Rare diseases, such as AADC deficiency, may take a long time to accurately diagnose and the journey to achieving a diagnosis can be challenging. 

Ivana Badnjarević is the parent of a daughter living with a rare disease: tyrosine hydroxylase deficiency (THD). She knows all too well about the journey to diagnosis and the realities of living with this rare condition. Listen to her discuss her experiences, including an explanation of the steps needed to confirm the diagnosis, which medical professionals might be involved, and some tips to help you get the support you need for your child.

Listen to the podcast for important information and who you can turn to for support.

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