You may have noticed that I have not been around as much

We have been at our Panama City Beach condo since Aug 2nd… Hurricane Michael took the metal roof off of our complex … some say that it was Michael’s Cat-5 status others have stated that it was a tornado that did the damage.  We have a top floor unit and our ceiling is a concrete slab… so water ran down the conduit runs and penetrations in that slab. The picture below is a satellite of our complex post Michael’s landfall Oct 10,2018 and the part of the roof missing – center left – is over out unit.  It is amazing how much damage a couple inches of water can cause..  it is also amazing how much damage that workman can do in the process of doing the repair work that they are in charge of doing…

The adjuster that the Association’s insurance company hired… – IMO – drug the Association’s Board of Directors around BY THE NOSE…  I am not going to mention any companies that were involved – not yet anyway… once everything is finalized… there will be another post… naming names..

The company hired as the primary remediation … brought in a moving company from 1000 miles away – from Michigan that was suppose to room center and wrap our furniture. Apparently the first company PROMISED the moving company a certain amount of $$ to be generated and when the legit business didn’t generate that amount they arbitrarily “pack out” units that it was determined that too much contents and too much dry wall damage… and we got chosen to be such a unit… and it was done without us signing a contract with the first company and they were the one who made the decision as to what unit were packed out…   I came down Dec 13th to find out unit COMPLETELY PACKED OUT… every piece of silverware, all dished, glasses & cups, the can goods in the pantry… they only thing left in the unit was a night stand and a dog bed…. and then we got a $25,000 moving bill… 

And they forced us to have our belonging moved back in Memorial Day week – before all the interior work had been done… they returned all of our “excessive belonging” and 170 boxes that they packed everything else in…

Luckily Florida has a “price gouging law” that goes into effect during a declared emergency and I have filed a complaint with the FL AG’s office and they are going after this company seriously and I may get a largest – or all  – of our money back for the moving expenses.

Our insurance company decided that since we did not have “wind insurance” – we have 150 MPH doors covered by 120 MPH metal hurricane shutters and nothing of any mass will get up this high… but our insurance denied any/all coverage – could have been as much as $120,000 because the water that got into our unit was INDIRECTLY WIND DRIVEN…

The people that did the drywall… only broke the kitchen sink faucet, broken half of our elec hurricane shutters and disconnected all of the R6 TV cables with WIRE CUTTERS..

I was able to hook up our TIVO system with the cable that comes into the unit and we have been able to STREAM shows from the TIVO and watched “TV” on our IPADS…

Because we didn’t know what monies that was going to come from the Association’s insurance… we built our own house 45 yrs ago… so the two of us have many VERY RUSTY skill sets … which we decided to start using… come to find out.. it is much like riding a bicycle… you never really forget the skill set.

BTW, the moving company brought back a RODENT INFESTATION back to the complex and the little varmints chewed the lines in the dish washer… causing it to leak…  looking at our dishwasher.. it was manufactured in 1998 ..but since we only stay here 2-3 months out of the year… so it was 20 yrs old… and decided to replace it…

I have not been posting much… and not been very prompt in responding to emails… and hope that everyone understands… we have been seriously preoccupied with all of the repair work on our condo. If I had the time… I could write a book … on how condo complexes and owners being on the Board of Directors – with limited experiences in a lot of areas – are “running the show “… and not doing a very good job…  But being only a single owner in a 134 unit complex… you have to go along with the crowd… and in our complex… the majority of the ownership … are more focused on what is good for their pocketbook and not what is good for the complex and the ownership as the whole.

About 100 units are rented by their owners, and since we are current been “closed” since Oct 10, 2018 and best estimate is that we will be back in the rental business Jan 1 , 2020… collectively the ownership has failed to generate AT LEAST 1.5 million in rental revenue… plus the cost of bringing their unit back to rental standards and not to mention the assessment – ours was $4700 – which may be the first of many.

USA: uses 2/3 of world supply of illegal opiates – mental health crisis ?

