Down Syndrome

Who We Help · Down Syndrome

down syndrome: what’s actually possible for your child

Most parents are told what their child with Down syndrome won’t do. For more than 47 years, NACD families have been writing a different story with dramatically different and better outcomes. Outcomes that are the reflection of very different opportunities. Individuals with Down syndrome have the potential to read and do math like their “typical” peers, to be independent, to work at real jobs, to contribute, live on their own, drive, have relationships, and lead long and happy lives. To do well, if really given the opportunity.

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Child learning through an individualized NACD home program
For Parents

A label need not be a prognosis

If you are here, you have probably heard the standard story: manage your expectations, plan for limits, try not to compare. Be grateful your child can get a session or two of therapy a week and receive special education. The people who deliver that story and provide those “opportunities” mean well, but it describes the failure of the system, not the potential of your child. Perceived limitations have defined “appropriate” opportunities. All of our children grow and develop as a reflection of the opportunities we provide for them. The historic failure of the system has not only limited opportunities; year after year it has confirmed the low expectations of those providing the services and perpetuated the broken system. This need not be the picture of your child’s future. It does not describe your child, and it does not describe what is possible.

Since 1979, NACD has worked with more than 50,000 families with every kind of child, and children with Down syndrome have been central to that work from the beginning. We design individualized, home-based programs built for each whole, unique, specific child. This page explains what we do differently, and why targeted input provided by the right people, your family and caregivers, can refine opportunities and outcomes. Read about the NACD approach

Understanding The Diagnosis

What is Down syndrome?

Down syndrome is a genetic condition in which a child is born with a full or partial extra copy of chromosome 21. There are three subtypes of Down syndrome: Mosaic, which comprises about 1 to 2 percent of the group; Translocation, about 3 to 4 percent; and Trisomy 21, the most common form, comprising about 95 percent of cases. Regardless of the subtype, every child is unique, as are their needs and those of their family.

Our chromosomes affect our bodies through our DNA, as they do with Down syndrome. Our DNA determines physical traits such as eye and hair color, height, and sex, and has some effect on how we grow and develop. How everyone grows, develops, learns, and functions is, however, primarily determined by what happens in our lives: our opportunities. Development responds to input, and the amount and quality of input a child receives every day is something a family needs to control.

Understanding Your Child

The individual’s unique profile is a starting point

Common real strengths we build on

  • Strong visual learning and visual memory
  • Social warmth and connection with people
  • Determination and persistence when engaged
  • Responsiveness to routine and daily input

Common challenges we target

  • Auditory processing, working memory, and cognition
  • Speech clarity and expressive language
  • Muscle tone and motor development
  • Health and nutrition factors that affect learning
  • Targeted educational input and opportunities
What NACD Does

A program built for your child, not a category

There is no Down syndrome program in a box, because the profiles and needs are unique to every individual. Every aspect of a specific child’s development and function is unique. Effective targeted input demands an understanding and appreciation of the individual’s strengths, inefficiencies, specific level of function, and needs: the whole child. Being a member of a category, a label, or a class does not define nor determine an individual child’s or adult’s needs.

1

Individualized programming

There is no Down syndrome program in a box. Your child is evaluated across every aspect of how they function, from self-help skills, behavior, speech and language, and fine and gross motor abilities to all aspects of cognitive function and education. Their program is assembled from a toolbox of over 1,000 techniques to fit the child in front of us: your child, within the context of your family.

2

Daily frequency, parent-delivered

An hour a week cannot change how a developing brain processes the world. Short, targeted activities done daily at home can. We train and coach you to deliver them. Our programs are dynamic, and with ongoing communication and support from our staff, your program is tweaked and modified on an ongoing basis to keep it as targeted as possible.

3

The whole child

Development, education, behavior, health, and nutrition are all part of one unique person. Your program addresses all of these together and more, and undergoes a comprehensive assessment and update three times a year.

Inside The Program

What your child’s program can address

Every program is assembled from a toolbox of over 1,000 techniques. These are the areas most Down syndrome programs draw from, in whatever mix your child actually needs.

