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“ Most patients with Type 1 diabetes have to monitor their blood glucose levels carefully and inject themselves with insulin at least once a day.” Once a day l
by dave8088 3y ago
“ Most patients with Type 1 diabetes have to monitor their blood glucose levels carefully and inject themselves with insulin at least once a day.”
Once a day lol. Tell me you don’t know anything about Type 1 diabetes without telling me you don’t know anything about type 1 diabetes.
- deleted 3y ago[deleted]
- terminalcommand 3y agoAnother T1 here, fast-acting insulin wasn't invented until recently. One large dose of mixed insulin and a fixed diet may have been prescribed back in the day.
- consp 3y agoBefore fast acting there was human analog, this is also somewhat short term. What was quite common for a while was the mixed insulins (the cloudy ones you would have to make sure mixed before injecting) which you took twice a day. The same could be achieved with individual doses of course. In general the very long acting insulins are highly variable and not much subscribed (as in they work between 12 and 48h, good luck if it varies a lot). Long story short, NPH insulins for medium length (about 18h to a day but still lots of variation) was available since the 50's and was usually combined with normal human analog in either a mixture taken twice a day or in separate doses. I was on the twice a day regime of mixtard for most of the 90's.
- terminalcommand 3y agoThank you for enlightening us, I was diagnosed around 2004. At that time, fast acting insulin was the norm. But I knew that some patients used mixed insulin. I still know T1Ds who continue to use mixed insulin, because it works for them.
- eep_social 3y agoLantus was approved in 2000. Diagnosed in early 2001, I spent maybe six months on NPH before they got me switched over. There’s also regular which is a mix of nph and fast acting, I still hear of people using that now as it works okay and is very cheap.
- eep_social 3y ago> Another T1 here There are dozens of us! Dozens!
- t-writescode 3y agoHeya! You seem knowledgeable about this. What is a normal amount? Thanks!
- terminalcommand 3y agoOne fast acting insulin per meal and one long term insulin a day, 4 at minimum if you eat 3 meals. Most of us use insulin pumps where we can get insulin any time we want.
- stranded22 3y agoBefore being on an insulin pump, my wife would be injecting 1-2 times a day with long acting insulin (to manage background levels) and then at least 3 times a day with food - not just meals, snacks too (and if levels running high). So realistically, 8-10 times a day would not be uncommon. That’s after 3-5 times a day finger pricks too. Now, she just has the pain of the libre once a fortnight and pump every few days (along with finger pricks when the libre is out). People do not realise how all consuming T1D is - she has to be on the ball all the time. If she isn’t, then her numbers screw up and she can’t drive (or live, tbh). This project could make a huge difference to her life - but there are always 5-10 years away
- kakoni 3y agoAt the moment open source artificial pancreas systems are way to go. Have you checked androidaps or loopkit?
- stranded22 3y agoI had a look over the years - the libre can pretty unreliable with levels, so I am concerned about someone else’s life being in jeopardy if I made a mistake (would be different if it was my own - I’d have done it a long time ago) She’s waiting for a closed loop system from her hospital - should be within the next few months (omnipod is due an upgrade). That said, I’ll check out androidaps and loop kit, thank you!
- epilys 3y agoIf you have type 1, you too can lead a normal life if you don't do any physically demanding activity, eat nothing, have no stress, do not get any common infection like the common cold, do not have any natural metabolic rate changes.. etc etc /s. There are so many things that affect blood sugar both in the short and long run. T1D treatment is constant correcting for the past hours, not just the moment and future. I wish it was easier to communicate this to people and journalists, because there are so many misconceptions like the one quoted here that makes T1D an even more invisible disability.