190: An Interview With Nikki McIntosh, Founder of Rare Mamas and SMA Patient Advocate
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190: An Interview With Nikki McIntosh, Founder of Rare Mamas and SMA Patient Advocate
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About this listen
Larry Luxner, senior correspondent for Rare Disease Advisor, interviews Nikki McIntoch, mother of a boy with spinal muscular atrophy (SMA) and founder of the advocacy group Rare Mamas.
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In the spirit of reconciliation, Audible acknowledges the Traditional Custodians of country throughout Australia and their connections to land, sea and community. We pay our respect to their elders past and present and extend that respect to all Aboriginal and Torres Strait Islander peoples today.