If We Knew Then - Down Syndrome Podcast
A podcast by Stephen and Lori Saux
184 Episoade
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163. Revisiting Patience In The New Year with Maezen Miller
Publicat: 15.01.2024 -
162. Living In The Moment and Taking the Time to Reflect On Life
Publicat: 23.10.2023 -
161. Down Syndrome Awareness Month 2023: Bringing Awareness to Our Community’s Potential
Publicat: 16.10.2023 -
160. The Inclusive Hub: A Gym For People of All Abilities with Liam Starkey
Publicat: 09.10.2023 -
159. DSALA and DSC2U: Supporting Our Spanish-Speaking Community
Publicat: 02.10.2023 -
158. Best Buddies with Katelyn Quintero
Publicat: 25.09.2023 -
157. Ruby’s Rainbow with Liz Plachta
Publicat: 18.09.2023 -
156. GiGi’s Playhouse with Nancy Gianni
Publicat: 11.09.2023 -
155. Using Your IEP to Make the Most of Middle School
Publicat: 04.09.2023 -
154. Revisiting Our Interview with Megyn Price
Publicat: 28.08.2023 -
153. Revisiting Jad Issa’s Story: A Man with Down Syndrome Raises a Family - An Interview with Sader Issa
Publicat: 21.08.2023 -
152. Revisiting The Canadian Down Syndrome Society’s Project Understood - Training Speech Recognition Technology
Publicat: 14.08.2023 -
151. The New York City Buddy Walk and Times Square Video with Abby Brandon-Livits and Misty Adams
Publicat: 07.08.2023 -
150. Down Syndrome Research, Ableism and The Right To Just Be with Dr. Eric Rubenstein
Publicat: 31.07.2023 -
149. Down Syndrome and Alzheimer’s Research with Dr. Tom Mahan
Publicat: 24.07.2023 -
148. RODS Heroes - Our Interview with Brady Murray
Publicat: 17.07.2023 -
147. T21 Coffee - Giving Back to the Down Syndrome Community - Johan Lindborg
Publicat: 10.07.2023 -
146. Down Syndrome Diagnosis Network (DSDN) with Ben Hughes
Publicat: 02.07.2023 -
145. A Grassroots Movement to Change the Narrative: A Conversation with Ted Green
Publicat: 27.06.2023 -
144. Non-Speaking Is Not Non-Communicating - Vaish and Sid Sarathy
Publicat: 20.06.2023
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.