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Health
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Title: Amish grandpa farmer found guilty on ALL counts involving his homemade salves - faces up to 48 years in prison
Source: Health Nut News
URL Source: https://www.sott.net/article/344894 ... faces-up-to-48-years-in-prison
Published: Mar 11, 2017
Author: Erin Elizabeth
Post Date: 2017-03-11 10:00:56 by Ada
Keywords: None
Views: 444
Comments: 15

Fri, 10 Mar 2017 18:15 UTC We are SHOCKED and saddened to report that on March 2nd, Amish farmer (and father and grandfather) Samuel Girod- who we have reported on before - was found guilty by a federal jury for making and distributing herbal products on his family farm. The FDA requires manufacturers of defined drugs to register their facility with them and the Girod farm is not registered. He will be sentenced by a judge on June 16 at 10 a.m.

Watch this video I made below:

In the end, the government charged Girod with conspiracy to impede an officer, obstruction of a proceeding before an agency, failing to register with the FDA, eights counts of causing misbranded drugs to be introduced into interstate commerce, tampering with a witness and failure to appear. The jury found Girod guilty on all 13 counts, but not only did they find him guilty, "they found Sam guilty of each separate part of each count, even when only one part would be needed to make Sam guilty of that count against him," reports Health Impact News. It's almost like it was personal.

From Health Impact: Sam described the FDA coming to his home in Indiana and objecting to the skin cancer claim so he removed that from the label. Sam asked if they had any other concerns and was told they would like to think about it for a week. They never responded. After a few weeks, Sam contacted them and they didn't reply.

Sam refuted the claim that the Amish were physically intimidating. He explained that they would never intimidate or threaten anyone. Anybody with even a passing familiarity with the Amish would know that to be the truth. He also stressed that nobody cursed at the FDA agents, as that is something they do not do.

Sam stated that he never harmed anybody and never acted to deceive anybody.

Sam explained that he never threatened or intimidated Mary Miller to prevent her from providing evidence to a grand jury. They had discussed the matter because she had no prior dealings with the FDA and in fact that was the last thing this Amish woman wanted, and Sam felt bad that his actions had inadvertently drawn the FDA's attention to Mary. Sam followed up with a letter to several customers and business associates in a letter addressed to "Friends". He stated in the letter that everyone was free to do whatever they wanted to do. From the federal government's perspective it was inappropriate for Sam to contact them, but he was reaching out to confused and very worried friends with whom he had a close personal business relationship. He was trying to explain what was happening to the best of his understanding. A subpoena from the federal government is a terrifying thing to an Amish person. It was obvious from the testimony of all of the FDA's subpoenaed witnesses that they did feel threatened and intimidated... by the FDA. They were clearly on Sam's side, even though they were being compelled to testify against him.

When the problems first surfaced with the FDA, some time around 2003, Sam hired a lawyer and his lawyer hired an FDA approved lab to test Sam's products. The FDA also tested Sam's products in their own lab using liquid chromatography and mass spectroscopy. Both labs reached the same conclusions. The ingredients matched the label's ingredients list, the samples did not contain any drugs as commonly defined or any alkaloids or poisons, and the samples from different containers of the same product were consistent. In 2003 and 2004, the FDA requested more label changes and Sam made the changes, removing all health claims and only listing the ingredients on the label. We cannot believe the FDA has gone to these lengths to silence someone becasue they are making a natural health product. Do not believe for one moment they are trying to save or protect anyone from harm- they are silencing and potentially putting an Amish man in PRISON for healing people without the help of pharmaceuticals. That is the extent of it. Quite frankly is shameful.

Please consider writing the judge to let him know a) what you think of this travesty and b) that Sam Girod deserves grace and time served:

The Honorable Danny C. Reeves United States District Judge US District Court 101 Barr Street Lexington, KY 40507

You can also sign the Change.org petition for Sam Girod. [Here's a link to copy and share:bit.ly/freeamishsam]

Click for Full Text!

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Begin Trace Mode for Comment # 11.

#9. To: Ada (#0) (Edited)

When the problems first surfaced with the FDA, some time around 2003, Sam hired a lawyer and his lawyer hired an FDA approved lab to test Sam's products. The FDA also tested Sam's products in their own lab using liquid chromatography and mass spectroscopy. Both labs reached the same conclusions. The ingredients matched the label's ingredients list, the samples did not contain any drugs as commonly defined or any alkaloids or poisons, and the samples from different containers of the same product were consistent. In 2003 and 2004, the FDA requested more label changes and Sam made the changes, removing all health claims and only listing the ingredients on the label. We cannot believe the FDA has gone to these lengths to silence someone becasue they are making a natural health product. Do not believe for one moment they are trying to save or protect anyone from harm- they are silencing and potentially putting an Amish man in PRISON for healing people without the help of pharmaceuticals. That is the extent of it. Quite frankly is shameful.

"Not FDA approved" should have been enough of a label change to stop the FDA from wasting the time and money of taxpayers in this prosecutorial pursuit to preserve its Medicinal Monopolization. For many thousands of years before the FDA, people relied on natural remedies to help them medicinally but now they are expected to just suffer and maybe even die if they can't afford the exorbitant costs of the FDA's Pharmaceuticals Protection Racketeerings.

FDA: Food and Drug Administration | Criticisms - Wikipedia

Nine FDA scientists appealed to then president-elect Barack Obama over pressures from management, experienced during the George W. Bush presidency, to manipulate data, including in relation to the review process for medical devices. Characterized as "corrupted and distorted by current FDA managers, thereby placing the American people at risk," these concerns were also highlighted in the 2006 report on the agency as well.

The FDA has also been criticized from the opposite viewpoint, as being too tough on industry. According to an analysis published on the website of the libertarian Mercatus Center as well as published statements by economists, medical practitioners, and concerned consumers, many feel the FDA oversteps its regulatory powers and undermines small business and small farms in favor of large corporations. Three of the FDA restrictions under analysis are the permitting of new drugs and devices, the control of manufacturer speech, and the imposition of prescription requirements. The authors argue that in the increasingly complex and diverse food marketplace, the FDA is not equipped to adequately regulate or inspect food. In addition, excessive regulation is blamed for the rising costs of health care and the creation of monopolies, as potential competitors are unable to get FDA approval to enter the market to compete and keep health care costs down.

However, in an indicator that the FDA may be too lax in their approval process, in particular for medical devices, a 2011 study by Dr. Diana Zuckerman and Paul Brown of the National Research Center for Women and Families, and Dr. Steven Nissen of the Cleveland Clinic, published in the Archives of Internal Medicine, showed that most medical devices recalled in the last five years for "serious health problems or death" had been previously approved by the FDA using the less stringent, and cheaper, 510(k) process. In a few cases the devices had been deemed so low-risk that they did not need FDA regulation. Of the 113 devices recalled, 35 were for cardiovascular health purposes.

GreyLmist  posted on  2017-03-15   2:48:03 ET  Reply   Untrace   Trace   Private Reply  


#11. To: GreyLmist (#9)

The FDA also tested Sam's products in their own lab using liquid chromatography and mass spectroscopy. Both labs reached the same conclusions. The ingredients matched the label's ingredients list, the samples did not contain any drugs as commonly defined or any alkaloids or poisons, and the samples from different containers of the same product were consistent.

IF that is true,the FDA/government has no case. If it can not be legally defined as a drug,it's none of the FDA's business,and the FDA should be sued for wasting taxpayer dollars.

sneakypete  posted on  2017-06-09   7:32:57 ET  Reply   Untrace   Trace   Private Reply  


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