If We Knew Then - Down Syndrome Podcast
Un pódcast de Stephen and Lori Saux
184 Episodo
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183. The Adolescent Brain with Christina Aries
Publicado: 3/4/2025 -
182. World Down Syndrome Day - March 21, 2025
Publicado: 21/3/2025 -
181. Olivier and Hilda Bernier and Their IEP Experience
Publicado: 3/3/2025 -
180. Liam Turns 15: What Have We Learned In This Journey?
Publicado: 25/2/2025 -
179. Forget Me Not: Inclusion in the Classroom Documentary - Hilda & Olivier Bernier
Publicado: 10/2/2025 -
178. The 2025 DSDN Rockin' Dad Retreat with Ben Hughes
Publicado: 3/2/2025 -
177. Showing Up For The Challenges - Karen Maezen Miller
Publicado: 27/1/2025 -
176. Revisiting 10,000 Maniacs Founding Member Steven Gustafson
Publicado: 20/7/2024 -
175. Communicating Our Stories with Sid and Vaish Sarathy
Publicado: 17/6/2024 -
174. Advocating For Speech Therapy - Julie Picot
Publicado: 10/6/2024 -
173. The Endless Possibilities of People with Down Syndrome: Revisiting Jake Pratt
Publicado: 27/5/2024 -
172. Happy Mothers Day: We Celebrate You
Publicado: 12/5/2024 -
171. Alzheimer’s Disease In People with Down Syndrome - Dr. Elizabeth Head
Publicado: 29/4/2024 -
170. Celebrating The Life of Carl Erskine with Ted Green
Publicado: 21/4/2024 -
169. The Annual DSDN Retreats with Ben Hughes
Publicado: 15/4/2024 -
168. Liam's 14th Birthday: Sharing Some Insight
Publicado: 8/3/2024 -
167. A Discussion About Using The R-Word with Lynette Louise
Publicado: 26/2/2024 -
166. Finding The Right Supports Without Shame - Julie Picot
Publicado: 19/2/2024 -
165. Picking The Right Pediatrician with Dr. Ilona Kleiner
Publicado: 29/1/2024 -
164. Charlotte and Riley: Not Taking No For An Answer
Publicado: 22/1/2024
We are Stephen and Lori Saux and welcome to the If We Knew Then Podcast. We are parents of two children and one of them has Down Syndrome, Liam. When Liam was born we didn’t know very much about Down Syndrome and most of the information we did have didn’t seem very hopeful and positive. Well this podcast aims to share honest and useful conversations about supports, therapies, education and society as it pertains to Down Syndrome advocacy and parenting.