In the very first scene in the award winning show, “The Newsroom,”
Jeff Daniels, who is playing a cable newscaster, is appearing as a guest
speaker at Northwestern University. A young college student
asks him the following question, “Can you sum up in one sentence or less ...
what makes America the Greatest Country in the World?” After first dodging
the question, he is pressed for an answer by the moderator of the event. His
candid response follows:
And you—sorority
girl—yeah—just in case you accidentally wander into a voting booth one day,
there are some things you should know, and one of them is that there is
absolutely no evidence to support the statement that we're the greatest country
in the world. We're seventh in literacy, twenty-seventh in math, twenty-second
in science, forty-ninth in life expectancy, 178th in infant mortality, third in
median household income, number four in labor force, and number four in
exports. We lead the world in only three categories: number of incarcerated
citizens per capita, number of adults who believe angels are real, and defense
spending, where we spend more than the next twenty-six countries combined,
twenty-five of whom are allies. None of this is the fault of a 20-year-old
college student, but you, nonetheless, are without a doubt, a member of the
WORST-period-GENERATION-period-EVER-period, so when you ask what makes us the
greatest country in the world, I don't know what the fuck you're talking
about?! Yosemite?!!!
We sure used to be. We stood up for what was right. We fought for
moral reasons, we passed and struck down laws for moral reasons. We waged wars
on poverty, not poor people. We sacrificed, we cared about our neighbors, we
put our money where our mouths were, and we never beat our chest. We built
great big things, made ungodly technological advances, explored the universe,
cured diseases, and cultivated the world's greatest artists and the world's
greatest economy. We reached for the stars, and we acted like men. We aspired
to intelligence; we didn't belittle it; it didn't make us feel inferior. We
didn't identify ourselves by who we voted for in the last election, and we
didn't scare so easy. And we were able to be all these things and do all these
things because we were informed. By great men, men who were revered. The first
step in solving any problem is recognizing there is one—America is not the
greatest country in the world anymore.
That scene is one of the most impactful opening scenes of any
television show in recent memory. And although fictional, is there any
legitimate doubt as to the accuracy of those remarks ringing true today?
Especially in the field of mental health and more specifically in the eating
disorder industry.
But, we are not here today to bury America. Instead, we are here
today to praise Australia.
On Sunday, December 9, 2018, Christine Morgan, the CEO of the
Butterfly Foundation issued a press release stating that the Prime Minister of
Australia announced an amendment to Australia’s Medicare Benefits Scheme
designed to improve access and affordability of appropriate eating disorder
treatment across Australia. One executive stated, “The socio-economic impact
of eating disorders on a person’s life is one of the most severe and enduring
in Australia. The introduction of a Medicare response into the health system is
the most significant and necessary reform. Without a Medicare response other
system reforms that are still needed could not be considered.” [emphasis
added]
Australia’s new benefit scheme in part provides:
· A dedicated single Medicare
Benefits Scheme item number for eating disorder treatment for those with severe
and complex illness, delivering up to 60 Medicare funded sessions of treatment
– 40 psychotherapeutic and 20 dietetic across the range of eating disorders –
anorexia nervosa, bulimia nervosa, binge eating disorder and atypical
presentations.
· Diagnosis by a GP and mental health
practitioner recognizing that these psychiatric illnesses have a significant
physical impact and integrated treatment is essential.
The Press Conference announcing this new law was momentous as
well. It included politicians, foundations, counselors, and family members all
united as one. The transcript from this Press Conference can be found here:
Standing by itself, this achievement is incredibly note worthy.
But, this is only the latest event in what now appears to be a
concerted government – private enterprise collaboration to address this
insidious disease. Australia along with New Zealand has a recent history of
being progressive, of confronting a problem head on and objectively seeking to
find solutions. In 2014, The Royal Australia and New Zealand College of
Psychiatrists issued new Clinical Practice Guidelines for the treatment of
eating disorders. These Guidelines included policies and procedures for the
admission of children and young adults, guidelines addressing in-patient
management and outpatient care, hospital care, residential care. It was free of
corporate bias with no specific economic agenda. Treatment will be made
available for groups of people who previously would not have been able to
obtain help.
Australians have been given hope. They know that their government
listened to their concerns and fears and took affirmative, strong action.
Research and treatment are not being driven by private corporations whose
interest begins and ends with their profit margin.
Meanwhile, back in the
United States
Status quo ante reigns, no progressive, affirmative bold conduct
is being undertaken and our children continue to die. In the halls of Congress,
strengthening and increasing the financial gains of the private equity
overlords predominates lobbying efforts. Nowhere is this more obvious than in
analyzing the 2018 payments to the eating disorder lobby and the specific bills
being lobbied.
In 2018 alone through the end of October, the Eating Disorder
Coalition, the Residential Eating Disorder Consortium (“Consortium”) and the
National Eating Disorder Association (“NEDA”) paid their now unified lobbyist a
combined $250,000.00. This number is expected to exceed $325,000 by years end.
And what did the eating disorder industry buy with this money? The specific
bills and resolutions the lobbyist was instructed to lobby involved:
1. On behalf of NEDA,
H.R. 1625, the “Consolidated Appropriations Act of 2018,” related Labor and
Defense Appropriations Acts and House Resolution 428 and Senate Resolution 419
both of which recognize February 26, 2019 – March 4,2018 as “eating disorder
awareness week.” NEDA paid the lobbyist $60,000 for this work.
