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:
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
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#126 Ask Me Anything about FASD with Jeff Noble ROUND 2
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#123 BONUS Episode: FASD Day Extravaganza
#122 Essential FASD Back To School T.I.P.S. with Danna Ormstrup
#121 Audrey McFarlane Breaking FASD News
#120 Marj Wingrove Talking to Kids with FASD about Death
#119 Miranda Eodanable Photovoice: young people’s experiences and views of FASD
#118 Mark Courtepatte- FASD & IEPs
#117 Rhonda & Shawn: How to love someone with FASD who’s hurt someone
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