We are honored to sit down with Megan Tanna, founder of Little Sparks Project and Amanda Sarkis, board member, about motherhood, resilience, and turning unimaginable challenges into purpose. Megan shares her journey as a mom of three boys and opens up about how the birth of her second son, Brooks, and his diagnosis with Apert Syndrome, a rare genetic condition, changed her family’s life forever.
We discuss the emotional and financial realities families face when navigating complex medical diagnoses, what inspired Megan and her husband to create Little Sparks Project, and how the nonprofit is now helping countless families access support during some of their hardest moments. We also dive into how parents can talk to their children about differences with compassion and curiosity, helping raise kinder, more inclusive kids. This conversation is raw, inspiring, educational, and a reminder that even the smallest spark can create meaningful change.
Please help us raise awareness for this amazing non-profit by sharing Megan and her families story with your friends and family, and consider donating to The Little Sparks - there's no donation too small to help make a huge difference for a family in need.
We'd also love for you to join us at Trillium in Canton on June 7th from 11-2 for a family friendly event to help raise awareness!
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