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I, ADONIS; A powerful film on Muscle Dysmorphia

I, Adonis paints an excruciating vision of the poorly understood condition known as Bigorexia (Muscle Dysmorphia) in this visually striking short film. 

I, Adonis, written and directed by Angelo Raaijmakers, offers a gripping and unfiltered look into the reality of living with Muscle Dysmorphia. This powerful film draws from personal experience to shed light on a condition that is often misunderstood and overlooked.

With a mission to increase awareness and empathy, I, Adonis reveals the intense struggle and profound pain endured by those affected by Muscle Dysmorphia. The film delves into the hidden world of sufferers, uncovering the obsessive behaviours and rituals that dominate their lives behind closed doors.

Muscle Dysmorphia is a severe and often debilitating condition, one that can be difficult to recognise in loved ones until it reaches a critical point.

Don’t miss the premier —visit Alter on the link shared below.

Watch Here

Carrie-Ellise’s Recovery Story

“I still have a way to go before I can sit in a hair salon and not blur my eyes in front of the mirror; however, I no longer stress over bad hair days, I just swish my glasses into the hairband position.”

Once an impossible dream, here I am lounging outside in the midday sun.

I’ve not checked the mirror today, though I’m not quite bare-faced because I’m still wearing yesterday’s makeup. I haven’t gotten so far in my recovery that I can just grin and bear it all. Day-old makeup is a step in my desensitisation process. Still, I’m acutely aware that someone could stroll up the path and see me raw.

My husband approaches and I fight the instinct to shrink away. Instead of increasing facial camouflage, I slip my glasses up to form a hairband. This is not entirely innocent, rather a reconfiguration because I’m covertly concealing my hair parting. My hands jerk to cover my face, though I keep them on my book until the sensation fades.

Seven years ago, four layers of window-dressing shrouded me in perpetual darkness. Facing daylight demanded days of preparation, fighting through rituals, as I struggled to make my face publicly acceptable. I would wash and reapply makeup until my skin burned, rendering me housebound and without groceries for yet another day.

At the height of my struggle, I wore sunglasses until friction blistered my nose and ears, their arms hooked on for dear life. Even those lesions became part of my camouflage, a temporary deformity I rationalised as diverting attention from my perceived imperfections. But instead, BDD was trying to manifest itself in physical ways, to prove, look, I am deformed.

When at my local Sainsbury’s, the security guard asked, “Why the sunglasses indoors?” I replied with a rehearsed excuse, “I’m recovering from surgery.” Then I avoided that store for a year, driving 45 minutes out of my way for a pint of milk.

After waiting 22 years to “grow out of it,” as my friends assured me I would, I self-prescribed an exposure exercise: a bodybuilding competition, because once I’m lean then I’ll be happy, right?

Over four months, I trained six days a week. Then, during peak week, I chugged 6 litres of water daily and tapered my calories down to 450. I stepped on stage, abs defined, my face thinned out, and I made it into the top ten, only to realise I’d built a body as unhealthy and unsustainable as the pills I popped. My bikini sparkled, my skin glistened, and my stage makeup concealed a dark truth; my lips had turned grey from injecting myself with unregulated tanning agents.

BDD learned to exist on a new frequency, and I judged myself on an unreasonable scale, measuring body fat by the millimetre whilst swallowing dodgy fat burners and diuretics. After I binged my way back to normal, a real medical crisis erupted one morning and sparked a dilemma: Do I call an ambulance or apply makeup?

I imagined the paramedics, revolted by my face, and decided to leave them something nicer to look at. It’s better to be dead wearing makeup than to show my raw face in public.

I wobbled to the bathroom and set out my instruments. If I died doing eyeliner, it would be the most honest way to go.

Stumbling into the GP’s office the following day, the medical form asked, “What is your eye colour?” I had no idea; I hadn’t seen my eyes in daylight in over two decades since I closed my curtains at thirteen. And with nobody to call because I had ghosted myself into reclusivity, I had to guess the answer: blue?

Lacking a proper vocabulary, I shared how I injected myself and took under-the-counter supplements, meanwhile remaining silent about my two-decade mirror obsession because, to me, it was nothing more than a “vanity curse,” my shameful, dirty little secret.

Discovering The Broken Mirror by Dr Katharine Phillips finally put a name to my situation: Body Dysmorphic Disorder (BDD). I was eager to consult Dr Phillips, except she was in America and I was tethered to my mirror in Britain. Even if I could get beyond my pre-travel rituals, flying had become an excess baggage nightmare, requiring me to stow mirrors, lights, and window coverings.

My recovery began with a single decision: to peel away the layers from my windows. Inch by inch, I unravelled the blinds and peeled back the curtains, shielding below a ball cap or behind sunglasses, taking small steps forward and then retreating, until I could finally face myself. All the while, audiobooks, movies, and music distracted my self-criticising voice.

