actually causes people to gain weight in the long run. In the middle of all this is a liver that grows, quite literally, fattier and more sluggish by the day.

Liver Cleanse

 

The liver has two distinct and highly important functions. First, it is the body's chief blood detoxifier. Secondly, the liver is the body's primary fat metabolizer. Once the liver becomes sluggish and fatty it performs neither job well and we begin to pack on the pounds in earnest and have great difficulty losing the weight once it is on.

What are some causes of a fatty liver
A high fat diet (primarily animal fat) will most likely cause the liver to malfunction over time. Animal fats tend to contain toxic materials that were trapped by the animals body. When we ingest these fats the toxins are released in the liver where they have the ability to cause damage, inducing poor liver function.

Another cause of fatty liveris artificial sweetener use. Artificial sweeteners have been touted by industry as a zero calorie marvel that will help consumers reduce calories and lose weight. What is not revealed is that artificial sweeteners generally lead to long term weight gain. How, do you ask? Artificial sweeteners completely bypass the normal digestive stages and are immediately taken into the liver. The liver basically shuts down all other metabolic processes, including metabolizing fat, to contend with the sweetener. The fats in the liver are either released – without being fully metabolized – into the blood stream to be stored as unprocessed material or theyattachthemselves to the liver. Either way,this is bad news for your weight and health.

An additional prevalent culprit behind fatty liveris excessive alcohol use. Before the alcohol causes cirrhosis it makes the liver fatty, which is the beginning of the road to dysfunctional health and weight gain.

Finally, prescription and over-the-counter medications have adverse effects on the liver. Notice that almost all of the pharmaceutical commercials mention the liver and liver function. It is because they know how detrimental their medications areto the liver and the healthdysfunctions, like weight gain, cirrhosis and liver failure that will occur when using their products. Continue taking your prescriptions but seek a holistic health professional who can assist with eliminating the underlying cause(s) of your condition which would eliminate the need for the medication.

How to avoid or reverse a fatty liver
Here are a few helpful tips that can get you started or keep you on the road to healthy liver function.

• Avoid artificial sweetener use
• Restrict or eliminate alcohol consumption
• Nourish the liver with fresh citrus juices, milk thistle, and licorice. A mixture of cayenne and lemon juice or cayenne and vegetable juice is a great liver nutritive
• Detoxify the colon to keep the digestive system flowing which increases metabolism and aids the liver in its proper functioning

It is clear that poor liver function will most likely lead to a malfunctioning and fatty liver, in turnmaking weight gain probable and weight loss unlikely. If you are working diligently at exercising and eating right but still struggle to lose weight have your liver function checked to shed light on this little-known aspect of weight management.

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Uncategorized

Ten Tips For A Spring Detox to Rejuvenate Your Liver

by: Paul Fassa

(NaturalNews) Spring is upon us, and the concept of “spring cleaning” our domiciles comes to mind. It can apply to the health conscious as well for cleaning out the body’s master cleanser, the liver, while increasing supportive nourishment.

Liver Cleanse
Detox Protocol

Coincidentally, Chinese medicine associates spring with the liver and gall bladder; both work together as blood cleansers. It’s like they’ve worked to keep our other organs and blood relatively free of toxins all winter, now it’s time to clean them out so they can function to their fullest. Liver dysfunction leads to chronic poor health, disease and death.

The symptoms of a sluggish liver can be vague, but chronic fatigue and/or increased irritability may be indicators. Mainstream medical liver tests only spot major problems such as hepatitis, sclerosis and fatty liver. Chinese and Ayurvedic medicine practitioners are better at diagnosing troublesome liver problems in their early phases.

There are several methods that can be utilized to cleanse and strengthen the liver and gall bladder system. Ten will be pointed out here with some links to give you details.

(1) Coffee enemas: There’s no better assurance of efficacy and safety than knowing Max Gerson used coffee enemas to detox the liver while curing cancer. The Gerson health protocol uses it daily still, and so does Dr. Nicholas Gonzalez with his alternative cancer therapy based on Dr. William Donald Kelley’s earlier groundbreaking cancer therapy.

If you’re not dealing with cancer, the coffee enema can be used as infrequently or frequently as you wish.

(2) Liver-gall bladder flush: This one is controversial. Whether it actually eliminates gallstones or fatty globules is the issue.

(3) Alpha lipoic acid (ALA): ALA, especially R-ALA, has been used to treat serious liver diseases.

(4) Glutathione: The master antioxidant. You must ingest precursors to synthesize glutathione in the liver because it can’t get past the GI.

(5) Milk thistle and dandelion root: These two natural herbs are commonly used to protect and cleanse the liver. Milk thistle is the protector, and dandelion root is the cleanser. They can be taken separately, but many liver supplements contain both. These herbs can be taken regularly over time with or without obvious liver issues.

(6) Vitamin C: Vitamin C is great for liver health. Earlier studies have shown large quantities of vitamin C flush out fats and repair liver damage. Here’s how to make your own mega dose encapsulated orally consumed C.

(7) Lecithin: This helps the liver emulsify fats. You can use sunflower lecithin if want to avoid soy based lecithin, but non-GMO soy lecithin granules are used for encapsulating ascorbic acid in (6) above.

(8) B complex: All the Bs are helpful, especially B12, which has been used to help hepatitis patients. But you need the right type of B12 administered the right way separately from other B supplements.

(9) Lemon water: Start out the day with a half glass of warm strong lemon or lime water without any sweetener. Chinese medicine promotes sour tasting food as conducive to liver health. The warm lemon/lime water stimulates a sluggish liver.

(10) Avoid or minimize alcohol and all over the counter and prescribed pain suppressant drugs containing acetaminophen, a known liver toxin.

This toxic world stresses our livers. Restoring a tired liver and maintaining its healthy cleansing functions are vital for overall health.

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Featured Articles

Health Authorities Now Admit Severe Side Effects of Vaccination

by Karin Munsterhjelm-Ahumada, M.D.

(OMNS, March 20, 2012) The swine flu pandemic of 2009 was caused by a type A influenza (H1N1) virus. This virus was originally referred to as "swine flu" because many of the genes of this new virus were very similar to influenza viruses that normally occur in pigs in North America. The H1N1 virus is genetically similar to the 1918 pandemic virus, as determined from victimes of the latter who were buried, and later disinterred, in Svalbard. It was responsible for most of the outbreaks up until 1956 and then disappeared.

However, this new virus was actually quite different from the typical swine flu viruses. This virus first caused illness in Mexico and the United States in March and April, 2009. This novel H1N1 flu spread from person to person, unlike typical swine flu. In 2009 vaccines were being developed for the prevention of swine flu in humans. http://www.medterms.com/script/main/art.asp?articlekey=99584

On 11 June 2009, the World Health Organization (WHO) declared that the swine flu had developed into a full scale world epidemic – a pandemic alert to Phase 6. Margaret Chan, the Director-General of WHO, commented on the situation in a somewhat ambiguous way. While stressing that the swine flu had reached a serious pandemic level, she declared later in the same statement that the illness seemed to be mild and that most of the patients would recover without medical intervention. http://www.who.int/mediacentre/news/statements/2009/h1n1_pandemic_phase6_20090611/en/index.html

The world chose to listen to the first part of her message.

Two pharmaceutical companies GlaxoSmithKline (GSK) and Novartis had, under considerable time pressure, developed a vaccine against the swine flu. Since the cultivation of an adequate amount of virus to generate the vaccine requires time, GSK and Novartis decided to formulate a weaker vaccine but strenghten it with an adjuvant that contains squalene. Immunologic adjuvants are substances, administered in conjunction with a vaccine, that stimulate the immune system and increase the response to the vaccine http://www.who.int/vaccine_safety/topics/adjuvants/squalene/questions_and_answers/en/. Although squalene is a natural substance found in methabolic pathways of the body, its inclusion in a vaccine is controversial and it is not in use in the USA.

On 25 September 2009, the European Medicines Agency (EMEA) approved Pandemrix, the swine flu vaccine produced by GSK and Focetria produced by Novartis. http://justthevax.blogspot.com/2009/09/eu-approves-gsk-pandemrix-and-novartis.html The vaccine would be ready for use that October.

