Wednesday, August 28, 2013

The Powers That Beat From amazon.com: http://amzn.to/12GylaP





From amazon.com: http://amzn.to/12GylaP


Posted by Picasa

Editorial Reviews

Product Description

Bringing you the best of the best from the Autism and Asperger's support community. Hear from parents, professionals, advocates and people with Autism Spectrum Disorders. Additional posts about health law, technology applications, research developments and education.

Kindle blogs are fully downloaded onto your Kindle so you can read them even when you're not wirelessly connected. And unlike RSS readers which often only provide headlines, blogs on Kindle give you full text content and images, and are updated wirelessly throughout the day.


Product Details

  • Publisher: Elyssa D. Durant, Ed.M. (February 18, 2013)
  • Sold by: Amazon Digital Services, Inc.
  • Language: English
  • ASIN: B00BHUVCDG

5.0 out of 5 stars Unique and insightful

This review is from: Powers That Beat (Kindle Edition)
Ms. Durant has drawn on her sterling academic background and extensive experience in health services policy development and actual service in the field to present a comprehensive analysis of the organ transplant situation in the United States. She thoroughly discusses all aspects of the situation - not only legal and medical, but also moral, social and ethical aspects and the dilemmas faced when this topic is addressed. Ms. Durant raises significant questions that must be addressed as organ transplants become more commonplace in today's times. A thought provoking book that should be read by everyone as this question touches every American. Highly recommended.

J. D. Yencharis
NASA Mission Planning & Mission Control 


When Elyssa writes something, you should read it. She is one of the most intelligent and articulate people I have ever known. She is an amazing researcher and really digs deep for the important facts on any topic she focuses on. If you want to learn details about a topic and get some cutting edge viewpoints related to it, read anything Elyssa Durant writes.
Stuart Silverberg, Ed.D.
Columbia University

Ms. Durant has a talent for explaining complex legal issues in interesting, accessible format. Her level of expertise on the subject matter is impressive and comes through on every page.

Rick Silver, Esq.

Ms. Durant has drawn on her sterling academic background and extensive experience in health services policy development and actual service in the field to present a comprehensive analysis of the organ transplant situation in the United States. She thoroughly discusses all aspects of the situation - not only legal and medical, but also moral, social and ethical aspects and the dilemmas faced when this topic is addressed. Ms. Durant raises significant questions that must be addressed as organ transplants become more commonplace in today's times. A thought provoking book that should be read by everyone as this question touches every American. Highly recommended.

Ray Harris
Advocate for People with Disabilities

Ms. Durant has an amazing ability to discuss complex policy issues in easy to understand language. She has a tremendous grasp of her topic and of her audience. Easy to read and understand; Ms. Durant explains difficult concepts and evolving health care law and policy issues in a user friendly manner. A real eye opener!

Karen Baker, MSW 


I just want all to know what a Hero for the Autism community Elyssa has been for us and how much we appreciate her advocacy and intelligent posts. AutismAid has been a dream of mine for ten years. my heart was just about broken when others took advantage of us. I know that in the end we meet people who we connect with and do the right thing. The 13 Service non profits under the AutismAid Umbrella and many others are in the fight for their life in this economy and environment. This Web and viral traffic is great. Thank you providing the support, documentation and logistics are needed to make the event happen.

Tim Welsh, Executive Director
AutismAid.org



From amazon.com: http://amzn.to/12GylaP

Tuesday, August 27, 2013

UNWRITTEN: Patient File and Formal Apology

August 2006

Elyssa - thanks for continuing to update us on DB. I received an email from Eric Henderson who has been looking into DB's case. 

According to his information there was a CFTM schedule for DB, transitional living staff, etc. on 9-6-06 and she did not attend. In the email, Eric states that DB signed for a certified letter regarding the meeting in August. 

This meeting might have been a way for DB to meet everyone face to face to discuss her needs, etc. From her past experience with DCS, I wondered if she was discouraged about meeting with them or felt it might be more of the same old, same old." 

You probably have the best rapport and insight into how she if feeling with the situation.

Is DB at the place where she can follow a program, rules, or guidelines that might be required by certain programs, etc. to receive housing, services, etc.? 

In my experience working with many older foster children they can be so tired of all this with the system, that they basically shut down when needing to access services, etc. after aging out. 

Does she need a case manager or support that she can partner with for these meetings and contacts that will provide the consistent "cheerleading" when perhaps she cannot she the forest for the trees (needing to attend meetings, follow expectations, file forms, etc)? 

My reason for asking these questions is to get your perspective on where DB is in being able to access resources and then maintaining them (again relating to following a program, etc.) 