DOJ’s Aggressive Effort to Combat Opioid Crisis Places Everyone in the Crosshairs

DOJ’s Aggressive Effort to Combat Opioid Crisis Places Everyone in the Crosshairs

https://www.jdsupra.com/legalnews/doj-s-aggressive-effort-to-combat-90992/

A wave of recent indictments unsealed against opioid distributors and their executives signifies that the U.S. Department of Justice (“DOJ”) has embarked on a criminal crackdown after years of civil enforcement efforts failed to staunch America’s opioid epidemic. In particular, the DOJ appears to have broadened its investigatory and enforcement activity to encompass not just customary bad actors, such as “pill mills,” drug trafficking organizations, and rogue prescribers, but also companies involved in the drug supply and distribution chain. Such companies include manufacturers, wholesale distributors, and retail pharmacies. In addition, the DOJ is increasingly pursuing criminal charges against senior executives at companies allegedly responsible for the overutilization or diversion of opioids. Recent victories in the DOJ opioid crackdown, such as the convictions of five top executives at Insys Therapeutics, Inc. (“Insys”), an opioid manufacturer, for racketeering conspiracy, as well as a related settlement by Insys with the federal government to resolve, in part, criminal investigations into the company’s marketing practices, likely will encourage and embolden federal prosecutors.

The increase in enforcement actions taken against these companies and their senior executives follows from the Trump administration’s public commitment to end the improper diversion and distribution of addictive opioids and deter similar malfeasance in the future. In October 2017, the Trump administration officially declared the opioid crisis a public health emergency.[1] Alex Azar II, Secretary of the U.S. Department of Health and Human Services, most recently renewed the public health emergency declaration on July 17, 2019.[2] As a result, the Trump administration has prioritized enhanced regulatory enforcement, including the investigation and prosecution of high-impact individuals and companies, as a tool to fight the opioid epidemic. For example, in February 2018, the DOJ announced the creation of a new task force, the Prescription Interdiction & Litigation Task Force, charged with “aggressively deploy[ing] and coordinat[ing] all available criminal and civil law enforcement tools to reverse the tide of opioid overdoses in the United States, with a particular focus on opioid manufacturers and distributors.”[3] More recently, on August 8, 2019, the DOJ announced the immediate suspension of the Certificate of Registration issued by the U.S. Drug Enforcement Administration (“DEA”) to Oak Hill Hometown Pharmacy (“Oak Hill”), a West Virginia pharmacy alleged to have improperly filled large volumes of an addictive controlled narcotic, on grounds that the pharmacy posed an “imminent danger to the public health or safety.”[4]

Furthermore, according to the DEA’s Automation of Reports and Consolidated Orders System, which tracks all opioid purchases in the United States, 15 percent of pharmacies handled almost half of opioids that were distributed — a total of 35 billion opioids.[5] These pharmacies, largely comprised of small independent pharmacies in rural areas, “had annual double-digit growth in pain pills and bought far more opioids than competitors in the same counties.”[6] Although some of the pharmacies were previously subject to disciplinary actions or warnings from regulators, it is not clear whether all high-volume pharmacies were similarly sanctioned.[7] The pharmacies, some of which now operate under new ownership, are located in Kentucky, Idaho, Kansas, Illinois, Tennessee, West Virginia, Nevada, Utah, Oregon, Michigan, and Oklahoma. Government agencies are increasingly relying on data analytics in order to target so-called “bad actors” for further investigations. Accordingly, pharmacies that dispense opioids or other controlled substances in volumes or patterns that are aberrant to those of similarly situated pharmacies are at increased risk of government inquiries into their internal business operations and practices. A similar example of the current government focus on facilities or actors believed to be large contributors to the crisis involves Purdue Pharma, which is reportedly offering $10–$12 billion to settle all of the cases and a recent raid in which the DOJ charged 41 people for allegedly running a “pill mill” in Texas.[8]

In response to this increased government scrutiny, companies conducting business at any stage of the supply and distribution chain in the opioid space and investment firms that own portfolio companies in the industry should carefully evaluate corporate compliance programs, particularly with respect to marketing strategies, utilization review, and communications with health care prescribers, to determine whether they are effectively implemented or mere “paper programs.”

The Past

In the past, the DOJ’s enforcement efforts primarily involved civil settlements that included substantial fines. For example, in 2008, McKesson Corporation (“McKesson”), a distributor of pharmaceutical drugs, agreed to pay a civil penalty of $13,250,000 in order to settle alleged violations of the Controlled Substances Act.[9] The DOJ alleged that McKesson failed to properly report to the DEA suspicious purchases of controlled substances by pharmacies and clinics. In 2017, the DOJ alleged that McKesson again violated federal reporting requirements pertaining to suspicious orders for controlled substances it received from third parties. As a result, McKesson entered into another settlement agreement with the DOJ whereby the distributor agreed to a $150 million civil penalty and the suspension of controlled substances sales from certain noncompliant distribution centers, as well as adherence to an enhanced compliance program.[10] While this civil penalty constituted the largest settlement amount at that time, no criminal charges were filed against McKesson’s executives in either settlement.

