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Tag: Issue-11 - Organic Lifestyle Magazine Tag: Issue-11 - Organic Lifestyle Magazine

Issue 11- Vitality

Short Sighted – Diminishing Returns – Letter From the Editor

Ask OLM

Sprouting to Remove Enzyme Inhibitors

Enzyme Supplementation

Swine Flu Vaccine Health Concerns

Robert F. Kennedy Jr. – Green Our Vaccines Rally

Generation Rescue – Company Profile

Alzheimer’s

Natural Cures for Cataracts

Pure Sleep – 11 Tips for Better Sleep

Monsanto Company Profile part IV of IV

Homemade Papaya Enzyme Supplement

Tips to Look Younger, Feel Younger, Be Younger, and Live Longer

80% Raw Food Diet

Lentils

Lentils and Wild Mushrooms In Savoy Leaves

Lentil Burger Recipe

Olm Interviews Seth Leaf of Living Nutz




Short Sighted – Diminishing Returns – Letter From the Editor

Studies showing that GMOs work and work well are accurate, to a point. Initially, yields are higher and farmers don’t need to spray as many herbicides or pesticides. In the long run, we read reports from all over the world claiming yields decline, super weeds are growing, and soil degradation is rampant.

Our society is one of short sighted vision. Our consumption model, which drives our people and our government, is also short sighted, resulting in increased debt and reliance on non-sustainable resources. It can’t last.

Pharmaceutical medications work the same way. You treat the symptoms (short term) not the cause (long term).

Companies are set up to make as much money as they can, as quickly as possible. When a company can no longer sustain its practices, it finds new ways, often corrupt ways, to maintain its profits. These methods often result in harming people and our environment in the long run.

Consider the fact that if Americans saved, spent money on what they needed, and refused to go into debt to buy “extras,” our economy would completely collapse.

Our society is comprised of pleasure seeking, quick fixing, short term results oriented, greedy consumers. That’s how we work. It can’t last forever.

 

Michael Edwards

Signature

Editor in Chief




Ask OLM

Loose Skin

Dr. Tim O’Shea,

I lost a lot of weight. I have loose skin. It was recommended that I take a systemic enzyme. I am also considering taking the collagen supplement you recommend. I have been told that systemic enzymes somehow eat foreign protein. Is this true and will they cancel each other out?

~ Sean

DR. TIM O’SHEA: For some collagen products that’s true, but the one that I sell at thedoctorwithin.com (Hydrolyzed Collagen Protein Hydrate) one is completely bioavailable. You must do it for two months every day to see the good effect. For more information check out thedoctorwithin.com/collagen.

Something in Common with Francis

Dear Raymond Francis,

I’ve read your book, Never Be Sick Again, and was astonished by how similar our stories are. I too had my immune system collapse, and suffered from many environmental sensitivities (though not as severe as yours). Through diet and naturopathic medicine I have recovered much of my health. One thing I discovered was a severe sensitivity to gluten. Do you believe that I can reverse my inability to digest gluten when I completely restore my health?

~ Carol

RAYMOND FRANCIS ANSWERS: It is impossible to predict if gluten sensitivity can be reversed in a particular person. Whether this can happen depends on too many individual factors, including genetic makeup. That being said, I have observed numerous people overcome gluten sensitivity by rebuilding their immunity, and very importantly, rebuilding the integrity of their gut tissue. Damaged gut tissue and leaky gut are a sure-fire prescription for food allergies. Repairing gut tissue with diet, stress reduction, and supplements will often make food allergies and gluten sensitivity go away. At the very least, as you improve your health, your sensitivity will be reduced, and it will take exposure to higher amounts of the allergen to get a reaction.

Receding Gums

I have a problem with receding gums. My dentist says I need to have surgery. Is there a way I can fix this with naturopathic medicine?

~ Sara

DR. SHILLINGTON ANSWERS: Absolutely! My “Tooth & Gum” Formula works wonders in this area. Below is a success story for you to read. The stuff IS AMAZING!!!

All the best,

Doc (Ian Shillington)

Success Story: When I moved to Clearwater in October 1997, I had advanced periodontal disease. Very deep pockets existed in all of my teeth and I had been told by 3 dentists that I would lose all of my upper teeth and at least 4 of my lower teeth. In December, my friend Valorie gave me the Tooth & Gum formula to use on my gums. At the time I had a very deep and painful abscess in my upper gums extending into my sinus cavity. I swished one dropperful of Tooth and Gum formula around in my mouth and within 20 minutes the pain (that large doses of pain medication would not handle) was gone! I used the formula in this manner for the next couple of days along with Echinacea and the abscess was gone within 3 days. Daily over the next couple of months, I diluted the tooth and gum formula and used the water-pick. This was all in an effort to save some of the lower teeth. I still expected to lose all of the upper teeth and at least 4 of the lower ones.

When I went to the dentist in April 1998 to have a final evaluation and get the necessary teeth extracted, we discovered that all the pockets in the lower teeth had shrunk from 7, 8 and 9 mm back to the depth of about 3½ mm and I was able to keep all of my bottom teeth. Additionally I was able to keep 4 teeth on the top, save myself $1500, and now eat the raw veggies which I love. I was astounded!! So was my dentist. In a nutshell this tooth and gum product tightened my gums, restored the bone loss and returned the above mentioned teeth and surrounding gums to a healthy state. All the best,

Mary O – WA

Fingernails

A few years ago I noticed ridges in my fingernails from root to tip. Then my thumbnails thickened. They break in chunks. What causes this, and what can I do to reverse it?

