Marijuana Today: Sen. Jeff Sessions confirmed

Marijuana Today: Sen. Jeff Sessions confirmed

Plus, pot slows brain cancer; and the weed gender gap is closing; …

http://www.sfgate.com/news/article/Marijuana-Today-Sen-Jeff-Sessions-confirmed-10920803.php

TOP NEWS
Sen. Jeff Sessions was confirmed in a split 52-47 vote yesterday.
 
 … Here’s what I think you can count on: Jeff Sessions is going to do his worst. But, if history is any guide, it will matter little. … Sessions has a bb gun, and he is shooting at a glacier.
 
This former DEA agent understands. It’s a resources game. Sessions has 5,500 DEA agents, and a couple billion dollars in budget. But only a fraction of that can go to cannabis. Meanwhile, 21 percent of the U.S. population is in a legalization state; about 76 million people; the industry employs 122,000 people; and is worth maybe $50 billion per year in total retail sales alone.
 
Remember — President Obama spent hundreds of millions of dollars interfering in state-legal medical cannabis systems. His DOJ attacked the best, brightest, most state-legal actors, in order to make the point that no one was safe from federal law. And what happened? The California crackdown of 2011 engendered a backlash that drew in unprecedented new allies. Cannabis will have even more this time. 
 
Mark my words — there will be raids, forfeiture threats, regulatory intimidation, propaganda, new sentencing, everything that happened under President Obama. And if the People are more upset about it than ever — then the people will win, again.
 
More on that thread: “John J. Hudak of the Brooking Institute, last weekend at the Virginia Cannabis Conference, explained how ‘you’re insane‘ if you think the marijuana industry is too big and popular to be a target of Republican wrath”.
 
Meanwhile, the MPP is “cautiously optimistic”. The NCIA said “We look forward to Attorney General Sessions maintaining …[the status quo]”… TheDCMJ is “hopeful”. … NORML said “we will never stop fighting.” … And theDPA said attacking pot will leave Trump and Co. “even less popular than they are now.”
 
OTHER BIG NEWS
Yup, pot helps treat brain cancer. … GW Pharma is almost done bottling it up.
 
Nevada is set to kick California’s butt in the race to implement recreational. … They’re going to do temporary regulations by July.
 
There might be almost 300 pot-related patents already on the books.
 
The L.A. Times endorses Measure M to catch the city up to where San Francisco was in 2005 — you know, actually regulating dispensaries.
 
Weed app data shows the gender gap closing, and cannabis replacing alcohol.
 
JUST A BILL ON CAPITOL HILL
Congressional bill HR 715 would legalize CBD.
 
Another bill would shield state-legal pot activity from federal drug laws.
 
HIGHLY DUBIOUS
There is something deeply wrong in the Personnel Review Board of Orange County, CA.
 
MEDICINE
pot for PTSD trial gets underway, via Army Times.
 
SURPRISING DISCOVERIES
Style brands Vanderpop and Tokyo Smoke merge.
 
Moxies Meds makes it into Cosmo Mag.
 
High Times out-Cosmos Cosmo with ‘How To Make Weed Lube for V-Day’.
 
The inventor of Ganga Yoga is throwing an Easter retreat to Yosemite.

And Puff, Pass, and Paint comes to San Francisco.

When you dig down “into the weeds”

Appeals Court Keeps Block on Trump Immigration Order in Place

http://abcnews.go.com/Politics/appeals-court-deliver-ruling-trump-executive-order/story?id=45386342

While this may appear way off topic for my blog… please follow the logic..  These judges would not reinstate the ban because it was determined – by them – that a certain group of people were being discriminated against because of their religion…

Could this logic be extended that the passage of the CDC opiate dosing guidelines and various states that have passed similar laws… be a discrimination AGAINST a group of HANDICAPPED PEOPLE  – covered by the ADA ?… and thus ILLEGAL..

But even though our President is the final authority on laws being enforced or not… but .. in this particular incident… a single person – a judge – in the  judicial district that has a history of having the most ruling being over turned on appeal.  So they whole issue will go back to the court system to be determined.

This is just an example of how our judicial system is not always “just” and does not always follows the letter of the law… It could also be a good example for the chronic pain community to unite … develop a “legal war chest” to challenge the constitutionality of many of the laws that are harming those in the chronic pain community.

Those who pass rules/laws/regulations/guidelines… have no mandate that what they pass … is in fact constitutional… they pass it… and it is up to those being affected/harm to take the bureaucracy to court to prove that they have exceeded their authority and their actions are unconstitutional.

A panel of federal appeals court judges ruled to keep a restraining order against Donald Trump’s controversial immigration action in place, according to court documents.

“We hold that the Government has not shown a likelihood of success on the merits of its appeal, nor has it shown that failure to enter a stay would cause irreparable injury, and we therefore deny its emergency motion for a stay,” the panel, from the 9th Circuit Court of Appeals, wrote in the decision Thursday.