[Redacted] CMSW 
Assistant Statewide Program Coordinator 
Office phone: 615-269-7751 
1315 8th Ave. South
Nashville, TN. 37203 
Mark Your Calendar's Now !!!!!!!! 
TVC's State of the Child Conference 2006 
October 16-18, 2006. For more info, visit our website, www.tnvoices.org



 



 
 

POST SCRIPT: Transportation never showed up to take DB to the meeting. As a member of the team and DB's primary counselor, CM and the person who requested the meeting to help advocate and secure services for my former client, I was not at the meeting because the state conveniently forgot to tell me when and where it was. 

DB later informed me that did go to a meeting and sat alone on one side of the long table in the conference room and had no one there to defend, advocate, or support her throughout the meeting.  

She was not offered ANY post custody services and was too intimidated to speak or advocate for herself with five to seven state employees sitting on the other side of the table blaming her for their mistakes and denying services that she was legally entitled to under state and federal law. 

She left that meeting with no services, no benefits, no hope, and no recourse. 


DB if you are reading this, please know that your story needs to be heard. 

In a court of law. I saved your records and gave them to an attorney for your protection. 

I hope you sue those fuckers for what they did to you and so many others. 

Your file was audited and I submitted a report to TVC and TCCY that your case file had been falsified by the for profit agency that pimped you out for $60/day. The court knew this because I called Carrie and told her. 

She told me that she was too busy to be bothered bringing you in two months before your eighteenth birthday. 

I did pick you up much to everyone's horror, and they were pissed that I managed to locate you just in time to benefit from post custody benefits that would entitle you to educational expenses, housing, transportation, healthcare, and transitional funds to get you started.  

That was an illegal placement and when I resigned, I left the agency because they refused to comply with federal laws and I refused to sign a false treatment report. 

Your file was audited and my signature was forged by KM. 

He used white out and didn't even try to color between the lines or match my handwriting. 

Two of us quit that day. Both of us will testify on your behalf. 

I'm sorry I couldn't do more. Your file is available if you need it. 

Be well, sweet girl and Happy Birthday. 

-Miss Elyssa

Wednesday, February 20, 2013

The Last Goodbye

I can no longer protect the one who hurt me the most, and I officially declare myself as independent and free.

Goodbye for now to The Powers That Beat, I am growing so tired ofthat nightmare where I cannot move my feet.

I am one today, but I am not alone; my DNA and birthright does not make me a clone.

Any genetic disorders, whatever they may be; will never again stand in the way for my fight to be free.

My bloodline alone comes right back to you, and your ridiculous denials are nothing new.

I must protect myself from your twisted mind, never forget, late last night, you left me behind.

You may think I have forgotten all your hysterical pleas, but I am legally required to remind you of these.

I hope you are ready for what lies ahead, because I do not think anyone else will agree this was all in my head.

You may dispose of my photos, writings, and more, I am sorry you do not realize you have officially now escalated funny money into a full-fledged war.

You declared this yourself, on March the Fourteenth, and I will expect it in writing before the next April 15th.

You no longer manipulate my ID or actions and blame; for I am not the one who falsely claims to be poor.

You may find it a little bit harder to blame it on crazy and point the finger at me; I am posting it here for the whole to see.

Do not blame my siblings or my father's new wife; material wealth should mean more value than your own child's life.

I got excluded from the human genome, stop feeding me crazy, just bring it back home.

The suicide note I once left in your possession, should no longer be guarded as your greatest protection.

I defy the heritage that left me broken inside; any tears I have shed will finally subside; I no longer will allow myself to be tried by the ridiculous facade that has given YOU a false sense of pride.

I am now on my own, as was always the case; it is so very sad you thought of this as a race.

I will honor your request to sever all ties; it is long overdue that I be free from your lies.

I never signed on to your game of deception, there was much more at stake than a strangers' perception.

So just as you once photographed my tattoo, sadly but surely, this one joke is on you.

I doubt you heard my very last words, but they were words of sincerity I hope that you'll review because my concern was genuine; just too familiar, we discussed nothing new.

I defy my heritage and reject your faith; I think I am worth more than an aborted mistake.

I declare my freedom and reject your "good faith" I am sorry you believe I was your biggest mistake.

You are so transparent it is easy to see, I hope you leave this behind the same way you left me.

My bloodline runs deeper than your maternal pride; I pray for your sake psychosis is real, for I see no other way your pain will ever be healed.

I am over and done with this stupid game, I gave you more than one warning to amend your tax claim.

So as I fight for my freedom, my health and my name, I hope your psychosis protects you from shame.

I must no longer allow trauma to guide me through life; I cannot worry about details as you become a new wife, you are correct in your assessment that you have earned all the "things" you cling to for dear life.
 
