On this Dad to Dad podcast host David Hirsch talks to Shane Lee, of Louisburg NC, a systems administrator. Shane and his wife, Jennifer, have been married for 14 years and are the proud parents of five children: Trey (8), Nathan (6), Asher (4), Kiera (2) and Jocelyn who was born in 2007 and died at age 4 ½ from complications related to SMA Type 1 or Spinal Muscular Atrophy.
We’ll hear the amazing story of the Lee family, their travails and triumphs over SMA on this SFN Dad to Dad Podcast.
Email - gixxer31@yahoo.com Cure SMA Foundation - www.curesma.org
Special Fathers Network - SFN is a dad to dad mentoring program for fathers raising children with special needs. Many of the 500+ SFN Mentor Fathers, who are raising kids with special needs, have said: "I wish there was something like this when we first received our child's diagnosis. I felt so isolated. There was no one within my family, at work, at church or within my friend group who understood or could relate to what I was going through."
SFN Mentor Fathers share their experiences with younger dads closer to the beginning of their journey raising a child with the same or similar special needs. The SFN Mentor Fathers do NOT offer legal or medical advice, that is what lawyers and doctors do. They simply share their experiences and how they have made the most of challenging situations.
Special Fathers Network: https://21stcenturydads.org/about-the-special-fathers-network/
Check out the 21CD YouTube Channel with dozens of videos on topics relevant to dads raising children with special needs - https://www.youtube.com/channel/UCzDFCvQimWNEb158ll6Q4cA Please support the SFN. Click here to donate: https://21stcenturydads.org/donate/
On this Dad to Dad podcast host David Hirsch talks to Shane Lee, of Louisburg NC, a systems administrator. Shane and his wife, Jennifer, have been married for 14 years and are the proud parents of five children: Trey (8), Nathan (6), Asher (4), Kiera (2) and Jocelyn who was born in 2007 and died at age 4 ½ from complications related to SMA Type 1 or Spinal Muscular Atrophy. We’ll hear the amazing story of the Lee family, their travails and triumphs over SMA on this SFN Dad to Dad Podcast. Email - gixxer31@yahoo.com Cure SMA Foundation - www.curesma.org Special Fathers Network - SFN is a dad to dad mentoring program for fathers raising children with special needs. Many of the 500+ SFN Mentor Fathers, who are raising kids with special needs, have said: "I wish there was something like this when we first received our child's diagnosis. I felt so isolated. There was no one within my family, at work, at church or within my friend group who understood or could relate to what I was going through." SFN Mentor Fathers share their experiences with younger dads closer to the beginning of their journey raising a child with the same or similar special needs. The SFN Mentor Fathers do NOT offer legal or medical advice, that is what lawyers and doctors do. They simply share their experiences and how they have made the most of challenging situations. Special Fathers Network: https://21stcenturydads.org/about-the-special-fathers-network/ Check out the 21CD YouTube Channel with dozens of videos on topics relevant to dads raising children with special needs - https://www.youtube.com/channel/UCzDFCvQimWNEb158ll6Q4cA Please support the SFN. Click here to donate: https://21stcenturydads.org/donate/
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