Propriospinal myoclonus was first described in 1991 as axial jerks of spinal origin.1 The myoclonus differed from segmental spinal myoclonus in that many spinal segments were involved, putatively linked by activity in the axially focused propriospinal pathways that link distant spinal segments within the cord. As such, two additional key features of the myoclonus were that it spared the distal limbs and face, and that myotomes were recruited into the jerks from a spinal focus with relative latencies that were consistent with conduction in slow propriospinal pathways. This original description of propriospinal myoclonus was followed by a gamut of anecdotal and rather speculative reports relating this condition to diverse causes ranging from vitamin deficiency to cannabis exposure.2 These dominated over a steady trickle of more credible reports of propriospinal myoclonus related to causes already associated with spinal segmental myoclonus, such as spinal tumors, syringomyelia, spinal dural arteriovenous fistula, and infective myelitis.