The Sky is the Limit

July 26, 2019 BAHA, Craniofacial, Family Stories, hearing loss, July 2019 Feature - Craniofacial, microtia, older child adoption, Sensory System 0 Comments

Ever since I was a young girl, I knew that I wanted to someday get married and to be a mom. I dreamed of having children born from my womb and children born from my heart. After college, I met the man of my dreams and we married in March 2006. A year and half …Read More

Our Leap of Faith: Adopting Our Son With Bilateral Microtia and Atresia

December 1, 2017 adopting a boy, ASL, BAHA, December 2017 Feature - Sensory, early intervention, Family Stories, hearing aids, hearing loss, microtia, Ponto, Sensory System, sign language, speech therapy 0 Comments

About five years ago, my husband and I began considering international adoption. We had two biological daughters, yet we both started feeling like our family wasn’t complete. During that time we researched many countries and decided China’s program would be the best fit for our family. However, the process was daunting and there was still …Read More

Seeing Things Differently

September 9, 2017 BAHA, Craniofacial, Family Stories, hearing loss, limb difference, microtia, Orthopedic, Sensory System, September 2017 Feature - Visible Special Needs, visible special need 0 Comments

Recently someone reached out to ask what I would tell a group of Boy Scouts if I could speak to them as a special needs mom. This friend, who works everyday as a speech therapist, had been invited to speak to a local Boy Scout troop about interacting with children with special needs. Upon reading …Read More

Please Don’t Poke the Bear

July 23, 2017 adopting as first time parents, BAHA, Craniofacial, declining a referral, Family Stories, hearing loss, hemifacial microsomia, July 2017 Feature - Craniofacial, medical needs checklist, microtia, referral, speech therapy, waiting for referral 1 Comments

I call my daughter baby bear. For my first Mother’s Day, my husband presented us with matching mama bear/baby bear bracelets. SJ saw them and exclaimed: “SJ. Mama. Same!” Though I’ve never considered myself a shrinking violet by any means, this process, this crazy-beautiful, seemingly impossible way of becoming parents, has seemed to draw out …Read More

Cool Hats and Shaggy Haircuts: Adopting a Child with Microtia

July 18, 2017 adopting a boy, BAHA, Craniofacial, Family Stories, hearing loss, July 2017 Feature - Craniofacial, medical needs checklist, microtia, Sensory System, visible special need 2 Comments

(Let me start by saying I are so far from an expert on the topic of microtia and atresia. Just know that I am a loving mother with a son who happens to have this special bonus feature, not an ENT doctor.) When my husband and I filled out a medical checklist in February of …Read More

When God Honors Our “Yes”: Our Sign Language Journey, Part Two

August 21, 2016 ASL, Attachment, August 2016 Feature - SIgn Language and Adoption, BAHA, cl/cp, cochlear implants, hearing loss, profound deafness, Sensory System, sign language 4 Comments

In Part one I described how the adoption of our daughter, Ava, born with cleft lip and palate and deafness, set us on a journey to become skilled in sign language. Our desire to support her ability to communicate with others led us on a roller-coaster of experiences and emotions, which culminated in our decision …Read More

A Little Piece of a Big Plan

July 16, 2016 adopting a boy, BAHA, Craniofacial, Family Stories, hearing aids, hearing loss, July 2016 Feature - Craniofacial, microtia, older child adoption, Ponto, Sensory System 0 Comments

“I just spoke to the director. He will call me when they’re about five minutes away.” It’s almost time. My heart is almost uncontainable. Everything. All of this. It’s about to happen. So many months, years, planning for this moment… Even though I shouldn’t be surprised, being a part of and seeing just a tiny …Read More

Undiagnosed Hearing Loss: Wisdom from the Journey

January 28, 2016 BAHA, Education, Family Stories, hearing aids, hearing loss, Nager Syndrome, speech therapy, undiagnosed SN 1 Comments

We always knew there were unknowns, as all adoptive parents do. But the moment we saw their faces we knew they were ours. This is important to always remember. Most of us who adopt realize that the medical records we receive are not always accurate or trustworthy. But sometimes, you just don’t know the right …Read More

Microtia. What?

July 23, 2015 BAHA, Craniofacial, Family Stories, hearing loss, hemifacial microsomia, July 2015 Feature - Craniofacial, microtia, Sensory System, speech therapy, velopharyngeal Insufficiency 6 Comments

“My ear hurts mommy.” “Which ear honey? Do both ears hurt?” “No, silly. This one doesn’t hurt. It’s not open. It’s teeny tiny.” Olivia was 3 and this was the first time that I knew of that she noticed that her right ear didn’t match the left. We had never made a big deal out …Read More

When the voiceless break into song (from Isaiah 35)

May 19, 2014 a father's perspective, BAHA, hearing loss, microtia, Mike, Sensory System 1 Comments

As a dad of six, I know that I am not objective in assessing my own kids. Often, I see them in too favorable of a light, and I find myself measuring our family room mantle to see if it will hold six Nobel Prizes, six Olympic medals, and six Academy Awards at the same …Read More

Dealing with the Undisclosed Need

May 27, 2011 BAHA, hearing loss, Sensory System, Wife of the Prez 0 Comments

Let me preface this post by saying that in all reality, hearing loss is NOT a total shock (or it shouldn’t be) when a child also was born with cleft lip and palate. In fact, I asked the audiologist we saw today and she confirmed to me that many of her patients have cleft lip …Read More

Our First Birthday Together!

January 14, 2010 BAHA, Education, hearing loss, homeschool, Laine, microtia, older child adoption, speech delay, speech therapy 4 Comments

Last year she celebrated with her beloved foster mama… but this year she celebrates with her forever mama and forever family! 😉 Thank you Jesus! We brought our 7 year old, Candie, home on Halloween of 2008. Her birthday is 8/23/00. Her special need is bi-lateral microtia/atresia. Candie is a happy little girl and for …Read More

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