The DOJ’s prior reliance on civil penalties to ensure compliance with drug control laws was not limited to McKesson. For example, in 2017, the DOJ announced a settlement with Mallinckrodt LLC (“Mallinckrodt”), one of the largest manufacturers of generic oxycodone, to resolve allegations that Mallinckrodt did not appropriately detect and report orders for controlled substances that were suspicious due to their frequency, size, or other factors. In announcing the settlement, then-Attorney General Jeff Sessions stated:

. . . as a result of today’s settlement, we are sending a clear message to drug companies: this Department of Justice will hold you accountable for your legal obligations and we will enforce our laws. I believe that will prevent drug abuse, prevent new addictions from starting, and ultimately save lives.[11]

While past settlements have signaled the DOJ’s willingness to resolve opioid cases with a company “cutting a check,” those days appear to be long gone. The recent wave of criminal prosecutions shows that the DOJ is developing a playbook to charge companies and executives involved in over-prescribing and over-distributing opioids.

Recent and Ongoing Cases Reflect DOJ’s New Game Plan

Several ongoing cases demonstrate federal prosecutors’ aggressive new approach. Earlier this year, the DOJ pursued for the first time felony criminal charges against a pharmaceutical distributor.[12] In United States v. Rochester Drug Co. Operative, Inc., prosecutors brought drug-trafficking charges against two former executives and Rochester Drug Co. Operative, Inc. (“RDC”), one of the largest pharmaceutical distributors in the United States, alleging that RDC shipped millions of oxycodone pills, fentanyl, and other opioids to pharmacies that its executives knew were distributing the drugs illegally.[13] In particular, the DOJ charged RDC with conspiring to distribute drugs, conspiracy to defraud the United States, and failing to file suspicious order reports.[14] The company paid $20 million in penalties and entered into a deferred prosecution agreement.[15] During a press conference discussing the case, U.S. Attorney for the Southern District of New York Geoffrey Berman noted, “[t]his country is in the midst of a prescription drug abuse epidemic . . . [t]his epidemic has been driven by greed.”[16] The former CEO of RDC faces related charges and is scheduled for trial in May 2020.[17] The former chief compliance officer has pled guilty and is cooperating with prosecutors.[18]

Shortly after announcing charges against RDC and its executives, the DOJ pursued a criminal case against Miami-Luken, Inc. (“Miami-Luken”), an Ohio-based distributor, its former executives, and two pharmacists for an alleged scheme that resulted in the distribution of millions of opioids throughout various states.[19] Specifically, the DOJ alleged that Miami-Luken and its executives distributed “more than 2.3 million oxycodone pills and 2.6 [million] hydrocode pills” to a single pharmacy located in a town with a population of approximately 1,394.[20] According to the DOJ, “[the two executives] and Miami-Luken sought to enrich themselves by distributing millions of painkillers to doctors and pharmacies in rural Appalachia, where the opioid epidemic was at its peak.”[21] The indictment further alleged that the two executives and Miami-Luken “ignored obvious signs of abuse and diversion . . . .”[22] In connection with its investigation, the DOJ similarly charged two West Virginia pharmacists whose pharmacies had received significant amounts of opioids from Miami-Luken; the pharmacists now face 20 years in prison.

The two cases have striking similarities. First, both cases involve criminal charges against the compliance officers of opioid distributors. Second, both cases involve companies that serviced pharmacies that were previously terminated by other distributors or wholesalers. Third, both cases involved allegations that the distributor shipped opioids to pharmacies that were under investigation by the DEA. Finally, in both cases, the facts indicate that the compliance officer or other executives had knowledge of the opioids being provided illicitly or otherwise were aware of red flags.

