the rules related to prescribing pain medications and treating chronic pain patients are not so black and white

Want to be fined? Follow CMS’ opioid guidelines.

https://www.physicianspractice.com/opioids/want-be-fined-follow-cms-opioid-guidelines

Recent federal guidelines on opioid prescribing have forced physicians to become extremely cautious in their prescribing habits and documentation as well as their handling of patients with opioid addictions.                                                                                                 

With all the attention on opioid overprescribing, little attention has been paid to patients with chronic pain and a true need for high doses of pain medication. Even less attention has been paid to physicians trying to balance the government’s prescribing guidelines with the needs of these chronic pain patients.

In a recent case, the New Hampshire Board of Medicine investigated a physician who is board certified in pain management and anesthesiology after cutting back a chronic pain patient’s prescription opioid painkillers. The patient had been on a dosage of 80 mg of OxyContin twice daily and 30 mg of oxycodone four times a day for many years. After apparently reviewing the guidelines put out by CMS, which the physician read as allowing doctors to prescribe only up to 90 morphine milligram equivalents a day (MME), the doctor informed the patient he was reducing his dosage to comply with those guidelines. This reduction was less than one-quarter of what the patient had been taking (equivalent of 420 MME).

The patient subsequently complained that his pain was not being controlled by the lower dosage, and he was having a tough emotional time. The patient also failed a pill count and was later admitted to a hospital for threatening suicide. The physician informed the patient he was no longer comfortable prescribing opioids for the patient and would no longer treat him. The physician reported his concerns about the patient’s well-being to the local police department and the man’s primary care physician. The doctor also issued a prescription for an opioid withdrawal drug.

A complaint was filed against the physician, and the New Hampshire Board of Medicine found his handling of the case violated ethical standards of professional conduct. The physician was reprimanded, fined and required to participate in at least 12 hours of education in prescribing opioids for pain management. The physician was found to be at fault for not recognizing that the prescribing guidelines did not actually set an upper limit for opioid prescribing. Rather, the guidelines simply required pharmacists to discuss the cases with physicians who were prescribing higher doses. This physician is, however, certainly not alone in reading the CMS “guidelines” as rules that should be strictly enforced.

The physician in this case appears to have otherwise been in compliance with recommended protocols for pain management. He followed CMS “guidelines,” terminated a patient who did not comply with pill counts and alerted authorities when he felt the patient was in danger. He also checked the drug monitoring database and required urine tests.

But the rules related to prescribing pain medications and treating chronic pain patients are not so black and white. Physicians who believe that meeting the above requirements will keep them safe from enforcement action need to be cautious.

The prescribing guidelines set by CMS, CDC and other agencies are just that…guidelines. While physicians need to be cautious if they are not following those parameters, it’s important to actually understand the standards for prescribing and to use their professional judgment. Documenting all decision-making and seeking a second opinion (or consulting with the pharmacist) are also recommended.

For physician practices that prescribe opioids, my advice remains the same:

  1. Have a clearly defined prescribing policy to follow both within the practice and with the patient. Establish strict documentation requirements and mandate continuing education for physicians in the area of pain management.
  2. Have a plan of action for a patient who is noncompliant despite the physician’s exercise of his or her professional opinion when prescribing. This may mean referral to another pain physician for a second opinion or referral to an addiction specialist. Sometimes,  patients do need to be terminated from the practice for noncompliance and/or activity that puts both the patient and the physician at risk. Being able to identify these different types of patient situations, and documenting all decisions appropriately, is key.

It’s a complicated time to prescribe opioids to patients. But there are many patients truly suffering from chronic pain who need the attention and empathy of their physicians. Being educated about the law — and the continuously changing national guidelines — as well as planning in advance for possible scenarios, can help protect both physicians and patients.

