An Interview With Nikki McIntosh, Founder of Rare Mamas and SMA Patient Advocate

Rare Care Podcast
16/09/2025 11 min Temporada 1 Episodio 190
An Interview With Nikki McIntosh, Founder of Rare Mamas and SMA Patient Advocate

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Episode Synopsis

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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