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Beating BDD
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Beating BDD

Author: BDD Foundation

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Information and inspiration for people living with body dysmorphic disorder, from the BDD Foundation in the UK. To learn more about the show and the work of the BDD Foundation, visit http://bddfoundation.org
44 Episodes
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The author, speaker and therapist Scott Granet has lived with BDD for many decades, but he's now learnt to manage the disorder so it's 'no more than a minor nuisance'. He tells us about the childhood roots of his condition, the serious episodes that have marked his life, and how his daughter has changed his perspective on what matters.
Our guest, Rachel Moore, lived with undiagnosed BDD for around 30 years before finally receiving a diagnosis in her late thirties. She talks candidly about childhood bullying, family comments, and how the disorder affected her relationships and confidence. Today, Rachel lives a full and enjoyable life, which includes performing in a band and volunteering with the BDD Foundation.
Our guest, Mia Hill, describes how an obsession with perceived flaws took over her life during the COVID-19 lockdown. Today, Mia works for OCD-UK, serves as an ambassador for the BDD Foundation and openly shares her experiences to help others find hope and recovery.
Sheila Paul reflects on the role cultural expectations and painful childhood experiences played in her developing body dysmorphic disorder. And she describes how sharing her experiences within the African Caribbean community is helping to shine a light on mental health issues.
Sam Milburn, mum to Jack, is a passionate advocate for more awareness and better access to treatment for BDD. In this episode, she shares her hard-won advice for other parents, including how to navigate the system on behalf of your child while also looking after yourself.
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