The Purpose of the study was to understand the experience of chronic renal failure
patients for the qualified individual care for them. The purpose of this study was to
explore the experience of patients living with chronic renal failure and to identify the
meaning and structure of their experience.
The subjects were four patients, two females and two males. The age range was from
21 to 54. Data was collected with a few in-depth interviews by the authors until the
data was fully saturated. The framework and methodology of this study was based on
Parse's "Human Becoming methodology," an existential phenomenological research
method
ology.
The findings of this study were as follows. Three experience structures of chronic renal
failure patients were :
1. Sufferings and conflicts originated in the frustration caused by uncurable disease.
2. Dependence upon God and significant others with complex emotions.
3. Acceptance of sufferings, emerging hope for serving people, and gratitude for living.
In conclusion the experience of chronic renal failure patients could be described from the
findings (three structures) as "Experiencing the sufferings, conflicts originated in the
frustration caused by uncurable disease, dependence upon God and significant others
with complex emotion, acceptance of the suffering and hope for serving people, and
gratitude for living." The three structures of the lived experience of patients with
chronic renal failure, the findings of this study, could be explained by the three concepts
of "Theory of Human Becoming," the first structure could be explained with values, the
second with revealing-concealing, and the third with transforming.
The purpose of this study was to explore the experiences of Korean mothers in parenting children with Hunter's syndrome, an X linked recessive genetically inherited disease usually affecting boys.
Data were collected from 14 mothers having children with Hunter's syndrome, through two focus group interviews and individual in-depth interviews. Qualitative data from the field notes and transcribed notes were analyzed using the grounded theory methodology developed by Strauss & Corbin (1998).
The core category about the process of rearing children with Hunter's syndrome was identified as "navigating in the maze". The process of rearing children with Hunter's syndrome passed through three phases; 'entering an unknown region', 'struggling to escape from the unknown region', 'settling down in the unknown region'.
In this study "navigating in the maze", as the core category deeply showed joys and sorrows of mothers in the process of rearing their children with Hunter's syndrome. In this rearing process they gradually adjusted themselves to their given condition. Also they gained initiatively coping strategies to care for, and protect their children. Therefore health care providers can establish supportive programs in the clinical field to empower these mothers by reflecting their proactive coping strategies.
The purpose of this study was to identify and describe phenomenological structures of the lived experience of struggling against an illness for patients with Amyotrophic Lateral Sclerosis (ALS).
The participants were 7 patients with ALS recruited by snowball sampling who agreed to participate in this research and could verbally communicated with the researcher. Data were collected by long term-repeated interviews with participants in their own homes. Data were analyzed using Colaizzi's method of phenomenology.
Four categories were extracted as follows: 'Being seized with fear of death', 'Living a marginal life', 'Accepting hard fate', and 'Clinging to faint life'. Seven theme clusters were identified as: 'Wandering to find a healing method with ominous signs in the body', 'Having a diagnosis of ALS is like a bolt from the blue and struggling against illness with faint hope', 'Being forced out to the edge of life with anguish', 'Filling one's heart with hatred and longing toward becoming estranged from the world', 'Living with stigma as a stumbling block with bitter grief in one's heart', 'Accepting every things as one's fate with self controlled fear of death', and 'Attaching to desire to live'.
The results of this study can be used to develop the programs to support patients with ALS and their family.