Friday, February 24, 2012
Monday, February 6, 2012
Picture just in! A living room conversation with Secretary of HHS, Kathleen Sebelius, January 2012.
EDC Policy Director Jeanine Cogan, speaks with Kathleen Sebelius about the enormous challenges people with eating disorders face in trying to access life saving care. She let the Secretary know that things have not improved since the federal parity law passed as people with eating disorders are still regularly denied treatment and as a result some die. Jeanine asked the Secretary if there is anything she could do to address these gaps in coverage for people suffering from eating disorders through the essential health benefits and other implementation of the Patient Protection and the Affordable Care Act. The Secretary responded with concern and informed her that she would have her staff look into the matter.
Monday, January 30, 2012
24 Hours to Make a Difference
Action Alert! Send your comments by midnight (EST) on January 31, 2012
The Eating Disorders Coalition for Research, Policy & Action asks you to respond to a Bulletin by Heath and Human Services (HHS) that outlined their strategy for implementing the essential health benefits (EHB) of the Patient Protection and Affordable Care Act (ACA).
The EDC was optimistic that with the passage of ACA and the inclusion of mental health as an essential health benefit, the continued and widespread insurance discrimination experienced by people with eating disorders would come to an end.Join us in asking HHS to capitalize on this moment in history and incorporate the following 3 recommendations so that people with eating disorders will finally have access to the life saving treatment they are often denied.
Please send comments to EssentialHealthBenefits@cms.
Urge the Secretary of HHS to:
1. Replace the sizeable flexibility given to the states with national uniform standards for the EHB categories.
When Congress passed the ACA and created the EHB they intended to create a uniform minimum benefit standard that would apply to all States in order to correct existing disparities. Providing national standards that include the treatment of eating disorders would guarantee uniformity across states.
Currently the options for eating disorders treatment are highly variable based on where a person lives. A state such as Rhode Island with a comprehensive state parity law requires insurance companies to provide eating disorder treatment so that individuals in that state have options for care. Contrast this with states like Wyoming and Arkansas that have no parity law and no eating disorder treatment available within the state, yet based on national prevalence data, these two states alone likely have over 75,000 individuals with eating disorders within their borders.
In the absence of a uniform standard, we believe there is a significant risk that eating disorders will continue to be inadequately covered in many States.
We urge HHS to provide concrete language defining the EHB for mental health, which requires the coverage of eating disorders.
2. Provide a federal definition of medical necessity that is broad and inclusive.
The degree to which Americans enjoy full access to covered services within the ten EHB categories will depend, to a large degree, on the medical necessity standards that plans use to determine whether a service within these categories is covered.
Few regulations address the definition of medical necessity: there is no federal definition, and only about one-third of states have any regulatory standards for medical necessity. Consequently, the definition of “medical necessity” is most commonly found in individual insurance contracts that are defined by the insurer. As a result, the standard of medical necessity is most often controlled by the insurer, not the treating professional.
This has dire consequences for people suffering from eating disorders who are continually discharged from treatment or denied treatment based on erroneous and shifting definitions of medical necessity, per insurers.
We urge HHS to offer a federal definition of medical necessity that 1) is broad enough to include all clinically necessary levels of care for eating disorders and 2) requires insurers to use well respected, clinically proven or evidence based criteria for the effective treatment of mental illness.
3. Eliminate eating disorders from exclusion lists.
Exclusion of eating disorders is all too common on the part of insurers seeking to limit interventions deemed non-essential. Despite being biologically based mental illnesses with severe physical health complications, including death, eating disorders are all too often found on lists of benefit exclusions.
We urge HHS to ensure that eating disorders treatment is no longer specifically excluded and end the discrimination against individuals with eating disorders.
Please send your comments outlining the need for these 3 recommendations and include examples from your personal and/or clinical experiences as relevant.
Send comments to EssentialHealthBenefits@cms.
**Please also send your comments to: kmacdonald@eatingdisorderscoalition.org
Tuesday, January 10, 2012
Action Alert -Petition to End Discrimination

The EDC supports the efforts of this petition and encourages you to sign your name today. Then spread the word!
http://www.change.org/petitions/childrens-healthcare-of-atlanta-end-the-stop-sugarcoating-obesity-campaign
Together we can stop the dangerous trend of shaming people because of their weight, shape, size.