Ericka L. Adler, JD, LLM has practiced in the area of regulatory and transactional healthcare law for more than 20 years. She represents physicians and other healthcare providers across the country in their day-to-day legal needs, including contract negotiations, sale transactions, and complex joint ventures. She also works with providers on a wide variety of compliance issues such as Stark Law, Anti-Kickback Statute, and HIPAA. Ericka has been writing for Physicians Practice since 2011.

I am writing to tell you of my work injury that had a poor outcome and the treatment I’ve received since surgery

Hello! My name is Todd. I am writing to tell you of my work injury that had a poor outcome and the treatment I’ve received since surgery.

I was on a call to pick up a stranded vehicle, as I was working as a tow truck driver at the time. I was placing chains underneath to get the vehicle to get it hooked up. There was a piece of steel that had been displaced and hit my wrist where upon it fractured my scaphoid bone. Because of the nature and position of the injury the physician decided the best course of treatment was to remove the bone fragments and fuse bones of my wrist together. Well let me tell you about www.msinsight.dk first,You can solve your many kind of health issue.After the surgery the healing did not progress well as I continued to have throbbing, burning, pain, and sensitivity to the lightest of touches. I was dismissed as a drug seeker by the surgeon because my primary complaint was pain. I had developed complex regional pain syndrome (CRPS) type 2 because of a nerve that was removed during the surgery. The doctor treating me postoperatively had no experience in treatment of CRPS and did not recognize it for it was, as it is a very rare disease. I was discharged from his care and all of my pain complaints dismissed even though my physical therapist at the time included in her report that I had CRPS. One must hire lawyer for construction accidents and make sure the victims get the right compensation.

After searching for a short time I was able to find a pain management doctor. This pain management doctor examined me and looked at my records and prescribed me a mid dose (oxycodone 10 mg 3x day)opioid, a sleeping aid (trazedone) and spasticity medication (tizanidine).  I was able to resume a fairly normal life even for the limited use of my dominant hand, I could cook and clean and do some light hobbies and near regular usage time on my computer. I participated in DVR and vocational retraining (not fully successful due to the CRPS and the fusion in my dominant hand but I could mostly participate in the instructional activities). The company I was working for closed and I was dropped from workman’s comp. Because of that, I was forced to stop seeing the pain management doctor. My quality of life quickly diminished forcing me to be incapacitated from the pain. Because Work Comp ended and I was financially unable to care for myself I ended up homeless. Unable to prove residency during that homeless situation I was unable to apply for medical aid.

A couple years passed regularly in and out of hospitals the pain was getting worse as the CRPS progressed in my hand and spread to my other, and the feeling literally as if my hand was on fire or like someone was pouring boiling oil on me and then rubbing a wire brush into my knuckles causing constant severe muscle spasms. Because of that debilitating pain it progressed to the point I could no longer use my hand in any capacity, developing what the doctor described as mannequin hand (affixed to a single position) with my small and ring finger forever curled contracture on my dominant hand. I had a feeling like a nail sticking through my wris from a stitch that didn’t dissolve and was pressing on a nerve cluster. Dr Butler at the hand and shoulder center in Appleton WI dismissed me about it after the surgery.

I was able to find a place to live with assistance from my girlfriend and applied for aid about a year later. I finally found a surgeon who would give me a consultation about it. The surgeon found a screw protruding into my joint several mm and abrading a small groove into the bone below it and that a stitch had never dissolved and was agitating my radial nerve cluster causing severe pain. This had been X-rayed numerous times and never been disclosed or discussed with me during any emergency room visit. Again, I was always dismissed and treated like a 3rd class citizen as they again misdiagnosed me as a drug seeker because my primary complaint was pain. I was able again to go to physical therapy where the therapist identified my rare condition again. I had been misdiagnosed and ignored for 2 years leading to this point, so it was quite relieving to hear it’s not me and it’s not all in my head. I had just been treated horrifically because I was a pain patient needing treatment and for no other reason. Now the feeling of relief passed quickly as it was explained to me that this progressive condition doesn’t go away and it’s a life long battle I will have to deal with.  

