This week’s episode is sponsored by Freedom Concepts, creators of custom adaptive tricycles, Chill-Out Chairs, and early intervention equipment that help individuals of all ages and abilities experience mobility, comfort, and dignity. Heather shares the powerful stories of two families whose children’s lives changed dramatically after being matched with Freedom Concepts equipment. From new levels of independence to moments of pure joy, this episode is about what happens when kids finally get the tools they need to thrive.
This episode is sponsored by Freedom Concepts, a company designing innovative, customizable mobility and seating solutions that empower individuals of all abilities to live with dignity, independence, and joy.
Check out Freedom Concepts: https://freedomconcepts.com/
Find Heather and Jake’s Help from Heaven:
❤️ APOY Instagram: https://www.instagram.com/aplaceofyespodcast/
❤️ Heather’s Instagram: https://www.instagram.com/heathersstraughter/
❤️ Jake’s Help from Heaven: https://jakeshelpfromheaven.org/
❤️ Jake’s Help from Heaven IG: https://www.instagram.com/jakeshelp/
❤️ Facebook: https://www.facebook.com/jakeshelpfromheaven
❤️ Our YouTube Channel: https://www.youtube.com/@APlaceofYesPodcast
Listen on Apple Podcasts | Spotify | iHeartRadio
FIND HEATHER & JAKE’S HELP FROM HEAVEN ⬇️
❤️ Heather’s Instagram: https://www.instagram.com/heathersstraughter/
❤️ Jake’s Help from Heaven: https://jakeshelpfromheaven.org/
❤️ Jake’s Help from Heaven IG: https://www.instagram.com/jakeshelp/
❤️ Facebook: https://www.facebook.com/jakeshelpfromheaven
❤️ Our YouTube Channel: https://www.youtube.com/@APlaceofYesPodcast
Connect with us on social media:
• Heather’s Instagram
• Jake’s Help from Heaven
• Jake’s Help from Heaven IG
• Facebook
• Our YouTube Channel
Keep scrolling for the episode transcript.
Checkout our other episodes
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A Late Diagnosis: Losing My Mom to Rare Disease
“We kept asking doctors what was wrong. No one had answers. And then, just like that, I was 19 years old and saying goodbye to my mom.”
Losing a Son to Rare Disease: Parental Isolation & Grief
“When you’re a rare parent, it’s not just the disease—it’s the loneliness, the constant feeling that no one really gets it. And when your child is gone, that grief is even more complicated. Jack taught me so much. I want other parents to know they’re not alone.”