Farming, Latest Post, Marijuana-Cannabis-Hemp, Petition, Politics

The Industrial Hemp Farming Act, S.134, only has nine (9) cosponsors and "VOTE HEMP" needs signatures now!


VH Report header

 

 

The Industrial Hemp Farming Act, S.134, only has nine (9) cosponsors. The most recent cosponsors are Senator Bennett (D-CO), Senator Tester (D-MT) and Senator Baldwin (D-WI). We are grateful for their support but we need many more.

This important legislation would greatly benefit opportunities in terms of jobs and economic development in legal hemp states by removing industrial hemp from the Controlled Substances Act.

Together we can pass this legislation, but we need your support today. Add your name to show the Senate the overwhelming grassroots support behind the Industrial Hemp Farming Act.

 

 

Sign the Petition Today!

As always, thank you for your continued support of this effort to restore industrial hemp as an agricultural commodity. Please share this with friends, family and any network that is willing to help with our cause.

About Vote Hemp

Vote Hemp is a national, single-issue, non-profit organization dedicated to the acceptance of and a free market for industrial hemp, low-THC oilseed and fiber varieties of Cannabis, and to changes in current law to allow U.S. farmers to once again grow the crop.

Web Site: http://www.VoteHemp.com

Support Vote Hemp

Vote Hemp depends entirely on donations to support our work. Please consider making a donation today.

Contribute Here: http://www.VoteHemp.com/contribute

Vote Hemp, Inc.

Colleen (Sauvé) Keahey

National Outreach Coordinator
email: colleen@votehemp.com

Join Our Mailing List

 

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Vote Hemp, Inc. | P.O. Box 1571 | Brattleboro | VT | 05302

*This post for “Vote Hemp” is a free service from Sheree Krider.

Latest Post, Marijuana-Cannabis-Hemp, Petition, ShereeKrider, SHEREEKRIDER

IMMEDIATELY STOP FEDERAL FUNDING for a pharmaceutical drug to treat "MARIJUANA ADDICTION". THIS IS PREPOSTEROUS!


 

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The Washington Times reported on 6/26/15 that the Federal Government is “fast tracking” Pharma research for a Marijuana addiction drug. The research gets $3 million grant as Obama encourages legalization of Cannabis.

This is just too much! We do not need a “drug” to detoxify us from Cannabis! We need more Hemp and Cannabis Oil for Medical use,

Stop the funding effective immediately and give that $3 Million to a better cause.

Fact: GW Pharma has concluded that “Cannabis is not addictive” according to their ad for SATIVEX (which has not been approved for marketing in the U.S. as of yet — And SHOULD BE!). It additionally states that it does not appear to have withdrawal effects when stopped suddenly”…

Stop the INSANITY NOW! Stop the funding for an addiction drug for Cannabis!

Published Date: Jun 26, 2015

Issues: Civil Rights and Liberties, Disabilities, Health Care

 

https://petitions.whitehouse.gov//petition/immediately-stop-federal-funding-pharmaceutical-drug-treat-marijuana-addiction-preposterous

 

PLEASE SIGN PETITION ABOVE!!!

Latest Post, Petition, Politics

Make the FDA Advisory, Not Mandatory


You should control what medicines you use, not the FDA. The FDA should make advisory recommendations only. It should NOT have the power to mandate which drugs you can buy, and which you cannot.

  • If pharmaceutical companies value the FDA seal of approval, then they can pay the FDA to evaluate their drugs.
  • If consumers value FDA approval, then they can decide to only buy FDA approved drugs.

If the FDA’s seal of approval is really so valuable, then it does NOT need to be mandatory. No coercion is necessary. Instead, the FDA should be able to sell its services through voluntary means, just like Underwriter’s Laboratory does.

Consumers and doctors should be free to consult available science, and make their own decisions about which treatments to try.

All human beings are unique. Treatments that might be dangerous for one person, could be the only possible solution for another. There is zero chance that one-size-fits-all dictates can possibly account for the vastness of human variability. Patients and doctors must have the flexibility to deal with individual human uniqueness.

The FDA should serve, not rule.

Talking Points:

There are thousands of reasons why the FDA should lose its power to coerce you and your loved ones. Some of these reasons will be listed below, so that you can use them when writing to Congress, or when asking your friends to contact Congress on this issue . . .

The FDA gives consumers a false sense of security. Americans assume that the FDA is actually protecting them, but it is not. For instance . . .

The Union of Concerned Scientists surveyed 6,000 FDA scientists in 2006, and 1,000 of them responded with the following disturbing admissions:

  • 17% admitted that they had been “asked explicitly by FDA decision makers to provide incomplete, inaccurate, or misleading information to the public, regulated industry, media, or elected/senior government officials.”
  • Less than half agreed that the FDA “routinely provides complete and accurate information to the public.”
  • 47% admitted to being aware of instances “where commercial interests have inappropriately induced or attempted to induce the reversal, withdrawal, or modification of FDA determinations of actions.”

The FDA is constantly attempting to expand its powers. The people in that agency are relentlessly pushing into areas that are NOT part of their mandate — even where there is NO problem that needs to be fixed.

For Example: The FDA has made repeated attempts to regulate vitamins and supplements, even though there is no evidence that these things present any danger. Quite the contrary — vitamins and supplements are a powerful example of how health outcomes can be improved, without FDA involvement. The website of the Life Extension Foundation is full of scientific citations to demonstrate this. For instance . . .

A review of 2009 information for “adverse events” reported to the national control center’s data system shows that, NO major adverse events or deaths were reported for . . .

  • Botanical supplements like St. John’s wort, ginseng, and Echinacea
  • Hormone supplements like DHEA, melatonin, and pregnenolone
  • Phytoestrogen supplements
  • The joint- and cartilage-support supplements glucosamine and chondroitin
  • Vitamins A and E, and only one adverse event each was reported for vitamin B6 and C

In total, 41 major adverse events were reported for the entire spectrum of supplements including botanicals, amino acids, and vitamins, and only one was a death.

In contrast, more than 7,000 major adverse events were reported for pharmaceutical drugs, including a total of 496 deaths. And based on previous studies, we know the overall death rate for physician prescribed drugs to be far higher.

The Downsize DC position is pro-choice. The FDA should serve, not rule.

Use the form at right to send your elected representatives a letter about this issue. It’s easy!

  • Your position will be counted by each Congressional office,
  • Will educate the Congressional staffer who reads it,
  • May be passed up the chain of command,
  • May receive a reply (many DC Downsizers get them). If you receive such a letter, please share it with us at Comments@DownsizeDC.org.

 

Send a letter to Congress

We provide the first few words of the letter so that Congressional offices will see the most important point

right at the start, and so that no one can hijack our system for another purpose.

Here’s the part we provide . . .

Make the FDA advisory, not mandatory.

LINK

CONTINUE READING….