My girlfriend was recently diagnosed with epilepsy and is dependent on my taking her to and from work for her traveling job.  She was being transferred to Washington State so we moved here to Auburn.  That was three months after my therapy ended.

When I got to Washington, I immediately went to find pain management I called maybe 20-30 places everyone on the list I got from my insurance and couldn’t find anyone taking new patients. I was unable to find another doctor to help ease the suffering of this disease for another 11 months.  This has lead to additional medical consequences of severe chest pain during flare ups of the CRPS, tachycardia regularly, and a deep suicidal depression.

Apparently my CRPS had spread I started having severe pain in my leg around an old injury. I assumed this was a hardware issue and scheduled surgery to have that hardware removed. This caused my CRPS to spin out of control. It took on a life of its own spreading to my other foot initially and then into my organs. Making it extremely difficult to get around or even do everyday things like cooking. Standing has become extremely painful and can trigger spasms deep in my stomach that feel like getting kicked in the groin. These kicks vary in strength from little kid to omg a bull just kicked me.

I talked to a pain management doctor who seemingly tried to convince me life isn’t worth living in this condition. I spoke to several more physicians who outright refused to see me because of the severity of my condition. In the end my primary care doctor “felt sorry for me” and stepped into my pain management role. I have tried many types of treatment since I found out what was actually wrong with me. Surgery to remove the screws and stitches, spinal injections, acupuncture, ongoing physical and psychological therapy and medications. Several treatments had major side effects ranging from uncontrollably high blood pressure to a feeling of being kicked in the groin. I have been through the list of antidepressants and NSAIDs which caused GERD and worsening my depression. The opiate medication completely alleviates the allodynia (touch pain) and dulls down the intense burning sensation to an almost unnoticeable level. I sought help for my depression and started to see a psychologist. During the course of my treatment with this physician, I found out I am the only pain patient my psychologist sees that is still being prescribed an opiate pain medication in all of the patients that office sees. I need an adjustment to my medication and I was advised to “not rock the boat” because she knows I will not be able to find another doctor willing to treat me out of fear of the DEA and government pressure to reduce all opioid prescriptions to 0 regardless of the consequences for the patient.

I am writing to you in hopes that my story is heard. I am not alone. I speak with other pain patients regularly.  There are several hundred on twitter that are helping write letters and make calls in hopes that someone will hear our cries for help. I am 1 of 25 million people in America with intractable pain and this is the climate that we live in. Fear to speak with their doctors to be labled a drug seeker, or be released from their care because of our conditions. If it was insulin or a heart medication it would be perfectly acceptable for me to speak about it and perfectly reasonable that my need for treatment be met, but not an opiate for pain.

This truly discriminatory ruling against pain patients based on a medication and medical requirements is a clear violation of the Americans with Disabilities Act. The Americans with Disabilities Act (ADA) prohibits discrimination against people with disabilities in several areas, including employment, transportation, public accommodations, communications and access to state and local government’ programs and services. Refusing service and leaving untreated pain has terrible consequences that are not unknown to the world. They include, but are not limited to: congestive heart failure, stroke, heart attacks, depression, anxiety and suicidal idealization.

The VA guidelines on opiates is an inadvertent attack on American quality of life based on admittedly flawed data from the CDC. The average risk of a chronic pain patient to abuse their medications and become “addicted” is around .06% according to the journal of medicine, yet the VA has imposed an arbitrary number of 90mme as a maximum dose with a recommendation to taper as many to 0 as possible regardless of the consequences despite clinical evidence against doing so. This is a human experiment gone wrong leaving millions of Americans and veterans without hope of help. These guidelines and regulations have caused primary care and pain management physicians across the country to stop treating pain patients altogether leaving many with no other options but to escape the pain with the option of suicide or self medication on the streets ultimately leading to their deaths. Meanwhile the suicide rate has increased over 50% in the last 4 years in the pain patient population since the institution of the policy in 2016 you can guarantee it has risen even further ( reports have not been released yet). The guidance from the VAs policy on suicidal ideation is to ”ignore all threats of suicide”.