The three-judge panel heard arguments from a lawyer representing the state of Washington Tuesday who argued that the executive order — which temporarily halted immigration from seven predominantly Muslim countries in the Middle East and Africa and temporarily shut down the refugee program — discriminated on the basis of religion among other claims.

Department of Justice lawyers claimed that the order was made on national security grounds and that Washington District Court Judge James Robart’s issuance of a temporary restraining order pausing the ban nationwide was “overbroad.”

Trump unleashed a series of attacks on Robart following the judge’s initial decision to interrupt his order last week. On Twitter, the president called Robart a “so-called judge,” said his decision was “ridiculous and will be overturned,” and added that “[i]f something happens blame him and court system.”

Those comments were later condemned by members of both major political parties. Trump’s Supreme Court nominee Judge Neil Gorsuch classified Trump’s criticisms of the judiciary as “demoralizing” and “disheartening” in conversations on Capitol Hill, according to a spokesman, but the White House insisted he was not referring to a specific case.

The administration has denied that the order is a Muslim ban.

Where health is EVERYTHING… RPh didn’t get that memo ?

I’m a 57 year old disabled man. I have been going to CVS STORE #2990 here in Las Vegas, NV for over 4 years with no problems what so ever. On the 8th of February I went to CVS to fill my prescriptions at which time was accepted and I was told to come back in two hours.  Express leaving a new pharmacy manager came up named jerry that I never seen stated that he doesn’t feel comfortable filling my prescriptions and to go elsewhere. This man had a smile on his face and was taking his time giving me back my prescriptions so I could leave and every time I would ask he would chuckle and say no. This man made copies of my prescriptions stopped in front of me with a smile on his face and with my prescriptions and copies of my prescriptions said no when I asked why can’t you just use the copies ? I became very upset and scared. Being disabled and on social security I didn’t know where to go because of the actions of the predigest pharmacy manager that I never had seen in my over 4 years of never having a problem with. I called the corporate office at 1800cvs pharmacy and all I got was a “we will talk with him”. This manager stated that I was never allowed in ANY CVS and that he was going to notify the state about my abuse of my medications. I informed him that my prescriptions where for the 8th of February as stated on my prescriptions at which time he stated I was always coming in early and he could refuse anyone at any time. I had gone to 6-7 other pharmacies who stated no and the only one who would I had to wait tell the 10th. As of today’s date I have been unable to take my medication and have had several seizures I feel very depressed and unable to function properly and I’m in so much pain right now that I cry and get angry that this pharmacy manager purposely caused this.

 

Here is my response to this abused/discriminated pt:

           Pharmacist Jerry … gets paid every week.. regardless if he fills your prescription or not..  and from what I have heard back from other pts.. the major chain stores.. could care less.

I would suggest that you contact a local independent pharmacy.. here is a website to help you find one by zip code http://www.ncpanet.org/home/find-your-local-pharmacy

 

I ran the zip code of 89108 and it shows 40 stores within 10 miles…

 

You will be dealing with the Pharmacist/owner… who depends on filling legal prescriptions to put bread/butter on his/her table and will not start first looking for a reason not to fill your prescription(s)… Like Pharmacist Jerry did.  I would suggest that you have a talk with the Pharmacist/owner at the independent and tell them that you are willing to transfer all your prescription business to them… presuming that they will not “play games” on your refill dates.

 

Presuming that you can fine a pharmacy… ask the pharmacist about syncing up all your refills so that you will be getting all your Rxs filled on the same day each month… will be able to save you a lot of time/trouble over the long run and most independent pharmacies are more than happy to do so.

 

http://bop.nv.gov/Services/complaint/

Here is the complaint form for the NV board of Pharmacy… file a grievance with the BOP… since you have been patronizing the pharmacy for some time.. there should be little reason for the pharmacy/Pharmacist to reject your medications to be filled. The store has a PIC ( Pharmacist in charge) who is responsible for the legal operation of the Rx dept to the BOP… if Jerry is not the PIC.. file the grievance against Jerry, the PIC, & CVS (permit holder).. your grievance should be “denial of care”, pt/senior abuse, intentionally throwing a pt into cold turkey withdrawal, medical battery

 

I presume that you are on Medicare/Medicaid/Medicare Advantage… suggest that you file a grievance with that entity against CVS for failing to honor their contract – to fill legal/medical necessary Rx – with the insurance company.  If the insurance company refuses to do anything… then you need to file a grievance with

 

www.cms.gov (800-MEDICARE)… even If the insurance company does something positive… I would still file a grievance against CVS with CMS (Center Medicare & Medicaid Services)

 

You may also want to file a grievance with https://www.ada.gov/filing_complaint.htm because it is consider a civil rights violation of the American’s with Disability Act for discriminating against disabled pts… for refusing to fill a legit/on time/medically necessary prescription.

