being denied medicine: Email us at eyewitnessnews@13wmaz.com

http://www.13wmaz.com/news/opioid-epidemic-may-be-keeping-legitimate-patients-from-getting-pain-meds/454309714

Almost every morning is the same for Lauri Nickel — the pain may fluctuate, but it is always there.

“Some days are better than others,” said Nickel.

A staunch advocate for people with chronic pain, Nickel is upset with her leaders and elected officials.

She believes their effort to combat opioid abuse is having a negative effect on people who desperately need the drugs.

“You are sentencing people to an early death,” she said.

She is convinced the extreme focus has scared doctors from prescribing opioids to longtime patients who desperately need pain medication.

The result, according to Nickel, is that many patients will simply give up and take their own life.

Barby Ingle has not given up but it has been a difficult and often gut-wrenching journey.

The former college cheerleader and coach has battled chronic pain more than 20 years.

“Chronic pain devastated my life,” Ingle said. “It took everything away.”

At one point the pain was so bad and the prospects ahead so dire she contemplated suicide.

“I did think about it,” she said.

For the millions of people like Ingle and Nickel, opioids serve a critical role in their lives.

“It’s about quality of life, about surviving day to day, minute to minute, second to second,” said Ingle.

The two women say they know of several friends who have been denied access to opioids by doctors afraid to continue to prescribe the medication.

“They don’t want the DEA to come knocking on their door,” said Ingle.

“The people suffering from chronic pain should be mad at the people abusing the system,” said Doug Coleman, the Special Agent in Charge of the Arizona DEA office.

The longtime DEA agent says his office doesn’t target doctors who are prescribing opioids to legitimate patients.

Ingle and Nickel are not blind to the opioid problem but are worried this intense focus to curb the unlawful distribution of opioids could end up with many of their friends suffering in silence.

Do you know someone suffering from chronic pain who is being denied medicine or is worried about not getting the medicine they need? Email us at eyewitnessnews@13wmaz.com

Legality of CBD oil on trial in federal courts

With DEA digging in its heels on “marijuana extracts,” legality of CBD oil on trial in federal courts

www.thecannabist.co/2017/07/05/cbd-hemp-dea-marijuana-extracts-federal-lawsuit/82623/

Cannabist Special Report: CBD, TBD || Outcome of lawsuit pitting the hemp industry against the DEA could chart a new course for CBD — and a booming new agricultural sector.

Cannabidiol is a non-psychoactive cannabis compound touted for its medicinal promise — but marijuana- and hemp-derived extracts rich in CBD and low in intoxicating THC are facing a future yet to be determined.

The Cannabist’s special report “CBD, TBD” explores a regulatory and legal landscape pockmarked by federal-state conflicts, and examines national drug policy, pioneering research efforts and disparate avenues toward the compound’s full legalization. This is the third installment in an ongoing series.

Part I – Forbidden medicine: Caught between a doctor’s CBD advice and federal laws

Part II – How advocates are inspiring congressional action on CBD legalization


There are two wildly different views on how the federal government has classified cannabidiol (CBD) with a new drug code for marijuana extracts:

It was a mere administrative maneuver meant to bring the U.S. in line with international drug control treaties and to better track medical research.

It was the opening salvo in a federal offensive against the emerging American hemp industry.

A proposed final rule notice posted to the Federal Register last December by the U.S. Drug Enforcement Administration established a Controlled Substances Code Number for “marihuana extracts.” The rule notice, which was finalized in January, maintained cannabis-derived extracts’ Schedule I status under the Controlled Substances Act (CSA).

What the DEA saw as innocuous, the hemp industry saw as an existential threat.

Overnight, a pall was cast across an industry pumping out products ranging from hemp seed butter to bio-plastics used in automobiles to CBD oil, a non-psychoactive cannabis compound that has been highly touted for its potential medicinal benefits.

Hysteria and confusion swelled after initial reports erroneously asserted that a scheduling action occurred and that CBD was now illegal and in the crosshairs of the government.

