Wednesday, January 3, 2007

HPV vs. cervical cancer vs. Gardasil

Have you read the vaccine package insert?
http://www.merck.com/product/usa/pi_circulars/g/gardasil/gardasil_pi.pdf

Gardasil contains only four strains of HPV: Types 6, 11, 16, 18 (note that there are over 120 strains of HPV)

"HPV also causes approximately 35-50% of vulvar and vaginal cancers.... HPV also causes genital warts (condyloma acuminata) which are growths of the cervicovaginal, vulvar, and the external genitalia that rarely progress to cancer. HPV 6, 11, 16, and 18 are common HPV types.
HPV 16 and 18 cause approximately:
• 70% of cervical cancer, AIS, CIN 3, VIN 2/3, and VaIN 2/3 cases; and
• 50% of CIN 2 cases.
HPV 6, 11, 16, and 18 cause approximately:
• 35 to 50% of all CIN 1, VIN 1, and VaIN 1 cases; and
• 90% of genital wart cases."

So, of the 35-50% (leaving 65-50% of the cervical cancers being caused by other things) of cervical cancers that are diagnosed as being caused by HPV, HPV 16 and 18 cause approximately 70% of the 35-50% of cervical cancers caused by HPV.

Say 100 women are diagnosed with cervical cancer:
--50-65 of them will have gotten cervical cancer from a different cause
--35-50 of them will have gotten cervical cancer from HPV
--of the 35-50 who have cervical cancer from HPV, only ~70% of them would have been protected from HPV causing cancer (strain 16 and 18 are the cancer causing strains in gardasil)--24.5-35 of the women (in a 100) "could" have been protected against cervical cancer--that's if the vaccine were effective in them--or if the vaccine didn't wear off...or that they could receive the vaccine at all (because most people have adverse events following vaccination due to allergies or an over-response from the immune system).

Vaccine package insert: "As for any vaccine, vaccination with GARDASIL may not result in protection in all vaccine recipients."

"This vaccine is not intended to be used for treatment of active genital warts; cervical cancer; CIN, VIN, or VaIN.
This vaccine will not protect against diseases that are not caused by HPV.
GARDASIL has not been shown to protect against diseases due to non-vaccine HPV types.
As with all injectable vaccines, appropriate medical treatment should always be readily available in case of rare anaphylactic reactions following the administration of the vaccine. The decision to administer or delay vaccination because of a current or recent febrile illness depends
largely on the severity of the symptoms and their etiology. Low-grade fever itself and mild upper respiratory infection are not generally contraindications to vaccination.
Individuals with impaired immune responsiveness, whether due to the use of immunosuppressive therapy, a genetic defect, Human Immunodeficiency Virus (HIV) infection, or other causes, may have reduced antibody response to active immunization (see PRECAUTIONS, Drug Interactions).
As with other intramuscular injections, GARDASIL should not be given to individuals with bleeding disorders such as hemophilia or thrombocytopenia, or to persons on anticoagulant therapy unless the potential benefits clearly outweigh the risk of administration. If the decision is made to administer
GARDASIL to such persons, it should be given with steps to avoid the risk of hematoma following the injection."

"GARDASIL is not recommended for use in pregnant women."

"GARDASIL has not been evaluated for the potential to cause carcinogenicity or genotoxicity."

"Because many drugs are excreted in human milk, caution should be exercised when GARDASIL is administered to a nursing woman."

"The safety and efficacy of GARDASIL have not been evaluated in children younger than 9 years....The safety and efficacy of GARDASIL have not been evaluated in adults above the age of 26 years."

See pages 11-13 in vaccine package insert for adverse events table.

Keep in mind HPV is a sexually transmitted disease--a preventable disease (without vaccination). Practice safe sex people...

This is one, of many, vaccine I would NEVER recommend.

Comparison

FDA calls for pain reliever warning; Updated 12/20/2006 12:01 AM ET; By Julie Schmit and Julie Appleby, USA TODAY
The warnings don't stem from new data regarding health risks and NSAIDs, Ganley says. But he added there may be increasing evidence of liver risks with acetaminophen. A study published last year in Hepatology concluded that liver damage caused by acetaminophen exceeded other causes of U.S. drug-induced acute liver failure, but that most of the cases stemmed from accidental overdoses or suicide attempts. About 100 people in the USA die each year after accidental acetaminophen overdoses, the FDA says.