In Sweden, Finland, Norway and Iceland, the authorities explicitly set the goal of vaccinating the entire population http://www.svd.se/nyheter/inrikes/massvaccinering-raddade-sex-liv_6851143.svd. In this respect, it is of interest that the governments of these countries, already before the outbreak of the swine flu, had concluded an agreement with GSK, according to which they were assured the delivery of pandemic vaccines, if needed. In addition, the contract stipulated that, in a situation characterized as a pandemic by the WHO, the same Nordic countries would have ten days to decide whether or not to accept delivery of the vaccine in question. Hence, the purpose of the agreement was to assure that the entire populations of these countries would receive vaccinations. Finally, the contract protected GSK from any claim for financial compensation in case the delivered vaccine would have any side effects.

When WHO declared the swine flu to be a Phase 6 pandemic, the agreement referred to above was automatically activated.

Mass vaccination started in Finland and Sweden in October 2009. In order to cover the largest possible percentage of the population, the authorities initiated an enormous public relations campaign, which could be described in terms of a "moral persuasion." Solidarity became the slogan: "Be vaccinated to protect your fellow citizens." Those who questioned the vaccination program (small groups of vaccine opponents or just people who were hesitant) were looked upon with disapproval.

In contrast to these vaccine – enthusiastic countries, the politics of vaccination within the rest of the European Union varied immensely among its member states. Poland, for example, decided not to buy vaccines at all due to the strict agreement conditions required by the pharmaceutical companies. Denmark's order covered only "risk groups". http://www.svd.se/nyheter/inrikes/svd-granskar-sveriges-vaccinering-mot-svininfluensan_6843475.svd

The expected second wave of the influenza never appeared. The epidemic gradually declined during the first half of 2010. The same year, on 10 August, WHO officially declared the end of the epidemic. The European Center for Disease Prevention and Control (ECDC) stated that the swine flu was less dangerous and had a lower mortality rate than the seasonal influenza. Thus, apparently the swine flu would not have been a dangerous epidemic even without the mass vaccination. Interestingly, also that same year, vitamin D was shown to prevent influenza in children. (1)

In Sweden, 60% of the population had been vaccinated, while in Finland 50% was covered. In contrast, the figures in Germany and Poland were only 8 and 0% respectively. In the history of Swedish health care this pandemic campaign amounted to one of the most expensive ever. Enormous amounts of taxpayer money were at stake. http://www.svd.se/nyheter/inrikes/svd-granskar-sveriges-vaccinering-mot-svininfluensan_6843475.svd

Meanwhile, the media had become silent on this issue ; there was no further discussion about the swine flu anymore.

Then the blow came:

"The absolutely worst thing that could happen," commented Richard Bergström, the Director – General of the European Federation of Pharmaceutical Industries and Associations, EFPIA. "The worst nightmare of both the industry and the health authorities is an illness that turns out to be mild, while the vaccine that was supposed to prevent a dangerous epidemic causes a severe side effect that was previously unknown." http://www.kostdemokrati.se/nyheter/files/2012/02/SvD-sid-14-19.pdf

In August 2010, Finland reported an increased occurrence of narcolepsy in children and youngsters vaccinated with Pandemrix. On 1 September 2010, Finland stopped all Pandemrix vaccinations. http://articles.mercola.com/sites/articles/archive/2010/09/10/swine-flu-vaccine-may-have-caused-narcolepsy.aspx

Narcolepsy is a severe chronic neurologic disease that not only results in a disabling fatigue, which typically results in the patient falling asleep anywhere and at any time. It might also lead to panic attacks and a state of exhaustion. For many, the worst consequences are the symptoms of cataplexy. This condition causes the narcolepsy patient, when expressing strong feelings such as laughter or crying, to suddenly lose muscular control. The legs give way, speech gets slurred, the gaze goes unfocused and the person gives the impression of being drunk. In some patients, frightening hallucinations appear when falling asleep or waking up.

On 1 September 2011, the Finnish National Institute for Health and Welfare (THL) admitted, that for Finnish children and youngsters age 4-19, there was a new and obvious connection between Pandemrix and narcolepsy. As stated in THL's press release, "The increased risk associated with vaccination amounted to six cases of narcolepsy per 100,000 persons vaccinated in the 4-19 age group during the eight months following vaccination. This was 12.7 times the risk of a person in the same age group who had not been vaccinated." http://www.thl.fi/en_US/web/en/pressrelease?id=26352 This statement was made almost exactly two years after the THL's earlier statement made in the midst of the swine flu hysteria that everyone should be vaccinated with Pandemrix and that it would be safe. In that original statement, the director of the THL emphasized that the squalene adjuvant could increase the side effects of the vaccine to some extent. However, he stated, these side effects would not be dangerous. http://www.tohtori.fi/?page=5833192&id=0169960

In Sweden, at least 150 children are now suffering from narcolepsy caused by Pandemrix vaccine. In Finland, the number is approximately 100. In both countries the number is probably growing. Narcolepsy is a disease with lifetime consequences, and the risk that Pandremix may have caused other neurological illnesses has not yet been excluded. Many have already began to compare this tragedy with the thalidomide catastrophe. http://www.svd.se/nyheter/inrikes/medicinsk-tragedi-med-ett-absurt-slut_6861775.svd

No European countries had a particularly high rate of deaths due to the swine flue. Germany had the same death rate as Sweden, which was 0.31/100 000, although Sweden vaccinated 60% and Germany only 8%. This implies that the vaccine did little to prevent deaths. The responsible authorities have not yet commented on this matter of fact. http://www.svd.se/nyheter/inrikes/massvaccinering-raddade-sex-liv_6851143.svd

Last year the Finnish government promised full compensation for those who have developed narcolepsy as a consequence of the vaccination. http://www.bloomberg.com/news/2011-10-05/finnish-government-to-compensate-pandemrix-narcolepsy-victims.html. While Sweden did, indeed, follow the Finnish THL in admitting the connection between the vaccine and the disease, the Swedish authorities have not yet decided whether and how to provide appropriate compensation.

In February 2012, Svenska Dagbladet, a widely read newspaper in Sweden, presented an informative and accurate series of articles on this theme. They describe some of the affected children narrating how difficult it is to live with narcolepsy http://www.svd.se/nyheter/multimedia/artikel_6840743.svd

According to the authorities, much research is still underway concerning the details of the vaccine injury. Taking the pressure from the public and the affected families into account, it will be difficult for them to avoid carrying out a thorough investigation. Let's hope so.

References:

1. Urashima M, Segawa T, Okazaki M, Kurihara M, Wada Y, Ida H. Randomized trial of vitamin D supplementation to prevent seasonal influenza A in schoolchildren. Am J Clin Nutr. 2010 May;91(5):1255-60.

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Editorial Review Board:

Ian Brighthope, M.D. (Australia)
Ralph K. Campbell, M.D. (USA)
Carolyn Dean, M.D., N.D. (USA)
Damien Downing, M.D. (United Kingdom)
Dean Elledge, D.D.S., M.S. (USA)
Michael Ellis, M.D. (Australia)
Martin P. Gallagher, M.D., D.C. (USA)
Michael Gonzalez, D.Sc., Ph.D. (Puerto Rico)
William B. Grant, Ph.D. (USA)
Steve Hickey, Ph.D. (United Kingdom)
James A. Jackson, Ph.D. (USA)
Michael Janson, M.D. (USA)
Robert E. Jenkins, D.C. (USA)
Bo H. Jonsson, M.D., Ph.D. (Sweden)
Thomas Levy, M.D., J.D. (USA)
Stuart Lindsey, Pharm.D. (USA)
Jorge R. Miranda-Massari, Pharm.D. (Puerto Rico)
Karin Munsterhjelm-Ahumada, M.D. (Finland)
Erik Paterson, M.D. (Canada)
W. Todd Penberthy, Ph.D. (USA)
Gert E. Schuitemaker, Ph.D. (Netherlands)
Robert G. Smith, Ph.D. (USA)
Jagan Nathan Vamanan, M.D. (India)

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The Best Years In Life

Naturally Relieve and Heal Toothaches and Tooth Infections

by: Tony Isaacs

(NaturalNews) Toothaches generally occur when a tooth’s nerve root becomes irritated. The most common causes of toothaches are infection, decay, injury, or loss of a tooth. Pain may also occur after a tooth has been pulled. While no one enjoys a painful tooth, the good news is that tooth pain and infections can usually be relieved and healed naturally.

