Natural Solutions Foundation
Your Voice of Global Health & Food Freedom™
www.GlobalHealthFreedom.org
www.GlobalFoodFreedom.org
Dr. Rima Reports: Every Thursday Night
10 PM to Midnight
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From Dr. Rima:
Report on Gen. Bert’s Broken Hip
Vitamin C Wars: Your Money or Your Life
General Bert and I are in Chile, sourcing Southern Hemisphere organic-and-better foods for North America and beyond, to replace the Fukishima-contaminated foods of the entire Northern Hemisphere. (Yes, it is that bad! And North America’s 40+ leaking reactors are making it worse.)
More about what you can do about that here: http://tinyurl.com/radprotect
While here in Chile we thought we’d enjoy the winter snows in the high Andes and catch some skiing, which we dearly love and which, truth to tell, Panama lacks totally, even in the temperate Eternal Spring of the Highlands where we have sited the Valley of the Moon Eco Demonstration Project, www.MyVAlleyoftheMoon.org.
First ride up the lift, first run, first day, Bert fell and broke his left hip and did some serious damage to his femur. We were helicopter-lifted to the Clinica Alemana in Santiago….
When the same thing happened 10 years ago in Wyoming, in order to get the IV Vitamin C (50 Grams every 12 hours) and other nutrients into him immediately following surgery, I had to smile sweetly and threaten to “Sue the S***” out of the surgeon if he refused to order that treatment.
After telling me that the use of nutrients to speed healing was “not how we do it here,” Dr. Alva Forbes, the orthopedic surgeon for the US ski team, saw the burning beauty of my logic, illuminated brilliantly in he harsh glare of my very serious threat and allowed as how he would do it that way, this time.
So I was prepared for the same thing this time, but in Spanish.
Imagine our delight and surprise when the doctors all, to a man and woman, said, “Well, I never heard of that, but why not? Vitamins can only be good, after all!” It was like music to our ears…
The plan was that as soon as the surgery was over, Bert would receive the first of the 12 hour IV bags, each containing 50 Grams of Vitamin C and other nutrients including calcium, magnesium, biotin, Vitamins A, D3, etc.
Great plan except for the fact that that first bag contained 500mg, 1/100th of the required dose, of Vitamin C.
You could hear it, clear as day: somebody in the Pharmacy department said “50 GRAMS???? Has Dr. So and so lost his MIND???” And then they “corrected” the doctor’s “mistake”.
Bert not only had his wife with him, he had his own MD. That stands for “Medical Dragon” Along for the ride. And she roared.
Two and a half hours later, another bag arrived from the pharmacy with not 50 Grams, but 14 Grams of Vitamin C because, allegedly that was the entire stock of Vitamin C for the entire hospital and they would have to buy more in the AM.
What happened next was that we got told that there is nowhere in Chile where that much Vitamin C can be purchased.
Horse puckey!
So now, with the good will and wishes of the entire medical and nursing staff, who are totally astounded that a hip surgery patient has zero pain, zero inflammation and zero complications from the meds that generally mess up people in the post surgical period, and acknowledging that it is unheard-of to see this kind of post surgical wellness so it has to be due to the Vitamin C he received, they have arbitrarily reduced his 24 hour dose from 100 Grams to – ready for this? – 10 Grams, 1/10 the dose that I, the nutritional medicine expert, have told them, the totally uneducated-in-nutritional-medicine doctors that the patient needs.
Why?
No reason in particular. No fears of toxicity, no evidence that it is bad, dangerous or does not work.So much for “evidence based medicine” which is, all too often, based on exactly the evidence “I already believe in or get a nice reward for believing in.”
Now, to confuse the picture, they have no idea about the nutrients and anti-inflammatories which Bert is being given by the Dragon Doc, me.
So they are not going to realize that their absurd 10 Grams of Vitamin C in 24 hours is not doing the trick.
But my other nutrients are covering the inflammatory waterfront and the reason that he simply cannot get an infection is because I am dosing him with nanosilver — never travel without a supply!
www.nutronix.com/naturalsolutions
People with broken hips die from the consequences of inflammation: pain and subsequent lack of movement, drugs for these situations and the terminal stints in the nursing homes that result where they go downhill, get under stimulated and over medicated and die in short order.
Unless they get post operative IV nutrition.
Why not try it? Why not demand it?
Because then Big Pharma is not in control of your life and death. You are.
Because then the government has to keep making payments to you when you are old instead of stopping the payment when you conveniently die prematurely.
And then the money for the absurd drugs and obscene markups stays in your pocket, never making it to the Uber Cartel’s pockets.
So here, in the Clinica Alemana in Santiago, Chile General Bert and I are engaged in a skirmish in the great, and deadly, Vitamin C wars.
The Fraud and Death Administration, whose tentacles reach very far, has already declared that IV Vitamin C is an unapproved NEW DRUG!
As such, it is subject to severe restriction leading to sharp price increases and further demonization. After all, in the land of malpractice litigation, what doctor is willing to risk using an “unapproved drug”?
What can you do about it?
Take the following Action Items demanding the FDA abandon its disastrous anti-nutritional supplement Guidelines and honor the law passed by Unanimous Congressional Consent in 1994, DSHEA, the Dietary Supplements Health and Education Act, which says that supplements are foods and, as such, their use, form and manner are totally up to you.
Stop FDA Power Abuse!
http://tinyurl.com/FDApowerabuse
Leave our Vitamins Alone!
http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=5448#Action
Then forward the link to every one you can reach.
Yours in health and freedom,
Dr. Rima
You may recall that General Bert took a tumble and while all the King’s Horses and all the King’s Men did not get into the act, two trauma surgeons, a helicopter airlift pilot and nurse and 6 days in the hospital later, he emerged on a walker with a much stiffer, swollen and difficult-to-move hip and thigh than he should have.
Why do I say that? Because despite their great lip service and lovely personal bedside manners, the doctors at Santiago’s famed (and very nicely managed) Clinica Alemana gave me a lot of ‘look ‘em straight in the eye when you lie’ nonsense about giving Bert the Vitamin C that he needed (50 G every 12 hour in an IV bag) but wound up giving him a ridiculous 10 G every 24 hours, or 1/20th the dose that he needed to prevent the pain and swelling of a broken hip and the following traumatic surgery.
I was told that there was no IV Vitamin C in Chile (ABSURD) and other fantastic nonsense. When I complained (loudly, you can be sure!), I was finally told that the truth was that the gerontologist who told me that he knew NOTHING about vitamins and minerals but that he knew they could not hurt anything, so why not do what I suggested was the one who wrote the order for a dose that Gen. Bert could have safely exceeded by MOUTH.
The result, of course, was that he had far more difficulty and movement restriction than he did 10 years ago when he did the same thing to his right thigh bone and hip. That happened in the US and my deadly serious threat to sue the surgeon worked like a charm – Gen. Bert got his 100 G per day of IV vitamin C.
Note: it is not the hip surgery that kills the elderly who suffer these fractures: it is the pain and immobility which restricts their motion and leads to complications, incarceration in nursing homes and, ultimately, death. All of which would not occur if enough Vitamin C were used!!!!
But WAIT! There’s more. Gen. Bert tends toward a very low blood pressure on his own. That is why salt is essential, and in pretty good quantities, too, for him to eat along with lots of water. He also lost a huge amount of blood during the accident and the surgery so his hematocrit was low – dangerously low. In fact, the recommendation of the doctors was to give him several transfusions. On his behalf, I refused. Why not give him iron, I said, and let the body create more hemoglobin, instead of exposing him to all the dangers of transfusions?
The doctors agreed and ordered an iron supplement by mouth. The hemoglobin started to crawl up and Gen. Bert was spared the transaction. But we all agreed that the supplement was critically important to his well-being at this point.
The iron supplement he was given in the hospital did not make it home with him so since last Friday he has been without iron supplements. He cannot eat red meat because he gets gout when he does, which is sad because he is an enthusiastic red meat sort of guy.