 

Take care of yourself first, by finding a independent pharmacy to take care of ALL YOUR MEDICATIONS… because all those entities that you will be filing a grievance with… will move at the speed of cold molasses

 

Tell your story abt being harmed by CDC opiate guidelines…

Calling all chronic pain warriors who have been hurt by the CDC’s guidelines for PCP’s. Many states are making laws & our pain management practices are doing us harm. Please send your stories to Sherman.sherry224@comcast.net. I’m meeting with representatives on 2/28 & leaving 2/27 for hotel. I’m asking for personal stories from all who’ve been affected including your friends, significant other & all who have been affected. Please title it “CHRONIC PAIN STORY.” We must be heard & this is the time to have our voices heard. Thank you

Per Forrest Gump: Stupid is as stupid does

Georgia bill would require new ADHD prescriptions every 5 days

(CNN)A bill meant to curb the abuse of prescription opioids in Georgia has stirred outrage in the ADHD community because a provision requires adults and children on medications for attention deficit hyperactivity disorder to get new prescriptions every five days.

“It’s clearly a cause for concern,” said state Sen. Nan Orrock, an Atlanta Democrat who wants the provision struck from the bill. “The argument is pretty hard to debunk: that families coming in every five days for ADHD prescriptions is impossible. There’s just a panic list of questions this creates.”
News of the measure spread rapidly across social media on Tuesday after a post from a parent about the restrictions on medications for ADHD was shared on Facebook.
“What I understand is that, if this bill passes, prescribers will only be able to write 5-day prescriptions and will have to review their patients in a database every 90 days. That would require getting a new prescription weekly,” said the post, which was widely shared.
In this era of rapid-fire “fake news” posts, it seemed almost absurd.
But it is true. “Every five, days the patient would have to come back in,” said Orrock, a member of the Georgia Senate’s Health and Human Services Committee, which held a hearing last week to receive input on the bill. “That’s absolutely what would happen if that bill became law in its current form.”
Across Georgia, doctors, state senators and advocates for people with ADHD began fielding a flood of phone calls. Their inboxes filled with questions about the bill, known as SB 81 (PDF), and worried parents sent messages over social media.
The bill is meant to curb the abuse of prescription opioid painkillers, such as OxyContin and Vicodin. It was drafted by Sen. Renee Unterman, a Republican committee chairwoman from the suburbs of Atlanta, in an effort to stop the state’s growing opioid epidemic.
It would allow over-the-counter sales of an opioid blocker called naloxone, an emergency medicine that can save people from dying during an overdose. The bill also allows doctors to see whether a patient has recently received an opioid prescription, allowing them to determine that patients are going from doctor to doctor.
“What it does is prevent doctor-shopping. It prevents these legal drugs from becoming street drugs and sold at exorbitant prices,” Unterman told The Telegraph newspaper in Macon, Georgia.
Unterman has not responded to CNN’s request for comment.
The controversial provision of the bill deals with the limiting of doctors’ ability to write prescriptions on controlled substances to only five days. The main medications to treat ADHD, such as Adderall, Ritalin and Vyvanse, are listed as Schedule II drugs, and the bill makes no exclusions for those with ADHD.
Although the loudest outcry came from the ADHD community, the bill would also apply to other vital medications, including some used to treat seizures, that are listed as controlled substances. Patients have been taking many of those medications for years, and there are already strict measures for getting refills.
The bill does make exceptions for medications “necessary for palliative care or to treat a patient’s acute medical condition, chronic pain or pain associated with a cancer diagnosis.” In those cases, the prescriber must “indicate that an alternative to such controlled substance was not appropriate to treat such medical condition.”
Dr. Jennifer Shu, an Atlanta-area pediatrician, said the bill lumps ADHD medications “in with opioids, which are the main concern of the bill.”
“I would hope that the legislators focus strictly on the narcotics and not on ADHD medications if they pass such a law,” Shu wrote in an email.
Elaine Taylor-Klaus, who helps coach parents of children with ADHD and runs the counseling and education company ImpactADHD.com, had never heard of the provision until Tuesday, when the social media post made the rounds and she was hit with a deluge of people seeking guidance.
“My Facebook Messenger blew up,” she said.
Addicted? How to get help

If you’re addicted to prescription drugs, help is available. You can call the Substance Abuse Mental Health Services Administration 24/7 hotline at 1-800-662-HELP(4357) or visit their website.

Taylor-Klaus advocates across the nation to educate people about ADHD, but even she was surprised by the provision. She credited the social media post with raising awareness and rallying the community.
She said she immediately called her legislators to find out the details of the bill and was assured that there is “some awareness of the problem” of the provision and that changes will probably be made.
“I hadn’t heard about (the provision) because there’s no organization specifically focused on ADHD that’s advocating and lobbying on a local level,” she said. “Unless there’s somebody watching out very closely, this is one of those obscure pieces of legislation that could pass through quite easily without anybody realizing what the full implications are.”
She noted the irony of the measure: The bill would require new prescriptions weekly, but people with ADHD struggle with organization skills.
“Not only would it be impossible for a family to manage,” she said, “but it would be impossible for a physician’s office to manage that kind of onerous requirement.”
Orrock, the Democrat seeking changes to the bill, said she’s confident the measure will be revised. However, she hasn’t seen a new bill yet. She said she hopes a revised version is presented Thursday, when the committee meets again.
“There’s nothing close to look at yet,” she said. “The work is still going on.”
Join the conversation

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Efforts to get comment from several Republicans on the Health and Human Services Committee, including Vice Chairman Dean Burke and Bill Cowsert, were unsuccessful.
Tom Krause, Cowsert’s chief of staff, said the state senator is closely “monitoring” the progress of the bill. He added that Unterman is working with two senators who are physicians and has said she “expects changes to the legislation.”
“Sen. Cowsert said it would be premature to comment on SB 81 until after he sees the changes,” Krause said.
 