Shortly after the rule was announced, DEA officials reiterated to The Cannabist that no scheduling action took place. None was necessary — CBD oil and other extracts derived from marijuana and hemp “have been and will continue to be Schedule I controlled substances,” officials said.

The DEA has not changed its stance.

Hemp industry lawyers claimed the rule instantly subjected what were presumed lawful operations to DEA registration and drug code assignation, effectively treating their products as controlled. The coding also amounted to the DEA acting outside of its authority by attempting to schedule cannabinoids, or even marijuana extracts, which are not explicitly listed in the Controlled Substances Act, attorneys alleged.

A federal lawsuit filed in January by Denver’s Hoban Law Group on behalf of the Hemp Industries Association, Centuria Natural Foods and RMH Holdings LLC was intended to protect an American agricultural revival, attorney Bob Hoban told The Cannabist.

“The entire industry hinges on this,” Hoban said.

Now it’s up to the 9th U.S. Circuit Court of Appeals to make a decision that could chart a new course for the hemp industry.

Uncertain times, booming business

At least 16 states, including Colorado, have laws allowing cultivation of hemp for research and/or commercial purposes, according to the National Conference of State Legislatures.

In 2016, the hemp industry notched an estimated $688 million in U.S. sales, setting a new record, according to an analysis by the Hemp Business Journal. Hemp-derived CBD accounted for an estimated $130 million share of that total, the Denver-based trade publication reported.

However, questions have continuously swirled around the legality of the sourcing, manufacturing processes and distribution of the plant’s products and extracts.

Central to the issue are the parts of the cannabis plant that are refined into products. In the Controlled Substances Act, the government defines marijuana as:

“all parts of the plant Cannabis sativa L., whether growing or not; the seeds thereof; the resin extracted from any part of such plant; and every compound, manufacture, salt, derivative, mixture, or preparation of such plant, its seeds or resin. Such term does not include the mature stalks of such plant, fiber produced from such stalks, oil or cake made from the seeds of such plant, any other compound, manufacture, salt, derivative, mixture, or preparation of such mature stalks (except the resin extracted therefrom), fiber, oil, or cake, or the sterilized seed of such plant which is incapable of germination.”

What has been excluded from the CSA definition — mature stalks and unviable seed — is considered to contain only traces of cannabinoids such as psychoactive THC. Foods such as hemp-seed hearts and cooking oil made from seed fall into this category.

DEA officials confirmed to The Cannabist last December that the new code number would have no effect on the slew of hemp products not intended for human consumption that are already exempt from the CSA. That included the likes of lotions, shampoos, solvents, ropes, clothing and bird seed, officials said.

Questions arise when hemp plants that are naturally low in THC are used to make CBD oil.

“The uncertainty, frankly, is what has created this industry,” Hoban said. “Economics and business thrive in uncertainty.”

Surviving in uncertainty, however, is another matter.

Hoban said the industry can’t sit on the sidelines assuming state legalization and existing case law will shield producers, retailers and consumers of hemp-derived products.

He noted how companies in Texas and Kentucky had their CBD products seized by state police. He expressed concern that operations by the U.S. Customs and Border Patrol could lead to seizures of CBD oil and other hemp-derived products under the auspices of the DEA’s marijuana extract coding.

CBD oil’s legality has been questioned in places like Orchard Park, New York, where officials for a state-run special care facility said federal law prohibited them from administering doctor-recommended CBD oil for a patient.

“There’s no black and white about this,” Hoban said, and added that the fight in the courts is critical.

The U.S. Court of Appeals in San Francisco provides a familiar battleground for the DEA and the Hemp Industries Association. Nearly two decades ago, the 9th Circuit set precedents on hemp foods and cannabinoids that play heavily into this year’s case.

