To the Editor: Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder, by which 2 in 100,000 individuals are affected each year,1 that affects primary motor neurons in cerebral cortex, brain stem, and spinal cord.2 Degeneration of motor neurons will hinder sending cerebrum impulses to the muscle fibers, impairing voluntary movements. Muscle twitching and spasticity, difficulties in speech, swallowing, and breathing are most commonly known symptoms of ALS. One of the most salient features in determining disease severity and appropriate treatment is gait disorder in form of increase in mean stride interval and decrease in mean speed of walking.3 Stride-to-stride fluctuations in healthy adults show alteration in a chaotic manner; these have a fractal (self-similar) structure more than a random one,4,5 which would approach a stochastic state.5