If there ever was a time to say, "This too shall pass...," then please go ahead and kiss my tattooed fat ass!





ELyssa Durant, Ed.M. © 2009-2013

Tuesday, February 19, 2013

New York Voices: A Letter To My Former Therapist

A Letter To My Former Therapist
Elyssa D. Durant, Ed.M.
« Article 1 of 29 »
Hi Elyssa,
It's nice to hear from you, I had just been thinking of you. Is there a reason why you sent me two copies? Talk to you soon—Elyssa's Former Therapist

Now how can you call yourself a qualified therapist and ask me such a stupid question? I have at least two of everything!

So my alter-ego as a "cyberwhore" is no longer a secret! I always send duplicate copies of every outgoing e-mail to myself to a number of free-mail accounts. Most have probably expired and I can't even remember most of the passwords to access them, which leads me to wonder what happens to my written works that I have so carefully created? Do they just float around in cyberspace forever? Are my words now immortal? Does that make me grandiose or paranoid?

I had my first appointment with my new psychiatrist on Wednesday and he seems very "eager" to help. He is a very young resident, and I think he is kind of psyched that he got placed at Vanderbilt in Nashville rather than some community mental health center in rural Tennessee. For his training, he needs a number of hours conducting therapy—so I graciously agreed to be one of his guinea pigs. I negotiated a one-hour session every other week.

I hate therapy. It seems so staged and rehearsed. I actually spend hours before a session trying to think of what I should say.

That never seemed to work with you. That kind of annoyed me, because I wanted you to play the game with me. This is the way it is supposed to work: I'll tell you what happened as a child, and you tell me the source of my insanity.

I would try to remember the random things that happen each day and let you know that I was telling you the truth about my life, my world, and my family. On many occasions, I would forget my zinger, my "punch-line" if you will, and I would be so disappointed in myself. I would drop these little tidbits of information hoping you would recognize that I was not completely beyond help, and you might understand the method to my madness. Would that make it okay to be so fucked up? Loony. Crazy. Nuts.

You never once said, "Aha!" Instead, you would listen impatiently as I reflected on childhood traumas. Even the most elaborate reports of my childhood experience did not make you flinch—well, maybe a few times! At what point did you realize that there was some truth in what I was telling you? I would say the same thing over and over because I knew it to be true, to be fact, to be far more cruel and evil than anything I could I make believe as a child. I want to stop playing those games. I am ready to be a person. I am ready to love. I am ready to be "normal."

As I grow, I would like to become more direct, more assertive, and more sure of what I am saying and how it is being received. In the past, I would sit with silence and ambivalence and just fall into situations by default. I don't want complacency to guide me through life. I am not incapable of protecting myself anymore. I hated being such a passive participant in my own life not knowing where I would be living, with whom, and for how long. Learned helplessness. I wonder how things might have been different...if only.

I will never know how events shaped my life and broke my mind. What caused my mind to break? Was I too weak? Was there some point where I should have thrown in the towel and taken my own life? Was there anything, anything I could have done differently to survive? Is there a "normal" breaking point? Did I put up a good fight? Did I do okay?

I want to act with purpose, speak with conviction, and be confident in my decisions. I want to choose action rather than inaction and feel comfortable with the choices I have made. No more ruminating over what I should have, might have, or almost done.

How did you manage to put my mind back together again without knowing what went wrong? Is my head okay? Can I have children?

You were a good therapist, you are a great therapist-- the best! 

Monday, February 18, 2013

Trapped

Have you ever been trapped?

I am not talking about your every day run-of-the-mill subway congestion or an elevator that is filled beyond capacity.  

Trapped.

No way out.

Paralyzed.

Frightened, frustrated, angry and desperate.

Like any ordinary "normal" person, you are going about your daily activities and the next moment you are drowning in unfamiliarity.  In reality, little has changed.  Sadly, nothing has changed.  Minutes, hours, years have passed... but nothing has changed.

Despite evidence to the contrary, your actions seem to have no consequence.  

This is how I feel.  Not as often as I used to, but more often than I care to admit and more often then I would like.  It leaves me paralyzed-- much like a deer frozen by the illuminating light of oncoming traffic.

It is a short journey from the trigger back to the beginning.  

I wonder what I may do if my task was completed.  It is my greatest hope to find a place where I can end this debilitating madness.  Just break the cycle. Free. Free from the need to provide objective verification of my physical existence and a rational basis for a seemingly bizarre obsession.

I know these things.  I organize my life in a sequential, numerical, historical, logical order where everything has a designated beginning, middle and end.

There must be a place where reason and purpose replace obsessions and insanity.  

Can anyone understand this madness?  Why can't you see how simple everything is for me?

I need things to be simple.

