State Rep. Tricia Byrnes Is Looking for the Filmmaker Who’ll Investigate FND
Missouri State Rep. Tricia Byrnes is seeking a filmmaker to investigate Functional Neurological Disorder. She says hundreds of families report children were labeled with FND before doctors fully checked seizures and loss of mobility, and that second opinions were blocked.
Maddie Aumann: From an FND Diagnosis to Maddie’s Law
Maddie Aumann was diagnosed with FND before genetic testing identified a rare SCN9A disorder. Her mother, Christine Aumann, describes how the FND label continued to affect Maddie’s care even after that discovery, ultimately helping inspire Maddie’s Law.
The Falsification Problem: FND Resolved After CSF Leak Repair
A patient diagnosed with FND recovered completely after surgical repair of a CSF leak. Why did the diagnosis remain? This article explores what the case reveals about comorbidity, diagnostic reasoning, and the falsification problem in FND.
When Nursing Education Reinforces a Diagnosis
Does this nursing guide teach observation, or does it teach reinforcement of a diagnosis? A critical examination of how skepticism, alternative diagnoses, and diagnostic uncertainty are presented to nursing staff.
The Common Phenotypes Hypothesis
An exploration of FND, positive rule-in signs, comorbidity, predictive processing, diagnostic closure, and whether functional symptoms may reflect common phenotypes arising from multiple underlying conditions.
ALS or FND? The Troubling Case of Tanea "Rebel" Brooks
Tanea "Rebel" Brooks has faced a devastating battle with lymphoma and a terminal ALS diagnosis. This piece explores her difficult medical journey and raises the question I’ve been wondering about: Could Functional Neurological Disorder (FND) be playing a role in misdiagnosis or diagnostic confusion?
The Medical Journey of Megan Dixon: FND and Severe Disability
Megan Dixon became severely disabled following childhood illness, with progressive loss of mobility and speech leading to prolonged hospitalisation. She was later reportedly diagnosed with FND and underwent extended rehabilitation after years of severe impairment.
ANTIBIOTICS CURED ME OF FND !
Personal account of complex neurological and systemic symptoms following a tick bite, with a clinical diagnosis of FND made after extensive negative or inconclusive investigations. The author proposes an infectious origin involving Lyme disease and other tick-borne infections and reports improvement following targeted antibiotic treatment.
Hoping one day we each will recover
An 18-year-old developed severe neurological symptoms after a concussion, was diagnosed with FND after inconclusive testing, and later found to have tethered cord syndrome requiring surgery.
The Belief Prerequisite: How FND Treatment Echoes Faith Healing
One of the most striking things you notice when you first start reading the literature on FND is how crucial it is considered for patients to accept and believe in the diagnosis. Without that belief, treatment is often regarded as futile. They simply will not get better.
Living in France, stuck in the FND Trap
Miranda’s health collapsed almost overnight, progressing from difficulty walking to seizures, psychosis, and rapid neurological decline. Despite abnormal findings and worsening symptoms, she was quickly labelled with Functional Neurological Disorder, and further testing was repeatedly refused. Her story raises serious concerns about missed conditions like Autoimmune encephalitis and the risks of diagnostic overshadowing blocking proper care.
What Makes a Doctor a Good Doctor?
A reflection on what makes a good doctor in the context of complex chronic illness, focusing on collaboration, systems thinking, and clinical humility.