• Resources
    • Videos/Speeches/Articles
    • The Art of Health Freedom
    • Good Books
    • Recommended Videos
    • Recommended Links
    • Radio Show Archives
    • Trustee Interviews
    • Newsletter Archives
    • Internet Links
  • Rave Reviews
    • Testimonials
    • Video Testimonials
  • Take Action
    • Create Pushback
    • Tell Your Friends
    • Become an Organizer
    • Send Letters
  • Wellness Stores
    • Buy our products
    • Valley of the Moon Coffee
  • 5 Big Lies
    • Drugs & Vaccine
    • Chemtrails
    • G.M.O.
    • Radiation
    • Food
  • Home
  • Support
    • Support Health Freedom
    • Coffee
  • Events/Press/Media
    • POD Casts/Radio Shows
    • Webinars
    • Press Release
  • About Us
    • Mission Statement
    • Accomplishments
    • Board of Trustees
    • NSF History/Vision
    • Contact Webmaster
    • Customer Service
  • Dr. Rima’s Blog/Vlog
    • GDS
    • Codex Alimentarius
  • eBook Download

Archive for Government Agencies – Page 2

Support the Ear Candlers Case Against FDA Dictates!

By Administrator on March 23, 2011 No Comments

Natural Solutions Foundation
Your Voice of Global Health & Food Freedom™
www.GlobalHealthFreedom.org
www.GlobalFoodFreedom.org

Please Donate Here and receive your holistic gift!

earcandleimage

After sitting on the case for nearly a year, the Federal Judge hearing the Ear Candlers case dismissed the lawsuit because he determined that the FDA’s “cease and desist” letters of February 2010 were not “final agency actions” and the companies therefore do not have “standing to sue” until the FDA takes enforcement action. The Ear Candlers intend to file a Motion to Reconsider since the facts, as they’ve developed while the Court held the motion, is that the couple companies that did NOT join in the law suit as plaintiffs did have enforcement action taken against them, so the Judge has invoked the infamous Catch 22: our lawsuit protected the plaintiff companies from FDA persecution, so that “means” the plaintiffs cannot sue, since there has been no enforcement action against these particular parties.

What can we do?

In order to bring this matter forward, by filing the Motion to Reconsider and then, if that is rejected, a full appeal, we need to raise needed legal expense funds. None of the companies that make the NonMedical Devices Formerly Known as Holistic Ear Candles (FDA says they cannot be called anything that uses the words “ear” or “candle” or “holistic”) is a big company; all are small family businesses. While they cannot afford the costs of fighting the Federal Government in its own courts, they can offer you a gift of 6 Ear Candles (our use of the term “Ear Candles” herein should be considered short-hand for said NonMedical Devices Formerly Known as Holistic Ear Candles). So PLEASE DONATE GENEROUSLY!

Our prior posting on the case: http://drrimatruthreports.com/?p=5210


JUDGE THROWS EAR CANDLE CASE OUT OF COURT:
“TARGET EAR CANDLE COMPANIES HAVE NO STANDING TO DEFEND THEMSELVES AGAINST BEING PUT OUT OF BUSINESS”

Our employee, the FDA is, once again, wreaking havoc and terror on you and me – on We the People!

Having declared Ear Candles a Medical Device, the Fraud and Death Administration then stated that under no circumstances could Ear Candles ever be APPROVED as a Medical Device and issued “Cease and Desist” orders against the manufacture or sale of Ear Candles.

Whether or not you use Ear Candles, it is clear that this assault on a safe, time-honored and danger-free modality is the first in a new campaign of terror –yes, terror – against the manufacturers, marketers and consumers of anything but dangerous, expensive and easily replaced pharmaceuticals.

FDA is vigorously attacking Ear Candle Manufacturers while, for example, supporting Pfizer and reversing the FDA position on antibiotics: Pfizer new vaccine “for” ear infections killed 4 more children in Japan shortly before the Tsunami. AMA has reversed their long held, science based position against antibiotics in ear infections and now are claiming that antibiotics “cure” ear infections despite the lack of clinical evidence to suggest that it is true. The press, however, is not touting this “breakthrough”.

Although claims are sharply prohibited by FDA in this war of terror, the truth as Dr. Laibow and other holistic practitioners know from their clinical experience is that Ear Candles have a significant efficacy rate in ear infections. None of the companies adopt this position, of course.

And the Supreme Court tells us, in the leading case of Thompson vs Western States (535 U.S. 357, 2002) that –

“If the First Amendment means anything, it means that regulating speech must be a last – not first – resort … We have previously rejected the notion that the Government has an interest in preventing the dissemination of truthful commercial information in order to prevent members of the public from making bad decisions with the information… Even if the Government did argue that it had an interest in preventing misleading advertisements, this interest could be satisfied by the far less restrictive alternative of requiring … a warning that the [device] had not undergone FDA testing and that its risks were unknown.”

