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    • 11 hours, 51 minutes ago
      Gerald Oefelein likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I've tried twice and was rejected both times because I control my diabetes as best I can. As others have already stated, if immunosuppressing drugs are involved, count me out. I'm not interested in something worse than what I already have.
    • 11 hours, 51 minutes ago
      Gerald Oefelein likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      Not if it requires immunosuppressant drugs. Been there done that time to move on to something much better.
    • 11 hours, 52 minutes ago
      Gerald Oefelein likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - 👍 immunosuppression needed - 👎
    • 17 hours, 39 minutes ago
      Natalie Daley likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I answered “Very Unlikely” not because I woud not want to participate but because, at age 75, I think it very unlikely that any researcher would want me in their patient panel.
    • 17 hours, 39 minutes ago
      Natalie Daley likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - 👍 immunosuppression needed - 👎
    • 18 hours, 39 minutes ago
      Marthaeg likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - 👍 immunosuppression needed - 👎
    • 18 hours, 49 minutes ago
      kristina blake likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I answered “Very Unlikely” not because I woud not want to participate but because, at age 75, I think it very unlikely that any researcher would want me in their patient panel.
    • 18 hours, 58 minutes ago
      Mike S likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - 👍 immunosuppression needed - 👎
    • 19 hours, 18 minutes ago
      Eve Rabbiner likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I answered “Very Unlikely” not because I woud not want to participate but because, at age 75, I think it very unlikely that any researcher would want me in their patient panel.
    • 19 hours, 21 minutes ago
      Marty likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - 👍 immunosuppression needed - 👎
    • 19 hours, 33 minutes ago
      John Barbuto likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I answered “Very Unlikely” not because I woud not want to participate but because, at age 75, I think it very unlikely that any researcher would want me in their patient panel.
    • 1 day, 14 hours ago
      Kristi Warmecke likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      not for those of moderate income.
    • 1 day, 14 hours ago
      Kristi Warmecke likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I am hopeful- it may not be in my lifetime, but they have already made great strides in the research. The autoimmune response and need for immunosuppressants is still a pretty big sticking point.
    • 1 day, 14 hours ago
      Kristi Warmecke likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      But probably not in my lifetime.
    • 1 day, 16 hours ago
      dholl62@gmail.com likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I don't see how a cure will be possible without islet cells as they are what produce insulin. Using immunosuppressants or not is what will determine what the first "cure" will be like. If safe immunosuppresants are used, then it is actually a "functional cure". If they can infuse islet cells without needing immunosuppressants nor other meds, then I would call it a "cure".
    • 1 day, 16 hours ago
      dholl62@gmail.com likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I am hopeful- it may not be in my lifetime, but they have already made great strides in the research. The autoimmune response and need for immunosuppressants is still a pretty big sticking point.
    • 1 day, 17 hours ago
      Bruce Schnitzler likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I don't see how a cure will be possible without islet cells as they are what produce insulin. Using immunosuppressants or not is what will determine what the first "cure" will be like. If safe immunosuppresants are used, then it is actually a "functional cure". If they can infuse islet cells without needing immunosuppressants nor other meds, then I would call it a "cure".
    • 1 day, 17 hours ago
      Steve Rumble likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I think that a functional cure is the most viable scenario as far as a "cure" is concerned. It seems like the most progress is being made with islet cell therapies.
    • 1 day, 18 hours ago
      Natalie Daley likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I don't see how a cure will be possible without islet cells as they are what produce insulin. Using immunosuppressants or not is what will determine what the first "cure" will be like. If safe immunosuppresants are used, then it is actually a "functional cure". If they can infuse islet cells without needing immunosuppressants nor other meds, then I would call it a "cure".
    • 1 day, 18 hours ago
      Marty likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I am hopeful- it may not be in my lifetime, but they have already made great strides in the research. The autoimmune response and need for immunosuppressants is still a pretty big sticking point.
    • 1 day, 18 hours ago
      Marty likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      But probably not in my lifetime.
    • 1 day, 18 hours ago
      Kathy Hanavan likes your comment at
      If islet cell transplantation is proven safe and effective, how likely would you be to consider it a treatment option?
      Very likely provided immunosuppressants aren't required. Also younger people should receive the treatment first.
    • 1 day, 18 hours ago
      Kathy Hanavan likes your comment at
      If islet cell transplantation is proven safe and effective, how likely would you be to consider it a treatment option?
      as long as it doesn't require immunosuppression, I'm interested
    • 1 day, 18 hours ago
      Kathy Hanavan likes your comment at
      If islet cell transplantation is proven safe and effective, how likely would you be to consider it a treatment option?
      I was going to comment that there's always a trade off. Am I trading insulin replacement with some other daily treatment? If so, what's the difference? Is the new daily grind more harmful than the old?
    • 1 day, 18 hours ago
      Kathy Hanavan likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I am hopeful- it may not be in my lifetime, but they have already made great strides in the research. The autoimmune response and need for immunosuppressants is still a pretty big sticking point.
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    Do you have any programmed diabetes-related “reminders” on your phone or other technology? For example, a reminder to take your long-acting insulin every night at 10 p.m., or a reminder to bolus every day at 1 p.m.?

