| “What my life looks like”
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Existing routines and the impact of disruption |
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People’s understanding of their condition |
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Relationships with others |
“I mean they seem to concentrate more on the insulin dependent ones and us tablet controlled ones seem to be left to our own devices.” [Male participant; aged 62 y; >5 y since diagnosis]
“I mean if we’re out and something is available to eat, she gives me the nod if I should eat it.” [Male participant; aged 80 y; <5 y since diagnosis]
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What it “means” to live with T2Da
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“I’ve got it, can’t do anything about it, it’s under control, I’m not worried about that.” [Female participant; aged 73 y; >10 y since diagnosis]
“I always call it the fat diabetes when I say I’ve got diabetes, it’s not insulin, it’s the fat one.” [Female; aged 56 y; >5 y since diagnosis]
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Changes in self-management of T2D over time—what and how
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The “drip drip” effect |
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Take what you need—and stick with it |
“No, no nothing was unhelpful. I enjoyed getting them and where it was needed, I changed things. But there wasn’t a lot to change because I was doing the right thing and I realised that because of the messages.” [Female participant; aged 74 y; >5 y since diagnosis]
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The system as a vehicle between then and now |
“The variety of messages was good the way they suggested different ways to remind yourself. Make a note of it somewhere, ask someone, make sure a family member is watching over you if you don’t think you’re going to remember. I think there was about nine or 10 different ways, but you can only say it so many times. By differently wording it sometimes—as I said before—it makes you read it again.” [Male participant; aged 54 y; >5 y since diagnosis]
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