In addition to the imposition of criminal charges, the government also is relying on administrative enforcement mechanisms to crack down on the opioid epidemic. This is most clearly demonstrated in the DOJ’s suspension of Oak Hill’s DEA registration due to allegations of improper dispensing activities dating back to December 2016. According to the DOJ, Oak Hill continued to fill 2,000 prescriptions of Subutex, a Schedule III controlled substance, despite multiple prescription abuse and diversion indicators.[23] In particular, the DOJ noted the frequency of prescriptions written by out-of-state physicians, cash payments, and long travel distances made by patients, as well as multiple prescriptions written on the same date. In its press release, the DOJ discussed pharmacies’ obligations and role in combating the prescription drug abuse by stating:

Every pharmacy that fills prescriptions of scheduled narcotics has a corresponding responsibility to assure that those prescriptions do not include unresolvable red flags and are for a legitimate medical purpose. It is the proper role of law enforcement and the Drug Enforcement Administration to ensure public safety with respect to the dispensing of controlled substances by pharmacists and providers. We take this responsibility seriously.[24]

The DOJ’s recent use of criminal as well as administrative actions against individuals and companies reflects that multiple factors and industry stakeholders contributed, and continue to contribute, to the opioid crisis. The DOJ approach further reflects the government’s view that various mechanisms and strategies are necessary to punish and deter future harm.

Massachusetts at the Forefront

The aggressive prosecution of key actors in the opioid industry may be most evident in Massachusetts. As noted, the U.S. Attorney’s Office for the District of Massachusetts brought criminal and civil charges against Insys, which agreed in June 2019 to a $224 million settlement in connection with various civil and criminal investigations into the company’s promotion of its drugs.[25] To resolve the criminal investigation, Insys agreed in part to enter into a deferred prosecution agreement and pay $30 million in criminal penalties. A subsidiary of Insys also agreed to plead guilty to mail fraud. The government alleged that Insys violated the federal Anti-Kickback Statute, among other allegations, by utilizing a “sham speaker program” as a mechanism to bribe physicians and other health care practitioners into prescribing opioids.[26] Through these speaker programs, prescribers received kickbacks for generating new prescriptions for and increasing dosages of Subsys, a highly addictive opioid painkiller.[27] The DOJ settlement with Insys comes after a jury convicted five former Insys executives, including the company’s founder, of racketeering conspiracy charges.[28] In its press release regarding the convictions of the Insys executives, the government reiterated its focus on this new enforcement strategy. In particular, U.S. Attorney Andrew Lelling stated:

Just as we would street-level drug dealers, we will hold pharmaceutical executives responsible for fueling the opioid epidemic by recklessly and illegally distributing these drugs, especially while conspiring to commit racketeering along the way . . . . This is a landmark prosecution that vindicated the public’s interest in staunching the flow of opioids into our homes and streets.[29]

Massachusetts also provides an example of how state agencies are getting involved in the opioid crackdown. In one of the first cases of its kind, the Massachusetts Attorney General brought charges against eight members of the Sackler family and Purdue Pharma (“Purdue”) for misleading doctors and patients about OxyContin. The complaint alleges that Purdue is responsible for 671 deaths in Massachusetts due to opioids manufactured and marketed by Purdue.[30] Specifically, the complaint states, “Purdue promoted its opioids to Massachusetts patients with marketing that was designed to obscure the risk of addiction and even the fact that[?] Purdue was behind the campaign.”[31] The case is currently pending, after a recent motion-to-dismiss hearing where the judge took the defendant’s motion under advisement.[32]

Conclusion

As the government ramps up enforcement efforts against business entities alleged to have contributed to the opioid crisis, all industry stakeholders are impacted. Continued success by the DOJ or state agencies in these areas undoubtedly will result in increased investigations of key pharmaceutical companies, not just “bad actors” that directly interact with patients. Businesses involved in the controlled substances supply chain, particularly relative to opioids, would be wise to thoroughly review existing compliance programs to ensure that appropriate and robust safeguards are in place to prevent the improper diversion and distribution of such drugs.

‘Profits over patients’: DEA Agents discuss how traditional pill mills are on a decline


 

‘Profits over patients’: DEA Agents discuss how traditional pill mills are on a decline

https://www.foxchattanooga.com/news/local/profits-over-patients-dea-agents-discuss-how-traditional-pill-mills-are-on-a-decline

Tennessee will receive $25 million in federal funding to help fight the opioid crisis.

We’re continue our 8-week series highlighting the opioid epidemic.

Just last month, a former doctor received a lengthy prison sentence after being convicted of running a pill mill in Hixson.

A Drug Enforcement Administration Assistant Special Agent says the owner was definitely one of the main contributors to the opioid crisis here in Hamilton County.

‘Profits over patients’: DEA Agents discuss how traditional pill mills are on a decline{p}{/p}

Fred Clelland is an attorney in Hixson.

