44 pupils sick after hepatitis B vaccination

44 pupils sick after hepatitis B vaccination
http://www.chinadaily.com.cn/china/2010-04/23/content_9768719.htm
By Zhang Jiawei (chinadaily.com.cn)
Updated: 2010-04-23 16:26

A total of 44 pupils became sick and was taken to the hospital after receiving the hepatitis B vaccine at school on Thursday in Huilai county, in Jieyang of Guangdong province, the Guangzhou Daily reported Friday.

On Thursday morning, 84 pupils got the injection, and some felt ill half an hour later, and 44 had been taken to the hospital as of 5:00 pm, the newspaper said.

The disease control center of Huilai county said they have used more than 90,000 doses of the same batch of hepatitis B vaccine but did not have any abnormal reactions. The rest of the vaccine has been sealed up.

“The vaccine was transported here by the special refrigerated truck of Jieyang’s disease control center,” said Wu Junqiu, head of the disease control center of Huilai county. He said it was impossible that there were any problems in the storage and transportation process of the vaccine, he said.

The newspaper said the vaccine was produced by a Shenzhen-based biological product company and was valid until Sept 1, 2012. And the syringes, which are valid until October 2012, were produced by a Shanghai-based company.

As of 5:00 pm Thursday, 39 of the pupils didn’t have any obvious symptoms and five suffered from throat congestion, Wu said, adding that experts had checked them one by one.

The cause of the reactions is still being investigated.

VRM: Australian Vaccine Scandal

VRM: Australian Vaccine Scandal
http://vaccineresistancemovement.org/?p=3377
24th April 2010 – By Joel Lord

THE REAL REASON SO MANY YOUNG CHILDREN ARE BEING ADVERSELY AFFECTED BY AUSTRALIA’S 2010 FLU SHOT COCKTAIL (WHICH INCLUDES THE PANVAX VACCINE)?

CONTENTS: A STAGGERING 50 MICROGRAMS OF MERCURY IN THE SHOT (MOST CURRENT MULTI-DOSE VACCINES AVG 2.5), H1N1 SUBUNITS (LIVE VIRUS SLIGHTLY MODIFIED WITH DETERGENT), NEOMYCIN (HAZARDOUS TO PREGNANT WOMEN) & POLYMYXIN (ANTIBIOTICS ASSOCIATED WITH KIDNEY FAILURE), BETA-PROPLOLACTONE (CARCINOGEN).

Most multi-dose vaccines currently average 2.5 micrograms of Thimerosal Mercury. Based on EPA standards this is considered a safe level of exposure for a 250 pound adult. Australia’s 2010 Flu vaccine Panvax contains 50 micrograms of Thimerosal; technically a safe level of exposure for a 5000 pound adult. Unless you were born a Mack Truck this is tantamount to attempted murder. Time for the Australian community to rise up against this tyranny with a massive Class Action law suit.

‘Included in the ingredients are two antibiotics, Neomycin and Polymyxin B Sulphate. Both are noted for serious side effects, predominantly kidney failure. It is warned both these antibiotics not be used by pregnant women. Neomycin is in the FDA pregnancy category D. This means that it is known to be harmful to an unborn baby. In the “first tier” of candidates to receive this unregistered, unapproved vaccine, pregnant women are on top of the list. Beta-Propiolactone is another listed ingredient. Ranked as one of the most hazardous compounds (worst 10%) to humans and “reasonably expected to be a human carcinogen” (International Agency for Research on Cancer – IARC, 1999). ?eta-Propiolactone is a disinfectant. Panvax is formulated using chick embryos (Ovalbumin). People who suffer allergy to eggs or anaphylactic reactions may experience problems.’
http://contribute.abc.net.au/_Panvax/blog/718273/32422.html

‘The Australian is reporting that clinical tests were never carried out on this particular vaccine, which was a first-time combination of seasonal flu with Panvax, a vaccine against the H1N1 strain. Australia was the first country to use this type of vaccine, the report said. Panvax was tested on 400 children before its release last year, but the combined shot was not subjected to any clinical trials.’
http://www.newsinferno.com/archives/19877

EARLY VACCINE TRAUMA REPORT (HIGH TEMPERATURES & FEBRILE CONVULSIONS) – The Australian Health Minister, Kim Hames, says 45 children have been taken to hospital suffering high temperatures and febrile convulsions after receiving the vaccination. Dr Hames says the program will be suspended until the department finishes its investigation. He says parents who have had their children vaccinated should take precautions.”If it’s longer than 12 hours ago then there is no risk. But if it’s in the last 12 hours they should make sure that they give their child paracetamol and then take every effort to make sure that the temperature of their child is settled.”
http://www.abc.net.au/news/stories/2010/04/22/2880521.htm?site=news

Febrile convulsions occur in young children when there is a rapid increase in their body temperature. It affects up to 1 in 20 children between the ages of one and four but can affect children between six months and about five years old.

