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    • 8 hours, 28 minutes ago
      Bob Durstenfeld likes your comment at
      What part of managing T1D takes the most mental energy for you right now?
      It is the most ironic of ironies. Just as I have seemingly mastered the technical intricacies of gewgaws like CGMs, correction factors, insulin sensitivities, pancreatic enzymes, Kaplen-Meier curves, etc. that I must board the mystery train of insurance/logistics as my favorite form of conveyance. Befuddlement may end up being my BFF. જ⁀➴
    • 8 hours, 47 minutes ago
      Anneyun likes your comment at
      What part of managing T1D takes the most mental energy for you right now?
      Resolving sticky highs (especially when I had the flu) and coping with the erratic data in the first 24 hours of a sensor change.
    • 8 hours, 47 minutes ago
      Anneyun likes your comment at
      What part of managing T1D takes the most mental energy for you right now?
      Post meal spikes!!!
    • 8 hours, 54 minutes ago
      TEH likes your comment at
      What part of managing T1D takes the most mental energy for you right now?
      Resolving sticky highs (especially when I had the flu) and coping with the erratic data in the first 24 hours of a sensor change.
    • 8 hours, 55 minutes ago
      TEH likes your comment at
      What part of managing T1D takes the most mental energy for you right now?
      Replacing failed sensors from the manufacturer.
    • 8 hours, 55 minutes ago
      TEH likes your comment at
      What part of managing T1D takes the most mental energy for you right now?
      It is the most ironic of ironies. Just as I have seemingly mastered the technical intricacies of gewgaws like CGMs, correction factors, insulin sensitivities, pancreatic enzymes, Kaplen-Meier curves, etc. that I must board the mystery train of insurance/logistics as my favorite form of conveyance. Befuddlement may end up being my BFF. જ⁀➴
    • 9 hours, 22 minutes ago
      John Barbuto likes your comment at
      What part of managing T1D takes the most mental energy for you right now?
      Resolving sticky highs (especially when I had the flu) and coping with the erratic data in the first 24 hours of a sensor change.
    • 9 hours, 22 minutes ago
      John Barbuto likes your comment at
      What part of managing T1D takes the most mental energy for you right now?
      Post meal spikes!!!
    • 10 hours, 4 minutes ago
      Gerald Oefelein likes your comment at
      What part of managing T1D takes the most mental energy for you right now?
      Replacing failed sensors from the manufacturer.
    • 10 hours, 11 minutes ago
      Vicki Andersen likes your comment at
      What part of managing T1D takes the most mental energy for you right now?
      Other. Trying to find a blood glucose balance or equilibrium, while dealing with gastroparesis, and celiac disease take a lot of mental energy. I'm on a constant roller coaster. It is exhausting.
    • 10 hours, 12 minutes ago
      Vicki Andersen likes your comment at
      What part of managing T1D takes the most mental energy for you right now?
      Replacing failed sensors from the manufacturer.
    • 10 hours, 12 minutes ago
      Vicki Andersen likes your comment at
      What part of managing T1D takes the most mental energy for you right now?
      Preventing highs? I found truly waiting for 15 minutes before eating helps a lot. Sometimes it’s not practical. And exercise. I worry as I age that I will get lazier. Keeping my mouth shut also prevents many highs. Nope, for me, Medicare has just been a nightmare, throwing wrenches into my routine.
    • 10 hours, 12 minutes ago
      Vicki Andersen likes your comment at
      What part of managing T1D takes the most mental energy for you right now?
      It is the most ironic of ironies. Just as I have seemingly mastered the technical intricacies of gewgaws like CGMs, correction factors, insulin sensitivities, pancreatic enzymes, Kaplen-Meier curves, etc. that I must board the mystery train of insurance/logistics as my favorite form of conveyance. Befuddlement may end up being my BFF. જ⁀➴
    • 10 hours, 26 minutes ago
      Lawrence S. likes your comment at
      What part of managing T1D takes the most mental energy for you right now?
      Replacing failed sensors from the manufacturer.
    • 10 hours, 26 minutes ago
      Lawrence S. likes your comment at
      What part of managing T1D takes the most mental energy for you right now?
      Preventing highs? I found truly waiting for 15 minutes before eating helps a lot. Sometimes it’s not practical. And exercise. I worry as I age that I will get lazier. Keeping my mouth shut also prevents many highs. Nope, for me, Medicare has just been a nightmare, throwing wrenches into my routine.
    • 10 hours, 31 minutes ago
