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Ep 23: Caregiving the Caregivers with Sarah Giddings
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Το περιεχόμενο παρέχεται από το Williams Syndrome Association. Όλο το περιεχόμενο podcast, συμπεριλαμβανομένων των επεισοδίων, των γραφικών και των περιγραφών podcast, μεταφορτώνεται και παρέχεται απευθείας από τον Williams Syndrome Association ή τον συνεργάτη της πλατφόρμας podcast. Εάν πιστεύετε ότι κάποιος χρησιμοποιεί το έργο σας που προστατεύεται από πνευματικά δικαιώματα χωρίς την άδειά σας, μπορείτε να ακολουθήσετε τη διαδικασία που περιγράφεται εδώ https://el.player.fm/legal.
In this episode, Jen, Brendan, and Producer Joel delve into the crisis in this country surrounding parents and caregivers of individuals with developmental disabilities - specifically Williams syndrome.
After watching the documentary "UNSEEN: How We're Failing Parent Caregivers & Why It Matters" (which you can watch at www.caregiverdoc.com), they share their reactions for the first time in the recording.
Then, WSA Vice-President of Programs and Services, Sarah Giddings, joins to talk about how the WSA makes an intentional effort to provide education and resources to our community in an effort to alleviate the stress felt by parents and caregivers. She also shares her experiences as a parent to Matthew, her son with WS.
We hope that this episode helps spark conversations about how this country can do better for families and caregivers.
Also, please check out the 2023 WSA Holiday Gift Guide this giving season.
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