My patterns seem so obvious. Pay attention!  What seems like chaos to you serves as my salvation.  Don't you see how resourceful I am?  I know my methods are rigid but they are clearly consistent with my "mission" in life.  

Few can be bothered with the elegant simplicity of my rituals.  My behaviors are rational! They protect my delicate foundation. I do not have far to fall.

I need an out!

Why question my methods? 

By collecting physical evidence of my experiences and transient existence, I can be someone. Someone with a past, a present, maybe even a future.

I collect, therefore I am.

Look! I have proof! History. References.
I want to be part of your world.  Really I do.  

I want roots, consistency and foundations.  I want high school reunions and a hometown.

My task must be finished!  It is destroying my relationship with my future self.  My soul is withering away beneath this desperate facade.  

Please give me a moments consideration and see me.  

I am not cruel.  I am not evil.  Nevertheless, I am so alone and isolated.  I am here and I am ready.  I am ready to end this endless search for home.  But how?

I need you.  I need you to help me find a place where I can feel comfortable ending this vicious cycle.  

I am looking to you... the collective you of humanity to help me through this time of need and uncertainty.  

All I seek is compassion, empathy, and understanding. I continue my search hoping I am not completely alone in my quest.

Restoring order dominates my very existence.  Keeping me trapped in the past; invading the present; dictating my actions through repetition, ruminations, anxiety and fear inhibiting my growth and progress.  I do not have it in me to climb out of another depression.  

Don't you see how this life is breaking me?

If only I had the same resignation and grace of that lone Buck crossing a quiet country road, I would cherish the instant where I am faced with certain death or total salvation.  I would search for a sanctuary where forgiveness replaces damnation.

For one instant, I would welcome the challenge to live freely in this brave new world...  to explore and run free on a distant, winding path.

I would stand proud, defiant, and free.

Really, truly, trapped.  

Elyssa D. Durant, Ed.M.  © 2002-2013

Take the Long Way Home: Lost on Long Island

Naked.

Raw.

Exposed.

I am ashamed and embarrassed, yet I am strangely in control.

And such are my insecurities-- for whatever it's worth, and that may be quite a bit, this was the original message I wrote, but I sent it to myself and sent you an abbreviated version.

I think the uncensored version was better. 

I try to articulate.

I try to be interesting.

I try to be normal.

I need someone to hear what I'm not saying-- sometimes-- I don't like talking in riddles all the time.  I don't like talking in riddles all the time. I don't like obsessions and ruminations.

I don't like explaining the obvious.  I don't understand why it must be so complicated. 

I have one task. I have no idea how to complete my task, but I must keep searching.  

I developed new skills last night.  My car is still having problems and then my phone locked up.  I was completely lost on Sunrise Highway and could not find my way home (though I wasn't quite sure where my final destination would be.)  

I finally realized that I needed to pull over every twenty minutes to gather my bearings and plan a short term traffic route.  Forcing myself to stop for about forty minutes each time I got lost allowed me to process the emotions of the whole thing.

I pulled over at a diner in Long Beach and they were able to reconnect my phone so I could call for directions or support, or whatever!  

As I sat on the phone with tech support for over an hour, I started noticing that there were people sleeping in parked cars a few spaces away.  I couldn't tell if the couple that just emerged from a car just two spots away were committing an underage indiscretion or a felony in the back seat.  

As I noticed others around me, I wasn't so frightened anymore and I settled into my home for the night.  I did not feel so uncomfortable shuffling around in my somewhat respectable Honda Civic.  I almost forgot for a while that I was lost so I took a baby step to the next place and what an experience.  I was still lost but closer to my destination.  

This time I settled into a "execustay" type of hotel/motel.  This was working, so why rush. 




Why so frantic? 

Even with the phone now working, the car situation had not improved and I simply could not think of anyone to call.  Even if someone could come and get me, where would I go? Where would I put my things?

So finally, I made it over to Starbucks on the perimeter of the Hofstra Campus.  I was the only car in the lot, and I boldly parked facing forward and watched the police race by me without notice.  

I became very sad for this world just around then.  They were racing all around me and it took about 30-35 minutes before a cop car pulled into the parking lot.

Saddened by the reality that my suspicious activity did not invite further inquiry, I had already decided to tell them the truth before they pulled up to me in the lot.  

I did not even bother to park in a space.  I boldly parked horizontally taking up two or three spaces placing myself in a precarious situation.

Do you think they knew it wasn't the first time? 

Do you think they saw through my decidedly in in-your-face tactics and saw this as a thinly disguised effort to feign temporary homelessness? 





Would they be back tomorrow night? Would I?

