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SFN Dad To Dad 396 - Olivier Cortambert, London, Head Of Solutions Architecture at Yospace & Father Of A Son With A Rare Undiagnosed Disease

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Manage episode 507272990 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://podcastplayer.com/legal.
Our guest this week is Olivier Cortambert of London, UK who is head of solutions architecture at Yospace and father of a son with a rare undiagnosed disease.
Olivier and his wife, Feng, have been married for seven years and are the proud parents of Antoine (3) who has a genetically tested undiagnosed disease, which presents with; low muscle tone, hearing loss, non-verbal as well as difficulty swallowing and walking.
We learn about Small Steps, a UK based agency that provides free services to those who are unable to walk and the pros and cons of having an undiagnosed rare disease. We also learn about Olivier's involvement with the SFN Mastermind Group.
The Cortambert family story is one filled with hope and optimism all this episode of the SFN Dad to Dad Podcast.
Show Notes -
WhatsApp – +44 7801 120520
Email – [email protected]
LinkedIn – https://www.linkedin.com/in/cortambert/

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/

SFN Mastermind Group - https://21stcenturydads.org/sfn-mastermind-group/
  continue reading

396 episodes

Artwork
iconShare
 
Manage episode 507272990 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://podcastplayer.com/legal.
Our guest this week is Olivier Cortambert of London, UK who is head of solutions architecture at Yospace and father of a son with a rare undiagnosed disease.
Olivier and his wife, Feng, have been married for seven years and are the proud parents of Antoine (3) who has a genetically tested undiagnosed disease, which presents with; low muscle tone, hearing loss, non-verbal as well as difficulty swallowing and walking.
We learn about Small Steps, a UK based agency that provides free services to those who are unable to walk and the pros and cons of having an undiagnosed rare disease. We also learn about Olivier's involvement with the SFN Mastermind Group.
The Cortambert family story is one filled with hope and optimism all this episode of the SFN Dad to Dad Podcast.
Show Notes -
WhatsApp – +44 7801 120520
Email – [email protected]
LinkedIn – https://www.linkedin.com/in/cortambert/

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/

SFN Mastermind Group - https://21stcenturydads.org/sfn-mastermind-group/
  continue reading

396 episodes

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