The Rare Life

100: Raising Awareness | Disabled People (and Their Parents) Do Not Owe Society Anything


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So often, we feel that as parents, we need to be raising awareness about issues relating to disability. Maybe we’re sharing our lives on social media in an effort to show that our child really isn’t that different from the next and deserves inclusion. Or perhaps we’re teaching about the importance of being an organ donor because our child wouldn’t be here today without generous donors. Or maybe we’re shouting the symptoms and definition of our child’s rare syndrome in the hopes that they’ll finally get the funding needed to research a cure.

There are many causes to fight for and many reasons for doing so. But it’s important to remember that we are not obligated to raise awareness about anything. Becoming a parent to a child with a disability does not require it.

In this episode, I invite parents to evaluate their cause and their “why” against the question: “is this serving me? Is it serving my child?” Because at the end of the day, that’s what really matters.

Links:

Children’s book What Happened to You? by James Catchpole

Demystifying Disabilityby Emily Ladau

Ep. 85 w/ Emily Ladau and Amanda Griffith-Atkins

Ep. 23: Disability Advocacy w/ Jenny McLelland

Follow me on Instagam.

Disabled adults on Instagram whom I love learning from:

cathyreaywrites

EmilyLadau

Sitting_Pretty

DisabilityReframed

TheCatchpoles

Wheelchair_Rapunzel

Wheel.Life.in.the.Wheel.World

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The Rare LifeBy Madeline Cheney

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