In South Carolina, the parents of an adopted intersex child are suing a hospital and its employees for surgically assigning "M. Now around 10 years old, the child identifies as a boy.
The 29-year-old from Chicago has Androgen Insensitivity Syndrome (AIS), a very rare disorder affecting 1 in 20,000 which prevents a womb from growing and causes testes to grow in the abdomen or other unusual places in the body.
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One in every 2,000 babies is born intersex – and it's thought that doctors continue to operate on these newborns to 'assign' gender.
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As a result, the person has some or all of the physical traits of a woman, but the genetic makeup of a man.
Complete androgen insensitivity prevents the penis and other male body parts from developing. The complete form of the syndrome occurs in as many as 1 in 20,000 live births. A person with complete AIS appears to be female but has no uterus, and has very little armpit and pubic hair.
Previously, she had spent time at an all-boys school; not the easiest place for someone who describes herself as "super-feminised" from a young age.
But she always knew who she was, and had support from her family, including her younger brother.
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Vocal: Using social media to voice her thoughts, she recently tweeted: 'Diagnosed [with] testicular feminization (AIS) & labeled male pseudo-hermaphrodite exist in the gray.
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