No Child is Hopeless

Our goal is for every hurt child to have a fighting chance to be well.

Since 1955, we’ve been pioneering better ways to grow the brain to use the vast capacity that is presently unused.

We Treat the Problem

Treating the symptoms of injury to the brain without addressing the brain itself will fail. Surgery and medication are often used to try to eliminate a distressing symptom. Medical treatment of the brain-injured child must be aimed at brain maturation, in order to be safe and eﬀective. The answer is not to be found in the medicine cabinet—but in stimulation and opportunity. This is a more conservative treatment, a safer treatment, a cost-eﬀective treatment, and most important of all a treatment that works.

"We don’t agree with everyone about brain-injured children. Our disagreement begins with diagnosis, extends to classiﬁcation, identiﬁcation, treatment, technique, methods, philosophy, and ends up with objective. We are positive the goal should be to make brain-injured children well, and we sometimes do. The world believes that to be impossible and therefore never does."

- Glenn Doman, Founder of The Institutes for the Achievement of Human Potential

When A Good Brain Gets Hurt

There are probably 100 ways for a good brain to get hurt and, by now, we have probably seen all those ways. It does not matter whether that path began shortly after conception, six months before delivery or after birth, in the end, the child is left with the injury and its consequences.

The good news is that the brain has tremendous plasticity. It can recover, it can get better – it is only hurt. Brain-injured children are hurt: not damaged, not diseased, they are hurt. That is why we often used the term “hurt kids”. It is a softer, more accurate and, we hope, more civilized way to introduce the brain-injured child who has been tragically called by so many names that are libels more than labels.

Is Your Child Brain-Injured?

There are more than 300 symptomatic labels used to describe children who have problems in the central nervous system. These labels rarely include the brain. This is tragic for parents who waste precious time treating the symptoms and limited resources chasing after a proper diagnosis.

The children with these frightening labels are brain-injured children. Their problems originate in the brain, not the periphery. All treatment to be eﬀective must begin with a real diagnosis. If your child has one of these symptomatic labels your child is brain-injured.

Our Treatment Programs

All of the treatment of our children is done at home with mother and father. The program covers all aspects of the child’s physical, physiological and intellectual development. Parents are taught how the brain develops and how injury to the brain disrupts that development.

Parents attend our courses, read our books and bring their children to The Institutes for evaluation and a program. Between visits parents have the support of the staﬀ when they have a question or a problem.

On Campus and Online

What To Do About Your Brain-Injured Child

After taking this world-renowned course, you’ll understand your hurt child like never before, and leave with a real plan for the future.

Upcoming Courses

For Parents of Hurt Children

What To Do About Your Brain-Injured Child

A life-changing course. Parents learn what to do, how to do it and why it works. Presented in English & Spanish

Get to Know Our Kids

Our parents have proven, beyond a shadow of a doubt, that hurt children have tremendous potential. Meet the brain-injured kids getting better every day:

Jay – Age 64

Cerebral Palsy

Jay – Age 64

Cerebral Palsy

I was born with a congenital speech impairment. A pediatrician and neurologist concluded that I was a brain- injured child. Today, I’m 64 years old, married, and living a good life with my condition.

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Caleb- Age

Cerebral Palsy

Caleb- Age

Cerebral Palsy

When Caleb’s parents were told that their son had Cerebral Palsy, doctors told them that his prognosis was bleak. His parents refused to accept that Caleb could not improve and made plans to attend the What To Do About Your Brain- Injured Child course.

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Elisa – Age 8

Developmental Delay

Elisa – Age 8

Developmental Delay

Doctors agreed with the parents’ observations that Elisa was experiencing learning difficulties. Her parents began to look for ways to help Elisa catch up with her peers. The Institutes helped her do just that...and more.

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Alice – Age 4

Down Syndrome, Trisomy 21

Alice – Age 4

Down Syndrome, Trisomy 21

“We no longer worry about her future as we did. We still do not know what the future holds for Alice, but now we know it is a bright and happy future.”

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Floyd – Age 6

Trisomy 21

Floyd – Age 6

Trisomy 21

At about 4 months, Floyd started showing symptoms of Trisomy 21. His parents worried he would not recover. That is when they discovered The Institutes and began implementing a treatment program at home when Floyd was 6 months old. The rest is history.

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Sara

Down Syndrome, Immobility, Trisomy 21

Sara

Down Syndrome, Immobility, Trisomy 21

On the day of Sara’s birth, her parents were told that she had Trisomy 21. This began the family on a search to find answers for Sara, leading them to The Institutes. Today, Sara goes to school, and is above age level in academics, athletics, and in social situations, too.

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