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    • 9 hours, 54 minutes ago
      ConnieT1D62 likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I usually bolus for breakfast right at the time I start eating. But I prefer to bolus 15 minutes before. Better results. But I always forget.
    • 11 hours, 50 minutes ago
      KarenM6 likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I said 15-30, but it may have been more than 30. I wasn't watching the clock this morning. I just checked my pump bolus history. It was about 30 minutes. I need to bolus early in the morning because my blood sugars shoot up high after breakfast. Bolusing sooner seems to help keep my BG from going off the charts. But, if I bolus too soon, I have serious low BG's. It's all an art ... and luck.
    • 11 hours, 53 minutes ago
      KarenM6 likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I am able to pr bolus for Breakfast and dinner as I am at home. I never know when I am going to eat at work so bolus is at start of meal.
    • 14 hours, 44 minutes ago
      Mick Martin likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      Question is misleading until type of insulin is understood. I said 15 because I use Fiasp insulin.
    • 15 hours ago
      Kris Sykes-David likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I said 15-30, but it may have been more than 30. I wasn't watching the clock this morning. I just checked my pump bolus history. It was about 30 minutes. I need to bolus early in the morning because my blood sugars shoot up high after breakfast. Bolusing sooner seems to help keep my BG from going off the charts. But, if I bolus too soon, I have serious low BG's. It's all an art ... and luck.
    • 15 hours, 57 minutes ago
      Ernie Richmann likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I said 15-30, but it may have been more than 30. I wasn't watching the clock this morning. I just checked my pump bolus history. It was about 30 minutes. I need to bolus early in the morning because my blood sugars shoot up high after breakfast. Bolusing sooner seems to help keep my BG from going off the charts. But, if I bolus too soon, I have serious low BG's. It's all an art ... and luck.
    • 16 hours, 18 minutes ago
      Robin Melen likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      My most recent meal was breakfast and, during the work week, I am far better at bolusing ahead of time. The rest of my meals in the day though end up receiving the bolus as I start eating or part at the start and more later on (depending on what I am eating and whether I know how much I'll eat.)
    • 1 day, 11 hours ago
      KarenM6 likes your comment at
      Of the people in your life, who (if anyone) makes you feel judged or criticized for your T1D management (for example, what foods you eat, where or when you check your blood glucose, etc.)? Select all that apply to you.
      Insulin, meters, diabetic tech are not magic wands. Its usage does not guarantee only "positive" results. Negative events can and do occur, period. Non -D- typically (incorrectly) equate negative events as being total user failure, severe user errors. As diabetics we get blamed, despite having made zero mistakes on our part. We make seriously educated best guesses, despite that truth, we can and do fail anyway sometimes! Outsiders falsely need to believe inulin, our tech are complete-total cures, rather than tiny bandages at best. When confronted for using (sic. my) "drugs" in public, no matter how invisibly done... it is their self righteousness , poor assessment which is the issue. I gladly squash such insects...
    • 1 day, 16 hours ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      The more important question is 'how well does the clip work'. For me, the Medtronic clip worked very well, but the Tandem clip is quite ineffective and the pump falls off my belt during things like yard work or other bending movements.
    • 1 day, 16 hours ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      I answered never. I always use a clip -- I wear my t:slim x2 on my belt -- but not the Tandem clip. I use the black t:Holster Rotating Belt Clip. Very pleased.
    • 1 day, 16 hours ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      I am rough on pumps and use a Tandem X2 but dont use the Tandem clip/holster. I use a neoprene case and a pouch with a metal clip. Thenmetal clip is uncomfortable while I sleep. Looking for a different solution for wearing my pump at night.
    • 2 days, 12 hours ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I answered that nobody wants to be screened, but I was answering based on my immediate family. I did let my deceased type-1 diabetic cousin's 35 year old son know he can be tested for his likelihood of becoming type-1 diabetic. He said he may be tested as he was always curious if he had a chance.
    • 2 days, 12 hours ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I have T1, and when my oldest grandson got T1, the other 3 grandkids got screened. The grandson who's the brother of the one with T1, showed a strong possibility of being a future T1 diabetic. It sadly came true about a year later.
    • 2 days, 13 hours ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I have LADA, and the idea of screening has not come up, either by me or my adult children. I guess I need to present the opportunity to them so they can make the decision.
    • 2 days, 13 hours ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 2 days, 16 hours ago
      Samantha Walsh likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I was born in 1939 and had many childhood illnesses. Three different kinds of measles and tonsils removed before I was 5 years old, then mumps and chickenpox when I was 5. While recovering from the mumps and chickenpox, I began showing the symptoms of very high blood sugar. Three doctors examined me and they were not able to make a diagnosis. I had lost much weight, and I had stopped eating. I did not have an appetite. It was almost impossible for me to walk. A fourth doctor had my blood tested and he made the diagnosis. While receiving pork insulin I finally began to recover a few days after my sixth birthday. I did not have ant relatives with diabetes. I think the childhood diseases caused internal damage and that was the cause of my diabetes. At the present time there are still no type one diabetics among my relatives. I do not believe it is necessary for my children and grandchildren to be screened for T1D autoantibodies.
    • 3 days, 11 hours ago
      KarenM6 likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 3 days, 13 hours ago
      Katie Bennett likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 3 days, 13 hours ago
      Kate Kuhn likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 3 days, 14 hours ago
      Karen DeVeaux likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I was born in 1939 and had many childhood illnesses. Three different kinds of measles and tonsils removed before I was 5 years old, then mumps and chickenpox when I was 5. While recovering from the mumps and chickenpox, I began showing the symptoms of very high blood sugar. Three doctors examined me and they were not able to make a diagnosis. I had lost much weight, and I had stopped eating. I did not have an appetite. It was almost impossible for me to walk. A fourth doctor had my blood tested and he made the diagnosis. While receiving pork insulin I finally began to recover a few days after my sixth birthday. I did not have ant relatives with diabetes. I think the childhood diseases caused internal damage and that was the cause of my diabetes. At the present time there are still no type one diabetics among my relatives. I do not believe it is necessary for my children and grandchildren to be screened for T1D autoantibodies.
    • 3 days, 14 hours ago
      Kelly-Dayne likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 3 days, 15 hours ago
      William Bennett likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 3 days, 16 hours ago
      Jneticdiabetic likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I have led a team for the JDRF OneWalk annually since the late 1990's. We have been able to raise a lot of funds for JDRF...and I have enjoyed doing it. Good cause!
    • 3 days, 16 hours ago
      Lawrence S. likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      my siblings & parents are older (like me) and they've never expressed any interest in getting tested. my nieces and nephews have never said anything either
    • 4 days, 3 hours ago
      Karen Newe likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I participated in several ADA walks not long after being Dx with T1D. As Ahh Life points out large $ are rased, but where do they go? I stopped supporting ADA for that reason. I think JDF is much more open on where the funding goes.
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    If you wear an insulin pump, how do you decide how much insulin to fill it with during a site change?

