Subscribe Now

[hb-subscribe]

Trending News

T1D Exchange T1D Exchange T1D Exchange
  • Activity
    • 1 hour, 18 minutes 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!
    • 1 hour, 19 minutes 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.
    • 1 hour, 19 minutes 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.
    • 3 hours, 31 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.
    • 3 hours, 32 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
    • 3 hours, 33 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!
    • 4 hours, 15 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.
    • 5 hours, 38 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.
    • 7 hours, 35 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
    • 22 hours, 58 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.
    • 23 hours 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.
    • 23 hours, 1 minute 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.
    • 23 hours, 2 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
    • 23 hours, 10 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 ´ )⎠⎞
    • 1 day, 1 hour 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, 1 hour 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, 1 hour 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, 5 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, 7 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, 7 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, 8 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, 8 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, 8 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, 8 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, 8 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.
    Clear All
Pages
    • T1D Exchange T1D Exchange T1D Exchange
    • Articles
    • Community
      • About
      • Insights
      • T1D Screening
        • T1D Screening How-To
        • T1D Screening Results
        • T1D Screening Resources
      • Donate
      • Join the Community
    • Quality Improvement
      • About
      • Collaborative
        • Leadership
        • Committees
      • Centers
      • Meet the Experts
      • Learning Sessions
      • Resources
        • Change Packages
        • Sick Day Guide
        • FOH Screener
      • Portal
      • Health Equity
        • Heal Advisors
    • Registry
      • About
      • Recruit for the Registry
    • Research
      • About
      • Publications
      • COVID-19 Research
      • Our Initiatives
    • Partnerships
      • About
      • Previous Work
      • Academic Partnerships
      • Industry Partnerships
    • About
      • Team
      • Board of Directors
      • Culture & Careers
      • Annual Report
    • Join / Login
    • Search
    • Donate

    If you use an insulin pump, on average, how often do you bolus an amount that is different from the suggested dose from the pump’s bolus calculator? (I.e., entering a number of insulin units without using the calculator at all, editing the bolus calculator’s suggested dose to be higher or lower, etc.)

    Home > LC Polls > If you use an insulin pump, on average, how often do you bolus an amount that is different from the suggested dose from the pump’s bolus calculator? (I.e., entering a number of insulin units without using the calculator at all, editing the bolus calculator’s suggested dose to be higher or lower, etc.)
    Previous

    Do you ever purchase candy labeled “sugar-free”?

    Next

    How often does your T1D health care provider screen for neuropathy with a monofilament, tuning fork or pin prick on your bare feet?

    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.

    Related Stories

    Advocacy

    Blue Circle Health: A Free Virtual Program Expanding Support for Adults Living with Type 1 Diabetes 

    Michael Howerton, 3 days ago 4 min read  
    News

    Thyroid Eye Disease (TED): What You Need to Know 

    Jewels Doskicz, 5 days ago 4 min read  
    News

    Immunosuppressants in T1D Research: Expert Opinions from Diabetes Pharmacist Diana Isaacs 

    Jewels Doskicz, 1 week ago 5 min read  
    2025 Learning Session

    The 2025 T1DX-QI Learning Session: Driving Better Diabetes Care 

    Sarah Howard, 2 weeks ago 7 min read  
    Lifestyle

    Barriers to Care in Aging: Voices from the T1D Community 

    Jewels Doskicz, 3 weeks ago 7 min read  
    Lifestyle

    When T1D Becomes a Calling: Stories From our Team 

    Jewels Doskicz, 4 weeks ago 11 min read  

    30 Comments

    1. Cheryl Weaver

      After I’ve had my pump on for a couple days the insulin I bolus with it doesn’t bring my blood sugar down, or prevent it from going high. I have to inject using a syringe and needle to bring it down. The insurances say to change your site every 3 days, but between that 2nd and 3rd day something seems to happen, where it isn’t being absorbed as well. So the blood sugars go up, and I have to bolus the old fashioned way, with a syringe.

      4
      4 years ago Log in to Reply
      1. LizB

        Ask your doctor to write a new prescription that says to change every 2 days instead of every 3 days. Not every insurance will go for that, but sites sometimes don’t last 3 days for everyone.

        4
        4 years ago Log in to Reply
      2. Sherolyn Newell

        I sometimes have that issue as well, but it’s not consistent. If I see the insulin not working as well, I will adjust my bolus amounts up by 0.1 or so.

        2
        4 years ago Log in to Reply
      3. Larry Martin

        You need to change your carb ratio or insulin sensitivity to fix those issues. Carb ratios and sensitivity vary widely throughout each day.

        2
        4 years ago Log in to Reply
    2. Greg Felton

      I don’t think the tandem’s calculator is aggressive enough when my BG is rising and arrows are pointing up. I will often over bolus.

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

      I often make adjustments for exercise, other physical activities, which works out to most days.

      2
      4 years ago Log in to Reply
    4. GLORIA MILLER

      My pump will do this but I chose not to use that function. I feel I can calculate the necessary bolus better than my pump.

      1
      4 years ago Log in to Reply
    5. Sherolyn Newell

      I sometimes have a few days or a week when the insulin seems to be less effective. When I see that happening, I will raise my bolus calculation a bit. I don’t change my settings because it always goes back to normal. Less often, the insulin seems to be supercharged and I have to back down bolus for a couple days. And it varies by time of day, sometimes lunch insulin doesn’t seem to work, other times it supper.