~ Janie

RYAN HARRISON, MA: Many women spend a good deal of time and money on their nails. Unfortunately, cosmetic care isn’t necessarily the best way to keep your nails healthy. In fact, nail polish itself can actually remove the natural fat found in nails, leading to brittleness.

Keratin is the component responsible for a nail’s firmness and if a person is experiencing nail brittleness or splitting, a deficiency of keratin is typically the underlying cause. This deficiency can be caused by malnutrition, malabsorption, or a metabolic defect such as low stomach acid. Your body will synthesize keratin, but you need to be sure you’re giving it the nutrients it needs to do so. These include calcium, molybdenum, sulfur, and zinc. Increase your intake of whole grains, organic dairy products, legumes, and toxin-free fish to ensure you’re getting these nutrients. Get an extra nail-healthy boost of the vitamin biotin from brewer’s yeast, saltwater fish and soybeans, as well.

Another way to increase your nail-enhancing mineral intake is to make and drink a tea made from nettle leaves, horsetail herb, chamomile, and yarrow flowers. Pour 1 cup of boiling water over 1 tbsp of a mixture of these herbs. Let it steep for 15 minutes and then drink 1 cup up to 3 times, daily. Finally, be sure that you are caring for your nails in an appropriate manner. Filing your nails is gentler than clipping, but don’t exert too much pressure when filing. And never push back your cuticles with a hard or sharp object, which may cause the nail to develop grooves or break off faster. Instead, oil or soak your cuticles and push them back gently with your fingertips.

Sensitive Teeth

I have very sensitive teeth. I can’t eat cold foods at all. What’s wrong with my teeth and what can I do? I take calcium supplements, and I do eat veggies and drink milk. Can I still be low on calcium?

~ Patricia

RYAN HARRISON, MA: Sensitive teeth can have several causes. Most commonly, as a person’s gum line recedes, the roots of teeth can end up exposed. These roots can be very sensitive to hot and/or cold or to pressure. Another cause is the exposure of a tooth’s root when the tooth’s enamel is broken, cracked, or chipped. Finally, as with many other health issues, there can also be an emotional or psychological component; the pain manifests in the teeth, but really starts somewhere else.

For teeth that are sensitive due to receding gums or pores in the tooth itself, most dentists prescribe a toothpaste that contains potassium nitrate, which fills pores and helps numb the pain. Unfortunately, like many other components of standard dental care, potassium nitrate is a toxic chemical. Its MSDS registration lists it as “harmful if swallowed, inhaled, or absorbed through the skin” and states that it “causes irritation to skin, eyes and [the] respiratory tract.” Is this really something you want to put in your mouth, where chemicals are quickly and easily absorbed through oral membranes?

More natural approaches to calming sensitive teeth include herbal, nutritional, and energetic recommendations. As far as herbs go, you might find a blend of nervine (nerve-calming) herbs to be very helpful. Capsules containing equal parts of herbs such as lavender, hops, valerian, chamomile, and skullcap, when taken regularly, can help decrease pain and soothe irritated nerves. Be careful, however, in your dosage and usage of these herbs. They can also have sedative effects. Check with a knowledgeable herbalist before starting any herbal regimen.

There is anecdotal evidence to suggest that tooth enamel can be “rebuilt” – a process referred to as “remineralization” – if the proper steps are followed. In large part, this requires adherence to some dietary instructions that reduce the acidity of saliva while also introducing foods and/or supplements high in calcium, magnesium, and vitamin D.

Additionally, some essential oils such as myrrh, clove, and goldenseal may be used to help cleanse the mouth and safely reduce pain. Speak with a qualified naturopath to determine what would work best for you.

Finally, I would suggest that your first step be approaching the issue from a psychological angle. While it may seem strange, it’s well proven that a person’s state of mind can affect her physical wellbeing. And though we are making great strides in understanding the mind’s relationship with the body, it’s still pretty hard to tell when a physical ailment is (or isn’t) caused by some kind of mental/emotional stressor. There’s a very powerful, efficient, and surprisingly simple energetic technique that helps alleviate a host of physical conditions by removing mental/emotional charges called EFT (Emotional Freedom Techniques). It has an impressive track record for calming the body and mind and reversing even deep-seated complaints, sometimes within minutes. A professional EFT practitioner will be able to help you explore this possibility.

Email your questions to questions [at] organicmail.net. Questions may be edited for clarity or length.




Sprouting to Remove Enzyme Inhibitors

If you were to leave a kernel of spelt, hard red winter wheat, rye, barley, or any other grain on your dining room table for the next five years, it wouldn’t rot or decompose. Grains were found  in the pyramids. Not only were they intact after two thousand years, but when water was added, some of the kernels grew. There is a reason why grains don’t easily decompose. Grains, seeds, tree nuts, and most beans, contain a live, biochemical agent called an enzyme inhibitor. Enzyme inhibitors stop enzyme activity until the right conditions exist for germination. This is nature’s way of preserving the life force in a seed so it can reproduce.

Foods with enzyme inhibitors are very difficult to digest, and they slow down the naturally occurring enzyme activity in your body. Every time you eat regular pasta, bread, cake, cereal, and all other grain products, or nuts, seeds and beans, you are slowing down the communication processes throughout your entire body and suppressing your body’s ability to function at peak performance. Ingesting enzyme inhibitors causes obesity, lethargy, gas, bloating, high blood pressure, gastrointestinal difficulties, an enlarged pancreas, diabetes, destruction of the body’s own natural production of enzymes, and an overall general condition of poor health.