New Warnings Proposed For Over–the–Counter Drugs; The New York Times, 12-20-06; Editor's Notes: or read it straight from the story: Warnings Proposed for Over-the-Counter Drugs; By STEPHANIE SAUL; Published: December 20, 2006
But Dr. Ganley said that when the drugs are used by so many people rare problems could add up. Doctors have raised concerns about overdoses from drugs containing acetaminophen, a leading cause of acute liver failure. More than 200 million Americans a year take products like Tylenol with acetaminophen, and overdoses cause up to 450 deaths a year from acute liver failure.


Approximate deaths per year from varicella: 100 (CDC's MMWR publication).

That would put Tylenol on the same level of safety as the varicella infection--wouldn't it?

Since the beginning of the Varicella vaccine: Found 28274 records with Vaccine contains 'VARCEL' (singular varicella vaccine) plus, Found 293 records with Vaccine contains 'MMRV' (Proquad) reported cases to VAERS...which does more harm...varicella, or the vaccines that "protect" against varicella?

Which is safer: Tylenol, varicella, or the varicella vaccine?

Tuesday, December 26, 2006

Herd Immunity

How can herd immunity exist in our world today?

Vaccines do not provide life-long immunity. How could vaccines create herd immunity then? Plus, there are vaccines that shed--therefore spreading the disease (well, a weaked form of the disease, but spreading the disease nonetheless)--how can herd immunity exist with vaccines keeping the disease in circulation.

As far as I know, this is still a theory--with plenty of mathematical equations to recreate what the scientific community/medical community believe to be happening. I still haven't seen evidence that PROVES this theory.

My understanding was that herd immunity could only happen when a disease went through a population naturally. Those who survive will have natural immunity--and their children will gain basic immunity and be able to handle the disease and have natural life-long immunity themselves.

Vaccinated immunity leaves adolescents with waning "immunity" (if they have any at all) and leave them susceptable as adults--instead they should be acquiring natural immunities as children by experiencing these childhood diseases. Vaccinated immunity cannot be passed from mother to infant/child--leaving the infants more susceptable to disease--whereas, natural immunity CAN be passed from mother to infant, giving the child basic immunity so they can survive disease. Vaccinating leaves a hole for another strain or serotype to step forward and become a menace--creating the need for more and more vaccines--which makes the community at large more susceptable to disease--creating an unhealthy environment. And I guess you could view boosters as a cure to the vaccinated immunity problem--but does it solve the problem?--no!

Vaccinated immunity wears off--natural immunity does not wear off.

Some interesting reads:
The concept of herd immunity applied to the evaluation of vaccination programs

Increased Susceptibility to Measles in Infants in the United States

Decay of Passively Acquired Maternal Antibodies against Measles, Mumps, and Rubella Viruses

Analysis of epidemiological peculiarities of rubella based on a mathematical model (according to observations over 10 years in Moscow).

Measles, mumps and rubella: control by vaccination.

Rubella among the Amish: resurgent disease in a highly susceptible community.

A great compilation of quotations about immunity by lilithx: natural vs. vaccination immunity

Sunday, December 24, 2006

rBGH/rBST

Milk--it does a body good?

What if the cows are treated with rBGH/rBST?

If you don't want cancer then don't drink milk that is from cows injected with rBGH/rBST

rBGH -- Recombinant Bovine Growth Hormone -- It's Bad News

more info

CFS
For over 10 years, bovine growth hormone, or rBGH, has been a staple in the dairy products consumed by Americans. Since these products are not labeled as containing rBGH, most consumers have no idea that a growth hormone intended to induce dairy cows to be more productive is in much of their milk, cheese, and yogurt.

After approving the use of rBGH in 1993, the Food and Drug Administration has turned a deaf ear to the pleas of consumers, food safety organizations and scientists to reverse its approval of the hormone, or to simply require labeling of foods containing rBGH. Even a legal challenge by CFS could not force FDA to reexamine the health threats of rBGH. The FDA's decision stood despite regulatory bodies in both Canada and Europe rejecting the hormone due to numerous animal and human health concerns.