Colloidal Silver

If your toothache comes from an abscess or other infection, combine the use of 1) oil of oregano topically and internally; 2) colloidal silver topically, internally and for swishing; and 3) warm salt water for alternate swishing as follows:1. Take several drops of oil of oregano under the tongue. Hold for a few minutes and then swish with lots of colloidal silver as frequently as once every hour.

2. Spit out the colloidal silver and then swallow additional colloidal silver (up to 8 ounces total in a day).

3. Gently rub some colloidal silver into the gum area around the tooth.

4. After a few minutes, rub oil of oregano onto the gum area.

5. In between the colloidal silver swishes also do a fairly vigorous warm salt water swish (preferably sea salt) and follow that up with more oil of oregano rubbed into the gums.

More natural remedies which can relieve and heal painful toothaches
1. Purchase some ginger root. Cut off a piece of the ginger root and remove the skin. Put the piece in your mouth on top of the painful tooth and bite down on it. The pain should subside very quickly. Keep the rest of the ginger in a container in the refrigerator and replace the piece in your mouth periodically as needed.

2. Relieve a throbbing tooth with clove essential oil (Syzygium aromaticum). The aromatic chemical in clove called eugenol numbs pain and kills bacteria. To apply the clove oil, soak a cotton ball or swab with the oil and use it to wipe on and around your sore gums and tooth. Repeat as needed.

3. Take one teaspoon of blackseed oil (Nigella sativa) and 1/2 cup of vinegar and boil. Cool and then use as a mouth rinse to reduce inflammation and infection. Rinse every couple of hours until the pain and/or swelling is gone.

4. For tooth abscess and infection, put two level teaspoons of salt in a cup. Pour a small amount of boiling water on the salt in a cup to dissolve it and then fill the cup with enough cool water to make the solution warm. Rinse your mouth slowly and well, using all the salt water. Repeat at least twice a day (the more often the better). If this does not work at first, try increasing the amount of salt.

5. Use a cold pack or other cold items to relieve pain. When you have a toothache, pressing something cold on the outside of your mouth can often give temporary relief, especially if you are having problems sleeping. If you don’t have a cold pack, no need to worry about ice that will melt in the middle of the night – simply grab anything from your fridge or freezer. You can use a jar of mustard, a bottle of water, you name it. If the container is frozen, cover with a wash cloth before placing on the skin. Note: Do not take a food item to bed which will spoil.

6. Supplements which may help clear infection and speed healing include olive leaf extract and bromelain.

Note: If your tooth pain worsens or persists more than a few days, see a qualified dentist – preferably a holistic one.

 

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Morgellons Disease, The Mysterious Skin Disease

by Anne Gordon, RN

Why would tens of thousands suffer from odd symptoms of fibers, and worm like debris sprouting from skin sores, and other symptoms, without knowing the cause? Unexplained constellations of symptoms from general fatigue, concentration difficulties, fibromyalgia, neurocognitive disorders, and skin lesions seem are continuously reported. This disturbing trend prompted a research project.

Researchers, from the Centers for Disease Control (CDC) in combination with Kaiser Permanente Health System in Northern California studied the accelerating numbers of cases between 2006 and 2008. After $360,000, and 115 people studied, Morgellons is still described as ‘unexplained dermopathy’.

It is also strange that the largest clusters of cases appear to be in regions of California, Texas, and Florida, although all 50 states have experienced complaints, according to: (http://www.healthsciences.okstate.edu/morgellons/index.cfm)

Symptoms appeared to be from crawly tingly pins and needles prior to seeing a rash, or ulcerative sores. One theory is that clothing could be the culprit, although that in itself sounds crazy. Another theory suggests that Morgellons victims may suffer from an old disease called ‘delusional infestation’. But why would those numbers of sufferers be growing?

The Centers for Disease Control and Prevention (CDC) issued the results of their multi year findings in January of 2012. It was indicated that no disease organisms were present in Morgellons and that normal clothing fibers suggested that the sensations of sufferer’s were due to their own ‘delusional infestations.’

However, some people do not agree. For example Richard Fagerlund, entomologist, stated that he takes Morgellons disease seriously. He believes that whatever is causing ‘delusional infestations’ is reaching epidemic proportions. He suspects that it maybe caused by pesticides, or other pollutants.

Jan Smith, owner of Morgellons Exposed.com, hosts a site which hosts her theories on causes of Morgellons, including nano technology, and believes ‘something is being hidden.” Randy Wymore, presently director of the Oklahoma State Health Sciences' Center for the Investigation of Morgellons Disease, claims that Morgellons patients have submitted masses of dark fibers visible at 60x magnification under the unbroken skin. 

An article about Morgellons published by the American Journal of Clinical Dermatology in early 2006 stated  that "Morgellons disease may be linked to an undefined infectious process," and reported that many patients with Morgellons disease have positive Western blots for Borrelia burgdorferi, the causative agent of Lyme disease.

In 2008 the Washington Post Magazine reported that Internet discussions about Morgellons include conspiracy theories about the cause, including biological warfare, nanotechnology, chemtrails (persistent contrails) and extraterrestrial life.

In conclusion, the numbers are increasing, the symptoms are varied, yet, no cause is determined. Again, the question might be: why would an increasing amount of people have this ‘delusional disease’ while being able to pull fibers from ‘sores’ that suddenly appear?  This mysterious condition might warrant more study. Perhaps a new organism will emerge as a result, or something chilling.

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Health & Freedom

Doctor From MMR Controversy Wins High Court Appeal

by: Ethan A. Huff

(NaturalNews) The U.K. General Medical Council's (GMC) rash and unfounded decision to strike Professor John Walker-Smith, who had helped Dr. Andrew Wakefield in treating desperately-ill children with regressive autism symptoms and severe gastrointestinal problems, off the medical register for alleged "professional misconduct" has been exposed as a fraud. During a recent High Court appeal, Mr. Justice Mitting ruled that Prof. Walker-Smith's striking "cannot stand" because of serious misconduct in the way GMC handled the case against him, and that the entire council needs to be reformed.

For many years now, Prof. Walker-Smith has had to endure having his reputation tarnished by the likes of freelance journalist Brian Deer, GMC, the British Medical Journal, and the lapdog American media who have together conspired to destroy the legitimate work of Dr. Andrew Wakefield and his colleagues on the gastrointestinal problems they observed in young children, many of whom had received the combination measles, mumps, and rubella (MMR) vaccine. And caught in the fray of this malicious crusade against independent thought and honest medical inquiry was the life and career of Prof. Walker-Smith, who had already retired from his medical practice when the controversy began.

Prof. Walker-Smith had been head of the department of pediatric gastroenterology at the Royal Free Hospital (RFH) in London where Dr. Wakefield was making observations about children's health that would later be published, and retracted, by The Lancet. During this time, Prof. Walker-Smith was helping to treat these suffering children, the parents of whom had directly approached both him and Dr. Wakefield for help after being ignored by their own general practitioners.

"There has been a great burden on me and my family since the allegations were first made in 2004 and throughout the hearing that ran from 2007 to 2010," said Prof. Walker-Smith in a recent statement about the case. "I am relieved that this matter is now over."

Since GMC's handling of the entire case has been proven fraudulent, it is now Dr. Wakefield's turn to be exonerated
Mr. Justice Mitting's scathing indictment of GMC's unprofessional and dishonest handling of the Dr. Wakefield case is telling, as it once again calls into question the legitimacy of any of the claims made against Dr. Wakefield and his colleagues concerning their observational, peer-reviewed study. It only further reinforces what has already come to light about the blatant fraud that is the continued witch hunt against Dr. Wakefield for his independent work.

"The welcome decision to exonerate Prof. Walker-Smith is a clear indication that the GMC's case against the Royal Free doctors was manufactured to discredit any association between bowel disease, autism conditions and some of the parents' reported link to the MMR vaccine," writes Age of Autism. "The allegations leveled at Prof. Walker-Smith and the Royal Free team now have to be viewed with total skepticism as nothing more than a witch hunt by vested interests at the highest levels in government, media and the pharmaceutical industry."

This ruling will clearly bolster the efforts of Dr. Wakefield to vindicate his own reputation and career, including his recent lawsuit against Brian Deer, BMJ, and BMJ editor Fiona Godlee, all of which have repeatedly spread lies and slander about Dr. Wakefield and his paper.