Enzyme inhibitors make meat protein more difficult to utilize, while causing animal fats to concentrate, and cholesterol and triglyceride levels to rise.

So does this mean we should eliminate all of these foods because they’re bad for us? Absolutely not! All we have to do is to prepare them correctly to release the enzyme inhibitors. Once the enzyme inhibitors are gone, grains, seeds, tree nuts, and beans are some of the most perfect foods. They are very high in assimilable amino acids (proteins) and extremely rich in the exact kinds of enzymes
our bodies need to keep us in good physical condition.

So, how do you get rid of enzyme inhibitors? The answer is simple. Sprouting! Water unlocks enzyme inhibitors. Soaking these foods in water sends them into “sprout mode” and starts the germination process.

Put sunflower seeds in a sprouting jar, add water, and let them soak. Empty the water at the end of 8 hours and place the jar out of direct sunlight. Prop it at a 45 degree angle so it can drain. Rinse your seeds twice during the next 12 to 16 hours. To allow for air circulation, be sure the seeds do not cover more than half of the jar lid. After 24 hours, drain your seeds well and spread them on unbleached paper towels on a cookie sheet and let them dry. The enzyme inhibitors will be gone and your seeds will be bursting with flavor!

Sprouting not only eliminates enzyme inhibitors, it also turns acidic grains, nuts and seeds into alkaline foods.

Only eat breads and pasta made from sprouted grains. Soak and sprout your seeds, nuts, and beans. A great book with charts on germination times for various foods is Dining in the Raw by Rita Romano.

Recommended Supplements:



Enzyme Supplementation

Human glyoxalase I. Two zinc ions that are needed for the enzyme to catalyze its reaction are shown as purple spheres, and an enzyme inhibitor called S-hexylglutathione is shown as a space-filling model, filling the two active sites.

There are several different kinds of enzymes. The ones I focus on typically are digestive enzymes and systemic enzymes.

Digestive enzymes like hydrochloric acid and pepsin are the primary things you need in your stomach to help digest proteins and minerals. They also help to sterilize the stomach and kill parasites, bacteria, mold, micro spores, etc. Ideally your stomach is the only place in your body that’s acidic, and it should be extremely acidic. After the mouth the stomach is the beginning of all chemical and digestive reactions in your body. You need all the atomic energy in there to break up the molecules and to get things ready and assembled for digestion. If you put protein like meat in water it will just set there; it won’t break down. Put the same protein in a strong hydrochloric acid and it will dissolve relatively quickly, and that’s what you want to have happen. You want things to dissolve relatively quickly. You don’t want food just sitting there rotting in your stomach. That’s the reason you need to avoid drinking fluids during your meals. They will dilute the acids. As you can imagine, taking antacids while you are trying to digest foods pretty much puts a stop to everything.

Digestive enzymes work in the stomach to digest food, while quality systemic enzymes are enterically coated to prevent contact with the stomach acid. This way they pass through the stomach into the intestines where they are absorbed by the body.

We are born with the ability to produce a certain amount of systemic enzymes. Systemic enzymes fight
inflammation, fibrosis (scar tissue), and viruses; modulate the immune system; and cleanse the blood. These enzymes are a kind of scavenger hunter. They go after foreign protein, things that shouldn’t be there. They’ll go after scar tissue, a cyst, bacteria, parasites, viruses. Virtually anything that doesn’t belong in your body is like food to these enzymes. We’ve even seen systemic enzymes kill heartworms in cats. And when you are young you can bump into things, fall, scratch yourself, and your body healed easily, and quickly, often not leaving a scar when you thought it would. You
didn’t have aches or pains, you healed so easily. But as they get older, the typical person does not ingest enough systemic enzymes and the body realizes it’s running out of them. So it begins to ration them, because if you completely run out, you can’t survive. Three days after you run out of enzymes you are dead. Your body always needs enough in reserve for the unexpected.

So you get into your 20’s and you don’t heal as quickly. You get into your thirties and you notice you scar more easily. You may even be developing permanent aches and pains. The reason you are running out of
these enzymes and not replenishing them is because you are not doing what you used to do, what all other animals do in nature, you aren’t eating living things.

When you pick an apple off of a tree, you get enzymes. When you eat an apple fallen from the tree a few days ago, you’re getting fewer enzymes. If you eat an apple off the shelf at the grocery store, well, you get the idea. It’s not rotten, it may have everything else you need, but the enzymes are gone.

Fish eat other fish, giraffes eat leaves, lions eat living prey, and we eat dead food. And we don’t heal like we should and we don’t digest our food like we should. We need these enzymes.

In Germany and Japan, two countries with the best healthcare in the world, you would be given systemic enzymes for almost any treatment. If you had kidney problems, they would include these enzymes in your treatment. If you were in an auto accident driving on the autobahn and sustained a spinal cord injury they would give you a retention enema with the equivalent of about 300 enzyme capsules to save you from major damage and reduce the possibility of major paralysis.

Dr. Kelly recommends Betaine HCl and Pepsin from Thorne for digestive enzymes and Vitälzym X for systemic enzymes.




