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Tilly’s Recovery Story

“Finding a support group was the real game changer. It helped me begin to accept that I might actually have this thing called BDD. The way we would all describe certain experiences almost verbatim made it hard to deny that a common thread linked us together.”

At its worst, BDD made me feel like an amorphous alien blob of flesh and body parts whose loosely formed features wouldn’t stay in their own distinct shape when I didn’t pay attention. I believed that I spread to fit my clothing no matter the shape or size, like jelly in mould, so that garments would fit tight to my formless body, or worse, create a bulge. The areas of concern were broad ranging. Depending on the day it might be my hair, my body shape and size, or my face. I remember likening myself to a Picasso, feeling that my facial features were ‘all over the place’, and that ‘I look like I’ve been hit by a bus’. That one was a particularly nasty judgement that really took me into despair. The only parts of my body that I liked were my feet, hands, forearms and ears.

I was hyper aware of how I looked from different angles, making public and group situations extremely difficult, I couldn’t effectively control my body for all the angles needed at any given time. I’d be facing someone trying to focus on how I look to them, and on the conversation, whilst frantically worrying about how I look to someone else passing by! Just walking to and from work became a huge ordeal, with every person that walked towards me sending a spasm of shame through my body for fear of what they could see when they looked at me. Holding back tears, thoughts spiralling way out of control, and hyperventilating until I reached somewhere ‘safe’ was a daily experience.

The feeling of people looking at me ‘noticing how ugly I was’, brought about a set of physical symptoms. I became instantly hot and flushed, breathless, and panicked. Often parts of my body would begin to really hurt, like a hot and painful lower back, or sore legs or arms. I don’t know how but the thoughts, and perhaps the associated tension, quickly brought on this physical pain. I would often become bloated if the area of concern in that moment was my tummy. If my top wasn’t baggy enough I would be concerned that my tummy contours could be seen against the clothing, and this mental anxiety would trigger painful physical bloating that made me completely unable to focus on anything else.

I first sought professional help when I was at university age 21 and received some low cost counselling for what I thought was general depression. But I didn’t have the words to describe what I was experiencing and I didn’t know that BDD was even a thing. So the cycle of insufficient short term attempts at counselling continued for a number of years with a variety of practitioners. I was around 27 years old before a psychologist raised the possibility of me experiencing BDD and started treating me with CBT for BDD. At first I didn’t fully believe I had BDD, but I was happy for my emotional pain to be taken seriously and to receive specialist support. The belief I held was ‘I’m just ugly, and this psychologist, seeing this to be true and unable to resolve my appearance, is just trying to make me happy by telling me it’s a mental problem instead’ I was afraid that if the work was successful I’d end up living my life like someone whose appearance wasn’t deficient, and make a huge fool of myself by not being aware of my true ugliness.

Finding a support group was the real game changer. I still needed to work one to one in therapy but meeting others experiencing the exact same concerns and behaviours was eye opening. It helped me begin to accept that I might actually have this thing called BDD. The way we would all describe certain experiences almost verbatim made it hard to deny that a common thread linked us together.

I cope with challenges now by separating myself from the BDD, seeing it as something ‘other’ that tricks me into feeling and believing certain things that aren’t helpful. Maybe BDD is a bit like the opposite of ‘rose tinted glasses’. If I hear myself making unfair judgments in the mirror, I take off my BDD tinted glasses, and try really hard to adjust my vision back to reality. Blink a few times, step back and get some distance, look in a different mirror with natural lighting, or just simply walk away and do something else. I stop engaging with the thoughts because I know that ruminating and looking closer will not help at all.

I feel most proud of a recent experience I had, that I didn’t even notice until after the event, and that in itself is the beauty of it. I was going out to a gallery for an evening event, mingling and art etc.. the sort of thing that can terrify me. I had to wear what I had on from the day, which was not a good outfit, and I had to do my makeup in super low lighting. I expected to feel wretched when I got there, I promised myself I’d show my face and then head off as soon as I felt too uncomfortable. Skip forward 2 or 3 days, sitting in my car, and the realisation hit me hard!… a smile crept onto my face as I realised that I don’t even remember thinking about my appearance the whole evening at the gallery. When I arrived I asked my friend if I had panda eyes from doing my makeup in low light, she responded that I did a little bit but not that bad. And somehow that was enough for me. I stayed a couple of hours, I chatted and laughed and met new people. I didn’t hold my body at weird angles, or think about how I looked from behind. It was an incredible moment of realisation that filled my body with happiness and hope. If I can do that once, surely I can do it again!

