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Parental Experiences in Pediatric Multiple Sclerosis: Insights from Quantitative Research
Samuela Tarantino1, Martina Proietti Checchi1, Laura Papetti1
1Developmental Neurology Unit, Bambino Gesù Children's Hospital, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), 00165 Rome, Italy.
Children (Basel, Switzerland)
|January 23, 2024
Summary
Pediatric multiple sclerosis (MS) significantly impacts families, reducing parental quality of life and increasing mental health risks. Addressing parental well-being is crucial for child treatment adherence and overall family adaptation.
Area of Science:
- Neurology
- Pediatric Neurology
- Psychology
Background:
- Multiple sclerosis (MS) is a chronic, inflammatory central nervous system disease.
- Pediatric MS presents with physical, cognitive, and psychological challenges, affecting quality of life.
- The impact of pediatric MS on families, particularly parents, is not fully understood.
Purpose of the Study:
- To review the impact of pediatric MS on parental well-being.
- To highlight the psychological and social effects on parents of children with MS.
- To emphasize the need for research into family adaptation and parental support.
Main Methods:
- Literature review of existing studies on pediatric MS and its family impact.
- Analysis of evidence regarding parental quality of life and mental health.
- Synthesis of data on the relationship between parental factors and child treatment adherence.
Main Results:
- Pediatric MS negatively affects parental quality of life, even with low child disability.
- Parents of children with MS face an increased risk of mental illness, especially mothers.
- Inadequate MS information exacerbates parental anxiety and reduces perceived competence.
Conclusions:
- The burden of pediatric MS extends to parents, impacting their mental health and quality of life.
- Parental psychological well-being is linked to the child's treatment adherence.
- Further research is needed to understand and support family adaptation to pediatric MS.
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