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127: Season 7 Finale + 3 Year Anniversary | How This Podcast Has Changed My Life w/ Juston Cheney
It’s the very last episode of Season 7! We have clips from every episode this season, listener take-aways, and a very special guest: my husband Juston. This finale is a little different from seasons past because we’re not just celebrating another season, it’s also the third anniversary of the podcast.
To honor that milestone, I’m answering a ton of questions with Juston from this community about what it’s like behind the scenes, how I plan and run the
podcast, and how I handle the sometimes heavy topics and stories that I bring to you all week after week.
Not going to lie, this last season and planning for Season 8 have been a little tougher than previous seasons. But this podcast is a labor of love. It’s for all of us: those who wished we had something like this when our children first received their diagnosis and the families who will come after us who can hopefully find space and hope here, instead of feeling scared and alone. And my goal for the future is that we share this podcast far and wide so everyone who needs it will have access.
Finally, make sure you catch our exciting announcement about ways you can connect with other listeners over the summer! If you’ve ever wanted to chat about the topics we cover each week, you’re in luck! Thank you for being here these last three years, and I feel so honored to create even more episodes for you next season.
Links:
Fill out our contact form to be added to our email list for Discussion Groups!
Listen to Ep 114 about grieving intellectual disability with Marci Dunning.
Listen to Ep 124 about living in survival mode with Suzy Boubion.
Check out Ep 77: To Those Who Cannot Say, “I Wouldn’t Have Them Any Other Way” one of my favorites.
Listen to Ep 19 and Ep 20 with Katie Peterson about her daughter’s terminal diagnosis and anticipatory grief.
Connect with Rebekah, Andie, and Emily!
Follow me on Instagram!
Donate to the podcast via Buy Me a Coffee.
Contact me about sponsoring the podcast.
Follow the Facebook page.
Join the Facebook group Parents of Children with Rare Conditions.
Access the transcript on the website here.
And if you love this podcast, please leave us a rating or review in your favorite podcast app!
View all episodes
By Madeline Cheney
5
149149 ratings
It’s the very last episode of Season 7! We have clips from every episode this season, listener take-aways, and a very special guest: my husband Juston. This finale is a little different from seasons past because we’re not just celebrating another season, it’s also the third anniversary of the podcast.
To honor that milestone, I’m answering a ton of questions with Juston from this community about what it’s like behind the scenes, how I plan and run the
podcast, and how I handle the sometimes heavy topics and stories that I bring to you all week after week.
Not going to lie, this last season and planning for Season 8 have been a little tougher than previous seasons. But this podcast is a labor of love. It’s for all of us: those who wished we had something like this when our children first received their diagnosis and the families who will come after us who can hopefully find space and hope here, instead of feeling scared and alone. And my goal for the future is that we share this podcast far and wide so everyone who needs it will have access.
Finally, make sure you catch our exciting announcement about ways you can connect with other listeners over the summer! If you’ve ever wanted to chat about the topics we cover each week, you’re in luck! Thank you for being here these last three years, and I feel so honored to create even more episodes for you next season.
Links:
Fill out our contact form to be added to our email list for Discussion Groups!
Listen to Ep 114 about grieving intellectual disability with Marci Dunning.
Listen to Ep 124 about living in survival mode with Suzy Boubion.
Check out Ep 77: To Those Who Cannot Say, “I Wouldn’t Have Them Any Other Way” one of my favorites.
Listen to Ep 19 and Ep 20 with Katie Peterson about her daughter’s terminal diagnosis and anticipatory grief.
Connect with Rebekah, Andie, and Emily!
Follow me on Instagram!
Donate to the podcast via Buy Me a Coffee.
Contact me about sponsoring the podcast.
Follow the Facebook page.
Join the Facebook group Parents of Children with Rare Conditions.
Access the transcript on the website here.
And if you love this podcast, please leave us a rating or review in your favorite podcast app!
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