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    • 16 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.
    • 17 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
    • 17 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!
    • 1 hour 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.
    • 2 hours, 23 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.
    • 4 hours, 20 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
    • 19 hours, 43 minutes 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.
    • 19 hours, 45 minutes 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.
    • 19 hours, 46 minutes 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.
    • 19 hours, 47 minutes 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
    • 19 hours, 55 minutes 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 ´ )⎠⎞
    • 21 hours, 47 minutes 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.
    • 21 hours, 48 minutes 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.
    • 21 hours, 50 minutes 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, 1 hour 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, 3 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, 4 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, 5 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, 5 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, 5 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, 5 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.
    • 1 day, 5 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I only knew a little . That is why I give grace to others who do not know anything or have misconceptions.
    • 1 day, 5 hours ago
      Lawrence S. 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, 5 hours ago
      KCR 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, 5 hours ago
      Gary R. 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 ´ )⎠⎞
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    If you wear a pump or CGM, when in your daily routine do you prefer to change your sites/sensors?

    Home > LC Polls > If you wear a pump or CGM, when in your daily routine do you prefer to change your sites/sensors?
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    If you wear a pump or CGM, do you usually change your site or sensor around the same time of day?

    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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    24 Comments

    1. Molly Jones

      I wish I could check my accuracy of CGM while sleeping or that eating did not interfere with setting up my CGM. I am grateful for it’s existence though.

      5 years ago Log in to Reply
    2. Greg Felton

      The good advice is to never change a pump site before bedtime, and if you change a CGM at the same time, never before a meal. Do I always follow this? No. I will swap out a pump site and CGM at 8 pm now and then. I have a BG meter and syringe available in case.

      5 years ago Log in to Reply
    3. Dennis Pataniczek

      I change when the device calls for it—when the insulin runs out in the case of the pump, and in the case of the CGM, when the sensor time period is up.

      5 years ago Log in to Reply
    4. Sherolyn Newell

      When I first started on pump and Dexcom, I picked a time when I am usually at home and not busy and started the first one then. That way the Omnipod/Dexcom always expires when it’s usually a good time to start another one. Doesn’t always work perfectly, but it’s been close.

      5 years ago Log in to Reply
    5. Jose Almodovar

      After a shower, Early, Mid morning, afternoon after work under the current COVID-19 environment.

      5 years ago Log in to Reply
    6. Gene Maggard

      A better question would have been “when is the worst time to change . . .” I don’t like changing an infusion set at bedtime in case the site isn’t a good one. I’ve had occasions where the cannula hits a piece of scar tissue or other impediment and the insulin doesn’t flow correctly. However, any other time of the day is fine. For the CGM, I like to change it when my blood sugar is least prone to jumps. So I don’t do the changeover right after a meal, for example.

      5 years ago Log in to Reply
    7. Tod Herman

      My CGM is changed in the morning every 10 days. The insulin pump is changed when it runs out which varies depending on a variety of circumstances.

      5 years ago Log in to Reply
    8. Alexandra Johnson

      Pump site= when insulin runs out CGM= Anytime during the day

      5 years ago Log in to Reply
    9. Diana Kasbaum

      I change both my pump reservoir and CGM whenever they run out or expire. Because the CGM is specifically timed, it’s in the evening, so that the 2 hr start is done before going to bed.

      5 years ago Log in to Reply
    10. Lynn Green

      This is a second question where you’re lumping CGM and pump sites changes together (10 days vs. 2-3 days?). The timing and preference of each type of site change is different to me. I rarely do both at the same time.

      5 years ago Log in to Reply
    11. Thomas Hatton

      I agree with others here. I change my pump infusion site when the insulin runs out usually. I will reload the resivor and reinstall the new infusion set before the resivor runs out if insulin would run out overnight or during a time when I can’t reset the pump, like driving. Insulin is too expensive to throw away if I can avoid it. And with my CGM sensor, i like to do it in the morning so I can get the “warmup” complete. Sensors are also too expensive to throw away.

      5 years ago Log in to Reply
    12. Maureen Helinski

      Sensor in the evening so I don’t have to worry about eating and bolusing. Site in the morning because then I can watch the effects, maybe go a little low.

      5 years ago Log in to Reply
    13. Dave Barden

      No CGM, pump only. I used to always change the canula and reservoir at the same time. When the insulin ran out. That meant the canula sometimes stayed in place a day or so longer than recommended. Lately I’ve been changing the canula site when the pump tells me to, but not the res, that I change only when empty and will refill it even, in order not to waste the 20-30 units of insulin in the tube n res, or if it will run out in the middle of the night.

