The BDD Foundation

Since 2006, the BDD Foundation has been dedicated to the relief of suffering from Body Dysmorphic Disorder. Together, we can change lives.

At the BDD Foundation, we aim to advance education and understanding of BDD. We support research into BDD and its treatments. Whilst we are based in the UK, our reach is international and we are proud to be the only charity for BDD in the world.

Together at the BDD Foundation, we aim to:

  • Raise awareness about BDD.
  • Advance the education of the public and healthcare professionals, supporting them to understand the nature of BDD and how it might best be treated.
  • Relieve suffering from BDD through support and high-quality information.
  • Reduce stigma, discrimination and isolation caused by BDD.
  • Help develop a sense of community for people affected by BDD. This includes individuals with BDD, their families, friends, partners and carers.
  • Provide information on relevant treatment options.
  • Support research into the understanding and treatment of BDD.

Mission

We are the leading charity for Body Dysmorphic Disorder. We shine a light on a condition that is misunderstood by raising awareness, providing support and fostering community to shatter stigma and shame. We alleviate suffering and inspire hope – because we know recovery is possible.

Vision

We envision a world where Body Dysmorphic Disorder is truly understood, and everyone impacted has timely access to support, care, and treatment.

Values

  • Hope
  • Community
  • Compassionate
  • Dedicated
  • Pioneering

Our Impact

Explore our impact reports to see how we’re making a difference, driving change, and creating a better future for those affected by BDD.


Our History

The BDD Foundation began in 2006 by Ruth Ryan assisted by Stuart Chandler and Matt Chappel and Stephen Hosking as a website providing information about BDD. It was set up by a small group of individuals with BDD but they were unable to keep it going. The current trustees resurrected the brand and registered it as a charity in September 2013.

Today, we have a Head of Operations to help run the day-to-day operations, a People and Projects Manager, E-helpline Manager and E-Helpline Coordinator as well as an excellent group of volunteers.


Our Constitution

We were registered as a Charitable Incorporated Organization (CIO) in September 2013. A CIO is a new incorporated form of a charity, which is not a limited company, or subject to company regulation. It does, however, have limited liability.


Policies

The Body Dysmorphic Disorder Foundation. Charity no. 1153753.