      Lawrence S. likes your comment at
      What part of managing T1D takes the most mental energy for you right now?
      I find your answers truly humorous but often very informative.
    • 11 hours, 22 minutes ago
      Kathy Hanavan likes your comment at
      What part of managing T1D takes the most mental energy for you right now?
      I find your answers truly humorous but often very informative.
    • 1 day, 3 hours ago
      kristina blake likes your comment at
      On days when T1D feels more demanding than usual, what helps you get through it?
      I just had a few days of inexplicable highs. I'm literally wiped out. But after brainstorming and problem-solving, I think I found the culprit. I took some airplane rides in rapid succession, apparently, the pressure changes caused a large amount of air to be drawn into the pen chambers. Learned two things: (1) remove all needle tips from pens before flying (2) check the barrels of the pens after each flight for air bubbles.
    • 1 day, 3 hours ago
      kristina blake likes your comment at
      How confident do you feel making diabetes-related decisions without input from apps, algorithms, or other people?
      Day to day I rely entirely on my self knowledge and understanding with over 60 years of experience living in a body with T1D. I do appreciate and rely on CGM technology that enables me to see current BG and trends on pump screen. Other than that, I don't use any bells and whistles apps, or crazy ass algorithms. When i need to I consult with my endo, or more likely, with another T1 PWD who may well have insights from their own real life experience to share.
    • 2 days, 4 hours ago
      Lawrence S. likes your comment at
      How confident do you feel making diabetes-related decisions without input from apps, algorithms, or other people?
      I've been making diabetes decisions for 70 years, long before there was any adjunct technology. I have been in situations where I had to drop back and manage manually. I worry about my granddaughter with T1D, she has been on a pump and CGM since being diagnosed. She might not have he management skills. I am not sure she has even had to draw up a shot and inject herself.
    • 2 days, 4 hours ago
      Lawrence S. likes your comment at
      How confident do you feel making diabetes-related decisions without input from apps, algorithms, or other people?
      I change all of my pump settings on my own as needed and override boluses for what I know I’ll need vs what the algorithm low-ball suggests.
    • 2 days, 4 hours ago
      Lawrence S. likes your comment at
      How confident do you feel making diabetes-related decisions without input from apps, algorithms, or other people?
      I definitely use less insulin using my pump's algorithm than I would using my own guess. However, since I know how much my pump would give me for my typical meal, I would be pretty close to what it deems necessary. My pump is usually pretty correct. However, I do override the bolus the bolus or basal rates as sometimes I know other factors that don't go into the pump's algorithm calculations.
    • 2 days, 4 hours ago
      Lawrence S. likes your comment at
      How confident do you feel making diabetes-related decisions without input from apps, algorithms, or other people?
      I said unsure. Before my pump and CGM, before using a glucometer, I would try to anticipate the answer. I was rarely spot on. But I see now that glucometer isn’t part of the unknown. Still, without my pump algorithm and especially CGM data which is basically on an app I am reading, I’m afraid my decisions would not lead me to where I am today where foot doc, eye doc, etc. say they would not be able to tell from those body parts whether I was diabetic. My Endo is probably way down the list. Yesterday, I was in-and-out in 10 minutes and ordered a script I told him I did not need.
    • 2 days, 4 hours ago
      Lawrence S. likes your comment at
      How confident do you feel making diabetes-related decisions without input from apps, algorithms, or other people?
      I have been on this journey for 45 years. I have lots of experience dealing with decisions.
    • 2 days, 4 hours ago
      Lawrence S. likes your comment at
      How confident do you feel making diabetes-related decisions without input from apps, algorithms, or other people?
      I took it that the assumption was having the test data and knowing what you've previously done already, how comfortable are you making a treatment decision. In that case, like you, after decades of doing it (even without the data), I'm fully confident. I'm sure you are too given what we've been through throughout the decades.
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    For insulin pump users: How long have you worn an insulin pump?

