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Psychosocial issues of the adolescent PI patient and the development of the PI Teen Outreach Program

Publication: LymphoSign Journal
20 February 2018

Abstract

Background: The effects of disruptions in the lives of the adolescent Primary Immunodeficiency (PI) patient require psychosocial staff involved in their care to find unique approaches to treatment. The demands of living with PI in adolescence complicates this already turbulent life cycle transition. Absence from school due to infections and treatment can lead to social isolation and in turn issues of self-esteem, creating challenges for teenagers with chronic diseases. The importance of maintaining social support with peers and developing a new network of social supports with teens with similar diagnoses is highlighted in the literature as an important factor in helping teens successfully cope with the demands of chronic illness.
Methods: To best meet the complex needs of this population, the PI Teen Outreach Program was created in 2010. The goal was to connect teens with PI to one another in an environment that engages them in “normal” activities while providing an opportunity to discuss diagnosis, coping, and the impact of living with PI. The program consists of group teen events that involve an activity for peers to connect followed by a meal for sharing of life experiences. Community peers are invited to assist teens in demystifying their PI disease to their community friends.
Results: At the conclusion of each outreach event, teens were given an anonymous evaluation utilizing both Likert scales and qualitative narrative comments. The positive feedback highlights the importance of providing creative and unique programs for this population.
Conclusion: A diagnosis of PI can be difficult for teenagers as they cope with the developmental tasks of adolescence alongside a chronic illness. The Teen Outreach Program has been successful in enhancing the psychosocial support and normalizing the experience of teenagers with PI.
Statement of novelty: There is a paucity of literature addressing the psychosocial issues that the PI teen population face and any novel programming to address their unique needs.

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REFERENCES

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Information & Authors

Information

Published In

cover image LymphoSign Journal
LymphoSign Journal
Volume 5Number 1March 2018
Pages: 29 - 33

History

Received: 19 January 2018
Accepted: 18 February 2018
Accepted manuscript online: 20 February 2018

Authors

Affiliations

Wendy Shama [email protected]
Hospital for Sick Children, Department of Social Work; Factor-Inwentash Faculty of Social Work, University of Toronto, Toronto, ON
Brenda Reid
The Hospital for Sick Children, Nursing and Immunology/Allergy, Toronto, ON

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Cited by

1. Physician–patient shared decision making in the treatment of primary immunodeficiency: an interview-based survey of immunologists

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