Daily activities |
Walking, sitting |
Restricted ability for exercising |
|
Symptoms due to HS |
Fatigue, pain |
Tired because of HS, fatigued because of HS, pain because of HS |
|
Emotional consequences |
Depression, anger |
Depression because of HS, fear because of HS, suicidal thoughts because of HS |
|
Psychosocial consequences |
Isolation from others |
Isolation because of HS, nervous to go out to meet other people because of HS, avoidance of social contact because of HS |
|
Restricted clothing choices |
Clothing choices to avoid flare-ups |
HS impact on clothing (to avoid flare-ups and to hide the disease) |
|
Coping |
Social coping |
Coping with HS |
|
Sexual functioning |
Embarrassment, pain during sex |
HS impact on sexuality, embarrassed because of HS |
|
Work/economic consequences |
Financial burden of HS management and treatment |
HS impact on job situation in general, HS impact on getting hired for a job, monetary cost of disease |
|
Interactions with medical personnel |
Inaccessibility to medical professionals |
The doctor's knowledge of HS, influence/participatory on own treatment |
|
Symptoms due to treatment |
Treatment side effects |
Side effects of treatment |
|
Concentration issues |
Trouble concentrating at work |
Ability to study with HS flares |