Understanding Intersex Children: A Guide for Non-Profits

Intersex children are born with physical sex characteristics that don’t fit typical definitions of male or female. These variations may involve chromosomes, genitals, hormones, or internal reproductive organs. It’s important to remember that being intersex is a natural variation, not a medical condition or disorder.

Key Points for Non-Profits:

• Prevalence: Intersex traits are more common than many people think, affecting approximately 1 in 100 births.
• Terminology: Use respectful and accurate language. Avoid outdated or stigmatizing terms like “hermaphrodite.”
• Support: Intersex children and their families need support and understanding, not judgment or attempts to “fix” them.
• Medical Interventions: Non-essential medical interventions on intersex children are highly controversial and can have lifelong negative consequences. Prioritize the child’s well-being and autonomy.
• Advocacy: Advocate for policies that protect the rights of intersex children, including their right to bodily autonomy and self-determination.

How Non-Profits Can Help:

• Education: Provide accurate information about intersex variations to staff, volunteers, and the communities you serve.
• Support Groups: Facilitate peer support groups for intersex children and their families.
• Advocacy: Advocate for policies that protect the rights of intersex individuals.
• Resources: Connect families with resources, such as medical professionals who specialize in intersex care and support organizations.

Remember:

• Every intersex child is unique.
• Respect their autonomy and right to self-determination.
• Create a safe and inclusive environment where they can thrive.