Nothing Is Impossible

July 17, 2018 apraxia of speech, cl/cp, Craniofacial, developmental delays, Family Stories, July 2018 Feature - Craniofacial, non-verbal, speech delay 3 Comments

We had been home with our Laura Cate for 12 months, when a family member made a statement that took my breath away: “Your adopted daughter just doesn’t have the same potential. She will never be able to do all the things your biological daughter can do.” /// We adopted Laura in October 2015, when …Read More

Say What? – Six Months Later

April 9, 2018 apraxia of speech, Brandie, early intervention, Education, hearing aids, hearing loss, sign language, speech delay, speech therapy, undiagnosed SN, velopharyngeal Insufficiency 1 Comments

Six months ago, I shared about our journey with Caston through his surprise diagnosis of hearing loss and severe speech delay. Six months! Half of a year. It seems like just yesterday that I sat down to write about our experience. Since then, I’ve seen so many parents with questions and concerns relating to speech …Read More

From “What If” to “What Is”

October 29, 2017 apraxia of speech, developmental delays, Developmental System, non-verbal, October 2017 Feature - Developmental, siblings, speech delay, speech therapy 4 Comments

The doors open, and all of the 3 year old preschoolers come running out… “Mama, I painted today!” “Mama, we ate cookies at snack!” “Mama, I played on the slide outside!” “Mama, I had so much fun today!” My little girl also comes running out. Her mega-watt smile is turned on high. She hugs my …Read More

1 in 1000: Adopting a Child with Childhood Apraxia of Speech

October 17, 2016 apraxia of speech, Central Nervous System, cerebral palsy, developmental delays, early intervention, Education, Family Stories, non-verbal, October 2016 Feature - Developmental, speech delay, speech therapy 0 Comments

Like so many of us who are part of the adoption community, we have learned so very much in the time our two youngest kiddos have been part of our family. Our son, Liam, who is now eight years old, joined our family at the age of 28 months. His special need was listed as …Read More

Our Non-Verbal World {hearing her "it" factor}

February 21, 2013 Angie, apraxia of speech, cl/cp, speech delay 8 Comments

Angie and her husband live in Pennsylvania with their 3 kids (2 bio boys and 1 daughter adopted in July 2011 from china – born with the cutest cleft lip you ever did see). They spend time working on crazy projects, taking far too many pictures and serving God to the best of their abilities. …Read More

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