Meet the Team
The BDD Foundation is a very small charity comprising of an active Trustee Board, Patrons, Associates and part-time staff.
Rob Willson – Chair of Trustees
Rob is a Cognitive Behaviour Therapist with a special interest in obsessional problems. He co-authored with David Veale and Alex Clarke the self-help book Overcoming Body Image Problems including BDD. He first became involved in research on BDD 20 years ago. Currently, he divides his time between private practice and conducting research on improving the understanding and treatment of BDD. Rob was indirectly involved in the original launch of the BDD Foundation through his participation in a BBC TV documentary Too Ugly for Love. Rob hopes that the foundation will help to raise a far greater level of awareness of BDD amongst people with the disorder, the general public, and healthcare professionals. He believes that there is a great deal to be done in terms of improving identification/diagnosis, understanding of how serious BDD can be, and that it can be successfully overcome. His personal website is http://robwillson.com/
Nicole Schnackenberg – Secretary
Dr Nicole Schnackenberg is a child, community and educational psychologist with lived experience of BDD. She is also a certified yoga teacher and has undertaken extensive training in yoga therapy. Nicole is a facilitator of Eat Breathe Thrive, a yoga programme for food and body image struggles. Nicole currently divides her time between working as an educational psychologist in Southend, Essex, her position as a Director of the Yoga in Healthcare Alliance and her position as a trustee of the Body Dysmorphic Disorder Foundation. She has authored books on transpersonal modes of healing from appearance-focused identity struggles: False Bodies, True Selves and Bodies Arising. She has also co-authored The Parents’ Guide to Body Dysmorphic Disorder and co-edited, Reflections on Body Dysmorphic Disorder: Stories of Courage, Determination and Hope. Nicole’s doctoral research was on young people’s lived experience of BDD. It was entitled, “The Only Way I Was Going To Be Lovable.” A Grounded Theory of Young People’s Experiences of Body Dysmorphic Disorder.
Joe Davidson – Treasurer
Professor David Veale
David is a Consultant Psychiatrist in Cognitive Behaviour Therapy at the South London and Maudsley NHS Trust, where he directs a national specialist service for people with BDD and The Nightingale Hospital London in Marylebone, . He is a Visiting Professor at the Institute of Psychiatry, King’s College London. He has co-authored with Rob Willson and Alex Clarke a self-help book on Overcoming Body Image Problems including BDD and with Fugen Neziroglu a treatment manual for BDD for professionals. He was chair of the NICE Evidence Update on OCD and BDD in 2013 and a member of the working group that produced the NICE guidelines on OCD and BDD in 2005.He has been a Trustee of OCD Action since 1993 and was actively involved in organizing user conferences for anxiety disorders for several years. He was a member of the World Health Organization’s International Advisory group for writing the new diagnostic criteria for OCD and related disorders such as BDD. He has been researching BDD for nearly 20 years and has published about 40 scientific and teaching articles in BDD. He was motivated to improve the care of people with BDD after the suicide of one of his in-patients with BDD in 1991. His personal website is www.veale.co.uk
Dr Amita Jassi
Amita is a Consultant Clinical Psychologist and lead for the National Specialist BDD service for young people at South London and Maudsley NHS Trust. She has worked with young people with BDD, OCD and related disorders since 2006. In her clinical role, she leads multi-disciplinary specialist assessments and develops and delivers individually-tailored treatment packages, including intensive, home-based and inpatient treatment, as well as offering consultation and joint work with clinicians around the country. Amita has taught and trained nationally and internationally and engages with media to help increase awareness and understanding of BDD and related disorders. She has authored several books on OCD and BDD and published peer-reviewed papers in this field. Amita has worked closely with OCD Action since 2010 as a clinical advisor and has actively been involved in their work for young people. Her ambition is to raise awareness of BDD, increase and facilitate access to mental health services for people who have it and improve treatments. Her hope is to utilise both her clinical role and position as a BDD Foundation Trustee to do this.
Scarlett grew up mainly in Germany and is bilingual in German and English. She has degrees in Italian and French. Scarlett worked for the Italian Trade Centre in Düsseldorf, Germany before working for American Airlines in various roles at Düsseldorf Airport. She has, over the years, been on various Nursery School and School committees. Since having children, Scarlett has been a stay-at-home mother of four, one of whom has suffered with BDD since 2010. She has had to fight the NHS system to obtain the treatment her daughter so desperately required. Scarlett has gained an extremely close insight into BDD and the struggles of living with and supporting a BDD sufferer.
Emily holds a Bachelors degree in English Literature and French Language from the University of Manchester and a Masters degree in Development Studies from the School of Oriental and African Studies in London. She worked for over 15 years in programme management and implementation for international development and humanitarian organisations such as Médecins Sans Frontières and Pact, including several years spent in sub-Saharan Africa. Emily relocated to the UK from Zambia in 2020, and she now works as a Family Worker for Cornwall Council, following a long-standing ambition to work in frontline social services.
Emily has clinically diagnosed obsessive compulsive disorder and body dysmorphic disorder, and was introduced to the BDD foundation as a patient of David Veale in 2014. She feels strongly that both conditions are widely misunderstood, and is delighted to now be a trustee for the BDD Foundation which is providing objective information and evidence-based support to those living with the condition and their family and friends.
Katharine A. Phillips, M.D.