So no supplement, no meat, and not enough spinach to put in your left eye, organic or otherwise. And the robust and vigorous Gen. Bert began to fail.
I emailed the hospital: no response. I took a prescription they had given me “just in case” to the two pharmacies I can reach from the hotel we are staying in and showed it to them. In both cases the girls behind the counter looked at me blankly and told me that they do not have iron. NONSENSE!!
As the few days wore on, he became deathly pale, terribly weak, frightfully cold and could not stay awake for very long.
I was very worried and deeply angry with myself because I ALWAYS travel with my blood pressure cuff and stethoscope – Always, that is, until this time.
But, I said to myself, that is not a problem because today we are going to pay a nurse from the Clinica Alemana 22,000 Chilean Pesos (about $44 US) to change the dressing from the operation in a visit to the hotel. She will, I reasoned, have a stethoscope and cuff with her. She was his nurse in the hospital and she will see the change in him and help him get the support he needs, including the dietary supplement which could, literally, save his life.
His pulse was hard to find, weak and thready. His heart beat was irregular and his status was deteriorating. But she’ll be here with the scope and pressure cuff shortly.
NOT SO! She walked in, smiled, obviously did not look clinically at her patient, whom she had nursed when he was in the Clinic, changed his bandages, smiled again and left. Gen Bert was, in my clinical judgment, in grave danger of a stroke, a myocardial infarction (heart attack) or death.
Low blood pressure, low blood volume, not enough iron? Time for folk medicine, pure and simple.
I brought bags of salted nuts and potato chips, neither of which are health foods, and presented them to Gen. Bert with the instruction to eat all he could hold and drink as much water as he could.
I poured ¼ teaspoon of salt in the palm of his hand, told him to lap it up and drink water. I went to the nearby store and bought red meat, which he cannot eat, but which is a dense source of iron and protein, and made a soup with organic onions, mushrooms, garlic, plenty of salt and cooked up a broth that I gave him no option NOT to drink, despite the fact that it will most likely give him gout. I gave him colchicine, a very old remedy for gout, to prevent the development knowing that he may get it anyway.
But you don’t die from gout. You can die from lack of oxygen because of lack of iron!
And you know what? He pinked right up, over the several hours the above took. His arrhythmia went away and his heartbeat became normal again. Color returned to his skin and life returned to his eyes.
Now there is a good side to the story: I badgered the nurse into calling the Physical Therapist who was coming tonight anyway, into bringing the iron preparation he needed this evening. 20 little bottles of iron supplementation walked in the door when he arrived. And I was, of course, very appreciative, but also very apprehensive about what was in the process of happening: Gen. Bert was shutting down through lack of good planning and follow-through.
Why am I telling you this? Several reasons: first of all, if someone you care about is in hospital, they are in grave danger unless there is someone staying with the patient AT ALL TIMES running interference, reading labels, demanding, yes, demanding, to know what is happening to the patient and why. It does not matter whether the doctors and nurses like you. It matters whether you can protect the person in the hospital because they cannot.
Accept nothing. Question everything. Hospitals are dangerous places.
Second, Do not discard what you already know for what the doctors and nurses seem to know. The salt water I gave Gen. Bert increased the volume of his circulatory system, apparently increased his blood pressure and may have saved his life. It wasn’t medicine. It was folklore applied to a medical situation, rapidly becoming an emergency.
Third, Do not discard what you already do despite what the doctors and nurses tell you. Gen. Bert received 6 capfuls of Silver Sol Nano Solution by mouth per day. Hospitals are dirty places and the infections people get in hospitals kill nearly 100,000 people in the US alone. I was determined that Gen. Bert was not among them.
I told no one. I just gave it to him.
I continued to give him the nutritional powerhouse array of supplements he receives every day, but when no one was looking. I told no one. I just gave it to him.
Fourth, Do not believe in the omnipotence, competence or diligence of the medical staff. Sometimes your skepticism will be unwarranted, but, going back to tip Number 1, all kinds of mistakes occur day in, day out. And they can be lethal.
Food. There was nothing to heal with or get well on in a single meal of the Clinica. Bring in food that the patient will like and will appreciate and that you know is wholesome. Say it is for you. Pretend you are taking it home to your pet iguana. Whatever you need to say, say it. Whatever you need to do, do it. Just get decent, tasty, nutrient dense food into your loved one or friend. And get out of that hospital the very minute that you can.
More to follow.
Yours in health and freedom,
Dr. Rima
PS: One more thing: I bought a stainless steel urinal for the General, called, in Spanish, a pavo masculinio, or male duck. It had three small holes in the body of it. When I called Diamed, the store that sold it to me, to ask them to replace it, that said that they did not have another one, that they did not care about my $45US, that they did not have to do anything about it and it was my bad luck.
So now we have a male duck with holes in it, but it is stainless steel!!! Tip number 5: take nothing for granted. REL
Natural Solutions Foundation
The Global Voice for Health and Food Freedom™
Health Freedom Advocates Ask Presidential Candidates Tough Questions
We’ll list here to whom the Questionnaire is being sent (as we obtain contact information) with send dates:
1. Dr. Ron Paul [GOP] – 6.16.11 via email to congressional office
2. Mit Romney [GOP] – 6.16.11 via web form at official site
3. Michelle Bachmann [GOP] – 6.16.11 – via email to press office
4. Herman Cain [GOP] – 6.16.11 – via web form to campaign site
5. Newt Gingrich [GOP] – 6.17.11 – via web form to campaign site
6. Gary Johnson [GOP]- 6.17.11 – via web form to campaign site
7. Barack Hussein Obama [Democrat] – 6.17.11 – via web form to campaign site
8. Tim Pawlenty [GOP] – 6.17.11 – via web form to campaign site
9. Wayne Allyn Root [Libertarian Party] – 6.17.11 – via web form to campaign site
10. Cynthia McKinney [Green Party] – 6.17.11 – via message to Facebook page
Candidate Questionnaire – 2011 Presidential Primaries
Questions About Health and Food Freedom
To All Declared Presidential Candidates,
This is an expressive association activity of the Natural Solutions Foundation, a Non-Governmental Organization (NGO) in part dedicated to educating decision makers regarding natural solutions to issues of health and food. Instructions to Candidates: Please answer each question either “Yes” or “No” followed, if you chose, by an explanation of any length. The more than 300,000 concerned health freedom advocates on our opt in list thank you in advance for your time and considered response. We will share the results of this Questionnaire with them and with the millions to whom our Action eAlerts are forwarded. Please email the response to our Counsel at ralph.fucetola[at]usa.net. All responses are due by July 4, 2011.
Yours for Health and Food Freedom,
The Trustees of the Natural Solutions Foundation
Maj. Gen. Bert Stubblebine (US Army, Ret.) – President
Dr. Rima E. Laibow MD – Medical Director
Ralph Fucetola JD – Counsel
www.HealthFreedomUSA.org
Questionnaire URL: http://drrimatruthreports.com/?p=9733
Food Freedom:
1. Do you support the mandatory labeling of foods as GMO or GMO Free?
2. Do you support a permanent ban on GMO food and ingredients products?
3. Do you support upgrading Organic Standards, so that USDA standards meet or exceed the private standards developed by international organizations of organic producers?
4. Do you support defunding the 4,000 FDA food inspector positions, duplicating state-level programs, created in the so-called FDA Food Safety Modernization Act of 2010?
5. Do you support Dr. Ron Paul’s Raw Milk Freedom Bill, HR.1830 which would reverse FDA’s current policies preventing interstate commerce in raw milk or raw milk products?Health Freedom:
6. Do you support legislation to reverse FDA’s current policies preventing interstate commerce in what are termed “alternative” health care approaches, including minerals, nutrients and herbs used for traditional wellness purposes, energetic devices used to support normal structure and function, and such folk remedies as ear candling?
7. Do you support legislation voiding all CDC vaccine recommendations (which then become the basis for state and private vaccine mandates)?
