Gender: Female
Status: Married
Age: 38
Sign: Cancer
City: Shipwrecked in
State: Oregon
Country: US
Signup Date: 5/13/2007
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Thursday, July 30, 2009
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http://thefeministbreeder.typepad.com/the_feminist_breeder/2009/05/a-cesarean-consent-form-for-the-ob-to-sign.html
I am so pissed off at the lack of patient choice and the asinine
mentality of doctors here. I am very, very frustrated. So, I thought I
would vent some of that frustration by doing something
semi-constructive. To that end, I wrote my own consent form. After all,
if the doctor wants me to sign theirs, they should sign mine first.
Here 'tis.
I,
the undersigned physician, have, in violation of the Consumer Bill of
Rights and Responsibilities, the Emergency Medical Treatment and Active
Labor Act, the Patient Self Determination Act, the ethical guidelines
of the American Medical Association and the American College of
Obstetricians and Gynecologists, Constitutional Law (the right to
privacy and self determination protected by the 1st and 14th
amendments), international tort law, and case law (of particular
interest "In re A.C.", 1987, "In re Fetus Brown, 689 N.E.2d 397, 400
(Ill. App. Ct. 1997)", and "In re Baby Boy Doe, 632 N.E.2d 326 (Ill.
App. Ct. 1994)") and the Patient Rights as determined by this
institution, deprived my client,________________, of her right to self
determination and her right to bodily integrity by ignoring her
repeated refusal for delivery by repeat cesarean section. I acknowledge
that by refusing to honor my client's denial of consent, I have not
only violated the above laws, but I also affirm that I have used
unwarranted and unethical pressure including emotional threats to my
client's and her unborn child's life and safety, in my attempts to
obtain such consent. I further affirm that I have stressed the risks of
vaginal birth after cesarean, but neglected to inform my patient of the
risks of delivery by repeat cesarean section. I further affirm that I
understand, that should I resort to physical force, including but not
limited to physical or chemical restraints to compel my client's
cooperation, I will be guilty of criminal battery, which is defined as
"any form of non-consensual touching or treatment that occurs in a
medical setting".
In compensation for the above violations of my client's rights, I hereby guarantee the following:
a
healthy baby, born in perfect condition, with no physical, mental or
developmental defecits whatsoever, whether arising from surgery or any
other cause
no complications for the infant, including but not
limited to: persistent pulmonary hypertension, transient tachypnea of
the newborn, respiratory distress syndrome, iatrogenic prematurity,
lacerations, or hematoma
a speedy, uncomplicated post-operative
recovery for my client. Specifically, I guarantee that my client shall
not experience nerve damage, organ damage, hemorrhage (whether
sufficient to require transfusion or not), disability or disfigurement,
intraoperative or postoperative infection of the wound or surrounding
skin and tissues, post partum depression and post partum post traumatic
stress disorder (PTSD), and other conditions not listed here.
Signed,
Note: this was written by a nurse!
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Monday, February 09, 2009
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http://www.mountainroseherbs.com/ I'm thinking of doing my herbology course through http://www.schoolofnaturalhealing.com. There's a correspondence option there, which, as anyone with small children knows, is essential for time management. Now, all i need is for God to rain the money down on me and i can get started!
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Saturday, August 09, 2008
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The Real Dangers of Disposable Nappies
We all know that modern disposable nappies are produced using valuable resources such as petroleum based plastics, and wood pulp, as well as adhesives and a host of chemical products- and we all know this is harmful to the environment. But as parents, it is also our duty to carefully evaluate these chemicals and assess their potential consequences when using them on our infants.
Taken from the a large disposable nappy manufacturers website, they list some of the components that make up their nappies:
'The inside absorbent padding on our nappies is made of wood cellulose fibre, a fluffy paper-like material, and a super-absorbent material called polyacrylate. Other materials used include polypropylene, polyester, and polyethylene. These are all synthetic materials designed to enhance the fit of the nappy and the help stop leaks. The elastic strands in all our nappies are made of synthetic rubber to provide a snug but gentle fit for baby. In addition, our nappies feature an all-over breathable outer cover"
This 'list' is described in a promotional manner, however these synthetic substances and plastic ingredients are hardly reassuring when you take a closer look….
Sodium Polyacrylate- Ever noticed little gel balls on your babies bottom after wearing a disposable nappy? Welcome to Sodium Polyacrylate - A Super Absorbent Polymer that turns urine into gel and can absorb 100 times its weight in liquid. This is a substance which was banned from use in tampons in 1985 due to its link with Toxic Shock Syndrome. Employees in factories producing Polyacrylate suffer from female organ damage, fatigue and weight loss. No long term studies have been conducted to assess the risks of 24/7 exposure to this compound on a babies vulnerable genitals.
Due to its extreme absorbency, this chemical has been found to draw moisture from the skin, causing severe nappy rash and bleeding of perineal and scrotal tissue. Sodium Polyacrylate is also lethal to cats when inhaled.
Dioxin- The most toxic of all cancer-linked chemicals, and a by-product of the paper bleaching process. Dioxin has been known to cause birth defects, skin disease and liver damage.
TBT (Tribulytin)- This substance was found in Pampers® Ultra Dry nappies in May 2000. TBT is one of the most toxic substances ever produced, it damages the immune system and impairs the hormonal system. There is also speculation of a link with male sterility.
Xylene, Ethylbenzene, Styrene & Ispropylene - These are some of the chemicals which were reported to be released from disposable nappies in a study published in the Archives of Environmental Health (1999). Anderson Laboratories exposed lab mice to various brands of disposable nappies and found them to suffer from asthma like symptoms, including bronchoconstriction and eye, nose and throat irritation as a direct result. Xylene and Ethylbenzene are suspected endocrine, neuro and respiratory toxins; Styrene is a suspected carcinogen and respiratory toxin; Ispropylene is a suspected neurotoxin.
Male Infertility- In 2000, a scientifc study was conducted at Kiel University in Germany which indicated that the widespread use of disposable nappies, which heat the testes above body temperature, is a significant factor in the declining fertility rates in Western European males.
Nappy Rash- Reported instances of nappy rash rose from 7.1% to a whopping 61% with the increased use of disposable nappies according to a review of Proctor and Gambles own studies (The Landbank Consultancy Limited, 1991). How very handy for Nappy Rash Cream manufacturers!
So, we can see that the petroleum based plastic and wood pulp compounds of the disposable nappy are harmful enough to us and our world, but adding chemicals such as Sodium Polycrylate and Dioxin into the mix, as well as allergy causing irritants like fragrances and deodorants, we could potientally have serious problems.
There has currently been no where near enough studies assessing the long term risks of the modern disposable nappy- especially because they are ever changing, and always being 'added to'- so really, is it worth taking that risk?
Article taken from www. babies-nappies. co. uk
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Saturday, August 09, 2008
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Hidden Dangers of Disposable Diapers
http://www. awchamburg. org/AWCH_GettingSettled/AWCH_Child_Family/AWCH_Diapers. html
* Researched by Jennifer M Submitted November 2000
Isn't it amazing to think that most of us were raised in cloth diapers, but most of our children have grown up in disposables? Believe it or not, it is not too late to reverse this trend.
With our first child, my husband and I were planning on using disposable diapers from the start; but our midwife encouraged us to look into using cloth diapers. After we went to the store (Rundum, Gertigstrasse 57, Tel. (040) 27 87 76 66) and got some advice and took a look at the cloth diapers out on the market, we decided to go with the cloth diapers after all. It did not look any more difficult than disposables, and it would save money, as well as do some good for the environment. Most of our friends reacted skeptically when we told them; but after our success story, most of those friends have ended up using the same cloth diapers on their children. At the time, the hidden dangers of disposable diapers were still hiding from me, but now I know the difference.
The Environmental Issue
There are those who claim that disposable diapers are better for the environment because no water, energy or soap is wasted on washing or drying them as with cloth diapers. The question is: how did the disposables get manufactured in the first place? Certainly a fair amount of water and energy were needed to produce them, not to mention valuable raw materials like wood and oil. And who walks to the store to buy their disposable diapers? Certainly not people pressed for time, which is the main argument against cloth diapers -- that they take up too much time. And what about waste disposal costs? Also, did you know that in the U.S. , it is illegal to put human fecal matter in residential garbage? Which person pressed for time shakes the poop out of his or her disposable diaper before disposing of it? Did you also know that experts speculate that a disposable diaper can take anywhere from 100-500 years to biodegrade in a landfill? This means that EVERY SINGLE disposable diaper ever used is still out there decomposing somewhere!
Even the argument that the soaps used in laundering cloth diapers are harmful and eventually end up in our ground water are exaggerated. Most people who choose cloth diapers also choose an environmentally friendly soap, and then the waste water from laundering a load of cloth diapers is benign. Take in comparison the impact of the waste water from the manufacture of disposable diapers which often contains dioxins, solvents, biocides and even heavy metals; and then a little environmentally friendly soap seems harmless.
What is better for your baby?
