Susan Ringwood is a Board member of F.E.A.S.T.,the global parent support network, and was Chief Executive of the UK charity Beatfor 13 years until 2015. Susan was a member of the National Institute of Health and Clinical Excellence guideline development groups for the treatment of Eating Disorderswhich set standards for evidence-based treatment, for example the Children and Young People’s Eating Disorder Access and Waiting Time Commissioning Guide, and has served on UK government committees and task forces related to eating disorders and mental health treatment.
Susan is a fellow of the Academy of Eating Disorders, she was a founder member of the AED’s Advisory Board, is a former Chair of the Academy’s Patient and Carers’ Committee and was the 2008 recipient of the AED Meehan/Hartley award of Leadership in Advocacy and Public Service. When she joined Beat in 2001 Susan knew absolutely nothing about the condition. What she learnt, very quickly, and mostly from those parents she met, was that this was a confounding, challenging and downright scary place to be. Fast forward 18 years, and she is serving on the F.E.A.S.T. board to do what she can to bring evidence-based treatment to all — in a way that involves, includes and respects families.
To mark the fourth annual World Eating Disorders Action Day on June 2, this story is the first in a series on the 2019 theme, “Eating Disorders: We Can’t Afford to Wait”. By Susan Ringwood We’ve been waiting for a long time. Anorexia Nervosa was first formally described by Sir William Gull, physician to Queen..

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The Australian Broadcasting Commission (ABC) Radio 774, in the Conversation Hour on January 13, discussed the effects of food shortages due to the pandemic. I describe the impact on people with eating disorders.
My segment starts 34.30 mark.
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