 

Federal Bill Aims to Decriminalize CBD and Reschedule Cannabis

Reschedule CannabisFederal Bill Aims to Decriminalize CBD and Reschedule Cannabis

http://ireadculture.com/federal-bill-aims-decriminalize-cbd-reschedule-cannabis/

A bill was introduced to the House of Representatives on January 27 that could change the future of medical cannabis in the United States. H.R. 715, also known as the Compassionate Access Act, aims to decriminalize cannabidiol (CBD) by excluding it from the definition of “marihuana.” H.R. 715 also requires the Secretary of Health and Human Services alongside the Institute of the National Academy of Sciences officially recommend for the Drug Enforcement Administration (DEA) to reschedule cannabis from Schedule I.

If the Compassionate Access Act is passed, the bill’s text requires the Administrator of the DEA to consider the recommendations the DEA has received and move to reschedule cannabis from its Schedule I status. The bill does not specify which section cannabis should be rescheduled to, leaving that decision to the DEA’s discretion.

Excluding cannabidiol from the definition of “marihuana” would be a huge win for many people battling debilitating conditions across the nation. According to the bill, “The term ‘cannabidiol’ means the substance cannabidiol, as derived from marihuana or synthetically formulated, that contains not great than 0.3 percent delta-9-tetrahydrocannabinol on a dry weight basis.” CBD is a non-psychoactive cannabinoid that is found in the cannabis plant.

CBD has been proven effective for stopping seizures in patients with Dravet’s Syndrome, intractable epilepsy and other rare seizures disorders. It has also been reported that CBD is great for treating Crohn’s disease, Multiple Sclerosis and Post-Traumatic Stress Disorder. It has even proven effective at healing and strengthening bones.

Representative Thomas Garrett of Virginia introduced the H.R. 715 to the Committee on Energy and Commerce. Garrett introduced the bill on behalf of himself and Representative Earl Blumenauer of Oregon.

CBD is being recognized as medicinal not only in the United States, but there is a global movement towards its acceptance as well. Earlier this year, The Medicines & Healthcare Products Regulatory Agency in the United Kingdom admitted that CBD is in fact medicine. Mexico recently approved the importation of CBD derivatives from American company Medical Marijuana, Inc. If H.R. 715 does pass, it will be a huge victory toward cannabis reform.

WV: Naloxone doses UP… OD deaths UP… bureaucratic stupidity – unchanged ?

A vial of NaloxoneWest Virginia distributing 8,000 overdose antidote kits

http://www.foxnews.com/health/2017/02/07/west-virginia-distributing-8000-overdose-antidote-kits.html

West Virginia health officials are responding to opioid overdoses by distributing more than 8,000 kits with an antidote — Naloxone — that can get people breathing again if administered in time.

Money for the kits comes from a $1 million federal grant to West Virginia, which has had the nation’s highest rate of overdose deaths.

“Naloxone is a lifesaving antidote that, if administered in a timely manner, can effectively reverse respiratory depression caused by opioid and opiate overdose and revive victims,” said Dr. Rahul Gupta, commissioner of the Bureau for Public Health. “This collaboration represents an essential step toward turning around West Virginia’s staggering overdose statistics.”

Federal data show West Virginia had 725 overdose deaths in 2015, the highest rate of any state at 41.5 per 100,000 people. Last year’s numbers are expected to show little improvement.

“We have seen a significant and steady increase in all drug overdose deaths in West Virginia over the last several years. Unfortunately, based upon the trend we are seeing, the number of overdose deaths has not yet peaked,” Gupta said. “We expect our preliminary data for 2016 to further increase as more toxicology results are recorded.”

Meanwhile local emergency medical services agencies administered 4,186 doses of Naloxone last year, up from 3,351 the year before and 2,165 two years ago. Gupta said that data doesn’t include uses by hospital emergency departments, urgent care centers, first responders and family members.

The project is funded with a $1 million federal grant managed by the state Bureau for Behavioral Health and Health Facilities and administered by Gupta’s bureau. West Virginia University’s Injury Control Research Center will implement and evaluate the project.

More than 4,000 of the two-dose kits will go out in the next few weeks to high priority areas, including needle-exchange programs and police and fire departments in the cities of Huntington, Charleston, Wheeling and Morgantown and other urban and rural areas.

Emergency medical personnel currently carry the antidote, but this project should make it more widely available to other first responders and to people at high risk, their family members, friends and caregivers, said Herb Linn, the center’s deputy director.