Even though disposable diaper manufacturers spend millions of dollars every year on advertising that their diapers feel "drier", no scientific evidence indicates that diaper rash occurs more often with cloth diapers than with disposables. In fact, because disposables feel drier, many parents postpone diaper changes too long and the bacteria from the urine remains in longer contact with the baby's skin causing redness and irritation. In addition, because the plastic in disposable diapers prevents the proper circulation of air, ammonia from the bacterial-breakdown of urine is unable to escape causing further irritation; whereas cloth diapers with a wool or micro-fiber cover allow the baby's skin to breathe, thereby eliminating this source of irritation. The best way to prevent diaper rash, however, is frequent diaper changes, regardless of which kind of diaper one uses.
What is most frightening about disposable diapers is the unknown or passively ignored presence of toxic chemicals. One such chemical is dioxin, a highly toxic by-product of the bleaching process. Secondly, sodium polyacrylate, the clear gel-like substance you often find on your baby's genitals after a diaper change, gives disposable diapers their super absorbant characteristic. Its use in tampons was banned in 1985 because of its link to Toxic Shock Syndrome. And most recently, TBT or Tributylin was found in disposable diapers in Europe. TBT is ranked by the World Health Organization (WHO) as one of the most toxic substances in use in consumer products in the world today. It is a biocide and is used in killing or preventing the growth of bacteria. And although the WHO has also revealed that the amount of TBT found in disposable diapers poses no threat to the health of a baby, the question still arises: Why is such a toxic substance needed in a diaper? And furthermore, even though the TBT in diapers does not adversely effect those wearing the diapers, what about the safety of ground water from decomposing diapers in landfills?
What's more, new scientific studies have linked disposable diapers and their harsh perfumes and toxic substances to the increase of asthma in today's society. Laboratory rats exposed to disposable diapers straight out of the package have suffered increased eye, nose and throat irritation, as well as bronchioconstriction similar to that of an asthma attack (according to Rosalind C. Anderson, lead author of the report "Acute Respiratory Effects of Diaper Emissions", Archives of Environmental Health, 54, October 1999).
The Convenience Issue
Admittedly, disposable diapers do have the appearance of being more convenient. Those who claim that disposables are more convenient and time-saving, however, seem to forget that someone has to go out to the store to buy them, carry them home, and take out the trash can when they are used up. And although you do have to wash cloth diapers, the few minutes it takes to start up a load of laundry (which you have to do more often with small children in the house anyway) is much less than the effort it takes to acquire and dispose of disposable diapers.
What's The Hype?
You ask yourself. My child wears disposable diapers and does not have asthma, nor do I notice any harmful side-effects from all the toxic substances. That may very well be true, but you should also ask yourself if the alleged "convenience" of disposable diapers is worth the cost to the environment and to the health of your child. Each purchase of disposable diapers is an economic incentive for disposable diaper companies to continue producing products found to be extremely harmful not only to our children, but also to our environment.
Environmentally Friendly Disposables
Such a creature does exist: Moltex Öko Disposable Diapers. They are rated by the German Öko-Test (Heft 28/99) Consumer Product Testing publication as "Empfehlenswert" or Recommendable. In America, look for the brand Tushies: they have been bleached via a non-toxic method and contain no polyacrylate granules. They are a good compromise when traveling. Who wants to lug around a suitcase full of moist, stinking cloth diapers?
Cloth Diapering -- Getting Started
Cloth diapers are not what they used to be! No one has to use pins or spend hours folding square pieces of cotton into complex origami-type contraptions anymore. The cloth diapers my family uses (from Mother-ease) are pre-formed, completely adjustable to fit babies from 3-18 kilograms, and are fastened via snaps and/or velcro tabs. A micro-fiber cover goes over the top to keep the moisture in, but at the same time, allows the baby's skin to breathe. In addition to a cloth inlay for extra absorbency, there is a paper inlay, which is then flushed down the toilet and with it, most of the fecal matter. Soiled diapers are rinsed out and stored in a diaper pail. Every other day, the diapers are washed with the rest of the baby laundry and voilá!
We use non-bleached, organic cotton diapers and inlays (that way we support sustainable cotton agriculture and are assured that no harmful pesticides or dioxins are present in our diapers). The paper inlays are also from organic raw materials and are bleached via non-toxic methods. We use a phosphate-free detergent, specially designed for washing at a lower temperature (Vollwaschmittel from the store, Spinnrad); and we hang our diapers out to dry. What's more, we have the peace of mind, knowing that we are offering our babies the best possible diaper care, as well as doing our part in protecting our environment.
cloth diaper outlet: clothdiaperoutlet. com for great prices on cloth diapers.
for Tushies and Seventh Generation diapers: diapers. com <~~~get $10 off your first order with this code:FIVE7697
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Wednesday, July 16, 2008
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"No one likes to hear the words, "I don't like you." Some people will do almost anything to be liked, even at the expense of their own happiness, values, beliefs and standards. Some people's overwhelming need to be liked is the very thing that makes them hard to like. In fact, for many people, the need to be liked is actually a significant barrier to personal and professional growth. Not everyone is going to like you, and that's OK. While it's normal to want to be needed, liked, loved and important to others, it's also crucial to get clear about who you are and what you stand for, and to live a life consistent with those values. When it comes to this issue, you might want to ask yourself: Do I speak the truth (while still exercising care, wisdom and understanding) even if it's not popular to do so? Do I live a life which is consistent with my core values? Do I operate with integrity? Do I believe that my motives are good? Is it my goal to be a positive influence in the lives of others? Am I happy to disagree with people I like? Do I (really) like me? If you answered no more often than yes, you may want to make a few changes. If you really want to be liked, then stop trying to be liked and start being you." ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
I found this article linked in my daily Mercola newsletter. Haha! It reminded me of several people i know, including myself, but I have to say that i'm doing much better on this subject now that i'm "old." After many years of being afraid of "rocking the boat" i've come to a place where i have peace. Seriously, it's not about whether i like myself of not, it's a matter of priority and practicality. I'm scum and i know it and that's what keeps me close to Jesus, but at the same time, that which draws me close to him also keeps me wanting to focus on faith, virtue, and truth, all being priority. There is an endless supply of things to argue about in life from issues of politics, the sanctity of life, and the meaning of the universe to who looks "hottest" in a bikini, which is better McDonald's or Burger King, or who spit on who first in the back seat of the car. One really has to get a grip on what is really worth fighting for or, as i like to put it, pick your battles wisely. That's practicality. So, really, does it matter if i am liked or not? Will the world suddenly stop turning if i am not liked? Will i end needless suffering if i am? HA! Nice thought, eh? The only thing that i take into this consideration is that i am setting the example for my faith and standard, by which i will ultimately be judged by my creator anyway. So, forgive me in advance if i take a turn and make a mistake that offends, know that i am not on this earth to please others, but am doing my best to live my life the way that i know will please my creator and, since i am scum, i am likely to make mistakes. If i attract by my show of the love and care for others (as my creator has for me), or by my attention to truth and freedom, then know that it comes as only a serendipitous kind of thing. I don't look for it, didn't ask for it, it just happens. It's like finding a $20 bill in the pocket of your favorite jeans. You don't know how it got there, you aren't going to question it, you just appreciate it! 
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Wednesday, April 23, 2008
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Please ask your doctor to sign this if he/she thinks Vaccines are safe
Physician's Warranty of Vaccine Safety
I (Physician's name, degree)_________________________, _____ am a physician licensed to practice medicine in the State of ________________ . My State license number is _______________ , and my DEA number is _______________. My medical specialty is ______________________ .
I have a thorough understanding of the risks and benefits of all the medications that I prescribe for or administer to my patients. In the case of (Patient's name) ___________________________ , age _________________ , whom I have examined, I find that certain risk factors exist that justify the recommended vaccinations.
The following is a list of said risk factors and the vaccinations that will protect against them: Risk Factor Vaccination: _____________________________________________________ ________________________ _____________________________________________________ ________________________ _____________________________________________________ ________________________ _____________________________________________________ ________________________ _____________________________________________________ ________________________ _____________________________________________________ ________________________ _____________________________________________________ ________________________ I am aware that vaccines typically contain many of the following fillers:
• aluminum hydroxide • aluminum phosphate • ammonium sulfate • amphotericin B • animal tissues: pig blood, horse blood, rabbit brain, • dog kidney, monkey kidney, • chick embryo, chicken egg, duck egg • calf (bovine) serum • betapropiolactone • fetal bovine serum • formaldehyde • formalin • gelatin • glycerol • human diploid cells (originating from human aborted fetal tissue) • hydrolized gelatin • mercury thimerosol • monosodium glutamate (MSG) • neomycin • neomycin sulfate • phenol red indicator • phenoxyethanol (antifreeze) • potassium diphosphate • potassium monophosphate • polymyxin B • polysorbate 20 • polysorbate 80 • porcine (pig) pancreatic hydrolysate of casein • residual MRC5 proteins • sorbitol • sucrose • tri(n)butylphosphate, • VERO cells, a continuous line of monkey kidney cells, and • washed sheep red blood
and, hereby, warrant that these ingredients are safe for injection into the body of my patient. Reports to the contrary, such as reports that mercury thimerosol causes severe neurological and immunological damage, are not credible. I am aware that some vaccines have been found to have been contaminated with Simian Virus 40 (SV-40) and that SV-40 is causally linked by some researchers to non-Hodgkin's lymphoma and mesotheliomas in humans as well as in experimental animals.
