Abstract

Loss of mobility is one of the most widespread and debilitating consequences of multiple sclerosis (MS). In the first of two articles, the results of a survey on MS patient mobility from the perspective of healthcare professionals (HCPs), specifically neurologists and MS specialist nurses who treat patients with mobility issues, are presented. The vast majority of HCPs stated that they specifically asked patients about mobility issues during consultation, or that the patients spontaneously raised the subject. Most HCPs rated loss of mobility as having a significant impact across all aspects of patients’ lives. Although 80 % of HCPs believed they had sufficient knowledge to identify mobility impairment, only 50 % felt they had the necessary tools available to fully assess the loss of mobility. Considerable differences existed between neurologists and MS specialist nurses, and across geographical regions, in the tools used to assess mobility impairment and the subsequent treatment options offered. This study shows that HCPs are aware of the potential impact of mobility difficulties on their MS patients, and highlights the need for novel or improved therapy options.

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