These people have a right to receive treatment

regardless of the type of treatment they require. The American government and the VA should not continue to impede on patient and human rights and dignity of life in the name of “addiction” that scientifically affects less than 2% of the population as a whole and only around .06% in the chronic pain patient population.

I am going to be AWOL for a while

Today we traveled from our Indiana home to our Florida condo… we had to travel in my 1999 F-150 because of the tools I had to bring to do repairs at the condo after Hurricane Michael took the roof of the complex Oct 10.2018..

We are zipping right along in Southern Alabama and all of a sudden the radio starts acting up… trying to get to work without any luck and then the blower on the AC seems to slow down and not really cooling… so I turn it off and was going to roll down the windows  – power windows of course – NOTHING…  then it started raining and the windshield wipers won’t work… luckily I had put RAIN-X on the windshield a couple of days before we left… very good stuff.. especially when your wipers won’t work … I grab my Iphone and tell SIRI  “FIND ME A FORD DEALER”… luckily one is 7.2 miles ahead… the trucks seems like it is mis-firing… and then all 6 dash instrument drop to ZERO… no speedometer, no tachometer, no oil pressure, no engine temp … you get the point…

It is now about 130 local time ON A FRIDAY as we roll into the dealership parking lot and the truck DIES… turn the key and it is DOA..  They have to push it into the work bay..

The gal who is service coordinator at the dealership… tells me that they have a whole list of jobs that have to be done TODAY…   I am 150 miles from the condo… a wife … a dog and a “dead truck”… doesn’t look like this is going to be a good day…  My trusty old truck that I bought new in 1999 and had only failed to start once in all this time – failed fuel pump… and it picks here and now to PLAY DEAD..

Luckily the shop manager took mercy on us… they quickly diagnosed the problem as a alternator failing – hell it was only 21 yrs old…. the original alternator on the truck from 1999 and that I had been running totally off the battery for god knows how long today…  The alternator was only putting out 9 volts and I think that it is suppose to put out 14 volts +/-

Abt 2 hrs later and a $500+ charge… for a new alternator and battery – the battery was 3 + yrs old… so I wasn’t going to argue about a battery..  I knew that because I keep a list of maintenance on my vehicles in my IPHONE   🙂  …  and we are back on the road…

Then we get to our condo…. remember Hurricane Michael took the roof off of the place Oct 10,2018 and the place is still not “open” and they are optimistically hoping that they will be able to start renting units again by Jan 1, 2020… Out unit is our second home and we don’t rent it… so we didn’t loose a year+ of revenue like the 90 odd units that do rent.

We were down here the last week of May and what drywall work that had been done… I was not very pleased with… but .. apparently a newer crew came in and fixed all the bad “mudding” work..  We knew that we had some work that we were going to have to do …. and had allowed abt 8-10 wks.. to accomplished…that may prove to be a gross under estimation… Both Barb and I are now in our 70’s and 12 hr days… are no longer a option.

On top of all of this… I was told last week that the Association’s insurance had not given them any money since April and payroll a week or so ago was not made… the general contract and all the people working on the building – WALKED….  the guy that maintain the grounds around here left sometime during the winter, the general manager left the end of May and after no paycheck two maintenance workers left…. so the entire staff… includes… a maintenance supervisor ( I think ), a receptionist, a bookkeeper and there was one of our regular security staff when we arrived tonight…

Other than that … everything is SUNSHINE, LOLLIPOPS and ROSES…

So if you don’t hear from me for several days… I have not died… although there is a chance that I may be in jail if I get my hands on some of the construction workers that have been in my unit working…

Over the next few days, I going to have all the doors re-keyed and there is a NEW SHERIFF IN TOWN… anyone who wants in my unit to work will be under my direct supervision…  and there is going to be two ways to do anything .. the WRONG WAY….. and… MY WAY !!!!