I hereby give my assurance that the vaccines I employ in my practice do not contain SV 40 or any other live viruses. (Alternately, I hereby give my assurance that said SV-40 or other viruses pose no substantive risk to my patient.
) I hereby warrant that the vaccines I am recommending for the care of (Patient's name) _______________ _______________________ do not contain any cells from aborted human babies (also known as "fetuses").
In order to protect my patient's well being, I have taken the following steps to guarantee that the vaccines I will use will contain no damaging contaminants.
Steps taken: ______________________________________________________________________________ ______________________________________________________________________________ ______________________________________________________________________________ ______________________________________________________________________________ ______________________________________________________________________________
I have personally investigated the reports made to the VAERS (Vaccine Adverse Event Reporting System) and state that it is my professional opinion that the vaccines I am recommending are safe for administration to a child under the age of 5 years.
The bases for my opinion are itemized on Exhibit A , attached hereto, "Physician's Bases for Professional Opinion of Vaccine Safety." (Please itemize each recommended vaccine separately along with the bases for arriving at the conclusion that the vaccine is safe for administration to a child under the age of 5 years.
) The professional journal articles I have relied upon in the issuance of this Physician's Warranty of Vaccine Safety are itemized on Exhibit B , attached hereto, "Scientific Articles in Support of Physician's Warranty of Vaccine Safety." The professional journal articles that I have read which contain opinions adverse to my opinion are itemized on Exhibit C , attached hereto, "Scientific Articles Contrary to Physician's Opinion of Vaccine Safety." The reasons for my determining that the articles in Exhibit C were invalid are delineated in Attachment D , attached hereto, "Physician's Reasons for Determining the Invalidity of Adverse Scientific Opinions.
" Hepatitis B: I understand that 60% of patients who are vaccinated for Hepatitis B will lose detectable antibodies to Hepatitis B within 12 years. I understand that in 1996 only 54 cases of Hepatitis B were reported to the CDC in the 0-1 year age group. I understand that in the VAERS, there were 1,080 total reports of adverse reactions from Hepatitis B vaccine in 1996 in the 0-1 year age group, with 47 deaths reported. I understand that 50% of patients who contract Hepatitis B develop no symptoms after exposure. I understand that 30% will develop only flu-like symptoms and will have lifetime immunity.
I understand that 20% will develop the symptoms of the disease, but that 95% will fully recover and have lifetime immunity. I understand that 5% of the patients who are exposed to Hepatitis B will become chronic carriers of the disease. I understand that 75% of the chronic carriers will live with an asymptomatic infection and that only 25% of the chronic carriers will develop chronic liver disease or liver cancer, 10-30 years after the acute infection. The following studies have been performed to demonstrate the safety of the Hepatitis B vaccine in children under the age of 5 years.
______________________________________________________________________________ ______________________________________________________________________________ ______________________________________________________________________________ In addition to the recommended vaccinations as protections against the above cited risk factors, I have recommended other non-vaccine measures to protect the health of my patient and have enumerated said non-vaccine measures on Exhibit D , attached hereto, "Non-vaccine Measures to Protect Against Risk Factors.
" I am issuing this Physician's Warranty of Vaccine Safety in my professional capacity as the attending physician to (Patient's name) ________________________________. Regardless of the legal entity under which I normally practice medicine, I am issuing this statement in both my business and individual capacities and hereby waive any statutory, Common Law, Constitutional, UCC, international treaty, and any other legal immunities from liability lawsuits in the instant case. I issue this document of my own free will after consultation with competent legal counsel whose name is _____________________________, an attorney admitted to the Bar in the State of __________________ .
__________________________________ (Name of Attending Physician)
__________________________________ L.S.
(Signature of Attending Physician)
Signed on this _______ day of ______________ A.D.
________
Witness: ___________________________________ Date: ________________________
Notary Public: ______________________________ Date: ________________________
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Friday, April 11, 2008
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Physician's Responsibility Form
I ………………(Physicians name)…………………. do hereby state I have advised the parent(s) of ............(Childs name)……........that
in my professional opinion the child should be given ………(Vaccine's name)………….include manufacturer name, serial
…………, batch……….….I have this day ...…(mm/dd/yy) ……………. administered this medication. I have advised the parents of the investigated the risks and benefits of the following vaccines and diseases. I am aware that there are documented cases of people contracting diseases for which they are clinically fully immunized and that the manufacturers of the vaccines do not guarantee 100% efficacy. I am also aware that VAERS (Vaccine Adverse Events Reporting System) documented cases of over 54,000 adverse reactions from vaccines in a 20-month period. The National Vaccine Injury Fund, created in 1986 to compensate those damaged by vaccines has paid out over one billion dollars in compensation to date.
POLIO: I understand and acknowledge the risk of the child developing paralytic disease and meningitis associated with poliomyelitis. I understand that even under epidemic conditions, natural polio produces no symptoms in over 90% of those exposed to it.(1) I understand that there have been no cases of wild polio in the US in the last 20 years and that those cases which have been documented have been caused by the vaccine.(2) I understand the following side effects for the vaccine are possible: Killed virus polio: temperature of *102° in up to 38%, sleepiness, fussiness, crying, decreased appetite, vomiting, Guillain-Barré Syndrome and allergic reaction in those allergic to neomycin, polymyxin B and streptomycin. Precautions include those who have had a previous negative reaction, pregnant women, and possibly those with HIV/AIDS or otherwise compromised immune systems.
Live virus polio: Reactions include contraction of polio by those who have received the virus and by those who have come into contact with body fluids and wastes of the immunized person. Paralytic symptoms may follow contraction of polio. Live virus is reportedly shed for up to 8 weeks after the inoculation. Guillain-Barré Syndrome has also been noted. Not recommended for use in households where someone has a compromised immune system, for pregnant women, or where a previous reaction has been reported.(3) Killed virus Ipol® is grown on monkey kidney cells, contains formaldehyde, and triple antibiotics. Poliovax® is grown ..s from an aborted baby, contains formaldehyde, cow serum and triple antibiotic solution.(4) The monkey kidney cells used in the original killed polio vaccine contains SIV-40 and has been found in tumor cells of children whose parent's were vaccinated against polio using the contaminated virus.(5) The live vaccine is grown on monkey kidney cells, antibiotics and calf serum.
HEMOPHILUS INFLUENZAE B: I understand and acknowledge the risk of the child developing meningitis (although this vaccine will not protect the child from meningitis from all other forms such as pneumococcus, and meningococcus, viruses, and fungi), pneumonia, and infections of the blood, joints, bone, and soft tissue associated with Hemophilus Influenzae B. I understand that this disease is most likely in children up to 15 months of age and is fatal in 3-6% of children who contract it. Incidence of this disease today is low and the vaccine has not proven to be highly effective in 41% of cases, according to some studies.(6) Treatment is available. The vaccine is often combined with the DPT which has the highest reaction rate of any vaccine available today. Reactions include: contracting HIB, localized pain, erythema and induration, fever >100.6°, irritability, lethargy, anorexia, rhinorrhea, diarrhea, vomiting, cough, when administered alone. Reactions occurred in up to 30% of patients. When administered in conjunction with the DPT, reactions include local tenderness erythema and induration, fever >100.8°, irritability, drowsiness, anorexia, diarrhea, vomiting, persistent crying, seizures, urticaria, hives, renal failure, Guillain-Barré Syndrome and death. Reactions occurred in up to 77.9% of patients.(7) The vaccine contains yeast, thimerosal (mercury derivative), and diphtheria toxoid when given alone.(8)
PERTUSSIS: I understand and acknowledge the risk of the child developing whooping cough, pneumonia, convulsions, inflammation of the brain, and death associated with pertussis. I understand the disease is rarely fatal, with a 99.8% recovery rate. It is most serious and life-threatening in children under 6 months old, but there are adequate methods of treatment available.(9) The vaccine is most often given in conjunction with diphtheria and tetanus as the DPT or as the DaPT. Pertussis vaccine may cause: fevers >106, pain swelling, diarrhea, projectile vomiting, excessive sleepiness, high--pitched screaming, inconsolable crying bouts, seizures, convulsions, collapse, shock, breathing problems, brain damage and SIDS. One in 600 suffer a severe reaction in one study (10) and 1 in 875 suffered shock-collapse and convulsions.(11) Those in the 2nd study were only tracked for the first 48 hours following immunization. A more recent study indicates that 1 in 100 react with convulsions, collapse, or high-pitched screaming and 1 in 3 of those cases sustained permanent brain damage.(12) In a study of 103 children who died of SIDS, 70% died within 3 weeks of the DPT vaccine and 37% of those died within the first week.(13) The DaPT is recommended as a safer option for vaccination. Side effects of the DaPT were only tracked for 72 hours and included: tenderness, erythema, induration, fever >102.2°, drowsiness, fretfulness, vomiting, upper respiratory infection, diarrhea, rash, febrile seizures, persistent or unusual crying, lethargy, hypronic-hyporesponsive episode, urticaria, anaphylactic shock, convulsions, encephalopathy, mono- and polyneuropathies and death.(14) Not recommended for children under 15 months or for those who have not had 3 injections of the DPT. Either form of the vaccine contains thimerosal (mercury derivative), formaldehyde, and aluminum phosphate.(15)
DIPHTHERIA: I understand and acknowledge of the risk of the child developing paralysis, heart failure, or respiratory failure associated with diphtheria. I also understand and acknowledge that there have only been 5 cases reported annually since 1980.(16) I am also aware that diphtheria is rarely fatal and treated with antibiotics and bed rest. (17) The Diphtheria component is most often given within the DPT or DaPT and includes the same side effects and reactions as those listed for pertussis.
