Skip to Page Content (will bypass menus and search fields)
Seeing Through His Eyes: The Beauty of Medically Fragile Motherhood
Published May 10, 2020
For Maria, motherhood hasn’t always been easy. But it is always beautiful. Her older son, Darian, was born premature and lives with cerebral palsy. Maria had to go home from the hospital without Darian soon after he was born. She then watched for mo…
Rémi's Occupational Therapy Journey: With Us Every Step of the Way
Published April 17, 2020
By Alecia, Rémi's Mom Rémi was born a twin on January 23rd, 2017 weighing 5 pounds, 15 ounces. She was diagnosed in utero at 23 weeks with Hypoplastic Left Heart Syndrome (HLHS). She underwent her first open heart surgery at just ten days old, fo…
Javier's Occupational Therapy Journey: Building a Bridge to My Son
Published April 10, 2020
By Denny, Javier's Mom In April of 2017, our son, Javier, was diagnosed with Autism and required substantial support. Unsure and confused about what exactly this meant, I felt a big piece of my heart go numb. As parents, we try to study and learn ev…
Life with Trisomy 21: Catalena's Story
Published March 20, 2020
By Priscilla, Cat's Mom When people tell you that you don't know love until you're a parent, it's true. When Catalena first looked up at me with her little baby eyes, it was like time stopped. The world was still. I knew she was going to make my lif…
Life with Trisomy 18: Dawson's Story
Published March 13, 2020
Dawson is an amazing little boy! He brings such joy to our lives. He has the most perfect little smile. Although he is non-verbal, he communicates with his eyes and hands to make us feel so loved. Whether he is hanging out in his bed or his wheelch…
Life with Trisomy 21: Ally's Story
Published March 6, 2020
By Margaret, Ally's Mom As we approach World Down Syndrome Day on March 21st, we were asked to share a little about our daughter Alison (Ally). There is so much to write about, but I think our focus should be about how such a small little girl has m…
Jeremiah Takes His First Steps
Published Nov. 29, 2019
By Kim, Jeremiah's mom My son Jeremiah has grown not only physically but emotionally as well with physical therapy. When Jeremiah was born, we already knew he would have a harder time with simple things such as eating, talking, and walking. Even cra…
Increasing Saylor's Independence
Published July 5, 2019
Saylor is a 20-month-old little girl with a rare mitochondrial disease and Fanconi Syndrome. Because of these conditions, Saylor depends on a central line with TPN for nutrition and, until recently, she required frequent hospitalizations. During the…
Finding the Perfect Therapy Team for My Son
Published June 28, 2019
By Maira, Erik’s mom Although my son, Erik, has always been a sweet boy, when he turned three his behavior began to change. I noticed a delay in his speech when he turned three years old, which was a bit odd to us since my older daughter had been ve…
The Beauty of a Father's Love
Published June 16, 2019
When Doug and Tina’s fourth son, Anthony, was born with muscular dystrophy, they faced new challenges as parents. “We didn’t know what to do,” Tina recalls. “We didn’t know what kind of life he could have. We had no idea how to parent a child who de…