Pediatric Lyme Disease Care: Addressing Challenges and Solutions
$23.79
To develop workable solutions that close the care gaps that parents report experiencing, this study attempts to better understand how families of kids and teenagers with Lyme disease experience the illness. To learn more about how parents highlighted certain medical and psychological difficulties when describing their family's experiences with Lyme illness, this study especially looks at the written correspondences of 23 parents of children and adolescents with Lyme disease. Parents spoke of feelings that included concern for their child as well as anger and resentment against the healthcare system. Researchers discovered four therapy phases where families believed they received subpar care. In addition to the interactions between the doctor and the medical staff and the kid, parents, and family, these phases also involve testing, diagnosis, treatment, and care of the affected patients. The researchers then put forward several therapeutic choices as well as additional prospective remedies that might enhance the lives of parents and families of kids and teenagers with Lyme disease in similar regions. Some of these recommendations were modified from strategies used to treat kids with other chronic conditions more effectively. Researchers think that more research into how doctors may enhance the paradigms of care and treatment for kids with chronic illnesses, in general, can lead to discoveries about how to enhance the patient and parent experience while coping with Lyme disease in kids and teenagers.