Archive for the ‘Activism’ Category

CDC Widespread Abuse of Knowledge

This entire article was taken from:  https://lifebiomedguru.wordpress.com/.  It is one more example of how the CDC and others make public policy, and it should frighten all of us.

https://jameslyonsweiler.com/2016/05/17/science-and-policy-on-vaccine-safety-scienceabsence-of-evidence-abused-as-evidence-of-absence-part-1/

Science and Policy on Vaccine Safety Science:’Absence of Evidence’ Abused as ‘Evidence of Absence’: Part 1
by jameslyonsweiler

THERE IS A DISTURBING AND CONSISTENT trend in the vaccine safety literature for government-affiliated researchers in the misinterpretation of negative results from studies of specific, serious adverse events from vaccines, such as autism, encephalopathy, ADHD, and other serious neurological injuries.

Here’s the (il)logic flow:

*Conduct a retrospective epidemiological study (case/control, or cohort) with a relatively small samples size (few patients).

*Do not publish any power analysis showing that you had sufficient sampling effort to conduct significant effect.

*Analyze the data (we won’t go into cherry picking results here, but that, as well as “analyzing to result” both happen when a positive association is found, but the researchers wish to keep the result from public view).

*Find no or weak association.

*Lament the high confidence interval.

*Conclude something sciency-sounding, like:“The relative risk of severe neurologic disease in the 0–7 day risk period after meningococcal C conjugate vaccination was estimated at 1.28 (95% CI, 0.17–9.75). As evidenced by the wide confidence interval, the sample size is not large enough to get a more precise estimate of the relative risk. The authors concluded that administration of meningococcal C conjugate vaccine is not associated with an increased risk of severe neurologic disease within 0 to 7 days of vaccination” [1]

*Issue a official policy-sounding statement, such as:
Weight of Epidemiologic Evidence
The committee has limited confidence in the epidemiologic evidence, based on one study that lacked validity and precision, to assess an association between meningococcal vaccine and encephalitis or encephalopathy.[1]

*Create a policy of adoption of the vaccine, and give the following rationale:“There is no scientific evidence of serious neurological disease as result of this vaccine”.

If you don’t the flaw in the logic of steps 1-7, you’ve been duped.

Scientific studies, whether they are prospective studies, or retrospective studies, are supposed to provide proof that the sample size – the number of patients included in the study – was large enough to detect a specific effect if it did indeed exist. This property of a study is called “STATISTICAL POWER” and the analysis they SHOULD be including in their publications is called “POWER ANALYSIS”. Statistical power is the ability of a test to detect a significant (difference, increase in relative risk, increase is odd ratio) and is a function of:

-Sample Size in each sample group (N1, N2)

-Stringency of the test – the p-value required for a result to be considered ‘significant’ – this is generally 5%

-The degree of intrinsic variability in the data within and between the two groups (population variance)

-The effect size (the size of the actual difference in the measure of interest between two groups).

In randomized prospective studies of adverse events of drugs, a power analysis is par for the course. Showing the no adverse reactions were found is easy with small sample sizes, because the variability estimated within and between the two groups (say, treated vs. untreated) is a mathematical function of sampling effort N1 and N2.

Any qualified data analyst, epidemiologist, statistician, or scientist knows this.

Any study in vaccine safety that demonstrates a negative result for any given adverse event may show a negative result for two reasons:

(1) No difference exists between the two populations under study with respect to rates of the adverse event of interest, or

(2) The study was conducted with a sample size that was too small to ensure detection of a difference in the frequency of adverse events between the two populations under study.

That is, the study had insufficient power.

Unless a power analysis is conducted, no one – NO ONE – interpreting the results has any position to choose between the two reasons as their interpretation of the results.

Any qualified data analyst, epidemiologist, statistician, or scientist knows all of this, too.

It is flabbergasting why, then, so many studies from the CDC and CDC-affiliated scientists make conclusions such as:

“The relative risk of severe neurologic disease in the 0–7 day risk period after meningococcal C conjugate vaccination was estimated at 1.28 (95% CI, 0.17–9.75). As evidenced by the wide confidence interval, the sample size is not large enough to get a more precise estimate of the relative risk. The authors concluded that administration of meningococcal C conjugate vaccine is not associated with an increased risk of severe neurologic disease within 0 to 7 days of vaccination.”[1]

And then issue a official policy-sounding statement, such as:
Weight of Epidemiologic Evidence
The committee has limited confidence in the epidemiologic evidence, based on one study that lacked validity and precision, to assess an association between meningococcal vaccine and encephalitis or encephalopathy.[1]

Leading to a policy of adoption of the vaccine, based on the rationale:“There is no scientific evidence of serious neurological disease as result of this vaccine” or “No scientific study has shown…”

The Safety Assumption

There is an expression that is sometimes a fallacy, and sometimes not. It goes like this:

“The absence of evidence is not evidence of absence”.

