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    • 14 hours, 37 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.
    • 14 hours, 39 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.
    • 14 hours, 40 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.
    • 14 hours, 41 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
    • 14 hours, 49 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 ´ )⎠⎞
    • 16 hours, 41 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.
    • 16 hours, 42 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.
    • 16 hours, 44 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 ´ )⎠⎞
    • 20 hours, 45 minutes 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
    • 22 hours, 47 minutes 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".
    • 23 hours, 32 minutes 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 ´ )⎠⎞
    • 23 hours, 56 minutes 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.
    • 23 hours, 57 minutes 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".
    • 23 hours, 57 minutes 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.
    • 23 hours, 58 minutes 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.
    • 23 hours, 58 minutes 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 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 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 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 ´ )⎠⎞
    • 1 day ago
      ConnieT1D62 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 ago
      eherban1 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, 12 hours ago
      NANCY NECIA 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, 15 hours ago
      Anita Stokar likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I won't use the word "diabetic" as a noun. It's as simple as that, an adjective, yes. I didn't refer to a good friend with MS as a "sclerotic". When I was working with first responders, I tried to remember to say "schizophrenia is involved", or "there's alcoholism at play here".
    • 1 day, 15 hours ago
      Anita Stokar 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, 15 hours ago
      Anita Stokar likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      No one has said (in seriousness) you can't eat that, but I have gotten the question "Can you eat that?"
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    If you use an insulin pump, which of these options best describes when you most often change your pump site?

    Home > LC Polls > If you use an insulin pump, which of these options best describes when you most often change your pump site?
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    At your current job (or most recent, if you are not currently working), do the coworkers with whom you regularly interact know you have T1D?

    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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    31 Comments

    1. Carol Evans

      My response was “other.” I only use 25 units of insulin a day, so I fill the reservoir (Tandem x-slim) with a week’s worth of insulin, but I change my infusion site every three days. I have been doing this for years with no issues. Medicare makes me get infusion sets and cartridges in the same quantity, even though I only need half the number of cartridges. I won’t enumerate the waste and cost of this system. Medtronic sells infusion sets without the tubing for exactly my situation, but Tandem has decreed that everyone must change out the cartridge every three days.

      1
      2 years ago Log in to Reply
      1. Marty

        I change my infusion set every 2-3 days after I exercise and shower, late morning or early afternoon. I fill my cartridge every 5-6 days at the same time as I switch sets. Somehow, I don’t have any problem getting the right number of sets and cartridges for my routine even though Medicare pays for them. Maybe it has to do with the way my endo writes my prescriptions.

        2 years ago Log in to Reply
    2. terrih57@msn.com

      No specific routine but I prefer earlier in the day when reservoir gets low

      1
      2 years ago Log in to Reply
    3. Greg Felton

      No routine – whenever the reservoir is low and the time is convenient. I used to have a set evening time but now that I can see an accurate number of insulin units left, I try to use it up. In fact, I’m so reluctant to waste insulin that before changing my site I will often eat something and bolus for it, even when I’m not hungry, just to use those last few units of insulin!

      2
      2 years ago Log in to Reply
      1. TEH

        💯
        Totally agree!

        2 years ago Log in to Reply
      2. Jennifer Bounds

        I’ve do the same thing if needed. Insulin is so expensive!

        2 years ago Log in to Reply
      3. ConnieT1D62

        We all have our quirks!

        2 years ago Log in to Reply
    4. Janice Bohn

      Start of my day which means I am woken up every 3 days at 3:30am by the reminder alarm around

      2 years ago Log in to Reply
    5. Daniel Bestvater

      I change my infusion set(steel) every 1-3days depending on how it is working. I change my insulin cartridge (Tandem X2) every 7-12 days. Depending on my activity level I use 15-25 units of insulin per day.

      2
      2 years ago Log in to Reply
    6. T1diabetic

      I don’t change sites until my reservoir is empty.

      2 years ago Log in to Reply
    7. stillarobyn

      Because I need to calibrate it so many times the first day, I do it as early in the day as possible.

      2 years ago Log in to Reply
    8. Joan Benedetto

      I answered end of day, but my son showers before dinner, and charges his pump then. After showering, he changes his pump site so that we know it’s working well before bed.

      1
      2 years ago Log in to Reply
    9. Jennifer Bounds

      No specific routine but also if I have any insulin left in the reservoir I’ll keep the pump on for the allotted up to 8hrs that my pump allows so not to waist the insulin.

      2
      2 years ago Log in to Reply
    10. Sherolyn Newell

      My pods expire every three days with several hours of grace period before they stop working. At the beginning, I picked a time of day when I am usually home, so around 5:30. Sometimes it’s later, but then I try to get back to my regular time.

