The July 2012 issue of the International Journal of Eating Disorders arrived in my mailbox yesterday and on the front cover were the words: The Challenge of Treatment Refusal. Because I had just written two posts here having to do with treatment against the will of a person with a severe eating disorder, I suspected that this article might be of the same ilk.
The title of the article is The Stigma of "Mental" Illness: End Stage Anorexia and Treatment Refusal 45.5 627-634 2012 and, in fact, the authors -- Amy T. Campbell, JD, MBE and Mark P. Aulisio, PhD -- propose (they write "argue") "....psychiatric patients should sometimes be allowed to refuse life-sustaining treatment in favor of comfort care for a condition that is caused by that psychiatric disorder and [we] articulate the core considerations that should be taken into account when such a case arises." (p. 627
Their conclusion contradicts that reached by the judge in the Wales case so fully discussed by the media recently in the UK.
This paper and the authors' conclusion also brought me to full attention because I have wondered "when is enough enough". It seems dreadful to even think this when one is a parent. It feels immoral, disloyal, unloving, inhumane and even criminal.
At the very beginning of this second round about 9 years ago, a wise therapist said to me, "hope for the best and prepare for the worst." I do and I have. This disease is life-threatening. And I, for one, continue to hang in there.
But, what does one do if one's loved one sinks back down again (and again) into the morass of the eating disorder without any glimmer of the desire to change their behavior; to stop it and turn around despite utilizing and/or offering every single known method to bring about a return to the path to recovery and the stability of staying on it?
Let go and Let God?
What does one do when one observes a beloved human being endangering their life with a multitude of behaviors not the least of which is not eating and sees the pain they are in, both physically and psychologically. What kind of life is this?
This is the dilemma being faced by many people whose daughter/son/patient/ward/family member has an eating disorder so entrenched that there appears to be no way out. This is the dilemma that confronted the medical team of the woman (an adult) in Wales who sought the opinion of the judge. This is the dilemma discussed by Dr. Tomas Silber in this paper.
This is tough stuff.
I want to pause here and take you to a thought that appeared in a post a few years ago written by a young woman I know who is in recovery and who makes it clear repeatedly that her recovery depends on constantly taking advantage of tools she has gained as well as the support of a therapist and a steadfast family. She wrote in that post that if she had known those who she thought "had her back" were talking about end of life care rather than recovery, she might have thrown in the towel and given up.
Think about this. I sure do. Every day.
Now I turn to the article under discussion here in which the authors look at two women, both having been fighting an eating disorder for 40 years and 25 years respectively. The former, who is 55, has declared she doesn't want to do this anymore and the latter, who is 40, has stated she wants to live but she isn't willing to again take on the necessary treatment to get on the path to recovery.
They ask, by way of introduction, "....is there such a thing as an 'end stage psychiatric disorder' and if so, what are the conditions, if any, under which an individual might be able to legally and ethically choose to refuse further treatment for this disorder and opt for comfort care?" (p. 627)
Like Dr. Silber, the authors focus on issues related to what they call "capacity" and Dr. Silber calls "competence" and they go on to propose a "framework to guide systematic analysis of issues raised by this [their] article." (p. 627) The authors discuss entrenched eating disorders.
There have been papers and a book, actually, referring to entrenched eating disorders as Severe and Enduring Eating Disorder (SEED) by Paul Robinson (Wiley-Blackwell, 2009) and I could go on about this condition. But here, I want to focus on the topic of this paper and, as well, put out a call or a heads-up to people in the field and in the trenches to pay attention and participate in this developing conversation. It is not going to go away.
The authors discuss the legalities involved including what informed consent means. They look at capacity/competence. They underscore that "....law and ethics also support an individual's right to refuse life-sustaining treatment" and then turn to philosophically explore what stand might be taken about those with psychiatric illness rather than physiological illness, for example, cancer.
The going gets tougher with their question, "Do Persons with Psychiatric Disorders ever get to Make Decisions to Refuse (Further) Life-Sustaining Treatment?" (p.629) They claim that in fact this is permitted and accepted. But, I wonder, what about those with serious mental illness. Should they be permitted to make such a decision?
Ultimately, after several interim steps looking at physical condition, the idea of an entrenched illness, the idea of what they call "psychic suffering," the authors believe that a person with a serious mental illness should be able to make such a decision and further, given the two case studies that they incorporate, they believe that any hesitancy actually "....perpetuates stigma directed towards persons with psychiatric disorders." (p.633) Further, they believe one should take a holistic approach, a look at the entire situation rather than "just" competence.