~yours from the Hill, the EDC
from BEDA --
Why This Is Important
The "Stop Sugarcoating" campaign developed to address childhood obesity sends several dangerous messages to both children and adults. It shames children who are larger, reinforces social prejudices around size by encouraging weight stigma, and rather than focusing on healthy behaviors it uses bullying style advertising to encourage kids to diet and exercise. In short, the campaign traumatizes children struggling with their own feelings about size and may even reinforce their use of food as a coping mechanism. See the campaign here: http://strong4life.com/#
Public bullying of kids and adults because of size is not acceptable. The campaign does not consider that kids of all sizes are susceptible to eating disorders, which have the highest rates of mortality with regard to mental health illnesses. Public shaming is archaeic, dangerous, and inexcusable. Weight stigma is extremely damaging and studies show it actually lends to increased weight. The public health officials who designed this campaign should be embarrassed and do everything they can to stop this campaign. They also owe an apology to the citizens of Georgia and the entire country. The Binge Eating Disorder Association (BEDA) sponsors the National Weight Stigma Awareness Week yearly during the last week of September. We encourage public officials and others to read the information provided about weight stigma on our website at http://www.bedaonline.com/2011WSAW/index.html. We also encourage them to consider the risk/benefits of the campaign they have designed. We ask you, CHOA, to stop sugarcoating your weight stigma, call a spade a spade, and do the right thing.
photo credit: http://barbaracolebythesea.com/wp-content/uploads/2010/10/discrimination.jpg
Wednesday, December 7, 2011
EDC Addresses All Treatment Denials
In early 2011 the EDC initiated the Hold Insurance Companies Accountable Campaign (HICA Campaign) as a response to a number of insurance companies that are categorically denying residential treatment for eating disorders.
We are now expanding the HICA Campaign to include all denials of eating disorder treatment.
Mental Health Parity requires that any group health plan that includes mental health and substance use disorder benefits along with standard medical and surgical coverage must treat them equally. According to the nationally recognized law firm of Patton Boggs, the statute is clear that limits on the scope and duration of treatment must be applied no more restrictively in the mental health benefit than in the medical/surgical benefit. The statute defines treatment limitations as "limits on the frequency of treatment, number of visits, days of coverage, or other similar limits on the scope or duration of treatment."
Not complying with the parity regulations is a calculated effort to avoid costs at the expense of people's health and lives. The EDC argues that treatment should be determined by severity and type of illness, rather than what is arbitrarily allowed by an individual's insurance company.
Through legal and political advocacy, the EDC's Hold Insurance Companies Accountable Campaign is working with specialized attorneys and experts in the field to put an end to such discriminatory and deadly practices.
IN ORDER TO HELP YOU, WE NEED TO HEAR ABOUT YOUR EXPERIENCE:
If you or a loved one has been denied insurance coverage for eating disorder treatment, please email us at: EDCHoldsInsuranceAccountable@yahoo.com
We will send you a short form to fill out and then work with you to alert Members of Congress and other people who could help address your situation (such as pro-bono attorneys if appropriate).
You deserve access to care and we look forward to helping you gain justice in that regard.
Monday, November 21, 2011
use your voice -Action Alert
EDC asks you to use your voice to make sure eating disorders get included in insurance coverage
If you haven't already: Please submit your comments today!
Deadline has been extended to November 30th
______________________________
A key component of the Affordable Care Act (ACA) is the requirement that all insurance plans offered through the exchanges must cover, at a minimum, a number of Essential Health Benefits. Mental health is one of these Essential Health Benefits (EHB) that must be included.
The Department of Health and Human Services (HHS) is tasked with promulgating regulations for how the EHB will be designed and implemented. The EDC is asking HHS to incorporate three recommendations into the EHB: 1) eating disorders should be specifically listed in the EHB, 2) all levels of treatment including residential treatment, as recommended by the APA Guidelines, should be part of the EHB, and 3) the definition of medical necessity should be broad and inclusive so that insurers cannot assign medical necessity at random.
Please add your voice by sending comments to HHS ) you urge them to support these above 3 recommendations and 2) some of your personal experience that underscores why these recommendations are important. For example: maybe you personally benefited from successful residential and/or other treatment ---include that in your comments. If you were denied residential and/or other treatment ---include that, and the consequences of being denied, in your comments. And include anything else about your experience or expertise that underscores the need for these 3 recommendations. We know that personal stories matter to HHS.Please then send an email to kmacdonald@eatingdisorderscoalition.org to inform us that you sent your comments.Thanks so much for taking a few minutes out of your day to make an important difference. Together we will improve the lives of those suffering from eating disorders!