•The attack often begins with the child losing consciousness, and shortly afterwards the body, legs and arms go stiff.
•The head is thrown backwards and the legs and arms begins to jerk.
•The skin goes pale and may even turn blue briefly.
•The attack ends after a few minutes and the shaking stops. The child goes limp, and then normal colour and consciousness slowly return.
•Some children regain consciousness faster than others.
AUSTRALIAN FLU VACCINE DEATH TOLL BEGINS –

‘A family is in mourning after their toddler unexpectedly died less than 12 hours after receiving a seasonal flu vaccination. Two-year-old twin Ashley Jade Epapara had been “perfectly fine” before dying at her home, on Brisbane’s southside, on April 9. Parents David & Nicole are shattered by the mysterious death of their baby girl. “It’s dreadful, it’s a very hard time,” Mr Epapara said. Ashley’s twin sister, Jaime, also received the flu jab at the same time and is believed to have been vomiting the night before her sister died.’
http://www.news.com.au/national/flu-shot-fatality-toddler-dies-12-hours-after-having-vaccination/story-e6frfkvr-1225857872979

‘Queensland police are preparing a report for the coroner into the death of a Brisbane child who had earlier received the seasonal flu vaccine. The two-year-old girl from Upper Mount Gravatt on the city’s southside died earlier this month, the day after she was immunized.’
http://au.news.yahoo.com/a/-/local/7106652/police-investigate-girls-death-after-flu-vaccine/

‘Drug regulators are urgently investigating whether the seasonal flu vaccine is safe for children, after the nation’s top doctor said they shouldn’t receive it. Australia’s chief medical officer Jim Bishop today said health professionals should stop immunizing children under five years old with the vaccine immediately. Professor Bishop is concerned about a spike in the number of West Australian youngsters experiencing fever and convulsions after getting the shot.’

“This is a precautionary measure while the matter is being urgently investigated by health experts and the Therapeutic Goods Administration,” Jim Bishop
http://www.smh.com.au/lifestyle/wellbeing/dont-give-children-flu-jab-chief-medical-officer-20100423-tig6.html

Look how the Vaccine Manufacturer & Australian Government have insulated itself from prosecution:

‘The Australian Government has granted an exemption allowing the dispensing of this vaccine, without it being approved by the Therapeutic Goods Administration (TGA). That means that client consent must be obtained and recorded in detail on special Commonwealth consent forms prior to injection.’

PANVAX: PACKAGE INSERT
http://secure.healthlinks.net.au/content/csl/pi.cfm?product=csppanva11209
http://preventdisease.com/news/pdf/CSL_PANVAX_H1N1_SEPT2009.pdf

MERCURY CHART
http://www.prisonplanet.com/mercury-in-australian-approved-h1n1-vaccine.html

CSL LABORATORIES: VACCINE PROPAGANDA
http://www.h1n1vax.com.au/s1/cs/auvx/1255922570499/content/1255922570467/content.htm
http://www.h1n1vax.com.au/s1/cs/auvx/1249870357676/content/1249870357436/content.htm
http://www.csl.com.au/s1/cs/auhq/1217017237558/Web_Product_C/1253567277997/ProductDetail.htm

Vaccines: Veterinarians Are Better Than Human Doctors

Vaccines: Veterinarians Are Better Than Human Doctors
http://www.huffingtonpost.com/dr-sherri-tenpenny/vaccines-veterinarians-ar_b_533505.html
Dr. Sherri Tenpenny
April 16, 2010

Veterinarians and pediatricians have a great deal in common. Both are highly qualified medical professionals with similar years of education. Both often struggle to determine what is wrong with their patients since pets, like little people, cannot communicate what hurts. Their jobs are not easy, but the premise of their work is simple: Support the health of those in their care and abide by the oath: “First, do no harm.”

Wellness checkups for babies and pets are often synchronized with routine vaccination schedules. Before a shot is given, the consent of the caretaker is required. For human patients, this is where discussions with the doctor can turn dark. Parents are aware of others who have been discharged from a medical practice for questioning vaccines and are wary of bringing up their concerns. Their fears are not unfounded. According to a 2005 survey of the American Academy of Pediatrics (AAP), when faced with parents who refuse immunization, pediatricians reported that they always (4.8 percent) or at least sometimes (18.1 percent) tell parents that they will no longer serve as the child’s physician. Pet owners, on the other hand, have latitude to discuss their vaccination concerns. In many cases, refusing a vaccination has the full support of their vet.

When it comes to dogs, veterinarian professionals can tailor the vaccination schedule to the pet. The Canine Vaccine Guidelines and Recommendations offer suggestions about shots for puppies and adult dogs. Vaccines are categorized as core (recommended for all dogs); non-core (those that are optional); and not recommended (due to poor efficacy and unacceptable risk of side effects). The guidelines recognize vaccination as a medical procedure that needs to be individualized based on the animal’s geographic and lifestyle exposure. Veterinarian professional organizations allow flexibility and encourage doctors to extend vaccination intervals whenever necessary for the safety of the pet.

