For Families
Everything a Parent Needs Before the First Phone Call
How to get started, what insurance really involves, honest answers to the questions families ask us most, and plain-language reading for when you have ten spare minutes.
Getting Started, Step by Step
You should never need a decoder ring to begin. Here is what reaching out actually looks like — and what it does not commit you to.
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Connect With Us
Tell us about your family and what support you're looking for. One short form, or one phone call — whichever is easier for you.
No referral or diagnosis required to simply ask a question.
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Explore Your Options
We discuss your needs, our current service availability, and potential next steps, including what we can and cannot support right now.
Availability and coverage are confirmed, never assumed.
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Develop a Personalized Plan
When appropriate, we complete the necessary assessments and collaborative planning with you, informed by your child's strengths and your family's priorities.
You review and approve goals before services begin.
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Begin Your Journey
We work together on individualized goals in relevant home and community settings, with regular communication along the way.
Plans are reviewed and adjusted as your child grows.
Reaching out does not commit you to services. Availability, assessment requirements, insurance coverage, and authorization are confirmed individually and are never guaranteed by this website.
When you call, it helps to know
- Your child’s age and roughly what support you think they need
- Who is in the household and who will be available during sessions
- Any evaluations, diagnoses, or school plans that already exist
- Your general area, so we can speak to availability and travel
- Three changes you would genuinely like to see at home
What we ask you not to do
- Do not send diagnosis details, reports, or medical records through this website form.
- Do not share your child’s full name and date of birth together in a free-text message.
- Do not assume coverage — we confirm it together with your payer, in writing.
- Do not wait for a formal diagnosis to ask us a question.
Insurance, Coverage, and Funding — Stated Plainly
Insurance and funding questions are some of the first families ask. We want to be straightforward about what we can and cannot confirm.
Community Horizons ABA works with families to understand their specific benefits and funding pathways. Coverage for ABA services varies widely by plan, by state, by the child's diagnosis and medical necessity documentation, and by the authorizations a payer issues. We do not want to imply that any particular plan, network status, or coverage outcome is guaranteed.
- We can review your benefits with you and explain what our team sees in your plan documents.
- We can help organize the documentation a payer typically requests for an ABA authorization.
- We can talk through other funding pathways that may exist in your state or region.
- We will always tell you plainly what is confirmed, what is pending, and what is not covered.
Nothing on this website constitutes an insurance eligibility determination or a guarantee of coverage, authorization, or payment. Confirm your own benefits directly with your payer.
Plans we have worked with
Verified from the Accepted Insurance Plans list published on chaba.care. The site notes networks change frequently and invites families to ask if a payer is not listed.
Lists like this go out of date. If your plan is not shown, ask us — we would rather check than have you assume.
Documents we usually need
- Insurance card and any plan or benefit documents you have
- Prior evaluations, reports, or a diagnostic letter if one exists
- School or IEP information where relevant
- A list of other providers currently involved with your child
Do not upload these to the website. Bring them, or send them by the secure method our intake team confirms with you.
Frequently Asked Questions
Answers to what families actually ask us, written plainly. If your question is not here, asking is always free and carries no obligation.
Getting started
No. You can contact us with a question, a suspicion, or just a hunch that your child could use more support. A formal diagnosis is often needed before an insurer will authorize ABA services, but it is not needed to start a conversation, ask us what we think, or ask us to help you figure out the next step.
A member of our intake team reviews it and follows up using the contact method you chose. That first conversation is a conversation, not an assessment: we ask what you are seeing and what you want to be different, tell you honestly what we can support, and explain the possible next steps. We never ask for detailed clinical information through the website form.
Wait times depend on current staffing capacity, the hours and settings you need, and your location within our service area. We do not publish a wait time on a website because it would be out of date within weeks — we will give you the real answer when you call, including whether we can offer a reduced schedule in the meantime.
ABA is one approach, and it is not the only one, nor automatically the right one for every family. It tends to be a good fit when a family wants structured, data-informed support delivered in real environments, and is comfortable collaborating closely with the team. If we do not think we are the right fit for your child, we will say so and try to point you somewhere better.