In cows treated with rBGH, significant health problems often develop, including a 50 percent increase in the risk of lameness (leg and hoof problems), over a 25 percent increase in the frequency of udder infections (mastitis), and serious animal reproductive problems, i.e., infertility, cystic ovaries, fetal loss and birth defects.

Because rBGH use results in more cases of mastitis, dairy farmers tend to use more antibiotics to combat the infections, the residues of which also may end up in milk and dairy products. These residues can cause allergic reactions in sensitive individuals and contribute to the growth of antibiotic resistant bacteria, further undermining the efficacy of some antibiotics in fighting human infections.

Furthermore, recent research has shown conclusively that the levels of a hormone called "insulin-like growth factor-1" (IFG-1) are elevated in dairy products produced from cows treated with rBGH. Canadian and European regulators have found that the FDA completely failed to consider a study that showed how the increased IGF-1 in rBGH milk could survive digestion and make its way into the intestines and blood stream of consumers. These findings are significant because numerous studies now demonstrate that IGF-1 is an important factor in the growth of cancers of the breast, prostate and colon.


News and Views
on rBGH & rBST

Aspartame

Well, you gotta love the artificial sweetners, right? It's been almost a year now that I've been Diet Coke free...part of the reason I quit is because of the artifical sweetner Aspartame.

Analysis Shows Nearly 100% of Independent Research Finds Problems With Aspartame
October 17, 1996

An analysis of peer reviewed medical literature using MEDLINE and other databases was conducted by Ralph G. Walton, MD, Chairman, The Center for Behavioral Medicine, Professor of Clinical Psychiatry, Northeastern Ohio Universities College of Medicine. Dr. Walton analyzed 164 studies which were felt to have relevance to human safety questions. Of those studies, 74 studies had aspartame industry-related sponsorship and 90 were funded without any industry money.

Of the 90 non-industry-sponsored studies, 83 (92%) identified one or more problems with aspartame. Of the 7 studies which did not find a problems, 6 of those studies were conducted by the FDA. Given that a number of FDA officials went to work for the aspartame industry immediately following approval (including the former FDA Commissioner), many consider these studies to be equivalent to industry-sponsored research.

Of the 74 aspartame industry-sponsored studies, all 74 (100%) claimed that no problems were found with aspartame. This is reminiscent of tobacco industry research where it is primarily the tobacco research which never finds problems with the product, but nearly all of the independent studies do find problems.

The 74 aspartame industry-sponsored studies are those which one inveriably sees cited in PR/news reports and reported by organizations funded by Monsanto/Benevia/NutraSweet (e.g., IFIC, ADA). These studies have severe design deficiencies which help to guarantee the "desired" outcomes. These design deficiencies may not be apparent to the inexperienced scientist. Healthcare practitioners and scientists should print out the all of the documents on the Monsanto/NutraSweet Scientific Abuse web page, the Scientific FAQs web page and the Aspartame Toxicity Reaction Report Samples. Please refer scientific questions to mgold@holisticmed.com.


Abuse of the Scientific Method Seen in Monsanto Aspartame Research

Which lead me to the following link: SURVEY OF ASPARTAME STUDIES: CORRELATION OF OUTCOME AND FUNDING SOURCES

Scientific Abuse in Methanol / Formaldehyde Research Related to Aspartame

Scientific Abuse in Seizure Research Related to Aspartame

Scientific Abuse in Migraine/Headache Research Related to Aspartame

Scientific Abuse in Parkinson's Disease Research Related to Aspartame

Independent Analysis of the
"Opinion of the European Commission, Scientific Committee on Food:
Update on the Safety of Aspartame / E951"


Reported Aspartame Toxicity Effects
Q. What are the reported reactions to aspartame ingestion?

How often are such effects seen?

Answer
------

==> What are the reported reactions to aspartame ingestion?

We will limit our discussion in this FAQ to reported toxicity
reactions to aspartame ingestion. Controlled studies showing
problems with aspartame ingestion will be discussed in another
FAQ. Toxicity reactions to aspartame can be divided into three
types:

1. Acute toxicity reactions occuring within 48 hours of ingestion of
an aspartame-containing product.

2. Chronic toxicity effects occuring anywhere from several days of
use to appearing a number of years (i.e., 1-20+ years) after the
beginning of aspartame use.