      2 years ago Log in to Reply
    11. KIMBERELY SMITH

      On through the day

      2 years ago Log in to Reply
    12. Mig Vascos

      I don’t have a special time or a especial number of days. If it’s the site is working I might let it be up to the 4th day. If it’s not I might have to change it more often.
      After many years of injections I’m sure I have a lot of scar tissue even though not visible but many times the site just doesn’t absolve week enough to keep my BG where I want them.
      The tandem pump is great but it’s infusion sets really suck. All pumps give you a diagram of all the places you could input a set but in reality can you? No. The connection is not easy to hook up unless you can see and align the trident with the openings. So the back is out. If you’re a side sleeper can you lay on the site all night without getting bruises? can you use your arms if you do a lot of exercises and play sports? And so the list goes on.
      I visited my nurse practitioner who helps
      Me
      Manage the pump and she changed the correction feature on my settings and it seems to be working better. Now when the Control IQ is trying to keep my highs it’d be given more insulin and it’ll work faster. This way I might be able to avoid trying to do the corrections myself by bolusing and ended up with a low 2 or 3 hours later.
      Another problem as someone else mentioned is MEdicare and the rule that you have to get the same amount of infusion sets as of cartridges and syringes. It’s a complete absurdity.

      1
      2 years ago Log in to Reply
      1. Mig Vascos

        Meant to say “the site doesn’t absorb well.

        2 years ago Log in to Reply
      2. Marty

        I’m on Medicare but I get more sets than cartridges with no problem.

        2 years ago Log in to Reply
    13. Trina Blake

      I change my infusion set evrey 3 days – although the time of day varies with my schedule. I fill the cartrdge to the full 300 units, and change it when it is empty. Again, since my schedule is so varied I wouldn’t dare to try to come up with a 3-dyas-worth of insulin to change both out every 3 days. There are days when I don’t eat anythng but a small green salad for lunch and nothing else, days when I am very physically active, and dyas that my work requires sitting at the desk for 12+ hours. So insulin requirements vary greatly.

      1
      2 years ago Log in to Reply
      1. Trina Blake

        Adding, that since I am not qualified for Medicare, I can order just infusion sets which I do about every other order.

        2 years ago Log in to Reply
    14. Donald Cragun

      I change my infusion set just before I take a meal bolus (usually for breakfast).

      2 years ago Log in to Reply
    15. Becky Hertz

      No specific routine. When the site goes bad, after a certain amount in insulin has been infused, when the reservoir runs out, when I won’t make it through the night with what insulin is left, painful site.

      1
      2 years ago Log in to Reply
    16. Louise Robinson

      I’m retired. so have greater flexibility in my schedule. Because I have high insulin sensitivity and am required to load my Tandem t:slim X2 cartridge with more insulin than I will use in 3 days, I tend to change my cartridge when it runs out but will change my infusion site every 3 days or sooner rather than doing both at the same time. Otherwise, too much insulin is wasted.

      1
      2 years ago Log in to Reply
    17. William Bennett

      One thing I liked about my old dumb Paradigm pump was that you could choose to have the low reservoir alert go by time rather than units remaining. With an AID pump that’s more of a moving target, but with an old dumb pump it would just calculate out your basal rates. I found if I set it to 12 hrs I’d usually get warned during normal waking hours rather than the 3am pumps would just natural prefer. “Hey, if I’m not jerking you out of a deep sleep how do you know I care?”

      2 years ago Log in to Reply
    18. Chris Albright

      I found that it is never good to change anything (as it relates to diabetic medical devices late in the day…….. ) I like time to ensure everything is working right so earlier is better. I also leave my existing infusion set in place in the event that I need to go back to a known working site. Once the new site is verified, I remove the old set.

      1
      2 years ago Log in to Reply
    19. Stephen Woodward

      What does a resevoir amount have to do with site changes. There is no clinical reason I’ve found or studies to that say that you have to change site and resevour at the same time. Never done that in over 25 yrs of pump use. Why do T1Ds get told this, it’s not written in the pump guides.

      2 years ago Log in to Reply
    20. Carol Meares

      The pump runs me most of the time. I sometimes run it beyond the specified expiration if I am still getting good numbers. Sometimes I will change early if my daily plans will not coincide conveniently. Mostly I just change when it says to change, or close.

      1
      2 years ago Log in to Reply
    21. T1D4LongTime

      I chose: “No specific routine – whenever the site expires or the reservoir is too low”. However, I also look at my schedule for the next 24 hours. If I have an early morning, I will try to extend the site till later the next day or change it after supper. I don’t like to change right before bed nor when I need to leave home immediately after the change.

      2 years ago Log in to Reply
    22. Bill Kast

      I use an omnipod from Insulet. There is a hard failure wired into the electronics at the end of 3.00 days plus 8 hours. At that point the pump, and the injection point, stop working and the pump starts to squawk loudly. Because I am on medicare, I pay for my pump out of pocket. I usually try to utilize every moment of my allotted time with the pump. I end up being a slave to a sliding time-of-failure that is usually inconvenient for me.

      2 years ago Log in to Reply
      1. Teresa Schnoor

        Same here, I like to get every minute.

        2 years ago Log in to Reply
    23. KSannie

      I do it either 2 hours before lunch or supper, so I have a follow up period to make sure the set is working. (I am not up early enough before breakfast to do it 2 hours before.) And then a follow up period of a couple hours after the meal to make sure it handles the meal before going to bed. Which time I choose depends on where I am and what is scheduled. If I have a class two hours before lunch, I will do it 2 hours before supper. If I have a late afternoon dental appointment, I will do it before lunch. And so on.

      2 years ago Log in to Reply

    If you use an insulin pump, which of these options best describes when you most often change your pump site? Cancel reply

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