In 2003, the court ruled against the DEA’s “Interpretive Rule” banning all naturally occurring THC, including the trace amounts found in hemp seed and oil. In 2004, that same appellate court established bounds on the DEA’s authority related to natural and synthetic THC, according to court records:

The DEA’s Final Rules purport to regulate foodstuffs containing “natural and synthetic THC.” And so they can:  in keeping with the definitions of drugs controlled under Schedule I of the CSA, the Final Rules can regulate foodstuffs containing natural THC if it is contained within marijuana, and can regulate synthetic THC of any kind. But they cannot regulate naturally-occurring THC not contained within or derived from marijuana-i.e., non-psychoactive hemp products-because non-psychoactive hemp is not included in Schedule I. The DEA has no authority to regulate drugs that are not scheduled, and it has not followed procedures required to schedule a substance.

A decade later, Congress passed the Agricultural Act of 2014, also known as the Farm Bill, which allowed states to set laws on hemp production. The act defined industrial hemp as “the plant Cannabis sativa L. and any part of such plant, whether growing or not, with a delta-9 tetrahydrocannabinol concentration of not more than 0.3 percent on a dry weight basis.”

Under that legislation, a state department of agriculture or university could produce industrial hemp for research purposes, and others could grow the versatile crop under state-sanctioned pilot programs.

Poking the bear

Past circuit court rulings and hemp-friendly federal legislation have offered legal precedent for producers, retailers and consumers of CBD-rich extracts, but they didn’t necessarily provide security or stability to all.

Some advocates for CBD oil in therapeutic and medical applications said they prefer a clear-cut approach — the stakes are far too high for too many people and businesses to solely rely on the courts.

Paige Figi, a Colorado Springs-area mother, credits CBD oil with drastically reducing her daughter Charlotte’s seizures caused by Dravet syndrome, a type of epilepsy. She founded the nonprofit Coalition for Access Now to lobby for CBD laws.

CBD oil’s legality ultimately needs to be decided in the halls of Congress, Figi said.

Figi and Coalition for Access Now are supporting Congressional efforts to exclude CBD — and plants rich in cannabidiol and low in intoxicating THC — from the definition of marijuana in the Controlled Substances Act.

Beyond the need for full federal legality, Figi said she is concerned that continued court battles could ultimately backfire against the entire industry.

The DEA’s enforcement priorities have been elsewhere, she said, noting that agents have mostly taken a hands-off approach toward producers that adhere to state laws and consumer safety standards.

“When you poke the bear, the DEA can come back and say, ‘It’s scheduled,” and increase enforcement actions, Figi said.

DEA spokesman Russ Baer did not respond to The Cannabist’s requests for interview about the pending lawsuit and the broader debate involving CBD oil.

Last December, Baer told The Cannabist via email that the new rule on extracts would not change the DEA’s enforcement priorities, which are focused in the widely abused areas of heroin, fentanyl, meth and cocaine.

A decision in the 9th Circuit would be legally binding in only a collection of states and territories in the western United States, Hoban said. The 9th Circuit consists of Alaska, Arizona, California, Guam, Hawaii, Idaho, Montana, Nevada, Northern Mariana Islands, Oregon and Washington.

Still, he said, a legal victory in the 9th Circuit would both clarify the DEA’s rule notice in the interim and further set precedent for the future.

“This is the first inning of a very long ballgame,” he said.

 

Each lawsuit names the West Virginia Board of Pharmacy

Four drug distributor lawsuits removed to federal court

http://wvrecord.com/stories/511144093-four-drug-distributor-lawsuits-removed-to-federal-court

CHARLESTON – Four lawsuits against drug distributors for allegedly contributing to the opiate epidemic have been removed to federal court.

The lawsuits were filed by Mayor Charles Sparks, on behalf of the town of Kermit; Mayor Vivian Livinggood, on behalf of the town of Gilbert; Mayor Reba Honaker, on behalf of the city of Welch; and the Lincoln County Commission.

 

Each lawsuit names the West Virginia Board of Pharmacy; McKesson Corporation; AmerisourceBergen Drug Corporation; and Cardinal Health 110. Miami-Luken is also named in Gilbert, Lincoln and Kermit’s lawsuits. Dr. Harold Anthony Cofer Jr. is named in Welch’s. Chip RX and George W. Chapman III is named in Lincoln’s. Cameron Justice was also named in Kermit’s.