This nonmedical device example is just one in a long, long line of shameful distortions and persecutions of natural products health and wellness manufacturers and those who disseminate and purvey the information about what they are and how to work with them. Because Ear Candles are less known than other modalities like, for example, Chelation therapy or Vitamin C drips for treatment of cancer, we believe that the FDA sees them as a good place to start this new assault. The strategy is to declare them untested medical devices and then prevent them from being made or sold through Cease and Desist orders without taking a final action. It is this lack of final action which the Judge says prevents the companies from having standing to defend themselves.

We believe that if we do not file a successful appeal, we, the health freedom community, will see a blizzard of these Cease and Desist orders, none of them final action, but all of them definitive: “Keep making the product, or selling it, and go to jail.”

We have no choice but to fight as long as it takes to stop the FDA. Ear Candles are the tip of the iceberg: fighting and winning the Ear Candle issue is identical to fighting and winning a major portion of the health freedom battle: the right to decide what methods you use to gain and maintain health.

Please Donate Here to fund the appeal process which we must begin within the next couple weeks.

For every 25 dollars donated, we will send you 6 free ear candles from your preferred vendor:

Harmony Cone Ear Candles
Beck Ear Candles
Lees Ear Candles
Coning Works
So Fine Distributor

Please indicate in the “comments” section of the donation page the vendor from whom you would like to receive your “thank you” gift of 6 Ear Candles.

Thank you in advance for your donation to help win this peaceful health freedom revolution!

Ear Candlers’ Association
Natural Solutions Foundation
Citizens for Health

Please Donate Here:





We know it’s really hard out in America right now. We know you are working hard just to make ends meet. We know how all your expenses have been going up; we buy groceries too. Frankly, there is no one else to whom we can turn for the resources to make a difference. So it is up to you.

How important is the fight? What do you care about some holistic device?

What we can tell you is, this FDA “cease and desist” order to these companies sets a precedent, a dangerous one… But, we can Push Back through the courts and seek redress of grievances that can protect all of our access to natural means to achieve and maintain health.

Protest this gross violation of civil rights:
http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=2521

Categories : 01 Food ebook, Activism, Blog / Vlog, Declaration of Health Independence, Disinformation, Get Involved, Government Agencies, health freedom

Educate Congress: NO Federal Debt Ceiling Increase; No Funding for Food Control Law!

By Administrator on March 9, 2011 No Comments

Natural Solutions Foundation
Your Voice of Global Health & Food Freedom™
www.GlobalHealthFreedom.org
www.GlobalFoodFreedom.org

Action item: http://TinyURL.com/NoDebtIncrease

Update:
LET’S HELP MAKE THIS ACTION ITEM GO VIRAL!
Please circulate this video:No Increase in the Federal Debt Ceiling!
http://www.youtube.com/watch?v=Y-h6o1tGlL0

This message from Natural Solutions Foundation President (and Oath Keeper) Maj. Gen. Bert Stubblebine (US Army, Ret.):

“This is a crucial moment in the history of the Republic.

“HHS Secretary Sibelius just admitted the “Obamacare” law, passed but not read by Congress in 2010, includes a $105 Billion authorization for the nationalization of health care and also a $16 Billion slush fund for the Secretary to use. To prevent Sibelius from using her slush fund, which has to be funded by borrowing (since the government is running 40% in the red) we urge you to help educate Congress to NOT increase the debt ceiling to prevent the back-door funding of the evil Food Control Law (misnamed the FDA Food “Safety” Modernization Act of 2010.”

See: http://teapartyorg.ning.com/profiles/blogs/rajjpuuts-folly-105464-billion

The Federal Govt’s control over the States has been predicated on two factors: the Carrot (Federal spending) and the Stick (overwhelming military force, as it’s had since the 1860s).

Where does the Fed Govt get the money it needs to exercise control over state and local govt employees, such as food safety officials? How does it have the power to force us to accept GMO “Phude” (it looks like food; maybe even smells and tastes a bit like food… but it is not!)?

Not so much from taxes anymore. It was John M. Keynes who opined that governments didn’t need taxes to run, since central banks (like the Federal Reserve) could print up all the money they needed; taxes were needed in this view to “sop up” all that fiat currency in order to slow price inflation. No doubt, the Federal authorities will opt for more fiat money creation to maintain the control dollars create.

