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About Sydra
Sydra is federal IDR software built out of a working revenue cycle operation, founded by Dr. John M. Abrahams, MD, a board certified practicing neurosurgeon in New York.
Founder, Board Certified Neurosurgeon
Fellow, American Association of Neurological Surgeons · President, New York Brain & Spine Surgery · Founder, Sydra
Dr. John M. Abrahams, MD is a practicing neurosurgeon in New York. He built the original federal IDR submission process for his own neurosurgical practice after the No Surprises Act took effect in 2022, and it produced consistently better outcomes than the contingency model the practice had used before.
The clinical coding framework, the determination library curation criteria, and the clinical necessity narrative structure in Sydra are all built from that work. He reviews every piece of medical content Sydra publishes.
Director of Revenue Cycle
Heisha brings over 15 years in revenue cycle management and has worked with the No Surprises Act regulations since they took effect in 2022. She leads revenue cycle strategy and IDR operations for Sydra clients.
Director of IT
Chelsea leads Sydra's IT and integration architecture — including ModMed, Stedi, and EMR connectivity — and manages the product roadmap.
Lead Programmer
TJ leads Sydra's software engineering, owning the platform's core build, releases, and deployments.
Associate Programmer
Michael-Paul builds and maintains application features across the Sydra platform.
IDR Specialist
Camilla manages federal IDR submissions, determination tracking, and account reviews for Sydra clients.
IDR Specialist
Robert handles IDR submissions and escalations, keeping every dispute on deadline.
Most software in this category is built by people who read the regulation. This was built by someone who missed deadlines, argued market rate, and watched a contingency take 20 percent of recoveries he had already done the clinical work for.
That is why Sydra defaults to one claim per CPT, why the eligibility check runs before drafting, and why nothing files without a human approving it. Those are not product decisions made in a planning session. They are scar tissue.