On this episode, my guest is Marie-Louise Goode, a midwife from the United Kingdom and author of The Modern Midwife’s Guide to Pregnancy, Birth and Beyond and The Modern Midwife’s Guide to the First Year. Both books share a clear and important message: early life works best when we understand physiology rather than fight against it. Pregnancy, birth, feeding, sleep, movement, and development all become less frightening when parents receive clear, practical, evidence-based guidance.

That idea connects directly to hip health. Hip dysplasia is a developmental condition, and the newborn hip is shaped not only by genetics and anatomy, but also by early positioning, swaddling, carrying, and how parents are taught to care for their babies.

In this conversation, Marie-Louise helps us understand what midwives do and the central role they play in pregnancy, birth, and the early postnatal period. We talk about why midwives are often overlooked in conversations about early detection and prevention, even though they are frequently among the first professionals to guide new parents.

We discuss pregnancy, birth, newborn development, baby carriers, swaddling, infant positioning, and how simple, calm education can help families support healthy hip development without creating unnecessary fear.

This was a thoughtful and very practical conversation about prevention, trust, and the enormous value of educating parents early, before problems are missed and before anxiety takes over.

In this special season recap of Straight From the Hip, I reflect on nine conversations that explored hip dysplasia from multiple perspectives: patients and families, psychology, clinical decision-making, trust, innovation, and the future of care.

Drawing on discussions with Betsy Miller, Gemma Barber, Sammy Krathen, Dr. Kelly Rabenstein, Dr. Maurizio De Pellegrin, Dr. Joel Warsh, Dr. Tom Youm, Dr. Manoj Ramachandran, and Dr. Jacob Jaremko, this episode examines the themes that connected the season and answers questions submitted by listeners.

Topics include the lifelong impact of hip dysplasia, parental anxiety and resilience, borderline dysplasia, shared decision-making, the role of innovation in orthopedics, and how artificial intelligence may transform screening and diagnosis in the years ahead.

From patient stories to system design, this episode explores a central idea that emerged throughout the season: hip dysplasia is not just an anatomical condition; it is a developmental condition that requires long-term thinking.

Whether you are a parent, patient, clinician, researcher, or advocate, this episode offers a chance to step back, connect the dots, and look ahead to the future of hip preservation and hip dysplasia care.

My guest today is Dr. Jacob Jaremko, and we are discussing a topic that may change how we diagnose developmental dysplasia of the hip around the world: artificial intelligence.

For decades, hip ultrasound has been central to early detection. Yet despite its value, it remains highly dependent on the person performing and reading the scan. Small differences in image acquisition, landmark identification, probe position, and measurement thresholds can lead to very different interpretations—and, ultimately, different treatment decisions.

But what if we could standardize that process?

Recent advances in artificial intelligence, machine learning, and three-dimensional ultrasound are challenging many of our assumptions about how hip dysplasia should be diagnosed. New multicenter studies suggest that AI-assisted ultrasound can approach expert-level diagnostic accuracy, improve reproducibility, and expand access to high-quality screening far beyond specialized centers.

In this episode, we discuss the latest evidence behind AI-assisted hip ultrasound, the role of 3D imaging, how these tools may reduce variability, and whether the future of DDH screening will focus less on measuring angles and more on predicting risk and guiding clinical decisions.

We also explore practical implementation: scan quality, handheld ultrasound, global screening programs, and the potential impact on patients and families worldwide.

Today’s episode is a conversation with Dr. Joel “Gator” Warsh — a pediatrician who has written extensively about trust, communication, and decision-making in modern pediatrics. He is the author of Between a Shot and a Hard Place, which explores the vaccine conversation through the lens of informed consent and respectful dialogue, and Parenting at Your Child’s Pace, which focuses on development, environment, and long-term health.

But this episode is not a vaccine debate. It is a conversation about something deeper: how pediatricians communicate uncertainty, how we balance prevention with overmedicalization, and how we think about conditions that begin early in life but may not manifest consequences until decades later.

Hip dysplasia is one of those conditions. It is developmental. It can be silent. And when missed, it can lead to arthritis in early adulthood. So the themes of trust, screening, parental agency, and long-horizon thinking are not abstract — they are deeply relevant to orthopedics.

In this discussion, we explore how pediatric medicine navigates nuance, how to talk to families about risk without coercion, and how early structural and environmental factors shape adult health. This is a conversation about development, transparency, and building healthier adults by thinking earlier.

Today’s episode is about innovation in orthopedics — where it works, where it fails, and how ideas actually move from theory into clinical practice.

My guest is Manoj Ramachandran, a pediatric orthopedic surgeon who has consistently positioned himself as an innovator operating at the intersection of surgery, technology, and systems design . Over the years, he has explored artificial intelligence in medicine, surgical innovation pathways, and the broader ecosystem that connects clinicians, engineers, startups, and hospitals.

