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Billie’s Recovery Story

“I’ve come to find a beautifully complex depth in my identity that reaches far beyond the cage of shame it was confined to for about 10 years.”

Think about all the times you’ve been drifting off to sleep and all of a sudden, you’re jolted awake by a memory of that really embarrassing thing you did 3 years ago. Maybe you wallow in the shame for a bit before eventually drifting back off to sleep, albeit a little humbled. But what if that feeling of shame never drifted away? What if it coiled itself around your identity like a snake, binding you to the feeling 24/7? What if shame was the lens through which you interacted with the world? One thing’s for sure, you don’t get much sleep.

I’ve already said so much about what my appearance anxiety meant to me without mentioning the word appearance. A diagnostic manual would tell you that BDD is a preoccupation with a ‘flaw’ in appearance that is either not visible at all to others, or visible but not to the same degree of intensity. But to me, attaching these complicated and uncontrollable feelings of shame onto my physical appearance was a way for me to try and control what I ultimately couldn’t. My mind was coopted by the unhelpful cultural expectations we place on young women and girls to look and behave a certain way. To be beautiful was to have worth. So in my head, I wasn’t struggling emotionally, I was just ugly. I just had to make sure my skin cleared up. I just had to be a bit taller. My nose a little smaller and less pointy, my lips a little thicker, my smile less creepy, my hands less stumpy, my head needed to be a different shape, my face needed to be a little less shit. And while we’re there, how about we stop being so stupid and uncomfortable to be around too? At my worst, I was using sandpaper, nail files, and bleach to smooth out my skin, I felt incapable of being loved, I felt guilty for others who had to look at me. Every day, I felt like ripping my face off, and I felt so worthless that I might as well be dead.

I would avoid mirrors or reflective surfaces at all costs when out of the house so as to not write off the rest of the day. Instead, I would cover my face with my hands and constantly ask my friends if I looked alright. I would make self-depreciating jokes in a desperate bid for reassurance and validation that I wasn’t as disgusting to look at as I thought I was. At home, on the other hand, I would stare at my face in the mirror for hours, dissecting it, interrogating it, picking at it. It makes me so sad to think of the friends and memories I missed out on whilst my appearance anxiety ate up all my time.  It breaks my heart that there are no pictures of me and my partner in the first year of our relationship because I couldn’t bear to be in front of a camera.

After googling ‘why do I feel so ugly all of the time?’, I came across the term ‘body dysmorphia’. I learnt about people who were so afraid to be seen by themselves or others that they had multiple cosmetic surgeries, were housebound, or would have frequent panic attacks. But I was still going to school. I was still going to work. I wasn’t having panic attacks. Convinced this was all just normal teenage angst, I continued my way of life without seeking any professional help or support.

Over the next 5 years, I went through phases of considering whether or not I had body dysmorphia. I did some of the self-assessment questionnaires and scored highly, but then again, I was making new friends at University, I was going out, I was studying. At a shallow glance I was functioning perfectly fine. The problem for me was that it wasn’t just the preoccupation with appearance, it was everything… my self-esteem, my self-confidence, my entire identity was bound by shame. By the time I was 21 I had developed a mask that hid all of that away from people. When the mask worked I felt like the most beautiful and lovable person in the world. When the mask slipped, I felt dirty and hideous and reminded of how lonely I really was and how impossible I had made it for anyone other than my partner to get close to me.

I was 22 when I went to the BDDF conference and heard Nicole Schnackenberg talk about the shame-bound identity that many BDD sufferers face. She described how with BDD, you assume judgement and criticism and all the things that you as a shameful individual should receive from others. This paired with an unconscious ability to see yourself through the eyes of others makes the world a very scary place. Under the perception of others, you see yourself and your shame from all angles, you are utterly exposed. This was the first time I had ever heard anyone relay my own experience back to me. This is also the only time I’ve ever been so moved by a conference talk that I’ve cried. Most of the time, I’m asleep by the end of them.

Since then, I have worked on trying to being more comfortable being myself without the mask. A big part of this journey has been my role as a lead peer facilitator on the Overcoming BDD Programme. This is a 20-week structured peer support group based on CBT for BDD, so every week, we go through some new psychoeducation or some CBT-based tools focused on managing BDD. Using the tools I learnt from facilitating these groups has really helped me to practice existing as myself in the real world, particularly the tools on how to train my focus of attention, exercise self-compassion, and expose myself to situations that trigger my BDD in a slow and steady way in order to get out of my comfort zone. I’m so grateful that for the 4 years that I’ve volunteered on this programme, I’ve been able to be a part of something that helps others understand that they are not alone, that there is no shame in suffering, and that there is hope that things will get better.  