      5 years ago Log in to Reply
    14. Eve Rabbiner

      Insulin site: change whenever it’s close to out. Rarely have a problem. CGM: change it in the morning since after warming up it often goes nuts and sends out non-stop alerts that would make sleeping impossible. By dinner time it straightens itself out. Dexcom support reassured my not to be concerned, this is not unusual.

      5 years ago Log in to Reply
    15. Nicholas Argento

      I agree with at least one other that grouping CGM and pump sites is not a good idea because they are on differnt schedules and serve different functions. I prefer Dexcom CGM early evening so the countdown warnings don’t awaken me. I wish I could shut those off entirely, or make them silent. For pump, I change in the AM so I can see that it is working well in the day, not at night. Bad site would escape detection longer. I see many people commenting that they change the site when the pump runs out of insulin. I am not crazy about this approach for several reasons- 1) some who do this leave them in longer than the site is still absorbing well, leaving a period of high blood sugars- I see this in downloads all the time; 2) it might run out at night, then there is a risk of delayed change and high BG levels; 3) Insulin in a reservoir can be removed if you don’t want to lose insulin, or figure out how much you need for the period you find good function (number units per day x days + number needed for priming + some extra), understanding that 20 + units is not counted in T-Slim.

      5 years ago Log in to Reply
    16. AIMEE MCGUIRE

      I change them when they expire or if close to expiration and I am not going to be home when they do expire.

      5 years ago Log in to Reply
    17. connie ker

      This question is very similar to yesterdays question. I change the 14 day Freestyle Libre when it times out, or when it becomes loose, or when it stops reading accurately, or when it quits reading and tells me to change. It is never the same time, same day, or same reason. Sometimes it goes for 14 days and I change when it prompts me to change sensors.

      5 years ago Log in to Reply
    18. Carol Meares

      I change infusion sets when I have the time, or if they pull out every 2-3 days. I change CGM when it expires or shortly thereafter, sometimes before when it is too late in the evening because I like to be receiving readings before I go to sleep.

      5 years ago Log in to Reply
    19. Ceolmhor

      I didn’t notice, when I answered this, that you seem to be asking about both sensors and infusion sets. My answers to those are very different. I tend to change sensors in late morning. I like it to be as far as possible away from bedtime, so the sensor will stabilize a bit and let me sleep. But I also want the old sensor still working while I exercise, so on sensor days I have breakfast, then exercise, then change sensors. On the other hand, I change infusion sets just before I go to bed. No special reason for that, though.

      5 years ago Log in to Reply
    20. Donald Cragun

      I change sensors two to three hours after dinner (so it is stable before I go to bed and so I can still see any changes in levels after dinner). When possible, I change infusion sets just before a meal bolus.

      5 years ago Log in to Reply
    21. Steven Gill

      Although I indicated “it doesn’t matter,” I wait until l have less than 5-6 units in my cartridge. If it’s in the morning I’ll change it than, in the evening than. If l start the day with less than 20 units will carry a prefilled cartridge, switch it out appropriately. Generally at lunch although there’s been times I’ve just taken a break and switched cartridges as needed (follow all the steps except inserting another insert). But I’m using 38 units a day, this may not work for others.

      5 years ago Log in to Reply
    22. Janis Senungetuk

      I don’t change them at the same time. My CGM expires every 10 days at approximately 10:30 am. I try to apply a new sensor at that time. I change the pump when the cartridge has less than 16 units of insulin left, but aim for early afternoon because I want time before dinner to make sure it’s working correctly. I don’t keep a riding schedule because my activities change during the week and I want it to be a convenient time for me.

      5 years ago Log in to Reply
    23. Ahh Life

      No preference. You can advise and advise and advise, but, as one person said, “When the devil calls for it . . .” Oops, sorry. When the device calls for it, you do it 😘😘

      5 years ago Log in to Reply
    24. Megan L

      Pump- whenever it either tells me it’s out of insulin (I know that’s bad; sometimes I just forget it told me there’s only 10 units left). CGM – usually in the morning so it’s done calibrating completely by the time I go to bed.

      5 years ago Log in to Reply

    If you wear a pump or CGM, when in your daily routine do you prefer to change your sites/sensors? Cancel reply

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