8. Do you support, on the federal level, legislation to assure to all Americans the right to exercise religious and philosophical objections to mandated vaccination?
9. Do you support repealing the special liability privileges drug companies were granted by Congress in the Vaccine Injury Compensation Program?Health & Food Freedom:
10. Do you support legislation mandating revisions to US Codex Alimentarius policies, protecting American health and food freedoms from “harmonization” with international restrictions?
11. Do you support First Amendment rights to share information concerning the health benefits of food and components now limited by FDA and FTC regulatory criminalization of such speech?
Natural Solutions Foundation
Your Voice of Global Health & Food Freedom™
www.GlobalHealthFreedom.org
www.GlobalFoodFreedom.org
Dr. Rima Reports: Every Sunday Morning
10 AM to 1 PM EDT
www.HealthFreedomPortal.org
New Video: A Weaponized World – a Warning from Gen. Bert and Dr. Rima
They tell us the “Super bug E. coli 0104:H” is terrorizing Germany, causing otherwise healthy people to develop Hemolytic-Uremic Syndrome (HUS) in which their kidneys fail, their red blood cells explode and then, tragically, they die.
Germ sleuths and clinicians alike have been even more horrified than the average Spanish cucumber eater (the vegetable pinned with the blame for the lethal outbreak). The general public just wants the disaster to go away. The doctors want to know why, what and, now, WHO is responsible.
E. coli is found in the guts of every mammal and is generally harmless. In fact, it is present in massive quantities: half of the volume of the normal bowel excretion is made up of their huge numbers. But when a good germ goes wrong, it can cause disease in the host or anyone who picks it up through contamination or lack of hygiene.
And E. coli 0104:H4 has gone very, very wrong, with, it would appear, quite a bit of help from its friends.
Mike Adams, the intrepid Health Ranger, revealed to the English speaking world that this extraordinarily aggressive E. coli (from a family of bugs which are normally passive and non-aggressive in the extreme) had been systematically genetically altered through laboratory manipulation, to be totally resistant to 8 classes of antibiotics.
Natural News Article Link: http://www.naturalnews.com/032623_ecoli_fresh_vegetables.html
“European health authorities are leaping at the opportunity to spread fear about organic foods while ignoring the obvious true cause of the contamination in the first place — the widespread abuse of antibiotics in animal farming operations… The e.coli blame game has become a circus of musical chairs. First, they blamed the Spaniards as a form of retaliation for Spain’s resistance to accepting GMOs. This act drove Spanish farmers into bankruptcy through a savage campaign of rumor-mongering. After ravaging the Spanish vegetable farmers, they began to randomly instill widespread fear about a variety of vegetables: First it was cucumbers, then lettuce and then finally tomatoes. And now, the blame has come full circle and is now being cast upon organic sprout growers in Germany!”
Learn more: http://www.naturalnews.com/032623_ecoli_fresh_vegetables.html#ixzz1OjU2qjYz
He pointed out, quite correctly, that without sustained and careful laboratory manipulation there would be no way for this organism to acquire total resistance to these drugs since the drugs are not used in agriculture and the bacteria would not encounter all eight of them in nature.
The only reasonable conclusion is that colonies of normal E. coli had been intentionally, systematically exposed to each of the antibiotics in turn and the surviving colonies had been propagated and then exposed to the next antibiotic. The surviving germs were now resistant to both of the antibiotics to which they had been exposed. The process was repeated until a super bug was created which would not yield to any of the antibiotics that doctors would customarily use to treat the infection.
This is the only rational conclusion to which the evidence points.
Of course, by who, and why, the altered organism was deployed has not yet been established. A psychotic graduate student with aspirations to be a mass murderer? A corporate ploy to discredit independent agriculture and force the total industrialization of food to keep it “safe” from contamination (that is, the organized intentional contamination of all food by the folks who make the agrochemicals and GMOs which allow more of them to poison us and the drugs that you take when you get sick from the food)? A dedicated globalist loyally pursuing the “great culling” of us “useless eaters”?
So what we knew was that a forced natural selection had been used to create killer super-super bugs. Now we know that genetic manipulation of the GMO sort has been used, as well. Truly, a weaponized bug if there ever was one…
Helge Karch, the director of the Robert Koch Institute (Germany’s CDC). who heads a consulting laboratory at the Münster University Hospital in Germany says that he has discovered that the super killer contains DNA from E. coli, which is what he expected. It also contains (unexpectedly for those who don’t expect such genocidal manipulations) DNA from the organism that causes plague, responsible for wiping out a quarter of Europe’s population during the Black Death (1348-1351).
Please pay attention here: we are talking about the Black Death. Seriously.
Bubonic plague is caused by Yersinia pestis and is one of the most feared of all disorders. So when Dr. Karch blithely assured the German population that there is little danger of an outbreak of plague from this organism, he is clearly whistling through his Spanish cucumber.
Although we all love to be reassured, there is no one on planet Earth who can reassure us that we are not already facing a new plague. This one, however, rather than resulting from an unplanned, but wildly toxic combination of rats, lice and history, would be the intentional outcome of an unnatural selection process and a high-tech genetic manipulation to create a death bug. A weaponized bug.
Deny the genocidal agenda at your peril. I, for one, can see no reasonable option to the conclusion that the mad [wo]men at the helm of the realm are consummate murderers, killing randomly for their own unspeakable ends.
A bright note, however: there is no way in which any organism can become resistant to nano silver. None. Faced with the presence of a plague, a weaponized super plague, an ordinary infection or a genocidal assault through organisms of death, I want nano silver on hand, lots of it. Nano-silver is a nutrient that supports normal immune system function.
Ah, yes, nano silver was declared illegal in Europe on January 1, 2011. Can’t use an illegal substance, now can we. The good people of Europe are expected to be good citizens of the New World Order and… just die.
Civil disobedience, anyone? Or perhaps the people are ready to fight for their silver!
I get mine, which is called “Silver Sol” at www.Nutronix.com/NaturalSolutions. You should, too.
Yours in health and freedom,
Dr. Rima – www.DrRima.net
Rima E. Laibow, MD
Medical Director of the Natural Solutions Foundation
NATURAL SOLUTIONS FOUNDATION
Your Global Voice of Health & Food Freedom™
www.HealthFreedomPortal.org
You can read our previous Petitions here:
2009 Swine Flu Petition
FDA Docket No. FDA-2009-P-0418 http://drrimatruthreports.com/?p=3429
2008 False Vaccine Advertising Petition
FTC Miscellaneous Matter No. P002501 http://drrimatruthreports.com/?p=507
Petition mailed for filing December 17, 2010: Express Mail Tracking Number: EG 743479923 US. FDA notified us by letter dated December 22, 2010 that our Petition has been received and has been given FDA Docket No. FDA-2010-P-0651-0001/CP. It is posted here: http://www.regulations.gov/#!documentDetail;D=FDA-2010-P-0651-0001
You can comment on the Petition here: http://www.regulations.gov/#!submitComment;D=FDA-2010-P-0651-0001 or use our Action Item to send you comment to the FDA with copies to your representatives: http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=5708
Index:
Introduction
Petition
How You Can Help
Before the
United States of America
Food and Drug AdministrationPETITION
FDA Docket No. [To be Provided]
In the Matter of the 2009/2010 A-H1N1-09 “Swine Flu”
And 2010/2011 Season Influenza Vaccines
To: Dockets Management Branch }
Food and Drug Administration
Room 1061 }
5630 Fishers Lane HFA-305
Rockville, MD 20852 }Dated: December 17, 2010
Petition Index:
Introduction
Actions Requested
Statement of Grounds
The Park Doctrine
Disclosures Requested
Conclusion
Introduction
Petition IndexPursuant to the Constitution of the United States of America, First Amendment, Right to Petition for Redress of Grievances, the Federal Food, Drug and Cosmetic Act (FFDCA), 21 U.S.C. §§ 321 et seq., the Administrative Procedure Act (APA), 5 U.S.C. § 553(e), 21 C.F.R. 10.20 and 10.30 (Citizens Petition) and, to the extent applicable, 21 C.F.R. 10.35, to amend the FDA’s rules respecting the safety, effectiveness and availability of influenza vaccines, including the 2009/2010 Swine Flu (A-H1N1-09) and the 2010/2011 Seasonal Influenza Vaccines which includes A-H1N1 viral materials (herein, the Vaccines) the undersigned Petitioners PETITION the United States, to wit:
1. This Petition is brought before the Executive Authority of the United States of America, mindful of the President’s call for transparency in government and science-based decision-making. Petition is grounded in the Constitutional Right to Petition which may not be in any way abridged by Government and therefore any regulatory requirements are subordinate to that primary source of authority for this Petition. Additionally, in so far as any of the Petitioners are protected under the RFRA, all rights are reserved under the Religious Freedom Restoration Act of 1993 (RFRA – P.L. 103-141).
