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. 2021 Jan 7;57(1):43.
doi: 10.3390/medicina57010043.

Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS): Major Impact on Lives of Both Patients and Family Members

Esme Brittain  1 , Nina Muirhead  2 , Andrew Y Finlay  1 , Jui Vyas  1
Affiliations

Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS): Major Impact on Lives of Both Patients and Family Members

Esme Brittain et al. Medicina (Kaunas). .

Abstract

Background and objectives: To explore the impacts that Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) has on the patient and their family members using the WHOQOL-BREF (Abbreviated World Health Organisation Quality of Life questionnaire) and FROM-16 (Family Reported Outcome Measure-16) quality of life assessments. Materials and Methods: A quantitative research study using postal questionnaires was conducted. A total of 39 adult volunteers expressed an interest in participating in the study: 24 returned appropriately completed questionnaires. Patients with ME/CFS completed the WHOQOL-BREF and up to four of their family members completed the FROM-16 questionnaire. Results: ME/CFS negatively affects the quality of life of the patient (median scores WHOQOL-BREF: Physical health = 19, Psychological = 44, Social relationships = 37.5, Environment = 56, n = 24) and their family members' quality of life (FROM-16: Emotional = 9.5, Personal and social = 11.5, Overall = 20.5, n = 42). There was a significant correlation between the patient's reported quality of life scores and their family members' mean FROM-16 total scores. Conclusions: This study identifies the major impact that having an adult family member with ME/CFS has on the lives of partners and of other family members. Quality of life of ME/CFS patients was reduced most by physical health compared to the other domains. Quality of life of family members was particularly impacted by worry, family activities, frustration and sadness. This highlights the importance of measuring the impact on the lives of family members using tools such as the FROM-16 in the ME/CFS clinical encounter and ensuring appropriate support is widely available to family members.

Keywords: FROM-16; ME/CFS; QoL; WHOQOL-BREF; family impact.

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Conflict of interest statement

A.Y.F. is joint copyright holder of the FROM-16. N.M. has given testimony to NICE and Ono Pharmaceutical, N.M. is also Chair of the Education Working Group of the CFS/ME Research Collaborative (CMRC) and is a member of Forward ME. J.V. has been on a paid advisory board for Amgen and has received honoraria from L’Oréal outside of this submission. E.B. has no conflicts of interest to declare.

Figures

Figure 1
Figure 1
Bar Graph to illustrate the number of family members who completed the FROM-16 (Family Reported Outcome Measure-16) questionnaires within each family (n = 42).
See this image and copyright information in PMC

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