Swine Flu Vaccine Health Concerns

ALERT Canadians: Toxic Ingredients in the Arepanrix H1N1 Vaccine Harm Your Health

Health Canada has authorized the sale of Arepanrix™ H1N1 vaccine based on no conclusive clinical testing. The authorization is based on the Health Canada review of available data on the quality, safety and immunogenicity of similar vaccines, which established the benefit/risk profile in favour of inoculating the Canadian population.

Read the Notice of Decision issued by Health Canada. The decision by the Health Minister was based on a belief (not qualified or informed) that immediate action is required to deal with the H1N1 risk. The assertion that the decision is based on limited clinical testing is being misapplied. There have been NO conclusive results from any clinical trials on the Arepanrix H1N1 vaccine.

This report is designed to inform you how the risks outweigh the benefits of the vaccine. It will demonstrate how the Health Canada assessment is flawed and contradictory to established research on the detrimental health effects of the vaccine ingredients contained in Arepanrix.

Swine Flu Vaccine Description and Composition

Arepanrix™ H1N1 (AS03-adjuvanted H1N1 pandemic influenza vaccine) is a two-component vaccine consisting of an H1N1 antigen (as a suspension), and an AS03 adjuvant (as an oil-in-water emulsion). The virus is inactivated followed by formaldehyde treatment and disrupted with sodium deoxycholate.

Preservative content:

5µg (micrograms) Thimerosal USP per 0.5mL dose or 2.5 micrograms organic mercury (Hg) per 0.5mL dose

Adjuvant:

The AS03 adjuvant system is composed of DL-α-tocopherol, squalene and polysorbate 80 in a 3mL vial:

DL-α-tocopherol: 11.86 milligrams/0.5mL dose

Squalene: 10.69 milligrams/0.5mL dose,

Polysorbate 80: 4.86 milligrams/0.5mL dose

Analysis of Ingredients

Formaldehyde

According to the Australian National Research Council, fewer than 20% but perhaps more than 10% of the general population may be susceptible to formaldehyde and may react acutely at any exposure level. More hazardous than most chemicals in 5 out of 12 ranking systems, on at least 8 federal regulatory lists, it is ranked as one of the most hazardous compounds (worst 10%) to ecosystems and human health (Environmental Defense Fund).

Formalyn a 37 percent solution of gaseous formaldehyde which includes methano (used in vaccines as a tissue fixative) is considered a hazardous compound, and its vapor is toxic. In the body, formaldehyde can cause proteins to irreversibly bind to DNA. Laboratory animals exposed to doses of inhaled formaldehyde over their lifetimes have developed more cancers of the nose and throat than are usual, as have workers in particle-board sawmills… Formaldehyde is classified as a probable human carcinogen by the U.S. Environmental Protection Agency and as a known human carcinogen by the International Agency for Research on Cancer.

Sodium Deoxycholate

Sodium Deoxycholate is a water soluble ionic detergent/bile salt which causes cell death and symptoms such as burning, redness, and swelling. It has been shown to weaken the blood-brain-barrier (BBB) and subsequently activate seizures. It has demonstrated synergistic toxicity with antifungal drugs.

Detergents and emulsifiers promote tumors and cause cells to leak or explode by weakening their walls, with no mechanism for regulating destructive activity. These chemicals are not completely purified out of the final vaccine product, so they enter the body at the time of injection.

Detergents are used extensively in cell research precisely because of their ability to break cells open for further analysis. This catastrophically mimics the membrane attack complex (MAC). Detergents hit cells at random and continue destroying cells regardless of which call off the attack.

Sodium Deoxycholate is completely foreign to the relationships that define and make up the delicate balance of the immune system. It systematically disrupts these relationships to negate the optimal function and design of immune responses.

Thimerosal

Thimerosal has powerful and damaging effects on cells of the nervous and immune systems in mammals including humans. Its effect may vary depending on the dose, the genetics of the individual, and the timing of exposure. The mercury dose from thimerosal produces acute and often deadly ethylmercury blood levels.

Organic forms of mercury are well-known neurotoxic agents and far more dangerous than inorganic mercury sources. Exposure to organic mercury produces predominantly central nervous system (CNS) effects that are commonly severe and can induce prolonged unconsciousness, coma, and death. (See: Acta Chim. Slov. 2004, 51, 361-372)

After only 2 hour exposures, thimerosal at micromolar concentrations causes neuronal membrane damage and alterations leading to cell death in immune T-cells. Thimerosal alters the functioning of critical neurotransmitters necessary for proper brain functioning.

Thimerosal causes DNA fragmentation of neuronal cells and disrupts neuronal growth factor signaling at micromolar and even nanomolar concentrations. It also causes DNA methylation and attentional pathways at nanomolar concentrations, leading to alterations in brain function.

Squalene in AS03 adjuvant

Too dangerous for human use, Squalene is not officially licensed for use in the United States or Canada. Oil adjuvants like squalene have been ordinarily used to inflict diseases in animals – for experimentation and study. According to anthrax vaccine expert Gary Matsumoto and other reliable sources, the US military used an unlicensed, experimental anthrax vaccination laced with squalene, with disastrous consequences, including Gulf War Sydrome.

“There are now data in more than two dozen peer-reviewed scientific papers, from ten different laboratories in the US, Europe, Asia, and Australia, documenting that squalene-based adjuvants can induce autoimmune diseases in animals, observed in mice, rats, guinea pigs, and rabbits. Sweden’s Karolinska Institute has demonstrated that squalene alone can induce the animal version of rheumatoid arthritis. The Polish Academy of Sciences has shown that in animals, squalene alone can produce catastrophic injury to the nervous system and the brain. The University of Florida Medical School has shown that in animals, squalene alone can induce production of antibodies specifically associated with systemic lupus erythematosus,” writes Matsumoto.