Most veterinarians agree house pets should be assessed yearly and vaccines – if given at all – should be tailored to an animal’s age, health, and lifestyle. For example, Dr. Matthew J. Toia, Chief Veterinarian Officer for PetLabsMD.com (“Pet-Labs”), a national direct to consumer animal health wellness testing laboratory staffed by licensed veterinarians and veterinary technicians, concurs. “An indoor cat with limited exposure to some diseases may never need some of the common vaccinations. For instance, Lyme’s disease, a regional illness for outside pets in endemic areas, is not necessary for unexposed animals in low risk regions of the country. Cats can forgo this vaccine without an issue.”

His comments are supported by two veterinary associations, the American Association of Feline Practitioners (AAFP) and the Academy of Feline Medicine (AFM). The Advisory Panel on Feline Vaccines (APFV) has guidelines for the selection and administration of vaccinations for cats. Feline shots fall into two basic categories: core vaccines (those recommended for most cats), and ancillary vaccines (those recommended for only a small percentage of cats.) Both of these organizations encourage cat owners to develop a good relationship with their veterinarian so their cat’s vaccination schedule can be openly discussed.

Veterinarians limit the number of vaccines given to puppies on a single visit. A study of more than 1,200 dogs found evidence that the risk of a vaccine-associated adverse event was significantly increased as the number of vaccine doses administered per office visit increased; each additional vaccine significantly increased risk of an adverse event by 27 percent in dogs under10 kg (22 lb) and 12 percent in dogs over 10 kg. Vets are cautious about giving multiple vaccines on one office visit.

Unlike their animal doctor counterparts, the American Academy of Pediatrics (AAP), endorses universal immunization and follows a one-size-fits-all vaccination schedule. The AAP not only assumes that all vaccines are necessary, pediatricians assume that children can all equally tolerate all vaccines given in the standard schedule. As many as six doses – and 18 vaccine antigens – can be given at the same time. The Advisory Committee of Immunization Practices (ACIP) recommends that if a dose is not administered “on time” at the routine two, four and six month checkups, the shot should be given at the next visit. Every dose is considered to be so essential that the ACIP has created a ‘catch up’ schedule for children who have missed even one shot.

Parents have become alarmed by the large number of injections given at one time. To by-pass their psychological concerns, manufacturers have created combination vaccines, such as Pediarix and Comvax, to trick parents into believing that their baby is “only” getting one shot at a time. Pediarix is actually three vaccines in one shot (DTaP, hepatitis B and polio) and Comvax combines the hepatitis B and HiB vaccine into one shot. The ACIP states that, “The use of combination vaccines is preferred over separate injections of its equivalent vaccine components”. The AAP backs up this recommendation, urging combination vaccines to “improve timely vaccination coverage.” Both ACIP and AAP overlook a potentially serious problem with combination shots: If a reaction occurs, it is impossible to determine which vaccine caused the side effect. Animal doctors have figured this out. The Association of Feline Practitioners (AAFP) recommends using single dose vaccines because “increasing the number of antigens in a vaccine also increases the probability associated adverse events.”

Most pediatricians seem to have a “vaccinate no matter what” approach to childhood immunizations rather than ensuring the safety and appropriateness of the individual child. The AAP encourages pediatricians to “work individually and collectively at local and national levels to ensure that all children receive all childhood immunizations on time.” This includes giving vaccines to children, even when they are sick. According to the most recent “General Recommendations for Vaccination”, published in 2006 by the Centers for Disease Control (CDC), there are few reasons for delaying vaccination. In fact, the guidelines state, “Among the most common conditions often inappropriately considered contraindications are diarrhea, minor upper-respiratory tract illnesses (including otitis media) with or without fever, mild-to-moderate local reactions to a previous dose of vaccine, current antimicrobial therapy, and the convalescent phase of an acute illness.” Pediatricians, at the behest of the CDC and the AAP, follow the CDC’s instructions to use of every encounter as an opportunity to vaccinate.

When animals are sick, most vets choose to err on the side of safety. Vaccines are delayed until the pet is healthy to minimize the risk of a reaction. According to PetEducation.com, the decision to vaccinate a sick animal should be made on an individual basis. The vet determines if a shot is appropriate by performing a physical examination and possibly obtaining laboratory tests to aid in the decision. Not so with children. According to the CDC, a routine physical exam and taking a temperature is no longer a prerequisite before vaccinating. If a child appears in the doctor’s office, vaccination should proceed.

Avoiding over-vaccination: Vaccine Titers
Many vets are concerned about the potential for side effects and complications from unnecessary shots and boosters. They order a blood test, called a titer, to determine the need for additional vaccinations. A vaccine titer is test that measures the level of an antibody in the blood, a component usually induced by vaccination. A titer is reported as a ratio of one to a number. The higher that number, the better. For example, a titer of 1:5 is a low titer, and generally implies a susceptibility to disease. A titer of 1:1,000,000 is a very high titer, and implies immunity. It is generally accept that a high titer indicates further vaccination is unnecessary.