We discuss where surgical innovation really comes from — whether it begins in the clinic, in industry, or in engineering labs — and why so many promising ideas never make it into day-to-day practice . We examine the tension between innovation and evidence, and whether innovation inevitably moves faster than validation . We talk about AI in orthopedics, separating hype from practical value, and ask where artificial intelligence will genuinely change musculoskeletal care in the next decade .

We also explore the role of the entrepreneurial physician — how surgeons can shape technology development, advisory work, and innovation platforms without losing clinical credibility. And we look ahead: what ideas seem unrealistic today but may become routine in the near future.

This was a transformative conversation because it challenges assumptions. It forces us to think critically about what innovation actually means, what problems remain unsolved in orthopedics, and how surgeons should engage with technology responsibly.

If you care about the future of musculoskeletal medicine, about artificial intelligence, about surgical innovation, and about how ideas become reality, this episode will push you to think differently.

This episode is part three of this mini-series dedicated to Patient Leadership. Today, we approach hip dysplasia from a different, essential perspective: behavioral health.

I’m lucky to be joined by Dr. Kelly Rabenstein, a Clinical Assistant Professor in the Department of Psychiatry and Behavioral Sciences at the Medical University of South Carolina in Charleston. She is a licensed psychologist working in Bio-Behavioral Medicine, and our conversation explores the psychological dimensions of developmental hip dysplasia that are often present but rarely addressed directly.

We discuss parental anxiety at the time of diagnosis, the behavioral challenges surrounding treatment

 adherence in infancy, and the longer-term psychological impact on adolescents and young adults living with hip dysplasia. We talk about how uncertainty is processed, how medical language shapes perception, and how clinicians can communicate in ways that reduce fear while preserving clarity.

This episode is forward-looking. If hip dysplasia is a condition that can span decades, then behavioral health cannot be peripheral to care. It must be integrated from the beginning. I think you will find this discussion thoughtful, practical, and deeply relevant to both clinicians and families navigating this journey.

In this mini series, of episodes, I’ve been exploring the lived experience of hip dysplasia, not just the science, but what it actually feels like to live with this condition.

Today’s guest is Samantha “Sammy” Krathen, one of the founders of a community called 

The Hipsters: the-hipsters.com

Sammy brings a perspective we don’t hear often enough in medicine, the voice of a teenager navigating hip dysplasia while still figuring out who she is, what matters to her, and what life should look like.

For Sammy, this journey isn’t only about doctors’ visits or recovery from surgery. It’s about being a high school student, going to summer camp, building friendships, and forming an identity while dealing with something that many people around her can’t see or fully understand.

That perspective matters. For other young people going through the same experience, it can be reassuring to hear that they’re not alone. And for clinicians, it’s a reminder that behind every diagnosis is a person whose life continues far beyond the clinic or the operating room.

This episode is part of a Patient Leadership Series, where I highlight the voices of individuals who have lived with hip dysplasia and chosen to turn that experience into action.

Today I’m speaking with Gemma Barber from the United Kingdom. Gemma has lived with developmental dysplasia of the hip and has become a powerful advocate within the UK community. Through her advocacy work and her recent Springtime fundraising ball in the Wirral, near Liverpool, supporting hip dysplasia awareness, she has helped build support networks for families navigating diagnosis, treatment, and long-term uncertainty.

In this conversation, we talk about what it means to grow up with hip dysplasia, how different healthcare systems shape the patient experience, and why peer support remains essential even in countries with universal healthcare. It is a discussion about resilience, community, and the importance of making sure no family feels alone when they hear the words hip dysplasia.

This is a special video episode of the podcast meant as a public service announcement to help parents understand what matters for baby hips!

On this podcast, I've explore developmental dysplasia of the hip from every angle: the science, the evolution of treatment, the lived experience, and how patients and families make sense of a diagnosis that can follow them across decades.

Today’s episode is a wide-ranging conversation with Betsy Miller, author of The Parents’ Guide to Hip Dysplasia, (https://betsymillerbooks.weebly.com), a book she published nearly twenty years ago, around the same time the International Hip Dysplasia Institute was founded. Betsy wrote that book not as a physician, but as someone who had been treated for hip dysplasia as an infant and later realized how little practical, accessible information existed for parents facing a brace, a cast, or surgery. With a background in technical writing, she set out to create the resource she wished had existed.

Although she did well for many years, she was later told she had residual dysplasia, something that came as a surprise. We discuss how hip dysplasia can remain silent for decades, why some people do not realize they have it, and how the field of hip preservation emerged in response to these late presentations.

We also talk about how people get their information in 2026, whether books still matter, the challenges of nonprofit education, and what happens when hip preservation is no longer enough. Betsy ultimately underwent bilateral hip replacements and is now writing a new book, Hip Replacement at Any Age, aimed at younger patients who often feel alone in a space dominated by older adults.

It is a thoughtful conversation about information, identity, and how a diagnosis in infancy can echo throughout a lifetime.