Beating BDD Podcast #38 – Malise Honey

“What you see isn’t the true version of who you are. BDD has taken over your brain.”

Just a couple of years ago, Malise was in a wheelchair after spending three and a half years in hospital being misunderstood and mistreated. Today she is in recovery, volunteering for the BDD Foundation and even training for the Manchester Marathon. She shares the devastating impact of misdiagnosis and how finally receiving the right support changed everything.


You can download the transcript for this episode here:

3 Peaks Fundraising Team

On 16th May, our incredible 3 Peaks fundraising team are taking on the mountains, one step at a time, to help raise funds for the BDD Foundation.⁠

With a collective target of £7500, their efforts will make a huge impact in supporting our work, and the services we offer to those suffering with BDD.⁠

THANK YOU, Team! 💙

Meet the Team ⬇️

Rebecca Robinson

I’m both incredibly excited and slightly apprehensive about the 3 peaks challenge. I’m most looking forward to the beautiful scenery, time with great people as well as the sense of accomplishment I will feel upon completion.

As part of my job role as a CBT therapist, I am encouraging people to get comfortable with the uncomfortable and do things that feel challenging. I believe it is important to demonstrate I am willing to do the same and what better wat than to do something in aide of this fantastic charity!

I support people with BDD with CBT therapy, and have provided teaching on this subject for NHS trainee therapists too. It is an area I feel passionate about and really enjoy working with. I have seen people reclaim their life from BDD so want to continue to instil the hope that overcoming BDD is possible.

Most my training at the moment involves increasing my distance with running as well as going to HIT classes at the gym. The 3 peaks team did a practice hike up Watlington Hill and are potentially planning a trip to Snowdonia at the start of next year.

Rebecca’s Fundraising Page


Samuel Herbert

I’m really excited to be taking part in the National Three Peaks Challenge for the BDD Foundation in 2026. This is the first big fundraising challenge that I’ve signed up for and I’m so pleased to be taking on this epic challenge to help raise funds for such an incredible charity.

Working as a psychotherapist is a real privilege and provides unique insights into how debilitating mental health conditions such as Body Dysmorphic Disorder can be. I’ve seen first-hand how the BDD Foundation provides invaluable support, advocacy and advice for patients, professionals and loved ones – and know how important this money will be to help them in continuing to do such vital work.

The prospect of climbing the 3 tallest mountains in the UK consecutively and all within a 24 hour period is a rather daunting prospect (especially for someone with very limited hiking experience!) but I’m really looking forward to the challenge so please donate what you can and wish me the best of luck.

Samuel’s Fundraising Page


Rob Willson

It has been very fulfilling to hold the role as Chair of the BDD Foundation for the past 11 years. As a Cognitive Behaviour Therapist with a special interest in BDD, I have witnessed the inspiring courage and perseverence of those living with BDD, particularly when engaging in exposure challenges in treatment.

I am proud to support the BDDF and of course, hope we can help raise some funds and awareness along the way.

I’ve never done anything like this before, so I’m training hard!

Rob’s Fundraising Page


Thomas Gagen

Until a few months ago, I had never heard of Body Dysmorphic Disorder. Although I don’t work in therapy, I think this says a fair bit about how this isn’t highlighted widely enough as I didn’t know about any of it until my partner said she was doing the three peaks challenge and I wanted to get involved.

Living at the bottom or Barnet Hill for most of my life, I feel fully prepared for the uphill struggle of the three peaks. I’m a enthusiastic amateur runner so regular hill reps along with a marathon this past December and a series of half marathon training runs should stand me in good stead.

My potential highlights for the challenge are going to be the snacks, the overall challenge and (most importantly) leaving work early at 12.30 on the Friday to make it up to the start line in Fort William.

Tom’s Fundraising Page


Arzum Gulsar

In my work as a mental health practitioner, I see how incredibly tough life can be for those living with Body Dysmorphic Disorder, a condition that’s still so misunderstood.

I’m taking on this hike because I’m determined to help shine a light on BDD and raise the funds needed for proper, specialist support. It’s about more than just the miles; it’s about showing people they aren’t alone and helping to break down the shame that often stops them from reaching out.

Every donation goes directly towards life-changing resources, and I’d be so grateful if you could help me support this brilliant charity.

Male Research Participants Needed

UCL Researchers are seeking male participants who worry about the size, definition or tone of their muscles. They are exploring symptoms of Muscle Dysmorphia, how symptoms might relate to the sex assigned at birth, and experiences in social settings.

Taking part includes a brief 15 min online survey, and a chance to win one of ten £25 vouchers.

You can take part if:

  • You identify as male
  • You worry about your body and self-identify as having BDD or muscle dysmorphia
  • Age 18+
  • Fluent in English

If you are interested in finding out more or taking part, follow the link or contact:

  • amelia.peck.23@ucl.ac.uk
  • chloe.andrews@ucl.ac.uk

This is a doctorate of Clinical Psychology research study

More info & take part

Beating BDD Podcast #37 – Mark Brown

“Don’t give up. You deserve to be happy in life.”