While useful as a guide, titer levels have limitations. They only measure one component of the immune system so the level of full protection is unknown. Antibodies cannot be distinguished between those generated by vaccination from those developed after recovery from a disease. Except where vaccination is required by law, all animals can have serum antibody titers measured to determine the need for booster shots. Testing is especially important for pets that have previously experienced an adverse reaction. While not all vets agree with checking antibody titers, the test is available for pet owners who prefer not to follow the conventional practice of annual boosters.

While veterinary medical associations are advocates of vaccination, they insist that immunization is only one component of an individualized, health-care plan for pets. One organization that wants to assist owners in their quest for healthy pets is PetLabsMD.com, the first and only national company to offer consumer-direct laboratory testing. Pet owners can actively participate in the health and wellness for their pets. Tests can be ordered directly through the internet by owners at substantial savings. PetLabsMD.com offers hundreds of screening tests, from preventive profiles for cancer, to tests for infectious diseases, diabetes, nutritional deficiencies, and vaccination titers.

Most importantly, owners will have the added convenience of having their pets’ blood tests done in the privacy of their own homes, avoiding the added stress of taking a pet to the vet. PetLabsMD.com is expanding their nationwide network of veterinarians and veterinary technicians who will come directly to your home to draw the necessary samples. Pet owners without access to a holistic veterinarian can order important health tests directly from Pet-Labs.

Vets vs Peds: A Interesting Comparison
Unlike the AAP that routinely denies any connection between vaccines, adverse events and side effects, the Council on Biologic and Therapeutic Agents (COBTA) at the American Veterinary Medical Association concludes that vaccines can cause problems and should be individualized. The following is an excerpt of their policy:

“There are insufficient data available to scientifically determine a single best vaccination protocol regimen for application to all animals globally. Despite significant advances in our knowledge of antigens and antigen presentation, gaps still remain in our under-standing of the immune system’s acute and chronic reaction to multiple vaccinations. The body of knowledge surrounding the genetic variability within individual breeds or species and the resulting idiopathic responses to vaccination (including vaccine-associated adverse reactions), is increasing but remains too inconclusive to make specific recommendations appropriate for all patients. Consequently, COBTA believes that a customized approach to recommended vaccination protocols is the safest and most effective method to medically address the increasing diversity in patients presented for immunization.”
It appears that veterinarians are more prudent about vaccination than their pediatrician counterparts. A comparison of Vets to Peds can be summarized as follows:

•Veterinarians consider pets as individuals. Vaccines are customized to their needs and lifestyles. For example, dogs that have allergies are often vaccinated less, given smaller doses or not vaccinated at all. If any adverse reaction was experienced from a vaccine, vets are cautious about future vaccines. Unfortunately, the same level of individual tailoring and caution is not found in the pediatric community.
•To avoid over vaccinating, vets often request vaccine titers. Pediatricians do not offer vaccine titers for children; in fact, all vaccines are mandated for all kids, at the risk of expulsion from the medical practice for refusing.
•Veterinarians acknowledge that vaccines can cause serious adverse reactions, including well-documented cancers in cats: feline leukemia and feline sarcomas. Pediatricians rarely, if ever, acknowledge an association between vaccines and asthma, eczema, seizures, gastric reflux, strokes, cancer and autism. Parents are told a side effect is not caused by a recent vaccine; tens of thousands of dollars of medical tests and procedures are ordered to prove it.
•Most veterinarians seem to understand that a one-size-fits-all vaccine policy is not appropriate. Not so for people doctors.

It’s time for pediatricians, the AAP, the CDC, the ACIP and all others involved with human vaccination programs to acknowledge that vaccines have risks and can cause serious harm, including death. If animal doctors can work with owners to individualize vaccination schedules, to avoid over-vaccinating though vaccine titers, and to encourage participatory care, human doctors need to start doing the same. Parents need to demand care that is as good for their children as it is for their pets.

Flu jab fears grow as toddlers hospitalised

Flu jab fears grow as toddlers hospitalised
http://www.theaustralian.com.au/news/nation/flu-jab-fears-grow-as-toddlers-hospitalised/story-e6frg6nf-1225857634415
April 24, 2010

CLINICAL tests were never carried out on the latest seasonal flu vaccine – a first-time combination of seasonal flu with the feared swine flu H1N1 – that has left a baby girl fighting for her life in a Perth hospital and sparked fits, fevers and vomiting in up to 60 toddlers across the country.
Health officials were last night trying to determine what had caused the reactions in the children, mostly in Western Australia.

The country’s chief medical officer, Jim Bishop, yesterday ordered doctors in all states to stop giving the flu vaccine to children under five.

Professor Bishop said non-swine flu strains in the vaccine may have caused the reactions.

For the first time in the world, the flu shot rolled out in Australia last month combined two strains of seasonal flu, as well as H1N1.

Professor Bishop said the Panvax vaccine – the swine flu jab – was “safe”, but said the combined flu shot had been suspended for young children as a “precautionary measure” pending investigation by the Therapeutic Goods Administration, which approved its use last month.