TETANUS: I understand and acknowledge the of the risk of the child developing fatal neuromuscular disease related to tetanus. I understand that the incidence of tetanus is low, and there is an antitoxin, should parents decline the immunization. I understand that contracting tetanus does not provide life-long immunity, and neither does the vaccine. I understand that to prevent more severe reactions from the vaccine, the tetanus component has been so significantly "diluted" that it is clinically ineffective.(18) I understand that the death rate for properly treated cases of tetanus may be as high as 20%.(19) Side effects of the tetanus vaccine alone include: high fever, pain, recurrent abscess formation, inner ear nerve damage, demyelinating neuropathy, anaphylactic shock and loss of consciousness.(20) Tetanus given in the DPT or DaPT shot include the same side effects and reactions as those listed for pertussis.
RUBEOLA (MEASLES): I understand and acknowledge the risk of the child developing pneumonia, encephalitis (inflammation of the brain), degenerative disease of the nervous system with convulsions (subacute sclerosing panencephalitis) related to rubeola. I understand the death rate for measles is .03 in 100,000.(21) I understand that since 1984, over 55% of documented, confirmed cases of measles have been in fully immunized persons.(22) I understand that the greatest risk of the measles vaccine may be to push the incidence of this disease into the late teens and adulthood where it is more likely to be fatal or cause more adverse and long-term effects.(23) The measles vaccine is a live vaccine, and carries the risk that it will cause the patient to contract measles. Other adverse reactions include: stinging or burning at the injection site, anaphylaxis, fever up to one month following injection, rash, cough, rhinitis, erythema multiforme, lymphadenopathy, urticaria, diarrhea, febrile convulsions, seizures, thrombocytopenia, purpura, vasculitis, optic neuritis, retrobulbar neuritis, papillitis, retinitis, encephalitis and encephalopathy, ocular palsies, Guillain-Barré Syndrome, ataxia, and subacute sclerosing panencephalitis.(24) Measles vaccine is most often given as a part of the MMR which includes the following side effects: burning or stinging at injection site, malaise, sore throat, cough, rhinitis, headache, dizziness, fever, rash, nausea, vomiting, diarrhea, erythema, induration, tenderness, lymphadenopathy, parotitius, orchitis, nerve deafness, thrombocytopenia, purpura, allergic reactions, urticaria, polyneuritis, arthralgia, arthritis, anaphylaxis, vasculitis, otitis media, conjunctivitis, febrile convulsions, seizures, syncope, erythema multiforme, optic neuritis, retrobulbar neuritis, papillitis, retinitis, encephalitis and encephalopathy, ocular palsies, Guillain-Barré Syndrome, ataxia, subacute sclerosing panencephalitis,(25) and a recent study from Europe indicates that there may be a link between the MMR (measles/mumps/rubella) vaccine and autism and irritable bowel syndrome.(26) Measles vaccine contains chick embryo cells, neomycin, sorbitol and hydrolyzed gelatin. MMR contains all live vaccines, chick embryo, cells from aborted babies, neomycin, sorbitol and hydrolyzed gelatin.(27)
MUMPS: I understand and acknowledge of the risk of the child developing inflammation of the testicles, joints, kidneys, and/or thyroid, and hearing impairment related to mumps. I understand that mumps is rarely harmful in childhood, and that most of the above risks occur when mumps is contracted in adolescence or adulthood.(28) I understand that there is a Mumps vaccine which poses the following risks: contraction of mumps from the live vaccine, burning or stinging at the injection site, anaphylaxis, cough, rhinitis, fever, diarrhea, vasculitis, parotitis, orchitis, purpura, urticaria, erythema multiforme, optic neuritis, retrobulbar neuritis, syncope, encephalitis, febrile seizures, and nerve deafness.(29) Mumps is usually given in the MMR and may cause those side effects and adverse reactions as noted in the measles section above. Mumps vaccine is live and should not be given to pregnant women. It is cultured in chick embryos and contains sorbitol and hydrolyzed gelatin.(30)
RUBELLA (GERMAN MEASLES): I understand and acknowledge the risk of the child developing inflammation of the brain or joints, and of the risk of birth defects (including eye defects, heart defects, deafness, mental retardation, growth failure, jaundice, and disorders of blood clotting) in infants born to mothers who contract rubella during pregnancy, related to rubella. Therefore, I understand that the greatest risk to the child may be if she never contracts rubella as a child, but when she is pregnant and it damages her unborn child. If she contract rubella in childhood, she is immune for life, and prior to the vaccine 85% of the population was immune.(31) I understand that if she is not immune as an adult, she can choose to take the vaccine prior to becoming pregnant. I understand that many of those who contract rubella have been immunized (up to 80%). (32) Adverse reactions from the vaccine among teenage girls is 5-10% and 30% in adult women.(33) Adverse reactions include: contracting rubella from the live virus in the vaccine, burning or stinging at the site, lymphadenopathy, urticaria, rash, malaise, sore throat, fever, headache, dizziness, nausea, vomiting, diarrhea, polyneuritis, arthralgia, arthritis, local pain and inflammation, erythema multiforme, cough, rhinitis, vasculitis, anaphylaxis, syncope, optic neuritis, retrobulbar neuritis, papillitis, Guillain-Barré Syndrome, encephalitis, thrombocytopenia, purpura, and Chronic Fatigue Syndrome. (34) Rubella is most often administered in the MMR and may cause those side effects and adverse reactions listed under measles. Rubella is cultured on the tissue of an aborted child. This child was the 27th child aborted and tested by researchers due to exposure to rubella in a pregnant woman. It contains neomycin, sorbitol and hydrolyzed gelatin.(35)
HEPATITIS B: I understand and acknowledge the risk of the child developing Hepatitis B viral infection which can cause chronic inflammation of the liver leading to cirrhosis, liver cancer, and possibly death. I understand that the child's risk of developing Hepatitis B is low if I am not a carrier or infected, if the child does not engage in promiscuous sex or use drugs. I understand that there is antibiotic treatment for HepB and that most of those who contract it recover.(36) I understand that the HepB vaccine only contains strains of HepB and is not effective against HepA, C, D, E, F, or G. I understand that the HepB vaccine has the following side effect and adverse reactions: induration, erythema, swelling, fever, headache, dizziness, pain, prutitus, ecchymosis, sweating, malaise, chills, weakness, flushing, tingling, hypotension, flu-like symptoms, upper respiratory illness, nausea, anorexia, abdominal pain and cramping, vomiting, constipation, diarrhea, lymphadenopathy, pain or stiffness in muscles and joints, arthralgia, myalgia, back pain, rash, urticaria, petechiae, sleepiness, insomnia, irritability, agitation, anaphylaxis, angioedema, arthritis, tachycardia/palpitations, bronchospasm, abnormal liver function tests, dyspepsia, migraine, syncope, paresis neuropathy, hypothesis, paresthesis, Guillain-Barré Syndrome, Bell's Palsy, transverse myelitis, optic neuritis, multiple sclerosis, thrombocytopenia, eczema, purpura, herpes zoster, erythema modosum, alopecia, conjunctivitis, keratisis, visual disturbances, vertigo, tinnitus, earache, and dysuria.(37) The studies only followed patients for 4 days post-vaccination. The most commonly used HepB vaccine contains thimerosal, although a relatively new release does not contain thimerosal. The vaccine also contains: aluminum hydroxide, yeast protein, and phosphate buffers.(38)
VARICELLA (CHICKENPOX): I understand and acknowledge the risk of the child developing chicken pox which could potentially result in pneumonia, secondary skin or generalized infections, or, if caught during pregnancy, birth defects in the baby. I understand chicken pox is generally benign in children, but results in significant lost hours at work for parents. Chicken pox in adults often manifests as shingles, a chronic and painful condition. I also understand that contracting chicken pox later in life may increase my risk for herpes simplex. Side effects and adverse reactions for the chicken pox vaccine include: contracting chicken pox from the live vaccine (27%), pain and redness at site, swelling, erythema, rash, pruritus, hematoma, induration, stiffness, upper respiratory illness, cough, irritability/nervousness, fatigue, disturbed sleep, diarrhea, loss of appetite, vomiting, otitis, diaper rash/contact rash, nausea, eye complaints, chills, lymphadenopathy, myalgia, lower respiratory illness, headache, teething, malaise, abdominal pain, other rash, allergic reactions including rash and hives, stiff neck, heat rash/prickly heat, arthralgia, eczema/dry skin/dermatitis, constipation, itching, pneunonitis, febrile seizures, and cold/canker sore.(39) Varicella vaccine is cultured ..s from aborted babies, and guinea pig cell cultures. It contains live virus, monisodium glutamate (msg), sucrose, phosphate, processed gelatin, neomycin and fetal calf serum. (40)