Auditory processing & working memory

The foundation under language, learning, and following directions. Usually the highest-leverage target.

Expressive language & clarity of speech

Daily targeted input for receptive and expressive language, oral motor function, articulation, and communication.

Reading & academics

We teach to strength and remediate weakness. Building on strengths, we develop reading, math, and other academic functions without perceived limitations and with high expectations.

Gross & fine motor development

Addressing fine and gross motor function, coordination, strength, and fitness.

Health & nutrition

The physiological factors that affect energy, attention, and learning, coordinated with your medical team.

Attention, behavior & independence

Practical daily structure, chores, responsibilities, initiative, self-regulation, and other executive functions are all part of producing success and real-world independence.

Bob Doman Discusses Down Syndrome Issues
(Free Seminar)

How To Get Started

Three steps, starting free

1 · Free application and interview 2 · Evaluation and your child’s program 3 · Coaching and follow-ups, three times a year
Start Your Free Get Started Program

Testimonials From NACD Clients

Martin Family Testimonial

Jake was a beautiful baby, unusually so, who had a rough birth, low initial apgars and trouble breastfeeding. He was ...

Kelly Family Testimonial

The Kelly Family sent us this amazing video for their testimonial! Watch it below: ...

Acevedo Family Testimonial

We began our journey at NACD after finding a school system unable to help our daughter with Down syndrome to ...

Thorup Family Testimonial

Nine years ago, I gave birth to a precious baby girl. Her Daddy, two year old sister Claire, and I ...

Goad Family Testimonial

I knew when my husband and I adopted Jonathan as a newborn with Down’s Syndrome that he would face challenges ...

Gardner Family Testimonial

Jacob was born at home with a birth diagnosis of down syndrome. From the moment the NICU doctor mentioned the ...

Simmons Family Testimonial

Our family first heard about NACD in August 2023. We immediately decided that this is the program we have been ...
David

David’s Story, A Family’s Journey

Below is a message from Dawn Zachmann, a superstar mother of a young man with Down syndrome and autism. Dawn ...

Breaking Down Stereotypes: Gabriel is a Winner!

It has been a few years since I have seen Gabriel although he has been a part of NACD since ...

Jennie

Jennie – 33 years old 9-28-2017 Six years ago my daughter Jennie and I moved to St. George, Utah from ...
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Questions

Common questions from parents

Many NACD children with Down syndrome can not only learn to read and do math, but can learn to do it sooner and better than their “typical” peers. NACD has been successfully developing unique, individualized educational programs for children from preschool into college. NACD’s huge toolbox permits very targeted, individualized, successful educations.
The brain changes at every age, so it is never too late to start. NACD works with infants through adults with Down syndrome. Starting earlier gives you more time, but starting now beats waiting, whatever your child’s age.
No. NACD works with families across the world. Evaluations happen at evaluation sites and remotely, and your coaching and program support are available wherever you live.
Two things: individualization and frequency. Your child gets one integrated program built specifically for them instead of disconnected pieces, and it runs daily at home instead of an hour here and there. NACD also helps you coordinate everything your family is doing into one coherent plan designed to fit your child and your family.
Speech clarity is one of the most common goals in Down syndrome programs, and one where daily targeted input matters most. Your program addresses the pieces that produce good speech, from oral motor function to auditory processing, with activities that are integral to your child’s needs. Needs are individual, which is why the program is.
Yes. Although home education through NACD is often optimal, many NACD children attend school while running their program at home before, after, and at times within school. NACD also helps families coordinate everything their child is receiving into one coherent plan, and many families use their evaluations and NACD programs to develop their school’s plan.
Your NACD Developmentalist works directly with your child and with you, looking at processing, language, motor development, learning, behavior, and health factors. You leave with a full evaluation, and within days you receive your comprehensive program of daily activities with clear instructions, and a coach who supports you from day one.
Every child is different, and we do not make promises. What we can say is that our expectations are high. Our families do not need us to tell them of change; it’s obvious, and they tell us. Progress is reported to us and measured concretely at follow-up evaluations three times a year, so you always know what is moving and what the program targets next.