S. Amdt. 2222
"Bipartisan Health Care Stabilization Act of 2018" to H.R. 1625
"Consolidated Appropriations Act, 2018," all provisions. H.R. 4666
"Premium Relief Act of 2017," all provisions. S. 1835 "Lower
Premiums Through Reinsurance Act of 2017," all provisions. Issues
pertaining to Association Health Plans- 29 CFR Part 2510, RIN 1210-AB85, all
provisions. Issues pertaining to Short-Term, Limited Duration Insurance- 26 CFR
Part 54, RIN 1545-BO41, all provisions. P.L. 114-255 "21st Century Cures
Act," all provisions. H.R. 6311 "Increasing Access to Lower Premium
Plans and Expanding Health Savings Accounts Act of 2018," all provisions. S. J. Res 63 "A joint resolution
providing for congressional disapproval under chapter 8 of title 5, United
States Code, of the rule submitted by the Secretary of the Treasury, Secretary
of Labor, and Secretary of Health and Human Services relating to
"Short-Term, Limited Duration Insurance", all provisions.
H.R. 6898 "Maintaining Protections for Patients with Preexisting
Conditions Act of 2018", all provisions. [emphasis added]
3. The ED Coalition paid $90,000 on the following issues: Senate
Bill 3158, deemed the 2019 Department of Labor Appropriations Act and the
aforementioned H.R. 1625, the “Consolidated Appropriations Act of 2018.
That is the totality.
That is what almost 1/3 of a million dollars in lobbying bills
gets you. No additional treatment funding. No additional university based
research funding. No mandatory increase in training on eating disorders in
medical schools and internships. No new laws policing the out of control
private equity firms who are running amuck in the eating disorder
industry.
So what do you receive? Lobbying to cut off much needed help for families.
Short-term, limited-duration insurance is a type of health insurance coverage that is primarily designed to fill gaps in coverage that may occur when an individual is transitioning from one plan or coverage to another plan or coverage, such as when they are between jobs.
The Rule proposed by the Secretary of the
Treasury, Secretary of Labor and Secretary of Health and Human
Services provides consumers with more affordable options for health
coverage. Under this Rule, consumers would have the ability to purchase
short-term, limited-duration insurance policies that:
1.
Are less than 12 months in duration;
2. Contain important language to help consumers understand the
coverage they are receiving, and;
3.
May be renewed for up to thirty-six (36) months.
Parents, moms, dads, families … The Residential Eating Disorder
Consortium paid the unified lobbyist to oppose short term, limited duration
insurance policies. You read that correctly. To reiterate, the Consortium paid the lobbyist to oppose short term,
limited duration insurance policies.
These insurance policies could provide the ability to pay for life
saving treatment for our loved ones. And yet, the Consortium opposes it? To
double check, I looked at the specific language utilized in the Senate Joint
Resolution 63. The totality of the language states:
Resolved by the Senate and House of
Representatives of the United States of America in Congress assembled, That Congress disapproves the rule submitted by the Secretary of the
Treasury, Secretary of Labor, and Secretary of Health and Human Services
relating to “Short-Term, Limited Duration Insurance” (83 Fed. Reg. 38212
(August 3, 2018)), and such rule shall have no force or effect.
To triple check, I then looked at the language of the Rule
submitted by the Secretaries and recorded at 83 Fed.Reg. 38212. The exact
language summarizing this rule
states:
This final rule amends the definition of short-term, limited- duration insurance for purposes of its exclusion from the definition of individual health insurance coverage. This action is being taken to lengthen the maximum duration of short-term, limited-duration insurance, which will provide more affordable consumer choices for health coverage.
And all of the treatment centers who are included in the
Residential Eating Disorder Consortium not only oppose this provision, but are
paying a lobbyist to oppose short-term, limited duration insurance policies
which would potentially provide payment for life-saving treatment.
Is it because if this type of insurance passed and became law, it
would reduce the profits for the insurance providers while increasing their
costs? Is it because it could make treatment decisions in accordance with
insurance policy language and the DSM V more problematic for treatment centers?
Is it because the private equity firms which now control the Consortium and ED
Coalition are in bed with the insurance industry?
Whatever the reason, the daunting obstacles confronting families
who suffer from eating disorders are being exacerbated by the greed of the
private equity firms which own the treatment centers and the insurance
industry. And the cost to pay for this greed? The lives of our loved ones at
the rate of one death every 62 minutes. At this point, you may use whatever
word you wish … reprehensible, unethical, disgusting, or vile to define the
state of the eating disorder industry in the United States.
As the mantle of leadership and insight into treating and
researching eating disorders is firmly grasped by Australia, they are to be
commended and even admired for their vision and wisdom. And as for us? The
reality of why America is not the greatest country in the world comes more into
focus.
You have a point. However, let's not forget that most of the research on eating disorders is coming out of the United States, paid for by American taxpayers, and then disseminated around the world, including to Australia.
ReplyDeleteAlso, I'm not convinced that psychotherapy and nutritional counseling are the best approaches to treating anorexia nervosa, so I'm skeptical that the new policy in Australia, which provides funding for those two things, will have much impact. A better use of money, in my opinion, would be for the government to fund the dissemination of scientific information about anorexia nervosa directly to parents, bypassing professional psychotherapists and nutritionists.
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