Episode Six- Isaac Miller/Trisomy 18 Foundation
In this episode we hear from Victoria Miller, mother of Isaac and Executive Director of the Trisomy 18 Foundation. 

Also discussed:
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Category : General | Tags : medical children genetics parenting heal |
In this episode we hear from Victoria Miller, mother of Isaac and Executive Director of the Trisomy 18 Foundation. 

Also discussed:
In this episode we hear from Dana Tehako-Esser, founder of Noah’s Never Ending Rainbow. She talks about her nephew Noah, who had Trisomy 2. Dana also discusses how her organization helps families dealing with rare trisomy disorders.

Also in this episode:
Recommended books:
Changed by a Child by Barbara Gill
Married with Special Needs Children by Laura E. Marshak and Fran P. Prezant
A Very Special Baby Book by Rhonda DeBough-Insook
Waiting with Gabriel by Amy Kuebelbeck
Announcements:
New online support group for families dealing with a difficult pre-natal diagnosis
New Trisomy 13 Awareness Bracelet at livingwithtrisomy.org
Music by David Gielan
“Darkness (Leave the Light On)”