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H.R.3380 – TWO HOUSE SUPPLEMENT SUPPORTERS PRESS FDA

Press Release

Expressing regret with the FDA’s dismissal of Senators Hatch and Harkin’s written request for the FDA to withdraw the draft Guidance for New Dietary Ingredients for supplements, Congressmen Dan Burton (R-IN) and Jason Chaffetz (R-UT) have sent a similar letter to FDA Commissioner Margaret Hamburg, M.D.  Industry and consumers have been alarmed by this draft Guidance ever since last July when the FDA issued it amidst much fanfare but with the miserable intention of requiring thousands of “new” supplement ingredients to undergo expensive, drug-like safety testing.

   The Burton-Chaffetz letter references numerous examples where the draft Guidance requirements clearly run counter to the will of Congress and the Dietary Supplement Health and Education Act of 1994 (DSHEA).  A key feature of DSHEA is the watershed date of October 15, 1994, with all supplement ingredients marketed before that date being considered as safe. This “grandfather” date is the exact issue addressed by H.R.3380, the Dietary Supplement Protection Act. The bill would move the 1994 DSHEA grandfathering date forward from October 15, 1994 to January 1, 2007, so as to encompass and protect thousands of “new” dietary-supplement ingredients that are already safe but that the FDA would drive from the marketplace with its burdensome new testing requirements.

          The Guidance explicitly rejects these supplements and instead requires each manufacturer to shoulder the burden of showing use of a supplement prior to 1994 to classify them as being exempted from the guidance. In fact, 1994 has even been changed by the FDA to 1986 for exemption purposes. If a manufacturer is unable to supply this data – a difficult burden some 17 years after the fact – the Guidance allows FDA bureaucrats to re-characterize old ingredients and supplements as being new and subject them to the new regulatory burdens set forth in the NDI Guidance.

          For those companies that started manufacturing and selling supplements since 1994, these burdens would be cost-prohibitive and unnecessary because they have already been generally recognized as safe for human consumption. The NDI burdens illegally imposed by the FDA upon Americans will greatly increase the cost of supplements to the 53% percent of the US population who consume supplements, despite 17 years of historical use safety by millions of Americans for many of these “new” supplements. Just as importantly, it will also kill off innovation in the supplement industry.

          The Burton/Chaffetz letter forewarns that if the FDA does not withdraw the guidance, legislation will be considered. That legislation is H.R.3380. This bill would exempt many thousands of supplements not just from this guidance but also from future burdensome and unnecessary FDA regulatory policies. In Federal statute, it drastically closes the window against which unjustifiable bureaucratic actions can be taken in the future. H.R.3380 does not impact any other post-marketing regulations for protecting consumer safety.

          The Hatch-Harkin letter and the FDA’s blunt rejection of it – and the almost-certain rejection of the Burton-Chaffetz letter – are the start of an extended negotiation process with the FDA. The National Health Federation initiated the introduction of H.R.3380 with the intent not to engage in a process that will neither benefit the people nor the industry in the long term. As the most-experienced organization in the health-freedom community, we know all too well the history of what has happened and will not stand by to witness it again.

 

The Burton/Chaffetz letter can be downloaded from the NHF webpage at (Click Here)

Health-freedom advocates and supplement consumers need to proactively lobby their Congressional Representatives to cosponsor H.R.3380. This can be done at the NHF homepage atwww.thenhf.com.


CLICK HERE TO ACT NOW – http://www.thenhf.com/DSPA


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Natural Ways To Get Rid of Wrinkles

by: Kim Evans

(NaturalNews) Most people think that once you have wrinkles you're stuck with them, but there's actually quite a bit you can do about them. Of course, nutrition and being clean internally are key parts of the equation and it's not uncommon to find that with tons of juicing, eating lots of uncooked foods from nature and doing plenty of coffee enemas that wrinkles just go away. Actually, it's a combination that tends to keep us young and disease-free on many levels. However, there's quite a bit that you can do about wrinkles topically too.

Natural Remedies
Coconut oil, beet and carrot juice
Coconut oil is a wonderful oil that is known to rebuild our skin tissue and it can be used both topically and internally regularly for the elimination of wrinkles. Coconut oil is both hydrating and rebuilds our connective tissues, and damaged connective tissues are often the cause of wrinkles.

Using a little carrot and beet juice on the skin regularly helps remove wrinkles too and is in fact quite powerful. The vitamin A in carrot juice is wonderful for the skin. Beets are also known to repair our DNA, so using beet juice topically on wrinkle sites is a powerful way to rebuild the damaged skin which often causes wrinkles – possibly by repairing the DNA of the damaged tissue.

Using carrot and beet juice topically with coconut oil also increases the benefits of both. Coconut oil has absorptive properties that help pull the juices into the skin in addition to its hydration benefits. You'll only need a tablespoon or two of these juices each time and you can drink what you don't use. You'll want to leave these juices on your skin for about ten minutes before rinsing them off. You can apply and reapply the juices as they dry, rubbing them in each time.

Exfoliation
After you've spent some time repairing your skin with coconut oil and these juices, you'll want to exfoliate your skin to remove the dead skin. You can exfoliate with a washcloth or you can use the juice of a somewhat unripe pineapple. Pineapple contains the enzyme bromelain which naturally eats away our top layer of skin when applied topically and leaves the new fresh skin underneath. Pineapple juice easily rivals expensive spa exfoliation treatments.

To exfoliate with pineapple juice, just apply some of the juice with a little coconut oil or olive oil and rub it in, reapplying it as needed. After a few minutes of rubbing, you may find that dead layers of skin start to come off in your hands. And after doing this, just rinse and apply a layer of coconut or olive oil to hydrate the skin.

While you may not be able to get rid of all of your wrinkles this way, you might be able be get rid of 50 or 60 percent of them. Of course, the more you do the juices and the coconut oil, the more effective they are.

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Fetal Body Parts Being Used For Medical Research

by iwishart

It’s the hidden side of medical research. A massive industry harvesting pieces of dead children for experiments, or transplanting into animals. IAN WISHART discovers the University of Auckland has imported body parts from American babies for a research project, and asks some hard questions:

There are puddles of water in the gloomy corridors of Auck-land University’s School of Medicine, leftovers from a spring rainstorm and some bad building maintenance on this grey September afternoon. This nondescript urban edifice, now in the shadow of the new Auckland Hospital extensions, houses dark secrets. Or so Investigate has been told.

“They’re doing an undergraduate presentation next week in the Department of Optometry and Vision Science,” a source in Auckland’s optometry community confides in a cryptic email. “Thought you might be interested to investigate a research project involving tissue from aborted fetuses.”

Optometry. Eye doctors. Hardly the first branch of medicine that springs to mind as the cutting edge of macabre experimentation. But inside the Cole Lecture Theatre, safely sheltered from the weather and the waterlogged corridor, fifty or so medical students have filled the room almost to capacity as teams of fourth-year undergrads present the results of this year’s main research projects.

An American woman holds court, a scientific Mistress of Ceremonies taking clear pleasure in parading her protégés to their medical colleagues as they make audio-visual presentation after presentation. She is Dr Keely Bumsted O’Brien, and this is her baby, so to speak.

Across the road, in the big hospital’s emergency rooms and oncology units, specialists, intensivists, nurses and registrars are working frantically to save the living. Here, in the School of Medicine, it turns out O’Brien’s team has been dissecting the dead. And not just any dead.

“The title of the project,” tipped our source, “is ‘Photoreceptor-associated gene expression in human fetal and embryonic chicken retina’. As far as I am aware this project is unlikely to have received regional ethics approval from the Ministry of Health. The tissue has been obtained from elective abortions in the United States and was transported here for the experiments. This may be the first research of its kind in New Zealand and I am sure the public are quite unaware of it.”

Just how did body parts from a group of aborted American infants end up in New Zealand for students to conduct experiments on? To find the answers, we began investigations in the United States, and a controversy that blew up there six years ago.

***

It was an interview that shocked America. An Insider, spilling the beans on massive malpractice to a reporter on ABC’s 20/20. Only this time, it wasn’t Big Tobacco in the gunsights, it was the US abortion industry, exposed as harvesting the organs from aborted babies. According to former abortion clinic technician Dean Alberty, clinics were harvesting eyes, brains, hearts, limbs, torsos and other body parts for sale to the scientific market: laboratories wanting to test new drugs or procedures, or researchers trying to find the causes of genetic disorders or discover new ways of treating disorders like Parkinsons.

To make matters doubly embarrassing for authorities, the trafficking was taking place inside abortion clinics run by Planned Parenthood, the US affiliate of New Zealand’s Family Planning organization.

