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    • 1 hour, 34 minutes ago
      Amy Schneider likes your comment at
      Do you store your unopened insulin in the refrigerator?
      I keep my opened insulin in the refrigerator too. When traveling I use a FRIO evaporative pouch.
    • 3 hours ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      I want a thumbs down icon!
    • 3 hours ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      I seldom have any questions other than RX refill request which I submit through the patient portal. If I do have treatment questions, I typically do my own research, and if not satisfied with what I find out, I submit a question in the portal.
    • 3 hours, 1 minute ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      When I come up with a question between visits, I usually just do some research.
    • 5 hours, 13 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      I keep my opened insulin in the refrigerator too. When traveling I use a FRIO evaporative pouch.
    • 5 hours, 14 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Sorry. Of course I store unopened in frig. Opened in my room as I use it up in 30 days
    • 5 hours, 15 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      No, I keep it in the oven! ;) Same answer as the last time they asked this ridiculous question!
    • 5 hours, 57 minutes ago
      Becky Hertz likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Unopened yes, and now even opened just in case. I am getting a new health [lan (thank goodness a much better one - with better doctors and hospitals in network!) so it's worth it. But I can't get any appt - even for a PCP until September. I've been occasionally buying out of pocket insulin, pump and CGM supplies (in my mind, hoarding is a character asset for T1D people). I need to have my enough stuff to see me through, Of course, I am hoping there''s an appt cancellation.
    • 7 hours, 20 minutes ago
      Bruce Schnitzler likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Unopened yes, and now even opened just in case. I am getting a new health [lan (thank goodness a much better one - with better doctors and hospitals in network!) so it's worth it. But I can't get any appt - even for a PCP until September. I've been occasionally buying out of pocket insulin, pump and CGM supplies (in my mind, hoarding is a character asset for T1D people). I need to have my enough stuff to see me through, Of course, I am hoping there''s an appt cancellation.
    • 9 hours, 17 minutes ago
      alex likes your comment at
      Here’s What You Need to Know About the Dexcom G7
      This article explains the Dexcom G7 features in a clear and easy way, especially for people new to continuous glucose monitoring. Very informative and helpful. Sportzfy TV Download
    • 1 day ago
      KarenM6 likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      Long time ago - told there were certain occupations I would not be allowed to do because if T1D. Pilot, air traffic controller, military, etc.
    • 1 day ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I have been told many times "YOU CAN'T EAT THAT!" ONLY to frustrate them and eat it anyway and then bolus accordingly.
    • 1 day ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I think it is a common experience for most people with T1D. People do not understand anything about it. I do not take it personally. I try to educate when appropriate.
    • 1 day ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Lol hell when haven't they. Lol
    • 1 day ago
      KarenM6 likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day, 2 hours ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was only 2 when Diagnosed 70 years ago. My small town doctor admitted he didn't know much about T1D, and fortune for my parents and I he called what is now Joslin Clinic, and they told him how much insulin to give me. He taught my parents, who then traveled over 350 miles to Boston, to learn about how to manage T1D. My doctor learned more about T1D, and was able to help 2 other young men, that were later DX with T1D in our small town. I went to Joslin until I turned 18 and returned to become a Joslin Medalist and participated in the research study, 20 years ago. Still go there for some care.
    • 1 day, 2 hours ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was 7 when things changed in my home. My older brother was hospitalized for 2 weeks. When he came home, we no longer ate the way we had before. This was 1956. Dessert alternated between sugarless pudding or sugarless Jello. I learned that bread and potatoes had carbohydrates and that turned to sugar. There was a jar in the bathroom. It seemed my brother was testing his urine every time he went in there. There was a burner and pot on the stove designated for boiling syringes. I watched my brother give himself shots and I remember how hard it was to find someone to manage his care if my parents had to travel. Diabetic Forecast magazine came in the mail each month and there were meetings of the local diabetes association that my mother attended religiously. My brother got a kidney and pancreas transplant at age 60 and before he died lived for 5 years as a non-diabetic. A few years later I was diagnosed. Sorry he was not able to make use of today’s technology. I often wonder what he and my late parents would think about me, at age 66, being the only one in the family with type 1.
    • 1 day, 2 hours ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day, 6 hours ago
      kilupx likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      My brother was type 1 since an early age. I was only diagnosed in my late 40s
    • 1 day, 8 hours ago
      Phyllis Biederman likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Absolutely nothing. Diagnosed in late December 1962 at at the age of 8 years and was told I was going for a stay in hospital because I have "sugar diabetes".
    • 1 day, 9 hours ago
      Bill Williams likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day, 9 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was diagnosed in 1976 at the age of 18 while in college. One weekend, I was drinking a lot of water and peeing frequently. I remembered having read a Reader's Digest article on diabetes, and I told my friends I thought I might have it. Two days later, the diagnosis was confirmed.
    • 1 day, 10 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Absolutely nothing. Diagnosed in late December 1962 at at the age of 8 years and was told I was going for a stay in hospital because I have "sugar diabetes".
    • 1 day, 10 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I knew I couldn’t or shouldn’t have my two fav things in the world: Pepsi cola and chocolate. I was 42, and suspected very strongly that I had it, and ate a large piece of chocolate cake before my doctor’s appointment (sounds more like I was 12). Fast forward 25 years later: I never had a real cola again, but do occasionally have chocolate. I’m way healthier than I was back then in terms of diet. I no longer have irritable bowel, and I’m lucky to be able to afford what I need to combat the ill effects of this chronic disease. I’m blessed, and grateful for insulin.
    • 1 day, 10 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      It was 35 years ago for me. I had no experience with T1d. I was starting to show symptoms and my sister-in-law quickly researched T1d and told me what she found. I went to my GP a week or two later. My BG was over 600. He sent me to the hospital right away. Blood test confirmed it.
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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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    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
      2 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
      2 years ago Log in to Reply
    3. Nevin Bowman

      My pump reminds me to change sites.

      1
      2 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
      2 years ago Log in to Reply
    5. KIMBERELY SMITH

      Yes

      2 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
      2 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
      2 years ago Log in to Reply
    8. Kathleen Juzenas

      Yes: a reminder every 10 days that my CGM expires

      3
      2 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
      2 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.

        2 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.

      2 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
      2 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
      2 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
      2 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
        2 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).

        2 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.

      2 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
      2 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.

      2 years ago Log in to Reply
    17. Bob Durstenfeld

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

      1
      2 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
      2 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.

      2 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
      2 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.

      2 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)???

      2 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.

      2 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.

      2 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

      2 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.

      2 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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