“We’re looking at getting more naloxone out into a variety of individuals’ hands, who are in a position to be a witness to an overdose or get called and respond more immediately,” Linn said.

There may have been some recent progress in limiting fatalities from prescription opioids, but there’s been an upsurge in overdose deaths involving heroin and fentanyl, he said. “The problem remains huge in West Virginia, which likely continues to have the highest rate of overdose deaths. The naloxone distribution can only help to turn that epidemic around.”

West Virginia several years ago had one of the highest opioid drug prescription rates in the nation, which correlated with higher overdose deaths, Gupta said. The opioid epidemic is evolving, with prescription rates declining but the cheaper alternative of heroin available on the streets, sometimes contaminated with far more potent fentanyl and even the elephant tranquilizer carfentanyl, he said.

“We’re looking at addiction as a chronic relapsing disease rather than a stigma,” he said. The state response includes making more treatment, counseling and workforce training available, as well as screening pregnant women, whose cases and babies are treated as a priority, he said.

 

TORTURE …. BUREAUCRATIC AMERICAN STYLE

Pill mill crackdown has consequences for legitimate pain sufferers

http://www.abc-7.com/story/34438377/pill-mill-crackdown-has-consequences-for-legitimate-pain-sufferers

PORT CHARLOTTE – At first glance, it’s difficult to know exactly what Amanda Jakubowski is dealing with. The 36-year-old Port Charlotte woman moves slowly and deliberately, her small and frail frame accentuated by brightly colored short hair and dark glasses.

Without understanding her illness, you might jump to conclusions. Cancer? Drug addiction? Eating disorder? She said many people have wondered exactly that.

When she speaks, her soft voice is full of conviction.  

She is in pain and feels helpless to stop it. 

“It hurts because you’re begging for help and you can’t get it,” she said.

Amanda said she’s suffering in silence, as a nationwide pain pill crackdown is leaving patients like herself struggling to find options for relief.

For years, headlines have chronicled the rise and fallout of Florida’s prescription painkiller addiction.

But among the addiction rates, law enforcement crackdowns, and the subsequent rise of heroin use, there is another consequence that hasn’t gotten as much attention. Chronic pain sufferers, who say they’re still suffering and can’t get help, feel as though they’re slipping through the cracks.


Mark and Amanda Jakubowski at their wedding in 2005.

A devastating diagnosis

Amanda and Mark Jakubowski were just like any couple, both enjoying careers, their lives in Atlanta, and their marriage.

Everything changed on October 11th, 2010, when Amanda came home from work sick.

“Anytime she put anything in her mouth, within five minutes she was violently throwing up,” Mark explained.

Days of what she thought was a stomach flu turned into weeks, then months.

A never ending list of doctors offices and specialists brought up possible diagnoses of everything from Irritable Bowel Syndrome to gastric cancer, before finally revealing a devastating diagnosis: gastroparesis.

It’s a rare disease in which the stomach becomes paralyzed and unable to digest food.

In some, gastroparesis is brought on by complications from diabetes, but for many patients, doctors don’t know exactly what causes it. In either case, there is no cure.

It affects twice as many women as men, and it frequently happens among young adults, even children.

Amanda sees Dr. Raul Rosenthal, the director of Cleveland Clinic Florida’s Bariatric and Metabolic Institute, and a specialist on gastroparesis. He said the disease affects less than one percent of the population, but it will have a huge and lasting impact on a patient’s quality of life.

It’s been more than six years since Amanda has been able to eat a full meal. She has survived with the help of various feeding tubes, and small meals consisting of anything from a few goldfish to some ginger ale.

Rosenthal said because the disease is so rare, many other doctors don’t know just how devastating it can be.

“I think the number one reason why this disease is silent or invisible is the lack of knowledge and awareness,” he said.

Amanda thinks that lack of awareness explains why it took months to first be diagnosed, and why she still faces challenges in the medical community today.


Amanda Jakubowski receiving treatment in February of 2016.

The pain of pain management

As Amanda has struggled to fight this disease, slowly, her body has started to consume itself.

“It’s like from head to toe, everything just hurts,” she said.

“Malnutrition hurts. When your body consumes itself, your body is eating muscle and tendon and tissue you and things like that, that causes pain,” her husband Mark explained.

Treating that pain has not been easy.

As a chronic pain patient, Amanda feels as though she’s been slipping through the cracks of a state system trying hard to reduce prescription pill abuse.

Back in 2010, Florida was leading the nation in painkiller prescription sales, according to data from the CDC.

A statewide crackdown soon followed. Led in part by Governor Rick Scott and State Attorney General Pam Bondi, lawmakers and the DEA used newly-authorized money and resources to begin investigating and cutting off the state’s pill mills.

It worked. Prescription and drug deaths dropped dramatically. Florida was one of only two states to see a decrease in drug poisoning deaths from 2010 to 2014.

Today, Florida continues to track medications through their prescription drug monitoring program, E-FORSCE, an online database where doctors must report their prescriptions and monitor patients for potentially risky behaviors like doctor shopping.