Alberty worked for a Maryland agency called the Anatomic Gift Foundation, which essentially acted as a brokerage between universities and researchers seeking body parts, and the abortion clinics providing the raw material. Alerted by the clinics about the races and gestations of babies due to be aborted each day, AGF technicians would match the offerings with parts orders on their client lists. Alberty and his colleagues would turn up at the abortions that offered the best donor prospects to begin dissecting and extracting what they needed before decay set in.

“We would have a contract with an abortion clinic that would allow us to go in…[to] procure fetal tissue for research. We would get a generated list each day to tell us what tissue researchers, pharmaceuticals and universities were looking for. Then we would go and look at the particular patient charts—we had to screen out anyone who had STDs or fetal anomalies. These had to be the most perfect specimens we could give these researchers for the best value that we could sell for.

“We were taking eyes, livers, brains, thymuses, and especially cardiac blood…even blood from the limbs that we would get from the veins” he said.

Alberty told of seeing babies wounded but alive after abortion procedures, and in one case a set of twins “still moving on the table” when clinicians from AGF began dissecting the children to harvest their organs. The children, he said, were “cuddling each other” and “gasping for breath” when medics moved in for the kill.

Alberty had been asked by a pro-life group, Life Dynamics, to provide information about activities in the clinics, and the issue caused enough national scandal to see an episode of ABC’s 20/20 devoted to it in March 2000.

On that programme, as in this magazine, the imagery was highly sanitized so as not to upset sensitive viewers. The closest 20/20 got to screening images of trafficked human fetal tissue was a pea-sized fragment of unidentifiable tissue in a glass Petri dish.

Life Dynamics founder Mark Crutcher later told media:

“We are sympathetic to the explanation offered by the ABC producer who told us after the show that the network could not broadcast footage of dismembered babies, baggies full of tiny human eyes or any other accurate footage of the ‘commodity’ being sold by the baby parts merchants. But this should have been stated in the programme. Showing scientists poking at slivers of flesh in a Petri dish through a microscope was deceptive and it dehumanizes this debate.”

In America, late-term abortions are permitted, even up to 30 weeks gestation. It’s a three day procedure and involves forcing the mother to go into labour but killing the baby with a spike to the base of the skull before it leaves the birth canal. Even so, according to Alberty, it wasn’t unusual out of the 30 or 40 late-term abortions each week to see several babies born alive on the operating table before clinicians could perform the procedure.

“They were coming out alive. The doctor would either break the neck or take a pair of tongs and basically beat the foetus until it was dead.”

Alberty’s testimony was verbal, and in many cases it was challenged by abortion providers who questioned his motives and accused him of “embellishing” the sordid details of the abortion industry. But Alberty the whistleblower wasn’t alone. Another former clinic manager, Eric Harrah, gave a video interview disclosing live births as the abortion industry’s “dirty secret”:

“It was always very disturbing, so the doctor would try to conceal it from the rest of the staff.”

One incident in particular haunts him. The clinic had begun inducing a woman 26 weeks pregnant, but sent her overnight to a nearby motel to await the full procedure in the morning. Instead, in the middle of the night she gave birth to a child and was brought back to the abortion clinic with the baby wrapped in a towel.

“I was in the scrub room when I saw the towel move,” says Harrah. “A nurse said, ‘Eric, you’re just tired. It’s three in the morning.’ Then we both looked and a little baby’s arm raised up out of the towel and was moving like a newborn baby. I screamed and ran out. The doctor came in and closed the door and when we went back in to process the baby out of the clinic into the lab, [the baby] had a puncture wound in his chest.”

In the United States, trafficking in baby parts for profit is a criminal offence. But to get around the problem, universities and researchers pay a fee – not for the parts themselves but for the “cost of extraction”. Thus, there are different fees depending on the amount of work involved. And shipping and handling is extra.

Harvesting fetal tissue is not yet illegal in the US. In fact, the programme at five major universities including the University of Washington is part funded by the US National Institutes of Health. It is the University of Washington that has been supplying Keely Bumsted O’Brien at the University of Auckland, with some of her eyeball retinas of aborted children.

The reality of the ethical boundaries wasn’t lost on the stu-dents gathered in the Auckland School of Medicine lecture theatre when fourth year undergrads Tim Eagle and Kimberly Taylor wrapped up their presentation on genetic testing the eyeballs of chicken embryos and human fetuses. They told the audience they’d used tissue from a 10 week human embryo, a 12 week and a 16 week foetus. When Keely Bumsted O’Brien called for questions from the audience, the first was an ethical one, from a female student somewhere up the front of the crowded auditorium. Had Eagle and Taylor, she wondered, run their project past the Auckland University Ethics Committee?

“We have ethical approval under Keely as referee, which is obvious by itself. Her current ethical approval worked for what we were doing so we basically used hers, which was obtained as far as we’re aware from America,” Taylor responded.

When Investigate rang O’Brien to clarify, she confirmed her teams were working on something big.

“There’s a large ongoing project, and I don’t think I need to tell you when and where I actually do specific things. Are you aware that importation of human tissue into New Zealand does not require any sort of permit?,” she countered.

Apparently, she’s right. Under current New Zealand law, you can import body parts to your heart’s content as long as you do it in a biosafe manner. But what about seeking approval from the Ministry of Health’s Northern Region Ethics Committee? Surely there must be laws governing the carrying out of experiments on aborted human infants in the name of science?

“No,” says O’Brien emphatically, “because you’re not required to, because it’s tissue, not alive.”

In other words, thanks to a loophole in New Zealand law, it is perfectly legal to conduct experiments on aborted human embryos. For all we know, there may be dozens of experiments being carried out on aborted children in research labs throughout New Zealand. The fetal eyes, O’Brien says, arrive in the country having been “snap frozen cryogenically” just minutes after death, then placed in formaldehyde.

So who supplies Auckland University with infant eyeball retinas? O’Brien repeatedly talks of the “organizations” that supply her, but names only one, the University of Washington.

“These organizations, like for example the University of Washington has a tissue programme. The UOW oversees the collection of tissue, they have their own ethics committee. So they have to be overseen by another committee. So to use fetal human tissue in NZ I have to go through the local ethics committee, and in addition the tissue that I’m gathering has to be gathered under a separate ethics protocol. That ethics protocol is overseen by the ethics committee that’s on site.”

When Investigate suggests that the body parts could be coming in without mothers even realizing their aborted baby had been harvested moments after death, O’Brien is outraged.

“Working with human fetal tissue is not taken lightly. You have to have respect for the donation of the tissue. Now the child obviously cannot give consent, it’s the mother that’s giving consent.”

“Do you think they’re asking these women, ‘do you mind if we keep the baby for medical research?’,” we ask.

“You absolutely have to! You absolutely positively have to! Do your homework man! You simply cannot take fetal tissue from an aborted foetus without informed consent from the mother. Oh my goodness, I’m shocked to hear you suggest that. I’m upset and shocked that you suggest that. Totally off base.”

But is it really off base? O’Brien insists that women seeking abortions are asked to sign consent forms authorizing the use of their dead babies for medical research. It leads to a terse exchange with Investigate.

“There is an informed consent form that the mother signs. She is not coerced, she is not paid any money. She is informed of all of her options. That informed consent was part of my approval that was produced and shown to the ethics committee here [in Auckland].”

Great, we thought. So O’Brien actually knew the names of the mothers involved and had presented copies of their consent to her peers?

“Absolutely not! That is so unethical! All I know is that the tissue was donated by the mother, and the mother has signed an informed consent form.”

But hang on, we asked, how do you know, if you don’t have a signed form with a name on it?

“I don’t keep those records on site.”

No, but somebody must.

“Yes, they are kept by the organization that coordinates the donation.”

So what, physically, does O’Brien have that proves there’s been informed consent from the mother?

“You cannot collect the tissue without informed consent from the mother. It is unethical for the organization that coordinates the collection of the tissue to provide me with any sort of information that might link it back to the mother.”

In other words, there’s no signed paperwork for O’Brien or the ethics committee to see. It’s done on trust. To Investigate’s knowledge, O’Brien has never seen a signed informed consent form.

So for all you know, we pushed her, it could be somebody in an office somewhere chucking out these forms on a word processor saying ‘yeah, we do all this’ and of course they don’t. “If you’ve never seen a signed copy, how do you know?”