The Petitioners address the formal requirements of 21 C.F.R. 10.20 – 35, Section 10.30: A. Action requested; B. Statement of Grounds; C. Environmental Impact/Exemption and D. Economic Impact.
2. Petitioners are several NonGovernmental Organizations involved in health care civil rights and several individuals who are adversely impacted, have suffered particularized harms or legal wrongs by the Department of Health and Human Services (HHS), Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) (sometimes herein, the Agencies) actions referred to in this Petition, and all persons who join in this Petition hereafter.
3. This Petition is submitted to request specific action by the Department of Health and Human Services (HHS), the Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) within the scope of the mandated duties thereof, in order to exhaust administrative remedies.
4. Section 10:30 Statements
A. Actions requested:
Petition Index(1) The Petitioners request the enforcement of 21 U.S.C. 321, including Section k hereof, under the Constitutional Provision in Article II, Section 3, that the President “shall take Care that the Laws be faithfully executed…” with regard to the matters of the 2009/2010 A-H1N1-2009 Swine Flu Virus Influenza Vaccine and the 2010/2011 Seasonal Influenza Vaccines (which includes A H1N1 viral materials) and particularly the responsibility of drug company executives under the Park Doctrine for the foreseeable harms and legal wrongs arising from the Vaccines, including the miscarriages, injuries and deaths reported to the Vaccines Adverse Event Reporting System (VAERS).
(2) The Petitioners request that all approvals for the 2010/2011 Seasonal Influenza Vaccines that include the H1N1 virus be suspended forthwith, due in part to the large number of VAERS reported miscarriages, numbering at least 165 (which is to be compared to the typical number of such reports during a typical influenza season, zero to seven such reports).
(3) The Petitioners request that certain disclosure of vaccine dangers be made to the Public and that changes in public policy be made by the Agencies, as more fully set forth below in Paragraph 6 and thereafter.
(4) The Petitioners request that public hearings be held to make inquiry into the reason for the violations of the responsibility and legal charge placed upon the Agencies in order to”
a. Determine who shall be held accountable as permitted under the law in failing to perform a positive duty toward the public safety in the matter of approval of these vaccines and their purchase and dissemination,
b. Determine which administrative and regulatory procedures need to be changed, revamped, redesigned or abandoned in order to prevent this violation of the public trust from happening again
c. Determine whether conflict of interests lead to the design, purchase, approval, distribution and recommendations pertaining to these vaccines and, if so, what laws, statutes, regulation, codes of conduct or other limitations on Agency and industry personnel have been violated, if any and
d. What legal and regulatory responses, if any, should be taken to safeguard the public welfare.(5) The Petitioners further request that all findings from these public hearings be made public in a manner that makes them easily accessible to the public, inviting the public to participate in the development of suggestions, mandates and guidelines for reform, if indicated.
B. Statement of Grounds:
Petition Index(1) The 1976 Swine Flu Vaccine disaster resulted in hundreds of preventable deaths but none of the executives of the drug companies was punished, although the 1975 Park Doctrine* called for personal criminal responsibility.
(2) The 2009 Swine Flu Vaccine fiasco may have resulted in at least 165 (and perhaps as many as 3,000) vaccine-mediated, involuntary abortions in women who received the vaccine and whose unanticipated abortions followed shortly thereafter, as reported to VAERS, the government’s Vaccine Adverse Event Reporting System.
(3) The undersigned demand that the FDA investigate and refer to the Department of Justice all those drug and vaccine company executives who were involved in creating the un-safety tested H1N1 vaccine for an admittedly “novel” strain of the virus, providing the uninsurable and un-safety-tested drug to the public through the government Agencies herein, without ascertaining whether it would cause legal wrong or the deaths of unborn children and particularized harm, including death, to other protected persons.
(4) The undersigned further demand that all HHS, FDA and CDC officials who took part in the process whereby the government purchased, approved, recommended and distributed the deadly vaccines be suspended from their positions and be held accountable for the particularized harm and legal wrongs they have caused, without regard to any declared ‘public health emergency’, since these legal wrongs, deaths and other harms were foreseeable results of their actions and omissions.
5. The Park Doctrine:
Petition Index* United States v. Park, 421 U.S. 658 (1975) – Summary of the Supreme Court Decision:
The Act [21 U.S.C. § 331] imposes upon persons exercising authority and supervisory responsibility reposed in them by a business organization not only a positive duty to seek out and remedy violations but also, and primarily, a duty to implement measures that will insure that violations will not occur, United States v. Dotterweich, 320 US 277 (1943); in order to make food distributors “the strictest censors of their merchandise,” Smith v. California, 361 U.S. 147, 152 , the Act punishes “neglect where the law requires care, or inaction where it imposes a duty.” Morissette v. United States, 342 U.S. 246, 255 . Pp. 670-673.
21 U.S.C. § 331 – Prohibited Acts
“(k) The alteration, mutilation, destruction, obliteration, or removal of the whole or any part of the labeling of, or the doing of any other act with respect to, a food, drug, device, or cosmetic, if such act is done while such article is held for sale (whether or not the first sale) after shipment in interstate commerce and results in such article being adulterated or misbranded.”
C. Environmental Impact/Exemption
There is no significant environmental impact that can arise from the enforcement of 21 U.S.C. 321 against the individuals responsible for the particularized harms and legal wrongs suffered by Petitioners. The disclosures requested have no environmental impact. If any doses of vaccine are to be destroyed, this should be done in the standard manner for the disposal of any toxic medical waste, and particularly in a way in which the mercury contained in any multi-dose or other vial of the vaccine is not allowed to contaminate the environment.
D. Economic Impact
There is no significant economic impact that can arise from the enforcement of 21 U.S.C. 321 against the individuals responsible for the particularized harms and legal wrongs suffered by Petitioners, certainly since justice or the redress of grievances is intended to put the innocent victims in the position they would have been had there been no trespass.
6. Further Factual and Legal Grounds; Disclosures Required:
Petition Index(a) Petitioners petition the Department of Health and Human Services (HHS), the Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) to open and accept public comments and include, as part of any approval of the Vaccines, a clear requirement of strong warnings to the public, as mandated by the United States Supreme Court in another context, Thompson v. Western States Medical Center – 535 U.S. 357, 2002:
“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 each compounded drug to be labeled with a warning that the drug had not undergone FDA testing and that its risks were unknown.”
(b) The warning should therefore read: “This Vaccine has not undergone either FDA safety or efficacy testing required by law and its long and short-term risks are unknown in all age groups. The protective impact of this vaccine against seasonal influenza has not been established by significant scientific agreement. This Vaccine contains ingredients previously rejected for use in the United States and/or never evaluated by the FDA for safety or efficacy which have been shown in animal studies to cause significant adverse biological response when injected, including auto immune disease and permanent infertility.”
(c) The Petitioners petition the Department of Health and Human Services (HHS), the Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) to engage in a vigorous public information campaign, interleaved with their promotion of the Vaccines, and given equal prominence in type face, media announcements, web presence and other methods of public information used to promote the Vaccines, stating that the Vaccines contain ingredients previously rejected for use in the United States and/or never evaluated by the FDA for safety or efficacy which have been shown in animal studies to cause significant adverse biological response when injected including auto immune disease and permanent infertility.