The authors close by recommending, "....especially for psychiatrists, ....fuller contemplation of the limits of medicine, the nature of suffering, and the potentiality that a patient with an eating disorder may at some point make a rational decision to end aggressive treatment (which we very much distinguish from suicide.)" (p. 633) They also call for "...an expansion of the model of end of life care and palliative care to include patients with psychiatric-driven disorders, and an expansion of the model of integrated primary physical/behavioral health to end of life care."
They conclude that "....end of life planning including hospice and comfort care measures was the clinically, ethically, and legally appropriate path...." for the two women. (p. 633)
I found myself cringing as the analysis continued towards this their inevitable -- given their positions at each point -- conclusion.
I keep asking myself is there something about anorexia and the evidence
about the disintegration of ability of thought and meaningful action
gathered as a result of the Minnesota Starvation Experiment, headed by Dr. Ancel Keys - here in one interpretation that appeared in the online Psychology Today , that would argue in the direction of the position taken by the judge in Wales?
A difficult question worthy of further exploration and serious debate.
Information is provided about eating disorders, particularly of adults, to parents and other loved ones written by a parent who is in recovery from an eating disorder.
Welcome
When I created this blog, I was "getting on" in my early sixties, hence the blog name. However, my adult daughter's eating disorder and co-occurring emotional dysregulation disorder and other co-morbidities - ongoing for about 33 years - became and was our focus as we attempted to help her get into recovery. By learning about, reflecting on, reading about, attending conferences and writing about eating and brain disorders, I created a place to blog what I've learned. I hope this blog will be of use to others, especially families of and adult sufferers themselves to help them get into recovery. I update posts from time and the update date will be present at the top of the post.
Sadly, my daughter passed away in early October 2021 mainly because her body became so malnourished that she was immunocompromised, contracted a severe infection that was not properly addressed during an earlier hospital stay the month before, and developed an overwhelming non-covid pneumonia following surgery to save her life. I believe she should have been able to receive palliative care but Arizona, our country, and even the professionals trained in the treatment of eating disorders, particularly anorexia, are not "there" yet. I address the issue of palliative care in a recent post below, initially written in November 2021. I am not a certified eating disorder specialist. I am an Expert by Experience and college-educated with a BA in Community Work with an additional certificate in a one-year program in Business Administration from the same institution.
I am passionate about all of this because, as Shakespeare wrote in The Taming of the Shrew, Act 4, Scene 3: "My tongue will tell the anger [and sadness] of my heart or else my heart, concealing it, will break. And, rather than it shall, I will be free even to the uttermost, as I please in words."[2016]
Travel Guide
If you're new to my blog, I recommend you begin on the right side and take a look at the "Of Note" offerings. Read Dr. Cynthia Bulik's recent published interview (5/4/22) "Rethinking Eating Disorders" if you want to print an easy-to-understand professional's expert opinion about anorexia for your family doctor or the therapist. [Early intervention is absolutely critical. For those whose eating disorder is categorized as entrenched or severe and enduring, read the editorial comment by Stephen Touyz and Philipa Hay for a new approach about treatment. It is possible for your loved one to recover! I have also attached a link here for additional papers on the subject of severe and entrenched eating disorders. If you are a family member or friend of an adult with an eating disorder and have been at this for awhile, I refer you to the posts within the title "Adult Eating Disorders and Recovery Tools" found in the Index on the right hand side of this site. As well, in the "Of Note" section take a look at those posts with an asterisk. If you're a parent and need support, look for posts in the Index about parent support or parent toolbox.
In my opinion, the best book to buy, to refer to constantly and to share with members of the medical/psychiatric profession is "Sick Enough: A Guide to the Medical Complications of Eating Disorders" by Jennifer L. Gaudiani MD, CEDS, FAED. "Dr. Gaudiani aims to improve medical diagnosis and treatment, motivate recovery, and validate the lived experiences of individuals of all body shapes and sizes, while firmly rejecting dieting culture."
I recommend two groups who will support you on your journey - F.E.A.S.T and the National Alliance for Eating Disorders. Both maintain websites and Facebook private groups.