And when Investigate went searching, those are exactly the kind of discrepancies we began to find. Like this extract from the Seattle Post Intelligencer newspaper in the wake of a congressional visit to the University of Washington lab:

“Women who agree to the use of their aborted babies for research sign a simple “informed consent” document at the abortion clinic, which includes no information on where the particular “donation” will be sent or how it will be used. This oversight is inconsistent with the regulation requiring “informed” consent, according to a physician familiar with research protocols, and could be problematic for the University of Washington laboratory.”

The newspaper also discovered other discrepancies in the University of Washington paperwork, such as the University letting outside labs fill in forms instead of doing the paperwork themselves. Nor was the University of Washington doing the actual organ harvesting at the abortion clinics, so the University itself was one step removed from the informed consent process in terms of verifying whether the consent was genuine. In other words, the University of Washington’s ethical oversight could not have included whether the tissue was harvested ‘ethically’, because the University has never been in a position to know.

The congressmen went away sufficiently concerned that six separate pieces of legislation were drafted to combat the harvesting of tissues. But with a change in administration, those bills went onto the backburner.

Then there’s the issue of the other ‘organisation’ O’Brien refers to but doesn’t name. Investigate traced two scientific papers published by O’Brien in the past 24 months. One, “Expression of photoreceptor-associated molecules during human fetal eye development”, was published in the journal Molecular Vision in 2003 and can be found on the internet through a Google search. In the paper, O’Brien discloses she used body parts supplied by the University of Washington, but also by a private broking firm like the controversial Anatomic Gift Foundation referred to earlier; this one is named Advanced Bioscience Resources, or ABR, and is based in California. After Anatomic Gift Foundation was sprung thanks to the testimony of insider Dean Alberty, Advanced Bioscience Resources moved to fill the fetal tissue power vacuum. In an industry now estimated to be worth around $2 billion globally, ABR is believed to be a major player, particularly as it’s prepared to supply organs harvested from second trimester late-term abortions, which the University of Washington refuses to do.

Investigate has confirmed that an early second trimester baby was dissected for the Auckland University study, making ABR the likely supplier to O’Brien. And O’Brien has used babies up to the fetal age of 22 weeks, according to her published studies.

Her Molecular Vision paper describes how experiments were “prepared from snap frozen intact human fetal eyes ranging from fetal week 9 to fetal week 19…labeling was performed in a large number of eyes within an age group.”

There is no disclosure in the internet version of the paper how many eyes were harvested for the experiments. At least ten babies from fetal weeks 9 to 22 are known to have been harvested for O’Brien’s second scientific paper we found, published in Investigative Ophthalmology and Visual Science in August 2004. Again, suppliers were both ABR and the University of Washington. One paper on eyes supplied by ABR describes how the baby’s eyes are “enucleated” from the skull – medical talk for being scooped out with a knife.

Although she was working at the University of Auckland at the time, O’Brien has told Investigate the experiments detailed in her published papers were carried out “elsewhere”.

And what do we know of Advanced Bioscience Resources? According to O’Brien, her suppliers operate with transparent ethical rules and committees. But Advanced Bioscience Resources appears far from transparent. At least one American news report says the company has refused to comment on its body parts trade, making it impossible to ask whether ABR’s practices comply with federal US law.

“We’re a biotechnology firm, we don’t talk to the press,” a company spokeswoman is quoted as saying on another occasion.

Investigate has confirmed that ABR supplied aborted baby brains to be injected into mice, as part of experiments creating a part human/part mouse chimera. The genetically-engineered mice have been given – all courtesy of aborted fetuses from ABR – a human immune system, a human fetal thymus, liver and lymph node. The mice are then infected with HIV as part of AIDS research.

The US National Institutes of Health, which funded the grisly harvesting and experiment, has refused to provide any written proof that ABR holds informed consent forms, nor has the NIH confirmed that mothers were told by ABR that organs from their dead babies would be transplanted into genetically-engineered mice.
ABR has also supplied baby hearts for transplantation into pigs, and fetal stem cells.

We asked O’Brien whether she felt modern scientists were stepping into a dark pedigree.

“Do you see a correlation between the boundaries of science and experimentation on humans in this area, and the dreams of Nazi Josef Mengele and others back in World War 2 and the kind of experiments they were conducting?”

“No.”

Mengele had taken particular interest in dissecting live infants for medical experiments.

“You see no correlation?”

There was a pause as O’Brien drew in her breath. “What you’re trying to get me to say is that research on human fetal tissue is morally and ethically wrong, and I’m not going to say that. Because obviously I’m working on the tissue. I think the information to be gained is extremely valuable and it’s not something taken in lightly. I don’t think the information I use can be interpreted and used for eugenics. The reason that we have ethics committees is so we don’t have a scientific free for all.”

Other ethicists, like Paul Ramsey in the US, disagree however.

“Far from abortion settling the question of fetal research, it could be that sober reflection on the use of the human foetus in research could unsettle the abortion issue.”

Are human children, ask ethicists, any less-deserving of protection from medical experiments and execution than animals?

Pittsburgh-based researcher Suzanne Rini, who interviewed Ramsey and whose 1995 book Beyond Abortion: A Chronicle of Fetal Experimentation brought to light a body parts trade that’s existed since the 1950s, believes the very fact that scientists need the elixir of youth from fetuses may be the ethical catch-22 that kills the abortion industry. On the one hand, she says, medical researchers try to argue the foetus is not a live person. On the other, whether it’s a cure for Parkinson’s, diabetes, Huntington’s, MS or a range of other disorders, medical researchers claim the life in fetuses is the only thing that can save adults. But only if you kill the foetus first.

University of Auckland’s Deputy Vice Chancellor, Research – Tom Barnes – says it is ethical under current NZ law to harvest organs from fetuses for the sake of improving the lives of adults.

“As you know [Keely’s] research is looking at eyes. She’s trying to solve the problem of macular degeneration which is a disease that affects 60% of more of people who are 70 years old or over. She’s also trying to solve some problems to do with eye disease in younger people as well.”

It is a modern, relativistic idea that you can sacrifice the few for the good of the many. Indeed, this was one of the justifications Hitler used in whipping up hatred against Jewish, Gypsy and gay minorities. In 21st century form, the argument is more subtle: that if a cure for crippling diseases can be found by harvesting fetal organs from abortions, or growing human embryos in the laboratory for stem cell harvesting, then the deaths of those infants are justifiable because of the perceived greater good to the community at large.

Indeed, O’Brien makes a similar appeal when we ask what the ultimate benefit of dissecting children’s eyeballs is:

“You achieve knowledge, so that you can start to try and find therapies to help people regain their vision, or intervention so that you can help people who have congenital abnormalities that we might be able to fix them.

“Obviously I don’t think there should be a blanket ban on the use human fetal tissue because I think the information that you get out of the use of human tissue is very valuable in trying to help people.”

But is that a valid line of reasoning that justifies made-to-order abortions?

At the Nuremberg War Crimes trials, evidence was presented of horrific scientific experiments being performed on cap-tives in the concentration camps. The Nazi medics on trial attempted to justify it by saying the test subjects were due to die anyway and the knowledge gained would benefit the rest of humanity.

Needless to say, the Nazis were shot down in the courtroom (and later simply shot outside it) and Nuremberg issued a declaration condemning the role of the medical profession in experimentation and slaughter of innocents.

University of Auckland’s Keely Bumsted O’Brien resents modern scientists being likened to Hitler’s gruesome genetic engineers, and points out that when Germany’s Max Planck Institute for Brain Research recently discovered it possessed the brains of many Down’s Syndrome people slaughtered by the Nazis, the Institute did the decent thing.

“Rather than use [the brains for research], it was the decision of the Director to give those brains a decent burial. Which one could argue might be the ethical way to do it, if they were gathered by the Nazis in an unethical way dealing with eugenics. Now I don’t compare what I do to eugenics.”

But Investigate challenged O’Brien on her example.

“There is an arguable case that in 50 or a hundred years time society will look back and say the current Western practice of mass abortion was a similar sort of thing to what the Nazis did and they’ll look at it the same way, what’s your response to that?”

“I don’t think they will,” exclaims O’Brien. “And I think we take much more care in how we carry out the research than the Nazis did.”

It is clear to Investigate after an hour long interview with O’Brien that she is sincere in her beliefs, and she makes special mention of the fact that she respects the humanity of the tissue. She also attends an annual memorial service, she says, that the medical school has for the cadavers and tissue used during the year. Nonetheless, our inquiries into the baby parts business give no reason to think that the harvesting of organs in America from dead or dying infants is done more humanely than the Nazis did.