(d) The Petitioners petition the Department of Health and Human Services (HHS), the Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) to recommend to all implementing agencies, such as State Departments of Health, that these un-insurable, unproven and untested Vaccines not be subject to any legal mandate, whether direct or indirect, perceived or actual, requiring their use by any class of persons in order for such persons to receive government services, such as schooling or health care, or to work in particular employments, such as first responders or health care workers, or to travel or to attend any public places or for any other purpose.
(e) The Petitioners petition the Department of Health and Human Services (HHS), the Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) to recommend voluntary Self-Shielding at home in preference to vaccination or removal to FEMA or other relocation facilities in the event of a Declared Pandemic Emergency.
7. As an Executive Department Agency, the Department of Health and Human Services (HHS), the Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) must “Take Care that the Laws be faithfully executed” (Article II, Section3, United States Constitution).
8. This Petition is grounded in fundamental principles of inalienable right, law and equity.
9. The primary legal basis for submitting this Petition to the Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) is the First Amendment to the Constitution of the United States: “Congress shall make no law…abridging… the right of the people… to petition the Government for a redress of grievances.” Additionally, the First Amendment Freedom of Speech, requiring transparency in government, as well as Fourth, Fifth, Ninth, Tenth and Fourteenth Amendments impact the arguments herein.
10. Petitioners also cite: the World Medical Association 1964 Declaration of Helsinki. See: http://www.wma.net/e/policy/b3.htm. This Declaration has the force of International Law, to which the United States is a party, and it clearly forbids experimental medication or medication without fully informed consent, as does United States law, for example, 42 U.S.C. 289(a) (a section entitled, Institutional review boards; ethics guidance program
11. The United Nations Universal Declaration of Human Rights – Article 12 – “No one shall be subjected to arbitrary interference with his privacy, family, home or correspondence, nor to attacks upon his honor and reputation. Everyone has the right to the protection of the law against such interference or attacks.” See: http://www.un.org/en/documents/udhr/ and the Geneva Conventions: Protocol Additional to the Geneva Conventions of 12 August 1949, and Relating to the Protection of Victims of Non-International Armed Conflicts (Protocol II) – Article 17.-Prohibition of forced movement of civilians:
“1. The displacement of the civilian population shall not be ordered for reasons related to the conflict unless the security of the civilians involved or imperative military reasons so demand. Should such displacements have to be carried out, all possible measures shall be taken in order that the civilian population may be received under satisfactory conditions of shelter, hygiene, health, safety and nutrition.
2. Civilians shall not be compelled to leave their own territory for reasons connected with the conflict.”
See: http://www2.ohchr.org/english/law/protocol2.htm
12. Current law and regulations provide for involuntary Provisional Quarantine, with removal, following refusal of persons to submit to vaccination with the untested, un-insurable, non-voluntary “informed consent” Vaccines. The Agency regulations should be amended to provide for voluntary Self-Shielding, Self-Quarantine and Self-Isolation as permitted alternatives.
13. Bivens v. Six Unknown-Named Agents of Fed. Bureau of Narcotics, 403 U.S. 388, 396-397, (1971); Carlson v. Green, 466 U.S. 14, 18-19 (1980). – These cases construe “42 USC § 300aa-31” with its “more likely than not” evidentiary burden and its Daubert v. Merrell Dow Pharmaceuticals, Inc, 509 U.S. 579, 113 S.Ct 2786, 2797 (1993), prohibition against expert opinion reliance upon poor quality and flawed data, the surviving good quality data shows the Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) is statutorily required to reject the Vaccines approval since it “more likely than not” caused numerous neurological and immune system pandemics (e.g., autism, neurological disorders, autoimmune disorders, etc). Since the Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) know of this linking data and intentionally exposed the public to these serous risks of harm, while attempting to hide/alter the data that showed the harm, the Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) also violated the 14th Amendment’s “Constitutional Safety Guarantees.” Under these egregious and horrifying circumstances, both Sec. 300aa-31 and a 28 USC § 1331 “Bivens Action” would authorize injunctive relief, and where warranted, damages.
14. Jacobson v. Commonwealth of Massachusetts, 197 U.S. 11 (1905), in which the Supreme Court of the United States, prior to the establishment of the Food, Drugs and Cosmetics Act revisions that established Federal pre-emption of drug approvals, gave deference to the Supreme Court of Massachusetts in an involuntary vaccination matter, also contains clear language authorizing Federal intervention in circumstances that are clearly present with regard to the Vaccines involved in this Petition.
“It is easy, for instance, to suppose the case of an adult who is embraced by the mere words of the act, but yet to subject whom to vaccination in a particular condition of his health or body, would be cruel and inhuman in the last degree. We are not to be understood as holding that the statute was intended to be applied to such a case, or, if it was so intended, that the judiciary would not be competent to interfere and protect the health and life of the individual concerned. “All laws,” this court has said, “should receive a sensible construction. General terms should be so limited in their application as not to lead to injustice, oppression or absurd consequence. It will always, therefore, be presumed that the legislature intended exceptions to its language which would avoid results of that character. The reason of the law in such cases should prevail over its letter.” United States v. Kirby, 7 Wall. 482; Lau Ow Bew v. United States, 144 U.S. 47, 58. Until otherwise informed by the highest court of Massachusetts we are not inclined to hold that the statute establishes the absolute rule that an adult must be vaccinated if it be apparent or can be shown with reasonable certainty that he is not at the time a fit subject of vaccination or that vaccination, by reason of his then condition, would seriously impair his health or probably cause his death.”
15. The Acts establishing the authority of the Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) being herein petitioned are also a legal basis for the Petition. The Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) exist to protect the public, within the limits established by the Constitution of the United States of America. However, Article 16 of the original enabling legislation that created the Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) indicates, in effect, that a primary purpose is to promote, protect and promulgate the pharmaceutical industry.
16. Petitioners note the statute in the derogation of the common law and Constitutional limitations, establishing certain limited exemptions from liability for Vaccine Injuries, 42 USC 300aa-16 (and the Vaccine Injury Compensation Program, thereunder). This law is further cited as a law that must be strictly construed in favor of patients, guardians, parents and children even if such construction is against the economic interests of the drug industry and other persons claiming exemption thereunder.
17. Petitioners note that, given the exceptional limited exemption given to both manufactures of the Vaccines and employees of the Federal Agencies and their designees which purports to eliminate the possibility of redress of grievances through the Courts by the public in the event that individuals suffer irreversible harm or death, it is especially important that careful notification and protection be offered to the public in the face of instructions or compulsions to accept the use of the Vaccines which contain ingredients previously rejected for use in the United States and/or never evaluated by the FDA for safety or efficacy which have been shown in animal studies to cause significant adverse biological response when injected.
18. The total amount that the Vaccine Injury Compensation Program has paid in compensation since its 1989 founding is in excess of $1,884,145,255.29.
See: http://www.hrsa.gov/Vaccinecompensation/statistics_report.htm
19. Basic common law principles prohibiting forced acquiescence under duress and limited or intentionally distorted information, as exemplified by the United States Supreme Court decision in the case of Thompson v Western States Medical Centers – 535 U.S. 357 (2002). The Petitioners note with concern that FDA regulation permits a choice under duress upon limited and distorted information such that those refusing the Vaccines in a Pandemic Emergency situation face incarceration/quarantine under Provisional Quarantine regulations in violation of the prohibitions mentioned above against forced acquiescence under duress and limited or intentionally distorted information. The Swine Flu National Health Emergency declared by President Obama on October 25, 2009 has not been suspended despite the fact that the World Health Organization rescinded its Level 6 Pandemic Status on XXXXX, 2010.