The lawsuits all allege the defendants contributed to the opiate epidemic across the state by flooding pharmacies with Hydrocodone and Oxycodone. The BOP allegedly failed to timely investigate and resolve suspicious order reports.

The defendants played a significant role in creating what amounts to a public nuisance by flooding the area with excessive amounts of dangerous and addictive medications, according to the suits. The plaintiffs claim the defendants’ actions are a serious breach of the public trust, which has resulted in drug abuse, misuse, overdose deaths and untold expenses for the plaintiffs.

The plaintiffs claim as distributors of inherently dangerous products like prescription narcotics, the defendants bore a significant duty to ensure that the drugs did not end up in the wrong hands and failed to do so.

In exchange for promising to honor their obligations, each of the defendant distributors was licensed and/or registered by the Board of Pharmacy and ultimately received compensation in the form of millions of dollars per year for shipping volumes of drugs well beyond what a reasonably company would expect, according to the suits.

The plaintiffs claim they were there to enforce codes, clean up streets and neighborhoods and repair and/or replace damaged and destroyed property.

In the notices of removal, the defendants claim complete diversity exists between the plaintiffs and defendants.

The plaintiffs are represented by H. Truman Chafin and Letitia N. Chafin of The Chafin Law Firm; Mark E. Troy of Troy Law Firm; Harry F. Bell Jr. of the Bell Law Firm; and John Yanchunis, Patrick Barthle and James Young of Morgan & Morgan Complex Litigation Group.

The defendants are represented by Brian A. Glasser and Steven R. Ruby of Bailey & Glasser; Enu Mainigi, F. Lane Heard and Steven M. Pyser of Williams & Connolly; Thomas Hurney Jr. and Laurie K. Miller of Jackson Kelly; A.L. Emch and Adam J. Schwendeman of Jackson Kelly; Meredith S. Auten and Eric W. Sitarchuk of Morgan Lewis & Bockius; Russell D. Jessee and Devon J. Stewart of Steptoe & Johnson; and Geoffrey Hobart and Matthew Benov of Covington & Burling.

U.S. District Court for the Southern District of West Virginia case number: 2:17-cv-03369, 2:17-cv-03372, 2:17-cv-03366, 1:17-cv-03364

The vast majority of Boards of Pharmacy ( BOP) takes their primary charge to protect the public’s health and safety in a very limited manner.  If this BOP is found liable for contributing to the opiate epidemic  in WV.  This could open the flood gates for BOP’s to be sued for a number of issues that they have chosen to ignore  that should be within their primary charge.

Dayton Ohio area: 99% of opiate OD’s tested positive for ILLEGAL FENTANYL ANALOG

Dayton Ohio area: 99% of opiate OD’s tested positive for ILLEGAL FENTANYL ANALOG

 

 

 

 

 

 

https://ndews.umd.edu/sites/ndews.umd.edu/files/update-on-fentanyl-outbreaks-in-dayton-ohio-ou-r21-da042757-05-02-2017.pdf

 

Popular stomach acid blockers linked to higher death rates

http://media.spokesman.com/photos/2017/07/03/26_GAMBLE_PRILOSEC_OTC.JPG_I1jfV5p_t2500.jpg?6913dd5f0afa17a0b7a91a88b4e808d586264d13

Popular stomach acid blockers linked to higher death rates

http://www.spokesman.com/stories/2017/jul/04/popular-stomach-acid-blockers-linked-to-higher-dea/

A higher risk of death is associated with long-term use of popular stomach acid reducers known as proton pump inhibitors, according to a study of prescribed drugs published Monday.

These drugs are sold under brand names such as Prilosec, Nexium, Protonix and Zegerid, along with generic versions such as omeprazole, lansoprazole and pantoprazole. Originally sold only by prescription, they are increasingly available over the counter. The study didn’t examine over-the-counter use.

Previous studies have indicated elevated disease risks from PPI use. This study goes further by linking them to higher death rates.

Use of the drugs was associated with a 25 percent greater risk of death, compared with those using another class of acid reducers called H2 blockers. H2 blockers are sold under brand names including Pepcid, Tagamet and Zantac. They are also sold under generic names, including famotidine, cimetidine and ranitidine.