    Home > LC Polls > Do you have any programmed diabetes-related “reminders” on your phone or other technology? For example, a reminder to take your long-acting insulin every night at 10 p.m., or a reminder to bolus every day at 1 p.m.?
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    If you have experienced severe hypoglycemia that resulted in a loss of consciousness, when was your most recent experience losing consciousness during a low?

    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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    29 Comments

    1. Ahh Life

      Yes. I use that great invention by Ts’ai Lun, a Chinese court official–a technology called paper. Reminds me when 3 days are gone for pump & 10 days for sensor. 🕺

      3
      3 years ago Log in to Reply
    2. Lawrence S.

      No. I use the Tandem X2, Control IQ system with the Dexcom G6 sensor. The sensor and pump do all of the work. I just have to remember to take my insulin bolus before I eat meals. Nice system 🙂

      5
      3 years ago Log in to Reply
    3. Nevin Bowman

      My pump reminds me to change sites.

      1
      3 years ago Log in to Reply
    4. Ginger Vieira

      I would definitely forget to take my once-weekly injection Ozempic if my Amazon Echo didn’t announce it every Sunday night. “Ginger, this is your reminder. Take Ozempic.” It’s critical! :p

      2
      3 years ago Log in to Reply
    5. KIMBERELY SMITH

      Yes

      3 years ago Log in to Reply
    6. Janice B

      0n my Google calendar I have a reminder every 3 days to change pump site and a reminder every 10 days to change Dexcom. Then I have reorder supply reminders every 3 months.

      3
      3 years ago Log in to Reply
    7. Sherolyn Newell

      I like to change pods at around 5:30pm, so on that day I will set an alarm. Otherwise, time gets away from me and I get off schedule.

      1
      3 years ago Log in to Reply
    8. Kathleen Juzenas

      Yes: a reminder every 10 days that my CGM expires

      3
      3 years ago Log in to Reply
    9. Marty

      I have set, cartridge, and sensor change reminders on my laptop Calendar with alerts in addition to the reminders that come from my pump and the Dexcom app on my phone. I also have reminders every 90 days to check on insulin and supplies refills, which are supposed to happen automatically but don’t always. My Calendar also reminds me to make and keep appointments for routine care like labs and annual eye exams. I need all the help I can get keeping track of things!

      3
      3 years ago Log in to Reply
      1. TEH

        90 day event reminder is a great idea! Thanks for the idea! My sensors and pump supplies come at different times.

        3 years ago Log in to Reply
    10. Dennis Dacey

      I allow the two diabetes management devices I wear, t-Slim x2 and Dexcom G6 provide all relevant reminders.
      Tandem built-in reminder system alone is sufficient, providing: G6 expiry countdown [better than Dexcom], site change reminder, reminder if I don’t take a bolus within an hour after “usual” meal-time.

      3 years ago Log in to Reply
    11. Grey Gray

      I have a rise alert on double arrows… that reminds me I forgot to bolus for my carbs. I have alert b4 low alarms that remind me I need to eat. Goin on 40 years with T1D it’s not like I don’t know but I don’t feel the lows till their pretty bad now. And I lost my appetite years ago.

