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Case series of psilocybin self-medication for spinal cord injury

Robin Sandell, Adele Lafrance, Olivia Gosseries, Robin Carhart-Harris

SSRN Electronic Journal preprint DOI: 10.2139/ssrn.6718771 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Qualitative case series with semi-structured interviews Case report
Sample size 3
Population Individuals with incomplete spinal cord injuries (C4–C5, T7, T12; American Spinal Injury Association Impairment Scale grades B–D) who self-medicated with psilocybin
Intervention Psilocybin
Topics Psilocybin
Key findings Psilocybin self-administration was associated with improved motor function, muscle activation, and psychological wellbeing in three individuals with incomplete spinal cord injury.

Abstract

Current spinal cord injury treatments primarily manage symptoms rather than promote neurological recovery. Psilocybin enhances neuroplasticity through 5-HT2A agonism and brain-derived neurotrophic factor upregulation, suggesting therapeutic potential for spinal cord injury rehabilitation. We conducted semi-structured interviews with three individuals who had incomplete spinal cord injuries (C4–C5, T7, T12; American Spinal Injury Association Impairment Scale grades B–D) and self-medicated with psilocybin. Case 1 reported improved motor function and gait automaticity. Case 2 reported activation of a previously non-responsive hamstring muscle. Case 3 reported rapid strength gains with enhanced proprioceptive awareness. All participants reported psychological benefits including increased wellbeing, enhanced motivation for recovery and improved adjustment to their post-injury reality, suggesting that psilocybin may serve dual therapeutic purposes. Benefits seemed greatest in partially innervated muscles. Subjects reported both acute and sustained maintenance effects, with gradual diminishment of benefits following cessation. Adverse effects included temporary spasticity. These observations suggest that psilocybin may enhance motor recovery and sensory integration in incomplete spinal cord injury through amplification of existing neural pathways and warrant controlled clinical trials.