Скачать или смотреть Celebrating Matthew | Trisomy Awareness Month

In this episode of the No Foot Too Small Podcast, Kaleb and Haley Admire share their journey after receiving a Trisomy 13 diagnosis for their son, Matthew. They open up about the impossible choices they faced, the 33 precious hours they spent with Matthew, and how faith, family, and the NFTS community helped them find strength through grief.

From the unique challenges fathers face in loss to the critical need for bereavement suites in hospitals, this conversation sheds light on the importance of support, connection, and advocacy for families experiencing pregnancy and infant loss.

Kaleb and Haley’s story is one of love, resilience, and purpose—a reminder that even in grief, we can find joy.

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If this episode resonates with you, please like, share, and subscribe to help spread awareness. You are never alone. 💙👣

00:00 - Introduction & Advice for the Journey
00:19 - Meet Kaleb & Haley: Their Story
02:08 - A Life-Changing Ultrasound
04:21 - Processing the Diagnosis & Difficult Choices
08:28 - Finding Strength Through Faith & Community
11:12 - The Reality of a Trisomy 13 Diagnosis
12:35 - Preparing for Matthew’s Birth
16:33 - Cherishing 33 Hours with Matthew
22:17 - The Challenge of Saying Goodbye
30:28 - The Importance of Bereavement Support
40:21 - Matthew’s Lasting Legacy

𝘔𝘦𝘥𝘪𝘤𝘢𝘭 𝘋𝘪𝘴𝘤𝘭𝘢𝘪𝘮𝘦𝘳: 𝘕𝘰 𝘍𝘰𝘰𝘵 𝘛𝘰𝘰 𝘚𝘮𝘢𝘭𝘭 (𝘕𝘍𝘛𝘚) 𝘥𝘰𝘦𝘴 𝘯𝘰𝘵 𝘱𝘳𝘰𝘷𝘪𝘥𝘦 𝘮𝘦𝘥𝘪𝘤𝘢𝘭/𝘩𝘦𝘢𝘭𝘵𝘩 𝘢𝘥𝘷𝘪𝘤𝘦. 𝘈𝘯𝘺 𝘪𝘯𝘧𝘰𝘳𝘮𝘢𝘵𝘪𝘰𝘯 𝘱𝘳𝘰𝘷𝘪𝘥𝘦𝘥 𝘣𝘺 𝘕𝘍𝘛𝘚 𝘪𝘴 𝘧𝘰𝘳 𝘨𝘦𝘯𝘦𝘳𝘢𝘭 𝘪𝘯𝘧𝘰𝘳𝘮𝘢𝘵𝘪𝘰𝘯𝘢𝘭 𝘢𝘯𝘥 𝘦𝘥𝘶𝘤𝘢𝘵𝘪𝘰𝘯𝘢𝘭 𝘱𝘶𝘳𝘱𝘰𝘴𝘦𝘴 𝘰𝘯𝘭𝘺 𝘢𝘯𝘥 𝘴𝘩𝘰𝘶𝘭𝘥 𝘯𝘰𝘵 𝘣𝘦 𝘤𝘰𝘯𝘴𝘪𝘥𝘦𝘳𝘦𝘥 𝘢 𝘴𝘶𝘣𝘴𝘵𝘪𝘵𝘶𝘵𝘦 𝘧𝘰𝘳 𝘱𝘳𝘰𝘧𝘦𝘴𝘴𝘪𝘰𝘯𝘢𝘭 𝘮𝘦𝘥𝘪𝘤𝘢𝘭 𝘢𝘥𝘷𝘪𝘤𝘦. 𝘗𝘦𝘳𝘴𝘰𝘯𝘢𝘭 𝘶𝘴𝘦 𝘰𝘳 𝘳𝘦𝘭𝘪𝘢𝘯𝘤𝘦 𝘰𝘯 𝘪𝘯𝘧𝘰𝘳𝘮𝘢𝘵𝘪𝘰𝘯 𝘧𝘳𝘰𝘮 𝘕𝘍𝘛𝘚 𝘰𝘳 𝘪𝘵𝘴 𝘢𝘴𝘴𝘰𝘤𝘪𝘢𝘵𝘦𝘥 𝘢𝘤𝘵𝘪𝘷𝘪𝘵𝘪𝘦𝘴, 𝘪𝘯𝘤𝘭𝘶𝘥𝘪𝘯𝘨 𝘱𝘦𝘦𝘳 𝘪𝘯𝘵𝘦𝘳𝘢𝘤𝘵𝘪𝘰𝘯𝘴, 𝘪𝘴 𝘴𝘵𝘳𝘪𝘤𝘵𝘭𝘺 𝘢𝘵 𝘺𝘰𝘶𝘳 𝘰𝘸𝘯 𝘳𝘪𝘴𝘬. 𝘞𝘦 𝘴𝘵𝘳𝘰𝘯𝘨𝘭𝘺 𝘦𝘯𝘤𝘰𝘶𝘳𝘢𝘨𝘦 𝘺𝘰𝘶 𝘵𝘰 𝘤𝘰𝘯𝘴𝘶𝘭𝘵 𝘸𝘪𝘵𝘩 𝘩𝘦𝘢𝘭𝘵𝘩𝘤𝘢𝘳𝘦 𝘱𝘳𝘰𝘧𝘦𝘴𝘴𝘪𝘰𝘯𝘢𝘭𝘴 𝘳𝘦𝘨𝘢𝘳𝘥𝘪𝘯𝘨 𝘺𝘰𝘶𝘳 𝘪𝘯𝘥𝘪𝘷𝘪𝘥𝘶𝘢𝘭 𝘴𝘪𝘵𝘶𝘢𝘵𝘪𝘰𝘯 𝘢𝘯𝘥 𝘯𝘦𝘦𝘥𝘴.