HEPATITIS A (HAV): I understand and acknowledge the risk of the child developing HAV which could potentially result in prolonged or relapsed hepatitis, but will not result in chronic hepatitis disease. (41) HAV usually causes mild "flu-like" illness, jaundice, severe stomach pains and diarrhea; and, in rare cases may result in death. Infection confers lifelong immunity. (42) I understand that the CDC admits that good personal hygiene (handwashing) and proper santitation can prevent HAV. (43) HAV infection is spread by contaminated water or food, infected food handlers, unsanitary conditions following natural disasters, ingestion of raw or undercooked shellfish, institutionalized individuals, children not yet toilet trained, blood transfusions or sharing needles with infected people. Transmission is most likely in developing countries where sanitation is poor and infection rate of children under 5 is 90%. Fatality rate is less than .6% overall, and 70% of those in patients over 49 years, many of whom have underlying liver disease. (44) Other at-risk populations include those living on American Indian reservations and in Alaskan Native villages, homosexually active men, IV drug users, people using clotting factor concentrates and international travelers. (45) Side effects and adverse reactions from the vaccine include: injection-site soreness, headache, fever, malaise, induration, redness, swelling, fatigue, anorexia, nausea, pruritis, rash, utricaria, pharyngitis, upper respiratory tract infections, abdominal pain, diarrhea, dysgeusia, vomiting, arthralgia, elevated cratine phosphokinase, myalgia, lymphadenopathy, hypertonic episodes, insomnia, photophobia, and vertigo. (46) Aborted fetal tissue is an ingredient in the Havrix® Hep A vaccine, as is formaldehyde, aluminum hydroxide and 2-phenozyethanol.(47) There is currently a combination Hep A and B vaccine, Twinrix®, being tested in the UK. (48) Twinrix is grown in human cell cultures, contains 2-phenoxyethanol, neomycin sulfate, polysorbate, tromentamol and formaldehyde. (49)
PNEUMOCOCCAL: I understand and acknowledge the risk of the child developing pneumococcal disease which could result in meningitis, blood infection, pneumonia and/or ear infections. Iunderstand studies indicate that this vaccine may only decrease ear infections by 9%, and only result in a 20% reduction in chronic ear infections and ear tube insertion in that group. I understand that the child has a 7.5:5,000 chance of developing this disease if he or she is under age 2 and a 1:5000 chance of developing it if over age 2. Risk factors for developing this disease are: immunoglobulin deficiency, nephrotic syndrome, Hodgkin's disease, congenital or acquired immunodeficiency, some upper respiratory infections, splenic dysfunctions, splenectomy or organ transplant. This vaccine (PCV) was originally marketed for immunocompromised children. (50) This vaccine is contraindicated to children with thrombocytopenia, coagualtion disorders, or sensitivity to diphtheria toxoid.(51) Possible side effects and complications from the vaccine include: erythema, induration, tenderness, interference of limb movement, inflamation, fever, irritability, drowsiness, restless sleep, decreased appetite, vomiting, diarrhea, fussiness, rash, hives, bronchitis, asthma, pneumonia, otitis media (ear infection), sepsis, seizure, anaphylaxis and death.(52) Recipients were followed for 3 days and almost 10% of the subjects made a visit to the emergency room in the follow-up period. There were 8 cases of SIDS in the 17,066 subjects involved in the trial.(53) Note: Children in the studies' control group received another experimental vaccine, so there have been no trial studies done with children who received no vaccine.(54) Prevnar contains .125 mg of aluminum sulfate, protein polysaccharides from 7 strains of strep. pneumoniae bacteria, diphtheria toxin, casamino acids, yeast extract. Studies indicate that it may interfere with the safety and efficacy of other vaccines.(55)
I hereby do agree to take full responsibility should the child at any time suffer or develop any permanent condition deleterious or injurious to their health as a result of this treatment. I will pay any and all costs relating to the care and treatment of this child for the rest of his/her natural life. If death should be a result of this treatment, than no less than a total of $1,000,000 I agree to pay to parents of the child. I further agree that if my earnings are insufficient to meet these costs I will sell my home, my business, and all material possessions to put the proceeds towards meeting these costs.
Signature of responsible doctor.........................................................................................
Reference List
1. M. Burnet and D. White, The Natural History of Infectious Disease (Cambridge, 1972), p. 16. 2. Strebel, et al, "Epidemology in the U.S. One Decade After the Last Reported Case of Indigenous Wild Virus Associated Disease," Clinical Infectious Diseases, (Center for Disease Control, February 1992), pp. 568-79. 3. Physician's Desk Reference (PDR), 50th Edition; Medical Economics, 1996, p. 1388-1390. 4. Ibid, p. 885-886 and 891-892. 5. J. Butel, et al; "Molecular Evidence of Simian Virus 40 Infections in Children", The Journal of Infectious Diseases ; September 1999;180:884-887. 6. PDR, 50th Edition, p. 872-875. 7. Ibid. 8. Ibid. 9. Richard Moskowitz, M.D., "Immunizations: The Other Side," Mothering, (Spring1984),p. 34. 10. Immunization: Survey of Recent Research, (United States Department of Health and Human Services, April 1983), p. 76. 11. "Nature and Rates of Adverse Reactions Associated with DPT and DT Immunizations...," Pediatrics, Volume 68, No. 5 (November 1981). 12. Walene James, Immunization the Reality Behind the Myth, (South Hadley, Massachusetts: Bergin & Garvey, 1988), p. 14. 13. W.C. Torch, "Diptheria-pertussis-tetanus (DPT) immunization: A potential cause of sudden infant death syndrome (SIDS)," (Amer. Academy of Neurology, 34th Annual Meeting, Apr 25 - May 1, 1982), Neurology 32(4), pt. 2. 14. PDR, p. 875-879 and 892-895. 15. Ibid. 16. Robert Mendelsohn, M.D., How to Raise A Healthy Child...In Spite of your Doctor (Chicago: Contemporary Books, 1984), p.223. 17. Ibid. 244-246 18. Isaac Golden, Ph.D., Vaccination? A Review of Risks and Alternatives, (Geelong, Victoria, Australia: Arum Healing Centre, 1991), p. 31 19. Richard Moskowitz, M.D., "Immunizations: The Other Side," Mothering, (Spring1984),p. 34. 20. Isaac Golden, Ph.D., Vaccination? A Review of Risks and Alternatives; p. 71 21. R. Mendoholson; How to Raise a Healthy Child; p. 217. 22. John Frank Jr., M.D., et al. "Measles Elimination - Final Impediments," 20th Immunization Conference Proceedings, May 6-9, 1985, p. 21. 23. Infectious Diseases (January 1982), p. 21. 24. PDR, p. 1610-1611. 25. DR, p. 1687-1689. 26. Sara Solovitch, "Do vaccines spur autism in kids?", San Jose Mercury News, 5/25/99. 27. PDR, p. 1687-89, 1610-1611. 28. Richard Moskowitz, M.D., "Immunizations: The Other Side," Mothering, (Spring1984),p. 35. 29. PDR, 1708-1709. 30. Ibid. 31. R. Mendoholson; How to Raise a Healthy Child; p. 218. 32. Dr. Beverley Allan, Australian Nurses Journal, (May 1978). 33. Hannah Allen, Don't Get Stuck: The Case Against Vaccinations..., (Oldsmar, FL: Natural Hygiene Press, 1985), p. 144. 34. DR, p. 1697-1699. 35. Ibid and Attenuation Of RA 27/3 Rubella Virus in WI-38 Human Diploid Cells; Amer J Dis Child vol 118 Aug 1969 and Studies of Immunization With Living Rubella Virus ; Arch J Dis Child vol 110 Oct 1965. 36. John Hanchette, "Safety of controversial hepatitis B vaccine at center of debate" Gannett News Service, 5/18/99. 37. PDR, p. 1744-1747, 2482-2484. 38. Ibid. 39. PDR, p. 1762-1765. 40. Ibid. 41. CDC Viral Hepatitis A - Fact Sheet, 9/29/00; www.cdc.gov/ncidod/diseases/hepatitis/a/fact.htm 42. CDC Hepatitis A Vaccine Vaccine Information Statement; 8/25/98 43. CDC Hepatitis A Facts, 11/16/00 44. Mosby's GenRX®, 10th Ed., Hepatitis A Vaccine (003158) as posted on MDConsult website 45. CDC Hepatitis A Vaccine Vaccine Information Statement; 8/25/98 and CDC Hepatitis A Vaccine Vaccine Information Statement; 8/25/98 46. Mosby's GenRX@, Hepatitis A Vaccine 47. Ibid. 48. "Combined hepatitis A/B vaccine offers fast protection," Reuters Health, 4/12/00 49. Vaccines and Their Ingredients, 6/24/99; www.909shot.com 50. Michael Horwin, MA; "Prevnar: A Critical Review of a New Childhood Vaccine" 9/19/00. 51. Prevnar package insert, Wyeth Lederle, 2/17/00 52. Ibid. 53. Horwin; "Prevnar: A Critical Review" 54. Dr. Erdem Cantekin, Ph.D.; "Pneumocaoccal Vaccine and Otitis Media", NVIC's 2nd Intl. Public Conference, 9/8/00. 55. Horwin; "Prevnar: A Critical Review"
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Friday, April 11, 2008
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ACCEPTANCE OF RESPONSIBILITY
I, the undersigned, having assumed decision making power independently, or having been appointed to such, by a government bureaucracy or corporation controlled by such, do require the following individual(s):
_______________________________________________________________________
to receive the following vaccination(s):
_______________________________________________________________________
contrary to laws of this state that provide religious and philosophical exemptions.