Saturday, June 30, 2012
Sunday, June 24, 2012
Against Their Will - A P.S. with thanks to an article by Jeneen Interlandi in the New York Times Magazine, June 24, 2012
Today's New York Times Magazine (Sunday, June 24, 2012, pp. 25-29, 38, 46-7) carries an article written by Jeneen Interlandi about the journey their family took through emergency rooms, psychiatric wards, psychiatric courtrooms, and in their case jails.
The title of the article, linked here, A Madman in Our Midst, grabs the attention of the ordinary reader in a way that another title might not. I know I cringed at the title because it exacerbates stigma but I applaud Jeneen and her family for making this story public and for incorporating so much information about the history and the status of the mental health care system in our country, in some cases state by state, as well as the arguments pro and con about involuntary commitment and treatment.
I think Jeneen Interlandi's article highlights and vastly expands upon what I wrote in a previous post, "Against Their Will - Treatment for ED and Other Brain Disorders." The details she provides about the struggles her family had with the ethics of all of this reflect back to Dr. Tomas Silber's article, "Treatment of Anorexia Nervosa Against the Patient's Will: Ethical Considerations."
As Ms. Interlandi writes and as many of us caught in this cycle will tell you, "the absurdity of this situation wore on us. How was anyone with a diagnosed mental illness supposed to recover through a revolving door of emergency rooms, short-term psych wards and [in her father's case] jail?"
If you are interested in what's happening across the country, take a look at the website of the Treatment Advocacy Center, the purpose of which is to "eliminate barriers to the treatment of mental illness" and which is lobbying for broader involuntary commitment standards. Just released by the Center is A Guide for Implementing Assisted Outpatient Treatment, that [from the website] "includes 64 pages of practical information and instruction and appendices containing more than 30 sample forms and other documentation. For links to the guide, its appendices and samples, click here.
Change is needed for those who need to gain assured (meaning at least 6 months), not short-term, stability, in a safe place before consideration of next steps. As an advocate for those with entrenched eating disorders, I believe this placement with guided nutrition and therapy followed by a step-down program, must be available and is especially necessary.
The title of the article, linked here, A Madman in Our Midst, grabs the attention of the ordinary reader in a way that another title might not. I know I cringed at the title because it exacerbates stigma but I applaud Jeneen and her family for making this story public and for incorporating so much information about the history and the status of the mental health care system in our country, in some cases state by state, as well as the arguments pro and con about involuntary commitment and treatment.
I think Jeneen Interlandi's article highlights and vastly expands upon what I wrote in a previous post, "Against Their Will - Treatment for ED and Other Brain Disorders." The details she provides about the struggles her family had with the ethics of all of this reflect back to Dr. Tomas Silber's article, "Treatment of Anorexia Nervosa Against the Patient's Will: Ethical Considerations."
As Ms. Interlandi writes and as many of us caught in this cycle will tell you, "the absurdity of this situation wore on us. How was anyone with a diagnosed mental illness supposed to recover through a revolving door of emergency rooms, short-term psych wards and [in her father's case] jail?"
If you are interested in what's happening across the country, take a look at the website of the Treatment Advocacy Center, the purpose of which is to "eliminate barriers to the treatment of mental illness" and which is lobbying for broader involuntary commitment standards. Just released by the Center is A Guide for Implementing Assisted Outpatient Treatment, that [from the website] "includes 64 pages of practical information and instruction and appendices containing more than 30 sample forms and other documentation. For links to the guide, its appendices and samples, click here.
Change is needed for those who need to gain assured (meaning at least 6 months), not short-term, stability, in a safe place before consideration of next steps. As an advocate for those with entrenched eating disorders, I believe this placement with guided nutrition and therapy followed by a step-down program, must be available and is especially necessary.
Friday, June 22, 2012
Against Their Will - Treatment for ED and other Brain Disorders
Yesterday, while exploring the links that accompanied Laura Collins' recently posted presentation at the International Conference on Eating Disorders (ICED) in May 2012, I noticed a link to an article by Tomas J. Silber, MD, MAAS titled Treatment of Anorexia against the Patient's Will: Ethical Considerations.