This is largely considered a general fallacy – due in large part to Carl Sagan’s use of it in arguing for consideration of the likelihood that we just have not discovered all of the missing pieces of the evolution of the cosmos, but we can nevertheless deduce from other evidence that those missing pieces – the absence of evidence – nevertheless occurred. And we can certainly use the absence of evidence to deduce that some events that have not occurred have, in fact, not occurred.

But when it comes to science, especially epidemiological comparisons of rates of biomedical events in populations, there is a set of conditions in which the absence of evidence MAY NOT be used as evidence of absence.

Those conditions are when the study has low statistical power.

According to the committee statement, they concluded no evidence of the suspected increase in neurological adverse events from the vaccine due in part to a lack of precision.

“Lack of precision” means “high variability”, as in that reported in the sentence in the study:

“As evidenced by the wide confidence interval, the sample size is not large enough to get a more precise estimate of the relative risk.”[1]

The specific committee statement is carefully selected so as to allow the errant policy interpretation. They committee could have, and should have written:

The committee has no ability to rule out can association between meningococcal vaccine and encephalitis or encephalopathy based on the study, due to a lack of precision, resulting from a small sample size used to assess an association between meningococcal vaccine and encephalitis or encephalopathy.

In other words, a firm “We Don’t Know Because the Sample Size was Not Large Enough”.

This policy-like statement has a higher degree of fidelity to the limits of knowledge (LOK) imposed on interpretation of the study due to small sample size.

Policy based on a lack of evidence that results from a lack of statistical power, or destruction of validity of conclusions of studies via cherry-picking results after applying “kitchen-sink” statistics, is dangerous, because it requires the Safety Assumption: that a lack of evidence implies evidence of absence. The Safety Assumption only applies after a negative result has been found AND a power analysis has demonstrated that a positive result WOULD have been found given the sample sizes (N1, N2) and a priori estimate of the effect size.

Of course, if you control the sample size, you control the power…

ALERT!

There are many parents who know full well that their child suffered seizures, encephalopathy, and autism as a direct result of the vaccine – (aka “Vaccine-Induced Encephalopathy-Mediated Autism, or VIEMA). They know the vaccines cause their child’s autism as sure as they would be able to tell you their child was injured if they saw the child get hit by a moving car. They don’t need a significant result, nor a p-value, nor a power analysis. As the number of these parents in the population explode, an army of misled, misinformed parents are created. Fairly rapidly, however, these parents are waking up and becoming informed. When they attend courses to learn about statistical power – and how ridiculously simple is it to execute power analysis with available software, including many free online applications – they will have their time in the sun, their day in court, and they will re-dedicate their lives to righting the wrongs of the CDC and preventing further injuries. They, unlike scientists in academia, or not dependent on a culture of turning a blind eye to these willful acts of misinterpretation in the name of a ‘common good’ of vaccination. And, as I pointed out, they are growing in number every day, possibly by as many as 250,000 vaccine injured people/day.

Vaccine Safety Science as an Archery Contest

Imagine an archery contest in which a choice prize – a bag of gold – is given for hitting a hitting a bull eye’s on a target. In each round, a contestant gets a single draw. Each time a contestant hits hits the bull’s eye, they get another bag of gold.

A contestant lines up, draws, aims, and lets go. They miss the bull’s eye because their aim is not good. No bag of gold for them.

Another contestant lines up, draws, aims, and lets go. They hit the bull’s eye because their aim was good, and their pull was strong. All in witness of the tournament can see that the bag of gold is well-earned.

The CDC lines up, aims, draws a little, and the arrow flies about three feet, falling far short of the target. “Bullseye!” they claim!

In reality, they neither hit, nor missed the bull’s eye because they did not draw with sufficient power to enable an appropriate assessment of their aim.

