For more information you can contact Dr Tamara Shengelia : tamara.shengelia@bpp.com
The experts on the panel are:
Dr Barbara Rooney – Consultant Psychiatrist
Lou Lebentz – Founder at Trauma Thrivers, a psychotherapist, Speaker, EMDR and Trauma clinician
Dr Nicole Schnackenberg – Child, Community and Educational Psychologist. Yoga Therapist and BDD Foundation Trustee
Alanah Bagwell – BDD Recovery spokesperson, Trainee Psychologist
Anna Oliver – Highly Specialized Eating Disorder Dietician
Dr Ana-Maria Ilea, Consultant Psychiatrist, Clinical Director for Low Secure and Specialist Rehabilitation Services.
Tickets are £200 and all proceeds will be donated to the BDD Foundation, in memory of Tracy’s niece, Charlotte Franklin.
See formal invite below for more information about how to attend and purchase your ticket:
In 2021 media personality Charlie King announced on national television his struggle with BDD. From the start of his career in reality TV to a celebrity fitness trainer he has felt personal struggle increase due to media pressure. During the pandemic this intensified resulting in him undergoing cosmetic surgery (rhinoplasty) which incurred complications causing his BDD to spiral. The response to this interview on Channel 4 was overwhelming and highlighting that this is a condition which a lot of people are still naive to, especially men. The BDD Foundation continue to support Charlie and many others without government funding, so using his platform and story Charlie wants to assist in raising awareness and money for the charity.
Charlie has his own clothing line: By Charles King and he has kindly designed and produced an exclusive t-shirt with all proceeds going to the BDD Foundation.
By Charles King began with the intention to create pieces that you can wear and feel happy and proud to simply be yourself. With social media hashtags such as #ownyourcrown and #sharethelove we have seen customers relate and purchase all over the globe.
With the pressures of looking perfect on social media and with the use of filters it is very easy to lose sight of self-love. The t-shirt was designed by a 12 year old girl who was starting to question and not identify with what is looking back at her in the mirror. This was her first impression of what BDD Foundation does for this condition, cleverly using the logo with a heart felt image.
Raising awareness and understanding of the condition is extremely important to Charlie, due to his own experiences. This collaboration is very much aligned with the brand ethos. Through the sale of this t-shirt, we want people to learn about the condition as well as the help and support available to anyone affected by BDD through the work that the Foundation does.
Charlie is very aware that social media and reality TV photo editing can create a false idea of reality which can be very unhealthy. From Charlie’s own experience and feeling the pressures himself, this is exactly why By Charles King was founded. By Charles King is a fashion brand which is inclusive, celebrates all walks of life, and is transparent with their customers. All we want is to make people feel empowered while wearing our pieces, and our duty of care as a brand is to make conscious decisions when it comes to photography, marketing, representation, and even product. We want to create accessible aspiration, not unobtainable aspirations.
King’s College London aims to find out whether people with BDD think using Virtual Reality (VR) in treatment would be useful, whether they have concerns with such methods, and the effects of specific VR features on treatment. The information gathered will go towards investigating new treatment pathways and improving existing treatments for BDD.
If you choose to take part in this study, King’s College will invite you to a focus group with a small number of people who have BDD. You will be asked to discuss your thoughts and opinions with other participants on questions asked by the research team. The focus group session will last up to an hour and will be online on Microsoft Teams or Zoom.
If you are interested in participating and would like to find out more about the study, please contact the team using the contact form:
Please note that enquiring about participating and registering your interest does not commit you in anyway.
Dr Rob Willson, Chairman of the BDD Foundation shares his expertise:
Explaining the first signs and symptoms of BDD to look out for, Dr Willson tells us they usually see the “person spending more and more time thinking about, being distressed about and carrying out behaviours related to their appearance.”
Kitty Wallace, Head of Operations, shares her experiences:
From the moment I woke up, to the moment I went to sleep, my mind whirred with the same thoughts over and over. I worried that people would judge me for how I looked, but I was equally as worried that they were judging me because I cared about how I looked. I really couldn’t win. Some days the thoughts were so overpowering, I couldn’t leave the house. Everyone around me just thought I was going through a phase. Something I’d grow out of. I didn’t.”
Nightrider gives you the rare chance to explore the capital in the dark, on two wheels! You have the choice of a 50km or 100km route which will take you past the best sights in London, including Tower Bridge, Piccadilly Circus, the London Eye and Buckingham Palace. There’s full support along the route and regular breaks are provided. You’ll also be rewarded with a well-earned breakfast and medal at the finish.
You can choose to cycle either 50km (takes about 3-4 hours with stops) or 100km (6 to 8 hours).
It will cost you £58 to register. For this you will receive free water and snack stops, mechanical support and marshals along the route. You’ll also be rewarded with a well-earned breakfast and medal at the finish. You’ll make friends and hopefully lifelong memories. It begins and ends in the Velo Park in Stratford. Highlights include cycling through Queen Elizabeth Olympic Park, Tower Bridge, Canary Wharf, Piccadilly Circus, Trafalgar Square, the Royal Opera House and the London Eye.