Elyssa Durant, Ed.M.  © 2002

Monday, July 23, 2012

Barack Obama | Elyssa Durant: Applying Federal Law to Support Mandatory Coverage

Applying Federal Law to Support Mandatory Coverage

by Elyssa Durant, my.barackobama.com
July 25th 2009 9:59 AM

Underwriting the Social Contract: Distributive Justice & Health Care Reform

The Problem Statement

As health care costs climbed exponentially in the 1980's, so did the cost of health insurance plans. As a result, employers began to enroll their employees in managed care organizations, and many Americans were forced to leave their traditional indemnity type plans. With the advent of the health maintenance organization, there is a financial incentive for the underutilization of care. (Blumstein, 1996; Davis & Shoen, 1996).

In order to reduce financial risk, health insurance companies have restricted enrollment to individuals in poor health. By covering the minimal standards of treatment and excluding high risk groups altogether, major US insurance companies have realized that the health insurance market can a be an extremely profitable industry. The public sector absorbs the cost of unreimbursed care for chronic care in America (Robert Wood Johnson Foundation, 1996). Based upon these findings, it seems clear that the money being removed from the health care marketplace is fattening the pockets of CEOs and majority stockholders.

Recent trend towards localized government leaves individuals without a financial safety net. This is the least efficient manner to handle health care costs, and evades the premise that medical care is a natural right in a civilized society. Few Americans feel secure within the current system. The rising costs of medical care contributed to the recent market changes in both the administration and delivery of health services. The financial incentive to cover only the healthiest individuals ignores the fact that medical care is a social good.

Health Insurance Portability Act of 1996

Two years after the Clinton Health Plan was defeated in Congress, Senator Ted Kennedy and Nancy Kassebaum introduced the Kennedy-Kassebaum Bill in response to growing concerns about selective enrollment procedures used by health insurance companies in the private sector. In the final version of the Bill, insurance companies must limit preexisting condition clauses to twelve months. It has been estimated that this provision of the Bill will help an estimated 150,000 Americans obtain health insurance coverage.

There are many levels of the underinsured, including those without any coverage; effective policy must address the needs of the total population without shifting costs from one disadvantaged person to another. Kennedy-Kassebaum fails to address the cost issue—the primary concern for those at risk for losing their health insurance. It does nothing to help the uninsured acquire a decent health policy, and then provides no solution to the critical issue at hand— cost

Since Kennedy-Kassebaum does nothing to control the cost of health insurance and medical care in America, the Bill fails to respond to the issue of greatest concern to the citizens of this country: the cost of medical care. The Bill looks towards the states to develop consumer protections and weakens the regulatory role of the federal government. The majority of the American public is unaware of the fancy footwork involved with this legislation, and the demographics of the population it is intended to protect. In order to assess the utility of this Bill, it is critical to identify the populations at risk for loosing health insurance coverage and the underinsured.

Kassebaum-Kennedy focuses on a slim portion of the uninsured population, and those who would be eligible for COBRA continuation (Consolidated Omnibus Reconciliation Act of 1974). Of the 41 million uninsured Americans, only about 150,000 are expected to benefit from this legislation. The Health Insurance Portability and Accountability Act of 1996 is really nothing more than smoke and mirrors since it fails to address the true issue at hand—the simple fact that the cost of quality health care in America is becoming a privilege that only the wealthy can afford.

The Cost of Care for Pre-existing Conditions

An individual with high blood pressure may just require prescription medication. Cancer patients in remission may require chemotherapy, and a person suffering with a degenerative disease may be involved in treatment studies. Each condition requires individualized treatment that cannot be based upon the simple economic/cost-benefit analysis used in the utilization review process by large insurance companies. Clearly, the most effective treatment for one patient may not be the best for another. The time required for utilization review may present additional health risks and complications to a patient suffering from a chronic health condition.

Twelve months without insurance coverage may be financially devastating to some patients, and 63% of Americans have already forgone some type of medical treatment within the last year due to financial constraints. Publicity surrounding Kennedy-Kassebaum has hailed the bill as the "be all and end all in progressive legislation, however, in actuality it will only help about 150,000 people.

Recent studies have found that the majority of the uninsured population simply cannot afford to pay the premiums (Donelan et. al., 1996; Hoffman & Rice, 1996). According to their data, only 1% of the Uninsured population is due to current health status and exclusionary preexisting clauses, yet an overwhelming number of insured respondents reported an inability to receive medical care for chronic conditions. The majority of Americans with chronic illness are covered by some type of insurance, yet they are still subject to the utilization review process and access problems that deny or delay medically necessary treatment (Donelan, et. al., Hoffman & Rice, 1996).

Underwriting the Solidarity Principle

Traditional forms of insurance underwriting required that the contract explicitly state which illness or services are not covered by the policy, in advance. If the underwriter did not specifically state a certain condition in the contract, the insurer was held to the terms of the contract and required to pay for services utilized by the policyholder (Stone, 1994, as cited in Durant, 1996).

