Escape from Limbo Land

Jul 17, 2019 | Episode 47 | 21 mins

Parents of children who suffer from a rare disease can sometimes find it difficult to find a diagnosis, sometimes spending years living in a diagnostic limbo land. Heather Renton is the executive officer of Syndromes Without A Name (SWAN) Australia, and she joined me to discuss her daughter’s rare disease and the impact of NGS-based testing on her and her family.

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Escape from Limbo Land

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