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In this episode focused on cultural responsiveness, parents Tasha and Wolf share their experiences raising their daughter who has Spinal Muscular Atrophy (SMA) and the immense supports they have received along the way through their reservation, beginning with schooling at 6 months of age.
By Special Ed Tech Center4.4
55 ratings
In this episode focused on cultural responsiveness, parents Tasha and Wolf share their experiences raising their daughter who has Spinal Muscular Atrophy (SMA) and the immense supports they have received along the way through their reservation, beginning with schooling at 6 months of age.

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