Increasing numbers of for-profit and non-profit insurance companies began to control costs by refusing to insure individuals who they felt would utilize more services. Insurers began to require health survey status questionnaires (refer to attachment A), and even began implementing AIDS and genetic testing to identify high-risk individuals (Brunetta, as cited in Gutmann & Thompson, 1996). In the 1980s, large insurance companies began including sexual orientation as a high-risk category, by using actuarial sound criteria. Such criteria concluded that gay men were a higher risk for contracting AIDS virus and refused to write policies for anyone believed to be homosexual, (Stone, 1994 as cited in Durant, 1996).

By limiting enrollment to the healthiest members of society, selective enrollment undermines the solidarity principle of health insurance (Davis & Shoen, 1996; Snow, 1996; Stone, 1994). By eliminating those who were suspect of using more services than their healthier counterparts use, insurance companies are able to offer rock bottom prices for young, healthy individuals. By excluding preexisting conditions and requiring certain individuals to purchase high-risk policies, the number of uninsured and underinsured Americans continues to grow exponentially (Durant, 1996).

More individuals are choosing not to purchase insurance simply because they cannot afford it. Even among those with employer based health coverage, the policies frequently exclude coverage for long-term illness or care of chronic conditions (MSNBC News Forum, 1996). Without a standard definition of preexisting conditions, these clauses serve as "wildcards" since they allow insurers to deny coverage for any illness that "manifested itself before the issuing date of the policy (Stone, 1994 as cited in Durant, 1996).

This statement allows insurers to deny treatment for benefits and services for the policyholder for undiagnosed illnesses or conditions of which they were unaware. As a result, the insurers began to demand medical histories of applicants and their families in order to identify high risk individuals (please refer to attachment A).


Legitimacy of Distributive Justice

While there is a legitimate role of government to distribute scarce resources among the nation's neediest individuals, sadly this is not the cause for the mismanagement of medical dollars in the United States today. There is a big distinction between an individual being denied prescription medication at their local pharmacy due to a cost-effective formulary developed by their Managed Care Organizations (MCOs), than an individual being denied a liver transplant because healthy livers are a scarce resource. While both may have equally devastating consequences, it is more difficult to rationalize a lost life based upon rigid cost benefit analysis and utilization decisions made according to formulas and cost-benefit analysis of treatment protocols.

"The political controversy over the distribution of health care in the United States is an instructive problem in distributive justice. Good health is care is necessary for pursuing most other things in life. Yet equal access to health care would require the government to not only redistribute resources from the rich, healthy to the poor, and infirm, but also restrict the freedom of doctors and other health care providers. Such redistributions may be warranted, but to what level, and to what extent?" Gutmann & Thompson (Page 178).

Blendon and his colleagues have reported similar findings in public opinion polls from 1992 and 1994 (Blendon et. al., 1992; Blendon et. al., 1994). A recent study by the American Medical Association found cost to be of paramount concern to an overwhelming number of Americans (Donelan et. aI., 1996). Of the 40 million uninsured Americans, only 1% attributes their failure to acquire health insurance coverage to their preexisting conditions. Among the uninsured, cost is cited as the primary obstacle in obtaining health insurance coverage. Only 1% of the uninsured attributes their lack of coverage to a preexisting condition.

Based upon these democratic principles of distributive justice, consistent opinion polls demonstrate the legitimate role and public desire for government regulation of the health care industry. It has become obvious that the federal government must intervene in order to protect natural law rights, the social contract, and the Constitution of the United States. Regulation is needed to protect the individual freedoms, liberty, and the pursuit of "health, happiness, and the American Dream."

If America is to be the "Land of Opportunity," then clearly individual health and wellness should be an ideal to reach for. Current models of distributive justice emphasize public consensus as a legitimate role for government intervention. According to a number of studies by Blendon and his colleagues, the public has reported an overwhelming general concern about health care in this country, (1992, 1993, 1994, 1995, 1996).

State civil courts are backed up with cases where HMOs have violated the First Amendment (gag orders), the Fourteenth Amendment (due process), and the rights of protected classes under the Americans with Disabilities Act. Countless examples of "anecdotal" evidence appear as headlines everyday across the country. (New York Times, 1996; The New York Daily News, 1996; Long Island Newsday, 1996; LA Times, 1996; Picayne Times, 1996; Columbia Spectator, 1996; Columbia University Record, 1996; US News & World Reports, 1996; Newsweek 1996; Healthline, 1996; The Tennessean, 1996; The Albany Times, 1996; The Nashville Scene, 1996). In their entirety, these case reports represent the human tragedy that lies beneath the web of the very worst of American capitalism: corporate greed.

