Manifesto

The work begins with a different promise.

The New ABA is a statement of the standards we hold ourselves to, and an invitation to practice behavioral science in service of the child.

The Promise

We will listen for what silence may mean: overwhelm, shutdown, assent withdrawal, or recovery.

We will treat assent, refusal, hesitation, and distress as clinical data that shapes the plan.

We will measure progress by safety, access, communication, autonomy, connection, and quality of life.

We will use data to see more of what matters in the child's life.

We will use behavioral science carefully, humbly, practically, and ethically.

In service of safety, communication, autonomy, regulation, connection, dignity, and quality of life.

Why This Standard Matters

Behavioral science can help children build meaningful skills: communication, safety, daily routines, and access to school, healthcare, family life, and community. That is worth building on.

Autistic adults, families, and researchers have also documented harm when therapy prioritized compliance, normalization, or adult-defined goals over children's safety, communication, and quality of life, including suppression of self-regulation behaviors children needed, use of aversive procedures, and contexts where children could not refuse or signal distress.

The New ABA does not dismiss this record. It starts from the belief that behavioral science can help children and that the field can keep getting better.

Raising the standard means asking harder questions about goals, methods, assent, data, and what we are actually measuring when we call something progress.

The standard is not lower expectations. The standard is more honest questions about whose expectations we are serving and why.

What We Build Toward

The goal is not to make autistic children appear less autistic.

The goal is to help children become safer, more understood, more autonomous, more connected, and more able to participate in life as themselves.

That means building toward:

  • Safety — physical safety, emotional safety, and the safety of knowing that communication will be heard.
  • Communication — reliable ways to express needs, preferences, refusal, pain, confusion, and choice. Not as a reward. As a right.
  • Autonomy — the ability to make choices, refuse what is not working, and participate in decisions about one's own life and care.
  • Regulation — the capacity to recover, to feel supported, and to access learning and connection from a place of enough calm.
  • Connection — relationships with adults and peers built on trust, respect, and genuine responsiveness to the child.
  • Participation — access to school, play, healthcare, routines, and community life with more confidence and less distress.
  • Quality of life — a life that the child experiences as meaningful, safe, and increasingly their own.

Support should make life more accessible, not make the child less autistic.

What We Notice

Behavioral language can flatten experience.

A note might record that a child tried to get away from a task that felt difficult, overwhelming, or unwanted. A clinician might label that escape-maintained behavior. That may describe what happened on the surface. It does not tell us what the child experienced, whether the task was unclear, whether the room was overwhelming, whether the child lacked a reliable way to ask for help, whether an adult had missed earlier, quieter signals.

The New ABA keeps careful observation and adds a more complete question: what is the child telling us?

We notice:

  • What a child is communicating, even when there are no words.
  • How assent and assent withdrawal signal what is and is not working in real time.
  • What the environment is asking of the child, and whether that is fair given what the child can currently do.
  • Early signs of distress, before a situation has to escalate.
  • What changes for the child, not only what appears on the graph.

The better question is always: what support would make this behavior less necessary?

That question changes the work.

What We Measure

Data can be valuable. The New ABA does not reject data. It asks us to measure more of what matters.

A behavior decrease may reflect improved support, a better environment, a clearer expectation, a new way for the child to communicate. It may also reflect masking, fatigue, or a child who has learned that protest is not worth the cost.

Before we treat a decrease as success, we ask: what changed for the child?

Good data helps us see more of the child's life. It can include:

  • Communication — is the child more able to express needs, preferences, and refusal?
  • Distress and recovery — how often, how intense, how long, and how quickly does the child recover?
  • Autonomy — does the child have more choice, more agency, more ability to participate on their own terms?
  • Access — can the child participate more fully in school, routines, relationships, and community?
  • Trust — is the therapeutic relationship one of safety and responsiveness?
  • Quality of life — by the child's own indicators, is life better?

A graph can show an important pattern. It should not be the only story we use to define progress.

What We Ask of Practice

Many practitioners entered this field to help children. The New ABA holds that intention and asks us to raise the standard for how help is defined, measured, and delivered.

That means more than following a protocol. It means developing the clinical judgment to know when a protocol is working, when it needs to be adapted, and when it needs to be reconsidered entirely.

Protocols support practice. Judgment guides it.

We ask practitioners to:

  • Keep the child a full person, with experience, communication, preferences, distress, and agency, in every session and every note.
  • Treat behavior as information before treating it as a target.
  • Honor assent and assent withdrawal as clinical data, not disruptions.
  • Ask whether each goal has a clear child-centered reason, not only whether it is measurable.
  • Change the environment, the expectation, or the approach before asking more of the child.
  • Stay open to feedback from autistic adults, families, and the children themselves.
  • Pause when the child's communication tells us something important, and repair when we miss it.

The work is not to make children easier to manage.

The work is to make support more responsive, more respectful, and more useful.

Behavioral science in service of the child.

Autistic voices in this work

The New ABA is built in consultation with autistic advisors and draws on the work of autistic-led researchers, advocates, and community members. An advisory panel is forming. Autistic perspectives are not a footnote here, they are the starting point for asking better questions about what good support looks like.

If you are autistic and interested in contributing to this project, we'd like to hear from you.