I still have difficulties with BDD at times, but on the whole I am able to move through life without the constant knot of unworthiness in my chest. I am beginning to experience myself as more than my appearance. When I think I look crap it doesn’t have to stop me from enjoying the day or leaving the house, because I now know for certain that the image I conjure up with my BDD eyes is way worse than reality. I trust that even at my worst, I still just look like a human, a perfectly imperfect human just like all the others. So I don’t have to get hot and sweaty walking down the highstreet, because as it turns out I don’t actually look like an amorphous alien blob.

Seeking a Treasurer to Join our Board

The BDD Foundation is seeking a Treasurer to join our Board of Trustees and play a vital role in strengthening our impact, sustainability, and future growth.

This is an exciting opportunity for a financially skilled and strategically minded individual to contribute to an organisation making a real difference. As the only charity in the world exclusively supporting people affected by BDD, we provide specialist support, raise awareness, and advocate for better understanding and treatment of this serious mental health condition.

About the Role

As Treasurer, you will:

  • Provide strategic oversight of the charity’s financial health
  • Support the Board in fulfilling its financial governance responsibilities
  • Help ensure long-term sustainability and responsible growth
  • Work closely with fellow trustees and the leadership team

Why Join Us?

This is a unique opportunity to apply your financial leadership in a role where your expertise will directly support individuals and families affected by BDD. You will join a passionate and committed Board dedicated to driving meaningful, community focused change.

How to Apply

To find out more about the role and submit your application, please visit Charity Job

The Big Half Charity Places

We’re excited to share that we have 2 charity places remaining for the Big Half Marathon, taking place on 6th September 2026.

This iconic London half marathon is a brilliant opportunity to challenge yourself while raising vital funds and awareness for people affected by BDD.

Each charity place has a minimum fundraising target of £1,000, with full support from our team along the way.

📩 If you’re interested in taking part or would like more information, please email fundraising@bddfoundation.org to express your interest.

We’d love to have you on the team!

Beating BDD Podcast #36 – Dan Joseph

“Recovery begins the moment you allow yourself the possibility that life can be bigger than your rituals.”

For years, Dan Joseph’s life was governed by his BDD and a strict set of rules and rituals designed to camouflage his perceived flaws. Today, he truly believes it doesn’t matter how he presents to people – and the next day is no longer to be survived, but to be lived. In this episode, Dan speaks with remarkable openness about his experience and why spontaneity is now a defining marker of his recovery.


You can download the transcript for this episode here:

BDDF Speaks with Women’s Health Magazine

The BDD Foundation was recently featured in Women’s Health, where our Managing Director, Kitty Newman, and Vice Chair, Amita Jassi, contributed expert insights to an article exploring the growing pressures surrounding skincare culture and the impact on mental health.

Skin is one of the most common areas of concern for people experiencing BDD, and a significant proportion of individuals with BDD experience skin focused preoccupations and behaviours, often driven by intense distress about perceived imperfections that may appear minor or unnoticeable to others. Importantly, these concerns can persist even after a skin condition such as acne has resolved, with the emotional impact continuing long after the physical symptoms have changed.

As highlighted in the article, the naturally fluctuating nature of skin can intensify the urge to monitor, control, or ‘fix’ perceived flaws. At the same time, growing cultural pressure for rapid aesthetic transformation and extreme skincare may inadvertently worsen appearance anxiety and BDD for some people, reinforcing cycles of checking, reassurance-seeking, and avoidance.

Kitty explains: “The fluctuating nature of skin fuels the need to control it, while the fear of bad skin, new lines or flaws can be very intense.” These experiences underline the importance of compassion-focused approaches, realistic expectations, and access to evidence-based psychological support when appearance concerns begin to significantly affect daily life.

We are pleased to see increasing discussion about the psychological impact of BDD in relation to skin, and the importance of recognising when skin concerns may be linked to BDD.

Read the full article

Peer Support Group Expansion

We’re expanding our peer support groups!