Millions of veterans’ prescription records were examined across an average of nearly six years for the study. It was published in the journal BMJ Open. The senior author was Dr. Ziyad Al-Aly of VA Saint Louis Health Care System. Go to j.mp/acidppi for the study.

Doctors shouldn’t be deterred from prescribing these drugs when medically indicated, the study said, but only long enough to provide benefits that outweighs the risks. The increased mortality associated with PPIs was proportionately linked to their duration of use.

Acid reducers treat painful ailments including GERD (gastroesophogeal reflux disease), heartburn and peptic ulcers. According to prescription records, more than 15 million Americans are estimated to use proton pump inhibitors, a number that doesn’t include those who buy them over the counter.

For the study’s main analysis, Department of Veterans Affairs records of 349,312 patients were used. Of those, 275,977 were prescribed PPIs, and 73,335 prescribed H2 blockers. This produced the 25 percent increase in death rate among PPI users.

Two secondary comparisons were also made. One found a 15 percent increased death rate for PPI users compared to those who didn’t use PPIs but may have used another kind of acid suppressor. Records from 3,288,092 patients were examined for that comparison.

In the other comparison, the death rate was 23 percent higher among PPI users compared to those who didn’t use any acid suppressors at all. A total of 2,887,070 patient records were examined for that analysis.

The study’s comparisons were observational, so the conclusions are not as definitive as a randomized placebo-controlled study.

Another limitation is that the patients were “mostly older, white male U.S. veterans,” the study said, so the results may not apply to a larger population. Also, the study didn’t get information on the cause of deaths.

However, the study is consistent with previous ones finding long-term use of PPIs, but not H2 blockers, is associated with higher disease rates. These include kidney disease, dementia, infection by the antibiotic-resistant superbug C. difficile and other ailments.

Proton pump inhibitors work by a different mechanism than H2 blockers, explaining the differing responses. PPIs block stomach cells called parietal cells from releasing positively charged hydrogen atoms, or protons, into the stomach. This inhibits production of stomach acid, chemically known as hydrochloric acid.

H2 blockers stop the action of histamine, which stimulates parietal cells to produce hydrochloric acid. This indirect method is less efficient than that of PPIs, but is sufficient for many patients.

A 2016 study in JAMA Neurology found a 44 percent increased risk of dementia among those using PPIs.

PPIs can cause nutritional deficiencies, since acid is needed to release essential nutrients such as vitamin B12. Since stomach acid kills pathogenic bacteria; use of acid reducers has been linked to increased rates of food poisoning.

A 2015 study led by Stanford University researchers found that use of PPIs, but not H2 blockers, is associated with higher risk of heart attacks.

And in one of the most unusual side effects, proton pump inhibitors have been found to cause visual hallucinations in some patients with wet macular degeneration.

Dr. Anne Hanneken, a San Diego ophthalmologist, co-authored a 2013 study describing the phenomenon in the journal Investigative Ophthalmology & Visual Science. Go to j.mp/retinappi for the study.

It started with an 89-year-old patient who suddenly developed vivid hallucinations of little black polka dots. The hallucinations were severe enough to prevent her from living independently.

Hanneken couldn’t find a cause, but kept the record until she encountered another macular degeneration patient with a similar complaint, and found they were both taking PPIs.

After teaming up with retinal expert Wallace B. Thoreson, they figured out that the PPIs reached the retina through leaky blood vessels caused by wet macular degeneration. There, the PPIs interfered with proton pumps in retinal cells.

These hallucinations occur in a minority of patients, Hanneken said. Moreover, if people stop taking the PPIs quickly, the hallucinations dissipate readily.

In another twist, Hanneken discovered that the hallucinations can be suppressed with the drug gabapentin, sold under the trade name Neurontin. This drug reduces neuronal activity, and is used to treat epilepsy and neuropathic pain. However, the drug can also caused blurred vision, because it can also interfere with visual processing.