On one hand Federal grants to the states are tightening (“unfunded mandates”) while on the other hand, the central authorities seek to exercise even more control over the localities.

[Example: the new Food Control Law (misnamed the FDA Food Safety Modernization Act) provides for “contracts” between the FDA and local food safety officials to fund and control the local officials.]

So, if we are to give the States a chance to reassert state sovereignty, the Federal juggernaut needs to be held back.

How? By limiting its credit. More specifically, by no longer enabling its borrowing addiction. Yes, the Government of the United States of America is behaving exactly like any other addict… And with addicts, there is just one thing to do: JUST SAY NO!

All it takes is a House majority willing to say NO! and mean it.

NO INCREASE IN FEDERAL DEBT! ZERO ADDED DEBT TOLERANCE!

This Action Item allows you to send messages to your Congressperson and Senators.

It tells them the Federal Govt is addicted to borrowing ever more fiat dollars, and the only thing we can do when dealing with an addict is to say: NO!

Please send this link to all your contacts; take this Action Item viral!
http://TinyURL.com/NoDebtIncrease

This Action Item has been posted several places to help it “go viral” — please re-post widely and please “comment” on these postings to bring them to the attention of others:

http://www.campaignforliberty.com/blog.php?view=41079
http://drrimatruthreports.com/?p=8745
http://vitaminlawyerhealthfreedom.blogspot.com/2011/03/educate-congress-no-federal-debt.html
http://teapartypatriots.ning.com/forum/topics/action-item-no-increase-in
http://newworldwarriors.ning.com/forum/topics/action-item-no-increase-in

Categories : Activism, Blog / Vlog, Get Involved, Government Agencies, Legislation to Oppose

Researcher: Roundup or Roundup-Ready Crops May Be Causing Animal Miscarriages and Infertility

By Administrator on March 8, 2011 No Comments

Natural Solutions Foundation
Your Voice of Global Health & Food Freedom™
www.GlobalHealthFreedom.org
www.GlobalFoodFreedom.org

We are re-posting and disseminating this important article by Prof. Huber because it highlights the risks of GMO “Phude.” If these food substitutes are causing miscarriages among animals, what are they doing to people?

Ban GMOs – A Dangerous, Untested, Unnecessary, Globalist Technology
Before All DNA on the Planet is Contaminated — Forever! Action Item Here:

http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=2049
More information here:
http://drrimatruthreports.com/?p=6955

Researcher: Roundup or Roundup-Ready Crops
May Be Causing Animal Miscarriages and Infertility

http://farmandranchfreedom.org/gmo-miscarriages

One of the nation’s senior scientists alerted the federal government to a newly discovered organism that may have the potential to cause infertility and spontaneous abortion in farm animals, raising significant concerns about human health. Dr. Don Huber, professor emeritus at Purdue University, believes the appearance and prevalence of the unnamed organism may be related to the nation’s over reliance on the weed killer known as Roundup and/or to something about the genetically engineered Roundup-Ready crops. In a letter to Secretary of Agriculture Tom Vilsack, the professor called on the federal government to immediately stop deregulation of roundup ready crops, particularly roundup ready alfalfa.

Below is the full text of the letter. FARFA received an electronic copy of the letter from Dr. Huber and we have spoken with him directly to confirm its authenticity.

The letter was intended as to alert the government about preliminary research results that indicate serious problems. As Dr. Huber himself clearly states, more research is needed.

January 16, 2011

Dear Secretary Vilsack:

A team of senior plant and animal scientists have recently brought to my attention the discovery of an electron microscopic pathogen that appears to significantly impact the health of plants, animals, and probably human beings. Based on a review of the data, it is widespread, very serious, and is in much higher concentrations in Roundup Ready (RR) soybeans and corn—suggesting a link with the RR gene or more likely the presence of Roundup. This organism appears NEW to science!

This is highly sensitive information that could result in a collapse of US soy and corn export markets and significant disruption of domestic food and feed supplies. On the other hand, this new organism may already be responsible for significant harm (see below). My colleagues and I are therefore moving our investigation forward with speed and discretion, and seek assistance from the USDA and other entities to identify the pathogen’s source, prevalence, implications, and remedies.

We are informing the USDA of our findings at this early stage, specifically due to your pending decision regarding approval of RR alfalfa. Naturally, if either the RR gene or Roundup itself is a promoter or co-factor of this pathogen, then such approval could be a calamity. Based on the current evidence, the only reasonable action at this time would be to delay deregulation at least until sufficient data has exonerated the RR system, if it does.

For the past 40 years, I have been a scientist in the professional and military agencies that evaluate and prepare for natural and manmade biological threats, including germ warfare and disease outbreaks. Based on this experience, I believe the threat we are facing from this pathogen is unique and of a high risk status. In layman’s terms, it should be treated as an emergency.