But the problem is nationwide, and ongoing.

In March of 2016, the Centers for Disease Control issued new guidelines discouraging prescriptions of higher doses of opiates.

A local pain management specialist who declined an on-camera interview wrote in an email “…In addition, the DEA has made it clear that they wish to reduce the amount of opiate medication available by as much as 25%. These are factors contributing to the current climate of opiate-phobia.”

It can be difficult to quantify exactly how this “opiate-phobia” is affecting patients. But in 2015, a survey from the U.S. Government Accountability Office found that more than half of DEA registrants – like drug distributors, pharmacies, and pain management clinics – “have changed certain business practices as a result of DEA enforcement actions or the business climate these actions may have created.”

The survey also found many pharmacies reported stricter limits placed on them from distributors have limited to a “great extent” their ability to supply drugs to those with legitimate needs.

The Jakubowskis said it’s created a climate where patients like Amanda can’t get the help they need.

Mark said they’ve been met with disbelief and reluctance as they try to find pain management specialists willing to help.

Amanda said she’s experienced morphine withdrawal twice as doctors told her they wanted to try lowering her dose of medication to limits they felt were considered acceptable by the state.

She said one clinic closed up shop overnight, while another office turned them away after accusing them of doctor shopping.

“The frustration of trying to explain to the doctor that your wife is dying, and all I want is to know that, while I’m sitting in the chair on the other side of the room, that she’s resting comfortably,” Mark explained, “And she can’t do that because-“

“Because the abuse of all the other patients that might not have needed the medication has ruined it for the rest of us that do need it,” Amanda finished.

She has been to see three different pain management doctors in just the past four months.

She recently underwent surgery at Cleveland Clinic to implant a pacemaker in her stomach in an effort to quell some of the nausea and vomiting brought on by gastroparesis.

Meanwhile, she continues to struggle every day, still hoping for a pain management physician willing to take on her case in a system, she believes, is making it nearly impossible to get help.

“It’s been a necessity for doctors to have to be skeptical, but by the same token, there should be a step two – maybe we should somehow confirm that this patient does need it,” Mark said. “It should not be so difficult to not live in pain.”

In my opinion, kratom is safer than oxycodone and other narcotics.

Kratom and oxycodone

http://www.clinicaladvisor.com/your-comments/kratom-and-oxycodone/article/636257/

I think that kratom is much safer than some of the FDA- and US Drug Enforcement Administration–approved medications, such as oxycodone. I treat patients for opioid addiction, and I have a few who have stopped using opioids and are now on a stable, individualized dose that the patient decides. I know that this takes the control away from physicians and other governmental agencies, and there is also the loss of money for some drug companies. But so far, there have been no deaths or patients who needed to go to rehabilitation from using kratom. In my opinion, kratom is safer than oxycodone and other narcotics.—Anace Said, MD. 

Injections for back pain: An expensive placebo?

Injections for back pain: An expensive placebo?

https://www.psychologytoday.com/blog/unlearn-your-pain/201410/injections-back-pain-expensive-placebo

A large study on the effectiveness of injections for spinal stenosis was published in the New England Journal of Medicine in July of this year.  It was designed by top doctors in the field of pain management and funded by the Agency for Healthcare Research and Quality.  The patients were carefully selected to have pain in their legs and clear evidence of narrowing of the spinal canal on MRI examinations.  They were given an injection into the epidural space and were randomized to receive either an anti-inflammatory medication (corticosteroid) plus a local anesthetic medication (lidocaine) or just the lidocaine (which was considered a placebo as the effect is expected to wear off in a couple of hours). 

Before the injections, the patients had significant leg and back pain, with average self-reported pain levels of 7 on a 10-point scale.  Six weeks after the injections, their average pain level was reduced to 4.5, which is a significant drop, and suggests a good level of pain relief!  However, the reduction occurred equally in both groups.  The people who got the lidocaine injection obtained just as much pain relief as those who got the steroid injection.  In other words, the placebo treatment worked just as well as the therapeutic injections. 

What should we conclude from this study? Before answering that question, let’s review the relevant research from other studies on injection therapies for back pain and sciatic pain.

In 2009, Dr. Chou and colleagues reviewed 40 studies comparing epidural injections (and other types of injections or ablations) to placebo injections.  For back pain without pain radiating down the leg (sciatic type pain), their conclusion was this: “Evidence on efficacy of epidural injections specifically for spinal stenosis, low back pain without radiculopathy, or failed back surgery syndrome is sparse and inconclusive, but showed no clear benefit.”  For sciatic pain, a few of the studies showed some short term benefit, (within a few weeks) although the majority did not; and none showed longer-term benefit.

Dr. Staal (as part of the prestigious Cochrane Collaboration) also conducted a review of the available literature in 2008.  He reviewed 18 different research trials that included 1179 participants.  This was their conclusion:  “There is insufficient evidence to support the use of injection therapy in subacute and chronic low-back pain.”  These are hardly ringing endorsements for these procedures. 