      2
      3 years ago Log in to Reply
    12. Jim Andrews

      I do physical labor during the day which requires a zero basal profile. I have a reninder to turn my “normal” back on.

      2
      3 years ago Log in to Reply
    13. Mike S

      I mark every 10 days for the Dexcom in my calendar so that if I make a plan for that day, I’ll remember to take the new one with me. (I always have a backup omnipod on me, but the Dex is just too bulky to cart around)

      2
      3 years ago Log in to Reply
      1. TEH

        I do that too. I also have a recurring calandar reminder for cartridge/infusion sets for every 2 1/2 days.
        Then adjust it and future entries depending on exactly when i do change.

        2
        3 years ago Log in to Reply
      2. Gerald Oefelein

        I use Google calendar to remind me of site changes (3 days) and sensor changes (10 days).

        3 years ago Log in to Reply
    14. Shelly Smith

      As others have mentioned, my pump does the reminding. The only other part of technology I use for such things is that my pharmacy sends me a text when its time to refill my scripts.

      3 years ago Log in to Reply
    15. Laura G

      The only time I use a phone alarm is to remind me to deactivate daytime “sleep” or “exercise” mode on my Tandem control IQ. Those modes can’t easily be set to last for a select number of hours, so a phone alarm is my hack for remembering to turn them off… Important!

      1
      3 years ago Log in to Reply
    16. Tere North

      I sure used to! Before I got my pump I had 5 alarms each day centered around needing to each since the crossover of long/short insulin was always a problem.

      3 years ago Log in to Reply
    17. Bob Durstenfeld

      My only reminders are from my Dexcom Continuous Glucose monitor and that is plenty.

      1
      3 years ago Log in to Reply
    18. AnitaS

      My pump and CGM will remind me that my insulin has gotten to a low level and also that my CGM sensor or transmitter is about to expire.

      1
      3 years ago Log in to Reply
    19. Lori Lehnen

      When I was on Lantus, I had an alarm on my phone set for 7 am to remind me to take it. Now I use Tresiba for basal which is more forgiving if I’m a little early or late with my dosage, so I’ve removed the electronic reminders and just take it when I wake up.

      3 years ago Log in to Reply
    20. Kelly Wilhelm

      I started setting a daily reminder to check my settings because I often turn off my alarms when I am in meetings, etc. and forget to turn them back on

      2
      3 years ago Log in to Reply
    21. Cheryl Weaver

      I wear an insulin pump and my blood sugars are checked every 5 minutes by Dexcom.

      3 years ago Log in to Reply
    22. Jeff Balbirnie

      Save for the rawest, brad new diabetics, given the time periods long-acting insulins now cover why would such a reminder(s) be necessary? The entire purpose of modern insulins is complete and total flexibility rather than adherence to rigid schedule(s)???

      3 years ago Log in to Reply
    23. Mick Martin

      The regular reminder is set on my pump, a Medtronic 780G, to tell me when I’m due to change my infusion set. (I don’t possess a phone, so I can’t set reminders on that. lol.)

      Pumps work using fast-acting or rapid-acting insulins, so I have no need to have a reminder about taking long-acting insulin.

      I currently have 6 different basal settings that change within a 24 hour period, and should my blood glucose levels ‘stray’ outside of the range that I’ve programmed my pump to ‘stick to’ it does it’s best, using its inbuilt algorithm to maintain those levels.

      3 years ago Log in to Reply
    24. Wanacure

      I note on paper calendar when I can expect to change sensor. I write starting dates of new insulin vials there also.

      3 years ago Log in to Reply
    25. T1D4LongTime

      My insulin pump alerts me of highs and lows as well as delivers insulin when needed, so no need to set any other alarms

      3 years ago Log in to Reply
    26. Velika Peterson

      I set alarms to check bg in the middle of the night if my daughter’s sensor isn’t working well and sometimes when her Dexcom is warming up. Also, sometimes I set alarms for when she can eat after a prebolus, because sometimes we get carried away and she can crash.

      3 years ago Log in to Reply

    Do you have any programmed diabetes-related “reminders” on your phone or other technology? For example, a reminder to take your long-acting insulin every night at 10 p.m., or a reminder to bolus every day at 1 p.m.? Cancel reply

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