I further agree that the stated individual(s) are in excellent to perfect health prior to the administration of such immunization(s).
Consistent with this demand, is my personal acceptance of full responsibility for any and all damages resulting from such immunizations. As a result, I agree to provide compensation amounting to $1,000,000 to the family(s) of the persons you are requiring to receive the aforementioned vaccinations for each resulting vaccine related injury(s) and/or disease(s) as follows:
Death: http://www.909shot.com/Kids/richie.htm
Sudden infant death syndrome: http://www.909shot.com/Kids/nicky.htm
Shaken baby syndrome: http://www.vaclib.org/basic/sbsindex.htm
Cerebral bleeding: http://www.vaclib.org/basic/sbsrebut.htm
Cancer: http://www.sv40cancer.com/
Tumors: http://www.gulfwarvets.com/virus.htm
Asthma: http://vaccines.net/Asthma/allergie.htm
Auto-immune disease(s): http://healthresearchtoday.com/lupus/whatislupus.htm
Polio: http://www.909shot.com/Diseases/rotavirus.htm
Bowel blockage: http://www.909shot.com/rotaviru.htm
Autism: http://www.909shot.com/Diseases/Autism.htm
Brain damage: http://www.vaclib.org/news/2006/pentacel.htm
Mental retardation: http://www.vaclib.org/news/2006/pentacel.htm
Crippling arthritis: http://www.vaclib.org/intro/hepbinfo.htm
Paralysis: http://www.909shot.com/Kids/terry.htm
Mercury poisoning: http://www.gulfwarvets.com/kids.htm
Diabetes: http://vaccines.net/diabetes.htm
Blindness: http://www.vaclib.org/email/lymefda.htm
Loss of IQ: http://www.vaclib.org/email/autismviera.htm
Pain: http://www.909shot.com/Diseases/hepbcasereports.htm
Seizures: http://www.vaclib.org/email/seizures.htm
Chronic fatigue syndrome: http://healthresearchtoday.com/fibromyalgia/book_104.htm
*Note that virtually all of these conditions /diseases are incurable by modern medicine, but easily prevented by abstinance!
Name (print):_____________________________________Position:_____________________
Signature:____________________________________________________Date:___________
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Friday, February 29, 2008
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..> Acel-Immune DTaP diphtheria - tetanus - pertussis | Wyeth-Ayerst 800.934.5556 | diphtheria and tetanus toxoids and acellular pertussis adsorbed | | formaldehyde, aluminum hydroxide, aluminum phosphate, thimerosal, and polysorbate 80 (Tween-80) | gelatin | Act HIB
Haemophilus influenza Type B | Connaught Laboratories 800.822.2463 | Haemophilus influenza Type B, polyribosylribitol phosphate | | ammonium sulfate, formalin, and sucrose | | Attenuvax measles | Merck & Co., Inc. 800-672-6372 | measles live virus | neomycin | sorbitol | hydrolized gelatin, chick embryo | Biavax rubella | Merck & Co., Inc. 800-672-6372 | rubella live virus | neomycin | sorbitol | hydrolized gelatin, human diploid cells from aborted fetal tissue | BioThrax anthrax adsorbed | BioPort Corporation 517.327.1500 | nonencapsulated strain of Bacillus anthracis | | aluminum hydroxide, benzethonium chloride, and formaldehyde | | DPT diphtheria - tetanus - pertussis | GlaxoSmithKline 800.366.8900 X 5231 | diphtheria and tetanus toxoids and acellular pertussis adsorbed | | formaldehyde, aluminum phosphate, ammonium sulfate, and thimerosal | washed sheep RBCs | Dryvax smallpox (not licensed d/t expiration) | Wyeth-Ayerst 800.934.5556 | live vaccinia virus, with "some microbial contaminants," according to the Working Group on Civilian Biodefense | polymyxcin B sulfate, streptomycin sulfate, chlortetracycline hydrochloride, and neomycin sulfate | glycerin, and phenol -a compound obtained by distillation of coal tar | vesicle fluid from calf skins | Engerix-B recombinant hepatitis B | GlaxoSmithKline 800.366.8900 X 5231 | genetic sequence of the hepatitis B virus that codes for the surface antigen (HbSAg), cloned into GMO yeast | | aluminum hydroxide, and thimerosal | | Fluvirin
| Medeva Pharmaceuticals 888.MEDEVA 716.274.5300 | influenza virus | neomycin, polymyxin | beta-propiolactone | chick embryonic fluid | FluShield
| Wyeth-Ayerst 800.934.5556 | trivalent influenza virus, types A&B | gentamicin sulphate | formadehyde, thimerosal, and polysorbate 80 (Tween-80) | chick embryonic fluid | Havrix hepatitis A | GlaxoSmithKline 800.366.8900 X 5231 | hepatitis A virus | | formalin, aluminum hydroxide, 2-phenoxyethanol, and polysorbate 20 | residual MRC5 proteins -human diploid cells from aborted fetal tissue | HiB Titer
Haemophilus influenza Type B | Wyeth-Ayerst 800.934.5556 | Haemophilus influenza Type B, polyribosylribitol phosphate, yeast | | ammonium sulfate, thimerosal, and chemically defined yeast-based medium | | Imovax
| Connaught Laboratories 800.822.2463 | rabies virus adsorbed | neomycin sulfate | phenol red indicator | human albumin, human diploid cells from aborted fetal tissue | IPOL
| Connaught Laboratories 800.822.2463 | 3 types of polio viruses | neomycin, streptomycin, and polymyxin B | formaldehyde, and 2-phenoxyethenol | continuous line of monkey kidney cells | JE-VAX Japanese encephalitis | Aventis Pasteur USA 800.VACCINE | Nakayama-NIH strain of Japanese encephalitis virus, inactivated | | formaldehyde, polysorbate 80 (Tween-80), and thimerosal | mouse serum proteins, and gelatin | LYMErix lyme | GlaxoSmithKline 888-825-5249 | recombinant protein (OspA) from the outer surface of the spirochete Borrelia burgdorferi | kanamycin | aluminum hydroxide, 2-phenoxyethenol, phosphate buffered saline | | MMR measles - mumps - rubella | Merck & Co., Inc. 800.672.6372 | measles, mumps, rubella live virus | neomycin | sorbitol | hydrolized gelatin, chick embryonic fluid, and human diploid cells from aborted fetal tissue | M-R-Vax measles - rubella | Merck & Co., Inc. 800.672.6372 | measles, rubella live virus | neomycin | sorbitol | hydrolized gelatin, chick embryonic fluid, and human diploid cells from aborted fetal tissue | Menomune meningococcal | Connaught Laboratories 800.822.2463 | freeze-dried polysaccharide antigens from Neisseria meningitidis bacteria | | thimerosal | lactose | Meruvax I mumps | Merck & Co., Inc. 800.672.6372 | mumps live virus | neomycin | sorbitol | hydrolized gelatin | NYVAC (new smallpox batch, not licensed) | Aventis Pasteur USA 800.VACCINE | highly attenuated vaccinia virus | polymyxcin B sulfate, streptomycin sulfate, chlortetracycline hydrochloride, and neomycin sulfate | glycerin, and phenol -a compound obtained by distillation of coal tar | vesicle fluid from calf skins | Orimune oral polio | Wyeth-Ayerst 800.934.5556 | 3 types of polio viruses, attenuated | neomycin, streptomycin | sorbitol | monkey kidney cells and calf serum | Pneumovax Streptococcus pneumoniae | Merck & Co., Inc. 800.672.6372 | capsular polysaccharides from polyvalent (23 types) pneumococcal bacteria | | phenol | | Prevnar Pneumococcal 7-valent conjugate vaccine | Wyeth Lederle 800.934.5556 | saccharides from capsular Streptococcus pneumoniae antigens (7 serotypes) individually conjugated to diphtheria CRM 197 protein | | aluminum phosphate, ammonium sulfate, soy protein, yeast | | ProQuad measles, mumps, rubella and varicella | Merck & Co., Inc. 800.672.6372 | live measles (Enders' attenuated Edmonston), mumps (Jeryl LynnTM), rubella (Wistar RA 27/3), and varicella (oka/Merck) strains of viruses | neomycin | monosodium L-glutamate (MSG), potassium chloride, potassium phosphate monobasic, potassium phosphate dibasic, sodium bicarbonate, sodium phosphate dibasic, sorbitol, and sucrose | human albumin, human diploid cells, residual components of MRC-5 cells including DNA and proteins, bovine serum, hydrolized gelatin, and chicken embryo | RabAvert rabies | Chiron Behring GmbH & Company 510.655.8729 | fixed-virus strain Flury LEP | neomycin, chlortetracycline, and amphotericin B | potassium glutamate, and sucrose | human albumin, bovine gelatin and serum "from source countries known to be free of bovine spongioform encephalopathy," and chicken protein | Rabies Vaccine Adsorbed
| GlaxoSmithKline 800.366.8900 X 5231 | rabies virus adsorbed | | beta-propiolactone, aluminum phosphate, thimerosal, and phenol red | rhesus monkey fetal lung cells | Recombivax recombinant hepatitis B | Merck & Co., Inc. 800.672.6372 | genetic sequence of the hepatitis B virus that codes for the surface antigen (HbSAg), cloned into GMO yeast | | aluminum hydroxide, and thimerosal | | RotaShield oral tetravalent rotavirus (recalled) | Wyeth-Ayerst 800.934.5556 | 1 rhesus monkey rotavirus, 3 rhesus-human reassortant live viruses | neomycin sulfate, amphotericin B | potassium monophosphate, potassium diphosphate, sucrose, and monosodium glutamate (MSG) | rhesus monkey fetal diploid cells, and bovine fetal serum | smallpox (not licensed due to expiration) 40-yr old stuff "found" in Swiftwater, PA freezer | Aventis Pasteur USA 800.VACCINE | live vaccinia virus, with "some microbial contaminants," according to the Working Group on Civilian Biodefense | polymyxcin B sulfate, streptomycin sulfate, chlortetracycline hydrochloride, and neomycin sulfate | glycerin, and phenol -a compound obtained by distillation of coal tar | vesicle fluid from calf skins | smallpox (new, not licensed) | 617.494.1339 in partnership with Baxter BioScience | highly attenuated vaccinia virus | polymyxcin B sulfate, streptomycin sulfate, chlortetracycline hydrochloride, and neomycin sulfate | glycerin, and phenol -a compound obtained by distillation of coal tar | vesicle fluid from calf skins | TheraCys BCG (intravesicle -not licensed in US for tuberculosis) | Aventis Pasteur USA USA 800.VACCINE | live attenuated strain of Mycobacterium bovis | | monosodium glutamate (MSG), and polysorbate 80 (Tween-80) | | Tripedia diphtheria - tetanus - pertussis | Aventis Pasteur USA 800.VACCINE | Corynebacterium diphtheriae and Clostridium tetani toxoids and acellular Bordetella pertussis adsorbed | | aluminum potassium sulfate, formaldehyde, thimerosal, and polysorbate 80 (Tween-80) | gelatin, bovine extract US sourced | Typhim Vi typhoid | Aventis Pasteur USA SA 800.VACCINE | cell surface Vi polysaccharide from Salmonella typhi Ty2 strain | | aspartame, phenol, and polydimethylsiloxane (silicone) | | Varivax chickenpox | Merck & Co., Inc. 800.672.6372 | varicella live virus | neomycin | phosphate, sucrose, and monosodium glutamate (MSG) | processed gelatin, fetal bovine serum, guinea pig embryo cells, albumin from human blood, and human diploid cells from aborted fetal tissue | YF-VAX yellow fever | Aventis Pasteur USA 800.VACCINE | 17D strain of yellow fever virus | | sorbitol | chick embryo, and gelatin | ..> http://www.informedchoice.info/cocktail.html
