Dwarfism is a medical condition that lead to short Stature as a category of Disability. In Countries all round the world, persons affected by dwarfism still face social and physical barriers that can stand in the way of choices and opportunities.
There are more than 200 different types of dwarfism. 80% of persons affected by dwarfism have average height parents – their dwarfism can be the result of a spontaneous mutation, although some forms of dwarfism may be passed onto children. A child is born with dwarfism every 1 in 25,000 births. Despite this, very few doctors know much about dwarfism, so families often have to find a doctor that specializes in the type of dwarfism in their family.
A person with dwarfism will usually be 4ft 10inc or less in height. However, dwarfism is not just about height – other medical issues arise due to dwarfism, such as spinal stenosis, hydrocephalus, arthritis and more. Achondroplasia is the most common type of dwarfism and the word itself means ‘without cartilage formation’ or a bone growth disorder.
Challenges face by persons affected by dwarfism
In September 2021, FPAD-U with funding from DRF conducted regional survey on issues affecting people of short stature in Uganda that were used to develop an advocacy agenda as follows;
October 25th of every year, FPAD makes arrangements through mobilizing persons affected by dwarfism together with other development partners/ government to celebrate this day with an aim of creating and promoting awareness on dwarfism/short stature and different barriers they face to assert independence and their right to self-determination.
FPAD-U calls upon the government and other development partners to mainstream dwarfism to create awareness, protect people with dwarfism and enhance access to services for people with dwarfism.