His office is just a few doors down from where Tennessee Pain Institute once sat back in 2016.

“You would have an extra 5 to 10 cars mostly on a Monday mostly early that were dropping off people mostly stay in this parking lot or mostly move to different spots in the mall,” Clelland explained.

The owner, Timothy Gowder, was sentenced to more than a decade in federal prison last month.

Court documents say he prescribed narcotics in amounts and duration not medically necessary, advisable or justified for a diagnosed condition.

“Doctors who operate in this particular way are just the same as drug dealers on the street they are criminals,” said DEA Assistant Special Agent Brett Pritts.

Pritts says Gowder and the others in the case are responsible for distributing millions of illegal pills.

He says the result is communities filled with addicts not only in Tennessee, but in Kentucky where most of their clients came from.

“Profits, a lot of it is doctors putting profits over patient care,” Pritts added.

In Tennessee, Pritts says they removed more than 125 DEA registrations from medical professions since 2014.

DEA registrations are assigned to health care providers that allows them to write prescriptions for controlled substances.

“It could be just a doctor’s practice or a business owner decides there is a market for a certain area and they establish a business called a pain clinic, hire doctors to see patients and prescribe opioids outside of normal medical practices,” Pritts said.

Now, part of the goal is to educate doctors to show them what the DEA looks for and how it investigates to keep pill mills on a decline.

We asked Pritts what are pill mill signs. He says a waiting room filled with people in and out very quickly.

Also if doctors don’t offer any alternatives to your condition than pills, he recommends seeing another doctor.

 

Lady Gaga’s Fibromyalgia Puts Illness in the Spotlight

Lady Gaga’s Fibromyalgia Puts Illness in the Spotlight

https://www.vwscircle.com/index.php/2019/09/06/lady-gagas-fibromyalgia-puts-illness-in-the-spotlight/

THURSDAY, Sept. 21, 2017 (HealthDay News) — Last year, superstar Lady Gaga took to social media to announce that she has long struggled with fibromyalgia.

The news has put the painful and poorly understood illness center stage.

The singer postponed the European leg of her 2017 “Joanne” concert tour due to what she described as fibromyalgia-related “trauma and chronic pain.”

Gaga hasn’t offered up details of her condition, although it came just before a new TV documentary about the singer premiered on Netflix — reportedly highlighting some of her health concerns.

But one thing is already clear: the disease does, at times, pull the rug out from under the performer’s best-laid plans.

“The pain and disability seen in fibromyalgia is typically worse than almost any other chronic pain condition,” explained Dr. Daniel Clauw. He is a professor of anesthesiology, medicine/rheumatology and psychiatry at the University of Michigan.

“[The pain] doesn’t just affect one area of the body you can avoid moving, and often is accompanied by severe fatigue, sleep, memory and other issues,” Clauw noted.

Dr. Marco Loggia added that “it can be extremely debilitating.” Loggia is associate director of the Center for Integrative Pain NeuroImaging at Massachusetts General Hospital in Charlestown, Mass.

“Most of the patients we encounter in our research studies are significantly impacted by the disorder,” Loggia noted, “which sometimes prevents them from having normal work and social lives.”

Fibromyalgia was first recognized by the American Medical Association as a distinct disease back in 1987, and is “a relatively common chronic pain disorder,” Loggia said.

How common? The National Fibromyalgia & Chronic Pain Association (NFMCPA) indicates that the illness affects up to 4 percent of the world’s population, and anywhere from 5 million to 10 million Americans. It is much more common among women, who account for 80 percent of patients. Although it can affect children, it is most often diagnosed during middle age.

According to Loggia, the disorder is characterized “by persistent, widespread pain, fatigue, un-refreshing sleep, memory loss, poor concentration and other symptoms.”

The NFMCPA adds that it can also give rise to sensitivity to light and sound, as well as to a degree of psychological distress in the form of anxiety and depression.

But what exactly is it, and how does it develop?

The picture is murky, with the U.S. National Institute of Arthritis and Musculoskeletal and Skin Diseases flatly acknowledging that “the causes of fibromyalgia are unknown.”

But experts suggest that the disorder is likely driven by several factors, including exposure to a traumatic event (like a car crash) and/or exposure to repetitive injuries. Central nervous system disturbances may also play a role, as might a genetic predisposition to feel pain in reaction to stimuli that most people perceive as benign.

Struggling to find more in-depth answers, Loggia noted that American and German researchers have recently identified a subset of fibromyalgia patients who appear to have abnormalities in some of their peripheral small nerve fibers.