20. The Statutes authorizing the Department of Health and Human Services (HHS), the Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) contain general provisions that support the actions requested in this petition. Federal Law includes provisions that grant the responsible persons in the Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) broad authority to promulgate rules and regulations “necessary to carry out the Act[s].”
21. The Food, Drug and Cosmetics Act (FD&C Act) Mission Statement requires that “…(B) human and veterinary drugs are safe and effective…” (21 USC §393(b)(2)). The Act had been amended repeatedly, to require that no drug be approved unless it is proven “safe and effective.”
This clear legal requirement is explained by the Agency on its web site:
“In October 1962, Congress passed the Kefauver-Harris Drug Amendments to the Federal FD&C Act. Before marketing a drug, firms now had to prove not only safety, but also provide substantial evidence of effectiveness for the product’s intended use. Temple says, “That evidence had to consist of adequate and well-controlled studies, a revolutionary requirement.”
“Also critically, the 1962 amendments required that the FDA specifically approve the marketing application before the drug could be marketed, another major change.” The Kefauver-Harris Drug Amendments also asked the Secretary to establish rules of investigation of new drugs, including a requirement for the informed consent of study subjects. The amendments also formalized good manufacturing practices, required that adverse events be reported, and transferred the regulation of prescription drug advertising from the Federal Trade Commission to the FDA.”
See: http://www.fda.gov/AboutFDA/WhatWeDo/History/ProductRegulation/PromotingSafeandEffectiveDrugsfor100Years/default.htm
22. The Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) should issue the actions requested herein as an Interim Final Rule without first completing Notice and Comment, Risk Assessment, and Cost-Benefit Analysis. Additionally, the Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) should not issue the drug-industry requested vaccine approvals as an emergency matter.
23. Under ordinary circumstances, the Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) must comply with procedural requirements under the Administrative Procedures Act (APA) and the specific Acts authorizing the Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC), including the use of notice-and-comment rulemaking and the completion of a risk assessment and cost-benefit analysis before issuance of a new rule. However, both Acts provide for exceptions to those requirements for circumstances such as those present here (with regard to the Petitioners herein, but not with regard to the drug-industry applications), where the continuation of current policy (the emergency approval of the Vaccines) would constitute an imminent threat to public safety and any delay in the policy-making the Petitioners herein would be contrary to the public interest.
24. The Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) should only avail itself of those statutory exceptions with regard with Petitioner’s request herein and promulgate the requested policies while first providing the public with reasonable notice under these circumstances and an opportunity for comment and before completing a full risk assessment and cost-benefit analysis. The Department of Health and Human Services (HHS), the Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) should first adopt the policy as an “interim-final rule,” which would become binding upon publication (or within a time certain; for example, a week after publication) and subsequently provide for public comment and complete its risk assessment and cost-benefit analysis. If such a time period is provided for public comment and the completion of risk assessment and cost-benefit analysis, the Department of Health and Human Services (HHS), the Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) should make no declaration, take no action, approve no product or Vaccine related to this situation during such period.
25. The Requested Actions of Petitioners herein satisfy the “good cause” exception to the Administrative Procedure Act’s (APA) requirement for notice and comment, while the application of that exception should not apply to the Vaccine applications.
26. The Administrative Procedures Act (APA) provides that full notice-and-comment rule-making is not required when an agency “for good cause finds (and incorporates the finding and a brief statement of the reasons therefore in the rules issued) that notice and public procedure thereon are impracticable, unnecessary, or contrary to the public interest.” 5 U.S.C. Section 553(b)(B) The good cause exception “is an important safety valve to be used where delay would do real harm.” United States Steel v EPA, 595 F.2d207, 214 (5th Cir. 1979). According to the legislative history of the provision, “impracticable” means a situation in which the due and required execution of the agency functions would be unavoidably prevented by its undertaking public rule-making proceedings.” S. Rep. No. 752, 79thCong., 1st Sess., at 16 (1945). It has been held, determining “impracticality” requires analysis in practical terms of the particular statutory-agency setting and the reasons why agency action could not await notice and comment. American Transfer & Storage Company v. ICC, 719 F. 2d 1283, 1295 (5th Cir. 1983).
27. The same urgency which motivates the Department of Health and Human Services (HHS), the Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) to move forward with excessive rapidly and inappropriate zeal, in the light of an alleged influenza threat (which was declared despite the mild nature of the disease) should motivate the Food and Drug Administration (FDA) and/or the Centers for Disease Control (CDC) to move forward with the measures proposed by Petitioners herein to protect both the public’s welfare and their right to fully informed consent and transparency. Inclusion of the H1N1 Swine Flu vaccine in the Seasonal Influenza shots for the 2010 flu season, in the light of a total lack of threat of either H1N1 pandemic or illness is particularly egregious and its use should be immediately halted.
28. Below are listed three of numerous instances in which courts have upheld an agency’s decision to invoke the “good cause” exception and issue a rule without providing notice and comment where a delay would threaten public safety or the environment. See: Hawaii Helicopter Operators Ass’n v. FAA, 51 F.3d 212, 24 (9th Cir. 1995) (good cause exception satisfied in view of “the threat to public safety reflected in an increasing number of helicopter accidents”); Northern Arapahoe Tribe v. Hodel, 808 F.2d741, 750-52 (10th Cir. 1987) (good cause exception satisfied in view of urgent need for hunting regulations where herds were threatened with extinction); Northwest Airlines v. Goldschmidt, 645 F2d 1309, 1321 (8th Cir. 1981) (good cause exception satisfied in view of urgent need to allocate landing slots at major airport).
29. The rationale underlying those decisions is that compliance with time-consuming procedural requirements would “do real harm” by delaying implementation of urgently needed policies to safeguard public health. Swine Flu causes a disease of low virulence and pathogenicity so that the need for current Agency displays of overwhelming haste in their approval is not present, but the Vaccines contain never-before-approved, but previously rejected, adjuvants and known toxins so that the need for caution in their approval is very much present. Clearly, the exigent circumstances necessary to satisfy the Administrative Procedures Act’s (APA’s) good cause exception are present with regard to Petitioner’s concerns as set forth in the Factual Basis for Relief. They are not present with regard to the Vaccine approval applications. On the contrary, such approval would harm the public health.
30. Vaccinations cause well-known and foreseeable harm. Autism, neurological damage, Guillian Barré syndrome, post vaccination Encephalitis, asthma, coma, juvenile ALS, adult ALS, oil-in-water adjuvant-induced poly arthritis, dermatitis, fibromyalgia, fatigue, malaise, death and other known consequences of vaccine injury are generally not reversible and the present danger from the Vaccines to children and adults is so great that the “good cause” exception referenced above is well warranted in this case. Consumers are being defrauded while children and others are being irreversibly damaged. Once a child collapses into autism or juvenile ALS, post vaccine poly arthritis, for example, there is a virtually irreversible path which the child and family follow, often leading to eventual institutionalization. These are, in most cases, preventable tragedies. The probable harm is immediate and irreparable.
31. In order to redress the perceived harm, there are several procedural matters that should be addressed by Agency Rule or Court interpretation. These are the need for:
(1) Clear and prominent Warnings as specified elsewhere herein,
(2) Due-process compliant procedures for opting out of involuntary vaccinations,
(3) Sound information to support informed consent if the vaccination is truly voluntary, and
(4) Due-process compliant procedures required to involuntarily isolate or quarantine any person who refuses to take an involuntary vaccine,
(5) Agency and congressional hearings into
1. the causes of behavioral and neurological vaccine damage and the repair of such damage
2. The cause and conduct of these approvals any conflicts of interest or other improprieties, if any,
3. The persons responsible for these improprieties, if any.32. Medical ethics, United States law regarding medical experimentation and treatment, and international legal standards require nothing less. These international legal standards are among the international standards the Agency pledged to harmonize to in a notice published in the Federal Register of October 11, 1995 (60 FR 53078), “FDA articulated its policy regarding the development and use of standards with respect to the harmonization of various national and international regulatory requirements and guidelines…”
See: http://www.cfsan.fda.gov/~lrd/fr970707.html
33. The Vaccines are advertised to the Public as “safe and effective” and as “approved” and “recommended” by the Agencies. This is false and misleading. The most complete and recent review of the literatures shows no proof of safety or efficacy. See: Geier DA, King PG, Geier MR. Influenza Vaccine: Review of effectiveness of the U.S. immunization program and policy considerations. J American Physicians and Surgeons 2006 Fall; 11(3): 69-74.
