If We Knew Then - Down Syndrome Podcast

Un pódcast de Stephen and Lori Saux - Lunes

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177 Episodo

  1. 176. Revisiting 10,000 Maniacs Founding Member Steven Gustafson

    Publicado: 20/7/2024
  2. 175. Communicating Our Stories with Sid and Vaish Sarathy

    Publicado: 17/6/2024
  3. 174. Advocating For Speech Therapy - Julie Picot

    Publicado: 10/6/2024
  4. 173. The Endless Possibilities of People with Down Syndrome: Revisiting Jake Pratt

    Publicado: 27/5/2024
  5. 172. Happy Mothers Day: We Celebrate You

    Publicado: 12/5/2024
  6. 171. Alzheimer’s Disease In People with Down Syndrome - Dr. Elizabeth Head

    Publicado: 29/4/2024
  7. 170. Celebrating The Life of Carl Erskine with Ted Green

    Publicado: 21/4/2024
  8. 169. The Annual DSDN Retreats with Ben Hughes

    Publicado: 15/4/2024
  9. 168. Liam's 14th Birthday: Sharing Some Insight

    Publicado: 8/3/2024
  10. 167. A Discussion About Using The R-Word with Lynette Louise

    Publicado: 26/2/2024
  11. 166. Finding The Right Supports Without Shame - Julie Picot

    Publicado: 19/2/2024
  12. 165. Picking The Right Pediatrician with Dr. Ilona Kleiner

    Publicado: 29/1/2024
  13. 164. Charlotte and Riley: Not Taking No For An Answer

    Publicado: 22/1/2024
  14. 163. Revisiting Patience In The New Year with Maezen Miller

    Publicado: 15/1/2024
  15. 162. Living In The Moment and Taking the Time to Reflect On Life

    Publicado: 23/10/2023
  16. 161. Down Syndrome Awareness Month 2023: Bringing Awareness to Our Community’s Potential

    Publicado: 16/10/2023
  17. 160. The Inclusive Hub: A Gym For People of All Abilities with Liam Starkey

    Publicado: 9/10/2023
  18. 159. DSALA and DSC2U: Supporting Our Spanish-Speaking Community

    Publicado: 2/10/2023
  19. 158. Best Buddies with Katelyn Quintero

    Publicado: 25/9/2023
  20. 157. Ruby’s Rainbow with Liz Plachta

    Publicado: 18/9/2023

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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.

Visit the podcast's native language site