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It’s All My Fault (Rebroadcast)
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.
This is a rebroadcast of Ep. 22 of Season 2.
Links:
The episode that released right after this one Ep. 23: Jenny’s Story.
Follow me on Instagram.
Follow the Facebook page.
Join the Facebook group Parents of Children with Rare Conditions.
Donate to the podcast via Buy Me a Coffee.
Check out our appointment day merch.
Check out our sponsor BetterHelp for online licensed therapy.
View all episodes
By Madeline Cheney
5
149149 ratings
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.
This is a rebroadcast of Ep. 22 of Season 2.
Links:
The episode that released right after this one Ep. 23: Jenny’s Story.
Follow me on Instagram.
Follow the Facebook page.
Join the Facebook group Parents of Children with Rare Conditions.
Donate to the podcast via Buy Me a Coffee.
Check out our appointment day merch.
Check out our sponsor BetterHelp for online licensed therapy.
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