“Every year I see about three people who come in for unexplained visual loss,” Hanneken said. “They say everything’s sort of blurry and they don’t know why. And it turns out that their neurologist started them on Neurontin for some leg pain.”

I Love FACTOIDS… they are typically so easily BUSTED

There was enough opiate prescriptions filled in ONE YEAR to give each resident a bottle of OPIATES

https://www.statista.com/statistics/261303/total-number-of-retail-prescriptions-filled-annually-in-the-us/

In 2016 there was 4.51 BILLION prescriptions filled in the USA… with a population of abt 320 MILLION that comes out to abt 14 prescription for EACH PERSON.

Let’s assume that the one prescription per person is a FACT… meaning that there would be 320 million opiate prescriptions filled..

BUT WAIT… a chronic pain pt would need – TWELVE PRESCRIPTIONS PER YEAR – presuming 30 days supply of each…  Suggesting that those 320 million prescription would only take care of abt 26 million chronic pain pts..  or about EIGHT PER-CENT OF THE POPULATION.

BUT WAIT… there are people having to deal with acute… surgery, broken bones and the like..  let’s presume that 15% of the 320 million are for acute pain…  subtract 48 million … leaving 272 million for chronic pain pts…or  some 22 million chronic pain pts get 12 prescriptions a year..

BUT WAIT… standard of care and best practices indicates that a chronic pain pt should be getting both a long action and short acting – for breakthru – opiate.  Which would mean that abt 11 million chronic pain pts would get opiate therapy that conforms to accepted best practices and standard of care.

BUT WAIT… there is an estimated 100+ million chronic pain pts…

BUT WAIT… when the bureaucrats state that having enough opiate prescriptions to furnish everyone a prescription…  IS A BAD THING…  Are they really saying that they support/endorse under treating/un-treating the vast majority of chronic pain pts is a GOOD THING or a BAD THING ?

Since PAIN is generally considered a part of TORTURE… are our politicians and bureaucrats encouraging the TORTURING of our citizens ?

FACTOID DISPELLED !!

 

 

This Congressman REPRESENTS WHO … not all the VOTERS ?

Vet With Chronic Pain Denied Access to his Congressman

www.nationalpainreport.com/vet-with-chronic-pain-denied-access-to-his-congressman-8833959.html

by Ed Coghlan

A veteran with chronic pain wants to talk to his Congressman—and another attempt to do that on Monday failed.

Robert Rose is a 51-year old Marine who believes the Mountain Home VA Center in Johnson City, Tennessee has been denying him care and has been quite vocal about it,

Congressman Roe was scheduled to speak at the Mountain Home VA Center at 11 am—and Rose–well known to the VA authorities because of his protests about his care—arrived early, he said, to speak with other veterans.

Rose called me and told me that he had been told by the VA law enforcement people that he would be arrested if he said anything at the Congressional hearing and asked me what I should do.

“I told him I was a reporter not an advocate and it wasn’t my job to advise him about that–but let me know what happened.”

That call came at 9:41 EDT.

My phone rang again at 9:57 and again it was Rose who told me he was being escorted into the building by three officers–and I asked him to put me on speaker. We were on the phone for nearly 30 minutes to hear the exchange between Rose and VA law enforcement.

A VA policeman, later identified as Sergeant King, said to Rose,

“You are not being arrested,” but he was being urged to come with them to discuss the situation.

Sgt. King wanted to know who I was and said I could not record a conversation on federal grounds and wanted to end the phone call. I assured him I wasn’t and if I was recording anything I would have to let him know that and he agreed to let me continue to listen.

Essentially Sgt. King told Rose that he had received a complaint about him yelling and being disruptive at the Congressman’s entourage.

Rose, with some passion, explained that he was 30 feet from the roadway (a fact confirmed by a VA official) and wasn’t even on the sidewalk and that he had been talking with a fellow vet and his wife.

Rose asked twice (and I asked a third time) who had made the complaint and Sgt. King said he couldn’t say.

Later when I asked him, the Sergeant said that the “Congressman’s staff felt on edge,” but did not elaborate.

