))
Ep 23: Caregiving the Caregivers with Sarah Giddings
Manage episode 386283460 series 3450428
Sisällön tarjoaa Williams Syndrome Association. Williams Syndrome Association tai sen podcast-alustan kumppani lataa ja toimittaa kaiken podcast-sisällön, mukaan lukien jaksot, grafiikat ja podcast-kuvaukset. Jos uskot jonkun käyttävän tekijänoikeudella suojattua teostasi ilman lupaasi, voit seurata tässä https://fi.player.fm/legal kuvattua prosessia.
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.
46 jaksoa
Jaa
