The RGA is a UK based charity that provides vital information and support to improve the quality of life for persons of restricted growth (dwarfism), and their families.
There are estimated to be over 200 different forms of restricted growth, also known as dwarfism or short stature. The most common of these conditions, affecting around 70% of our full members, is Achondroplasia, a condition that causes disproportionate short stature. For more information about some of the conditions our members have experience of please see our page 'What is Restricted Growth?'.
The RGA aims to support individuals and families that are affected by any restricted growth condition by providing telephone support, opportunities to come together on equal terms, a quarterly magazine and provide a wider public awareness of the conditions to increase understanding.
The committee of the RGA is made up of members that represent the views and needs of the membership.
Living with Restricted Growth
You can now download the full report completed by Tom Shakespeare, Michael Wright & Sue Thompson from Newcastle University. This report is a research project carried out on behalf of the Restricted Growth Association and funded by the Big Lottery Fund in 2007.
Restricted growth affects approximately 6000 individuals in the UK and their families. Around 200 rare genetic or developmental conditions cause disproportionate short stature (dwarfism), known medically as skeletal dysplasia. But restricted growth is more than a medical condition: myths and legends have always provided imagery and stories about dwarfs or little people. This fascination is expressed today in staring and name-calling, and through media stereotypes........