For a start, the death toll alone from abortion far eclipses anything Hitler was able to achieve. In fact, one estimate of the abortion tally in the West in the past 30 years is that more than 58 million lives have been lost. Once you kick in the figures for the rest of the world including China, more people have been killed by abortion in the past 30 years than in all wars in recorded history. For the record, international studies like a 1999 paper from International Family Planning perspectives suggest 46 million lives a year are taken throughout the world.

At the Mayfair Women’s Clinic in Aurora, Colorado, staff admitted under cross examination in court that they had so many aborted babies to get rid of that clinician Dr James Parks used to put the bodies of larger babies (up to week 22) into meatgrinders so the remains could be reduced to the consistency of toothpaste and flushed down sinks.

Leaked documents from inside abortion clinics have hit the headlines across the US, and they make dark reading. They’re order forms from scientists to agencies like Advanced Bioscience Resources, instructing what parts they need and how to get them.

“Dissect fetal liver and thymus and occasional lymph node from fetal cadaver within 10 (minutes of death).” “Arms and legs need not be intact.” “Intact brains preferred, but large pieces of brain may be usable.”

Or this, from a scientist studying the “Biochemical Characterization of human type X Collagen,” who requests “Whole intact leg, include entire hip joint, 22-24 weeks gest.”

The harvesting technician is asked to “dissect by cutting through symphasis pubis and include whole Illium [hip joint]. To be removed from fetal cadaver within 10 minutes.”

Another, from University of Colorado’s Gary J. Miller, a professor of pathology, seeks the prostate glands of 24 fetuses from the first and second trimesters. The glands, he says in his request to Anatomic Gift Foundation on November 10, 1998, are “To be removed and prepared within 5 minutes … after circulation has stopped.”

According to World magazine in the US, which broke the story, other specifications state that they are to be “preserved on wet ice,” “picked up immediately by applicant,” have “low risk no IV drug abuse or known sexually transmitted diseases,” and no prescription medications used by “donor” mother. The contract is signed both by Dr. Miller and, for the Regents of the University of Colorado, by “Sharon Frazier, Director of Purchasing.”

O’Brien refuses to believe there is anything dodgy about the fetal tissue harvesting operations in the US.

“I have to put my faith in the fact that the organizations that I’m obtaining tissue from are obtaining it in an ethical manner.”

But let’s look at that more closely. The American Society For Cell Biology, an association of cell biologists, lobbied hard against regulating the fetal tissue harvesting industry, including a suggestion that researchers should have to “verify that the tissue was obtained properly”. This condition, and others, were regarded as too onerous for the scientists to accept.

None of the many articles and papers Investigate has read on the issue suggest that the abortion clinics or tissue har-vesting organizations are subject to ethical oversight com-mittees. In fact, the Anatomic Gift Foundation, which is similar to ABR, openly puts the onus on its clients – the researchers – to get ethical approval before they make an organ purchase application. Investigate has found no evidence that AGF or ABR are themselves audited by anyone.

And how ethical is the behaviour of another big fetal tissue provider (until it was sprung in the ABC 20/20 programme), Opening Lines?

A division of Missouri and Illinois-based Consultative and Diagnostic Pathology Inc, Opening Lines made no bones about the fact it was in business to make money. A 20/20 producer, posing as a potential investor in the 11 year old company, visited its founder, pathologist Dr Miles Jones.

Jones, unaware he was being recorded on a hidden video camera, explained how his company obtained fetal parts from clinics across America for shipment to research labs.

“It’s market force,” Dr. Jones told the producer about how he sets his prices. “It’s what you can sell it for.” He said he was looking to set up an abortion clinic in Mexico in order to get more fetal tissue by luring women in with cut-price abortions.

“If you control the flow — it’s probably the equivalent of the invention of the assembly line.”

As to the financial benefits of his business, Jones was brutal about the demand from researchers: “If you have a guy that’s desperate for, let’s say, a heart, then he’ll pay you whatever you ask,” he said.

“That’s trading in body parts. There’s no doubt about it,” Arthur Caplan, director of the University of Pennsylvania’s Center for Bioethics, told the Alberta Report newspaper after reviewing Jones’ statements.

The Opening Lines corporate brochure reads more like a supermarket advertisement than an ethical, dignified approach to the death of a baby.

“The freshest tissue prepared to your specifications and delivered in the quantities you need it.”

Despite compiling a baby parts price list and charging fees, an FBI investigation concluded that Opening Lines had broken no laws in what it had done and how it had done it. So if the American ethical rules are tough, there’s been no evidence of it to date.

Then there’s the question of whether the University of Auckland Human Ethics Committee is tough enough in demanding proof of informed consent in cases like O’Brien’s.

You’ll remember O’Brien is insistent that she could not provide the University of Auckland with copies of the informed consent because it would be unethical for her to know the identities of the mothers who’d signed them.

“It is unethical for the organization that coordinates the collection of the tissue to provide me with any sort of information that might link it back to the mother.”

Contrast O’Brien’s statement with this extract from the ethical guidelines imposed on fetal tissue research by the University of Texas at Houston:

“An investigator proposing to use fetal tissue must complete an application form for full [Ethics Committee] review and approval. The application must include a copy of the consent form used to obtain consent for donating the tissue. [Ethics Committee] must be assured that the woman donating tissue has been given an opportunity to understand the procedures, any possible risks to her privacy and well-being, and to assure that she has an opportunity to give free and informed consent to the donation.” [emphasis added]

Additionally, the University of Texas requires that the consent form cannot be generic, and must relate to the actual research project that is planned, with “a short description of the reasons for the research.”

While O’Brien claims it would be unethical for her to know the donor or talk to them, the University of Texas requires its researchers to include on the woman’s copy of the consent form “the name and telephone number” of the researcher, so that the donor can make contact, ask further questions, and even withdraw their consent.

Implicit in this is that the researcher must take ethical responsibility for the collection of the tissue, and should know who the donor is. Both of these aspects corroborate the comments made about the flawed informed consent procedures of the University of Washington earlier in this report.

It is clear from O’Brien’s interview with Investigate that none of the women donating their dead babies’ eyeballs would have been able to reach her to withdraw their consent or ask questions.

But Investigate didn’t leave the issue there. Despite the fact that Advanced Bioscience Resources refuses to give media interviews, we obtained the cellphone number of its President, Linda Tracy, and we rang it. What we obtained is a world exclusive:

“We’re just doing a story on fetal tissue use over here in NZ, and one of the suppliers is ABR, and people tell us you guys are subject to ethical committee oversight, would that be right?”

“Who are you with again?”

“Investigate magazine.”

“OK, I don’t give any information to magazines or interviews to anyone.”

But just as Tracy was about to do what she’d done so many times before to American journalists – hang up – we reminded her that negative publicity could affect her business, and she had a responsibility to put her side of the story.

“In this particular case, the researcher says that the suppliers such as yourself are subject to ethical committee oversight. I’m trying to find out who is responsible for ethical oversight in terms of ABR, would it be you or is it the researcher who must seek approval?”

“Both.”

“What committee do you people report to, how does it work?”

“Well, we are overseen by the IRS, the Internal Revenue Service. As a non-profit organization we have guidelines to abide by, but that’s about the only regulatory committee that we are subject to.”

So much for ethical oversight. Is there, we asked, an external ethical committee that Advanced Bioscience Resources reports to or which oversees its baby harvesting operation?

“No.”

What about the actual extraction of eyeballs and other fetal tissue, who carries that out?

“It is our responsibility to collect the tissue,” confirms Linda Tracy.

“So you’re in control of the process all the way through?”

“No.”

This ‘ethical oversight’ is getting more fascinating by the minute. Which part of the process, we asked, was outside ABR’s control?

“The [abortion] clinic consents the patient.”

“And then the clinic provides you with the consent?”

“Yes.”

“Is there any possibility that the clinic may not properly consent the patient, the clinic may take the view ‘we’re never going to see the patient back through here, they’re never going to know’, and they’ll just write out the forms. How do you know the clinic is doing the informed consent properly?”

“We just have to trust them,” says ABR’s Linda Tracy.

Don’t forget, the abortion clinic gets paid money for providing ‘office space’ to the harvesters, and has a financial interest in the success of harvesting as an industry.