In 2019, I flew to New York to meet Dr Phillips. Her diagnosis gave me new self-awareness, and I came away with a surprising side diagnosis: non-purging bulimia, another bodybuilding souvenir.

Today, I’m happily married and settled in Washington, and my active recovery is structured around these core practices: I restrict my makeup routine to just 15 minutes, and I often glance in the mirror no more than twice a day, occasionally forgetting until evening. I avoid interacting with my reflection when outside my home, hyper-vigilant of every reflective surface. Headphones replace sunglasses, and audiobooks not only provide a distraction, but have given me back my voice.

A year ago, in my journal, I recognised a tone change. I called it “Bogey Maid,” inadvertently giving my BDD a name and separation. Now I turn my scars into stories.

Moments ago, I finally checked my mirror. Close to the window where I can see my blue-grey-green, colour-confused eyes. I recognise my face looks normal, adding another increment towards recovery.

Sitting here right now, the warmth I feel is not a flush of embarrassment or shame, just a friendly kiss from the sun.

Thirty-five years of worrying about my face, chasing superficial fixes, and hiding behind camouflage led to nothing but isolation where I tiptoed near death. But just one inch of daylight led me here, to my husband, my cat, and a life.

I still have a way to go before I can sit in a hair salon and not blur my eyes in front of the mirror; however, I no longer stress over bad hair days, I just swish my glasses into the hairband position.

I’m thankful for Dr Phillips, the BDD Foundation, and every researcher who studies and supports those of us living with this not-so-invisible and destructive disorder.

If my experiences sound like they could be your own, or if your feelings seem misaligned with what’s considered typical, don’t delay seeking help as I did. BDD isn’t something you simply outgrow, and it’s not a universal experience. With the right approach and support, freedom awaits you too.

About Carrie-Ellise Poirier…

In 2005, a bidding war on eBay unexpectedly launched Carrie-Ellise Poirier into the literary world.

Having navigated 30 years of Social Anxiety and Body Dysmorphic Disorder, and driven by a relentless pursuit of recovery, Carrie’s life has been a series of unexpected turns, from securing a coveted role as a flight attendant with a premier airline to competing in a bodybuilding contest.

Today, Carrie channels her unusual experiences into her writing, establishing Bogey Maid as her platform for promoting positive body image while finalising her forthcoming coming-of-age memoir.

School’s Project – Volunteers Needed

We are recruiting volunteers to support on an exciting new Schools Project!

The Project

The BDD Foundation, in collaboration with the specialist NHS team at the Maudsley Hospital, is soon to relaunch our Schools Project, designed to provide educational professionals with the knowledge and skills to identify signs of BDD. This is an early intervention programme, aimed at supporting adolescents to access timely support. We know that BDD commonly onsets in adolescence, and causes significant disruption to their education and social development. Understanding within schools still needs improvement.

Guided by clinicians, our volunteers will be delivering in-person interactive training workshops to school personnel, primarily in south London schools. Training will cover the signs and symptoms of both BDD and appearance anxiety, and will equip staff with knowledge on BDD as a condition, how to spot the signs in a young person, how to approach the topic, steps in helping them access treatment and support for the wider family network.

The Volunteer Role

We are looking for volunteers who are interested in supporting us to deliver this crucial work. The criteria for this role includes:

  • Direct or indirect lived experience of BDD (personal experience or caring for a child/ loved one)
  • Good understanding of the signs and symptoms of BDD
  • Ideally experience in one or more of the following: delivering training, public speaking, facilitating groups, professional presentations
  • Clear communicator, organised, and passionate about early mental health intervention

How to apply

Please submit a CV and a personal statement (max 700 words) which outlines the following:

  • Your (direct/indirect) experience with BDD
  • Why you would like to apply for this position
  • Your relevant experience (either as an expert-by-experience, an expert-by-training or both)
  • Your relevant skills and qualities

Please submit your CV and personal statement to gem@bddfoundation.org by 11.59pm on 22nd August

Interviews are due to take place week commencing 26th August

Volunteer Information Evening

Join us on Zoom, for a Volunteer Information Evening on 28th August at 6.30 – 8pm (BST)

REGISTER HERE


We are soon to be recruiting for a variety of volunteer opportunities across the charity. This online information session offers the chance to find out more about the following roles: ⁠

⭐ Overcoming BDD Programme Peer Facilitator⁠
⭐ E-Helpline Volunteer ⁠
⭐ Support Group Facilitator ⁠

There will be a short presentation about each of the projects/ roles available, followed by lots of time to ask questions about any of the positions you may be interested in. ⁠If you are interested in applying, you will still be required to submit a formal application. This is an information session only. ⁠

We look forward to seeing you there!

