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	Skala Jakości Życia w Chorobie Huntingtona (HD-QoL)	Kwestionariusz Jakości Życia w Stwardnieniu Rozsianym-54 (MSQOL-54)
Dziedzina	Neurologia	Neurologia
Rodzina	Process / pipeline	Process / pipeline
Rok powstania	2001	1995
Twórca	Helder et al., University of Leiden	Barbara G. Vickrey, UCLA
Typ	Self-report questionnaire	Self-report questionnaire
Źródło pierwotne	Helder, D. I., Kaptein, A. A., van Kempen, G. M., Weinman, J., van Houwelingen, H. C., & Roos, R. A. (2001). Living with Huntington's disease: Illness perceptions, coping mechanisms, and patients' well-being. Journal of Psychosomatic Research, 50(1), 1-7.	Vickrey, B. G., Hays, R. D., Genovese, B. J., Myers, L. W., & Ellison, G. W. (1995). Outcomes in Multiple Sclerosis: The Multiple Sclerosis Quality of Life-54 Scale. Health Psychology, 14(1), 34-42.
Inne nazwy	Huntington Disease QoL, HD-QoL Scale	MS QoL-54
Pokrewne	4	4
Podsumowanie	The HD-QoL is a disease-specific quality-of-life instrument designed to measure the multidimensional impact of Huntington's disease on patients' physical, emotional, social, and cognitive functioning. Developed by Helder and colleagues in 2001, it uniquely addresses the progressive motor, cognitive, and psychiatric manifestations characteristic of HD. The scale recognizes that HD burden extends beyond neurological deficits to profound impacts on identity, family relationships, and existential well-being.	The MSQOL-54 is a disease-specific quality-of-life instrument designed to assess the physical and mental burden of multiple sclerosis on patients' daily functioning and well-being. Developed by Vickrey and colleagues in 1995, it combines the widely-used SF-36 generic health questionnaire with 18 MS-specific items to provide comprehensive measurement of QoL in MS populations. This scale is a cornerstone tool in MS clinical research and patient monitoring.