Background: Sickle Cell Anaemia (SCA) is a haematological disorder of red blood cells, caused by mutation in the beta globin gene. Caring for patients with the disorder poses a significant psychological burden on the sufferers, the caregivers and their families, thereby affecting their quality of life. Family counselling has been suggested to be vital in relieving the psychological distress and improving the quality of life. The study aimed to determine the effect of family counselling on psychological distress on caregivers of children with sickle cell anaemia in order to improve the quality of care of the SCA patients.Method: The study was a single blinded Randomised controlled trial involving caregivers of children with sickle cell anae...
The overall theme of this dissertation is an examination of the relationship between family level fa...
Objective: To examine moderating effects of family functioning and social support on the relationshi...
We interviewed 170 sickle cell disease (SCD) patients (mean age 25 years) with a modified version of...
Aim/Background: Sickle cell anaemia (SCA) is the commonest haemoglobinopathy in Nigeria with an inci...
Background: The increased risk of psychological disorders constitutes one of the complications of si...
ABSTRACTBackground: Attention paid to psychological disorders of mothers or families of children suf...
The study sought to highlight the major challenges faced by families with Sickle Cell Disease (SCD) ...
Nigeria is a country with one of the largest number of sickle cell disease (SCD) patients in the wor...
There is limited information on knowledge, perceptions, and management of sickle cell disease (SCD) ...
Objective: The objective of the study was to assess the problems experienced by immediate families i...
Sickle cell disease (SCD) is an inherited red blood cell (RBC) disorder transmitted to the child thr...
Development remains an immediate problem of health concern in Uganda for children who are of lower e...
Background: Sickle cell anemia (SCA) is prevalent in Sudan in general, and in particular in the west...
Background of Study: Caregivers of the children with thalassemia often experienced a life with varie...
Children with Sickle Cell Disease (SCD) face medical, psychosocial, and cognitive challenges, which ...
The overall theme of this dissertation is an examination of the relationship between family level fa...
Objective: To examine moderating effects of family functioning and social support on the relationshi...
We interviewed 170 sickle cell disease (SCD) patients (mean age 25 years) with a modified version of...
Aim/Background: Sickle cell anaemia (SCA) is the commonest haemoglobinopathy in Nigeria with an inci...
Background: The increased risk of psychological disorders constitutes one of the complications of si...
ABSTRACTBackground: Attention paid to psychological disorders of mothers or families of children suf...
The study sought to highlight the major challenges faced by families with Sickle Cell Disease (SCD) ...
Nigeria is a country with one of the largest number of sickle cell disease (SCD) patients in the wor...
There is limited information on knowledge, perceptions, and management of sickle cell disease (SCD) ...
Objective: The objective of the study was to assess the problems experienced by immediate families i...
Sickle cell disease (SCD) is an inherited red blood cell (RBC) disorder transmitted to the child thr...
Development remains an immediate problem of health concern in Uganda for children who are of lower e...
Background: Sickle cell anemia (SCA) is prevalent in Sudan in general, and in particular in the west...
Background of Study: Caregivers of the children with thalassemia often experienced a life with varie...
Children with Sickle Cell Disease (SCD) face medical, psychosocial, and cognitive challenges, which ...
The overall theme of this dissertation is an examination of the relationship between family level fa...
Objective: To examine moderating effects of family functioning and social support on the relationshi...
We interviewed 170 sickle cell disease (SCD) patients (mean age 25 years) with a modified version of...