34. The A-H1N1 “Swine Flu” 2009/2010 vaccination deadly results are similar to the 1976 “Swine Flu” vaccination panic results: hundreds of unborn children and others have died (more than are alleged to have died from the 2009 “Swine Flu”) and hundreds of thousands or more will be injured. Other countries, including Finland and Australia, after purchasing and recommending the same vaccines, noted with alarm the increase in neurological disorders including narcolepsy and convulsions. Their response was to ban the vaccines, noting that they were not necessary since the risk of the vaccine outweigned the risk of seasonal or H1N1 influenza. The United States can do no less for its citizens.
35. Since the 2010/2011 Vaccines contain the A-H1N1 strain, hundreds if not thousands of more deaths, including preventable miscarriages, will occur. These deaths are a foreseeable result of the Agencies’ policies and of the failure of the company executives to obey the law requiring that vaccines be safe and effective. Since vaccines have not been shown to be either safe or effective with significant scientific agreement, the Vaccines are misbranded.
36. Therefore, the Petitioners petition the Agencies to fully enforce 21 U.S.C. 321 and hold those company executives and Agency employees responsible for these foreseeable deaths; for the particularized harms and legal wrongs they have and are imposing upon Petitioners and others similarly situated.
37. The Petitioners reserve all Rights including any Right any Petitioner may have to petition the other co-equal branches of the Federal Government, the Congress and the United States Courts, for redress of grievances, particularized harm or legal wrong in any case or controversy for which any may have standing.
Wherefore the undersigned certifies that to the best of his knowledge and belief the factual statements made herein are true, complete and not intentionally misleading.
The undersigned certifies, that, to the best knowledge and belief of the undersigned, this petition includes all information and views on which the petition relies, and that it includes representative data and information known to the Petitioner which are unfavorable to the petition.
December 17, 2010
By:
Ralph Fucetola JD – ralph.fucetola@usa.net
www.HealthFreedomPortal.org
Natural Solutions Foundation Trustee, on behalf of all Petitioners
Please support this action by:
[1] Taking the Action Item in support of the Petition
http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=5708
[2] Donate to help us cover our costs: http://drrimatruthreports.com/?page_id=189
Dr. Rima Reports, live chat, updates, Action Items and more…
Permalink: http://drrimatruthreports.com/?p=7191
OCTOBER 23 2010
10 DAYS ‘TIL THE ELECTION! UNDER TWO WEEKS! |
Index: Perfect Coffee Gift – HACKED A NEW WAY! – Election Push Back – Codex
Free 10/27 Panama Webinar – Short Takes – Dr. Rima Reports – Dr. Rima Recommends & Webinars
First, A Word From Our Sponsor:
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Sigh… Hacked and Attacked in a New Way…
If you are among the few who have made a donation to the Natural Solutions Foundation, we thank you. Your support makes our work possible. A couple folks, however, have recently found that their credit and debit cards are being used to make donations they did not intend, often in small amounts (such as our minimum donation, $5.00 or our suggested donation of $5.10).
These questionable charges are of grave concern to us since they represent an invasion of your privacy, a threat to your good will and, as our horrific interaction with the Merchant Services company that took our money out of our bank account last year [reported by use here: [http://drrimatruthreports.com/?p=2732] shows, a potent way to attack the Natural Solutions Foundation.
Funny, you would not think that giving us money could be a threat to us, but, of course, if it was not YOUR free and voluntary decision, but a hacker ‘bot’s decision to put that money into our account, it is a serious threat. You have a right to be free of coercive redistribution of your funds… whether by goverment, its crony companies, or some misguided “Robin Hood” or more sinister agent provacateur…
We need your help to uncover the malcreants since we cannot tell the difference between a legitimate $5.00 donation and a questionable one. If any questionable charge directed toward the Natural Solutions Foundation appears on any card or statement which you have, we urge you to notifiy our Trustee and Counsel, Ralph Fucetola, JD, at once. Please email him throug our contact email, dr.laibow@gmail.com with “Questionable” as the subject line. Give us as much detail as you can, including the date, your name and the amount of the charge. Of course we will refund your money. Having this information will allow us to investigate and, we anticipate, identify the source of this criminal behavior.
We want your donations and we need them to continue our vital work. And we want to put a stop to the attacks on us, which are, of course, attacks on you and your freedom.
Thanks for your help and cooperation.
Yours in health and freedom,
Ralph Fucetola, JD
Trustee and Counsel
—————————–
Please Help! Make Your Tax Deductible Donation Now
http://drrimatruthreports.com/?page_id=189
We need recurring donations so we cover our expenses and plan ahead. Whatever your recurring donation is, it will help to make the difference. We are hacked and attacked for a reason: because we are having an impact. Do you want us at Codex in 10 days to bring you eyewitness reports? Then you have got to pitch in now. The next meeting is about to begin. Whether we are there or not is up to you.
The other side has huge power. We have more. Together. You see, we have your Push Back power!
The other side has huge budgets. We do not need that much.
The other side deals in lies. We deal in truth. The other side is truly dangerous because they are wreaking havoc and leading people to disease and death.
We are “dangerous” solely because we are telling truth to power.
Thanks for your help. Please take the actions below and please, please make a donation. Your health and food freedom literally depend upon it.
http://drrimatruthreports.com/?page_id=189
Yours in health and freedom,
Dr. Rima
www.Dr.Rima.net
What can you do about the Uber Cartel?
Here are those Action Items so you can take them and share them for others to take:
Send Congress 4 Push Back Messages:
“Don’t You DARE!”
Use the Action Items Below; Email Everyone You Know Urging Them to Do the Same and Forward to Their Contacts!
Stop S.510! Stop S.3767!
http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=4613
NO! to S.3767: Support the Food Freedom Amendment Instead!
http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=4878
NO! to GMOs
http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=2049
NO! To Forced Vaccination
http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=4376
That’s why our visits to the offices of both incumbents AND candidates, when we come in groups, armed with the talking points, are so very important. That’s why viralizing the Action Items (see above) and the Talking Points (see below) is so very, very, important.
NO! to FOOD FASCISM Talking Points
http://drrimatruthreports.com/?p=6910
GMO DANGERS Talking Points
http://drrimatruthreports.com/?p=6955
NO FORCED VACCINATION Talking Points
http://drrimatruthreports.com/?p=7004
OF COURSE “they” are attacking us! If you were the Uber Cartel and the other side were this successful, wouldn’t you attack them this way if you had no scruples and no desire to see anything like freedom for anyone but yourself?
A bit of inspiration: The Uber Cartel and the Peasants of the Dawn: http://www.youtube.com/watch?v=SkNj00lBDHo
We can only take this level of attack as a powerful confirmation that we, you and the Natural Solutions Foundation, are exerting a meaningful force against globalization, genocide and the contamination of our food! And that is why we cannot let up!
We Need Your Help to Attend Codex!
The Natural Solutions Foundation cannot operate without your support. Right now we are nearly through the month of October we do not have enough funds to go to the Codex Committee on Nutrition and Foods for Special Dietary Uses meeting in Chile early in November. What that means is that you will be, where Codex is concerned, blind and deaf. Your eyes and your ears, Gen. Bert and I, will not be there bringing you the real scoop, not some watered down, balsamic happy nonsense. But to get there, we need your support. Now.
We need your recurring donations and coffee orders now! Donate here: http://drrimatruthreports.com/?page_id=189 Order your Valley of the Moon Coffee here: http://ValleyoftheMoonCoffee.org Visit our Online Mall www.Organics4U.org here |
Why Would You Buy a Ticket to Panama?