3. Potential toxicity effects that would be nearly impossible for
the user to recognize the link to aspartame.

In an epidemiological survey which appeared in the Journal of
Applied Nutrition (Roberts 1988), 551 persons who have
reported toxicity effects from aspartame ingestion were
surveyed. The adverse effects found cover a subset of reported
acute and chronic toxicity effects from aspartame.
What follows is a listing of the adverse health effects
which were found.

-------------------
# of
people (%)
Eye
- Decreased vision and/or other eye problems 140 (25%)
(blurring, "bright flashes," tunnel vision)
- Pain (or or both eyes) 51 (9%)
- Decreased tears, trouble with contact lens, 46 (8%)
or both
- Blindness (one or both eyes) 14 (3%)

Ear
- Tinnitus ("ringing," "buzzing") 73 (13%)
- Severe intolerance for noise 47 (9%)
- Marked impairment of hearing 25 (5%)

Neurologic
- Headaches 249 (45%)
- Dizziness, unsteadiness, or both 217 (39%)
- Confusion, memory loss, or both 157 (29%)
- Severe drowsiness and sleepiness 93 (17%)
- Paresthesias ("pins and needles," "tingling") 82 (15%)
or numbness of the limbs
- Convulsions (grand mal epileptic attacks) 80 (15%)
- Petit mal attacks and "absences" 18 (3%)
- Severe slurring of speech 64 (12%)
- Severe tremors 51 (9%)
- Severe "hyperactivity" and "restless legs" 43 (8%)
- Atypical facial pain 38 (7%)

Psychologic-Psychiatric
- Severe depression 139 (25%)
- "Extreme irritability" 125 (23%)
- "Severe anixiety attacks" 105 (19%)
- "Marked personality changes" 88 (16%)
- Recent "severe insomnia" 76 (14%)
- "Severe aggravation of phobias" 41 (7%)

Chest
- Palpitations, tachycardia (rapid heart action), 88 (16%)
of both
- "Shortness of breath" 54 (10%)
- Atypical chest pain 44 (8%)
- Recent hypertension (high blood pressure) 34 (6%)

Gastrointestinal
- Nausea 79 (14%)
- Diarrhea 70 (13%)
Associated gross blood in the stools (12)
- Abdominal pain 70 (13%)
- Pain on swallowing 28 (5%)

Skin and Allergies
- Severe itching without a rash 44 (8%)
- Severe lip and mouth reactions 29 (5%)
- Urticaria (hives) 25 (5%)
- Other eruptions 48 (9%)
- Aggravation of respiratory allergies 10 (2%)

Endocrine and Metabolic
- Problems with diabetes: loss of control; 60 (11%)
precipitation of clinical diabetes;
aggravation or simulation of diabetic
complications
- Menstrual changes 45 (6%)
Severe reduction or cessation of periods (22)
- Paradoxic weight gain 34 (5%)
- Marked weight loss 26 (6%)
- Marked thinning or loss of the hair 32 (6%)
- Aggravated hypoglycemia (low blood sugar 25 (5%)
attacks)

Other
- Frequency of voiding (day and night), burning 69 (13%)
on urination (dysuria), or both
- Excessive thirst 65 (12%)
- Severe joint pains 58 (11%)
- "Bloat" 57 (10%)
- Fluid retention and leg swelling 20 (4%)
- Increased susceptibility to infection 7 (1%)

-------------------

There are other clinical reports in the scientific literature of
aspartame-caused toxicity reactions including Blumenthal (1997),
Drake (1986), Johns (1986), Lipton (1989), McCauliffe (1991),
Novick (1985), Watts (1991), Walton (1986, 1988), and Wurtman
(1985).