Start of sidebar. Skip to end of sidebar.
Related CoverageLittle girl died in cot after flu jab
The Australian, 2 hours ago
Child critical from WA flu vaccine
Perth Now, 1 day ago
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Daily Telegraph, 2 days ago
Flu jabs upset Qld kids
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Fevers in 60 children linked to flu jab
Adelaide Now, 2 days ago
.End of sidebar. Return to start of sidebar.
Panvax was tested on 400 children before its release last year, but the combined shot was not subjected to any clinical trials.

CSL, which manufactures both vaccines, has stopped distributing children’s doses nationally “to reduce the risk of inadvertent administration in this age group”.

One angry West Australian mother, who only wanted to be identified as Sharon, said if officials had acted earlier, the one-year-old girl in critical condition in hospital may never have become sick.

Sharon had three of her four children vaccinated two weeks ago and all three needed hospitalisation after suffering from fevers, vomiting and fits. She said it was a frightening experience after her three-year-old, Alivia, turned purple and began shaking. One of her one-year-old twins, Lateesha, later started convulsing.

Peter Richmond, associate professor at the University of Western Australia’s school of pediatrics and child health, said the vaccine was not subjected to trials.

“As with each year’s seasonal influenza vaccine, this year’s seasonal influenza vaccine isn’t subject to specific trials in children before it’s used,” he said.

He added that three trials of different combinations of seasonal flu vaccines had been conducted in children and no concerns had been raised.

Professor Robert Booy, the director of clinical research at the National Centre for Immunisation Research and Surveillance – who helped supervise the swine flu trials – said the combination of flu strains could not be the cause of the problems.

Mercury linked to immune changes seen in autoimmune disease

Mercury linked to immune changes seen in autoimmune disease.
http://www.environmentalhealthnews.org/ehs/newscience/mercury-linked-to-immune-changes-in-gold-miners
April 13, 2010

Gardner, RM, JF Nyland, IA Silva, AM Ventura, JM deSouza and EK Silbergeld. 2010. Mercury exposure, serum antinuclear/antinucleolar antibodies, and serum cytokine levels in mining populations in Amazonian Brazil: A cross-sectional study. Environmental Research http://dx.doi.org/10.1016/j.envres.2010.02.001.

Synopsis by Jennifer F. Nyland

Mercury increases the risk of developing autoimmune symptoms – similar to those seen with arthritis – in miners from Amazonian Brazil who work with the metal.

A study in people adds to the growing evidence and concern that mercury can alter the immune system in ways that may promote autoimmune diseases such as arthritis and lupus. The researchers report that mercury increased levels of key signaling and antibody markers measured in the blood of Brazilian gold miners who use the metal to extract the gold from river sediments.

This is the first time mercury has been shown to affect in people the immune signaling proteins that are responsible for inducing inflammation. The results support recent animal studies that find similar changes to rodent immune systems after mercury exposure. The study adds to the few other human studies on the subject, which are less consistent in their conclusions.

Mercury is a well known toxicant. Exposure to even small amounts can damage the brain and nervous system in ways that reduce motor, verbal and attention abilities. This is especially true for developing fetuses and children.

Its effects on the immune system are still being teased apart.

In the United States, most people are exposed to mercury – by eating certain species of fish – most notably large predators such as tuna, swordfish and tilefish. Federal fish advisories warn against eating too much of certain species or too much fish caught from contaminated waterways so as to limit exposure to the metal.

The researchers studied five separate populations: a gold mining camp where mercury is used to extract the gold and two diamond and two emerald mining camps where mercury is not used. Mercury exposure was determined through questionnaires, urine samples and hair samples. Overall, mercury levels and the ranges were higher than what is reported for people who live in the United States.

When blood from gold miners was compared to diamond and emerald miners, changes were found. Levels of certain antibodies and proteins called cytokines were increased only in the gold miners. These increased protein levels are often used to help diagnose some autoimmune diseases like lupus or rheumatoid arthritis.

Even though the miners were exposed through their work to periodic and relatively high levels of mercury, the findings apply to others since mercury exposure from multiple sources is a global problem. Importantly, these changes were not related to whether the miners had malaria, giving the findings a broader application worldwide. Malaria is a common parasitic infection in many parts of the world, but not in the United States or Europe, and it too can cause changes in the immune system. Since the immune changes observed in this study were unrelated to whether or not the miners were infected, the authors can conclude that the effects are most likely from mercury exposure.

Alert: Protect Your Right To Natural and Bio-available Vitamin B-6!

Alert: Protect Your Right To Natural and Bio-available Vitamin B-6!
http://www.anh-usa.org/alert-protect-your-right-to-natural-and-bio-available-vitamin-b-6/

April 6, 2010

Human beings cannot live without vitamin B-6. It is also important for the prevention of cancer and the prevention and treatment of seizures, anemia, mental disorders including schizophrenia, carpal tunnel syndrome, and other conditions. Its effect on carpal tunnel can seem almost miraculous.