Keely Bumsted O’Brien may have expressed “shock” and outrage when Investigate suggested the harvesting programmes could be ethically shonky, but the evidence now appears pretty damning.

Not only is there no ethical oversight of the abortion clinics, there is none on the companies doing the fetal tissue harvesting either. All the way through, the process appears to be done purely on “trust”.

And just how good is the actual informed consent process that the ethics committees rely on? According to the University of Texas, informed consent forms had to spell out what kind of research was specifically planned.

We asked ABR whether, for example, donating ‘mothers’ would be told their child’s organs would be used for eye studies, or for transplantation into animals for experiments?

“The law requires that we always state that it is possible that it may be used for important stem cell research, and if the patient asks specifically what it might be used for then that is explained to her verbally. The consent itself is somewhat generic except for the pluripotent stem cell use.” [our emphasis]

Based on Linda Tracy’s interview with Investigate, it now appears certain that no donating mother gave informed consent for her baby’s body parts to be transplanted into human/mouse hybrids, or injected into the veins of rats. Little wonder the US Government National Institutes of Health refused to release informed consent forms from ABR regarding those projects.

There was another aspect we wanted to clarify: O’Brien’s insistence that it would be unethical for her to see a donating mother’s consent form.

“Are those forms available to researchers if they need them for ethical approval?”, we asked Tracy.

“Yes.”

Naturally, all these discoveries raised more questions than answers. We went back to the University of Auckland’s Tom Barnes, the man the university’s ethics committee reports to.

“Keely does have ethical approval from the University of Washington to do this and that ethical approval is current and has gone through their prescribed procedures.”

Barnes explained that the project is a collaboration with the University of Washington’s Anita Hendrickson, who was apparently the principal point of contact with tissue harvesters.

But Barnes was not aware that University of Washington’s ethical procedures were found wanting, as referred to earlier in the Seattle Post-Intelligencer report.

“I’m sorry, I can’t comment on that,” reflected Barnes. “I’d have to know exactly what the situation is before I comment.

“In terms of what this university knows, we have the ethical approval from Washington, and also the proposal has been examined by our ethics committee de novo [as if for the first time] as well.”

When we pointed out that neither University of Washington nor ABR had directly sought informed consent from women and instead relied on abortion clinics to get it, Barnes said the University of Auckland had to trust the paperwork in front of it.

“As I say, I understand the ethical approvals were granted over there and we have paperwork that backs that up. Whatever happened over there I can’t comment on.”

We explained to Barnes the stringent ethical conditions imposed on informed consent forms by the University of Texas, and asked whether he was satisfied that the University of Auckland’s ethical rigours were tough enough.

“Let me say that our ethics committee operates under guidelines that are set nationally, and those guidelines are approved by the HRC. I believe we have an ethics committee that is absolutely committed to research being done in the correct way and I believe they do an excellent job of that.”

Having said that, says Barnes, the University of Auckland will ponder Investigate’s allegations that the US ethical process is flawed.

And what about the overall ethical issue of whether human infants should be experimented on at all? Barnes says it is legal under current New Zealand law, and proposed new rules to control it have not yet come into effect. When we again raise the comparison with Auschwitz, Barnes rejects the analogy.

“I think that’s entirely inappropriate.”

“How?”

“Well it’s a totally different situation.”

“How?”

“If you accuse, by default, Keely of behaving like somebody in a Nazi death camp, I do think that’s unfair. If the issues you’ve raised about ethical approval in America are resolved satisfactorily, if the mothers are in fact giving informed consent for the use of their tissue, that’s really quite different to somebody who’s in a Nazi death camp being experimented on,” says Barnes.

But doesn’t the answer, we pointed out, really turn on whether the fetus is the ‘mother’s tissue’ to dispose of in the first place?”

“We make sure we fall within the ethical guidelines as they are laid down,” says Barnes. “Whether those guidelines are flawed or not or whether they’ll change or not is a matter for the future, and in the meantime we have to operate within those constraints.

“To be honest with you, I think that that [whether a foetus is an individual human life or just part of the mother] is a broader debate which would have to take place in the country at large.”

It’s a good point. Researchers talk of the baby simply being “the mother’s tissue”, but advances in DNA mean we now know the foetus has its own unique DNA and tissue, and is not merely an extra piece of maternal flesh. The mother, in real scientific terms, can no more “own” the foetus on such grounds than she can “own” her older children and consent to their execution and vivisection. Is it time for renewed public debate?

It’s an argument that the University of Auckland is sympathetic to.

“You have to sort of balance the tremendous potential of this research to solve some absolutely debilitating problems – people being blind for years and so on. So we do the best we can at balancing all these factors within the guidelines and the law as it stands, and we contribute to and take part in that ethical debate and we will abide by what comes out of that ethical debate. We’re not trying to cover anything up.

“If the result of that debate that you’re referring to is that it’s unethical to work with this kind of tissue, then we wouldn’t do. No question.”

Another who shares that view is Steven Bamforth, a Canadian geneticist harvesting fetal tissue at the University of Alberta for his research colleagues. Every day, his job entails sifting through aborted remains, searching for recognizable eyes, hearts, livers and other organs sought after by universities.

“The humanity is always before us,” Dr. Bamforth told Alberta Report magazine recently. “If society said this research is not acceptable, of course, we would immediately desist. It’s not something that I do happily.”

Nor does the “helping older people with their health” excuse carry water with Christopher Hook, of Illinois’ Centre for Bioethics and Human Dignity. He told World magazine the exploitation of pre-born children was “too high a price regardless of the supposed benefit. We can never feel comfortable with identifying a group of our brothers and sisters who can be exploited for the good of the whole. Once we have crossed that line, we have betrayed our covenant with one another as a society, and certainly the covenant of medicine.”

In New Zealand, the issue of conducting medical experiments on dead bodies – both adult and fetal – is currently the subject of an ethics committee review by the Ministry of Health. Keely Bumsted O’Brien was one of those who made submissions to hearings prior to the issue of a draft report last year, Review of the Regulation of Human Tissue and Tissue-based Therapies, available on the web.

The 131 page document records a majority of submissions believe research should be prohibited on bodies where the wishes of the deceased were not known prior to death, even if the family give their consent post-mortem. As a foetus cannot express its wishes, such a restriction could impact on the use of fetal tissue, especially if society eventually reaches a decision that a foetus is a human life.

Even so, the document also notes growing unease at the use of fetal tissue for experiments, and the fact that it currently falls outside of the regulations, and the Ministry is now considering giving fetal tissue fresh ethical protection. How far it goes will depend, ultimately, on public debate.

PRICE LIST FOR BODY PARTS (US$)

Opening Lines Fee for Services Schedule
> age greater than
< age same or less than Unprocessed Specimen (> 8 weeks) $ 70
Unprocessed Specimen (< 8 weeks) $ 50
Livers (< 8 weeks) 30% discount if significantly fragmented $150 Livers (> 8 weeks) 30% discount if significantly fragmented $125
Spleens (< 8 weeks) $ 75 Spleens (> 8 weeks) $ 50
Pancreas (< 8 weeks) $100 Pancreas (> 8 weeks) $ 75
Thymus (< 8 weeks) $100 Thymus (> 8 weeks) $ 75
Intestines & Mesentery $ 50
Mesentery (< 8 weeks) $125 Mesentery (> 8 weeks) $100
Kidney-with/without adrenal (< 8 weeks) $125 Kidney-with/without adrenal (> 8 weeks) $100
Limbs (at least 2) $150
Brain (< 8 weeks) 30% discount if significantly fragmented $999 Brain (> 8 weeks) 30% discount if significantly fragmented $150
Pituitary Gland (> 8 weeks) $300
Bone Marrow (< 8 weeks) $350 Bone Marrow (> 8 weeks) $250
Ears (< 8 weeks) $ 75 Ears (> 8 weeks) $ 50
Eyes (< 8 weeks) 40% discount for single eye $ 75 Eyes (> 8 weeks) 40% discount for single eye $ 50
Skin (> 12 weeks) $100
Lungs & Heart Block $150
Intact Embryonic Cadaver (< 8 weeks) $400 Intact Embryonic Cadaver (> 8 weeks) $600
Intact Calvarium $125
Intact Trunk (with/without limbs) $500
Gonads $550
Cord Blood (Snap Frozen LN2) $125
Spinal Column $150
Spinal Cord $325

Published in print November 2006, Investigate magazine