💡 Please note, we are currently only able to work with volunteers residing in the UK and aged 18+ due to insurance reasons.

Understanding BDD webinar in collaboration with OCD Action

Upcoming webinar: Join us on Tuesday 30th July at 7pm for a comprehensive webinar on Body Dysmorphic Disorder (BDD) in partnership with OCD Action

Accredited CBT therapist Rebecca Robinson will discuss the common signs and symptoms of BDD, its impact on daily life, and the links between BDD and OCD. She will also cover treatment options, including medication and cognitive behavioural therapy (CBT) for BDD. Adding depth to the discussion, Mia Hill and Andy Hall will share their lived experiences, providing personal insights and highlighting the impact of BDD. Don’t miss this opportunity to learn and gain support from both experts and those with lived experience.

Register for free.

Meet the Panel

Rebecca Robinson: Accredited CBT Therapist

Rebecca is an accredited CBT therapist, initially working as a registered mental health nurse working in both acute inpatient and community outpatient settings. She currently works with Prof David Veale and Dr Rob Willson in their specialist OCD and related disorders service, ‘Overcoming OCD’. Rebecca has a keen interest in BDD, providing training sessions on the subject as well as having seen numerous patients with the condition.

Andy Hall: BDD Foundation volunteer and lived experience expert

Andy developed BDD in his late teens and has been in recovery for over ten years. Since joining the BDD Foundation in 2016, Andy has passionately promoted hope for recovery by sharing his experiences with the community.

Mia Hill: BDD Foundation Youth Ambassador and OCD Action Youth Engagement Panel Member

Mia Hill is a 21-year-old psychology student and part-time staff member at OCD-UK, supporting young people with OCD. She is a youth ambassador for the BDD Foundation and a member of the OCD Action Youth Engagement Panel. Mia runs a mental health page on Instagram, sharing her journey with BDD and OCD to raise awareness and help others through her own experiences.

Register for Free

Staff & Trustee Away Day

The BDDF team come together in person to establish mission, vision and values

We are delighted to share that BDDF recently hosted a staff and trustee away day, where we had the valuable opportunity to connect in person. A huge thank you to our wonderful Patron Tracy Northampton who kindly provided a beautiful venue at The Falcon, Castle Ashby – we were so lucky. We were also joined by one of our wonderful volunteers, Holly, who has been supporting us with our impact measurement work and guiding lots of these important conversations and focus areas.

This gathering allowed us to come together to connect in person, re-connect with the needs of our service users, and formally establish the charity’s mission, vision, and values. Additionally, we laid the groundwork for the next stage of our strategic plan. We extend our gratitude to the community members who participated in our recent survey; your input significantly informed our discussions. Stay tuned for an update on our new mission, vision, and values very soon!

10K in May Roundup

An update on all the wonderful activities of our 10K in May team!

We are pleased to announce that our ’10K in May’ fundraising team; Liane, Rachel, Jem, Zosia & Gem, have collectively raised nearly £2000! This is an incredible achievement, and we are so grateful for the dedication, effort, and commitment each of you has put into your individual challenges.

We know the hard work hasn’t only been in the physical challenges. There has been wonderful awareness raising, rallying support, spreading the word, and keeping the momentum going – this all requires a lot of perseverance and enthusiasm, but your passion and dedication have made a real difference.

To all our fundraisers, thank you for your incredible effort. You have shown us what’s possible when we come together to collectively fundraise, and we couldn’t have done it without you. Your commitment not only helps us financially but also raises awareness and encourages others to join our cause.

Inspired? Contact fundraising@bddfoundation.org today!

Mark’s Ironman Fundraiser for the BDD Foundation

On 30th June, Mark is completing his first Ironman Triathlon!

A huge thank you to Mark for his current fundraising efforts for the foundation! Mark is training to do an Ironman at the end of June this year. This involves a 2.4 mile lake swim, followed by a 112 mile cycle, then a 26.2 mile run.

This is such an incredible challenge. Not only is Mark fundraising but he is also working hard to raise awareness of BDD by sharing facts and stats about the condition wherever possible. Mark is also challenging his own pre-occupations about his body throughout the training, which he shares more about in his videos.

THANK YOU Mark! We are behind you every step, peddle and stroke of the way 🏊‍♂️🚴‍♂️🏃‍♂️

SUPPORT MARK HERE

Broken Mirror Film by Indriyaan Theatre Group

Indriyaan Theatre Group and Performing Arts School Produce Film on BDD

Broken Mirror offers a poignant portrayal of Body Dysmorphic Disorder, exploring the tumultuous journey of those grappling with this often misunderstood condition. Directed by the talented Ashwin Agrawal from Indriyaan Theatre Group & Living Bread Production, this film stands as a testament to the power of cinema in shedding light on mental health struggles with empathy and authenticity.

