Background: We sought to understand the experiences of parents/caregivers of children with inherited metabolic diseases (IMD) in order to inform strategies for supporting patients and their families. We investigated their experiences regarding the management of disease, its impact on child and family life, and interactions with the health care system. Methods: From four Canadian centres, we conducted semi-structured telephone interviews with parents/caregivers of children with an IMD who were born between 2006 and 2015 and who were participating in a larger cohort study. Participants were selected with the aim of achieving a diverse sample with respect to treatment centre, IMD, and age of the child. Interviews emphasized the impacts of the ...
Abstract Background: Diabetes is a major health problem, which has a wide prevalence in the world. ...
Newborn screening enabling early diagnosis of medium chain acyl-CoA dehydrogenase deficiency (MCADD)...
Background: Diabetes mellitus type 1 (DM1) is the most common form of diabetes in children. Strict ...
Abstract Background: We sought to understand the experiences of parents/caregivers of children with...
Abstract Background We sought to understand the exper...
Background and Objective: Children with inherited metabolic diseases often require complex and highl...
Objectives: The objectives of this thesis were to: (i) understand the experiences of parents/caregiv...
Introduction Children with inherited metabolic diseases (IMDs) often have complex and intensive heal...
Background: Patient-centered health care for children with inborn errors of metabolism (IEM) and the...
Parents of children with inborn errors of metabolism (IEM) face numerous psychosocial challenges. An...
Introduction: Type 1 Diabetes Mellitus is a chronic disease that is expanding and increasingly affec...
Purpose: The diagnosis of diabetes in pre-school children poses a number of unique challenges relate...
Background: Insulin pumps have the potential to improve glycaemic control and health in childhood ty...
Newborn screening enabling early diagnosis of medium chain acyl-Co Adehydrogenase deficiency (MCADD)...
Primary ciliary dyskinesia (PCD) is an incurable, rare, inherited, chronic condition. Treatment incl...
Abstract Background: Diabetes is a major health problem, which has a wide prevalence in the world. ...
Newborn screening enabling early diagnosis of medium chain acyl-CoA dehydrogenase deficiency (MCADD)...
Background: Diabetes mellitus type 1 (DM1) is the most common form of diabetes in children. Strict ...
Abstract Background: We sought to understand the experiences of parents/caregivers of children with...
Abstract Background We sought to understand the exper...
Background and Objective: Children with inherited metabolic diseases often require complex and highl...
Objectives: The objectives of this thesis were to: (i) understand the experiences of parents/caregiv...
Introduction Children with inherited metabolic diseases (IMDs) often have complex and intensive heal...
Background: Patient-centered health care for children with inborn errors of metabolism (IEM) and the...
Parents of children with inborn errors of metabolism (IEM) face numerous psychosocial challenges. An...
Introduction: Type 1 Diabetes Mellitus is a chronic disease that is expanding and increasingly affec...
Purpose: The diagnosis of diabetes in pre-school children poses a number of unique challenges relate...
Background: Insulin pumps have the potential to improve glycaemic control and health in childhood ty...
Newborn screening enabling early diagnosis of medium chain acyl-Co Adehydrogenase deficiency (MCADD)...
Primary ciliary dyskinesia (PCD) is an incurable, rare, inherited, chronic condition. Treatment incl...
Abstract Background: Diabetes is a major health problem, which has a wide prevalence in the world. ...
Newborn screening enabling early diagnosis of medium chain acyl-CoA dehydrogenase deficiency (MCADD)...
Background: Diabetes mellitus type 1 (DM1) is the most common form of diabetes in children. Strict ...