Rose, who is in a wheelchair, was told that they didn’t want to arrest him and was asked essentially to behave.

During the speech, he behaved but he silently protested.

During Congressman Roe’s speech, Rose, sitting in his wheelchair, turned his back on the Congressman–who by the way in an Army veteran himself and–importantly–Chairman of the House Committee on Veteran Affairs.

After the speech, Rose said his path to the Congressman was blocked by the VA Police and he wasn’t allowed to speak to him.

I asked Rose if he had any photos and he said that he was told he would have been arrested had he taken any, although local media did attend and took photos and video.

Rose, who said he’s lost count of how many times he’s tried to speak with Congressman Roe, believes the VA Police were trying intimidate him and illegally detained him before the meeting.

The National Pain Report called Roe’s office in Kingsport, but received a recording because they are on holiday today and tomorrow (July 4).

If they call back, we’ll let you know what they say.

DOJ civil rights division: IS Dreiband “the wrong person for the job.” ?

Civil rights advocates concerned with Trump’s pick to lead DOJ civil rights divisionCivil rights advocates concerned with Trump’s pick to lead DOJ civil rights division

http://thehill.com/homenews/administration/340402-civil-rights-advocates-concerned-with-trumps-pick-to-lead-doj-civil

Civil rights advocates are raising alarm over President Trump’s nominee to lead the Justice Department’s civil rights division.

Trump nominated attorney Eric Dreiband, who has represented corporations on matters such as civil rights and employment discrimination, to lead the DOJ’s civil rights division on Thursday.

Dreiband has represented various corporations such as Bloomberg, CVS Pharmacy and R.J. Reynolds Tobacco Co. He also served in George W. Bush’s administration as general counsel for the Equal Opportunity Commission.However, the official who led the division under former President Obama issued a statement saying Dreiband is “the wrong person for the job.”

“He has opposed important legislation to safeguard our civil rights. And he has no known experience in most of the Civil Rights Division’s core issue areas, such as voting rights, police reform, housing, education, and hate crimes. He is the wrong person for the job,” Vanita Gupta, who now leads the Leadership Conference on Civil and Human Rights said in a statement.

“Dreiband’s nomination, however, continues the Trump administration’s disturbing trend of retreating from — if not outright undermining — fundamental civil rights priorities,” the NAACP Legal Defense Fund said in a statement on Medium.

The White House pushed back on the claims against Dreiband saying nominees are selected based “on the merits of their character and not on the clients they once represented as counsel.”

“Mr. Dreiband is highly qualified to run the civil rights division, and we are privileged to have his service,” White House spokeswoman Kelly Love told CNN.

Should all the those in the chronic pain community and others that are covered under the Civil Rights Act and the Americans with Disability Act start to align with each other… to CAUSE CHANGE ?

 

Cost Containment by the Insurance Industry ?

This was a post on a FB page for chronic painers today:

Our world is going to crap. An insurance company just proposed to a doctor that two patients that needed treatment in another state, that they wouldn’t pay for treatment but would pay for assisted suicide. Look out everyone. When our laws are willing to let someone die that is suffering from a disease called addiction and kill another two that needed expensive treatment we are all in trouble. Wake up Americans

 

What happened to the OBESITY EPIDEMIC ?

Image result for cartoon obesity empidemic

850 will die from OBESITY — TODAY 

Remember a year or two ago… nightly in the media… there was WARNINGS about our OBESITY EPIDEMIC ?

But it is estimated that  850 DIED EVERY DAY IN 2016 from OBESITY.  Obesity is the FOURTH LARGEST CAUSE OF DEATH.. behind Heart Disease, Cancer & Tobacco/Nicotine.

Since 850 deaths per day … would appear to be AT LEAST TEN TIMES the number of opiate OD death per day that is being reported…  as an EPIDEMIC

I guess that a EPIDEMIC is in the eye of the beholder and what they can get the media to believe

Does that mean that the MEDIA is pretty gullible or the public is pretty gullible about all the fake epidemic(s) that various parts of our society is allowed to fabricate and promote.