A natural form of the vitamin, Pyridoxamine, was recently yanked off the market by the FDA. Why? Because a pharmaceutical company, BioStratum, wanted sole use of pyridoxamine in a drug, a drug which may or may not ever appear. The company filed a so-called citizens petition and the FDA agreed, notwithstanding protests from ANH-USA, other organizations, and thousands of citizens. You might ask: how can Pharma take a supplement off the market and claim exclusive use of it as a prescription drug? The FDA does not presently feel obligated to answer this question.

Unfortunately, this isn’t all the bad news about vitamin B6. All forms of B-6, natural or synthetic, must be converted to P5P, another natural form, for the body to use it. Another drug company, Medicure Pharma, wants sole use of P5P and so has petitioned the FDA to ban its use as a supplement as well.

Medicure has yet to market a drug made from P5P, but wants the ban to take place now. And never mind that any individual unable to convert synthetic B6 to P5P would have to rely solely on Medicure’s product to stay alive.

How does Medicure think it can get away with this? Its petition states rather candidly: “Pharmaceutical companies developing new drugs must be protected from companies that may seek to market the ingredients in those drugs as dietary supplements. The marketing of such products has the potential to undermine the incentive for the development of new drugs because many people may choose to purchase the supplements rather than the drugs.”

This is not of course a case of supplement producers creating a product to compete with an existing prescription drug. It is just the reverse. P5P, the natural and bioactive form of B6, has existed in food for as long as there have been humans and has been available as a supplement for years. Medicure seems to be saying: If it seems profitable, let’s just turn a critical vitamin, one essential for human life, into a drug, make it available only by prescription, and mark up the price. This is truly outrageous.

The FDA has not yet responded to Medicure’s petition. We have asked you in the past to send a message to the FDA and Congress protesting Medicure’s P5P grab, and the time has come to send some more messages. So if you haven’t sent in a message to the FDA and Congress yet, or even if you have, please send one today.

While we are discussing Vitamin B6, here is the latest scientific report. An analysis of 13 U.S., European and Asian studies of vitamin B6 and colon cancer, conducted from 2002-2009, has been published in a special edition of the Journal of the American Medical Association. Studies of the range of B6 doses found that vitamin B6 taken in higher doses reduced the risk of colon cancer by 21 percent. In one study, Dr. Susanna Larsson and her colleagues at Sweden’s National Institute of Environmental Medicine reported an inverse relationship between the intake of vitamin B6 or pyridoxine and the risk of colon cancer. Dr. Larsson linked the effect to bloodstream levels of pyridoxal-phosphate (PLP), the main active coenzyme form of vitamin B6. Pyridoxal-phosphate is also known as pyridoxal 5-phosphate or (as we referred to it above) P5P.

Don’t let the FDA take away our access to the natural and most bioavailable form of B6, P5P. Please take action now.

Is Aborted Fetal DNA in Vaccines Linked to Autism

Is Aborted Fetal DNA in Vaccines Linked to Autism
http://housegalleryview.blogspot.com/2010/03/is-aborted-fetal-dna-in-vaccines-linked.html
Wednesday, March 24, 2010

Last Wednesday I was invited by Representative Laura Brod to a conference call meeting with Theresa A. Deisher, Ph.D. The purpose of the call was to discuss the vaccine-autism controversy and her recent studies.

Dr. Deisher has an impressive background and credentials. She is an internationally renowned expert in the field of adult stem cell therapies and regenerative medicine, brings 17 years of experience in scientific and corporate leadership positions involving research, discovery, production and commercialization of human therapeutics. Dr. Deisher’s penchant for groundbreaking scientific discovery and her distinguished scientific research has resulted in 23 patents issued. She has published numerous scientific manuscripts and is a frequent invited lecturer and guest speaker in the area of stem cell technology and regenerative medicine.

Throughout her career, Dr. Deisher has been recruited by some of the country’s top biotechnology companies, including Genentech, Repligen, ZymoGenetics, Immunex and Amgen. She has managed and mentored undergraduate honors students, post-doctoral fellows, scientific executives and over 20 research assistants/scientists at all levels of responsibility.

Dr. Deisher graduated with honors and distinction from Stanford University, and obtained her Ph.D. in Molecular and Cellular Physiology from Stanford University.

Subsequent to obtaining her Ph.D from Stanford, Dr. Deisher was recruited by Repligen Corporation (Cambridge, MA) and accepted a position as Research Scientist where she managed a staff of associates and scientists and directed the development of research and clinical assays in support of Phase I and Phase II clinical trials for various Repligen developmental efforts. Additionally, Dr. Deisher was selected by Sr. Management to participate in strategic alliance initiatives, including serving on the Repligen / Eily Lilly joint development committee.
Following Repligen, Dr. Deisher accepted a position at ZymoGenetics, Inc (Seattle, WA) as Sr. Scientist, Cardiovascular Biology. While at ZymoGenetics, Dr. Deisher’s research and discovery in the area of cardiovascular biology led to the filing of dozens of patents. Dr. Deisher was the first person world-wide to identify and patent stem cells from the adult heart, including what are now called ‘very small embryonic-like stem cells’. Her discovery remains one of the most significant discoveries in the area of stem cell research. Within the field of regenerative medicine, Dr. Deisher is also a patented inventor of the most potent mesenchymal growth factor ever identified (licensed to Serono for clinical development), and of the use of cytokines to mobilize adult embryonic-like cells.

