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Daniel | Trees

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Manage episode 331779336 series 2836113
Content provided by Susan Geoghegan. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Susan Geoghegan 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://player.fm/legal.

Happy Fathers Day to all the dads out there! This week, instead of having a mom share her story, we invited a dad to the show! Daniel introduces us to his family, he talks about what it feels like to be a rare disease father as he faces the ‘it’s not fair’ moments as well as the waves of grief. Daniel is one of the founders of the Rare Disease Film Festival and the Disorder Channel where they showcase rare stories.

Topics discussed that you do not want to miss:

  • What we felt when we heard our children could be nonverbal
  • Timing throughout the journey
  • “This isn’t fair” vs “why me” mindset
  • Career change for rare
  • Waves of grief

Links and resources:

Make sure you hit SUBSCRIBE so you don’t miss out on our upcoming stories from other members of our medical and disabled community.

And, if you enjoyed this episode, please leave us a 5 star rating and a review! Thank You!

  continue reading

150 episodes

Artwork
iconShare
 
Manage episode 331779336 series 2836113
Content provided by Susan Geoghegan. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Susan Geoghegan 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://player.fm/legal.

Happy Fathers Day to all the dads out there! This week, instead of having a mom share her story, we invited a dad to the show! Daniel introduces us to his family, he talks about what it feels like to be a rare disease father as he faces the ‘it’s not fair’ moments as well as the waves of grief. Daniel is one of the founders of the Rare Disease Film Festival and the Disorder Channel where they showcase rare stories.

Topics discussed that you do not want to miss:

  • What we felt when we heard our children could be nonverbal
  • Timing throughout the journey
  • “This isn’t fair” vs “why me” mindset
  • Career change for rare
  • Waves of grief

Links and resources:

Make sure you hit SUBSCRIBE so you don’t miss out on our upcoming stories from other members of our medical and disabled community.

And, if you enjoyed this episode, please leave us a 5 star rating and a review! Thank You!

  continue reading

150 episodes

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