Our BDD Foundation online peer support groups will now run 3 times per month, with a new session added every 3rd Monday.

🕡 6.30–8pm (UK time)
💻 Online via Zoom
📷 Camera use optional
👥 Open to all, age 18+

Upcoming 3rd Monday dates: 16 Feb, 16 Mar, 20 Apr, 18 May, 15 Jun, 20 Jul, 17 Aug, 21 Sep, 19 Oct, 16 Nov & 21 Dec

📩 To join, contact support@bddfoundation.org

If you already have the joining link for our existing Monday groups, you can use that same link. We look forward to welcoming you!

Rachel’s Recovery Story

I first realised I might have BDD, when I was receiving talking therapy. I reached out for this as I was in a really dark place after losing my sister in law who had been more like a sister to me, and had been in my life since I was 5 years old. My brother and her were high school sweethearts but we sadly lost her 8 weeks after her cancer diagnosis. It was towards the end of lockdown, so due to the rules in place I didn’t get to say goodbye to her, and at her funeral I had to sit completely separate from my family – just me and my son.

During my assessment for talking therapy, I was asked a lot of questions, and for the first time in my life I was completely honest with my answers, even finally admitting I had been in abusive relationships. One was physically abusive and two had been emotionally abusive. At the end, the assessor said I displayed the traits of someone suffering with grief, PTSD & BDD. The first of the relationships being the worst one, and the root of my BDD. He would call me fat, tell me that there’d be no point leaving him because no one else would want me, say if I wore make up that I was cheating on him or doing it to get attention from men, and tell me I looked like a prostitute if I wore a short dress. Among many other things, I carried his words with me for 26 years before realising what he had done to me mentally. I was only with him for 5 years but the damage lasted a lot longer.

Some of the behaviours I was carrying out were: I hated anyone taking my photo, and on the rare occasion someone did without me knowing and I saw it, I would feel absolutely devastated about how I looked – to the point in private I would cry my heart out about it. I am not able to look in a mirror or see my reflection in a window without tearing myself apart with negative thoughts about my appearance. I don’t avoid social situations but when I do go out even just shopping I feel like everyone is looking at me & thinking things like “Oh my god – she’s so fat, so ugly, looks so old, her skin and hair are awful, her nails are horrible, what’s she wearing…. etc.” I have a slightly discoloured tooth caused by the previously mentioned boyfriend who hit the bottom of a beer bottle while I was drinking it, hitting my tooth and causing nerve damage. I felt like everyone would be staring at it when they were talking to me, and my thoughts were having a big impact on my life because even though I still went out I wasn’t living my best life or enjoying it fully.

It felt like there was always a grey cloud hanging over me, I would constantly compare myself to others and wish I looked a certain way (an idea I had of perfect), I picked at the skin around my nails making them bleed. If I had a spot I couldn’t leave it alone I would be picking at it all the time making it ten times worse, which would then make my the negative thoughts about myself even worse. I never told anybody how I was feeling as I thought they would think I was being dramatic, stupid or looking for attention, so many a time when I got home I would sit and cry uncontrollably. My lowest point with it was when I’d lost my sister in law and most days I would think ‘it should have been me not her’. I felt like I didn’t deserve to be here and wished I wasn’t. The only thing that ever stopped me from taking those thoughts any further was my son, I couldn’t do that to him, he was my saving grace. Most days I would spend the biggest part of it deciding what negative things other people were thinking about me, I mostly wear hoodies and sweatpants as they are nice and baggy so cover up what I believe to be a disgusting body. I hate it when people make a compliment as I feel like they are lying and just trying to seem polite.

A few months after I separated from my sons father, I met some who I had know for years – we’d previously had a kiss 22 years previously, and I had always had a soft spot for him. He treated me like a queen, but not because of his actions or words, but because of my own insecurities – I didn’t feel good enough for him. I felt like he could do better, have a more attractive girlfriend, and felt like he would leave me for someone better. I constantly tried to push him away even though I loved him, yet the thought of losing him broke my heart. I really am lucky because he stayed and even though he had no idea what was going on with me, he wanted to help me and support me however he could. After releasing that my actions could actually one day cost me a good man, I reached out for help.

