If We Knew Then - Down Syndrome Podcast
En podkast av Stephen and Lori Saux
184 Episoder
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163. Revisiting Patience In The New Year with Maezen Miller
Publisert: 15.1.2024 -
162. Living In The Moment and Taking the Time to Reflect On Life
Publisert: 23.10.2023 -
161. Down Syndrome Awareness Month 2023: Bringing Awareness to Our Community’s Potential
Publisert: 16.10.2023 -
160. The Inclusive Hub: A Gym For People of All Abilities with Liam Starkey
Publisert: 9.10.2023 -
159. DSALA and DSC2U: Supporting Our Spanish-Speaking Community
Publisert: 2.10.2023 -
158. Best Buddies with Katelyn Quintero
Publisert: 25.9.2023 -
157. Ruby’s Rainbow with Liz Plachta
Publisert: 18.9.2023 -
156. GiGi’s Playhouse with Nancy Gianni
Publisert: 11.9.2023 -
155. Using Your IEP to Make the Most of Middle School
Publisert: 4.9.2023 -
154. Revisiting Our Interview with Megyn Price
Publisert: 28.8.2023 -
153. Revisiting Jad Issa’s Story: A Man with Down Syndrome Raises a Family - An Interview with Sader Issa
Publisert: 21.8.2023 -
152. Revisiting The Canadian Down Syndrome Society’s Project Understood - Training Speech Recognition Technology
Publisert: 14.8.2023 -
151. The New York City Buddy Walk and Times Square Video with Abby Brandon-Livits and Misty Adams
Publisert: 7.8.2023 -
150. Down Syndrome Research, Ableism and The Right To Just Be with Dr. Eric Rubenstein
Publisert: 31.7.2023 -
149. Down Syndrome and Alzheimer’s Research with Dr. Tom Mahan
Publisert: 24.7.2023 -
148. RODS Heroes - Our Interview with Brady Murray
Publisert: 17.7.2023 -
147. T21 Coffee - Giving Back to the Down Syndrome Community - Johan Lindborg
Publisert: 10.7.2023 -
146. Down Syndrome Diagnosis Network (DSDN) with Ben Hughes
Publisert: 2.7.2023 -
145. A Grassroots Movement to Change the Narrative: A Conversation with Ted Green
Publisert: 27.6.2023 -
144. Non-Speaking Is Not Non-Communicating - Vaish and Sid Sarathy
Publisert: 20.6.2023
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.