The other part of this journey has been grieving the loss of my dad who passed away 4 years ago. He was perhaps the most authentic person I’ve ever met, for better or worse, and he was very live fast, die young. He would be the first to say ‘you only live once’ and ‘life is too short’. For me, striving to step into my authenticity and genuineness and getting as much out of this life as I possibly can is my way of honouring him. It has given this journey a sense of vital importance and it has given me strength and determination whenever the going gets tough. All of this has helped me reach a point of acceptance around my appearance and a sense of control over my life. I’ve come to find a beautifully complex depth in my identity that reaches far beyond the cage of shame it was confined to for about 10 years.

Learning to be comfortable in your own skin is a lifelong process for all of us, and for me, appearance anxiety was a painful, but important part of that journey.

The Observer Article: Our Obsession with Skincare

Our Vice Chair, Dr Amita Jassi speak with The Observer about the growing obsession with skincare and how it may relate to BDD, particularly skin-focused preoccupations.

The dermatologist Dr Sasha Dhoat has seen it all: acne, psoriasis, unexplained rashes, flaky skin and rosacea. But lately she’s noticed a shift in her work: more and more patients presenting with problems caused by elaborate skincare regimes. Regularly, Dhoat tells me from her clinic on London’s Harley Street, she sees women in their 20s and 30s, sometimes young men, who’ve put on overnight masks that have caused an explosion of severe acne, or used retinol and found themselves suffering from eczema or burns.

Particularly alarming, she says, are the cases of children and teenagers using anti-ageing products and harsh chemicals which can cause permanent skin damage. Take the 12-year-old patient with a skin condition she treated yesterday. “She came in with at least 40 products that could have paid for a small family holiday. She said her peers had the same products and she’d seen them on TikTok. The mother felt pressured. She didn’t want her daughter to feel left out.”

Dhoat advocates a less-is-more approach to skincare. “Flawless skin is a completely unreasonable expectation for any of us,” she says. “I have two young girls. I’d never want them to lose their childhood to this pressure.”

Over the past five years the UK skincare market has exploded, expanding from £2.9bn to £4bn between 2019 and 2023, a growth of almost 38%. Men’s spending on skincare in the UK is increasing year-on-year. Gen Alpha – those born after 2010 – are driving 49% of skincare sales growth, while the British Association for Dermatologists has noted a significant rise in the use of anti-ageing products among teenagers. Reports show some 7.7 million people had an aesthetic treatment in the UK in 2023, including microblading, Botox or fillers. Teenagers are turning to “Baby Botox”: small doses marketed as preventative.

Continue reading…

Community Fundraising News

Scarlett Takes on the 2025 London Marathon for BDDF! 🏃‍♀️💙

We are incredibly proud to share that one of our amazing community fundraisers, Scarlett, will be running the 2025 London Marathon in support of BDDF!

Taking on 26.2 miles is no small feat, and Scarlett is doing it all to raise awareness and vital funds for the BDD community. Her determination and generosity mean a lot to us, and to everyone affected by BDD across the UK.

We’ll be cheering her on every step of the way, and we hope you will too!

👉 Want to support Scarlett’s marathon? Read her story and donate here.

THANK YOU, SCARLETT!

BDD Training Opportunity – 2 Day Course

Delivered by The National & Specialist OCD, BDD and Related Disorders CAMHS Team, this training offers valuable insights for those looking to enhance their understanding of BDD and improve their practice.

This training course is for qualified clinicians working with children, young people and families, who are looking to build skills and competencies inline with the current evidence base.

Further details:

  • 2-day training workshop
  • 21st & 22nd May, 10am -4pm (please note attendance at both days is mandatory)
  • £550 (excluding booking fees)
  • Delivered online

This course is for you if you are:

  • A qualified clinician with CBT supervision
  • Working with young people with suspected BDD
  • Interested in developing your skills and competencies with assessing and treating BDD
  • Happy to give feedback on the BDD Clinician Manual following training

Course Content:

Day 1

  • Identifying BDD
  • Assessment of BDD
  • Introduction to BDD treatment

Day 2

  • Treatment of BDD What to do when treatment isn’t working
  • Working with risk in the context of BDD

Your Feedback:

Following the training workshop, all attendees will be given access to a BDD Clinician Manual, for use with patients. All attendees will be asked to provide feedback on this manual to contribute to the evaluation and development of it.

