Dwarfism is a medical or genetic condition defined by the organisation 'Little People of America' as resulting in an adult height that is shorter than 4”10’ or 147 centimetres. It is not a disease, nor is it a ‘curable’ condition, but its symptoms can be alleviated and those who experience the condition can – with the proper care and education – expect to live long and happy lives.
One of the greatest challenges for those who are short of stature is the lack of education about the condition amongst the general public, and indeed, dwarfism in popular culture can often find itself as the punch line of a joke or as the novelty factor in a film or television series episode. This does little to educate the public and can in fact be seen as a hindrance to those who strive to improve knowledge about dwarfism within the community. Moreover, it can effect the self-esteem of those who have the condition.
One of the best ways the myths and stereotypes can be broken is through education, and through the support of the organisations and associations who work every day to improve the quality of life of those who live with dwarfism. Understanding the causes, types, symptoms and treatments of dwarfism can greatly improve the quality of life of those who have the condition, and can lead to a much easier integration into social environments.
One of the best ways the myths and stereotypes can be broken is through education, and through the support of the organisations and associations who work every day to improve the quality of life of those who live with dwarfism. Understanding the causes, types, symptoms and treatments of dwarfism can greatly improve the quality of life of those who have the condition, and can lead to a much easier integration into social environments.