Oil-based vaccination adjuvants like squalene have been proved to generate concentrated, unremitting immune responses over long periods of time according to a 2000 article in The American Journal of Pathology. The study demonstrated that a single injection of the adjuvant squalene into rats triggered a chronic, immune-mediated joint-specific inflammation, also known as rheumatoid arthritis. The researchers concluded the study raised questions about the role of adjuvants in chronic inflammatory diseases.

Polysorbate 80

Polysorbate 80 is similar to Sodium Deoxycholate in its ability to increase cell permeability, damage, and bursting. After injection it can rapidly metabolize into sorbitol and ethylene oxide which is much more toxic than the original chemical. When Polysorbate 80 breaks down there are 20 moles of ethylene oxide for every mole of sorbitol. These polysorbates have been shown to cause dangerous, sometimes fatal effects, when given through a needle. Changes in heart function can occur immediately. The blood-brain-barrier (BBB) can be weakened and penetrated, followed by seizures and even death. Polysorbates demonstrate synergistic toxicity with a wide range of chemicals.

Polysorbate 80 has been found to negatively affect the immune system and cause severe anaphylactic shock which can kill. According to Annals of Allergy, Asthma, and Immunology, Volume 95, Number 6, December 2005 , pp. 593-599(7), “it is of current relevance as a ‘hidden’ inductor of anaphylactoid reactions”, and “Polysorbate 80 was identified as the causative agent for the anaphylactoid reaction of nonimmunologic origin in the patient. The study included a pregnant woman who suffered anaphylactic shock after being given a IV drip of multi-vitamins containing polysorbate 80.

In addition to this, there have been studies in Food and Chemical Toxicology which showed that Polysorbate 80 causes infertility. Baby female rats were injected with polysorbate 80 at days 4-7 after birth. It accelerated the maturing of the rats and caused changes to the vagina and womb lining, hormonal changes, ovary deformities, and degenerative follicles.

According to the World Intellectual Property Organization, which is part of the United Nations, scientists from the organization are developing vaccines specifically to damage fertility as a method of contraception. A suggested ingredient for the vaccine is Polysorbate 80 (also known as tween 80). As it is a preferred ingredient, scientists are obviously aware of its ability to cause infertility.

National Center For Biotechnology Information

Discussion

There are currently NO clinical trials or results which have validated the long-term safety and efficacy of the Arepanrix H1N1vaccine and its integrated AS03 adjuvant. Regulatory health agencies are refusing to acknowledge this fact or the nature of toxicity levels associated with Arepanrix and its ingredients. The well documented toxicity evidence for each ingredient presented above is simply being ignored.

A simple search on the ClinicalTrials.gov website shows that three “Rapid Evaluation” studies for Arepanrix H1N1vaccine have not even initiated recruiting as of the date this article was published.

One of the most critical elements which defines the toxicity potential of any vaccine are its pharmacokinetic properties. GlaxoSmithKline (GSK) and Health Canada do not consider the study, analysis or evaluation of the pharmacokinetic properties of any vaccine including Arepanrix. This means that the bodily absorption, distribution,= metabolism and excretion of ingredients within the Arepanrix vaccine are not known or even considered in safety assessments. This in itself is a highly suspicious and negligent behavior which leaves many questions on the credibility and reputability of GlaxoSmithKline and Health Canada and their motives for marketing this vaccine to the Canadian population.

Adults Aged 18-60 years:

Dosage recommendations of 0.5ml are based on very limited clinical evidence of safety and immunogenicity data available from two 3-week studies. Neither study has validated the long-term immunogencity, safety, toxicity, or pharmacodynamics of the vaccine based on any dosage. Clinically, the shortest acceptable period to study the side effects of any vaccine is 6-8 weeks. The accepted studies noted by GSK and Health Canada are half this period.

Elderly (>60 years):

No clinical data are available for Arepanrix H1N1 in this age group including the effects of the AS03 squalene adjuvant. There is no data to justify any safe dosage in this age group.

Children and Adolescents aged 10-17 years:

No clinical data are available for Arepanrix H1N1 in this age group including the effects of the AS03 squalene adjuvant. No exact dosing recommendations can be made.

Children aged from 6-35 months:

No clinical data are available for Arepanrix H1N1 in this age group including the effects of the AS03 squalene adjuvant. No exact dosing recommendations can be made.

Pregnancy and Lactation

No data have been generated in pregnant or breast feeding women with Arepanrix nor with the AS03 adjuvant.

Fertility & Sterility

GSK suggests animal studies have not demonstrated harmful effects with respect to fertility which directly contradicts several scientific studies which show that Polysorbate 80 causes infertility.

Interactions With Seasonal Flu Vaccines

GSK claims that no data is available on the concomitant administration of Arepanrix H1N1 with other vaccines, including seasonal influenza vaccines.

A study based on research in British Columbia, Ontario and Quebec, has shown that people who received the seasonal influenza vaccine last year are at greater risk of contracting the H1N1 flu this year.

Adverse reactions may be intensified with co-administration with other vaccines.