It found it really hard talking to my therapist initially, as I always bottle things up. However, after a few sessions I felt comfortable with her so started to open up. She pointed out that the thoughts I have about myself have come from someone I trusted who used those words to make themselves feel more powerful by breaking me. She recommended telling my partner about BDD and the thoughts I have about myself, and to look for support from other people going through the same thing. I sat down with my partner and found it really hard as I thought even though he’s a kind and understanding man – he would think it was ridiculous and I just needed to get a grip and stop being silly. But, I opened up and that’s not what he thought at all. He asked me what he could do to help me, and we are now both working on my recovery together.

I found The BDD Foundation on Instagram and even though I didn’t interact with the posts, it was such a comfort to realise that it not just me being daft, silly or dramatic – but there are so many people out there who are affected by it too. I am only just starting my recovery journey, and still have some days where the BDD takes over, but each month they are getting fewer, so I know I am making steps in the right direction. I have slowly started to trust some of my family and a few of my closest friends with knowing what I am going through, and it has been so much more helpful than I thought it would have been. I’m still not comfortable with seeing myself but I’m having less thoughts about what other people are thinking, I don’t pick at my skin around my nails as much as my partner bought me an anxiety ring to fiddle with instead. This really is helping. I am taking each day as it comes but feeling hopeful about the road to recovery I am now on.

To anyone who is struggling with BDD – even if you haven’t officially been diagnosed but you feel you have the signs, I encourage you to reach out and look for support. You are not alone and even though you don’t feel anything can help as you think it’s just you feeling this way, more people will understand than you think.

Community Voice Survey

We want to hear from you!⁠

This year, our manager and trustee team will be coming together to develop the BDD Foundation’s next steps, and it’s really important to us that this work is shaped by the voices of our community.⁠

If you have lived experience of BDD, or support someone who does, we’d love you to share your thoughts through our Community Voice Survey.⁠

Your feedback will help guide our services, resources, and priorities, so that our charity strategy truly reflects the needs and experiences of those we support.⁠

🗓️ Please complete by 8 February 2026⁠. Thank you for helping us shape what comes next

Complete Here

Save the Date: 2026 BDD Conference

We are so excited to share the date of our upcoming in-person conference.

Centred on recovery tools, interactive workshops, lived experience speakers, community and the power of connection for those living with BDD, this conference is about coming together to inspire hope and support the next step in your recovery journey.

More to come very soon – watch this space!

Sign up to our newsletter for more updates.

Engaging Young People in Treatment: A session for Parents and Carers

This webinar brings together the perspectives of Dr Angie Lewis: a clinician working with young people with BDD, and Lucy de Garis: a parent with lived experience of supporting a child with BDD. Drawing on clinical expertise and personal insight, they share practical guidance on understanding non-engagement, reducing conflict, and finding constructive ways to support young people who are reluctant or feel unable to engage in BDD treatment.

Meet the Speakers

Dr Angie Lewis is a Principal Clinical Psychologist at the National and Specialist OCD, BDD and Related Disorders Service for Children and Young People (South London and Maudsley NHS Foundation Trust). She has worked at the service since 2013, providing specialist assessment and evidence-based treatment to children and young people with BDD across the country. Angie is a peer-reviewed author and has contributed chapters to books on both OCD and BDD. She is involved in leading multi-disciplinary specialist assessments and delivering weekly, intensive, and home-based interventions. Angie has a particular interest in improving access to treatment. She has been programme lead for CBT training on the Children and Young People’s Improving Access to Psychological Therapies framework at Exeter university. Angie is the lead for the first and only satellite clinic for the service, which she has overseen since inception in 2022. Based in the southwest of England, Angie leads on the provision for young people across Devon, Cornwall and Somerset.

Lucy is mum to a teenage daughter with BDD and has been learning about the condition since her daughter first became unwell with it four years ago. Developing an understanding of BDD has been central to Lucy’s role in supporting her daughter along her recovery journey.  Lucy has also recently completed a Masters in Psychology and chose to do her dissertation on parents’ perspectives of BDD in young people. For this she interviewed 13 parents about their experiences of supporting children with BDD and wrote a report outlining the key themes identified.  Lucy is passionate about raising awareness of BDD and is currently volunteering with the BDD Foundation’s Schools Project.

The Body Dysmorphic Disorder Foundation. Charity no. 1153753.