The CDC’s widespread abuse of knowledge – because that’s what it is – leads to the situation where it appears as if a positive study has been conducted upon which public policy is based, when, in reality, the study might as well not even ever been conducted.

In reality, the above analogy is better fit if the goal of the contestants is to MISS the bull’s eye (no positive result), but you get the idea: The amount of empirical information generated by underpowered studies with negative results is zero.

What is even more disturbing is that the practice of Steps 1-7 have been repeated over, and over… and over. And worse than that – there is a pattern of CDC analysts taking the extraordinary step of changing study designs by omitting specific patients from studies for arbitrary reasons – with the result being a reduction in the sample size, yielding a corresponding drop in statistical power – AFTER finding a positive association with the full sample available for analysis.

In Part 2, I will enumerate examples in which current public policy on vaccines are based on the illogical, unwarranted Safety Assumption.

In Part 3, I will review the evidence that CDC officials and collaborators committed scientific fraud by taking extraordinary steps to corrupt otherwise robust study designs to reduce statistical power, and publish only the final, negative results, with no reference to the initial positive association.

These abuses of science are widely known as ‘heinous crimes’ in the biostatistics literature. So far, the academic community of statisticians have been oddly silent on these issues, but I will be sharing this series of posts with them for their consideration.

Citation

[1] Committee to Review Adverse Effects of Vaccines; Institute of Medicine; Adverse Effects of Vaccines: Evidence and Causality. Stratton K, Ford A, Rusch E, et al., editors. Washington (DC): National Academies Press (US); 2011 Aug 25. Chapter 11. Meningococcal Vaccine. http:// http://www.ncbi.nlm.nih.gov/books/NBK190008/

jameslyonsweiler | May 17, 2016 at 7:53 pm | Categories: Cures | URL: http://wp.me/p5Qzty-13O

Tiny Tick Big Controversy ABC Special Report

  Published on Feb 4, 2016 WMDT-TV Channel 47 Documentary on Lyme.  Approx. 25 minutes

See local Lyme patients, hear interviews with specialists, as well as medical professionals who don’t necessarily believe in chronic Lyme disease. Emily Lampa, senior reporter for WMDT-TV, courageously took on this challenge and created the documentary, “Tiny Tick Big Controversy”.

The prevention of tick-borne illnesses is much more complicated than just avoiding ticks. One of the major reasons is that the diagnosis and treatment of the most common vector-borne infection, Lyme Disease, is still such a mystery and so often clouded by controversy.

 

Good News! Stanford Lyme Working Group

 

Forward Thinking! — Ticktalkireland’s Blog

Thanks to Sherry and Lair Cagan, founders of www.Stand4Lyme.com, there is some great research being conducted at Standford University who is collaborating with numerous institutions.

If you need some hope today, watch this 20 minute video.  Kudos to the Cagans!

More good news:  http://www.northeastern.edu/news/2016/03/researchers-investigate-four-promising-new-treatments-for-lyme-disease/  March 29, 2016

“Uni­ver­sity Dis­tin­guished Pro­fessor Kim Lewis, who leads the Lyme dis­ease research team, is now expanding that ther­a­peutic reach with the help of a $1.5 mil­lion grant from the Steven and Alexandra Cohen Foundation.

The team is pur­suing four arms of treatment-related research at Northeastern’s Antimi­cro­bial Dis­covery Center, which Lewis directs.

They are: a mouse study of a reg­imen that erad­i­cated the bac­terium in the test tube, set­ting the stage for human trials; antibi­otic cock­tails using existing drugs; strate­gies to dis­cover new drugs that selec­tively target the Lyme bac­terium; and ways to alter the com­po­si­tion of the microbiome—the com­mu­nity of microor­gan­isms inhab­iting the human body—to stop the autoim­mune reac­tions that char­ac­terize the disease.

All four show exciting promise. The grant, Lewis says, “will give us the flex­i­bility to test our approaches in par­allel, which will save us an enor­mous amount of time.”

“We are going at Lyme dis­ease with every­thing we have.”
— Uni­ver­sity Dis­tin­guished Pro­fessor Kim Lewis

We are rooting for all of you!

Fluoride – Not What You Think

Fluoridated water is another example of a medical disconnect that needs to be exposed.

MSIDS patients have weak immune systems due to stealth pathogens invading Killer T-Cells which cause the body to attack itself.  We need to hunt to ground everything that is weakening our bodies, and one of those “things” is fluoride.