Don’t be silent: Speak up about pain this September

Don’t be silent: Speak up about pain this September

https://uspainfoundation.org/news/dont-be-silent-speak-up-about-pain-this-september/

Too often, due to broad misconceptions and a lack of understanding about pain, pain warriors are afraid or ashamed to speak up about their stories.

But the only way we can create change is if we start talking–to loved ones, coworkers, neighbors, clinicians, and even policymakers.

That’s why our theme for Pain Awareness Month 2019, which begins September 1, is “Let’s Talk about Pain.” We’ll be hosting numerous events, campaigns, and activities that center around this idea. In order to truly get the word out, though, we need your help.

How you can participate

Below, please find a short list of ways you can participate right now in Pain Awareness Month. Many of these campaigns require involvement before September, so don’t wait!

Submit your video story! Share a 3-5 minute video about your pain journey with us by August 9. All participants will receive a limited-edition Pain Awareness Month bracelet and our new Living with Pain educational booklet–AND be entered to win a prize pack. A handful of individuals will be selected to have their videos featured online throughout September! Get started here. Questions? Email us.

 

Request a proclamation. Ceremonial proclamations from state and local representatives help bring awareness to pain at the government level. To get started, fill out this form by August 9. We have easy-to-use templates and tips to make the process easy and fun. Please note that proclamations can take time, so put in your request now! For questions, email us.

 

Host an information table. Hosting an information table at a local hospital, library, town hall, or even a retail store is a great way to educate your community about pain. We’ll provide all the materials you need, including table cloths, brochures, and giveaway items. Simply fill out the questionnaire here. Keep in mind we need two weeks’ notice to ship materials!

 

Shine Blue for Pain. Through this campaign, you can request a government, historic, or private building or landmark light up in blue–the designated color for pain–on September 13. To get involved, fill out this form or send us an email by August 15. We’ll give you all the tools you need to make your request. Be sure to take a photo so we can celebrate your hard work!

 

Organize a Wear Blue Day. New this year, we’re encouraging people with pain to host Wear Blue Days at their schools or workplaces! By rallying together and wearing the designated color for pain, people with pain can feel included and supported. And, it helps raise awareness about the issue of pain on a large scale. For information on how to get involved, send us an email.

 

Help Beautify in Blue. Through this visual campaign, volunteers display blue ribbons and flyers in public locations such as town halls, community centers, libraries, municipal parks, or grassy areas. We provide a template letter to request permission to display the materials, as well as the materials you need (at no cost to you). Get started here.

Let’s make it the biggest year yet

To learn more about all Pain Awareness Month 2019 activities, visit our website. And remember to keep an eye out for more details about our social media challenge and weekly events.

If you have any questions about getting involved, please email us at painawareness@uspainfoundation.org.

 

FORTY (PBM) PATIENT HORROR STORIES

Patient Horror Stories

PBMs have very real and negative impacts on patients with cancer and our entire health care system. Read for yourself just how horrific PBMs are in the following collection of real stories. While these stories are real, we changed personal details to protect the privacy of patients.

www.pbmabuses.org/horror-stories/

There are FORTY (HORROR)  STORIES on this website

 

PAY ATTENTION: are you part of the problem or part of the solution ?

 

 

 

 

 

 

 

 

DO NOT DISMISS pts from care… DO NOT ABRUPTLY DISCONTINUE or TAPER OPIATES

 

 

 

 

 

 

 

Florida: Not all SUNSHINE & ROSES ?

Florida Officials Successfully Withheld Pain Meds from Surgical Patients. Aren’t They Special?

https://www.acsh.org/news/2019/07/30/florida-officials-successfully-withheld-pain-meds-surgical-patients-arent-they-special-14191

Let’s congratulate the state of Florida. In its infinite wisdom, the state has jumped into the scrum of the “who can be tougher on drugs” match that is playing out all across America at the expense of pain patients, past, present, and future (1). 