For much of the time Mark Brown lived with BDD – around 30 years – he looked as if he was functioning from the outside. But inside he was living under what he calls “a dome of shame and disgust”. Now, after lots of hard work and therapy, he says he’s much more present in his life and his old life with BDD feels like a distant memory.


You can download the transcript for this episode here:

Brighton 10K Fundraisers

Meet our amazing Brighton 10K team!

With personal stories and powerful motivations, their journeys are what make this challenge so meaningful. Take a moment to read their stories and, if you can, support their efforts through their fundraising pages. Every donation helps make a difference. Thank you Christie, Stan & Tom – we appreciate your amazing support!

Stan Dru

Hey, I’m Stan, I’m 40 and this year, I decided to run the Brighton 10K for the BDD Foundation because their support genuinely changed my life.

Last year I was diagnosed with Body Dysmorphic Disorder, alongside an atypical eating disorder. For a long time, I didn’t fully understand what was happening in my mind, I just knew my thoughts about my body were intrusive, loud, and exhausting. The BDD Foundation gave me something I didn’t realise I needed so deeply: understanding, language, and community.

Through their resources and support groups, I began to recognise patterns in my behaviour and thinking. I jumped on zoom calls and spoke with people who felt the same shame, fear and obsession I’d been carrying for years. That feeling of “it’s not just me” was incredibly powerful. It helped me seek proper treatment and start being more open about my experience. Listening to the BDDF podcasts allowed me to identify patterns in my behaviour and enabled me to speak more candidly about my BDD to my boyfriend Tom, which has definitely brought us closer.

Training for the 10K has been a journey in itself. Over the past few months I haven’t been motivated to run, however, I’m now taking SSRI’s which has definitely helped reduce the feeling of being overwhelmed thoughts of my body and appearance , and I’m now motivated to get training and focus on the run, I did a 10K just a few days (I’m all or nothing 🤣) which was my first 10K in nearly 5 months, so I’m extremely happy I didn’t snap my leg. 

What I’m most looking forward to on race day is the sense of collective purpose. Knowing that every step is raising awareness for a condition that’s still so misunderstood means everything to me. If even one person feels less alone because of this, it’s worth it.

Taking part in the 10K is all about using my voice and my platform for something bigger than myself and I’m proud to do it for the BDDF ❤️

Support Stan here


Tom Sheard

I’m Tom, I’m 35 and I was inspired to run for BDDF as my partner was recently diagnosed with BDD. I’d never heard of it or understood it until now and the stats of 1 in 50 people suffering with this floored me. I’m running to help raise awareness and show people there really is some help out there and they’re not alone.

My training is going well, I’m already running 10k on weekends at home to prepare for the race.

I’m most looking forward to the atmosphere on the day, hearing other people’s stories and their journeys and to just be included to play a little part in something that could be life changing for people suffering with BDD.

Support Tom here


Christie- Luke Jones

I’ve been living with BDD since my pre-teens, and The Body Dysmorphic Disorder Foundation is the first dedicated BDD charity that I’ve ever come across. I’m currently taking part in their Overcoming BDD programme and cannot express how grateful I am for the superb wellbeing tools that they have provided me with, as well as the invaluable opportunity to meet others living with the condition.

My training for the Brighton 10k is going well, though I still have to remind myself to focus on post-run recovery – stretching, foam-rolling, etc. Not easy when all I want to do is crash out on the sofa and demolish a sharer pack of crisps! On that note, I’m really looking forward to my post-race meal – I absolutely love Brighton and the food options are top-notch!

Support Christie here

BDD Collection of Poetry

We are honoured to share 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 📩

BBC News Features BDD Stories

We’re incredibly grateful to Tilly and Charlotte for bravely speaking to BBC News about their experiences of Body Dysmorphic Disorder this month.

In the article, Charlotte shares how BDD began in her early teens, leading to hours spent trying to ‘perfect’ her makeup to be able to leave the house for school, social isolation, and eventually specialist treatment. Through therapy and songwriting, she rediscovered her love of music and has since created a concept album inspired by her recovery journey – offering hope to others living with BDD.

Tilly also speaks movingly about developing BDD as a teenager, the impact it had on her confidence and daily life, and how receiving specialist support, including attending a BDDF support group, helped her regain control of her thoughts and rebuild self-compassion.

Their stories powerfully highlight that BDD is a serious mental health condition, but importantly, that recovery is possible with the right support.

We thank Charlotte and Tilly for supporting us in raising awareness and understanding of BDD.

Read the Full Article

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!

The Body Dysmorphic Disorder Foundation. Charity no. 1153753.