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Thursday, February 07, 2008
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AUTISM CAN BE TREATED Dr. Carolyn Dean, MD, ND and Elissa Meininger November 13, 2007 NewsWithViews.com "All truth passes through three stages: First, it is ridiculed; Second, it is violently opposed; and Third, it is accepted as self-evident." --Arthur Schopenhauer We are in the midst of a catastrophe. As of February 2007, the Centers For Disease Control (CDC) has admitted that there are at least 1.5 million children with autism in the U.S. affecting one in every 150 children and one out of 90 boys. Even these figures are probably too low and may not take into account the other categories being created to describe our increasingly challenged children. Pervasive developmental disorder, Asperger's disorder are two other autism spectrum disorders that describe children with variants of autism. The incidence of ADHD (attention deficit hyperactivity disorder) is one in ten children. As the saying goes, it doesn't take a rocket scientist to figure out that something is seriously wrong. Government health experts claim autism is an incurable disease offering anticonvulsant and psychotropic drugs to control behavior and a behavior modification therapy called "applied behavior analysis (ABA)." They dismiss all other means of helping these children as "unproven." Meanwhile thousands of children are back to full functionality by treating the damage caused by mercury toxicity using natural health therapies. Our government's slow and even deceptive response to this catastrophe is a major part of the problem parents of autistic children face. The CDC does not publicize the fact that in the 1970s only one in 10,000 children were diagnosed with autism, however, in the 1980s, this figure rose to one in every 2,500. Nor does it mention that the massive escalation of cases started in the 1990s coincided with the addition of several new vaccines to the compulsory childhood vaccination lists. Currently, every American child is expected to have 36 shots by the time they are six years old. The sudden 11-fold increase in neurobehavioral disorders of all kinds pointed to vaccines and most importantly, the mercury component (thimerosal) as the main culprit. The drug industry lobbied for laws that now protect them from liability should these government-mandated vaccines damage or kill any of the children required to take them. To aid victims of vaccination a special government-run fund was set up in but a Vaccine Court decided to disallow autism claims as there was no "scientific proof" that vaccines caused autism. With increasing demands of parents of autistic children, in the summer of 2007, the court was forced to conduct special hearings to determine, not by science, but by reasonable legal probability whether or not there is a plausible link between vaccines and autism. If a link is established, the trust fund initiated in 1986 to pay claims could provide financial relief for families with autistic children. However, the annual cost of treating an autistic child ranges from $50,000 to $200,000. If the Vaccine Court decides there is no link, the parents of 1.5 million kids must fend for themselves. Even if claims are allowed, there are not enough funds to cover all damaged children. There are several good articles about the CDC's attempts to suppress information it has about the dangers of vaccines. The most comprehensive one is Deadly Immunity by Robert F. Kennedy, Jr., Kenneth Stoller, MD, FAAP and Anne McElroy Dachel in their reports speculate that because mercury products (mercury amalgams and vaccines) are connected with the fossel-fuel industry they are protected by government. The ferocity of the battle is seen in press reports from both sides of the debate including the government itself. In September 26, 2007, a CDC study entitled, "CDC Study Finds Kids' Mental Acuity Not Hurt by Mercury," was quickly followed on October 1, 2007, by a press release titled "Mercury (Thimerosal) in Vaccines: FDA and CDC 'Guilty' of Misconduct, Says Senate Report." issued by Senator Enzi, Ranking Member of the Committee on Health, Education, Labor and Pensions. Thanks to massive pressure from hundreds of thousands of parents and Congressional leaders like Dan Burton, whose own grandchild has autism, Congress in 2007 finally passed legislation to fund autism research. However, this has not satisfied all parents. Their fear is that most of this money will be poured into genetic research and behavioral research and not address "the environmental causes of autism" i.e., mercury and vaccines. Sidestepping the environmental aspects of autism would serve to protect the vaccine manufacturing industry as well as the validity of the national policy on compulsory vaccinations. It is important to note that autism first appeared in the 1930s, around the same time thimerosal, a mercury component, started to be put into vaccines. Not many cases were reported back then and the dozens of vaccines children now receive, had not been developed. In the 1956, Dr. Bernard Rimland, a Ph.D. in experimental psychology and research design welcomed his son, Mark, into the world of autism. In that era, the medical community, under the leadership of psychiatrist, Bruno Bettleheim, believed autism was a psychological disorder caused by unloving mothers. The treatment was psychotherapy for both mother and child. Dr. Rimland did not agree. By 1964, Dr. Rimland, wrote Infantile Autism describing eight years or research and personal observation of his son with scientific evidence that autism is biochemical in nature and not caused by unloving mothers. Finding no support from the medical scientific community, Dr. Rimland founded the Autism Society of America. Its members were and still are parents of children with autism, many of whom are health professionals. He encouraged them to become the primary experts formalizing their work by creating the Autism Research Institute, which has now has the largest database in the world on the issues of autism. The Institute collects data from parents on what works to help their children providing comprehensive surveys on results of dozens of therapies. DAN! (Defeat Autism Now) conferences occur annually where researchers and parents present information on successful therapies. The DAN! approach also includes applied behavior analysis aka ABA (a behavior modification program which Rimland pushed for 20 years before it was accepted by the medical establishment), dietary supplements (which are still not accepted by the medical establishment including the psychiatric community), special diets to eliminate casein (found in dairy products) and gluten (found in wheat products) and a mercury detox. Evidence of success with DAN! protocols has recently been featured on both Oprah and Larry King Live by two Hollywood authors and actresses who are mothers of recovered children. These wonderful and committed mothers effectively use their experience and notoriety to bring hope to hundreds of thousands of parents who have not heard that autism is treatable. One of the duo is Holly Robinson Peete, who, along with her husband, Roland Peete of NFL football fame, founded Hollyrod Foundation to help raise money and spread the word about autism. The other mom is Jenny McCarthy, who has just released a book about her experiences with bringing her son Evan back from autism . The book, entitled, Louder Than Words: A Mother's Journey in Healing Autism, was featured on the cover of People in the October 1, 2007, issue. She is spokeswoman for an organization called Talk About Curing Autism (TACA), which provides detailed information on what parents can do to help their children recover. During their interview on Larry King Live, Jenny pointed out that while vaccines might not be the sole cause of autism, she believes they are a trigger, much like obesity is a trigger for diabetes. She also pointed out that her son had candida, a yeast infection, and as soon as this was cleaned up with an antifungal diet and an antifungal drug, Max started speaking complete sentences and his social development was back on track. Jenny said Evan's experience is common among kids with autism. The DAN doctor who Jenny credits with diagnosing Evan's candida overgrowth is pediatrician, Dr. Jerry Kartzinel. He was also on the Larry King show and said, "this isn't in the books", meaning the treatment of yeast in autism. Dr. Kartzinel has a special interest in autism because his own child became autistic after an MMR vaccination. His wife's directive to him was pretty explicit. She said, "you broke him, you go out and fix him." He quickly realized that there was nothing in the pediatric medical literature to describe the cascade of problems