Having had the privilege of a private screening at the BDD Foundation, courtesy of Ashwin Agrawal, it’s evident that Broken Mirror has the potential to spark important conversations surrounding mental health. Its depiction of BDD and its impact on individuals and their loved ones is commendable and essential in bringing greater awareness and understanding of the condition.

From the opening scenes, the film demonstrates the pain and anguish experienced by individuals with BDD. The film follows a realistic trajectory, exploring the debilitating behaviours that accompany the disorder, the challenges of accessing treatment, and the solace found in support groups. Broken Mirror shows commitment to portraying the nuances of BDD without sensationalism or stereotype, allowing viewers to truly understand the internal battles fought by those affected.

Ashwin Agrawal’s direction is fantastic, navigating the delicate subject matter with extensive research, sensitivity and compassion. The performances by the cast are exceptional, with each actor embodying their characters with real authenticity.

One of the film’s greatest strengths lies in its portrayal of hope and resilience. As the female protagonist Ahana, played by the incredible Titiksha Taggar, navigates her journey towards self-acceptance and healing, the film beautifully illustrates the power of pursuing values unrelated to appearance. By highlighting the importance of support networks and seeking professional help, the film offers a message of hope to those grappling with similar struggles, reminding them that they are not alone in their journey towards recovery and there is so much more to them than appearance.

We are feeling lucky to have seen the film prior to it’s full release. Ashwin Agrawal and the entire team behind the film have created a piece of work that deserves recognition. The film has been nominated for multiple film festivals including LAFA 2024 and World Film Fest Cannes. With its powerful message of resilience and hope, Broken Mirror is a must-watch for audiences seeking meaningful and thought provoking cinema.

Watch this space!

‘Heart On Your Sleeve’ Chosen Designs – Pre order open

We are excited to share the outcome of the Tilted East x BDDF Design Opportunity

PRE-ORDER NOW OPEN

The chosen t-shirt & poster designs are now available on pre-order only until 18th April, and will be shipped from 29th April. 50% of profits will support the BDD Foundation. Don’t miss out!

At the start of this year, BDD Foundation and Tilted East teamed up to collaborate on a t-shirt design opportunity, offering those living with BDD a space to share their experience through creativity and design, with the chance to have their design featured on a Tilted East t-shirt. We’ve been totally overwhelmed with how many people engaged in the opportunity, and bravely and beautifully shared their artwork alongside narratives about their personal and unique experiences of living with BDD.

Throughout March, we’ve been sharing the amazing designs we’ve received and many of the BDD community have connected what they’ve seen. It’s been such a wonderful opportunity to give each and everyone of your experiences with BDD the best chance to be recognised and understood for exactly what they are.

We are now pleased to share 2 chosen designs – one will be featured on a Tilted East t-shirt, and one on a poster.

Featured T-shirt

We have selected ‘Til I Get Okay’ By Hazel San Jose to be featured on a limited edition Tilted East T shirt.

Inside the four walls of her room, she sits atop a wooden digital box printing out the diagnosis of mirror count #1104 that reads “Getting There.” Nobody knows the lengths she has gone down the rabbit hole of appearance issues, a journey of countless mirror gazing of her facial features, testing the mirror’s authenticity. She believed it, but the strewn papers of negative diagnoses constantly reminded her that soon enough, she would be “Okay.”

Hazel’s design and narrative resonates strongly with what many people experience in BDD, and really tells a story even without the narrative. We hope many of you will relate to Hazel’s amazing design and know it’s going to look great printed on a tee!

Featured Poster

In addition to the chosen t-shirt design, we are excited to share a chosen poster design from the ‘Heart On Your Sleeve’ design opportunity. We have selected ‘Patchwork’ By Kat Hall to be featured on a limited edition Tilted East Poster.

This design represents the experience I have with BDD-at times I can see my face as a jumbled up mixture of facial features, almost like Frankenstein’s monster or a patchwork face comprising of all the “wrong” parts.

Kat’s design really stood out to us as an eye-catching piece, and also strongly resonated with the BDD experience. That feeling of facial features looking out of place, or seeing things differently each time we see ourselves in the mirror is one we are confident many will connect with.

Thanks again to everyone that took part in the design opportunity. We appreciate every one of you, as well as everyone who engaged with the art on our social media. It means so much. We loved all your designs for different reasons and will continue to share more from the artists involved over the coming weeks 💙

The t-shirt & poster are now available to pre-order only until 18th April, and will be shipped from 29th April. 50% of profits will support the BDD Foundation. Don’t miss out!

PRE-ORDER HERE

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!