Making the Grade: Special Education and Adoption

September 30, 2016 agenesis of the corpus callosum, autism, brain damage syndrome, cerebral palsy, cognitive delay, developmental delays, early intervention, Education, hypothyroidism, IEP, institutional autism, non-verbal, public school, September 2016 Feature - Back to School 1 Comments

It’s September which means school is back in session. And this month at No Hands But Ours, it’s all about Education. From IEPs to OT, from homeschooling to Early Intervention, we’re covering the gamut of educational topics and how they relate to the unique needs of the children who have joined our families through adoption. …Read More

Adoption Infertility: When Not Now Feels Like Not Ever

June 17, 2016 adopting again, adopting later in life, adopting two at once, brain damage syndrome, Family Stories 0 Comments

“Come, sit amidst the ash heap; pick up your potsherd and pray.” That was a phrase borne in my heart from a season of personal lament… a time during which my own sorrowful meditations were keenly focused on the circumstances of the biblical saint of old, Job. How he must have pondered there in that …Read More

A Seed of Hope

April 6, 2016 ADD, April 2016 Feature - CNS, brain damage syndrome, Central Nervous System, cerebral palsy, cleft palate, Craniofacial, developmental delays, Developmental System, Family Stories, hemiplegia 1 Comments

Our adoption journey started in the summer of 2003. We attended an adoption fair. A family speaking that afternoon had brought their daughter with them to the meeting. The little girl, about seven years old, snuggled up to my husband with a large photo album and began to tell him her story. A story, and …Read More

Sorrow Turned to Joy

March 4, 2016 brain damage syndrome, cognitive delay, developmental delays, Developmental System, Family Stories, microcephaly, small head circumference 0 Comments

I hesitate to write about my daughter’s adoption story for fear I might scare others away. However, her story is one of sorrow that has turned into joy. I want to share her joy. My daughter has a brain injury and microcephaly. She also loves to eat jelly beans, tease her siblings, and prefers to …Read More

Worth It

January 13, 2016 brain damage syndrome, Developmental System, estropia, Family Stories, hypoxic ischemic encephalopathy, low muscle tone, oral-motor delays, speech delay 2 Comments

The words in Miao’s file were daunting. “Soften lesion of posterior horn” and “softening of bilateral ventricle” and “HIE”. I wasn’t sure how to pronounce them, let alone what they meant. And my trusty sidekick, Google, was having trouble explaining them as well. I had come across a picture and short description of Miao on …Read More

Adopting a Child with a Brain Damage Diagnosis: “Prepare to be Amazed”

December 15, 2015 brain damage syndrome, Developmental System, Family Stories, October 2015 Feature - Developmental, speech delay 2 Comments

On January 31, 2014, we were heading out to dinner when I noticed a missed call on my cell phone. It was a Colorado area code. The agency. I asked my husband to give me a minute as I listened to the message. This was it! The call came only eight days after our application …Read More

special need highlight: adopting a child with brain scan issues

March 16, 2014 brain damage syndrome, Central Nervous System, enlarged ventricle, Family Stories 5 Comments

We adopted our son, Jackzhen, in 2012. We met parents on that journey that were already talking about their next adoption, while still in China. I couldn’t fathom returning so soon. Jackzhen was our 4th child and all the adjustments that we were about to endure was all I could handle at that point, especially …Read More

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