1.What do you think are the unique needs of young adults diagnosed with sarcoma?

2.Do you feel your healthcare providers understand the unique needs of young adults?

3.How involved were you in making decisions about your treatment?

4.How comfortable did you feel discussing emotional concerns with your care team?

5.Do you feel your age-specific needs were considered in your treatment plan?

6.Where did you find or access support and resources throughout your treatment journey?

7.What kind of follow-up care or survivorship resources have you received?

8.What coping strategies have been most helpful to you?

9.What types of support do you wish had been available but weren’t?

10.What would you like healthcare providers to understand about the experience of an AYA sarcoma patient?

11.What resources or support can organizations like SFA provide that would help assist in the treatment journey?

12.What resources or support can organizations like SFA provide that would assist in survivorship?

13.What else would you like healthcare providers and others to know about being a young adult with a sarcoma diagnosis?