Despite the suggested evidence in unpublished studies that seasonal flu vaccines can increase the risk of H1N1 flu, Canadian provinces are recommending co-administration of both vaccines in as little as 60 days. This highly irresponsible recommendation by public health officials could potentially devastate the health of millions of Canadians. An example of the schedule of shots in Ontario is listed in the chart below released in a leaflet to all Ontarians in early October 2009.

Timing Vaccination Targeted Individuals
October 2009 Seasonal Flu Ontarians 65
and over
November 2009 H1N1 Flu All Ontarians
Dec/09 – Jan/10 Seasonal Flu Ontarians under 65

The people in Ontario need to call the ServiceOntario INFOline at 1-800-476-9708 and request information as to why Ontario is contradicting studies which demonstrate the risks of administering both the seasonal flu and H1N1 vaccine within short periods.

In addition, the Government of Ontario (and Canada) need to respond to direct queries from the public to justify why and how recommendations are being be made to administer the H1N1 vaccine to those receiving the seasonal flu vaccine, when the studies that test the safety and efficacy for the “Rapid Evaluation of Pandemic H1N1 Influenza Vaccine in Adults Receiving Seasonal Influenza Vaccine” have not yet started as of late October 2009 (with no participants even being recruited).

Adverse Reactions

Solicited adverse reactions were reported more frequently in the H1N1+AS03 group compared to the H1N1 group based on 2 studies which evaluated the safety of another AS03-adjuvanted vaccine containing HA derived from A/California/7/2009 (H1N1)v-like (Pandemrix) in healthy subjects aged 18-60 years.

Since 48.6 of the 50.4 million doses of Arepanrix ordered by the Canadian government contain the AS03 adjuvant, we will focus on those adverse reactions
documented which are as follows:

  • Pain
  • Redness
  • Swelling
  • Fatigue
  • Headaches
  • Arthralgia (joint inflammation)
  • Myalgia (muscle inflammation)
  • Shivering
  • Sweating
  • Swollen lymph nodes
  • Fever
  • Vomiting
  • Tingling or numbness of the hands or feet
  • Shortness of breath
  • Vasculitis (inflammation of the blood vessels)

Serious adverse reactions are as follows:

  • Blood and lymphatic system disorders (lymphadenopathy)
  • Psychiatric disorders (insomnia)
  • Nervous system disorders (dizziness, paraesthesia, inflammation of the central nervous system, inflammation of nerves, autoimmune disorders affecting myelin sheaths of nerves such as Guillain-Barré Syndrome)
  • Ear and labyrinth disorders (vertigo)
  • Respiratory, thoracic and mediastinal disorders (dyspnoea)
  • Gastrointestinal disorders (nausea, diarrhea, abdominal pain, vomiting, dyspepsia, stomach discomfort)
  • Skin and subcutaneous tissue disorders (pruritus, rash)
  • Musculoskeletal and connective tissue disorders (back pain, musculoskeletal stiffness, neck pain, muscle spasms, pain in extremity)
  • General disorders and administration site conditions (bruising, asthenia, chest pain, malaise)
  • Disturbing Concentrations of Squalene

The average quantity of squalene injected into the US soldiers abroad and at home in the anthrax vaccine during and after the Gulf War was 34.2 micrograms per billion micrograms of water. According to studies, this was the cause of Gulf War syndrome in 25% of 697,000 US personnel at home and abroad.

The soldiers developed a cascade of reactions including arthritis, fibromyalgia, lymphadenopathy, rashes, photosensitive rashes, malar rashes, chronic fatigue, chronic headaches, abnormal body hair loss, non-healing skin lesions, aphthous ulcers, dizziness, weakness, memory loss, seizures, mood changes, neuropsychiatric problems, anti-thyroid effects, anaemia, elevated ESR
(erythrocyte sedimentation rate), systemic lupus erythematosus, multiple sclerosis, ALS, Raynaud’s phenomenon, Sjorgren’s syndrome, chronic diarrhea, night sweats and low-grade fever.

The AS03 adjuvant in the Arepanrix H1N1 vaccine contains 10.69mg per dose. This corresponds to approximately forty times more squalene per dose than the anthrax vaccine.

How much more evidence is necessary to convince public health officials that the risks of the Arepanrix H1N1 vaccine exceed any benefits?

Please do not play roulette with your health. Do not listen to the Public Health Agency of Canada or any public health or medical official that advises you to protect yourself from the flu with this vaccine. Its design and toxicity will only destroy your health.

This article has been reprinted with permission from PreventDisease.com

Dave Mihalovic is a Naturopathic Doctor who specializes in vaccine research, cancer prevention and a natural approach to treatment. Article is reprinted with full permission of PreventDisease.com

Reference Sources www.novaccine.com, www.gsk.ca, www.hc-sc.gc.ca, www.nvic.org  October 26, 2009




Robert F. Kennedy Jr. – Green Our Vaccines Rally

The following is a transcript of Robert F. Kennedy’s speech for the Green Our Vaccines Rally in Washington, DC, June 4th, 2008. This speech, posted on the Generation Rescue website is reprinted with permission.

Thank you very much. I’m so happy to see all of you out here today, finally telling the truth to this congress which needs to hear the truth for the first time, and as Boyd Haley says, the press isn’t telling it to them. You know, the one exception is UPI, that has done a great job, and we need to give them an applause for what they’ve done, ‘cause they’re the only media outlet that is telling the truth on this issue.

