
Jack’s Story
Jack was one month old when we were handed the book. I can still see the cover etched in my mind, big and spiral bound, the one they give parents after discovering their child has hearing loss. The anxiety and fear were overwhelming. What now? How do you even read these charts? What is a BAHA? How accurate is this testing?
In addition to hearing loss, Jack was born with a rare and poorly understood chromosomal variant, EFTUD2, also known as mandibulofacial dysostosis with microcephaly (MFDM). Hearing loss is a shared trait among nearly all diagnosed individuals. There is not really a word big enough for how it felt in that moment. We had been thrown headfirst into a world we knew nothing about, and we needed to figure out how to navigate it.
Gretchen Krenn


Raiden’s Story
“Our son, Raiden, was diagnosed with Auditory Neuropathy Spectrum Disorder in his right ear shortly after birth. We are still understanding what this diagnosis means for Raiden, however, what we’ve learned so far is that there are certain pitches where he has moderate to severe hearing loss, and he is also slightly delayed in his speech and communication. While we continue testing and learning more about what Raiden can hear, he currently wears a hearing aid in his right ear to support his development.
We began with Listen & Talk in their Blended Classroom this past fall, and we have truly been impressed by the level of care, compassion, and dedication every member of the staff and faculty pours into the children each day.
Lace Yamamoto
