This episode explored the journey of Namata Biswal with her son Yash.
Yash has a very rare genetic condition called Pallister Killian Syndrome, PSK for short. Not more than 20 in Australia diagnosed with this condition.
The talk explores Namita's actions and initiatives in this space.

The Small Picture Podcast - 2026-7-19
59:59

The Small Picture Podcast - 2026-7-12
59:59

E15: Invisible burdens that parents of children with additional needs carry
59:59