I didn’t want to get involved in this issue, I got dragged into this issue because the truth became undeniable to me—and I was working on mercury issues from an environmental standpoint: coal burning power plants, which discharged an enormous amount of mercury, and about eight years ago, the EPA said that in nineteen states, because of mercury discharge from power plants, it is now unsafe to eat any freshwater fish in the state. In forty-nine states, at least some of the fish are unsafe to eat because of mercury. In fact, the only state where all the fish are still safe to eat is Wyoming—Dick Cheney’s home state, where the republican-controlled legislature has refused to appropriate the money to test the fish.In all the other states, at least some, most, or all the fish are unsafe to eat. Every state on the Atlantic coast has fish advisories; every state in the Gulf coast now has fish advisories; if you eat tuna fish, the FDA will warn you not to eat too much of it; swordfish, all these fish, and why?

Because it causes neurological injury in children.

So the government scientists are acknowledging that even tiny, infinitesimal amounts of mercury—parts per billion—will cause

profound neurological injury in children. And I was working on these issues, and mothers started coming up to me and said, “You know, the biggest exposure is not coming from power plants, or old mining claims, or old mining claims, as you might think. It’s coming from our own vaccines.” And they asked me to work on it, and to just look into it. And they were not hysterical people. They were scientists, they were doctors, they were psychiatrists, they were pharmacists, they were people that had their feet on the ground. They had attended the conferences, they had read the scientific literature, they had calmly and deliberately gone through this, and they had reached a conclusion. And the conclusion was that the vaccines were destroying the health, were making the sickest generation of American children in the history of our country. And I started looking into it, and somebody provided me with the Simpsonwood memo, which I then published in Rolling Stone.

Simpsonwood was the transcripts of a secret meeting that was held between CDC and seventy-five representatives of the vaccine industry, in which they reviewed a report that CDC had ordered, the Stratton study of the hundred-thousand children in the United States Vaccine Safety Database. And when they looked at it themselves, they said, “It is
impossible—” this is a quote, “It is impossible to massage this data to make the signal go away. There is no denying that there is a connection between and Thimerosal in the vaccines. And they said—this is what they said, I didn’t say this, this is their own scientists, their own conclusion of the best doctors, the top people at CDC, the top people in the pharmaceutical industry.

And, you know, when they had this meeting, they had it not in Atlanta, which was the headquarters of the CDC, but at Simpsonwood, at a private conference center, because they believed that that would make them able to insulate themselves from a court request under the Freedom of Information law, and they would not have to disclose the transcripts of these meetings to the public. Somebody transcribed the meetings, and we were able to get a hold of it.

You have them talking about the Verstratten study and saying there’s a clear link not just with autism but with a whole range of neurological disorders: speech delay, language delay. All kind of learning disorders: ADD; hyperactivity disorder and the injection of these vaccines [sic]. And they could tell because, as you know, vaccine protocols were dramatically increased.

When I was a little boy, we only got three
vaccines. But my children, five of my six children, got twenty-two vaccines. Beginning in 1989—that’s the Thimerosal generation. That’s the vaccine generation, and it’s the sickest generation in the history of this country. And I looked at these, I read, and I was astonished, because I have worked on environmental issues for twenty-five years, and I know what “captive agency phenomena” is. It’s the dynamic by which the regulatory agencies become captured by the industries they’re supposed to regulate. And there’s all kinds of mechanisms that encourage that, or provoke that, or promote that to happen.

But I was shocked, because I know many of these people in CDC, and I know the people in the FDA, and I know that when they entered those agencies, they entered with a good heart, intending to do the right thing. But something had corrupted them. They got sucked into a vortex because they made decisions that were wrong, and instead of admitting it to the public, they covered it up to protect themselves. And it was very clear, and then I got a hold of the correspondence between the doctors and between CDC, rebuking each other and saying, “Why didn’t we look at this? Why didn’t somebody do a mass loading before we did these, approved these protocols with twenty-two vaccines to these children? Why didn’t we do this?” Rebuking themselves, rebuking each other. And then, the Simpsonwood transcripts, after the first, maybe two hours in which they’re talking about the undeniability of the connection between autism and Thimerosal; the impossibility of massaging the data further in order to try and eliminate those
signals. That’s what they spend the first two hours.

The rest of the meeting they spend talking about, “How do we hide this?” from the press, from the public, and from what they call the “predatory bar,” all the lawyers out there who may represent people who were injured by their negligence. And the end of that meeting, they make a few decisions. One is, for Stratton, the man who designed, who constructed the study, is hired the next day by GlaxoSmithKline and shipped off to Switzerland. And six months later, he sends in a redesigned study that includes cohorts that are—predictably—who are too young to have been diagnosed as autistic.

So he loads the study down, the data down, and they tell the public that they’ve lost all the original data. This is what CDC says to this day, that it does not know what happened to the original data in the Verstratton study. And they publish this other study that is a corrupt and crooked what we call “tobacco science,” done by a bunch of “biostitutes, of crooked scientists who are trying to fool the American public.
Then Kathleen Stratton, of CDC and IOM,says, “What we need is, we need some studies that will disprove the link.” So, they work with the vaccine industry to gin up these four phony European studies that are done by vaccine industry employees, funded by the vaccine industry, and published in the American Academy of Pediatrics magazine, which receives eighty percent of its revenue from the vaccine industry. And none of these scientists disclose any of their myriad conflicts, which conventional ethics
rules require them to do. It’s not disclosed.