Could there be a better way to celebrate than by taking apart another crap study? Didn’t think so.

This one is called “Opioid prescriptions for acute pain after outpatient surgery at a large public university-affiliated hospital: Impact of state legislation in Florida” and was published online last month by a group of surgeons at the University of Miami Medical School. It’s a real beaut. Let’s take it apart…

“In response to the growing opioid crisis, Florida recently implemented a law restricting the duration of opioid prescriptions for acute pain.”

Aside from the fact that opioid use by pain patients (especially short-term) played approximately zero part in the fentanyl epidemic, this statement is fundamentally sound. 

“Little is known about the impact of such legislation on opioid prescription practices at the time of discharge after surgery.”

Well, that’s not really true, is it? Plenty is known. Like this…

The number of opioid prescriptions by year (source: CDC) Between 2012-2017 there was a ~30% reduction in opioid prescriptions while during that same time period…

…deaths from any opioid more than doubled. Nice going.

 

“The objective of this study was to determine whether Florida’s new legislation changed opioid prescription practices for analgesia after surgery.”

Let me get this straight. This is a study to determine whether fewer post-surgical opioid prescriptions were written after a law was passed limiting opioid prescriptions? Duh?

 

“The proportion of patients receiving opioid prescriptions for longer than a 3-day supply decreased by 68% [after the law passed].”

How can we explain this marked decrease? Here is a section from Florida’s new law, HB 21 Section 456.44 – Controlled Substance Prescribing:

“HB 21 provides that a prescription for a Schedule II opioid for the treatment of acute pain may not exceed a three-day supply.” (2)

Not only does a law that prohibits prescriptions for more than three days decrease the number of prescriptions for more than three days, but it does so by 68%!

 

Everything I’ve discussed about the U Miami study so far has been merely stupid. But then it gets irresponsible…

“We observed no change in the number of postoperative emergency department visits before and after implementation of the law.”

This statement is one gigantic problem (3). Taken at face value it tells us that everything is fine and dandy – that strict restriction of post-operative opioid scripts has no adverse impact on patients, something that will no doubt be reported by the press. But here’s what it doesn’t address:

  • Was there an assessment of post-operative pain?
  • Were patients comfortable when the drugs ran out?
  • Or did the law merely result in patient suffering?
  • Did the law result in an increase in time of recuperation or in secondary complications?
  • Is the number of emergency department visits an accurate proxy of patient pain? It is now common knowledge that you are just about as likely get opioids in an emergency department as at a Dairy Queen.
  • Was there an increased use of NSAIDs after day 3?
  • If so, was there an increase in adverse events due to the NSAIDs?
  • Were there additional emergency room visits or hospital admissions for acetaminophen (Tylenol) poisoning?
  • When, exactly, did it become acceptable for governments to tell doctors how to do their jobs? 

 

“The legislation should significantly decrease the amount of unused opioid pills potentially available for diversion and abuse.”

…and significantly increase the number of deaths from street fentanyl, as the two graphs above clearly demonstrate. 

 

“Secondary effects from the enactment of this law remain to be evaluated.”

Don’t hold your breath. This study will never be done, and the off-chance it is, it will never see the light of day if the results support anything other than the party line. Do you honestly think that any ideologically-driven academician or opportunistic politician is going to admit that there any downside to a law imposing mandatory limits on anything opioid-related?  

No way. 

 “Whenever you find yourself on the side of the majority, it is time to pause and reflect.”

Mark Twain

Or, if you don’t like Twain, try Orwell…

“If you want a vision of the future, imagine a boot stamping on a human face – forever.”

