Our 8-step process
A clear, measurable path from your first call to long-term maintenance. Every plan is personalized, every protocol is guided by qEEG brain mapping, and every step is supervised by our physician team.
The Treatment Journey
Hover or tap a step to read what happens in it. The same sequence applies to every patient — what changes is the brain map underneath.
Before your first visit we verify your benefits, explain coverage for qEEG and TMS, and outline any out-of-pocket cost in writing — so there are no surprises. Most major insurance plans are accepted and we handle the paperwork for you.
We start by listening. You share your concerns, history, prior treatments, and goals. A clinician explains how qEEG-guided care works and whether it is a good fit for your child or yourself. There is no obligation to continue after the consultation.
A non-invasive 19-channel recording of brain electrical activity — eyes open, eyes closed, and (when appropriate) during a task. The recording is compared to a normative database matched to age, producing color-coded maps that reveal exactly where the brain is over- or under-active.
Our medical team reviews the qEEG alongside your history, screening tools, and consultation notes. We look for the specific patterns associated with your concerns — anxiety, attention, mood, regulation, sleep — and confirm there are no medical contraindications to treatment.
You receive a written plan: the targets we identified, the protocols we recommend, the expected number of sessions, projected milestones, and how progress will be measured. We answer every question before treatment begins.
TMS sessions are conducted in our Lombard clinic. The patient is fully awake, can read, watch a show, or talk with the technician. Most children and adults tolerate sessions easily. Side effects are uncommon and usually minor (brief scalp sensation or mild fatigue early on).
We measure progress with validated clinical scales, parent or self-report tools, and clinician observation at every visit. Your team meets weekly to confirm the plan is on track and to adjust if needed.
A follow-up qEEG confirms the neurological change matches the behavioral change. We then create a maintenance schedule — periodic check-ins, refresher sessions if needed, and parent guidance for sustaining gains. Most patients do not need ongoing treatment, only occasional follow-up.
What Families Experience
Treatment is not a single moment. It is a transition — from concern, to measurement, to lasting change.
What we deliver
The Difference
Most behavioral health care starts with a guess. We start with a measurement.
The Reign-Bow treatment process is designed to remove guesswork. Instead of trying medications or behavioral strategies in sequence and waiting to see what happens, we measure what is actually occurring in the brain — and then design a treatment plan that targets exactly those patterns.
Most behavioral health care starts with a guess. A child has trouble focusing, so a stimulant is tried. If it does not work, a different one is tried. Months pass. The Reign-Bow process replaces guessing with measurement. A qEEG shows us the actual brain pattern, and that pattern becomes the treatment target. Read more about what brain mapping is.
The follow-up qEEG is the difference between "I think it helped" and "we can prove it changed." We compare the post-treatment map to the baseline and to the normative database. When neurological change matches behavioral change, families have lasting confidence that treatment worked.
Parents are part of every step for pediatric patients. We share findings in plain language, explain the rationale for every protocol, and provide guidance for home and school. Many families say this transparency is what made the process feel safe.
Verify your insurance benefits or request a consultation — most families hear back within one business day.
From consultation to course completion, most families spend 8–14 weeks. The treatment phase itself is usually 6–8 weeks of consistent sessions, with consultation and qEEG before and follow-up after.
No. After the physician review and treatment-plan visit you decide whether to continue. Many families take a week or two to discuss before scheduling treatment.
TMS sessions feel like a gentle tapping on the scalp. Patients remain fully awake, can read or watch a show, and there is no sedation. Most patients return to school or work immediately after.
We treat children as young as six, teens, young adults, and parents. The youngest patients are screened carefully and family-supported throughout.
We use validated clinical rating scales appropriate to the diagnosis, plus parent/self-report tools, plus clinician observation, plus the follow-up qEEG. Multiple measures together give us a complete picture.
We review weekly and adjust the protocol if data does not match the plan. In rare cases where TMS is not a good fit, we refer to other evidence-based options. You are never locked in.
Yes. We offer after-school and early-evening slots to minimize school disruption for pediatric patients.
The Reign-Bow Promise
Verify your insurance, schedule a consultation, and take the first measured step toward lasting change for yourself or your child.