His own research suggests that some degree of brain inflammation may be at play, given that brain inflammation is common among chronic back pain sufferers and most fibromyalgia patients suffer from chronic back pain.

Unfortunately, Clauw cautioned that the failure to identify a clear cause for fibromyalgia has given rise to the myth “that it is not real.” That, he said, is decidedly not the case.

Loggia agreed.

“Traditionally, patients with fibromyalgia have been met with a great deal of skepticism, stigma and even condescension, including by many physicians that are supposed to take care of them,” Loggia said. “Even today, their pain is often dismissed as ‘all in their head,’ not real,” he added.

“However, many studies — and particularly those using brain imaging techniques such as functional magnetic resonance imaging — have now provided substantial support to the notion that the excessive sensitivity to pain that these patients demonstrate is genuine. I think that it is time to stop dismissing these patients,” Loggia said.

What these patients need now are “better drug and non-drug treatments,” Clauw said.

“We’ve only begun to take this condition seriously from a research standpoint for about 20 to 30 years,” he noted, adding that there are no “really effective” drugs for fibromyalgia.

Loggia said that means a lot of the focus has been placed on pain management, with patients turning to interventions such as painkillers (opioids) as well as yoga and cognitive behavioral therapy. “But these interventions are rarely ‘completely curative,’” he added.

As for Lady Gaga, she likely faces a better prognosis than most.

“That this was diagnosed when she was younger is good, because many people go years or decades undiagnosed,” Clauw said. “But she also almost certainly got better recognition and treatment for her condition given who she is. Others in similar medical — but different social — situations would struggle to even find a doctor to see them and take them seriously.”

Note: This article was published more than one year ago. The facts and conclusions presented may have since changed and may no longer be accurate.

SOURCES: Daniel Clauw, M.D., professor, anesthesiology, medicine (rheumatology), and psychiatry, University of Michigan, Ann Arbor; Marco Loggia, Ph.D., assistant professor, radiology, Harvard Medical School, Boston, and associate director, Center for Integrative Pain NeuroImaging, A.A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Charlestown, Mass.

Resource: https://www.myfibroteam.com/resources/lady-gagas-fibromyalgia-puts-illness-in-the-spotlight?utm_source=facebook&utm_medium=organicsocial&utm_content=MyFibroTeam&utm_campaign=HealthDayFIBROladygaga

 

Pain Specialists Pile on CDC Opioid Guidelines

Pain Specialists Pile on CDC Opioid Guidelines

Chronic pain patients were left out to dry

https://www.medpagetoday.com/meetingcoverage/painweek/81995

LAS VEGAS — The 2016 CDC guidelines on opioid prescribing have had lasting consequences for patients with chronic pain, an expert said here.

In the 3 years since the guidelines were published, at least 33 states have enacted legislation that limits opioid prescribing, and although half of these states specify that the new limits are intended for patients with acute pain, many physicians have stopped prescribing opioids to chronic pain patients as well, according to Gary Jay, MD, of the University of North Carolina in Chapel Hill.

“[The guidelines] added to the burden of chronic pain patients who use — not abuse — medications,” Jay told a standing-room-only crowd here at PAINWeek. “Because without their medications, they’re unable to function.”

In April, the authors of the guidelines stated that the recommendations were not intended to force hard limits of opioid doses, abruptly taper or stop opioid use, or be applied to patients outside the guidelines’ scope, such as patients undergoing active cancer treatment or, in some cases, patients with chronic pain.

“The guideline is not intended to deny any patients who suffer with chronic pain from opioid therapy as an option for pain management,” wrote Deborah Dowell, MD, MPH, of the CDC, in Atlanta, in the form of a letter. “Rather, the guideline is intended to ensure that clinicians and patients consider all safe and effective treatment options for patients.”

Around the same time, the FDA also advised against rapidly tapering or ceasing opioid use based on the known harms of doing so.

But these announcements came as “too little too late,” Jay said.

In effect, the guidelines have left many high-impact chronic pain patients, who commonly have difficulty accomplishing work and self-care activities, “essentially function-less,” Jay said.

Thomas Kline, MD, PhD, a known advocate for chronic pain patients, has compiled a list of 40 patients who have died by suicide associated with forced tapering of opioids.

Jay said anecdotally that he has had patients who have done so.

