02/14/2026
I recently watched the documentary "My Kid Is Not Crazy" (2018) on YouTube. It outlines the history of PANS/PANDAS and examines how the “controversy” surrounding this condition emerged, while centering the lived experiences of families whose children changed abruptly overnight. There are some major updates to the research since then (i.e. proof of concept of why IVIG works for PANS kids - Han et al., 2025) but this does a great job capturing the history of PANS/PANDAS.
The film follows children with sudden-onset symptoms including severe OCD, ARFID requiring tube feeding, and intense behavioral aggression. It also captures the reality many families face while navigating a medical system that is unsympathetic to their plight. Throughout the documentary, leaders in PANS/PANDAS research and treatment share their clinical and research perspectives, with representation from institutions such as Stanford University, Massachusetts General Hospital, and Yale University.
So, why does PANS remain a point of debate?
In part, because it challenges long-standing divisions between “medical” and “psychiatric” care. Integrating PANS into pediatric medicine represents a significant paradigm shift—one that requires clinicians to work across disciplines and reconsider how immune processes, inflammation, and neuropsychiatric symptoms intersect. That level of integration is complex.
Families are often left feeling isolated in the gaps created by these divisions. Psychiatric settings focus primarily on symptom management, while medical settings prioritize conditions that are more easily captured through traditional testing. PANS exists in the space between these approaches. Research has documented immune activation on a cellular level, basal ganglia inflammation, and differences in gene expression and RNA sequencing in children with PANS (Han et al., 2025)
When a condition does not fit neatly into one category, the question becomes: Where do these children go?
As a pediatric OCD clinician and a mother with lived experience, I will be frank: it simply makes no sense at this point to dismiss PANS as “not real” given the accumulating research and the repeated, consistent experiences of families.
Good medicine asks hard questions. It tests hypotheses and demands rigorous evidence. It also remains open, curious, and willing to evolve. It knows when to say, honestly, “We need to update our best practices."
For families living this reality, willingness of physicians with boots on the ground (pediatricians, pediatric psychiatrists, etc.) to listen more closely to PANS/PANDAS families is an absolute necessity going forward.
Call to action:
I encourage clinicians, educators, and parents alike to watch My Kid Is Not Crazy - https://www.youtube.com/watch?v=WJQT9-cQwIw
If you’d like to learn more, here are several resources:
PANDAS Physicians Network
International OCD Foundation (PANS/PANDAS resources)
ASPIRE PANS
PANDAS Network
Neuroimmune Foundation
My Kid is Not Crazy tracks the journey of six children and their families as they become tangled in the nightmare of a medical system heavily influenced by t...