A diverse set of researchers working on this problem have contributed various pieces of the puzzle, which together presents the following disturbing scenario:

Unique Physical Properties

This previously unknown organism is only visible under an electron microscope (36,000X), with an approximate size range equal to a medium size virus. It is able to reproduce and appears to be a micro-fungal-like organism. If so, it would be the first such micro-fungus ever identified. There is strong evidence that this infectious agent promotes diseases of both plants and mammals, which is very rare.

Pathogen Location and Concentration

It is found in high concentrations in Roundup Ready soybean meal and corn, distillers meal, fermentation feed products, pig stomach contents, and pig and cattle placentas.

Linked with Outbreaks of Plant Disease

The organism is prolific in plants infected with two pervasive diseases that are driving down yields and farmer income—sudden death syndrome (SDS) in soy, and Goss’ wilt in corn. The pathogen is also found in the fungal causative agent of SDS (Fusarium solani fsp glycines).

Implicated in Animal Reproductive Failure

Laboratory tests have confirmed the presence of this organism in a wide variety of livestock that have experienced spontaneous abortions and infertility. Preliminary results from ongoing research have also been able to reproduce abortions in a clinical setting.

The pathogen may explain the escalating frequency of infertility and spontaneous abortions over the past few years in US cattle, dairy, swine, and horse operations. These include recent reports of infertility rates in dairy heifers of over 20%, and spontaneous abortions in cattle as high as 45%.

For example, 450 of 1,000 pregnant heifers fed wheatlege experienced spontaneous abortions. Over the same period, another 1,000 heifers from the same herd that were raised on hay had no abortions. High concentrations of the pathogen were confirmed on the wheatlege, which likely had been under weed management using glyphosate.

Recommendations

In summary, because of the high titer of this new animal pathogen in Roundup Ready crops, and its association with plant and animal diseases that are reaching epidemic proportions, we request USDA’s participation in a multi-agency investigation, and an immediate moratorium on the deregulation of RR crops until the causal/predisposing relationship with glyphosate and/or RR plants can be ruled out as a threat to crop and animal production and human health.

It is urgent to examine whether the side-effects of glyphosate use may have facilitated the growth of this pathogen, or allowed it to cause greater harm to weakened plant and animal hosts. It is well-documented that glyphosate promotes soil pathogens and is already implicated with the increase of more than 40 plant diseases; it dismantles plant defenses by chelating vital nutrients; and it reduces the bioavailability of nutrients in feed, which in turn can cause animal disorders. To properly evaluate these factors, we request access to the relevant USDA data.

I have studied plant pathogens for more than 50 years. We are now seeing an unprecedented trend of increasing plant and animal diseases and disorders. This pathogen may be instrumental to understanding and solving this problem. It deserves immediate attention with significant resources to avoid a general collapse of our critical agricultural infrastructure.

Sincerely,

COL (Ret.) Don M. Huber
Emeritus Professor, Purdue University
APS Coordinator, USDA National Plant Disease Recovery System (NPDRS)

Categories : 01 Food ebook, Activism, Blog / Vlog, GMOs, Government Agencies

Sibelius’ $16 Billion Slush Fund: Will She Use It to Fund the Food Control Law?

By Administrator on March 8, 2011 No Comments

Natural Solutions Foundation
Your Voice of Global Health & Food Freedom™
www.GlobalHealthFreedom.org
www.GlobalFoodFreedom.org

Patron: “Waiter, There’s a $16 Billion Slush Fund In My Soup!”
Waiter: “Shhh! Be Quiet! Or Every One Else Will Be Wanting One, Too!

How Will Sibelius Use Her $16 Billion Slush Fund?

http://teapartyorg.ning.com/profiles/blogs/rajjpuuts-folly-105464-billion
“In section 402 Health and Human Services Director Kathleen Sibelius was given a $16 Billion slush fund to use as she sees fit…”

Will this slush fund provide the cash needed to hire the 4,000 new FDA agents authorized by the lame-duck 2010 Congress when it passed S.510, the Food Control Law? Tell Congress, “No!” – Action Item here: http://tinyurl.com/ nofoodcontrol

Hey, Kathleen! Just how did you get a $16 Billion slush fund and can I have one, too?

I need to help farmers all over the world reclaim their food production to stop the failure of their farms and the resulting famins around the world. I need to fund natural health research which has not been funded because there is no way to patent natural products (unless, of course, one is a Biotech company like Monsanto, given permission by a scientifically illiterate court system and a massivly corrupt regulatory agency to do just that – and hide it from the American people).