Many pilots appear to be particularly susceptible to the effects of
aspartame ingestion. They have reported numerous serious toxicity
effects including grand mal seizures in the cockpit (Stoddard 1995).
Nearly 1,000 cases of pilot reactions have been reported to the
Aspartame Consumer Safety Network Pilot Hotline (Stoddard 1995).
This susceptibility may be related to ingesting methanol at altitude
as suggested in a letter from Dr. Phil Moskal, Professor of
Microbiology, Biochemistry, and Pathology, Chairman of the Department
of Pathology, Director of Public Health Laboratories (Moskal 1990),
or it may simply be that some pilots tend to ingest large quantities
of aspartame during a flight. Whatever the case, numerous warnings
about aspartame dangers have appeared in piloting journals including
The Aviation Consumer (1988), Aviation Medical Bulliten (1988),
Pacific Flyer (1988), CAA General Aviation (1989), Aviation Safety
Digest (1989), General Aviation News (1989), Plane & Pilot (1990),
Canadian General Aviation News (1990), National Business Aircraft
Association Digest (NBAA Digest 1993), International Council of
Air Shows (ICAS 1995), and the Pacific Flyer (1995). Both the U.S.
Air Force's magazine "Flying Safety" and the U.S. Navy's magazine,
"Navy Physiology" published articles warning about the many dangers
of aspartame including the cumlative deliterious effects of methanol
and the greater likelihood of birth defects. The articles note that
the ingestion of aspartame may make pilots more susceptible to
seizures and vertigo (US Air Force 1992).

Countless other toxicity effects have been reported to the FDA (DHHS
1995), other independent organizations (Mission Possible 1996,
Stoddard 1995), and independent scientists (e.g., 80 cases of
seizures were reported to Dr. Richard Wurtman, Food (1986)).
Samples of some aspartame toxicity reactions reported on the
Internet can be found on the Aspartame (NutraSweet) Toxicity Info
Center web page:

http://www.tiac.net/users/mgold/aspartame/

Frequently, aspartame toxicity is misdiagnosed as a specific disease.
This has yet to be reported in the scientific literature, yet it has
been reported countless times to independent organizations and
scientists (Mission Possible 1994, Stoddard 1995). In other cases,
it has been reported that chronic aspartame ingestion has triggered
or worsened certain chronic illnesses. Nearly 100% of the time, the
patient and physician assume that these worsening conditions are
simply a normal progression of the illness. Sometimes that may be
the case, but many times it is chronic aspartame poisoning.

According to researchers and physicians studying the adverse
effects of aspartame, the following list contains a selection
of chronic illnesses which may be caused or worsened by the chronic,
long-term ingestion of aspartame. (Mission Possible 1994, Stoddard
1995)*:

Brain tumors Multiple sclerosis
Epilepsy Chronic faigue syndrome
Parkinson's Disease Alzheimer's
Mental retardation Lymphoma
Birth defects Fibromyalgia
Diabetes Arthritis (including Rheumatoid)
Chemical Sensitivities Attention Deficit Disorder

*Note: In some cases such as MS, the severe symptoms
mimic the illness or exacerbate the illness,
but do not cause the disease.

Also, please note that this is an incomplete list. Clearly,
ingestion of a very slow poison (as discussed in other FAQs) is not
beneficial to anyone who has a chronic illness.

Finally, potential toxicity effects from aspartame including brain
cancer (as seen in pre-approval research) and effects on fetal brain
and nervous system development will be discussed in other FAQs.


http://www.holisticmed.com/aspartame/recent.html

Industry Funded Research
Non-Industry Funded Research

Monsanto Products to Avoid

http://www.holisticmed.com/aspartame/embalm.html
The following facts shown by recent scientific research:

1. Aspartame (nutrasweet) breaks down into methanol (wood alcohol).

2. Methanol quickly converts to formadehyde in the body.

3. Formaldehyde causes gradual and eventually severe damage to the neurological system, immune system and causes permanent genetic damage at extremely low doses.

4. Methanol from alcoholic beverages and from fruit and juices does not convert to formaldehyde and cause damage because there are protective chemicals in these traditionally ingested beverages.

5. The most recent independent research in Europe demonstrates that ingestion of small amounts of aspartame leads to the accumulation of significant levels of formaldehyde (bound to protein) in organs (liver, kidneys, brain) and tissues.

6. Excitotoxic amino acids such as the one which is immediately released from aspartame likely increases the damage caused by the formaldehyde.



Aspartame / NutraSweet Dangers in Pregnancy

The Secret Dangers of Splenda (Sucralose), an Artificial Sweetener

The Potential Dangers of Sucralose:
Reader Testimonials


The Dangers of Chlorine and Issues With Sucralose

Sucralose (Splenda®) U.S. Product List

http://www.truthaboutsplenda.com/