Following ZymoGenetics, Dr. Deisher was named Sr. Staff Scientist, Vascular Biology at Immunex (Seattle, WA) where she was the project leader for both the Antithrombotic division and the Inflammation and Myocardial Repair division.

Dr. Deisher was named Principal Scientist at Amgen, Inc. (Seattle, WA) following Amgen’s acquisition of Immunex. She led multi-disciplinary teams working on the biology and commercial development of novel co-stimulatory pathways involved in the initiation and progression of cardiac failure. Her research interests encompassed stem cell therapies for myocardial regeneration. Additionally, Dr Deisher introduced revolutionary non-invasive imaging technologies for pre-clinical research to the company, including ultrasound (echocardiography) and near-infrared imaging. As a result, the company was honored as an official ‘Site of Excellence’ by Philips Medical for her department’s pioneering work.

Most recently, Dr. Deisher served as Vice President of Research and Development for Cellcyte Genetics Corporation, a post she held until October 2007 prior to founding AVM Biotechnology.

Dr. Deisher spoke with us for nearly an hour and the first thing that struck me, was that most people had never heard that aborted fetal DNA was used in the manufacturing of vaccines. This is morally reprehensible to me and appeared to be to the other legislators in the room as well. Because there has been a concern with the increase in autism, recent literature suggests that l out of 100 children are now impacted by autism spectrum disorder. Dr. Deisher has been studying the link and wants to alert the public about the possible dangers, as well as the wrenching moral dilemmas for parents and consumers.

How could the contaminating aborted fetal DNA create problems? According to Dr. Deisher, “It created the potential for autoimmune responses and/or inappropriate insertion into our own genomes through a process called recombination. There are groups researching the potential link between this DNA and autoimmune diseases such as juvenile(type I) diabetes, multiple sclerosis and lupus.” Her organization, Sound Choice Pharmaceutical Institute is focused on studying the quantity, characteristics and genomic recombination of the aborted fetal DNA found in many of our vaccines.

Dr. Deisher also asks the following questions: “Could genomic insertion of the aborted fetal DNA, found in some of our childhood vaccines since 1979 be an environmental trigger for autism? Could the fact that genes critical for nerve synapse formation and nervous system development found on the X chromosome provide some explanation of why autism is predominantly a disease found in boys? Could the “hot spots” identified in these autism associated genes be sites for insertion of contamination aborted fetal DNA?”

These are important questions and I am glad that this issue has been brought to the attention of the legislature. I will inform you in the future of further developments.

Vaccine Near, So Fear Mongering Starts Over Another Mild Disease

Vaccine Near, So Fear Mongering Starts Over Another Mild Disease
http://gaia-health.com/articles201/000234-vaccine-near-so-fearmongering-starts-for-another-mild-disease.shtml

by Heidi Stevenson
19 April 2010

Have you ever heard of respiratory syncytial virus (RSV)? In all likelihood, you haven’t, though you’e probably had it. You or your parents most likely called it a cold. Now though, there’s an RSV vaccine on the horizon, so the fear mongering is starting. Of course, to back up the fear, a study was done to give the impression that the disease is terrible. It was funded by vaccine promoters.

The Lancet has just published the study, which was financed by the Bill & Melinda Gates Foundation and the World Health Organization (WHO). The WHO is now being examined for its handling of the swine flu so-called pandemic. They stand accused of being in bed with pharmaceutical corporations to promote the use of vaccines. One of the Gates Foundation’s primary goals is to promote vaccines.

So, it should come as no surprise that the study’s results refer to RSV in terms that imply a severe problem. The article refers to its “global burden”. Because it’s a mild disease in normally healthy people, it focuses on developing nations. The study’s result was, of course, a foregone conclusion:

“The development of novel prevention and treatment strategies should be accelerated as a priority.”

Hint: That means focus on vaccinations, not on poverty, the real issue behind most deaths from minor illness.

The fear mongering has already started. BBC News has reported on HSV, describing it as “the single largest cause of lung infection in children”. That sounds so very terrible, but the reality isn’t necessarily so bad. After all, if you have a chesty cough, you have a lung infection. Do you automatically panic over it? Usually, such infections are referred to as the common cold.

RSV is a common disease at all ages. Unlike most viruses, which provide lifetime immunity after infection, only limited immunity occurs. It’s usually a mild disease, generally called a cold. In those with weakened immune systems, such as premature babies, it can be a serious disease, even leading to death. However, that happens in only a minuscule percentage of cases.