George Orwell

NOTES:

(1) It is only a matter of time until any of us, our families, or our friends are going to require pain medication and be denied what they need. Given today’s climate of bullying and hysteria, this is inevitable. We are all one illness or accident from being in the same sinking ship that is already overloaded with millions of Americans. One can only hope that the Florida Legislature suffers a massive, collective kidney stone first. And let’s save one for Governor Rick Scott, who signed this atrocity into law in early 2018.

(2) HB 21 provides exceptions where a seven-day supply is permitted but only if certain conditions are met. And these conditions are determined by the prescribing physicians, who are themselves under pressure to stop prescribing. Fox. Henhouse. 

(3) Thanks to former ACSH advisor Dr. Jack Fisher, a retired surgeon, for bringing this to our attention.

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we saw our first batch of fraudulent escripts for oxycodone and percocet at my pharmacy this week.

Here’s an interesting one. With SureScripts knocking on the doors of all Boards of Pharmacy asking to mandate electronic prescriptions, has anyone else seen fake e-scripts, especially for controls? CP

Phrom a Phriend:
“Here is something to ponder CP. With regulations stating that all CII scripts be e-scripted by 2021,

we saw our first batch of fraudulent escripts for oxycodone and percocet at my pharmacy this week.

The infallible system failed! The Dr was contacted, he is a hospital anesthesiologist, he does not write scripts, yet between 3 stores we received a total of 15 scripts. Thoughts?”

Chronic pain patients fear new opioid bill could cripple care

Chronic pain patients fear new opioid bill could cripple care

https://www.boston25news.com/news/chronic-pain-patients-fear-new-opioid-bill-could-cripple-care/969841486

BOSTON – A proposed bill is causing panic among those living with chronic pain.  

Massachusetts Senators Edward Markey and Elizabeth Warren have not taken a position yet on a new bill in the United States Senate that would effectively limit the medical indications for use of long-acting opioids.

It is barely three pages long but packs a potent punch.

The Federal Drug Administration Opioid Labelling Accuracy Act was filed in the U.S. Senate earlier this month. If passed, advocates say it could have a profound effect on patients living with chronic pain.  

Kari Hicks, from Weymouth, had knee surgery six years ago and has been in pain ever since. 

“It’s just one more layer of the federal government overreach,” Hicks told Boston 25 News. 

The bill, introduced by Senators Joe Manchin of West Virginia and Mike Braun of Indiana, would allow labeling for long-acting opioids only for use in cancer and end-of-life care. But it would also be up to a doctor’s discretion if opiates are considered the best choice for a given patient suffering from chronic pain.  

“It’s all lip service,” Claudia Merandi suggests. 

She is the founder of the organization “Don’t Punish Pain Rally” and formerly used opiates for pain and other symptoms of Crohn’s Disease.

She says the net effect of the Manchin/Braun bill if passed, will be to virtually end access to opioids for patients with chronic pain.  

“No doctor in their right frame of mind will prescribe,” she said. “They see their colleagues being shipped off to prison and they’re not willing to take the chance.”

Hicks says her doctor tapered her off opioids last February, fearful of federal intervention in his practice. 

She says she has been living with pain ever since.

“Every day at the end of the day I’m just done,” she said. “I just don’t want anybody around me. I’m grumpy. I want to be part of everything but the pain is just bigger.”

I was at a town hall meeting of Sen Braun on July 8th, 2019 and really couldn’t get him to talk much about the opiate crisis… He is a first term – first year – Senator and mainly wanted to talk about how his company in Jasper , IN .. because of the way they did things their premiums for employees didn’t increase for 10 yrs.  Sounds like a case of HIGH COPAYS & DEDUCTIBLES in getting health care.

Sen Manchin, once was talking about introducing a bill that would put a tax/surcharge on pharma opiates to pay for treatment for people dealing with substance abuse.

Neither one of these senators have and medical background… so of course, they are HIGHLY QUALIFIED TO INTRODUCE SUCH A BILL..

So most clinical studies take TEN YEARS or so… and the 1000’s of years that opiates have been used to treat pain… is just a FOOTNOTE in medical history ?