Our services
Our model is home- and community-based, which means services are delivered in your home and in everyday community settings rather than in a clinic room. Some families also benefit from a more structured setting, and if that is what your child needs we will be straightforward about whether we are the right provider for that.
Recommended intensity is an individualized clinical decision based on assessment findings, your child's age and needs, the settings involved, caregiver availability, and what your insurer will authorize. Two families in the same situation can reasonably end up with different recommendations. We will explain the reasoning behind our recommendation rather than just hand you a number.
Direct therapy is typically delivered by a trained behaviour technician working under ongoing oversight from a qualified supervisor, with programme decisions made by the supervising clinician. You are entitled to know who is assigned, what their qualifications are, and how often supervision occurs — and you should ask us all three.
Yes, and we encourage it when the family wants it. Skills generalize faster when more of the child's regular caregivers share the same approach. We can schedule time to include grandparents, older siblings, nannies, and babysitters in the strategies your child relies on.
Insurance and funding
We cannot answer that reliably on a webpage, and neither can any honest provider. Coverage for ABA depends on your specific plan, your state, the diagnosis on record, the medical necessity documentation, and the authorizations your payer issues. What we can do is sit down with your plan documents and go through it with you.
Yes. Our team helps organize the assessments, goal sets, and progress reporting that payers typically request for an initial authorization and for re-authorization. We will tell you what we have submitted, what is outstanding, and what the payer has said.
Depending on where you live, other pathways may exist — state Medicaid or waiver programmes, early intervention for younger children, school-based funding, and in some regions charitable or grant-funded slots. Availability varies enormously, so we discuss what is realistic for your situation instead of promising a pathway we cannot confirm.
The initial inquiry and the first exploratory conversation are about helping you decide, and we do not use them as a sales gate. Any chargeable clinical service is always explained to you in advance, with the cost and the authorization status made clear before it begins.
During therapy
Less like a classroom than you may be picturing. Sessions are activity-based, follow the child's motivation, and move around — including out of the house on community days. There is structure and a plan, but a good session usually looks like a child genuinely engaged in something they want to be doing.
Goals are written so they can be measured, and therapists record data during sessions. A qualified clinician reviews that data, and you receive written progress summaries on a predictable schedule. If a goal is not moving, that is a signal to change the approach, and you should hear about it from us rather than discover it yourself.
You raise it, and we change the plan. Families are not required to be patient with an approach that is not producing meaningful change, and neither are children. Persistent distress, regression, or a goal that no longer matters are all legitimate reasons to stop and redesign.
Yes. Services should have an exit. We plan for fading support and reducing intensity as skills become part of daily life, so that independence — not dependence on therapy — is the endpoint.
Respect, safety, and your rights
That is a stated commitment in how we practise. We do not target self-stimulatory behaviour simply because it looks unusual, we do not train children to suppress self-expression to appear typical, and we treat autistic ways of communicating as valid. Our goals aim at communication, safety, autonomy, and participation.
No. Our programming teaches skills and changes the conditions that make behaviour necessary. Any behaviour plan we use follows current professional ethical standards, prioritises antecedent and skill-building strategies, and requires qualified clinical sign-off. Parents receive and approve behaviour plans.
We pay attention to that. A child's refusal is information, and honouring it is part of ethical practice — including the right to request a break. Where participation is genuinely necessary, we build tolerance gradually with real reinforcement and control handed back to the child, rather than by escalating demands.
Your child's records are confidential. We share information with schools, other therapists, or payers only when you have authorized us to, and only the information that is needed for that purpose. You can ask us at any time exactly who has received what.
You Are Allowed to Interview Us First
Choosing a provider is a serious decision and you should interrogate ours. Ask who supervises, how progress is measured, what happens when a plan fails, and whether we would ever target a behaviour only because it looks unusual to a bystander. Any provider that is uncomfortable answering those questions has answered them.
Questions worth asking any ABA provider
- Who supervises the programme, and what are their actual credentials?
- Can I see an example progress report?
- What do you do when my child refuses a task?
- Do you reduce self-stimulatory behaviour, and why or why not?
- How are caregivers trained and how often?
- What changes if the data shows the programme is not working?
Ready when you are.
One short form, or one phone call. Tell us who you are and what you are hoping for, and we will tell you honestly what we can offer.