By Rachel Taylor
The podcast currently has 7 episodes available.
September 9, 2021
In this episode, we talk to Jessica, mom to 10-year-old Caleb who was born with Pierre Robin Sequence, or PRS for short. PRS is a condition with several clinical features: a small lower jaw (micrognathia), displacement of the tongue toward the back of the oral cavity (glossoptosis) and, often but not always, an opening in the roof of the mouth (cleft palate). Jessica had to fight for the diagnosis because the doctors did not believe Caleb fit the criteria. She explains why it's so important to be a voice and advocate for our children. Follow us on Instagram -- @snconfessions. Visit us and give us a ‘like’ on our Facebook page https://www.facebook.com/SNCONFESSIONS/.
SPONSOR -- Amanda Jessup from @illuminatedsketchbook. Amanda is an author, illustrator, and digital artist who makes beautiful custom sketches. Check out her artwork on Instagram!
You can now support our podcast and help keep our show going by visiting https://anchor.fm/csnp/support. Monthly donations start at just $0.99 per month.
If you liked this episode, please share it with your family and friends!
You can go to https://anchor.fm/csnp/message to leave us a voice message and let us know what you think of the podcast, leave a confession, or just say hi!
Thanks so much for listening! ~Rachel
Date: December 30, 2020
Episode title: Liana and Zoey Part 2
In this episode, we talk to Liana, mom to 20-month-old Zoey who has Feingold's syndrome, which can manifest with a variety of symptoms ranging from mild to severe. Liana shares with us how her life has changed, her struggles with her mental health, and she shares her best tips for surviving life as a special needs parent.
Learn more about Liana and Zoey, and follow their amazing story on Instagram -- @zoey_goldengirl.
Follow us on Instagram -- @snconfessions.
Visit us and give us a ‘like’ on our Facebook page https://www.facebook.com/snconfessions/.
SPONSOR -- Our sponsor for this episode is Anchor, the easiest way to make a podcast. The Anchor app is free to download so you can start podcasting right from your phone. Visit anchor.fm, the app store, or Google play to try it out today.
SPONSOR -- We also work with Amanda Jessup from @illuminatedsketchbook. Amanda is an author, illustrator, and digital artist who makes beautiful custom sketches. Check out her artwork on Instagram!
You can now support our podcast by visiting https://anchor.fm/csnp and clicking the "Support" button to help keep the show going. Monthly donations start at just $0.99 per month.
If you liked this episode, please share it with your family and friends! You can also go to Anchor.fm and click the "Message" button to leave us a voice message. Let us know what you think of the podcast, leave a confession, or just say hi!
Thanks so much for listening!
Date: December 21, 2020
Episode title: Liana and Zoey
In this episode, we talk to Liana, mom to 20-month-old Zoey who has Feingold's syndrome, which can manifest with a variety of symptoms ranging from mild to severe. Liana shares with us how her life has changed, her struggles with her mental health, and she shares her best tips for surviving life as a special needs parent.
Learn more about Liana and Zoey, and follow their amazing story on Instagram -- @zoey_goldengirl.
Follow us on Instagram -- @snconfessions.
Visit us and give us a ‘like’ on our Facebook page https://www.facebook.com/SNCONFESSIONS/.
SPONSOR -- Our sponsor for this episode is Anchor, the easiest way to make a podcast. The Anchor app is free to download so you can start podcasting right from your phone. Visit anchor.fm, the app store, or Google play to try it out today.
SPONSOR -- We also work with Amanda Jessup from @illuminatedsketchbook. Amanda is an author, illustrator, and digital artist who makes beautiful custom sketches. Check out her artwork on Instagram!
You can now support our podcast by visiting https://anchor.fm/csnp and clicking the "Support" button to help keep the show going. Monthly donations start at just $0.99 per month.
If you liked this episode, please share it with your family and friends! You can also go to Anchor.fm and click the "Message" button to leave us a voice message. Let us know what you think of the podcast, leave a confession, or just say hi!
Thanks so much for listening! We'll be back again on December 30th with the rest of our interview with Liana.
Date: October 1, 2020
Episode title: Josh and Grayson
In this episode, we talk to Josh, the co-host of Confessions of a Special Needs Parent, and dad to 1.5-year-old Grayson who has microcephaly, intractable epilepsy, dysphagia, and global developmental delay. Josh talks about how his life has permanently changed since Grayson was born, and shares how his mental health, spirituality, and other areas of his life have been affected.
Learn more about Josh and follow his story on Instagram @mrrandomdad.
You can now support our podcast by visiting https://anchor.fm/csnp and clicking the "Support" link to help keep the show going. Monthly donations start at just $0.99 per month.
Visit us and give us a ‘like’ on our Facebook page https://www.facebook.com/SNCONFESSIONS/.
Follow us on Instagram @snconfessions.
Our sponsor is Anchor, the easiest way to make a podcast. Download the free Anchor app to your phone or visit anchor.fm to try it out.
If you liked this episode, please share it with your family and friends!
Thanks so much for listening!
The podcast currently has 7 episodes available.