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SFN Dad To Dad 341 - Nate Plasman of Lombard, IL Father of Three Including A Son With Duchenne Muscular Dystrophy

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Manage episode 440902350 series 2275115
Content provided by David Hirsch. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by David Hirsch or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ppacc.player.fm/legal.
Our guest this week is Nate Plasman of Lombard, IL, a vice president at family owned Monroe Transportation and father of three, including a son with a rare genetic disease.
Nate and his wife, Sara, have been married for 20 years and are the proud parents of three children: Grace (15), Jackson (12) and Andrew (10) who has Duchenne Muscular Dystrophy, a progressive and severe muscle-wasting condition that typically results in premature death.
Duchenne impacts around 15,000 individuals in the United States, predominantly males, and over 300,000 globally. It is a condition that transcends cultural, economic, and social lines, affecting families worldwide.
We learn about a host of organizations seeking cures and improving the lives of those living with muscular dystrophy, including; Parent Project MD, Cure Duchenne and Serepta Therapeutics.
It'a an uplifting story about faith, family and overcoming adversity all on this episode of the SFN Dad to Dad Podcast.
Show Notes
Phone – (630) 248-3220
Email - [email protected]
LinkedIn - https://www.linkedin.com/in/nathan-plasman-0a050149/
Facebook - https://www.facebook.com/nathan.plasman/friends
Monroe Transportation – https://monroe-trans.com/
Parent Project MD - https://www.parentprojectmd.org/
Cure Duchenne - https://cureduchenne.org/
Serepta Therapeutics - https://www.sarepta.com/
Special Fathers Network -
SFN is a dad to dad mentoring program for fathers raising children with special needs. Many of the 800+ 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.
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/videos
Please support the SFN. Click here to donate: https://21stcenturydads.org/donate/
Special Fathers Network: https://21stcenturydads.org/
  continue reading

376 episodes

Artwork
iconShare
 
Manage episode 440902350 series 2275115
Content provided by David Hirsch. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by David Hirsch or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ppacc.player.fm/legal.
Our guest this week is Nate Plasman of Lombard, IL, a vice president at family owned Monroe Transportation and father of three, including a son with a rare genetic disease.
Nate and his wife, Sara, have been married for 20 years and are the proud parents of three children: Grace (15), Jackson (12) and Andrew (10) who has Duchenne Muscular Dystrophy, a progressive and severe muscle-wasting condition that typically results in premature death.
Duchenne impacts around 15,000 individuals in the United States, predominantly males, and over 300,000 globally. It is a condition that transcends cultural, economic, and social lines, affecting families worldwide.
We learn about a host of organizations seeking cures and improving the lives of those living with muscular dystrophy, including; Parent Project MD, Cure Duchenne and Serepta Therapeutics.
It'a an uplifting story about faith, family and overcoming adversity all on this episode of the SFN Dad to Dad Podcast.
Show Notes
Phone – (630) 248-3220
Email - [email protected]
LinkedIn - https://www.linkedin.com/in/nathan-plasman-0a050149/
Facebook - https://www.facebook.com/nathan.plasman/friends
Monroe Transportation – https://monroe-trans.com/
Parent Project MD - https://www.parentprojectmd.org/
Cure Duchenne - https://cureduchenne.org/
Serepta Therapeutics - https://www.sarepta.com/
Special Fathers Network -
SFN is a dad to dad mentoring program for fathers raising children with special needs. Many of the 800+ 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.
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/videos
Please support the SFN. Click here to donate: https://21stcenturydads.org/donate/
Special Fathers Network: https://21stcenturydads.org/
  continue reading

376 episodes

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