Book Here

BDD Training Opportunity – Introductory Course

Delivered by The National & Specialist OCD, BDD and Related Disorders CAMHS Team, this training offers valuable insights for those looking to enhance their understanding of BDD and improve their practice.

This course is designed for professionals who are working with children and young people who have appearance concerns, but do not have the qualifications to provide an evidence- based treatment (e.g. CBT for BDD).

Further details:

  • Wednesday 23rd April, 10-1pm
  • £75 (excluding booking fees)
  • Delivered online

Attendees may include:

  • Care coordinators/ case managers working in CAMHS
  • Low intensity workers (CWPs, EMHPs, SWPs)
  • School counsellors
  • Educational psychologists/ professionals

Expert speakers will share the latest research updates in this area, discuss how to screen for BDD, and discuss ways to support these young people whilst they are waiting for BDD treatment to start.

Book Here

BDD Collection of Poetry

We are honoured to introduce a powerful collection of poetry exploring the complex realities of BDD, written by contributors from our creative community. Each piece offers an honest, authentic glimpse into the journey of living with BDD, from the darkest struggles to moments of profound healing. These writers, at various stages of their recovery, share their voices with courage and vulnerability, creating a collection of shared experience that we hope will resonate with you. It is our honour to present their work, and we invite you to connect with these words, finding comfort, understanding, and hope on your own journey of healing.

We would love for this collection to continue growing. If you are interested in contributing to the poetry collection, please email us on volunteers@bddfoundation.org 📩

Schools Project Volunteers

We’re recruiting volunteers to work remotely on our Schools Project – come and join the team!

About the Project

The BDD Foundation, in partnership with Maudsley Hospital, has recently relaunched our Schools Project to help educators identify and support adolescents with BDD. As an early intervention programme, it aims to improve understanding and ensure timely support.

Guided by clinicians, volunteers have been delivering in-person workshops in South London schools. To better meet schools’ needs, we are now evolving the programme to offer virtual online sessions, making training more accessible. Workshops cover BDD, appearance anxiety, spotting signs, approaching conversations, and accessing support for students and their families.

About the role

We are looking for volunteers to help us expand and deliver our Schools Project, a vital initiative aimed at improving understanding of BDD in education and ensuring students receive the support they need. As a Schools Project Volunteer, you will be supported to reach out to schools in your local area on behalf of the BDD Foundation, introducing the programme and encouraging participation. You will then deliver training sessions – either in person or online, depending on the school’s preference, to equip staff with the knowledge to identify BDD, support students, and facilitate access to treatment.

We are looking for individuals with:

  • Lived experience of BDD (personal or as a carer for a loved one)
  • Strong understanding of BDD signs and symptoms
  • Experience in training/ teaching, public speaking, group facilitation, or professional presentations (desirable)
  • Experience using online training platforms (e.g. Zoom)
  • Clear communicator, well-organised, and passionate about early mental health intervention

How to apply

Please submit a CV and a personal statement (max 600 words) to gem@bddfoundation.org which highlights the following:

  • Your (direct/indirect) experience with BDD
  • Why you would like to apply for this position
  • Your relevant experience
  • The relevant skills and qualities you have for this role

Please submit your CV and personal statement to gem@bddfoundation.org by 12 midday on 2nd April 2025

Please note, this post is open to those based in the UK, age 18+ and is subject to an enhanced DBS check.

Conference Announcement


This year we’re joining forces with IOCDF to bring you an online BDD conference. Join us on 31st May 2025.

Join us for a day of learning about BDD, treatment, recovery, and more. Open to clinicians, educators, students, trainees, those with lived experience, loved ones, and supporters.⁠

🎟️ Tickets now available!

More info on speakers and topics to come very soon.

Tickets Here

E-Helpline Volunteers Needed!

Come and join us! We are looking for new volunteers to support our E-Helpline service. This is a really rewarding role, with the opportunity to make a difference and provide crucial advice, support and guidance to those suffering with BDD.

The E-Helpline

The BDD Foundation’s email support service offers guidance for anyone affected by BDD or concerned about a loved one. We are the only email support project specifically for BDD in the UK, providing high-quality information, treatment options, and a non-judgmental space to discuss symptoms. Run by our Helpline Manager, Helpline Coordinator and a team of dedicated volunteers, the service offers empathetic support and signposting to resources tailored to individual needs.

