At least 1 million Australians right now are living with an eating disorder. But there may be many more, because the early signs often aren’t recognized, there is significant stigma and stereotyping associated with eating disorders, and there is insufficient research into the best ways to prevent, detect and treat these disabling and sometimes deadly mental health disorders.
That’s why patient advocates, people with eating disorders, clinicians and researchers came together to develop the National Eating Disorder Research Strategy. “We worked with over 480 people around Australia to develop the strategy and to define the Top 10 most urgent research priorities, that can make a real difference over the next decade,” says Dr. Sarah Maguire, Director of the InsideOut Institute at the University of Sydney.
“We know that early intervention can prevent severe illness, we know that many people can fully recover if they get the right therapy at the right time,” says Dr. Maguire. “But unless we discover the right treatments through research and translate them into the right therapies received at the right time, people don’t and won’t recover.”
The Top Ten Priority areas for research include; stigma and health promotion, risk and protective factors, prevention, early identification, equity of access, do no harm, early intervention, support families, individuals medicine and treatment outcomes.
“Eating disorders are poorly understood by the general public and medical professionals,” says Dr. Maguire. “70 percent of people with an eating disorder don’t get treatment, and of those who do, only 20 percent receive an evidence-based treatment.”
“We need to work with clinicians so they can intervene effectively, using the best research,” says Dr. Sian McLean, President of the Australian & New Zealand Academy for Eating Disorders and one of the researchers who contributed to the development of the Strategy. “And we all need to be aware of the early warning signs of eating disorders, especially in people who might not fit public stereotypes.”
“Eating disorder research has been historically very poorly funded. Government investment in this strategy marks a significant turning point,” she says.
Eating disorders can be associated with significant body changes, for example weight loss in anorexia nervosa, but most people who live with eating disorders don’t experience this, and so their struggle can be hidden, go unnoticed or even be dismissed by clinicians.
One of the many contributors to the strategy was Shannon Calvert, who has used her experience of living with Severe and Enduring Anorexia Nervosa (SEAN) to embed the “lived experience” in research and treatment for eating disorders and mental health.
“The best treatment for eating disorders is person-centered and compassionate, and that’s also true of research,” says Shannon. “We have to integrate research and clinical practice so that our experience can educate scientists and health professionals, and inform the questions that they pursue.”
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