Chloë is a Consultant Clinical Psychologist and Team Lead for the service, overseeing treatment for the most severe, treatment-resistant cases of young people with OCD. She is pioneering Multi-Family Group work with families of young people with OCD. With 2 colleagues, she published the clinic’s treatment manual and workbook OCD – Tools to help young people fight back! Turner, Krebs and Volz. OCD and related disorders cause high levels of distress and anxiety and it is not uncommon for children and young people suffering from OCD to become aggressive and challenging at times. Parents may report that this is “out of character” and it can be highly distressing for family members to have to witness and manage these episodes of challenging behaviour. This talk aims to help parents to understand what might be going on for their children and to help them think through how best to approach these situations.
Georgina is an Honorary Consultant Clinical Psychologist and Associate Professor of Young People’s Mental Health and Cognitive Behaviour Therapy, at University College London. Her research interests include developing novel, evidence-based methods for delivering cognitive behaviour therapy (CBT) for obsessive-compulsive disorder (OCD) and body dysmorphic disorder (BDD) in young people, and understanding factors that interfere with recovery in order to inform the development of new treatment approaches.
Cognitive behaviour therapy (CBT) is a highly effective treatment for OCD and BDD, but young people often require support from parents to get the most out of therapy. This talk will cover some of the factors that can interfere with young people fully engaging with CBT, and we will discuss what parents can do to promote engagement. The talk will also address some of the common concerns that families have about remotely-delivered therapy, which has become commonplace over the last 15 months due to the Covid-19 pandemic.
We hear too often that people with BDD fall through the gaps between primary and secondary care and are left unable to access this treatment which is vital for recovery from BDD. As a charity, we responded to the inconsistencies in statutory mental health care provision by establishing a Structured Support Group (Now known as Overcoming BDD Programme), where we deliver evidence-based CBT in a group format online. We also enable peer support both between participants of the group and from our team of Peer Facilitators who all have their own experiences of BDD. The pilot phase ran from 2018-2021, where we conducted three iterations of the pilot project. We collected lots of feedback from both our participants and our Peer Facilitators, so that we could evaluate its success and make improvements. This talk will explore the role of peer support in the BDD Foundation’s online CBT-BDD programme and will provide a chance to hear from former participants on how accessing peer support has been so vital for their recovery.
Hannah works at the BDD Foundation co-ordinating the peer-delivered group-CBT project for BDD. She is a PhD researcher at Queen Mary, University of London where she studies culturally inclusive prevention strategies for eating disorders and body dysmorphic disorder – both of which she has lived experience of.
Alanah has worked for the BDD Foundation as a structured support group facilitator. She is currently finishing her two-year MSc in Developmental Psychology and Clinical Practice at UCL and The Anna Freud National Centre for Children and Families. Alanah has lived experience of BDD and has raises awareness about BDD through newspaper/magazine articles, documentaries, podcasts and as a speaker for the BDD Foundation Conference in 2016.
Nicole is a child, community and educational psychologist; yoga teacher and yoga therapist. She is a trustee of the BDD Foundation and director of the Yoga in Healthcare Alliance. Nicole has authored the books ‘False Bodies, True Selves: Moving Beyond Appearance-Focused Identity Struggles and Returning to the True Self’ and ‘Bodies Arising: Fall in Love with your Body and Remember your Divine Essence’.
‘Narrative approaches view mental health struggles, including BDD, as a bid to make sense of painful, oppressive life experiences through ‘thin’ stories told about the self to the self.
In this session – which will appeal to people with lived experience, loved ones and therapists – we will consider how narrative approaches can be supportive in BDD including a short exploration of creative writing and reading to aid recovery and healing.’
As we return back to “the new normal” since COVID-19, it is natural to want to seek safety and hide from the things that scare us. However, it is crucial that we all embrace our discomfort and remember that fear only gets stronger when we resist, avoid or fight it. During this presentation, participants will gain powerful skills and tools to help them lean into their fears and practice self-compassion, instead of self-judgment and self-punishment.
Kimberley is a licensed Marriage and Family Therapist in the State of California and the founder of CBTschool.com, an online platform that provides courses for those with Obsessive Compulsive Disorder and Body-Focused Repetitive Behaviours who do not have access to mental health care. Kimberley is the host of Your Anxiety Toolkit Podcast.
“BDD used to take up about 95% of my being. Now, the parts of me that bring me joy are bigger than my BDD.”
Now a holistic therapist, Rachel is our first guest from across the pond, and hopefully the first of many! In this episode, she shares her experience of BDD and how everything from working at a cat hotel to learning ballroom dancing has helped her to manage the disorder and find joy.
You can download the transcript for this episode here:
We are proud to announce that the BDD Foundation is the charity partner of The Humanians.
The Humanians is a socially conscious NFT collection born on the Ethereum Blockchain led by the celebrated female artist Amber Day, creator of VISBII – bridging art and utility in the NFTverse, while bringing awareness to the growing mental health issue of Body Dysmorphia. Through their inclusive and supportive Web3 communities on Twitter and Discord, The Humanians celebrate everyone and anyone, free of prejudice and judgement.
