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. Author manuscript; available in PMC: 2010 Sep 1.
Published in final edited form as: J Clin Psychol Med Settings. 2009 Apr 22;16(3):209–215. doi: 10.1007/s10880-009-9164-9

Table 1. Items and Sample Responses from the TADS-A.

TADS-A Items Representative Comments
1. What is the hardest part about having diabetes when you are with your friends? “Time it takes away from being with them. It singles you out. They try to tell you what you cannot do.”
2. What would you like your friends to know about having diabetes that they DON'T know? “You can have sugar…its not all sugar free.”
3. What do your friends say about you having diabetes? “They don't really care, sometimes they have questions, but I don't mind (most of the time).”
4. What's the hardest part of telling your friends about your diabetes? “Some people just stop talking to me.”
“They might not think of you the same, if they know.”
5. How does having diabetes get in the way of having fun with friends? “You can't just eat or drink whatever you want.”
“Takes too much time.”
6. How does having diabetes get in the way of making friends? “It's just hard to tell them why I have to do some of the things I do.”
7. Are there any differences in your management when you're with friends? “I sometimes forget about it when I am with them.”
8. How do your friends help you manage your diabetes? “They ask if I have checked my sugar.”
9. What can your friends do differently to help with your diabetes management? “Help me with stuff.”
“Remind me to test.”
10. How do your friends make it harder to follow your regimen? “They sometimes hurry me and don't want to be patient enough to let me bolus or check.”
11. Does it bother you to take care of your diabetes in front of your friends? Explain. “They don't normally pay attention, most of them don't like blood.”
12. Does it bother you when your friends are eating/doing things you can't do because of your diabetes? Explain. “Sometimes it bothers me when they do something I can't.”