Katharine is Professor of Psychiatry at Weill Cornell Medical College, Cornell University, and Attending Psychiatrist at New York-Presbyterian Hospital in New York City, where she has her clinical practice. She is also Adjunct Professor of Psychiatry and Human Behavior at the Alpert Medical School of Brown University in Providence, Rhode Island.
Dr Phillips is a physician and scientist who has spent her career caring for patients and conducting scientific research studies on BDD and other psychiatric disorders. She is internationally renowned for her clinical expertise and her pioneering work on BDD. Her research studies on BDD have elucidated many key aspects of this severe disorder; much of her work has focused on finding and developing effective treatments, both medication treatment and cognitive-behavioural therapy (CBT) for BDD. Her scientific studies on BDD were continuously funded by the National Institute of Mental Health for more than 20 years.
Dr Phillips has received numerous honours and awards for her research, clinical work, and other academic contributions, including a Special Presidential Commendation from the American Psychiatric Association for her research studies on BDD. She has published more than 320 original scientific articles, review articles, letters, and book chapters. She has also published six first-authored or co-authored books and five edited books on BDD and other topics, including the first book on BDD, The Broken Mirror: Understanding and Treating Body Dysmorphic Disorder, and the first comprehensive edited volume on BDD, to which BDD experts from around the world contributed (Body Dysmorphic Disorder: Advances in Research and Clinical Practice, published by Oxford University Press in 2017).
Dr Phillips is an elected Fellow of the American College of Neuropsychopharmacology and a Distinguished Fellow of the American Psychiatric Association. She is a member of numerous editorial boards, the American College of Psychiatrists, and the Scientific Advisory Boards of the Anxiety and Depression Association of America and the International OCD Foundation. She serves on the Board of the American Society of Clinical Psychopharmacology, and she is a Director on the Board of Directors of the Canadian Institute for Obsessive Compulsive Disorders. From 2002-2006 she chaired the National Institute of Mental Health’s Interventions Research Review Committee (Scientific Review Group).
For more information about Dr. Phillips and her clinical services please visit https://weillcornell.org/katharine-phillips-md
For more information about Dr. Phillips and BDD visit http://www.katharinephillipsmd.com/
Tracy Northampton is an accredited and qualified Psychotherapist with over 25 years of experience in the field of mental health. Tracy has a great interest in the mind, body, somatic connection and is a committed student of yoga. Tracy became interested in BDD when one of her close relations was diagnosed with the illness while being treated by Professor David Veale and Rob Willson. She learnt at first hand what it was like having a member of her immediate family suffering from BDD and the devastating effect on everyone. For the last two years, she has raised money for the charity by completing an annual sponsored marathon walk with her sister. She feels very grateful to the charity for all their support and is delighted to have become a patron of this very worthy cause. She sees her role as raising awareness of the work of the charity and supporting its activities in whatever way she can.
Danny Gray is the founder of the UK’s leading men’s makeup brand, War Paint For Men. As someone who has suffered from BDD for 20 years, War Paint is about more than make up for Danny – it’s a movement to eliminate the stigma surrounding men wearing makeup and give men access to tools that can help them feel more confident. BDD has been a part of Danny’s life since he was 12 after being bullied in school. Although this has shaped his life and still affects him to this day he wants to try and help others when it comes to the illness and spread awareness. Speaking about his appointment as a Patron for The BDD Foundation, Danny says, “The Foundation and the vital work they do sit very close to my heart, I understand the daily struggle of living with BDD. There’s isn’t enough awareness out there about BDD, so I’m eager to help and thankful to be a part of the Foundation’s important work”.
Benedetta Monzani (Clinical Advisor)
Benedetta is a clinical psychologist at the National Specialist OCD, BDD & Related Disorders Service for young people at the Maudsley Hospital. Before completing her doctorate in clinical psychology at the Institute of Psychiatry (King’s College London), she completed her PhD at the same institution, examining neuropsychological deficits and genetic factors involved in BDD and OCD. Benedetta has gained clinical and research experience with BDD and OCD, having trained and worked at various national BDD and OCD clinics in the UK and USA, including the Centre for Anxiety Disorders and Trauma (CADAT) at the Maudsley Hospital (UK), the BDD Clinic & Research Institute at Massachusetts General Hospital (Boston, USA), and the OCD Institute in Boston (USA), which offers residential treatment for severe BDD and OCD. Alongside her clinical practice she continues to be actively involved in writing about, and research into, BDD, OCD and Related Disorders. She published a number of peer-reviewed articles on BDD and hopes to help raise awareness of BDD through teaching, media, and research.
Stuart Chandler (Technical Director and Founding Member)
After Stuart graduated from Manchester in 1999 and worked for several years in the City as a web designer, his BDD meant not being able to work for a prolonged period. He was eventually treated in the Priory by Professor Veale and later, Doctor Rob Willson and over the last ten years or so has returned to health (but still battles with BDD). Stuart currently runs his own business offering PC Support and web design and is webmaster for the BDDF website. Stuart was part of the charity’s inception in 2006 and helped to re-launch the charity a few years ago. He is very interested in raising awareness of this oft silent illness and is delighted with the way the charity has gone from strength to strength over the past few years. Specific hopes of Stuart’s are that, one day, a BDD information leaflet will be in every GP surgery in the country and that the illness will gain a wider understanding.