The Rare Life

201: Roya's Story | A Diagnosis Without a Map, Learning to Advocate + the Journey Back to Herself


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From the moment her daughter was born, Roya had an inkling that something was different. What followed was a long year of uncertainty, endless medical tests, and finally anofficial diagnosis of Schaaf-Yang syndrome... all on top of learning a new language of care no parent expects to need.

In this episode, Roya shares the disorienting early days of her daughter’s diagnosis journey, what tending to her own mental health looked like in the midst of caregiving, and how she eventually found purpose in advocacy and community. From becoming her daughter’s “historian” to learning that even the strongest caregivers break down, Roya’s story captures so many of the aspects that shape the lives of disability parents.

If you’ve ever had to rebuild yourself in the middle of medical chaos, this conversation will hit home.

Links:

Listen to Ep. 180: Does Disability Parenting Ever GetEasier?

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Access the transcript on the website here.

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The Rare LifeBy Madeline Cheney

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