    Home > LC Polls > If you wear an insulin pump, how do you decide how much insulin to fill it with during a site change?
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    Sarah Howard

    Sarah Howard (nee Tackett) has dedicated her career to supporting the T1D community 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 Manager of Marketing at T1D Exchange. Sarah and her husband live in NYC with their cat Gracie. In her spare time, she enjoys doing comedy, taking dance classes, visiting art museums, and exploring different neighborhoods in NYC.

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    22 Comments

    1. Bob Durstenfeld

      I put about 240 units in the pump. it takes about 20 units to fill the tubing and I run it until the ALARM tells me I need to refill it, usually, 3-4 units left. I wear my sites for about four days.

      3 years ago Log in to Reply
    2. LizB

      I fill the reservoir completely and keep using it until it is empty, but I change the set every 3 days.

      3 years ago Log in to Reply
    3. Ahh Life

      I fill with same amount, approx. 120 units for a 72 kg retired person changing out every 3-1/2 days. How anyone plans for the next 3 days is unfathomable to me. The difference between plans and real life is that with plans we can set the parameters as if they are known. In real life, these parameters are as clear as mud. ✍( ͡❛ ͜ʖ ͡❛) ( ͡❛ ͜ʖ ͡❛)👎

      3 years ago Log in to Reply
    4. Clare Fishman

      I put the same amount in my pod every time. It is enough for 80 hours which is the maximum lifespan of a pod. If there is some left in it I don’t stress about it. If it gets low at the end I will bolus with a pen instead of changing it early.

      3 years ago Log in to Reply
    5. Sherolyn Newell

      My pods require 80 units to work. I usually put in 85 to 95. Normally, that lasts 3 days easily. There are exceptions when I use more, usually holidays, but I have never totally run out. I think my lowest was about 7 units left when I changed it. I think I’m on year 8 of a late onset of Type 1. I have had to increase my carb ratio a bit once, but so far, I am still pretty sensitive to the insulin.

      3 years ago Log in to Reply
    6. Jeannie Hickey

      I’m with Liz B, fill Medtronic full and change site every 2.5 days. Insulin is fine, saves insulin in tubing and time!

