Introduction and objective:
Multiple sclerosis is an autoimmune disease that affects nearly 3 million people worldwide. It is a progressive condition which has a significant impact on various spheres of life. The aim of this study is to deepen practical knowledge about the subjective limitations in meeting the requirements of daily functioning by patients with multiple sclerosis

Material and methods:
The study involved 153 participants: 115 women and 38 men with a declared diagnosis of multiple sclerosis. An anonymous survey based on the MSQOL-54 Quality of Life Assessment Questionnaire was used as a research tool. This questionnaire is a multidimensional tool for assessing health-related quality of life specific to multiple sclerosis.

Results:
Multiple sclerosis affects both physical and mental health, and the overall quality of life reported by respondents was on a low level (median=50). Gender, age, time elapsed from diagnosis and the identified form of the disease exert a significant effect on the quality of life of patients (p<0.05). The wide range of replies suggests that patients evaluate their quality of life and health status differently. Depending on individual experiences and the diversity of symptoms, coping with the disease may be perceived at different levels. Over time, patients experience numerous difficulties and face increasing health problems.

Conclusions:
Conducting studies to assess the quality of life of patients with multiple sclerosis is necessary for proper management of the disease and coordination of the therapeutic pathway. People suffering from multiple sclerosis usually have a lower quality of life, than the rest of the population, and require an individual approach and understanding in order to tailor care to their needs.