Meanwhile, the discontinuation of prescription opioids may lead other chronic pain patients to turn to the street to obtain heroin or other illicit drugs to control their pain, Jay said.

“When nonfunctional patients as well as recreational drug users couldn’t access oxycodone, they found something else: heroin,” Jay said.

While overdose deaths from any opioid have increased dramatically since 2009, the number of prescription medication overdose deaths has remained low, Jay said, suggesting that other drugs, like synthetic fentanyl and heroin, are driving the epidemic.

The number of opioids being prescribed is also decreasing, despite the increase in opioid-related overdoses, he added.

“We have been told the ‘opioid crisis’ was secondary to the ‘prescription opioid crisis’ and an ‘addiction crisis,’ but these statements have never been backed up with evidence,” he said. “It is clear that the overdose deaths were the result of polypharmacy and illicit fentanyl or other illicit or illegally obtained drugs.”

All but one of the guidelines received category “A” recommendations, but are supported by the two lower categories of evidence, which rely on observational studies, randomized trials with severe limitations, or clinical observation.

According to the guidelines, they were designed to “reduce the risks associated with long-term opioid therapy, including opioid use disorder,” by reducing prescription opioids.

But while the National Institute on Drug Abuse reports that 8-12% of patients on long-term opioid therapy develop an opioid use disorder, the evidence supporting this association is mixed, Jay said. Other reports show rates of opioid abuse following long-term opioid therapy to be as low as 0.6%.

Addiction, a complex condition with a genetic basis, also differs from tolerance and physical dependence, Jay noted. In patients with genomic changes, opioid addictions can form immediately after their first exposure; just one pain pill will induce the addiction, he said.

However, in 2013, the American Psychiatric Association updated the Diagnostic and Statistical Manual of Mental Disorders, consolidating substance abuse and substance dependence into “substance use disorder.” Patients with high-impact chronic pain, therefore, may fall under this definition, since they are dependent on their medication to function, Jay said.

But despite the backlash the guidelines have received from professional organizations and patients, little has been done to change them, Jay concluded.

“Months after the FDA and CDC statements, pain physicians and pain patients are still not sure if anything changed,” he said. “While they stated the guidelines were used inappropriately, nobody has made them appropriate.”

When the right to die becomes the duty to die

Disabled 41-Year-Old Man is Euthanized After Funding for Home Health Care Runs Out

https://www.lifenews.com/2019/08/21/disabled-41-year-old-man-is-euthanized-after-funding-for-home-health-care-runs-out/

Canadian Sean Tagert, aged 41, was killed by assisted suicide after health officials decided to cut the funding for his in-home care hours.

Mr Tagert suffered from Motor Neurone Disease (MND) which is known in Canada as Amyotrophic Lateral Sclerosis (ALS). His illness reduced his ability to move his body, eat or speak, however his mental awareness remained unaffected. Doctors recommended 24-hour in-home care to support Mr Tagert.

However, Vancouver Coastal Health, initially only offered Mr Tagert 15.5 hours of care a day, which was then raised to 20 hours a day, meaning that Mr Tagert was forced to pay $263.50 a day for the remaining care that he needed to survive.

 Welcome to the great Canadian healthcare system

According to Grandin Media, on social media, Mr Tagert wrote a status which explained that two Vancouver Coastal Health officials visited his home and confirmed that they were cutting funding for his already inadequate care hours.

After receiving this news Mr Tagert wrote a number of devastating social media status’s which read: “So last Friday I officially submitted my medically assisted death paperwork, with lawyers and doctors, everything is in proper order. It’s been a month since I submitted my appeal to the Vancouver Coastal Health patient care quality department. They didn’t even respond….Welcome to the great Canadian healthcare system.”

Mr Tagert was killed by assisted suicide on August 6th.

Canada is home to some of the world’s most sinister euthanasia and assisted suicide laws, as even those without a terminal illness or those suffering from a mental illness are eligible to be killed by a medically assisted death.

Since Canada legalised euthanasia in 2016, there have been at least 6,749 cases of medically assisted deaths, with over 803 dead in the first 6 months of legalisation. 2018 saw Canada’s euthanasia figures soar with over 3000 Canadians killed by their doctor.

When the right to die becomes the duty to die

A ComRes poll found that nearly half of the British population is concerned that if the option of ending one’s life was made legal, some people would feel pressurised into killing themselves.

It is becoming increasingly evident that suicide laws could lead to vulnerable people seeing suicide as a treatment option, so as not to be a burden to others.

