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Empowering Practitioners: Enhancing Healthcare for Individuals with Down Syndrome

Empowering Practitioners: Enhancing Healthcare for Individuals with Down Syndrome
In the field of online therapy, particularly when working with schools, it’s essential to continuously improve our skills and understanding to provide the best care possible. A recent study titled "Quality of health care according to people with Down syndrome, their parents and support staff—A qualitative exploration" sheds light on the unique perspectives and needs of individuals with Down syndrome (DS), their parents, and support staff regarding healthcare quality. This blog will discuss the key findings of the study and offer practical ways for practitioners to implement these insights into their practice.

Understanding the Unique Healthcare Needs of Individuals with Down Syndrome

The study, conducted by van den Driessen Mareeuw et al., involved semi-structured interviews with 18 individuals with Down syndrome, 15 parents, and focus groups with 35 support staff members in the Netherlands. The results highlighted several critical aspects of healthcare quality for people with DS, which can be summarized as follows:

Implementing Research Insights into Practice

Based on these findings, here are some practical steps practitioners can take to enhance their skills and provide better care for individuals with Down syndrome:

Encouraging Further Research

While the study provides valuable insights, it also highlights the need for ongoing research to better understand the healthcare needs of individuals with Down syndrome. Practitioners are encouraged to stay informed about the latest research and to consider participating in studies that can contribute to the body of knowledge in this field.

To read the original research paper, please follow this link: Quality of health care according to people with Down syndrome, their parents and support staff—A qualitative exploration.

Citation: van den Driessen Mareeuw, F. A., Coppus, A. M. W., Delnoij, D. M. J., & de Vries, E. (2020). Quality of health care according to people with Down syndrome, their parents and support staff—A qualitative exploration. Journal of Applied Research in Intellectual Disabilities, 33(3), 496-514. https://doi.org/10.1111/jar.12692

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