In this special post-conference episode of Living with FASD, host Patti Kasper brings together two influential voices in the FASD community, Rebecca Tillou and Joel Sheagren, to unpack the recent happenings at the FASD United and Adult Leadership Collaboration of the FASD Changemakers conference in Seattle. As attendees, Rebecca and Joel offer their firsthand insights and experiences, discussing the power of connection, the importance of research, and the future of FASD advocacy.
Rebecca, an advocate and author who has lived with FASD, shares her involvement in a CDC documentary aimed at educating professionals about FASD and her participation in a unique track designed for individuals with FASD. She highlights the value of safe spaces where stories and successes can be shared openly.
Joel, a parent and documentary producer, reflects on the international scope of the conference and the energizing presence of ALC. He recounts his productive interviews with experts and researchers for a documentary project he is working on, offering a glimpse into the significant connections between FASD and various societal issues, including the criminal justice system and human trafficking.
If, like host Patti Kasper, you missed the conference, FASD United will be posting recordings of many of the sessions, at FASDUnited.org.
This episode is a must-listen for anyone involved in or affected by FASD, providing inspiration, camaraderie, and a shared vision for a more informed and supportive society. Don't forget to subscribe, share, and consider supporting the podcast through patreon.com/LivingWithFASDPodcast, where you can join the community and contribute to the show's production costs. Your engagement helps us bring these critical conversations to a wider audience.
Patti is available for professional development training or as a coach for parents or individuals with FASD; you can reach her at contact@patriciakasper.com.
Tune in to Living with FASD for more episodes that delve into the lives and experiences of those affected by FASD, and join us in spreading knowledge and compassion for this often-misunderstood condition.
Until next time, keep learning, keep sharing, and keep believing in the incredible potential of those living with FASD.
Show notes created by headliner.app