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22: It’s All My Fault

22: It’s All My Fault

FromThe Rare Life


22: It’s All My Fault

FromThe Rare Life

ratings:
Length:
32 minutes
Released:
Nov 12, 2020
Format:
Podcast episode

Description

Finding out I’m a genetic carrier for my son’s syndrome of CDPX1 was a very tough pill to swallow; and it has a whole slew of implications for my life.
It means I caused all of my son’s hugely challenging and life-threatening birth defects. And it also means that each of our children have a 50/50 chance of inheriting the unlucky genes.
Listen to find out what it was like to receive this life-changing news and what we’ve decided to do about it.
Released:
Nov 12, 2020
Format:
Podcast episode

Titles in the series (100)

This is the real, raw, and all the feels of loving a child with disabilities. Episodes feature parent-guests, professionals, and solo episodes with host Madeline Cheney. Their authentic conversations don’t shy away from the strong and mixed emotions that often accompany medically-complex parenting. Parents listen in to feel seen, validated, and receive much-needed solidarity. Professionals working with disabled people listen in to better understand what is often going on under the surface for a family living with disabilities.