that develop in an autistic child. This lack of information led him to the DAN group and he is now considered a top expert in the field. When you allow yourself to go beyond the behavioral model of autism you will find research showing that one pivotal metabolic insult to an infant who develops autism is damage to a specific kinase enzyme. In a vulnerable segment of the population, perhaps 10%, a particular gene sequence can be damaged by heavy metals (mercury in children's vaccines or flu shots and dental amalgams in the elderly), antibiotics, alcohol, and acetaminophin. This vulnerable gene sequence is found in people who have autism and Alzheimer's; it is the template for creating the kinase enzyme P13. Some researchers refer to this gene sequence as the Alzheimer's gene, which is damaged early in these children by of overwhelming metabolic insults. Why is kinase P13 so important? The body requires kinase P13 for many tasks, one of which is to help break down gluten (a wheat, rye, oats, and barley protein) and casein (a milk protein). This same enzyme allows the methylation (or biochemical modification) of certain B vitamins. Without proper methylation of B12 into methylcobalamin and folic acid into folinic acid, hundreds of functions are impaired. For example, if you don't have methylcobolamine, your liver can't make glutathione (a powerful antioxidant). Without glutathione the body is not able to detoxify heavy metals. The vicious cycle is complete. The heavy metal that causes the gene damage in the first place is not excreted as it should be and continues to accumulate and cause more damage. So intricate are these pathways that giving children the wrong kind of folic acid or B12 can make matters worse; consequently autism therapy must be overseen by knowledgeable parents and practitioners. The therapies used to successfully treat autism are similar to ones used for Alzheimer's patients who suffer mercury and aluminum toxicity and people with irritable bowel syndrome (IBS), hormone imbalance, allergies, yeast overgrowth, viral infections, nutritional deficiencies, and heavy metal toxicity, because autistic children suffer from all of the above. Treatment must begin with diet. Casein and gluten are eliminated because they are not digested or absorbed properly in a kinase P13-damaged body. When not completely digested casein and gluten produce brain-disrupting hallucinogens or brain depressants. In my telephone consulting practice, I tell parents that a proper diet for autism is not just a matter of giving your child healthy food, it's more important to eliminate foods that are poisoning them. Sugar is another important food restriction. Sugar feeds yeast in the intestinal tract, which is often stimulated by overuse of antibiotics to deal with chronic infections that plague autistic children. Yeast produces up to 180 different toxins that cause or aggravate rashes, brain irritation, hypothyroidism, and IBS. In many autistic children the MMR vaccine with live measles virus has produced an ongoing intestinal infection. Therapeutic supplements are added to the diet as needed. For measles infection and yeast overgrowth natural antibiotics can be used. Methylcobalamine (B12) and folinic acid are given instead of the more common cyanocobalamine or folic acid. Hyperbaric oxygen helps revive damaged and starving brain and nervous system tissues. Urinary porphyrin testing helps determine the mercury and lead burden in a child and IV chelation with glutathione, phosphytidyl choline or calcium EDTA helps reduce the load. I recommend food based organic vitamins and angstrom-sized minerals for superior absorption of missing nutrients. Homeopathy is used to treat minor ailments in children so they aren't exposed to unnecessary medication. Practiced by an experienced homeopath, homeopathy has the potential to heal autism and ADHD. Judyth Reichenber-Ullman has written several books about the treatment of ADHD and autism with homeopathy. Impossible Cure – The Promise of Homeopathy written by Amy Lansky, PhD, a former NASA computer researcher describes how the writer's son, Max, recovered from autism using homeopathy. To those of us in the thick of the effort to treat autism, it's a modern day battlefield and no single practitioner and no single therapy holds all the answers. The management of autism requires exquisite chorography between practitioners of diverse disciplines and the use of all manner of non-toxic products. The job is difficult and expensive but the rewards are great. In one family I work with, we began with simple dietary exclusion of sugar, gluten, and dairy. Within days the 2-year old's siblings exclaimed "Justin is back. Where was he?" Pulled back from gluten and casein-induced brain depression that kept him in a fog of withdrawal and apathy, Justin was, indeed, back among the living. In another family I worked with, magnesium and a simple homeopathic remedy were all that Allen needed to begin detoxifying and healing. For me, the most heartbreaking part of working with families with autistic children is that modern science and modern medicine do not acknowledge the need for nutritional intervention. Long-standing criticism in our culture of people following healthy diets being called 'health nuts' and self-help being labeled 'unscientific' has kept most people in the dark about the necessity to take care of themselves and their children. Such criticism has likely been promoted by the drug industry and processed food industry and has served them well economically but has led to a population struggling with chronic disease. I encourage the parents I work with to think of themselves as scientists who use safe therapies and through a process of trial and error, they can "scientifically prove" in their own clinical trial (with their child) what works and what doesn't work for them. In our local parents group, whose members have given themselves full permission to look to all corners of the healing arts industry, I am constantly learning new things. Most important to realize is that each of us is different, and each child has its own set of issues that need to be addressed on an individual basis. Pediatricians, however well meaning, are trained to follow a standardized treatment plan and usually have no means of individualizing care the way a mother would or the way a natural health practitioner always does. Hopefully this brief overview alerts you to the epidemic of autism and in the same breath assures you that there are viable treatments for this so-called incurable condition. Browse the links that Elissa has provided to further your research and please leave no stone unturned to help the next generation overcome autism. Resource list for article. ORGANIZATIONS –These sites offer videos of many children who have been restored to normal function as well as considerable help for parents and families. www.talkaboutcuringautism.org www.safeminds.org www.generationrescue.org www.childrenscornerschool.com/stankurtz.htm www.autism.com www.danconference.com www.autismmedia.org/media15.html TREATMENT RESOURCES ARI Summary of Biomedical Treatments for Autism ARI Mercury Detoxification Consensus Position Paper Laboratoire Phillipe Auguste – Testing available to doctors and direct to the public for health issues including autism. The Institutes for the Achievement of Human Potential – offers courses and other support to teach parents about the field of child brain development so that parents can use that knowledge to help their brain-damaged child toward wellness. TV TRANSCRIPTS Larry King Live Oprah Transcript Video BOOKS Louder Than Words: A Mother's Journey in Healing Autism By Jenny McCarthy. Blow by blow story of how the author's son was healed. Impossible Cure – The Promise of Homeopathy by Amy L. Lansky, PhD. Author's son was cured by homeopathy. Book covers details of his treatment as well as many other aspects of homeopathy useful to know. Judyth Reichenberg-Ullman - books about how to treat Aspergers Syndrome, ADHD and other related maladies with homeopathy. Evidence of Harm: Mercury in Vaccines and the Autism Epidemic: A Medical Controversy – by David Kirby. Carolyn Dean, MD, ND – three books covering health issues autistic children suffer. The Yeast Connection, IBS Syndrome and Magnesium Miracle and several soon-to-be published E Books on mercury, sugar, as well as a health encyclopedia of naturopathic interventions to use instead of medications for common health problems. ARTICLES DNA Is Not Destiny – The new science of epigenetics rewrites the rules of disease, heredity, and identity – by Ethen Watters. Discover Magazine November 2006. by Ethan Watters Autism: It's Not Just in the Head: – The devastating derangements of autism show up in the gut and in the immune system. That unexpected discovery is sparking new treatments that target the body in addition the brain - by Jill Neimark. Discover Magazine. February 2007. © 2007 Carolyn Dean - All Rights Reserved E-Mails are used strictly for NWVs alerts, not for sale Dr. Carolyn Dean is a medical doctor, naturopath, and nutritionist. She is a recognized authority in conventional and alternative medicine and author of a dozen books on health and healing. Dr. Dean offers private telephone wellness consultations through her website. Website: www.carolyndean.com E-Mail: holeopharm@pol.net Elissa Meininger is co-founder of Health Freedom Action Network, a grassroots political action group, as well as a health freedom political analyst who can be heard on the natural health radio show SuperHealth, broadcast twice weekly on Fox Sports Radio 1340 AM in Oklahoma City and on the internet.
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