Welcome to the Dwarfism Awareness Australia page.
Dwarfism Awareness Australia Inc. is a not for profit organisation and registered since 2014. We are a group of like minded individuals who all strive for the same thing. To educate Australia about dwarfism, whilst offering support to individuals and families affected with dwarfism.
Some Facts About Dwarfism:
Did you know that there is over 200 different types of dwarfism?
You cannot catch dwarfism. It cannot be passed onto someone else like a flu. It is a hereditary and non hereditary condition which can only be passed on through carriers of the mutated gene or developed spontaneously in utero by a genetic mutation of a gene.
Dwarfism refers to a group of conditions characterised by shorter than normal skeletal growth. This shortness can be manifested in the arms and legs or trunk.
Achondroplasia is the most common type of short-limb dwarfism, occurring in around one in 25,000 children in Australia with both sexes at equal risk. This type of skeletal dysplasia (abnormal skeletal growth) is usually diagnosed at birth.
The majority of children born with the disorder have average-sized parents. The child may experience delay developing motor skills, such as controlling the movements of the head, but intellectual development is normal in children with Achondroplasia. The average final height for a person with this condition is 130cm for men and 125cm for women. Short-statured people lead normal, fulfilled lives. Achieving higher levels of education and career and personal ambitions is not limited by stature.
In humans, dwarfism is sometimes defined as an adult height of less than 4 feet 10 inches (58 in; 147 cm). Dwarfism can be caused from over 200 distinct medical conditions, such that the symptoms and characteristics of individuals with dwarfism vary greatly. Disproportionate dwarfism is characterized by one or more body parts being relatively large or small in comparison to those of an average-sized adult, with growth variations in specific areas being apparent. In cases of proportionate dwarfism, the body appears normally proportioned, but is unusually small.
There is no single treatment for dwarfism. Individual differences, such as bone growth disorders, sometimes can be treated through surgery, some hormone disorders can be treated through medication, and by hormone replacement therapy; this treatment must be done before the child’s growth plates fuse. Individual accommodations, such as specialized furniture, are often used by people with dwarfism.
For people, in addition to the medical aspect of the condition, there are social and sociological aspects as well. For a person with dwarfism, heightism can lead to ridicule in childhood and discrimination in adulthood.
Hypotonia, or low muscle tone, is common in dwarfs, but intelligence and lifespan are usually normal. Defining dwarfism by height alone is problematic because short stature in itself is not a disorder. For example, pygmies have adult male heights of less than 150 cm (4 feet 11 inches) on average.
The word “midget” is considered offensive. It is considered most offensive when misused to describe those with dwarfism. Acceptable words to use are dwarf, little person, person with dwarfism, short stature. But most would like to be called by their name rather than their condition.