Coming Soon — Dallas, Texas

Every child with a complex brain deserves a simple path to care.

A new multidisciplinary clinic dedicated to children with neurological complexity. Coordinated. Collaborative. Built to last.

The Challenge

Families shouldn't have to manage it alone.

Children with neurological complexity — cerebral palsy, epilepsy, hypoxic-ischemic encephalopathy, and other rare conditions — require ongoing care across many specialties. Neurology, rehabilitation, nutrition, pharmacy, developmental pediatrics, and more.

Too often, parents become the ones holding it all together. Juggling specialists across different health systems, repeating their child's story at every appointment, filling the gaps the system wasn't designed to fill.

Dallas has exceptional programs working to change this — but demand continues to outpace capacity. There is room for more.

~500K Children in the U.S. living with cerebral palsy

8+ Specialists a typical family coordinates across

4th Largest metro in the U.S. — Dallas–Fort Worth

What We're Building

A neuro-focused clinic built around the whole child.

Kids Complex Care is building a multidisciplinary clinic in Dallas, TX — purpose-built for children with neurological complexity. Not broad complex care, but deep, coordinated expertise in the conditions that need it most.

Our goal is to work alongside the programs and institutions already serving these families — expanding capacity, not duplicating effort — while demonstrating that sustainable long-term funding for this kind of care is possible.

Neuro-Focused

Deep specialization in CP, epilepsy, HIE, and rare neurological conditions — one team, one plan.

Collaborative

Designed to partner with existing programs and stakeholders across Dallas — building on what works.

Sustainable

A proving ground for long-term funding models — demonstrating that this kind of care can be financially viable.

Neurology Developmental Pediatrics Rehabilitation Nutrition Clinical Pharmacy Family Navigation

Our Story

Born from a family's journey.

Our founder Ryan's son Connor was born with severe hypoxic-ischemic encephalopathy — APGARs of 0-1-1. Twenty-six days in the NICU. Therapeutic hypothermia. A G-tube. At six months, myoclonic seizures at over 100 a day at their peak.

What saved their family wasn't any single specialist. It was the team — coordinated care across neurology, nutrition, pharmacy, GI, and developmental pediatrics working in concert.

Connor is thriving today. But for most families navigating this world, that level of coordination is the exception, not the standard.

"We're not building this because nothing exists. We're building it because what exists works — and there needs to be more of it." — Ryan Kline, Founder

Ryan published a "Family Reflections" piece in Pediatric Research (2025) about the post-NICU experience and the care model that changed everything for his family.

Coordinated care doesn't just treat a condition — it gives families their lives back.