I need resources to hire staff to share real, scientific information with people who need to know that information about the cure, treatment and prevention of the huge cash cows of the illness management organization in the US, often known by the incorrect name “Health Care”. I need a modest amount, say, $100Million, to create urban sustainable, chemical-free food growing programs around the United States, giving the newly homeless, the newly poor and their long-time counterparts the seeds, soil and skills to grow their own clean food to feed themselves and share with others while the dollar is collapsed around their ears.

I need some funds to hire a team of researchers and international lawyers and communications folks to visit governments of the poorest.most nutritionally vulnerable people in the world and share with them the solution to the globalists’ genocidal agenda – Oh, but I have a question to ask you before I tell you what I would like you to make available some of your slush fund, perhaps 1/12 of it. That would be a billion dollars. Given that you already have a Health and Human Services Department budget of hundreds of billions, you probably have a bit more than even you need.

The question:”Ms. Sebelius, have you been, as they say in all the spy and national security novels, ‘read into the program’? Do you know about the genocidal agenda of the World Health Organization, with which your agency works so closely or are you an ignorant dupe, too besotted with the power you are allowed to wield and totally disconnected from common sense or honest analysis by the career trajectory you have followed to see what is really happening and protect the people of the country as you have taken an oath to do?”

Our vocal analysis of your inner realities shows that you really want to do the right thing but that you are, quite literally, besotted by misinformation and the deceit you have been handed. But, unlike many at various helms, it does not show you to be an evil, malignant or cruel person.

Given that, Secretary Sebelius, I would like to ask no only for a small portion of your slush fund (slightly more than twice the combined national budgets for the Pitcairn Islands, Zimbabwe, Wallis and Fortuna and Todelau combined). Now it is true that they are small countries, but how about if you do the following things, Secretary Sebelius:

1. Donate 1/12 of your discretionary slush funds to the Natural Solutions Foundation to promote healthy food, healthy choices and health promoting information in the US and abroad. After all, such health promotion is part of your Agency’s charter, which states “FDA is responsible for protecting the public health by assuring the safety, efficacy and security of human and veterinary drugs, biological products, medical devices, our nation’s food supply, cosmetics, and products that emit radiation.” on your official website, http://www.fda.gov/aboutfda/whatwedo/default.htm.

You are also concerned with food and medicine as a counter-terrorism strategy but seem to have neglected the connection between weakening the nation’s collective immune system through dangerous drugs, contaminated foods and irresponsible vaccinations, but everyone has those lapses!

INTERRUPTION OF PREVIOUS COMMUNICATION

[While writing this letter to Kathleen Sibelius, Dr. Rima, the Queen of Multi-Taskers, was also in a meeting with a Panamanian cattle farmer. You can see where the discussion went and then return to her letter to Secretary Sebelius, below.]

Alonso is here to talk about stuff and we need to get to the formulator we discussed to make a product sample for the udders of drying cows. We are talking about a masters project in which Alonso is involved. The project is that they want to study the influence of the levels of energy and protein from the feed we give to the cows and all the influences from food on reproduction.

They want to study how long it takes the cow to be breeder based on food inputs.
There are different things that influence this: most important is the precalving period.
They want to study how we do it and how long it takes the calf to become estrous
This is from National University: They want to measure the body condition, weight, blood samples, rectal palpation.

I think the food is important, but also the presence or absence of drugs, vaccines and similar.

Now, 20 days previous to calving, Alonso analyzes for worms, I put some vitamin E and selenium and magnesium injected into the cow. Then we feed it with a formula with minerals which makes the cows take calcium from their bones (anionic minerals) so that the cows have enough calcium to give birth. Then you get a lot of diseases like placental previa, if there is a calcium failure, they get “downed cow syndrome” and they will not be able to let down their milk. In t he 9 months previous they accumulate the calcium in the bones. The signal in the brain is from selenium to help her take Ca from the bones.

That is standard practice.

We feed with a ration that is similar to the milking cow but different becuase of the minerals and a lower energy level than milking cows. Milking cows get more energy because they are producing milk. IF there is too much energym they get too fat.

After calving we check the cow for placenta and if not expelled in 24 hours, give Ca and Vit B12, 3 different types of calcium. IF that does not work, then we use antibiotics intravaginally. Right now if the cow is doing fine, they only get feed and observation. If the cow has a problem, sometimes they expel the placenta but still get milk fever. In the 15 days after calving they can get detosis, then we use dextrose and calcium 5%, then 50% dextrose. Ketosis from previous programs. Previous partum problmes because they do not eat enough feed in the right way.