Silber's topic and the outcome of this kind of decision, referred to here in Arizona as Title 36, has continued to be a thorn for me because I and my loved one's team have made the decision to utilize this law several times as a last ditch effort to save her life. It's a wrenchingly difficult decision to make for reasons that Silber discusses. In all cases but one (and a month later she and we suffered the consequences of the judge thinking she was competent and could make it and at that point Title 36 was invoked) approval was granted, the most recent being almost six months ago. Only over the past two months has she begun to re-gain (the word is used to illustrate that once upon a time she was at a healthy weight and needs to return to it) the weight through balanced nutrition so that she (her brain/body) is able to do the work ahead. This initial process - to reach stability - can take six months to a year! She's never been able to do this for a variety of reasons. The most recent step is an attempt to give her another opportunity.
Yesterday, a well-educated scientist who is knowledgeable (because she is also in recovery) about eating disorders, took a thoughtful look at the recent situation in Wales in which a judge, at the urging of the care team, has ordered forced feeding for a woman who had given up the fight and whose immediate family agreed with her decision. The consequent at times thoughtful at times emotion filled discussion has raised, I think with great value, the topic of eating disorders, specifically starvation eating disorders to public consciousness at a much higher level than before. [The post referred to is no longer available on line.]
We need to keep this conversation going.
The bottom line, for me, that so many of us continue to state is that nutrition must come first, for without a return to nutrition, the brain and the body don't have a chance against a starvation eating disorder. And that return requires stability for quite some time afterwards, too. And, this is only the beginning. The hardest part is ahead for this young woman and for others who need to overcome entrenched feelings and behavioral patterns.
So, back to Dr. Silber's article which takes a look at the ethics of treatment against a patient's will. He includes in his introduction the point, which is well-known in the eating disorder community whether treatment occurs at home or in a hospital or in a residential setting, "....In many, if not most, instances of treatment for AN, patients receive some form of treatment against their will."(p. 283) One only needs to read Harriet Brown's important book Brave Girl Eating to learn that even at home getting a child in the clutches of a starvation eating disorder to eat isn't the simple matter of just placing a plate in front of her/him and pleasantly asking him or her to eat. Rather, it's a matter of loving yet firm persuasion met with screams, and thrown and/or spit out food, and so forth until the child is re-nourished enough to start to participate in the process.
Silber goes on to say, "....The situation can become even more difficult to address once patients reach the age of majority." (p. 283)
This is the situation for the woman in Wales. This is the situation for those entrenched in eating disorders. This is the situation for my family member.
As he notes, the patient's entire team (if s/he is lucky enough to have one) may not reach agreement on how to proceed and often the decision must be taken on by another family member or a doctor or ultimately a judge.
To approach a decision, Silber proposes what he calls Justified Paternalism (JP) (p. 284 of the article published in Adoles Med State Art Rev. 2011;22(2):283-8,x.) and he believes that JP must be wise, meaning that one must realize one violates a moral rule and second that there must be a compelling reason.
He refers to two papers the conclusions of which are similar to Title 36 with the addition of "c)the person is likely to be thankful for the treatment at a later time,.... and "d)the intrusion is generalizable, in the sense that those supporting it would wish the same on themselves."
[I actually wonder if the judge read Silber's paper because it's so compelling in its pro and con positions, particularly in regards to eating disorders.]
He next discusses autonomy and society's drift towards leaving decisions to the patient. He recognizes during this discussion that someone with an eating disorder is quite able to present pseudo competence, therefore meeting standards for competency as also outlined in Title 36.
Yet, as many of us in the trenches and as Silber then goes on to recognize, those with a starvation eating disorder aren't fully competent; their brains and their bodies have been compromised and will remain so until they are renourished and stabilized in that renourished state. He also recognizes the supreme importance of involvement of the patient's family and/or social network -- the team that Dr. Janet Treasure and others advocate.
Silber presents research that underscores his arguments and also highlights the difficulty of working with teenagers and more particularly adults, and closes his paper with an emphasis on values and the importance of how the person perceives herself/himself to be respected during the treatment process. In other words, as he writes, "....At the end it is always values that underlie and strengthen the good work. These include fundamental respect for the person, even as liberty is restricted; beneficence; and truth telling." (p. 286)
I have heard parents say that they and their family member(s) are regarded as "less than" in these kinds of settings and a balance must be found so that all concerned believe they are participating in the effort to help their family member recover. Silber speaks to this important need.