Hailed by the Centers for Disease Control as one of the top ten public health achievements of the 20th century, water fluoridation is something most of us assume to be safe and effective. But new science has upended this assumption, revealing that fluoride is a developmental neurotoxin and an endocrine disruptor. The CDC tells us that drinking fluoride decreases tooth decay, at best, by 25%. That is one-half to one cavity per person over a lifetime. Is one less cavity worth risking a child’s long-term brain and thyroid health? It’s time to rethink this very old practice.

In OUR DAILY DOSE, filmmaker Jeremy Seifert (GMO OMG) lays out the dangers of water fluoridation informatively and creatively, highlighting the most current research and interviewing top-tier doctors, activists, and attorneys close to the issue. Through thoughtful examination of old beliefs and new science, the film alerts us to the health threat present in the water and beverages we rely on every day. This is an eye-opening look at how we have less control over our health than we may have thought.

http://articles.mercola.com/sites/articles/archive/2016/05/21/our-daily-dose-fluoride-documentary.aspx?utm_source=dnl&utm_medium=email&utm_content=art1&utm_campaign=20160521Z1&et_cid=DM105855&et_rid=1494753110

“Scientific investigations have revealed that fluoride is an endocrine disrupting chemical, and a developmental neurotoxin that impacts short-term and working memory, and lowers IQ in children.

It has been implicated as a contributing factor in the rising rates of both attention-deficit hyperactive disorder (ADHD) and thyroid disease.

Indeed, fluoride was used in Europe to reduce thyroid activity in hyperthyroid patients as late as the 1970s, and reduced thyroid function is associated with fluoride intakes as low as 0.05 to 0.1 mg fluoride per kilogram body weight per day (mg/kg/day).  

Children are particularly at risk for adverse effects of overexposure, and in April 2015, the US government admitted that the “optimal” level of fluoride recommended since 1962 had in fact been too high.

As a result, over 40 percent of American teens show signs of fluoride overexposure — a condition known as dental fluorosis. In some areas, dental fluorosis rates are as high as 70 to 80 percent, with some children suffering from advanced forms.

So, for the first time, the U.S. Department of Health and Human Services (HHS) lowered its recommended level of fluoride in drinking water by 40 percent, from an upper limit of 1.2 milligrams per liter (mg/L) to 0.7 mg/L.

The HHS said it will evaluate dental fluorosis rates among children in 10 years to assess whether they were correct about this new level being protective against dental fluorosis.

But just what is the acceptable level of harm in the name of cavity prevention?

A number of studies have shown that children with moderate to severe dental fluorosis score worse on tests measuring cognitive skills and IQ than peers without fluorosis — a clear revelation highlighted in the film, as some still insist that dental fluorosis is nothing more than a cosmetic issue.

As stated, fluoride is a drug, and research into the health effects of fluoride are based on pharmaceutical grade fluoride. However, a majority of water authorities do not even use pharmaceutical grade fluoride; they use hydrofluosilicic acid, or hexafluorosilicic acid — toxic waste products of the phosphate fertilizer industry, which are frequently contaminated with heavy metals such as arsenic, mercury, cadmium, lead, and other toxins.

This is a key point that many fluoride proponents fail to address when arguing for its use.”

Interestingly, 97% of Western European countries have stopped or have never fluoridated their water and have seen the exact same reduction in dental cavities as the U.S., proving it’s not fluoride doing the work here.

The best way to prevent cavities is by eating real, fresh food, avoiding sugar and processed food, getting plenty of omega -3 fats, and keeping the mouth clean.

Holistic Doctors Mysteriously Dying – The Kate Show

https://w.soundcloud.com/player/?url=https%3A//api.soundcloud.com/tracks/263821614&auto_play=false&hide_related=false&show_comments=true&show_user=true&show_reposts=false&visual=true“>

Kate interviews Erin Elizabeth of Healthnutnews.com on her findings as to why so many holistic doctors are suddenly and mysteriously dying! Erin was the first to interview the family of the first deceased doctor- Dr. Jeff Bradstreet – to refute the reports that he committed suicide. Over 30 doctors have died since and Erin discusses what could be the reasons behind the horrifying deaths. Erin discusses vaccines, cancer treatments and so much more. Also- new findings about Tylenol and why studies say ingesting acetaminophen could be robbing you of feeling empathy!