      3 years ago Log in to Reply
    7. Gene Maggard

      My Medtronic pump reservoir holds 300 units which I fill to the max each time. Based on my typical usage this lasts me from 4 to 4-1/2 days. Occasionally it begins to lose its potency but if that happens I change it early.

      3 years ago Log in to Reply
    8. David Smith

      I’m a Medtronic Minimed 670G user, and I was surprised at how many people fill their pump reservoirs with less than the max amount of insulin it will hold. Trying to match the amount of insulin in the reservoir to the amount of time you plan to keep a new cannula in place seems like a lot of extra work. And what if you have to change the cannula earlier than expected? Much easier to just fill up the reservoir and continue using it until it’s empty, plugging the tubing into new cannulas when you change them. In over 20 years of doing that, I’ve never had a problem.

      3 years ago Log in to Reply
    9. Amanda Barras

      I use 120 U a day so I have to max fill and then refill at day 2 to get to day 3.

      3 years ago Log in to Reply
    10. George Lovelace

      My Tandem I fill with 2.75 ml. which lasts about 5 days. I never consider Site Change or Tubing Change, each part is changed when needed.

      3 years ago Log in to Reply
    11. Thomas Hatton

      I fill my resivor to about 220 units. This gives me 5 complete draws from one vial. The problem with drawing the full 300 units is the left over after the 4th draw. What do we do with that?

      3 years ago Log in to Reply
    12. Grey Gray

      I use to max fill every time. But now fill for normal 3 day requirements. After many years of wondering I am now sure that insulin in a pump loses potency quickly in the south Florida sun

      3 years ago Log in to Reply
    13. Abigail Elias

      Generally the same amount but with adjustments, such as whether I have or have not yet boluses from breakfast, or taking into account likely exercise or other physical activities. If I end up with too much, I delay my pump change by a 1/2 day and adjust the next fill upward a bit so that I stick as closely as possible to 3 days.

      3 years ago Log in to Reply
    14. Sally Numrich

      I use about 25 units per day, so I get just over 3 days. So I change every 3 to 3 1/2 days. But of course it depends on what I am eating. Some days need more insulin like pizza or burgers & fries!

      3 years ago Log in to Reply
    15. Becky Hertz

      I fill mine with the max amount (300). I do use quite a bit of insulin. It usually lasts 3-4 days, but as I use a steel needle I usually change my site after 2 days (out when my site starts hurting or not absorbing).

      3 years ago Log in to Reply
    16. Greg Felton

      I try to squeeze every last drop out of that cartridge!

      3 years ago Log in to Reply
    17. Lori COLLINS

      I fill my MiniMed 770G cartridge to capacity & just plug the same tubing into a new infusion set every few days. I use relatively little insulin so a 300 ml cartridge lasts 13 – 15 days. I’ve been doing it this way since I got my first insulin pump 25+ years ago. I live on Florida’s Gulf Coast and have never had a problem w/ insulin losing potency either from heat or hanging out in my pump for two weeks. For me, unexpected highs usually mean it’s time for a site change.

      3 years ago Log in to Reply
    18. Robert Brooks

      My endocrinologist mentioned a study that showed that by the third day in a pump resting against a 97.6-degree body, the insulin is about 23% less active than it is initially. This is a reason to load a cartridge with what you will use up in three or three and a half days.

      3 years ago Log in to Reply
    19. Nick Trubov

      Currently I don’t use a pump, but when I did I filled it with the maximum amount that the cartridge would hold.

      3 years ago Log in to Reply
    20. Lenora Ventura

      Filling my cartridge is an independent task from changing my infusion site. When the current cartridge runs out, I start over with a full, new cartridge.

      3 years ago Log in to Reply
    21. Mary Ann Sayers

      I liked Robert’s answer re: body temp. Mine is around 96, and I fill the “cartridge” a little above 1.5 which lasts me 3 and a half days. I KNOW I’m supposed to change it EVERY THREE DAYS, but I’ve let some activites get in the way of taking care of taking of me!!! I plan on recharging my battery on time!

      3 years ago Log in to Reply
    22. Cheryl Seibert

      I look at the next 3 to 4 days schedule and then decide how much to load. I prefer to change the Tandem cartridge along with the infusion site, although I could fill the entire cartridge and only change the infusion site. My preference is to change the cartridge at home so if I’m away from caregiving my sick relative, I load more to get through until I’m back home.

      2 years ago Log in to Reply

    If you wear an insulin pump, how do you decide how much insulin to fill it with during a site change? Cancel reply

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