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#108 Part 2 of Candid Conversation with Jessica Birch

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Manage episode 329389590 series 2781077
Content provided by Jeff Noble. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Jeff Noble 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.

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In Part 1 of my conversation with Jessica Birch, an FASD advocate and adult on the Spectrum, we covered her advocacy and journey to get a diagnosis. In Part 2 we talk about life after the diagnosis. She gives us insight on how she copes with her symptoms and what you can do as a caregiver to help your loved ones.

In Part 2 we cover:

  • interdependence, impulsivity, emotional regulation, expectations
  • struggles to be taken seriously as an advocate and be accommodated
  • importance of a diagnosis and consequences of not getting one

I want to thank Jessica for her honesty and openness in sharing her story. I hope that by listening to this episode, your learning curve will be lessened, you can build deeper relationships with your kids and see a hopeful future. But more importantly, understand that FASD doesn’t define a person.

With individuals like Jessica speaking up, and those who support and advocate alongside us, we are raising the voices and awareness. Change is coming.

Show Notes:

Check out our blog for all the links at FASD Success

Support the Show.

  continue reading

157 episodes

Artwork
iconShare
 
Manage episode 329389590 series 2781077
Content provided by Jeff Noble. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Jeff Noble 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.

Send us a Text Message.

In Part 1 of my conversation with Jessica Birch, an FASD advocate and adult on the Spectrum, we covered her advocacy and journey to get a diagnosis. In Part 2 we talk about life after the diagnosis. She gives us insight on how she copes with her symptoms and what you can do as a caregiver to help your loved ones.

In Part 2 we cover:

  • interdependence, impulsivity, emotional regulation, expectations
  • struggles to be taken seriously as an advocate and be accommodated
  • importance of a diagnosis and consequences of not getting one

I want to thank Jessica for her honesty and openness in sharing her story. I hope that by listening to this episode, your learning curve will be lessened, you can build deeper relationships with your kids and see a hopeful future. But more importantly, understand that FASD doesn’t define a person.

With individuals like Jessica speaking up, and those who support and advocate alongside us, we are raising the voices and awareness. Change is coming.

Show Notes:

Check out our blog for all the links at FASD Success

Support the Show.

  continue reading

157 episodes

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