Newest Eco Demonstration Project Development:
Duplex Participations in the Project!
http://drrimatruthreports.com/?p=7098
This includes a special free October 27, 2010 Webinar!
Chef Gail Holding A Hand of Chemical Free Bananas From Our Coffee Finca. Next Step?
World-Class Banana Bread!
There are a number of reasons, all of them good ones, that I can think of to buy that ticket to Panama!
Here are some of them, in no particular rank order:
1. You are interested in finding out more about the Natural Solutions Foundation’s Valley of the Moon™Eco Demonstration Project and how it might fit your needs. You have visited www.NaturalSolutionsFoundation.org and www.MyValleyoftheMoon.org and you are intrigued. Of course, you are welcome at any time but you might want to join Trustee Ralph Fucetola and a group of people for their next visit here (tentative dates: January 19 – 27, 2011). Contact us at dr.laibow@gmail.com, subject PANAMA, for more information.
2. You know that the US is in the process of seizing both IRAs and 401s and “guaranteeing” them with the “strength” of the US Dollar to provide you with an “annuity” of 3% interest and you are not at all happy with this option. You know that you can still place your retirement funds offshore and are seriously considering this option.
3. You want to live in a community of like-minded people with a secure, BeyondOrganic food supply, natural medical center and other services and you want to do it outside the US.
4. You want to help to reclaim the production of clean, unadulterated food around the world through your support of, and connection with, the Valley of the Moon Eco Demonstration Project in Volcan, Panama. You don’t have to be a farmer to do so!
5. You want to attend our outstanding seminars and workshops, like Angela Malek’s “Living, Eating and Healing with the 5 Element Theory” Workshop from January 9 – 15, 2011. Watch a short video with Angela here: http://www.youtube.com/watch?v=RKmOB6VdctQ to get the “flavor”. Interested? Contact us at dr.laibow@gmail.com with “5 Elements” as your subject line. More information: http://drrimatruthreports.com/?p=7035 — Space is strictly limited!
6. You love good food and the idea of reclaiming its production. You love eating it, too, and you can’t wait to eat at our gourmet organic restaurant!
7. You want to volunteer your time and talents at the Valley of the Moon! Again, use our dr.laibow@gmail.com address with “Volunteer” in the subject line.
Short Takes
www.HealthKeepersOath.org
Coffee Drinking Associated With Reduced Oral Cancer Risk
October 19, 2010 — Drinking coffee is associated with a 36% reduction in the risk for cancer of the oral cavity and pharynx, according to Italian investigators who performed a meta-analysis of observational studies.
These findings echo those published earlier this year by the same group of researchers, and reported by Medscape Medical News at that time. However, the scope of the new study is larger and includes other aerodigestive tract cancers, including those of the esophagus.
The researchers did not find any association between coffee drinking and the risk for laryngeal and esophageal cancers.
“There are no definite biological mechanisms of the potential favorable role of coffee on [oral cavity and pharynx] cancer,” the authors write in their paper, which was published online October 13 in the Annals of Oncology.
However, coffee has “many chemicals with antioxidant and antimutagenic activities,” they say. The concentration of these chemicals varies, “depending on type of coffee power (Arabica or Robusta), roasting, and preparation,” the authors add.
A number of compounds found in coffee, such as chlorogenic acids, cafestol, and kahweol, have been shown to reduce the genotoxicity of several carcinogens, they explain.
The authors also point out that coffee drinking has been inversely related to liver cirrhosis, liver cancer, endometrial cancer, and colorectal cancer.
http://www.medscape.com/viewarticle/730771?src=mpnews&spon=34&uac=117629CN
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From Medscape Medical News
Maternal Influenza Vaccination May Protect Infants From Flu
October 7, 2010 — Maternal influenza vaccination may be associated with protection from influenza in infants, according to the results of a nonrandomized, prospective, observational cohort study reported online October 4 in the Archives of Pediatric and Adolescent Medicine.
“The US Advisory Committee on Immunization Practices recommends that pregnant women receive influenza vaccine because of the increased risk of influenza complications in pregnant women,” write Angelia A. Eick, PhD, from Johns Hopkins Bloomberg School of Public Health in Baltimore, Maryland, and colleagues. “Maternal influenza vaccination may also confer a benefit to infants born during influenza season, as they are ineligible for vaccination until 6 months of age.”
[REL] Never mind that these very products have never, never been shown to be either safe or effective for pregnant women and have been shown to contain ingredients which pose severe threats to fetuses.
YES, YES!!!! Monsanto, the giant biotechnology agriculture company that created genetically modified corn, soybeans and herbicides, isn’t riding so high this year in the stocks department, as news comes in that its products aren’t working like they’d hoped.
According to the New York Times, weeds are becoming immune to Monsanto’s herbicide Roundup, and its latest genetically modified, 8-gene corn is a flop, producing yields no higher than the company’s less expensive corn, which contains only three foreign genes.
“Monsanto has already been forced to sharply cut prices on SmartStax and on its newest soybean seeds, called Roundup Ready 2 Yield, as sales fell below projections,” the Times said. “And the Justice Department is investigating Monsanto for possible antitrust violations.”
“Until now, Monsanto’s main challenge has come from opponents of genetically modified crops, who have slowed their adoption in Europe and some other regions. Now, however, the skeptics also include farmers and investors who were once in Monsanto’s camp.”
Monsanto was named “company of the year” by Forbes Magazine in December. Last week, television stock market commentator Jim Cramer said it “may be the worst stock of 2010,” the Times said. New York Times October 5, 2010 – Http://articles.mercola.com/sites/articles/archive/2010/10/23/monsanto-finally-reaping-its-just-desserts.aspx
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June 16, 2010 – C8 exposure linked to ADHD in children
Children exposed to higher levels of C8 are at an increased risk of developing attention deficit hyperactivity disorder, according to a scientific paper published this week.
By Ken Ward Jr.
The Charleston Gazette
Advertiser
CHARLESTON, W.Va. — Children exposed to higher levels of C8 are at an increased risk of developing attention deficit hyperactivity disorder, according to a scientific paper published this week….Researchers compared parental reports of ADHD diagnosis from Centers for Disease Control Data and blood samples for the chemicals. They found that, for example, for every additional 1 part per billion of C8 in the blood, children faced a 12 percent increased risk of ADHD.”
Rima Laibow, MD
Dr. Rima Reports
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We will have some surprise guests then too!
Click Here For More Information on Dr. Rima Reports:
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NATURAL SOLUTIONS CENTER WEBINARS Webinar Archives 1. Archived! CAUTIONS FOR CAM PRACTITIONERS – Ralph Fucetola JD (1.5 hr – $99) 3. Archived! The Five Elements: Video Intro for Free Webinar and more… 4. Special Free Webinar — the Valley of the Moon Eco Community
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Please don’t forget the universal remedy, Nano Silver, www.Nutronix.com/naturalsolutions |
And don’t forget to supplement with Cognitive Enhancement Nutrients to keep your brain healthy and focused… this message from our friends at Biologics Nutraceuticals, providers of the Cognitive Enhancement Nutrition:
http://www.biologicsnutra.com/affiliate/scripts/t.php?a_aid=20070ae0&a_bid=787b0a60
“Please let Health Freedom supporters know they can take advantage of our Double Dip Sale with $4.99 Economy Shipping to the entire US! All of the Dr. Rima Packs are discounted 10% with the additional option to buy 2 and get another pack of the same type added to your cart at checkout for free! You may also buy three of the same type individual bottles and receive a free bottle of the same type in your cart at checkout!”
Yours in health and freedom,
The Trustees of the Natural Solutions Foundation
Maj. Gen. Albert N. Stubblebine III (US Army, Ret.)
President – www.FoodFreedomeJournal.org
Rima E. Laibow, MD
Medical Director – www.DrRima.net
Ralph Fucetola, JD
Counsel and Trustee – www.NaturalSolutionsFoundation.org
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