Maybe sometimes when a cow has a higher condition score, that is the best. 5 is the best. If you get 4, you have ketosis and retained placenta and if it gets worse, then you get torsion and death.

We will have the opportunity to put our methods into practice and the student will study two types of rearing and feeding. He wants to know about our working and our minerals and about his shot. Minerals by mouth are fine, these are from Brazil. I want to make sure that the injection minerals are working in the organic way.

Most common worms in mature cows. They can have pulmonary worms.

Right now Alphonso is no longer treating with ivermectin because there were some complaints in the food industry about it; some cows get virus earlier, they get ivermictin, if later, we use something to which people do not have allergies.

Used to give ivermictin when they got dry because the time before milking is longer, now using f-albendisol which works against mature and eggs; both mature and immature forms. Only check the eggs in feces. The people who see the eggs in the lab tell us whether they are pulmonary or intestinal. We give the selenium as prevention because we know if they do not get it, some cows do not do well.

This is not a disease that effects humans now. It only effects the cows. The thing is that it lowers the defense of the cow so they lose the ability to fight pathogens.

END OF INTERRUPTION – The above is an example of what we mean when we say we are seeking to “discover, develop, document, demonstrate and disseminate natural solutions…

Anyway, Madam Secretary, the point is that as far as I can tell, health and health freedom are more like four letter words to your agency than concepts to be supported and developed.

Take vaccines, for example. Your agency appears to pretty much never have met a vaccine it did not like. Why, without a disease of note, you purchased half a billion dollars worth of an adjuvant, squalene, also known as Freund’s Adjuvant, to mix into 6 billion dollars worth of unapproved vaccines to make them go further and do more damage. We are talking about the biggest non event of the 21st century here, Swine Flu.

And then there is Rotovac, which causes pneumonia AND meningitis in babies who didn’t need the vaccine in the first place. And there’s the mrecury whiich is used in pediatric vaccines to “wash” the vials leaving dangerous “trace” levels, and is full strength in flu vaccines, which is allowed because of shameless corporate shenanigans back in the early 20th century when your agency was just a baby.

Rima Laibow, MD: And there is the pesky fact that the flu vaccines are associated with increased levels of dangerous diseases like asthma and neurological and learning problems in the young, the old, the middle aged, in us all, with an increased all-cause mortality in people who get them compared with people who do not. And the autism white wash.

Then there are the scientifically and physiologically disastrous GMOs and other poisoned “PHUDES” [“They look a bit like food; they may even smell and taste a bit like food, but they aren’t!”] with which your agency is literally killing us and spreading your contagion of false information and deadly profits around the world.

Your war on the wellness industry is simply breathtaking. You have teamed your agency, already a pit bull guarding Big Pharma and Big Agribiz, Big Biotech and Big Chema, all in the service of Big Medica, of course, up with the FTC to make sure that small and medium sized manufacturers of vitamins and supplements, healthy foods and other dangerous commodities would be driven out of business. After all, if they manged to survive your draconian and rather batty “Good Manufacturing Practices” regulations (against an industry without health problems in its products, instead of against the pharmaceutical industry that kills hundreds of thousands of people each year), they will go under in your 2 agency united front against them.

So I am proposing, in the interests of the First Amendment, fairness, common sense, common decency and the basic human right of self determination granted by the UN Charter on Human Rights (oops! scratch that one: the US is not a signatory to that document or to the Nuremberg Convention prohibiting experimentation on people without informed consent, which is what your sub agency, the CDC, now admits they and you have been doing with fluoride and other goodies) that you share the wealth provided to your agency by the Obamacare legislation and, since you have $16 Billion to play with in your slush fund, that you share the wealth and give the other side, the loyal opposition that wants to have the research and the tools to make their case to the people – and to you, if you will listen, for natural health and clean food and natural health care options (like cancer treatment that works, for example) even though, gasp, the money might must take profits out of the hands of the gigantic industrial forces that are killing us all.

One final note, Madam Secretary, your body, and that of your family and loved ones, will need natural treatments or already do. What will you do when the antibiotics you permit in the vicious factory farm industy and the out-of-control medical industry no longer work for the newly resistant organisms that are eating your flesh, or destroying your organs? Will you have made nano silver illegal as your counterpart in Europe has done?

What will you do when anti depressants do not work? Will you seek in vain for the nervine tonics an herbalist might have made for you had you not made the herbs needed illegal?

What will your daughters and sons do when they are injected with Gardasil or Cevarix and develop a brand new disease, never before seen on the planet: juvenile ALS?

Or when your mother develops Alzheimer’s Disease because of the ful shots she dutifully took – or you do – and you have driven the chelating doctors out of business by criminalizing their knowledge and communication about what they do and what they know?