Silber concludes, and I hope that the prolonged treatment the judge has ordered for the young woman in Wales and for others remanded to treatment evolves into, "....Treatment interventions for eating disorders need to include not only the biopsychoscocial and spiritual components that have enriched the field over the years, but also need to incorporate a philosophical dimension that takes into account a reflective understanding of patient autonomy; patients' rights; obligation to protect; respect for persons; right to treatment refusal; and, last but not least, justified paternalism and an expanded concept of autonomy." (p.287)
In closing, I want to thank the author known as Extra Long Tail and Laura Collins for their recent posts. The information provided I am sure, with dissemination, will improve the care of others who have starvation eating disorders, a term that I came across last night in a book by Doreen A. Samelson, ED.D., MSCP titled Feeding the Starving Mind (New Harbinger Publications, Inc., 2009).
Silber's topic and the outcome of this kind of decision, referred to here in Arizona as Title 36, has continued to be a thorn for me because I and my loved one's team have made the decision to utilize this law several times as a last ditch effort to save her life. It's a wrenchingly difficult decision to make for reasons that Silber discusses. In all cases but one (and a month later she and we suffered the consequences of the judge thinking she was competent and could make it and at that point Title 36 was invoked) approval was granted, the most recent being almost six months ago. Only over the past two months has she begun to re-gain (the word is used to illustrate that once upon a time she was at a healthy weight and needs to return to it) the weight through balanced nutrition so that she (her brain/body) is able to do the work ahead. This initial process - to reach stability - can take six months to a year! She's never been able to do this for a variety of reasons. The most recent step is an attempt to give her another opportunity.
Yesterday, a well-educated scientist who is knowledgeable (because she is also in recovery) about eating disorders, took a thoughtful look at the recent situation in Wales in which a judge, at the urging of the care team, has ordered forced feeding for a woman who had given up the fight and whose immediate family agreed with her decision. The consequent at times thoughtful at times emotion filled discussion has raised, I think with great value, the topic of eating disorders, specifically starvation eating disorders to public consciousness at a much higher level than before. [The post referred to is no longer available on line.]
We need to keep this conversation going.
The bottom line, for me, that so many of us continue to state is that nutrition must come first, for without a return to nutrition, the brain and the body don't have a chance against a starvation eating disorder. And that return requires stability for quite some time afterwards, too. And, this is only the beginning. The hardest part is ahead for this young woman and for others who need to overcome entrenched feelings and behavioral patterns.
So, back to Dr. Silber's article which takes a look at the ethics of treatment against a patient's will. He includes in his introduction the point, which is well-known in the eating disorder community whether treatment occurs at home or in a hospital or in a residential setting, "....In many, if not most, instances of treatment for AN, patients receive some form of treatment against their will."(p. 283) One only needs to read Harriet Brown's important book Brave Girl Eating to learn that even at home getting a child in the clutches of a starvation eating disorder to eat isn't the simple matter of just placing a plate in front of her/him and pleasantly asking him or her to eat. Rather, it's a matter of loving yet firm persuasion met with screams, and thrown and/or spit out food, and so forth until the child is re-nourished enough to start to participate in the process.
Silber goes on to say, "....The situation can become even more difficult to address once patients reach the age of majority." (p. 283)
This is the situation for the woman in Wales. This is the situation for those entrenched in eating disorders. This is the situation for my family member.
As he notes, the patient's entire team (if s/he is lucky enough to have one) may not reach agreement on how to proceed and often the decision must be taken on by another family member or a doctor or ultimately a judge.
To approach a decision, Silber proposes what he calls Justified Paternalism (JP) (p. 284 of the article published in Adoles Med State Art Rev. 2011;22(2):283-8,x.) and he believes that JP must be wise, meaning that one must realize one violates a moral rule and second that there must be a compelling reason.
He refers to two papers the conclusions of which are similar to Title 36 with the addition of "c)the person is likely to be thankful for the treatment at a later time,.... and "d)the intrusion is generalizable, in the sense that those supporting it would wish the same on themselves."
[I actually wonder if the judge read Silber's paper because it's so compelling in its pro and con positions, particularly in regards to eating disorders.]
He next discusses autonomy and society's drift towards leaving decisions to the patient. He recognizes during this discussion that someone with an eating disorder is quite able to present pseudo competence, therefore meeting standards for competency as also outlined in Title 36.
Yet, as many of us in the trenches and as Silber then goes on to recognize, those with a starvation eating disorder aren't fully competent; their brains and their bodies have been compromised and will remain so until they are renourished and stabilized in that renourished state. He also recognizes the supreme importance of involvement of the patient's family and/or social network -- the team that Dr. Janet Treasure and others advocate.
