ABSTRACT Retinitis Pigmentosa (RP) is a retinal dege nerative disease causing progressive blindness. Most research on RP is biomedical, and mostly from an observer perspective, therefore poorly reflecting the lived experience of having RP. Accordingly, the researcher conducted a retrospective qualitative self-study, to analyse reflections on his own experience of diagnosis and receiving a mobility cane, as contained in emails sent to friends and colleagues. This analysis yielded a number of interesting themes significant to the RP experience, namely diagnosis, impact and dealing with RP. Reference is made to literature encouraging ophthalmologists to be actively involved in the facilitation of adjustment to loss of vision. Other significant...
This study explored the experiences of individuals within the clinical genetic service in South Afri...
Purpose- To understand the emotional difficulties associated with living with the ocular conditio...
Retinitis pigmentosa is a chronic, progressive, hereditary disease of unknown aetiology. The symptom...
The majority of previous research investigating the impact of low vision on the completion of activi...
Retinitis pigmentosa (RP) are a group of incurable and inherited eye conditions, and the leading cau...
This study used phenomenological approach of qualitative research. The researchers conducted several...
Purpose To understand the emotional difficulties associated with living with the ocular condition Re...
Vision impairment and blindness are associated with disability and decreased social participation an...
Aim: To study Retinitis Pigmentosa as a cause of blindness in patients attending Regional Eye Hospit...
This article reviews the consequences of Retinitis Pigmentosa, a retinal degenerative disease with p...
Glaucoma is a major cause of preventable sight loss. As there are no obvious symptoms in the early s...
The term retinitis pigmentosa (RP) indicates a heterogeneous group of genetic rare ocular diseases i...
The term retinitis pigmentosa (RP) indicates a heterogeneous group of genetic rare ocular diseases i...
Introduction: RLBP1 RP is an autosomal recessive form of retinitis pigmentosa (RP), characterized by...
Objective: To explore the experience of vision loss, focusing on working age patients’ self-awarenes...
This study explored the experiences of individuals within the clinical genetic service in South Afri...
Purpose- To understand the emotional difficulties associated with living with the ocular conditio...
Retinitis pigmentosa is a chronic, progressive, hereditary disease of unknown aetiology. The symptom...
The majority of previous research investigating the impact of low vision on the completion of activi...
Retinitis pigmentosa (RP) are a group of incurable and inherited eye conditions, and the leading cau...
This study used phenomenological approach of qualitative research. The researchers conducted several...
Purpose To understand the emotional difficulties associated with living with the ocular condition Re...
Vision impairment and blindness are associated with disability and decreased social participation an...
Aim: To study Retinitis Pigmentosa as a cause of blindness in patients attending Regional Eye Hospit...
This article reviews the consequences of Retinitis Pigmentosa, a retinal degenerative disease with p...
Glaucoma is a major cause of preventable sight loss. As there are no obvious symptoms in the early s...
The term retinitis pigmentosa (RP) indicates a heterogeneous group of genetic rare ocular diseases i...
The term retinitis pigmentosa (RP) indicates a heterogeneous group of genetic rare ocular diseases i...
Introduction: RLBP1 RP is an autosomal recessive form of retinitis pigmentosa (RP), characterized by...
Objective: To explore the experience of vision loss, focusing on working age patients’ self-awarenes...
This study explored the experiences of individuals within the clinical genetic service in South Afri...
Purpose- To understand the emotional difficulties associated with living with the ocular conditio...
Retinitis pigmentosa is a chronic, progressive, hereditary disease of unknown aetiology. The symptom...