Seems like a good bet to me, Kathleen. You have so much money. Give us a $1Billion crumb and let us see what we can do to help you pick up the pieces when your disastrous, short sighted, unscientific and anti-physiological methods fail, as they already are doing.

Action Item here: http://tinyurl.com/ nofoodcontrol

Yours in health and freedom,

Rima Laibow, MD: Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
Protecting Your Health and Food Freedom!

Categories : 01 Food ebook, Activism, Blog / Vlog, Dietary Supplements, Disinformation, Divest Governement of Food Regulation, GMOs, Government Agencies

FDA Seeking to Outlaw IV Vitamin C, Other Nutrients

By Administrator on January 7, 2011 No Comments

FDA Seeking to Outlaw IV Vitamin C, Other Nutrients
Rep. Ron Paul, MD: As an agency, FDA engages in “abuse of power…”

“FDA: Leave Our Nutrients and Supplements Alone!”
Action item: http://tinyurl.com/saveIVNutrients

Archive of Emergency Web Meeting of January 9, 2011 here:
https://naturalsolutionsfoundation.webex.com/naturalsolutionsfoundation/ldr.php?AT=pb&SP=MC&rID=2625702&rKey=9f5c8c59f61ba89a

March 9, 2011 – We Dissect a Response from the FDA! Click Here.


The FDA (the Food Destruction Agency) not content with its new power to control and industrialize our entire food supply, is, quite predictably, increasing its attacks on nutrients. Although the mis-named Food Safety [sic!] Modernization Act excludes nutrients, the FDA’s rampage against natural health is by no means limited to degrading our food supply.

DSHEA, the 1994 Dietary Supplements Health and Education Act, which protects dietary supplements does not protect nutrients unless they are delivered in oral form. That means that intravenous, transdermal, nasal, suppository or other forms of nutrition are vulnerable to FDA assault in a particularly worrisome way. This latest action by the FDA makes that point clearly.

On December 28, 2010 FDA ordered certain small manufacturers to stop making IV Vitamin C and several other injectable nutrients which are always used under a (holistic or Advanced health Care) physician’s supervision by classifying IV Vitamin C, Magnesium and certain B Vitamins as “New Drugs”.

The nutrients under attack, which form the basis of the popular “Myers Cocktail” and countless therapies for serious diseases, may be provided ONLY by compounding pharmacies under a specific prescription for a specific patient. This means that the cost of these nutrients will increase sharply.

It also means that the FDA, always hostile to compounding pharmacies and the independent use of nutrients, bio-identical hormones (now banned at the request of Wyeth/Pfizer, which manufactures dangerous synthetic hormones), the biologically active form of Vitamin B-6 (also banned at the request of a drug company) can pick off individual substances and attack compounding pharmacies at their leisure. This is a result of the power granted FDA in 2007 (section 301(11) of the Kennedy FDA Enabling Act) to ban interstate sale of any “food” ever studied for medical use, even if never so used.

Why, you ask, does FDA need authority to ban safe foods? Why does Congress think it has the power to grant such authority? Where in the Constitution does Congress have that power? And please, don’t say it’s in the “Commerce Clause” which grants the Federal Government the power to regulate Interstate Commerce. “Regulate” does not mean the power to forbid foods that people have always had the fundamental human right to grow, trade and use. It merely means to make commerce regular; to make fair and neutral “rules of the road” for Interstate Commerce. Under the 9th Amendment, the People have retained the right to grow and trade foods, including vitamins and minerals. As we Restore the Republic, that right must be respected again.

Manufacturing companies wishing to make and sell the now restricted injectible, inexpensive and life-saving nutrients will be forced to engage in full-scale drug approval testing for products that cannot be patented; this, the FDA knows, is economically impossible. The attack on Vitamin C comes on the heels of efforts by FDA to ban other nutrients, including forms of Vitamin B6 banned under the Kennedy Enabling Act.

If these restrictions stand, what nutrient will be next?

Please take the Action Item at this link, which tells the White House and FDA to leave our nutrients alone! http://tinyurl.com/saveIVNutrients

Blog entry originally published at: http://vitaminlawyerhealthfreedom.blogspot.com/2011/01/fda-seeking-to-outlaw-iv-vitamin-c.html


ONE OF OUR SUPPORTERS GOT A REPLY FROM THE FDA
ABOUT IV NUTRIENTS; WE DISSECT IT…

— On Wed, 3/9/11, CDER DRUG INFO wrote:

From: CDER DRUG INFO
Subject: RE: Leave our Nutrients Alone!
To: “‘[redacted]'” Date: Wednesday, March 9, 2011, 8:53 AM

Dear P… B…

Thank you for your e-mail expressing concerns about FDA’s December 28, 2010 warning letter to an individual manufacturer (McGuff Pharmaceuticals Inc.) of intravenous (IV) vitamin C along with other prescription drugs.