Have we learned more since then?  In 2012, Cohen and colleagues reported on a randomized, controlled trial of epidural steroids for sciatic type pain due to ruptured discs.  There was some benefit in the short term (at 4 weeks), but this result was not statistically significant and there was no benefit at all in comparison to the placebo injections at 3 and 6 months.  Also in 2012, Pinto and colleagues once again reviewed the available literature on epidural steroid injections for sciatica.  From 23 research trials they found that epidural injections showed very small benefit at 1 month (roughly a difference of one-half of a point decrease in pain on a 10 point scale) and no differences at longer-term follow-up.

When studies show that the intervention being tested is no better than the placebo intervention, we usually conclude that the intervention would not be recommended.  If a medication works no better than a placebo pill, most doctors (and patients) would not use it. 

Of course, doctors must also consider the potential side effects of an intervention.  If the side effects are mild or rare, that treatment is more likely to be used even if it has only mild efficacy.  Consider, for example, glucosamine and chondroitin sulfate, two herbal supplements often used for osteoarthritis.  A recent study showed that they had mild effects on pain, but no effects on the progression of arthritis.  While the positive effects are small, the risk of harm is low.  There are few potential side effects of these products.  Since their costs are reasonable, it may make sense to try them.

What are the potential side effects of epidural and other spinal injections? 

The most significant risks include infections (leading to meningitis), paralysis or death.  Fortunately, these catastrophic events are rare.  In 2012, there was an outbreak of spinal meningitis after epidural steroid injections.  Over 20 states were affected.  Ultimately 751 serious infections were documented and 64 people died due to the infection.  A more common risk is loss of bone density in the vertebrae of the spine due to the effects of the steroid medication, which can lead to spinal fractures especially in older individuals who have multiple injections.

Having reviewed the literature, let’s return to the recently published study from the July issue of the New England Journal of Medicine on injections for spinal stenosis

Despite their results that these injections were not more effective than the placebo injection, the authors did not make any recommendations about the use of these injections.  Nor did they mention the overall healthcare costs.  Last year, the Journal of the American Medical Association published an editorial on the subject and the author noted that guidelines from the US, Europe, Italy and the United Kingdom all do not recommend injection therapy for low back pain. 

Given that these data do not show clear evidence of efficacy over and beyond a placebo treatment and that several clinical guidelines don’t recommend these injections, how many injections do you think are performed each year?  They’re probably decreasing, right?

Wrong. 

Deyo and colleagues published an article entitled: “Overtreating chronic low back pain: Time to back off?”  They documented that over a recent seven-year timeframe, the rates of injections for low back pain increased by 271%.  Costs per injection also increased by 100%.  This combination of increased injections plus increased cost per injection has led to a massive 629% increase in overall fees associated with these procedures.  This was not due to an aging population either because the number of new enrollees in Medicare (i.e. aging people) only increased 12% during the same timeframe.

Currently, it is estimated that at least 12 million injections per year are done for back pain in the United States alone.  Total costs of these injections are at least $500 million.  A study by Abbott and colleagues noted that there is great variability in the number of injections given by certain doctors.  Some doctors are more likely to give large numbers, from 10 to up to 50 per year to a single patient.  The authors found that 10% of the doctors accounted for 36.6% of all of the injections and 20% accounted for over half.   Thus, relatively few providers are performing a majority of all spinal procedures. 

How can this be happening?

Here are a few possible reasons.  First, patients often report improvement from injections.  As we saw in the New England Journal of Medicine study, the level of pain dropped from about 7 to 4.5.  When patients return and report that a procedure helped it can be difficult for doctors to believe their treatment is simply a high priced invasive placebo even if they review the research. 

Some physicians may even ask what’s the harm in using these injections even if it is a placebo response?  We know placebo effects can be incredibly powerful and this is especially true for pain (interestingly, more “invasive” placebo treatments are found to be have higher placebo responses). 

However most ethicists would argue that administering a placebo treatment to patients without their knowledge is not ethical.   Also, unlike many placebos, there are risks of significant complications associated with these procedures and there are obviously significant healthcare costs involved.   Healthcare dollars are not an unlimited resource and every dollar spent on an expensive injection is a dollar that can’t be used for other therapies.

A second reason may lie in the economics of injections.  Physicians who regularly perform injection treatments for back pain can make a lot of money.  An editorial comment on the Abbott study suggested that the doctors who are doing very large numbers of these procedures “may well be stretching the indications, accepting poor results, or be driven by profit.”  Most doctors are not performing excessive amounts of injections.  But if they took a careful and critical look at their practices, they might make some changes.  And, as a society, we are making these decisions on a daily basis.

Let me tell you about a friend of mine, Dr. Kevin Cuccaro, who resides in Corvallis, Oregon.  Dr. Cuccaro is an anesthesiologist who has completed a fellowship in pain management.  He is very knowledgeable in the current management model of back and leg pain because he was involved in it for years.  

For several years, Dr. Cuccaro worked as a pain specialist at the Naval Medical Center San Diego. There he treated active-duty service members with chronic pain—including many who had back and sciatic pain. 