The team behind Humania, Odd One Out Labs joined forces with Amber to make a real difference in the NFT space. Together they curate and collaborate relationships with organisations, people and communities, advocating for social change around mental health stigma especially focused on BDD.
The Humanians have partnered with The Be Well Collective and The Body Dysmorphic Disorder Foundation as co-charity partners with the aim to make a difference in the real-world – serving as the bridge between social causes, communities, cultures, creatives and the Blockchain.
In case you didn’t know, Non-fungible tokens (NFTs) are single one off cryptographic assets sitting on a blockchain with unique identification codes and metadata that distinguish them from one another. NFTs can represent real-world or digital assets like artwork, music even to things like real estate; “Tokenizing” these assets makes buying, selling, and trading them more efficient while reducing the probability of fraud as all transactions are fully transparent with the purchase agreements viewable and not editable via smart contracts on the blockchain.
The Humanians aims to help promote The BDD Foundation’s aim which is to relieve the suffering for people with BDD, while donating to the BDDF to advance research, treatments and awareness of the condition which is often under-diagnosed. The founders will also be video documenting the entire journey along the way.
The Humanians and the BDD Foundation will be working together closely to make a sustained difference built around the BDD Foundation’s three pillars of action which are Awareness, Information, and Support. The Humanians aim to be an advocate for change by tackling unrealistic body expectations perpetuated by social and modern media. As part of this support effort The Humanians have an in-house certified NHS Mental Health Nurse Ouma Cazaril who runs an interactive discussion every Tuesday / Wednesdays at 8-9pm GMT, and Saturday Mornings at 7-8am GMT, where she discusses tips on healthy coping mechanisms. You can attend this on The Humanians Discord Channel.
Amber Day the artist for The Humanians has endured her own battles with body self image – which can be seen in her art style, where characters have exaggerated physical traits and quirky designs and proportions. “The idea of the human form has always fascinated me, and I believe the work I create is my way of exploring and seeing just how far I can push the boundaries of what society and ourselves deem as normal,” says Amber, adding that she is forever exploring her world of emotions, mental states, hardships, struggles, and the possibilities to live a more balanced life.
“As an abstract expression of humanity, The Humanians depict the human form in all of its glory and beauty: You are perfect no matter your size or proportion.” Says Amber.
Working to raise awareness The Humanians will also be raising funds for BDDF which is greatly needed – The BDD Foundation is the only charity in the world exclusively dedicated to raising awareness and alleviating the suffering caused by Body Dysmorphic Disorder. The BDDF runs on a very limited budget. They have a dedicated and diverse board of trustees consisting of leading clinicians and individuals with lived experience of BDD.
Together our aim is to spread positivity and support for our amazing community with tools and resources that promote active support and research.
We are proud to announce that the BDD Foundation is the charity partner of The Humanians.
“For one of my final year university projects, I decided to base it around a subject close to my heart – Body Dysmorphic Disorder. I created these two posters in the hopes of shedding light on something that has truly affected my life for many years – skin picking. Growing up, I never knew it was part of a disorder to get help for as I had never seen or heard anyone talk up about it. It was almost pushed under the carpet. I felt ashamed and embarrassed at what I was doing yet I couldn’t stop and never understood why.
Fortunately, I was lucky enough to have parents who were understanding when I opened up to them about it five years ago and they have supported me ever since. However, I have become increasingly aware that there are many others out there who pick their skin and struggle alone because they think it is something to be embarrassed about. But I am here to tell them it’s not. I used a 3D print of my face as a canvas to display skin picking. At first I was scared about doing this because only my close friends and family know about it, but I am sick of hiding and want to be able to try and squash the stigma around it so that others don’t feel so alone the way I did growing up. There is a QR code that takes anyone who sees the posters to the best source of information (the BDD Foundation) to either read about and educate themselves on BDD or to find the best help if they are struggling.
My goal is to get the posters out in as many places as possible to help others like me and be a part of raising awareness for Body Dysmorphic Disorder!” – Evie Horrell
Kitty describes that finding the BDD website and reading the list of symptoms was “like someone had crawled inside my brain and written down everything they could find. The idea that what I had was a condition, that it wasn’t my fault, was like a huge weight disappearing from my shoulders. For years, I’d blamed myself for everything.”
After discovering what BDD was and seeking help, she began treatment with a CBT specialist for BDD.
“At the beginning, going into treatment was really tough but soon I was having these huge moments. I clipped my fringe back off my face for the first time and was able to walk down the street without believing that everyone was staring at me,” she says. “It was a slow release from the grip that BDD had held over me since childhood.”
After a BDD relapse in her late 20s she decided she wanted to get involved in helping others and made contact with the Foundation again.
‘In her job now, as the BDDF’s head of operations, Wallace is constantly in contact with people who have BDD and sees her story reflected in their struggles. “For me, it was an overwhelming belief that there was something wrong with the very core of who I was, inside and out, and that is really isolating,” she says. “At the BDDF, a lot of our work is trying to show people that they’re not alone and it’s not their fault.”