Unlike oral vitamin C-which could be a dietary supplement- these particular IV solutions are, by law, unapproved drugs. Moreover, the manufacturers neglected to follow current good manufacturing practices, potentially exposing users to unnecessary risks.

Such risks have occurred before. In the E-Ferol tragedy of 1983, premature babies received E-Ferol, an intravenous form of vitamin E. E-Ferol was associated with adverse reactions in 100 premature infants, forty of whom died. It is highly likely that this tragedy would have been prevented if the product had been reviewed and approved by the FDA before its introduction to the market.

Since FDA announced its Unapproved Drugs Initiative in June 2006, marketers of unapproved drugs have been on notice that addressing risks from unapproved drugs is a high priority for FDA, and that the Agency plans to systematically and responsibly ensure that all products on the U.S. prescription drug market become compliant with current FDA approval requirements for safety and efficacy.

The mission of FDA’s Center for Drug Evaluation and Research (CDER) is to ensure that safe and effective drugs are available to the American public. Drugs that have not been approved by FDA may not be safe and effective, may have been manufactured under sub-standard conditions, may contain too much or too little (if any) active ingredients, and may not have necessary labeling information and warnings.

FDA’s drug approval process ensures that drugs are safe, effective, of a suitable quality and purity, and are properly labeled. The Agency remains committed to assisting all firms with meeting these standards.

Again, we thank you for your input and hope that we were able to address your concerns.

Best regards,

Division of Drug Information – JD
Center for Drug Evaluation and Research
Food and Drug Administration

For up-to-date drug information, follow the FDA’s Division of Drug Information on Twitter at FDA_Drug_Info

This communication is consistent with 21CFR10.85(k) and constitutes an informal communication that represents our best judgment at this time but does not constitute an advisory opinion, does not necessarily represent the formal position of the FDA, and does not bind or otherwise obligate or commit the agency to the views expressed.

Please note: the above statement, in our humble opinion, misstates the law. The various laws passed by Congress over the decades continually adding to the FDA’s power all include “grandfather” clauses allowing products that existed when the various laws were adopted — IV nutrition has been used for a very long time. Andrew St Georgie received the Nobel Prize as one of the discoverers of Vitamin C in 1937. Frederick Klenner, M.D used IV Vitamin C in the 1940s. It was used IV well before the 1952 authorization by Congress giving FDA authority over the “safety and efficacy” of drugs (before that time, FDA only had authority over misbranded or adulterated drugs). rf

“From 1943 through 1947,” writes Robert Landwehr (3), “Dr. Klenner reported successful treatment of 41 more cases of viral pneumonia using massive doses of vitamin C. From these cases he learned what dosage and route of administration – intravenously, intramuscularly, or orally – was best for each patient. Dr. Klenner gave these details in a February 1948 paper published in the Journal of Southern Medicine and Surgery entitled ‘Virus Pneumonia and Its Treatment with Vitamin C.’ (4) This article was the first of Dr. Klenner’s twenty-eight (through 1974) scientific publications.”

It might be interesting to learn how poliomyelitis was treated in Reidsville, N.C., during the 1948 epidemic. In the past seven years, virus infections have been treated and cured in a period of seventy-two hours by the employment of massive frequent injections of ascorbic acid, or vitamin C. I believe that if vitamin C in these massive doses – 6,000 to 20,000 mg in a twenty-four hour period – is given to these patients with poliomyelitis none will be paralyzed and there will be no further maiming or epidemics of poliomyelitis.’ Levy concludes: “The four doctors who commented after Klenner did not have anything to say about his assertions.”

Klenner administered ascorbate by injection, and, as Lendon H. Smith describes in great detail in the Clinical Guide to the Use of Vitamin C: The Clinical Experiences of Frederick R. Klenner, M.D., Klenner found that “the most effective route was intravenous, but the intramuscular route was satisfactory. He gave at least 350 mg per kilogram of body weight.” That quantity per day is a dose of 25,000-30,000 mg or so for an adult. Yet, Smith adds, “With 350 mg per kilogram of body weight every two hours, he could stop measles and dry up chicken pox.”

http://www.doctoryourself.com/klennerbio.html

Categories : 01 Food ebook, 06 Health Strategies, Activism, Blog / Vlog, Disinformation, FDA, Government Agencies, health freedom
« Previous Page
Next Page »