Part of Backbench Business – in Westminster Hall at 3:33 pm on 29 February 2024.
I wish to begin, as others have, by congratulating Wera Hobhouse on bringing forward this debate in Eating Disorders Awareness Week. I am very glad to once again participate in this debate, as I have done in the past. When I have spoken in this debate previously, I have always begun by pointing out that I first became aware of eating disorder conditions in the 1980s, when Karen Carpenter died, and then again in 1999, when Lena Zavaroni died. Both women had struggled with eating disorders for a number of years and sadly succumbed to them, when they ought to have had so many years ahead of them.
An estimated 1.25 million people across the UK face a similar struggle. Eating disorders, as we have heard, do not respect age, ethnicity, gender or background. Indeed, a quarter of those with eating disorders are men.
The mortality rate is high, especially for those with anorexia, which has the highest mortality rate of any mental illness, and one in six people with binge eating disorder attempt to end their lives. Other mental health challenges can often accompany eating disorders, such as depression, self-harm, anxiety and obsessive behaviours. Eating is fundamental to survival, so those with eating disorders typically develop severe physical health problems. Yet we know that, with the right support and treatment, we can change lives, and early intervention provides the best chance for recovery.
Eating Disorders Awareness Week this year seeks to highlight avoidant/restrictive food intake disorder, or ARFID, which is a relatively new term. It is different from other restrictive eating disorders in that it describes a pattern of eating that avoids certain foods or food groups entirely and/or is restricted in quantity. Sometimes those with it eat very small amounts. Avoidant and restrictive eating is not related to a lack of available food, cultural norms or even fasting for religious reasons, and it is not related to a person’s view of their body shape or a specific purpose, such as losing weight. Nor does it feature some of the other behaviours that can be associated with anorexia or bulimia, such as over-exercising. ARFID is often dismissed as picky eating, but the crucial difference between what we might call a picky eater and a child with ARFID is that a picky eater will not starve themselves to death. A child with ARFID very well might.
While the exact causes of ARFID are unknown, it is thought that people who develop it do so because of sensory sensitivity, fear of negative consequences or a lack of interest in eating. For example, they might be very sensitive to the taste, texture or appearance of certain types of food, or have had a distressing experience with food, such as choking, vomiting, infant acid reflex or other gastrointestinal conditions. That may cause the person to develop feelings of fear and anxiety around food, leading them to avoid it. It does not discriminate; it can affect anyone of any age, including even babies, and can be diagnosed in children as young as three.
Researchers know much less about what puts someone at risk of developing ARFID, but it has been discovered that people with autism spectrum conditions are much more likely to develop the condition, as are those with attention deficit hyperactivity disorder and intellectual disabilities. In addition, children who do not outgrow what we might call “normal picky eating”, or in whom picky eating is severe, appear to be more likely to develop ARFID. Many children with ARFID have a co-occurring anxiety disorder, and they are also at high risk for other psychiatric disorders.
According to Beat, the UK’s largest eating disorder charity,
“There has been a sevenfold increase in calls to our Helpline” related specifically to ARFID over the past five years. The variable service provision for the condition is due partly to the lack of research into treatment. The Scottish Government have provided Beat with more than £600,000 to provide a range of support for those affected by an eating disorder, but performance still varies across health boards. There must be no complacency. To help tackle that, a consultation was undertaken on the draft national specification for the care and treatment of eating disorders in Scotland to ensure that support and services meet the needs of those living with an eating disorder, wherever and whoever they are in Scotland. The responses to the consultation will be considered carefully.
When a person has an eating disorder of any kind, they need compassionate support with their mental and physical health. Their loved ones also need support, because this is a condition that affects whole families and not just individuals. Indeed, very often, it is close loved ones who are the first to pick up on the fact that their beloved family member has an eating disorder. There is nothing worse for them than watching their loved one’s mental and physical health deteriorate before their eyes from a condition that is often not well understood and, sadly, not always sufficiently supported through prompt and sensitive treatment.
I am glad that we are once again having this important debate on this condition in Eating Disorders Awareness Week and taking the opportunity to raise awareness of eating disorders in general and, this year, of avoidant/restrictive food intake disorder. Much more research needs to be done into that, and I confess that I knew almost nothing about it before I started preparing for the debate. I hope debates like this one will help those living with an eating disorder and their loved ones to feel less alone, because it can be an isolating illness for individuals and their families, which can only compound the pain and fear that this condition often generates.