Perception of hospice |
Initial perceptions of hospice |
Hospice as a place where people die |
Subsequent perception of hospice |
Loss of anxiety about ‘hospice’ once attending regularly |
Supportive relationships |
Relationships with other patients, |
Comparing self with other patients |
Competition with other patients |
Sadness at deterioration/death of others/own mortality |
Receive a ‘boost’ |
‘Boring’ if on own |
Being with others in similar position |
Sharing experiences/information |
Relationships with staff |
Support/guidance of staff |
Being ‘pushed’/encouraged by staff |
Permission ‘not to have to do’/protected |
Taking part in classes |
Physical effect |
Ability to do things, maintaining current level, not returning to previous disability |
Back to previous self/ doing things used to do before illness |
Wanting to improve strength/fitness |
Independence |
Exercises at home |
Tiredness, aches |
Working to own level/exercises adapted /progressed gradually/ No. in group and time on equipment |
Physical/ psychosocial effect |
Therapeutic |
Psychosocial and emotional effect |
‘Day out’ |
Improved mood/given a boost |
Humour |
Increased confidence/Self esteem/self worth |
Opportunity to reflect |
Coping |
Expectations |
Response to suggestion of class participation |
Expectations/not knowing what to expect in classes |