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 exclusively focused on 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.

Body Dysmorphic Disorder is an under-recognised and under-diagnosed mental health condition. It is characterised by a disabling preoccupation with perceived defects or flaws in appearance. Individuals with BDD are excessively self-conscious, believing that they are ugly, deformed or disfigured. As well as the excessive self-consciousness, individuals with BDD often feel defined by their flaw. Sufferers tend repeatedly to check on how bad their flaw is (for example in mirrors and reflective surfaces), attempt to camouflage or alter the perceived defect and avoid public or social situations or triggers that increase distress. They may at times be housebound or have needless cosmetic and dermatological treatments. There is no doubt that the symptoms cause significant distress or handicap and there is an increased risk of suicide and attempted suicide.

We know that the help and support provided by our charity can be life changing, offering crucial assistance that not only saves lives, but also transforms them.

The BDD Foundation

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