Impact of Mobility Impairment in Multiple Sclerosis 2 - Patients’ Perspectives

Abstract

In the second of two articles, the impact of mobility impairment in multiple sclerosis (MS) is examined from the patients’ perspective. Nearly half (45 %) of patients reported experiencing mobility difficulties within a month of diagnosis and nearly all patients (93 %) report difficulties within 10 years. Three quarters of the patients surveyed considered mobility impairment to be a significant problem and two-thirds believed it had contributed toward loss of earnings. Mobility difficulties were consistently reported across all age groups, but were a greater issue for men than women. Geographical differences were observed, particularly in the type of healthcare professional (HCP) with whom problems were discussed, the prevalence of mobility symptoms and the treatment options offered. These findings support previous studies on the impact of mobility difficulties on patients’ quality of life and highlight discrepancies between HCPs’ and patients’ perceptions, particularly in the severity of mobility impairment and treatment options. Patients consider loss of mobility to be limiting, challenging and frustrating, highlighting the need for long-term management of their mobility issues and new or improved therapeutic options.