The role of Volunteer

The key tasks carried about by volunteers include:

  • Responding to questions and concerns of individuals that email the service
  • Offering a compassionate, understanding and safe online space for those struggling
  • Identifying other sources of support both within and outside of the charity
  • Working within the policies set by the BDD Foundation
  • Attendance of ongoing training and development sessions

Skills and Qualities

For this role, it’s important to have a good understanding of BDD and the impact it has. We look for individuals with a non-judgmental attitude, empathy and understanding, and strong written communication skills. Since the role operates remotely, we are also looking for individuals with a good level of IT literacy and confidence using a web based email system.

Training and induction will be provided. We require a minimum time commitment of 2.5 hours per week on a rota basis.

How to Apply

Download the Application Form below, and send completed applications to christian@bddfoundation.org by 12 midday on 7th March 2025

For any questions about the role, please contact christian@bddfoundation.org

Applications will be reviewed and responded to by mid -March 2024

Please note – due to insurance reasons, this opportunity is open to those aged 18+, based in the UK and is subject to an enhanced DBS check.

Flora’s Recovery Story

“I now have self-compassion and know I am worthy of happiness and a fulfilling life.”

I first contacted the BDD Foundation after realising that for my entire adult life of 20+ years, I had been suffering from BDD. I have always had a debilitating preoccupation with my perceived flaws, but had never approached the reality of potentially having BDD, due to not feeling ill enough to have it and not wanting to face the fear of accepting it and dealing with it.

When I first reached out for support, it was after 4 months of self-sabotaging, convincing myself I didn’t have BDD and wasn’t worthy of recovery. None of my friends or family understood or knew how to support me, and I had no idea how to navigate it. But I was at the point of not wanting to live a life of complete and utter destruction anymore, and knew something had to change. I felt completely alone, like a freak, helpless, hopeless and at a complete loss with life with no way out. My safety behaviours were dictating my life and I couldn’t escape the grips of BDD.

But, after finding the BDD Foundation online, I took the hugely scary step of attending the Zoom support groups, off camera and silent during the sessions. But hearing people’s identical feelings and experiences reassured me that I wasn’t alone. The BDD Foundation offered a 20-week, CBT-based structured support group (now known as the Overcoming BDD Programme) which I applied for and attended, and it was life-changing.

It was a small group led by facilitators who had lived experience of BDD, and we explored our past experiences that have shaped us developing BDD and learnt some incredibly transformational CBT-based practises, such as the Big I and Little I, the vicious flower, exposure exercises and behavioural experiments, Theory A vs Theory B, exploring personal qualities, and self-compassion – which was the turning point for me in being able to recover.

If it wasn’t for the help of the BDD Foundation, I would not have been able to value myself for who I am rather than based on my appearance, and I would never have been able to realise that the problem was the way I thought about my body, not my body itself. Thanks to the BDD Foundation and my recovery, I now appreciate myself for who I am, the energy I bring to life, and the qualities I have that make me who I am, rather than place all my self-worth and value in the way my body looks.

This is me, having a professional photoshoot done on holiday, with quite a few spectators… living my life, enjoying being present, in my ‘broken mirror’ dress that I made myself as an empowering take on the ‘broken mirror’ metaphor of the distorted view I had of my body.

I now don’t camouflage myself and instead, I wear (and even make) bright, vibrant and exciting clothes that make me feel good. I now go out to social events and enjoy them and can be present, rather than avoiding them and isolating myself away from everyone to avoid being seen. I now have self-compassion and know I am worthy of happiness and a fulfilling life, regardless of what I look like. And thanks to the BDD Foundation, I have the coping mechanisms and toolkit to be able to not let BDD overcome me when the thoughts come creeping back.

I have also gained the confidence to share my experiences and took part in the Beating BDD podcast, as well as participating as a volunteer in a self-compassion exercise at a BDD Foundation Conference. I would say that the most impactful thing I have gained from the BDD Foundation is knowing that recovery is possible and will always be worth it.

The Body Dysmorphic Disorder Foundation. Charity no. 1153753.

Online BDD Conference

An opportunity for professionals, researchers, students, and those with lived experience to find community and to learn more about BDD.

Join this virtual event on Saturday, May 31, 2025!