Identifying Populations At-Risk

A study by The Lewison Group in 1996 reveals insight into the private individual health insurance market. Clearly, individuals choosing to purchase health insurance policies for several hundred dollars each month expect their health care needs and expenditures to exceed that amount Regardless of health status, a young healthy 25 year old who purchases an individual health insurance policy can expect to pay well over $300.00 monthly for a health insurance policy with Empire Blue Shield Blue Cross (based upon 1996 rates, current rates available from the New York State Insurance Department).

Since individual policies are not addressed in the Health Insurance Portability and Accountability Act of 1996 (HIPA), an individual policy with Blue Cross Blue Shield of Tennessee excludes preexisting conditions for 24 months (enrollment booklet available upon request). The critical markets in need of reform are the adversely selected individual insurance market, and the state's most vulnerable populations: children; the elderly; the chronically ill; the uninsured; and the underinsured.

For the millions of individuals who have lost their employer based coverage, the cost of private health insurance is prohibitively expensive. Many individuals opt out of the individual market and apply for public assistance when the need arises. Those who have retained their health insurance coverage through their employers are being moved into managed care despite their efforts to retain their indemnity style plans (Davis & Shoen, 1996; The Lewison Group, 1996).

Access to Medical Care

As routine practice, HMOs deny or delay care for all services that are not outright medically necessary. Growing numbers of individuals have suffered irreparable harm, and many have died awaiting approval from their HMO's (The New York Times, 1996; Long Island Newsday, 1996; The Tennessean, 1996; Healthline, 1996). It is hardly a secret that HMOs have fallen short of their promise to provide comprehensive health care for the "whole" individual by emphasizing preventative medicine, using medical management to coordinate care. There is substantial evidence that individuals with chronic conditions receive substandard care in HMOs.

A four-year longitudinal study of medical outcomes found that the elderly, the poor, and persons with chronic conditions were in better health when covered by fee-for-service plans compared with a control group covered in HMOs (Ware et. al., 1996). New statistics released in Washington, DC by the American Medical Association and the Robert Wood Johnson Foundation revealed the direct costs of individuals with chronic conditions account for 75% of direct medical expenditures in the United States (Hoffman & Rice, 1996; based upon the National Medical Expenditures Survey; raw data available on CD from the Department of Health and Human Services Washington, DC). 45% of the American population suffers from at least one chronic illness.

If managed healthcare has been found to deliver inadequate care to this population, then we are looking at 100 million individuals who are potentially facing personal and financial crisis as they are moved into managed care. The public already accounts for the largest payment of direct medical expenditures, which means the millions of dollars being made by for-profit insurance companies are not being circulated into the economy to assist in public health costs care. The industry made a 14.8% profit in the 3rd quarter of 1996, however these medical dollars were removed from health care and used to fatten the pockets of CEO's and majority stockholders (Healthline, 1996).

Based upon a new report from the Robert Wood Johnson Foundation, the direct costs for persons with chronic conditions represent 69.4% of national expenditures in personal health care (Robert Wood Johnson Foundation, 1996). Their direct medical costs are estimated at $4672.00 annually compared with $817.00 annually for individuals with acute illness (Hoffman & Rice, 1996; based upon National Medical Expenditures Survey 1987, not adjusted for inflation). This population is the most vulnerable to complications in their health and with their source of payment. Large insurance companies only provide adequate coverage for acute illness (Donelan et al., 1996; Hoffman et. al, 1996).

Medicaid Managed Care

Following Tennessee's lead, many states have enrolled their medically indigent populations in Medicaid Managed Care Organizations (MCOs). In Daniels v. Wadley, (926 F. Supp. 1305), the court held that TennCare violated the Due Process Clause of the Fourteenth Amendment since such procedures eliminate fair hearings and independent medical review of disputes. The court found the pattern of routine denials of care by MCOs participating in the states TennCare program to violate the Medicaid Act since it compounded the problem of institutionalized waiting periods for medical appeals pending independent review by the Medical Review Unit (MRU), (42 U.S.C. § 1396 (a)(8)).

Furthermore, the court ordered federal injunctive protection to participants and beneficiaries because no state law may preempt federal law by depriving individuals of their constitutional rights. The Department of Health and Human Services (HHS) was ordered to revise its utilization review procedures for TennCare recipients in keeping with the Medicaid Act (42 U.S.C. § 1396 (a) (8)) ensuring due process protections for all covered beneficiaries by requiring "services are provided with 'reasonable promptness,'" (926 F. Supp. 1305).