The Lancet focused on a single year, 2005. The authors reported that, worldwide, 66,000-199,000 children under age 5 died from RSV that year. This was misreported by BBC as simply 200,000 deaths in children under 5 worldwide, with the claim that it’s an annual figure, though the study was clear in pointing out that it referred only to a single year. Only 1% of these deaths occur in industrialized modern nations. The rest happen in the developing world, where malnutrition, lack of water, and poor sanitation are rampant. In other words, health is already compromised.

Rather than focusing on the most obvious issue relating to deaths from RSV, poor health from lack of the basic needs, the goal is to trot out a new vaccine. To have it accepted requires that people in the wealthier nations see it as a good thing—and that requires developing a hefty fear of the disease.

Big Pharma is brilliant at manipulating the media and creating false impressions through the use of phony grassroots groups and bribing researchers and doctors. They’ve already started to create an atmosphere of fear around the respiratory syncytial virus and its cold-like symptoms.

Once the vaccine is routinely administered to small children in industrialized nations—at enormous profits, of course—it can be pushed on impoverished people elsewhere. Of course, one must question who will bear the cost—but there can be little doubt. The WHO’s budget ultimately comes from the wealthier countries, and that means you and me.

Through all of this, consideration for safety will be nonexistent among the producers of the vaccine or the mainstream media or government agencies pushing it or mainstream medicine administering it. Those who express safety concerns will be marginalized, as always. Bit by painful bit, the truth will come out. But how long will it take? The experience of the last hundred years suggests that no amount of ill health or lives damaged will curtail Big Pharma from making its profits.

Scientists fear MMR link to autism

Scientists fear MMR link to autism
http://www.dailymail.co.uk/news/article-388051/Scientists-fear-MMR-link-autism.html
By SALLY BECK

New American research shows that there could be a link between the controversial MMR triple vaccine and autism and bowel disease in children.

The study appears to confirm the findings of British doctor Andrew Wakefield, who caused a storm in 1998 by suggesting a possible link.

Now a team from the Wake Forest University School of Medicine in North Carolina are examining 275 children with regressive autism and bowel disease – and of the 82 tested so far, 70 prove positive for the measles virus.

Last night the team’s leader, Dr Stephen Walker, said: ‘Of the handful of results we have in so far, all are vaccine strain and none are wild measles.

‘This research proves that in the gastrointestinal tract of a number of children who have been diagnosed with regressive autism, there is evidence of measles virus.

‘What it means is that the study done earlier by Dr Wakefield and published in 1998 is correct. That study didn’t draw any conclusions about specifically what it means to find measles virus in the gut, but the implication is it may be coming from the MMR vaccine. If that’s the case, and this live virus is residing in the gastrointestinal tract of some children, and then they have GI inflammation and other problems, it may be related to the MMR.’

The 1998 study by Dr Wakefield, then a reader in gastroenterology at the Royal Free Hospital in North London, and 12 other doctors claimed to have found a new bowel disease, autism enterocolitis.

At the time, Dr Wakefield said that although they had not proved a link between MMR (measles, mumps, rubella) and autism, there was cause for concern and the Government should offer the option single vaccines – instead of only MMRs – until more research had been done.

The paper – and the confused interpretation of its findings – caused uproar and led to many parents withdrawing their co-operation for the triple jab. Ten of the paper’s authors also signed retractions on the interpretation but stood by the science.

This is the second independent study to back up Dr Wakefield. In 2001 John O’Leary, Professor of Pathology at St James’s Hospital and Trinity College, Dublin, replicated his findings.

Last night Dr Wakefield said: ‘This new study confirms what we found in British children and again with Professor O’Leary. The only exposure these children have had to measles is through the MMR vaccine.

‘They were developing normally until they regressed. They now suffer autism and bowel disease.

‘The Department of Health and some of the media wanted to dismiss our research as insignificant. The excuse was that no one else had the same findings as us. What they didn’t say is that no one else had looked.’

A spokesman for the Department of Health said they had not read the American report, but added: ‘MMR remains the best form of protection against measles, mumps and rubella.’

Read more: http://www.dailymail.co.uk/news/article-388051/Scientists-fear-MMR-link-autism.html

Pollen, pollen go away…

Nicholas’s poor eyes always seem to get the brunt of allergy season. He gets better, more managable once it rains, but until it rains, it’s brutal. The whites of his eyes get all distorted, swollen and puffy to the point of looking like they are cemented shut. This year, Claritin failed us. Last year, we did well on Claritin with the occasional dose of Benedryl, but Zyrtec failed us. I had to move to Benedryl to keep his eyes okay and this was on top of keeping him in the house on absolutely beautiful days where all he wanted to do was go outside and play. Benedryl quickly started to fail. We went from dosing 2x a day to almost every 2 hours and that’s when I decided to get off of this crazy roller coaster.

A homeopath recommended Euphrasia Officinalis 30C and it worked like a charm and in less than one hour. Boiron makes it and I found it at my local Whole Foods and Vitamin Shoppe for less than $7.00.

Just sharing in case it helps someone else.

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