In a recent debate in the House Commons, MP Lynn McInnes expressed her concern at the very realistic possibility of the vulnerable being pressurised to die. Ms McInnes said: “My concern is that in the current climate, at a time of over-stretched NHS budgets and massively under-funded social care, if assisted dying was legalised, it would begin to be seen as an alternative to treatment and to care. There is a very real risk of a subtle yet dangerous culture change, in which vulnerable, terminally ill patients, come to see assisted dying as a treatment option, and indeed the best way to stop themselves becoming a burden to their families, to the NHS and to wider society.”

MP Jim Shannon also stated during the debate, that “the ‘right to die’ for the eloquent and well off would become a duty to die for the poor and vulnerable.”

We have a duty to protect the vulnerable

Director of SPUC’s Patients First Network, Antonia Tully said: “If assisted dying is legalised in Britain it could lead to a reduction in the quality of healthcare and risks promoting death as an alternative to medical treatment. We have a duty to protect the vulnerable, who deserve good healthcare and respect.”

Ms Tully continued: “Mr Tagert’s story should serve as a glaring warning to our MPs that assisted dying can make vulnerable people even more vulnerable. Assisted suicide is an inhumane response to suffering. It is a dangerous route to go down.”

LifeNews Note: Courtesy of SPUC. The Society for the Protection of Unborn Children is a leading pro-life organization in the United Kingdom.

 

 

Kevin Hart In ‘OK’ Mood and Intense Pain ..he’s still on heavy pain medication

Prevent Prescription Opioid Overdose – based on PARTIAL TRUTHS

Prevent Prescription Opioid Overdose

https://www.cdc.gov/rxawareness/prevent/

Saving lives from opioid overdose through the Rx Awareness campaign relies on the efforts of state and local agencies and organizations across the country. By sharing the campaign materials in your communities, you can broaden the reach of the message that, “It only takes a little to lose a lot.”

Get the Facts

Prescription opioids (like hydrocodone, oxycodone, and morphine) can be prescribed by doctors to treat moderate to severe pain, but have serious risks and side effects.

From 1999 to 2017, more than 200,000 people died from overdoses related to prescription opioids, with more than 17,000 prescription opioid overdose deaths occurring in 2017.

The most common drugs involved in prescription opioid overdose deaths include:

  • Oxycodone (such as OxyContin®)
  • Hydrocodone (such as Vicodin®)
  • Methadone

Overdose is not the only risk related to prescription opioids. Misuse, abuse, and opioid use disorder (addiction) are also potential dangers.

Anyone who takes prescription opioids can become addicted to them.

There are TWO KINDS OF FACTS:

Those that support your agenda …. Those that work AGAINST your agenda…

Take the figure of 200,000 people dying in the 19 yr period of 1999 – 2017 … that comes out to 29 deaths PER DAY…  a LOT LESS than the normal claim of over 100 OD drug deaths per day… that is typically quoted to describe the OPIATE CRISIS.

So what caused the other 100/day deaths…they are seeming to ignore in this press release… COULD IT BE ILLEGAL DRUGS , especially one or more of the 1400 illegal fentanyl analogs ?

Even the deaths of 17,000 in 2017… again that is 46 deaths/day …far less than the usual quote of drug OD deaths per day.

Of course in that same 19 yr time frame… alcohol would have contributed to some 1.5 + million and Tobacco/Nicotine would cause 9+ million deaths.  Those two “DRUGS” are only contributing to 1500 deaths/day….  BUT… we don’t have any discussion of a crisis involving those two legal drugs.

YES… anyone taking a legal opiate can become addicted to them… but… addiction is a mental health issue…. so prescribing a opiate to a person who is already diagnosed/treated for certain mental health issues and/or the pt has undiagnosed/untreated mental health issues… they can possibly become addicted… or the NEW TERM – opioid use disorder.

Hampering the Treatment of Chronic Pain

https://www.c-span.org/video/?188771-1/hampering-treatment-chronic-pain

The Cato Institute held a half-day conference entitled “Drug Cops and Doctors: Is the Drug Enforcement Administration Hampering the Treatment of Chronic Pain?” Members of the forum discussed the Drug Enforcement Administration’s efforts to eradicate prescription painkiller diversion and the subsequent effects on doctors, patients, and the treatment of pain.

In the first segment, members of the panel discussed pain, diversion, and public policy. The panelists also responded to questions from members of the audience.