This case is one of 543 civil suits pending in the state courts for violations of the Medicaid Act (based upon a Lexis-Nexis search performed December 26, 1996). With the passing of H.R. 3507 into public law, (The Welfare Reform Bill) private citizens will find little reprieve in the federal courts, so any attempts to hold states accountable for violations of federal law will be feeble at best (Denkeret. al., 1996).

Managed care has shown itself to be a farce of "medical management" in light of all the condemning evidence to the contrary. Timothy Icenogle, a medical doctor in the state of Arizona commented in 1981, "We play sort of an advocacy role. I think the public demands something more from physicians than to just be a blob of bureaucrats, and I think we have to take a stand now and then. Our role essentially as patient advocate, is to tell them, well, just because the insurance company is not going to pay, that is not the end of all the resources," (Icenogle, as cited in Gutmann & Thompson, 1996). Never has this statement been needed more than it is today. Unfortunately, as more insurance companies refuse to pay for medical treatment, fewer resources become available for patients in desperate need of financial assistance. As Judge Kessler eloquently stated as she handed down her decision in Salazar v. District of Columbia, No. 93-452, December 11, 1996, "behind every fact found herein is a human face and the reality of being poor in the richest nation on earth, (936 F. Supp. Slip op. At 3).

Perhaps most distressing is the lack of accountability for mismanaged healthcare and improper denials of medically necessary treatment. HMOs claim immunity under ERISA, and leaving individuals without recourse in a sea contractual language and lengthy court calendars. It is evident that individuals protected under the Medicaid Act are not fundamentally different from other populations entrapped in the maze of managed care. They are simply those who have "had their day in court."

Due Process Protections

Since all Americans are theoretically entitled to due process protections under the constitution of the United States, it seems the federal courts are long overdue for making such a public statement. We are wasting precious time and losing millions in valuable human resources as we await decisions to be handed down from state courts. The Supreme Court of the United States has agreed to hear New York's request for an ERISA (Employee Retirement Income Security Act of 1985) waiver, making health maintenance organizations liable for medical malpractice in the state of New York.

When HMOs deny care from patients, it is ludicrous to hold individual physicians liable for the utilization decisions made by decentralized corporate review boards. It is time to take a serious look at tort reform, and demand action by the Supreme Court as they approach the date of New York's ERISA hearing. A blanket court ruling upholding Daniels v. Wadley, and Salazar v. District of Columbia is desperately needed to avoid an avalanche of liability suits filed in state courts. The court must uphold Daniels v. Wadley, and Salazar v. District of Columbia if further lives are to be saved in medicine rather than wasted away in the utilization review procedures. While we wait patiently for District of Columbia circuit court to order injunctive relief, the number of individuals suffering irreparable harm due to the systematic denial of medical care grows larger each day.

The history of Medicaid Managed Care does not provide a very optimistic look into the future of TennCare recipients and Medicaid beneficiaries in states around the country. Dating back to the implementation of the Arizona Health Care Cost Containment System (AHCCCS) in 1981, there are documented cases where "people reportedly died for lack of medical treatment before their eligibility was determined," (Varley, as cited in Gutman & Thompson, I 996). This leaves me to wonder why the states continue to enroll their most vulnerable populations into a system of managed care that has proven to be a disaster.

Perhaps worthy of comment is that Arizona is the only state to have voted Republican in every election since 1948—certainly provides insight into the conservative morale of the state. Although Arizona was the last state to accept the Medicaid cost sharing incentive proposed by the federal government in 1966, it was the first state to force its medically indigent population into managed care in 1981.

Violating Federal Law

Rigid pre-certification requirements and nonspecific utilization review procedures place strategic barriers to access medical treatment and services in Health Maintenance Organizations (HMOs). Pre-certification requirements are strategic barriers incorporated into the "black box" of utilization review that institutionalizes exclusionary waiting periods and routine denials of medically necessary treatment. According to federal law, "care and services are to be provided in a manner consistent with the simplicity of administration and the best interests of recipients," (42 U.S.C. § I 396a (a) (19)). Clearly, such rigid pre-certification requirements that complicate administrative processing and paperwork on the part of the enrolled beneficiaries is a violation of United States Code.

Furthermore, using primary care providers as a mechanism to limit access to specialists not only complicates administrative processing, but limits enrolled beneficiaries choice of health professionals beyond what is available to the general public in the geographic area (42 U.S.C. § 1 396a (a)(30)(A)). Certainly referral procedures do not "assure that recipients will have their choice of health professionals within the plan to the extent possible and appropriate," (42 U.S.C. § 434.29). Under this provision, it seems that any individual, especially those with chronic health conditions or disabilities should be allowed

Original Page: https://my.barackobama.com/page/community/post/elyssadurant/gGMP3Q

Shared from Read It Later



 אל