Silber presents research that underscores his arguments and also highlights the difficulty of working with teenagers and more particularly adults, and closes his paper with an emphasis on values and the importance of how the person perceives herself/himself to be respected during the treatment process. In other words, as he writes, "....At the end it is always values that underlie and strengthen the good work. These include fundamental respect for the person, even as liberty is restricted; beneficence; and truth telling." (p. 286)
I have heard parents say that they and their family member(s) are regarded as "less than" in these kinds of settings and a balance must be found so that all concerned believe they are participating in the effort to help their family member recover. Silber speaks to this important need.
Silber concludes, and I hope that the prolonged treatment the judge has ordered for the young woman in Wales and for others remanded to treatment evolves into, "....Treatment interventions for eating disorders need to include not only the biopsychoscocial and spiritual components that have enriched the field over the years, but also need to incorporate a philosophical dimension that takes into account a reflective understanding of patient autonomy; patients' rights; obligation to protect; respect for persons; right to treatment refusal; and, last but not least, justified paternalism and an expanded concept of autonomy." (p.287)
In closing, I want to thank the author known as Extra Long Tail and Laura Collins for their recent posts. The information provided I am sure, with dissemination, will improve the care of others who have starvation eating disorders, a term that I came across last night in a book by Doreen A. Samelson, ED.D., MSCP titled Feeding the Starving Mind (New Harbinger Publications, Inc., 2009).
Thursday, June 21, 2012
BPD and ED - a view from the trenches by Evelyn Sharnov in Psychology Today
Warning: as I write below, this links to a very powerful and potentially triggering article. The thing is, it's real.
Powerful and very real is this story - In Extremis Part One - by Evelyn Sharnov that was just posted on the Psychology Today website blog.
Here's the link if the above highlighted title link doesn't work.
http://www.psychologytoday.com/blog/notes-the-frontline/201206/in-extremis-part-one
I want to highlight two very important points:
First, that she acknowledges what so many baffled parents have struggled with:
"A borderline personality disorder sometimes forms in response to triggers like abuse or abandonment, real or perceived—but not always. The origins of the disorder are a mystery at its core."
And, second, that this illness is treatable and must be addressed as soon as possible for the person affected.
An excellent book just out is by Francis Mark Mondimore, M.D. and Patrick Kelly, M.D. titled Borderline Personality Disorder: New Reasons for Hope (A Johns Hopkins Press Health Book, 2011).
I reviewed this extremely informative book here.
I know it's hard to hang in there with someone who is fighting this what I believe at its basis is a biological brain disorder. And, as illustrated in the story, Annie also has an eating disorder - a common combination. But as Laura Collins relates in her talk - powerful with terrific visuals to accompany the text - she presented at the International Conference on Eating Disorders in Austin this past May 2012, we must not forget that, again, these are biologically based illnesses of the brain and not willful behaviors and for that reason the people who are overwhelmed by these illnesses need our help, not our abandonment nor our disdain.
Powerful and very real is this story - In Extremis Part One - by Evelyn Sharnov that was just posted on the Psychology Today website blog.
Here's the link if the above highlighted title link doesn't work.
http://www.psychologytoday.com/blog/notes-the-frontline/201206/in-extremis-part-one
I want to highlight two very important points:
First, that she acknowledges what so many baffled parents have struggled with:
"A borderline personality disorder sometimes forms in response to triggers like abuse or abandonment, real or perceived—but not always. The origins of the disorder are a mystery at its core."
And, second, that this illness is treatable and must be addressed as soon as possible for the person affected.
An excellent book just out is by Francis Mark Mondimore, M.D. and Patrick Kelly, M.D. titled Borderline Personality Disorder: New Reasons for Hope (A Johns Hopkins Press Health Book, 2011).
I reviewed this extremely informative book here.
I know it's hard to hang in there with someone who is fighting this what I believe at its basis is a biological brain disorder. And, as illustrated in the story, Annie also has an eating disorder - a common combination. But as Laura Collins relates in her talk - powerful with terrific visuals to accompany the text - she presented at the International Conference on Eating Disorders in Austin this past May 2012, we must not forget that, again, these are biologically based illnesses of the brain and not willful behaviors and for that reason the people who are overwhelmed by these illnesses need our help, not our abandonment nor our disdain.
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