And these studies—and you know, I’ve made a profession of reading phony science, of junk science, of “tobacco science,” because I see it every day. I’ve sued over four-hundred polluters, and this how they defend themselves. They hire these phony scientists, “tobacco scientists,” they produce these phony reports—so I know how to read them. So I did something that not a single member—you see the press here, and all there?—not a single member of this press corps, I can guarantee you, has ever read any of those studies. It has not happened. What they read was the CDC’s description of those studies, which has nothing to do with what’s in the studies. And you need to read these studies—and I’m talking to you guys, and you

need to read them critically, and that woman, I called that woman who wrote that TIME magazine article, and I called the editor of The Washington Post when they said, you know, “Well, this is the newest mythology, they’ve removed the Thimerisal from the vaccines and autism rates have not gone down.”

How many times have you read that repeated by these people from the press? That is an industry talking point that the industry knows is a lie—everybody knows that’s a lie. The amount of Thimerisal today in the flu vaccines is about sixty percent of what they claim to have removed from all the other pediatric vaccines. So, I looked at these, I read these studies, and I saw studies that weren’t even good—that wasn’t even high-quality fraud. It is low—these are low quality fraud, the worst—I mean, anybody, you don’t even need a scientist to advise you and tell you where the fraud is. And I’ll tell you what they—I’ll just tell you what one of them, the big one that they all rely on, the Danish study, where they said, okay, in 1992, Denmark banned Thimerisal. And after that, autism rates continued to climb. Therefore, there is no association between autism and Thimerosal. That’s the study.

What they didn’t tell you is that in 1992, Denmark was concerned about the connection between Thimerisal and autism, and about this huge rise in autism, and it began for the first time requiring registering autism as a reported illness in Denmark. So all the people who had autistic children suddenly had to register them for the first time. Plus, in Copenhagen, they founded a new clinic to treat autistic kids, which gave people a huge financial incentive and health incentive to register their children. So it’s the registry that went up, not the incidents of autism that went up. But they didn’t say that in the study. They never mention the Copenhagen clinic. They never mention the change in the rules in Denmark.

They just show you the graphs, of Thimerisal is banned here, and autism continues to go up. Well, the reason the autism rates rose was because—was an artifact of their data collection processes. It had nothing to do with the reality on the ground of the occurrence of autism. So, and you’ve heard all of their other studies, and you know, they all have this guy Paul Offit. You guys know him? And he is the poster child for the term “biostitute.” This a man who has made himself the spokesperson for the vaccine industry. He portrays himself as an independent scientist, he does not disclose the millions of dollars of transactions.

Let me just close up by saying this, that—and I started out by saying this—that, you know, they, these people, one of the worst crimes that they’ve done—and, you know, I’ve talked to The New York Times, and I said, you know, “You guys had Judith Miller, you know, talking for a year about the Iraq War, and saying how what a great thing it is and covering up the truth from the government spokespeople.” And I said, “There’s no difference what you’re doing, and then you had to come out and apologize,” and the Times publically apologized for that. And I said, “You’re going to have to apologize for this someday, for what you’ve done here. Because what you’ve done here, that war’s going to cost us three trillion dollars, but the treatment of these children, and cost to our society, from what you have done, from what you are doing to this generation of children, is going to far exceed the cost of the Iraq War.” And somebody is going to have to come to terms with that, and ultimately, the American press has completely let down our democracy.

And one of the things you see repeated again and again, is that these are, that the women, you know, who claim that their children—and I’ve gotten now hundreds and hundreds and hundreds and hundreds of letters, and that’s not hyperbole, that’s not exaggeration, from women who had the exact same experience. They bring a perfectly normal two-year old, who’s exceeded all of their milestones, to the doctor to get—who they trust—to get their pediatric flu shots, their MMR vaccines at the age of two.

They get that shot, the child goes into seizure, develops a fever that night, and over the next three months loses her or his ability to speak, to interact with his brothers and sisters, engages in stereotypical behavior—head-banging screaming, biting—and lose all capacity for social interaction. And they’ve lost this child, and they watch it happen, and it’s happened thousands and thousands of times, and you hear that story once or twice, and you say, “Well, maybe it’s an anomaly,” but you hear it a hundred times, and you have to say, “We’ve got to start looking at this.” And nobody—the CDC had said, “No, we’re not going to look at it. We’re going to cut off all funds to anybody that wants to look at it.”

Why isn’t the press asking that question? Why aren’t they asking CDC, “Why don’t you study the Amish, like UPI did? You know, why don’t you study these home-schooled kids?” Thirty-thousand studied by the UPI and no autism in that group. They studied all the Amish in Lancaster, Pennsylvania. There’s only—there should be a hundred and thirty autistic kids. There are four. And three of them were adopted after receiving their vaccines, and the fourth one lived downwind of a coal-burning power plant. So we know what the truth is, and what we’ve got to stop doing is blaming the mothers, which is what they’ve done.

These are not hysterical women. These are people I—you know, I have a child who has allergies, life-threatening anaphylactic allergies, and asthma. My wife knows better than any doctor. She can put her hands on that boy and she knows what’s wrong with him. She knows if his chest is tightening up, she knows exactly what allergen triggered his allergy. She knows what’s gone wrong with that child, and these mothers know what made their child sick.

Anyway, keep fighting, and ultimately we’ll get these people to move, too. You’ve got to not just show up here, this is a really important rally, you’ve got to contact your congresspeople and make sure they understand this issue and that they’re going to operate, and let’s not let them go one more day without some legislation banning this stuff and getting it out.