    Home > LC Polls > For insulin pump users: How long have you worn an insulin pump?
    Previous

    Do you feel that your blood sugar patterns are different during times of the year when there are fewer hours of daylight, compared to when there are more hours of daylight? If yes, tell us how in the comments!

    Next

    For CGM users: How long have you had a CGM?

    Sarah Howard

    Sarah Howard has worked in the diabetes research field ever since she was diagnosed with T1D while in college in May 2013. Since then, she has worked for various diabetes organizations, focusing on research, advocacy, and community-building efforts for people with T1D and their loved ones. Sarah is currently the Senior Marketing Manager at T1D Exchange.

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    19 Comments

    1. Bob Durstenfeld

      My first insulin pump was in 1987. it was the size and weight of a brick and most of that was the battery that barely lasted 24 hours. I designed my own car charger.

      5 years ago Log in to Reply
    2. MidnightSun 55

      Yup. Quite large. It was an “Auto-Syringe”. 1982.

      5 years ago Log in to Reply
    3. Kristen Clifford

      I’ve been on pump therapy since January 2012

      5 years ago Log in to Reply
    4. Greg Felton

      It would be interesting to know how long each respondent has had T1D, to see how long they have worn a pump. (In my case, 44 years T1D and 22 years with a pump.)

      5 years ago Log in to Reply
    5. Annie Wall

      I was on the pump for 24 years, 1995-2019. I went off the pump in 2019 because there was too much scarring from infusion site sets. I’m now using the InPen and will probably return to a pump after a two year vacation.

      5 years ago Log in to Reply
    6. Chip Brookes

      I have been on a pump since about 2010. Started with Medtronic now on T-slim. Switched because the Dexcom CGM was more accurate than the Medtronic CGM. I do like the Control IQ function very much. I really dislike the installation procedure for the T-Slim. The Medtronic was much simpler.

      5 years ago Log in to Reply
    7. Ahh Life

      1996. And in those days the procedure involved a 2-day hospitalization, one on saline solution and one on the real McCoy (insulin). Additional advice for abdomen users/abusers: switch to the legs. They’re great ( ͡◉ ͜ʖ ͡◉)

      5 years ago Log in to Reply
    8. Kristine Warmecke

      Only 23 years of pumping (started in February 1997) was diagnosed T1D 38 years ago (January 5, 1982). Would have been pumping sooner, but my parent’s wouldn’t give in on their rule not until I was over 18.

      5 years ago Log in to Reply
    9. Trish Seidle

      Diagnosed in 1972. Joslin Clinic put me on what I think was the very first portable pump in around 1983ish. Because my parents had very good insurance, I was able to go to Joslin Clinic every 2 years. I don’t think that the first pump had a name…although it probably did. I think the second one was the Eugly…… This is when I wish I kept a journal so I could look back at things. The advances have been incredible!! They don’t seem like much at the time but looking back, they have been huge!

      5 years ago Log in to Reply
    10. Loretta Rogers

      Pumping since ’98. I know what all of you mean about scarring. I weigh about 100 lbs with very little fat. Yes, I used the abdomen too much. Now I rotate everywhere. Probably where I shouldn’t…thighs, derriere, abs, flank, arms [in a pinch]. Will be 50 yrs. in Feb. for diagnosis. So, ROTATE!!!

      5 years ago Log in to Reply
    11. Cheryl Seibert

      Medtronic since 2000, just switched to Tandem TSlim with Control-IQ in August 2020.

      5 years ago Log in to Reply
    12. Tim Lors

      1997. I had recently switched from 2 shots a day to MDI, and concluded it gave me much better BG management, but that I needed flexibility in meal timing a a better way to deal with Dawn phenomenon. They shipped the pump to me house and I started using it immediately. At my training session, the doctor was floored that I had been already using it for days. I was floored when I realized he had no clue how to properly set basal rates. At that point, I realized it was up to me to figure out what works for me. I am now on Tandem C-IQ (after a very long hard fight with UHC) and my TIR = 90%.

      5 years ago Log in to Reply
    13. Tim Lors

      How do you edit your post to correct typos? (O prefer the previous format.)

      5 years ago Log in to Reply
    14. Patricia Dalrymple

      Agree with Tim. I answered wrong but no way to edit.

      5 years ago Log in to Reply
    15. Glen Heatherington

      Since 2000. Coming up on 56 years since diagnosis.

      5 years ago Log in to Reply
    16. Tina Roberts

      I answered 20-25 years. That’s wrong and I can’t go back and change it. It’s 14 years. I do not like this new platform. I can’t change my answers and I’m getting double every email and it shows one question then when I select answer it’s an entirely different question!!

      5 years ago Log in to Reply
    17. Molly Jones

      I started pumping about 3.5 years after diagnosis to help with a pregnancy. It had not been suggested previously. Medtronic was the pump I used for more than ten years, then I tried Omnipod, went back to Medtronic and am now on Tandem. I liked Omnipod but it did not have the small amount of doses I needed. I also liked Medtronic’s pump better than Tandem, but because it doesn’t pair with Dexcom I will stay with Tandem.

      5 years ago Log in to Reply
    18. Jillmarie61

      I’ve been pumping since 1978. Where’s my cure? In that amount of time you surely could have found one by now.

      5 years ago Log in to Reply
    19. Jim Witte

      @Jillmarie61 > I’ve been pumping since 1978. Where’s my cure? How many years (decades?) will it take to get through pre-clinical trials with the transgenic pigs? And then how many decades for Phase 1-3 with humans?

      5 years ago Log in to Reply

    For insulin pump users: How long have you worn an insulin pump? Cancel reply

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