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#SAVEKRATOM Petition #TRUMP for #KRATOM

This PETITION takes just seconds to sign. It is meant to complement, not replace, other efforts. Please share this far and wide.

Go to the AKA Facebook “like” PAGE where it’s a public post. Share it from there or copy the link http://petitiontrumpforkratom.org/.  On Twitter, the petition tweet is pinned on our PAGE.

Also, please consider a donation to the AKA.  Click HERE to donate.

We know it is the holiday season, money is tight, many of you have already donated. However, Just $5.00 dollars would be helpful, if everyone that receives this email donates, if everyone that you share it to gives $5.00…. we would be a long ways towards our needed amount. Just think, it could be YOUR $5.00 that WINS this fight!  Do it as an anonymous gift for someone you care about.

 This information brought to you by: www.legalherbalshop.com

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#SaveKratom by leaving your positive comments about #Kratom at kratomcomments.org

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Please read and TAKE ACTION to #SAVEKRATOM #IAMKRATOM #KRATOMSAVESLIVES

The clock is ticking. Act NOW to make your voice heard!

Help ensure that Kratom will not become a controlled substance. Any positive experiences, factual research, scientific studies or journals, stories about how this plant has affected your life or the lives of those around you, etc., need to be shared now, more than ever. 

Our community’s voice needs to remain as strong as possible during this crucial period of time. Less than 40 days remain in the open comment period. Join in the movement today! Share this link with your friends, family, customers, and coworkers. 

Three ways to comment:

A Project of the American Kratom Association and the Botanical Education Alliance:

http://www.kratomcomments.org/#/5/

The above link is a little simpler then the DEA’s comment website and is linked to the DEA’s site so your comment will be seen there, or use the DEA’s website link below: 

Click the “Comment Now” tab on link below to make your voice heard (upper right-hand side of page) :

https://www.regulations.gov/document?D=DEA-2016-0015-0006

Or If you would prefer to hand-write and mail in your comments, you may do so. Please make sure these are sent in by the middle of November, so that they arrive before the end of the comment period. Address and information is below.
Paper comments: Paper comments that duplicate the electronic submission are not necessary and are discouraged.

Should you wish to mail a paper comment in lieu of an electronic comment, it should be sent via regular or express mail to: Drug Enforcement Administration, Attn: DEA Federal Register Representative/ODW, 8701 Morrissette Drive, Springfield, Virginia 22152.

Time line:

The comment period is going on right now and ends December 1st 2016.  At the end of the comment period the DEA will review the comments and can choose to act 1 of 3 ways in regard to Kratom. 

The 1st option is that the DEA could leave Kratom alone, which that will mean Kratom will stay legal.

The 2nd option is that the DEA can choose to recommend to Congress to schedule Kratom.  Congress will take over and if they decided to act upon the recommendation it would have to go thru both houses and then the president.  This process could take years.

The 3rd option is that the DEA will issue another notice of intent to schedule Kratom under the Emergency Ban Statue.  This would put us in same place we were at the end of August.  Let’s not let this happen again. If the DEA issues another notice of intent to schedule Kratom then they will again give a 30 day notice and start the process all over again.

You may go HERE for the Highest Quality KRATOM products!

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The DEA Blinked! #SAVEKRATOM #KRATOMSAVESLIVES

From the DRUG POLICY ALLIANCE:

 

Last month, you were one of tens of thousands to message Congress about the DEA’s absurd decision to place kratom, a medicinal plant used for millennia in Southeast Asia and currently used by millions in the U.S., on the list of Schedule I substances.
I must admit, even after we sent over 70,000 messages to Congress, and placed thousands of phone calls, I didn’t think the DEA would back down. They never have before.

Finally, in an unprecedented move, the DEA blinked. This morning, the DEAwithdrew its plan to ban kratom from the federal register, and opened up kratom scheduling to public comment through December 1st.

It’s truly remarkable to see the DEA, an agency with a long track record of ignoring both science and public opinion, forced to reconsider their actions.

It was the advocacy of people like you that spurred 51 Representatives and almost a dozen Senators to ask the DEA to postpone its plan to ban kratom.

But the fight isn’t over. We only have until December 1st to submit public comments to the DEA, and if they think the public outcry has died down, they’ll try to place kratom in Schedule I again.