Here are some additional talking points the EDC has made:
In response to the Department’s stated questions:In terms of how to best balance comprehensiveness of included in essential health benefits and affordability; we believe that:o Ensuring access to comprehensive specialized eating disorder care, across all levels of care including outpatient, intensive outpatient, partial hospitalization, residential, and inpatient, will allow individuals to access adequate, effective, evidence-based care in specialized settings, and decrease their need to access less specialized, less effective, more emergent medical and psychiatric care. Decreasing use of high-cost emergent and/or on-going use of inadequate care will balance comprehensiveness and affordability. Eating disorders have the highest mortality rate of all psychiatric illness. Including comprehensive eating disorders treatment in EHB will safe lives.In terms of how the Department might ensure that essential health benefits reflect an appropriate balance among categories; it is important for the Department to know that:· Eating disorders affect up to 25 million Americans, across all age, gender, SES, and ethnicity groups. Ensuring access to treatment will have an appropriate balance across the population of sufferers, many who, without adequate access to specialty care would unduly access inappropriate, inadequate, but costly, care.In terms of what should be taken into account to prevent discrimination against individuals because of their age, disability status, or expected length of life; it is important to remember that:o Eating disorders do not discriminate. Eating disorders affect up to 25 million Americans, from as young as age 8 through the lifespan. Without adequate access to effective, specialized care, many end up seeking disability coverage due to their illness.In terms of what models HHS should consider in developing essential health benefits; there are some good model policies in effect currently:o Insurance policies that include adequate and comprehensive access to specialized and comprehensive eating disorder care at all levels of treatment offer their members the opportunity for full recovery. Many insurers currently offer this type of coverage to their members. This type of treatment access is effective in successful treatment and resolution of the eating disorder. A fully recovered individual contributes to the workforce, is a productive and successful member of society.In terms of what criteria should be used to update essential health benefits over time; we believe that the combination of research and clinical practice expertise yield the most comprehensive road-map for determining updates :o As advances in eating disorders treatment are made, updates to essential health benefits should be related to clinical utility and integration of research findings.
Jeanine Cogan, Ph.D.
Policy Director
Eating Disorders Coalition
202-352-3208
Wednesday, November 9, 2011
Over 200 Respond to HHS Action Alert! Thank You for Your Help
Dear EDC Advocates,

Before I began serving as the EDC's Policy Assistant I was an EDC Advocate who came to EDC National Lobby Days and participated in Action Alerts.
When I first became an EDC Advocate back in 2002, I admit, I did not firmly believe that my voice could make that much of a difference. I mean, every day I listened to NPR and watched CSPAN and heard endless stories of gridlock and spending cuts plaguing our Federal Government, so in the scheme of things I didn't think that one Kathleen MacDonald could make an impact. Today, I know better. I know that my voice matters. And I want you to know that your voice matters.
Last week the EDC invited you to raise your voice in a time-sensitive and highly important Action Alert. Over 200 of you wrote in to HHS, sharing your voice, your stories, your research, your knowledge, your loved one's memories and your specific requests regarding eating disorders and the soon to be determined Essential Health Benefits. You made an impact and you spoke for the countless millions who suffer, for the countless millions who try to access treatment only to be denied by their insurance company, for the countless whose lives have been cut far too short by these insidious diseases, and for future generations who can be prevented from suffering the most deadly of all mental illnesses.

Before I began serving as the EDC's Policy Assistant I was an EDC Advocate who came to EDC National Lobby Days and participated in Action Alerts.
When I first became an EDC Advocate back in 2002, I admit, I did not firmly believe that my voice could make that much of a difference. I mean, every day I listened to NPR and watched CSPAN and heard endless stories of gridlock and spending cuts plaguing our Federal Government, so in the scheme of things I didn't think that one Kathleen MacDonald could make an impact. Today, I know better. I know that my voice matters. And I want you to know that your voice matters.
Last week the EDC invited you to raise your voice in a time-sensitive and highly important Action Alert. Over 200 of you wrote in to HHS, sharing your voice, your stories, your research, your knowledge, your loved one's memories and your specific requests regarding eating disorders and the soon to be determined Essential Health Benefits. You made an impact and you spoke for the countless millions who suffer, for the countless millions who try to access treatment only to be denied by their insurance company, for the countless whose lives have been cut far too short by these insidious diseases, and for future generations who can be prevented from suffering the most deadly of all mental illnesses.
On a personal note - with each one of your emails to HHS you increased the flame of hope within me. You increased my hope that together we will change the way those affected by eating disorders are treated --including families, sufferers, researchers, and clinicians.
Thank you for each of your comments to HHS and for your continued advocacy. We look forward to continuing our other advocacy efforts with you as we work to ensure that eating disorders research, treatment and education and prevention are adequately and duly addressed, and that people suffering from eating disorders receive the treatment, services and compassion they deserve.
Yours from the Hill, Kathleen
Photo courtesy PDPhoto.org
Thank you for each of your comments to HHS and for your continued advocacy. We look forward to continuing our other advocacy efforts with you as we work to ensure that eating disorders research, treatment and education and prevention are adequately and duly addressed, and that people suffering from eating disorders receive the treatment, services and compassion they deserve.
Yours from the Hill, Kathleen
Photo courtesy PDPhoto.org
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