The charity will help you make a fundraising page and agree minimum target for you to raise with lots of tips. A lightweight road or hybrid bike is recommended. The minimum age for participants is 16. Those under 18 will need to provide a letter of consent from a parent or guardian.
Ben McLaughlin is a filmmaker from Philadelphia who has experienced body dysmorphia for 5 years now, and who now hopes to make a difference within the BDD community. He believes that the best way to do that is through a PSA campaign, titled ‘Strength in Numbers’, that shows the daily experiences of individuals that also deal with this condition.
“I have suffered from a hyperfixation on my body for years and it’s something that, at points, has dominated the state of my mental health. My goal with this project is to tell individual stories to broaden our communities’ knowledge on Body Dysmorphia and how it affects specific people. Your experience is unique to who you are, but you are not alone.”
McLaughlin and his crew of filmmakers are currently crowdfunding for the first PSA that showcases the stories of individuals with body dysmorphia. The film will tell John’s story- Ben’s best friend who inspired the campaign. It will follow his journey with muscle dysmorphia and the obsessive tendencies that come with it.
Not only are Ben and his team crowdfunding for the production of the piece, they are also donating 20% of each donation to the BDD Foundation.
This production is through Typo Film House, a start-up production company based in Philadelphia that McLaughlin has co-founded with four other passionate creatives. They need your help to share this important message with the world!
You can also stay up to date with the PSA and their other upcoming projects on Typo’s Instagram @typofilmhouse
MPs are examining the relationship between people’s perception of their body image and their physical and mental health. They will consider how far people’s perception of body image can hinder access to NHS services and whether NHS training and Government messaging should be altered.
As a charity we are incredibly supportive of this inquiry and we believe it could be the start of real change.
Kim Booker has bravely shared her experience of Body Dysmorphic Disorder and how idealised images in the media as well as cosmetic treatments have played a part in the development and maintenance of her BDD
Dr Georgina Krebs, who is an Honorary Consultant Clinical Psychologist and Associate Professor of Young People’s Mental Health and Cognitive Behaviour Therapy, at University College London. She speaks on eating disorders and Body Dysmorphic Disorder including Muscle Dysmorphia in her evidence.
Nyome Nicholas who was involved in our Monki campaign on Selfie Love and petition calling for transparency on altered images online, James McVey from the band the Vamps and others also gave evidence on this.
Charlie King, an ambassador for the BDD Foundation gave evidence on his experience of BDD, bullying in childhood and plastic surgery that went wrong. You can watch his evidence here.
Danny told how a crippling mental health issue caused him to drop out of school and become housebound for several months as he was convinced he looked like a ‘monster’.
The condition caused him to perform a number of daily rituals, including scrubbing his skin, spending hours in front of the mirror and taking endless photos of himself in an attempt to look perfect.
Danny, who is now studying towards a PhD in mental health policy, told the Mirror: “I couldn’t leave the house because I was worried that people would be terrified of me, and that prevented me from engaging in anything.“
“Because I was a man, I didn’t think I could suffer from a body image disorder. But I’m lucky that I got the help I did when I did. It enabled me to get my life back”
Danny believes that the lack of awareness around BDD has also led to an increase in common misconceptions – the main one being that the condition is born from vanity.
34-year-old Kitty Wallace, who developed BDD in her late teens and since turned her struggle towards campaigning as Head of Operations at the BDD Foundation, said that the condition dictated every decision and movement she made growing up.
“I would spend eight hours trying to get ready, and still wouldn’t feel like I could leave the house and be seen. I felt so grotesque, so unusual. It was really scary.”
On the BDD Foundation Kitty explained that “we’ve got people visiting our website from all over the world because we are the only charity and website fully dedicated to it.”
Kitty points to the importance of specialised treatment for those who are diagnosed with BDD.
“The recommended treatment for BDD is specialised cognitive behavioural therapy. The reason I highlight specialised therapy is that a lot of people are just referred for generalised CBT for anxiety or depression.”
We are looking for a remote admin assistant to work 1-2 days a week, over a 5 week period (mid-June to mid-July). One week of that will be training alongside our Head of Operations.
The main responsibilities will be fielding general email inquiries (media, fundraising, volunteering) whilst our Head of Ops is on leave. There will be some miscellaneous tasks such as overseeing social media posting and scheduling and website updates.
We invite applications from people with lived experience of BDD or OCD, or of caring for someone with BDD or OCD. Applicants should have excellent written and communication skills as well as experience of using Outlook, Word, Instagram and Twitter. Knowledge of Canva and Mailchimp preferable.
There is the potential for this role to be extended beyond the 5 week period.
Please submit your CV and a personal statement which highlights the following to info@bddfoundation.org :