When physical therapy and exercise weren’t enough to help his patients, he relied (as do most pain management specialists) on pain medications and injections.  Unfortunately, what he experienced was disheartening.  Instead of getting better with injections many patients appeared to get worse.  One injection led to another and then to another.  It wasn’t clear that he was actually helping to reduce pain in his patients.

However, continuity of care was difficult in a military environment and Dr. Cuccaro reasoned that perhaps this was contributing to lack of patient improvement.

So, after he left the military, he joined an upscale private medical group in Oregon.  Since he could now maintain continuity of care and deliver high quality pain management he expected his outcomes to improve.    

It didn’t turn out that way.  The results he saw in his private practice were no better than those in the military.  Basically, injections led to more injections and patients didn’t seem to improve overall. 

Frustrated he went back to the medical research to find what he could be missing.  What he found shocked him despite all of his training.  Studies consistently demonstrated poor long-term outcomes with injections for chronic pain.  A few papers reported brief improvement in pain but high quality studies did not find that these results were sustained for any significant length of time.

Even worse, the reasons used to support the use of injections for chronic back pain (like decreased medication use, increased activity or faster return to work) weren’t true at all.  In fact the opposite was found.  His patients were simply not getting better.

Most shocking of all, he learned that despite an astronomical rise in the number of injections (and surgeries) for back pain, outcomes in back pain in the U.S. appeared to be worsening—not improving.

However, injections were well reimbursed by Medicare and insurance companies and he was encouraged to continue using them.  Instead, Dr. Cuccaro made a bold decision: he decided to leave his practice. 

This is how he summarized his experience and why he decided to make a change:  

“Once I questioned the use of injections, I went down a very scary rabbit hole.  I realized much of what I was taught about treating pain simply wasn’t true.  Yet despite this evidence, everyone kept telling me to do more injections.  My group liked them because they were easy to schedule, didn’t take long and paid well.  Referring doctors wanted me to do them because they thought injections would keep people off of opioids.  Even patients were telling me to do more injections because they heard somewhere they needed a “series of 3” (a completely made up practice by the way).  

However once I took a harsh look at ALL the research on chronic pain I had a difficult choice to make: 

Do I believe I’m somehow better than every other doctor out there including those publishing the studies?   Did I think that my injections, despite the lack of evidence, were helping people live happier healthier lives?  If these injections aren’t helping much, do I turn a blind eye and pretend I’m not likely to harm anyone with these injections?  Or do I leave my medical group and a traditional pain management practice? 

These were the only options I had at the time and it would be nice to say leaving was an easy decision. 

It wasn’t.  I had (and still have) student loan debt, a mortgage, and a young family support.   My practice was my livelihood.  But it was the right decision to make.” 

(You can see what Dr. Cuccaro is up to now by visiting his website, www.StraightShotHealth.Com)

Innovative research demonstrates those with chronic back pain have changes in how their brains process pain.  These changes are similar to those found in other chronic pain syndromes like fibromyalgia.  Additional research shows many of the structures often blamed for chronic back pain like “bulging” or  “degenerative” discs aren’t abnormal at all.  They’re also found in patients who don’t have back pain.

By always focusing treatment on structures located in the back, we are likely looking in the wrong place for many people who have chronic back pain. 

So what then can be done for chronic back pain?  Injections aren’t the answer and surgery should be viewed with caution.  Pain medications, particularly narcotics, for chronic pain have their own set of problems.

There are better ways of treating most people (excluding those with fractures, tumors or infections) with chronic low back and sciatic type pain. These treatments require patients to be engaged and active in their recovery.  They work because they help patients change their brain to stop the pain.  They do not temporarily cover up the symptoms like injections or medications do.  For those willing to challenge themselves and take control of their own healing process there is hope. 

I have conducted an outcome study of patients with chronic back and leg pain (these data have been presented at 3 conferences, the full study will be published soon).  All of them completed the 4-week mind body program I run in Michigan.  The results, at a six-month follow up evaluation, showed that over 50% of patients had a greater than 50% reduction in pain.  Almost two-thirds had at least a 30% improvement in pain.  These reductions in pain are highly significant and occurred in individuals who had an average duration of back pain of over 8 years.  The average pain score was over 5 on a 10-point scale prior to the program and averaged 2.8 at the six-month follow up.  Although some continued to have significant pain, many were pain-free.  

The patients I see have been willing to look at how stress has affected them and how it has caused both emotional and physical pain.  They made a commitment to heal.  They stopped fearing pain and took control over it.  They often made important changes in their lives.  This can be hard work, but their stories show that recovery is possible.    

Dealing with chronic back (and other) pain can be overwhelming and I see the ravages of chronic pain on my patients and their families every day.  When one is in severe pain, it’s difficult to resist the advice of doctors to have invasive procedures.  As the research shows, spinal injections do reduce pain for many people and most doctors are well meaning and honorable.  However, the studies also show this: If you’re told you need an injection for your back pain you might be getting an expensive, and potentially risky, placebo.