Hi everyone, I am currently a Child life intern in WA. I am working on my intern project and wanted to focus on teenagers who are critically ill and Cystic Fibrosis came to mind.
so if you don't mind could you please reply to some questions or just give me some advice or thoughts. i won't use any names in my project and it will remain confidential. I would just like to create some sort of resource for teens here who are strugglin with this.
What motivates you to continue with your treatment and keep your spirits up? Is there anything that child life does or can do to help you?
what helps you get through?
thank you so much and once again, please feel free to add anything you feel would be important.
so if you don't mind could you please reply to some questions or just give me some advice or thoughts. i won't use any names in my project and it will remain confidential. I would just like to create some sort of resource for teens here who are strugglin with this.
What motivates you to continue with your treatment and keep your spirits up? Is there anything that child life does or can do to help you?
what helps you get through?
thank you so much and once again, please feel free to add anything you feel would be important.