Comments can be submitted through regulations.gov, though as of this afternoon comments have yet to open. Check back soon, and we’ll be sure to email you again once they are.

Thanks for your help in this fight — together we’ve accomplished something unprecedented. If you can, please chip in $25 or more to help us continue dismantling the drug war, one law at a time.

Sincerely,

Grant Smith
Deputy Director, National Affairs
Drug Policy Alliance

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We have WON a Battle to #SAVEKRATOM, But it is NOT Over!!

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The DEA Has Withdrawn It’s Notice of Intent to Ban Kratom For Now.

On August 31, 2016, DEA published in the Federal Register, a notice of its intent to place mitragynine and 7-hydroxymitragynine, two substances of the plant Mitragyna speciosa also referred to as kratom, in Schedule I.  Since publishing that notice, the DEA has received a number of comments from members of the public.  Some of the commenters offered their opinions regarding the pharmacological effects of mitragynine and 7-hydroxymitragynine.  To allow consideration of these comments, as well as others, the DEA has withdrawn its notice of intent to temporarily place Schedule I controls on Kratom and is soliciting public comments until December 1, 2016.

The DEA has also asked the Food and Drug Administration (FDA) to expedite its scientific and medical evaluation and scheduling recommendation for these substances, which the DEA previously requested.

With respect to mitragynine and 7-hydroxymitragynine, the DEA will consider all public comments received under the above procedures, as well as the FDA’s scientific and medical evaluation and scheduling recommendation for these substances.  Once the DEA has received and considered all of this information, the DEA will decide whether to proceed with scheduling of mitragynine and 7-hydroxymitragynine pursuant to the requirements of the Controlled Substances Act.

The DEA’s withdrawal notice and solicitation of comments may be found here:https://www.federalregister.gov/documents/2016/10/13/2016-24659/schedules-of-controlled-substances-temporary-placement-of-mitragynine-and-7-hydroxymitragynine-into

It looks like it will be published today or tomorrow.
Thank you everyone for there hard work.  We will need to keep on this hard if we plan to win this next stage of keeping Kratom legal.
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Would you look at that. #Kratom might help cure #cancer. There is research in progress. #SAVEKRATOM #KRATOMSAVESLIVES

Antioxidant value and antiproliferative efficacy of mitragynine and a silane reduced analogue.

Goh TB, et al. Asian Pac J Cancer Prev. 2014.

Abstract

BACKGROUND: To investigate the antioxidant value and anticancer functions of mitragynine (MTG) and its silane-reduced analogues (SRM) in vitro.

MATERIALS AND METHODS: MTG and SRM was analyzed for their reducing power ability, ABTS radical inhibition and 1,1-diphenyl-2-picryl hydrazylfree radicals scavenging activities. Furthermore, the antiproliferation efficacy was evaluated using MTT assay on K 562 and HCT116 cancer cell lines versus NIH/3T3 and CCD18-Co normal cell lines respectively.

RESULTS: SRM and MTG demonstrate moderate antioxidant value with ABTS assay (Trolox equivalent antioxidant capacity (TEAC): 2.25±0.02 mmol trolox / mmol and 1.96±0.04 mmol trolox / mmol respectively) and DPPH (IC50=3.75±0.04 mg/mL and IC50=2.28±0.02 mg/mL respectively). Both MTG and SRM demonstrate equal potency (IC50=25.20±1.53 and IC50= 22.19±1.06 respectively) towards K 562 cell lines, comparable to control, betulinic acid (BA) (IC5024.40±1.26). Both compounds showed concentration-dependent cytototoxicity effects and exert profound antiproliferative efficacy at concentration > 100 μM towards HCT 116 and K 562 cancer cell lines, comparable to those of BA and 5-FU (5-Fluorouracil). Furthermore, both MTG and SRM exhibit high selectivity towards HCT 116 cell lines with selective indexes of 3.14 and 2.93 respectively compared to 5-FU (SI=0.60).

CONCLUSIONS: These findings revealed that the medicinal and nutitional values of mitragynine obtained from ketum leaves that growth in tropical forest of Southeast Asia and its analogues does not limited to analgesic properties but could be promising antioxidant and anticancer or chemopreventive compounds.

PMID

25081682 [PubMed – indexed for MEDLINE]

Full text

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