      1
      4 years ago Log in to Reply
    6. Mark Schweim

      I normally don’t but I’ve been fighting a combination antibiotic resistant bacterial and fungal infection in my sinuses and throat since the beginning of April and with this stubborn illness I’m having to usually increase the Bolus amount as much as double what the pump calculates I need.

      4 years ago Log in to Reply
    7. Patricia Kilwein

      If I’m struggling with an illness or on a prescription that causes high BG, my doc or edu will give me instructions on a temp setting for basal. The only time the bolus changes take place is when there’s a trend change and A1C goes up.

      1
      4 years ago Log in to Reply
    8. Maggie Morgan

      I will often give less insulin if I know that I will be working out in the next 2 hours.

      6
      4 years ago Log in to Reply
    9. Angela Pennacchia

      My Dr. Did write me a new prescription for every 2 days, as I have the same problem. I am on Medicare and they accepted it.

      4 years ago Log in to Reply
    10. Linda Zottoli

      Often, for lots of reasons. Pump doesn’t know some things that I know: what I’ve already eaten to deal with a low or otherwise without bolusing, the walk I’ve just taken or exercise I am planning, come to mind. And, for correction boluses, I have the correction amount set to work fine for some bg variations, but for readings above maybe 200, or even lower if long lasting ones, I also have to consider a decrease in sensitivity. And, sometimes, if I know what I want bolused, it’s just easier to just plug in the amount. (though can’t use info about percentage basal/bolus then).

      4
      4 years ago Log in to Reply
    11. AnitaS

      I do at least a few times a week as sometimes my insulin isn’t working because of the infusion site may not be as responsive to insulin as other sites. I may not plan on exercising as I usually do at a certain time. I may bolus more for high fat foods or bolus less for an activity that I am about to do. The reasons are endless.

      1
      4 years ago Log in to Reply
    12. kristina blake

      I am very aggressive in my T1D mgt. For meal boluses, I take into account any FOB (food on board – as best I can guess), I also pay attention to trend arrows. As another response said, only I know what is ahead for the next couple hours. While I do have different settings for about 9 different time zones throughout the day, I also titrate up (or down) based on the bg reading (if bg is under 130, I use the correction setting in my pump, if I am between 130-160, I increase by 10%, etc). I also have this “lovely” symptom of rising bg (lovely, because it comes in handy) – I get heartburn as my bg rises. I use what I can!

      4 years ago Log in to Reply
      1. Patricia Dalrymple

        OMG: I have just started experiencing this when I am high. It feels like I need to burp. It can’t.

        4 years ago Log in to Reply
    13. Bea Anderson

      The pump wizard does not know if I’m exercising or factor in other life issues.

      3
      4 years ago Log in to Reply
      1. Karen Brady

        my system doesn’t have an exercise setting/profile either, so I have to adjust manually for this (or even if I’m at work where I’m active and walking around, vs sitting on the couch at home)

        4 years ago Log in to Reply
    14. dave hedeen

      I add fat ‘carbs’, if eating food high in fat, pizza or pumpkin pie

      1
      4 years ago Log in to Reply
    15. Leon Ullrich

      My pump does a good enough job estimating with all the factors included in the pump. If the factors are wrong they are reviewed with my doctor.

      1
      4 years ago Log in to Reply
    16. William Bennett

      Some stuff you just get a pretty good sense of after you’ve been at this long enough. Things I eat frequently I rarely bother with the Wizard for, and stuff that’s unusual or hard to estimate b/c of fat content I’ve just built up a routine of my own for (pizza, Chinese). Of course it was very different before CGM, when it was much riskier to guesstimate things.

      2
      4 years ago Log in to Reply
    17. Janis Senungetuk

      Since my pump doesn’t read minds or calendars I often need to change the suggested bolus amount.

      2
      4 years ago Log in to Reply
    18. Carol Meares

      I don’t really count carbs. It is difficult when eating low carb. I have my carb to insulin ratio set at 10 to be able to easily calculate insulin I need for a meal due to protein, fat for resistance and yes, some carbs, type of activity level, stress, health condition, etc. The estimate I give may need to be corrected later or maybe not.

      4 years ago Log in to Reply
    19. Carrolyn Barloco

      I respond to upward trend arrows by taking a 1-2 unit bolus

      1
      4 years ago Log in to Reply
    20. TEH

      I adjust the carb estimat based on the fat content and my experience with certain meals. Must dinners average 50 g of carbs…

      4 years ago Log in to Reply
    21. Patricia Dalrymple

      I lower it sometimes with fresh insulin but have started lowering my basal for that because it is very consistent. Every Sunday I visit my dad. Even though I eat the same thing most mornings, when I go there my BG always goes low so I have been lowering my bolus a couple points.

      4 years ago Log in to Reply
    22. mbulzomi@optonline.net

      Except when I’m sleeping, I always self-Bolus. Control IQ is too slow to react. I have no patience with Control IQ. Some time when I used it, it would take 4 hours to bring down my numbers. Good for new kids, not me.

      1
      4 years ago Log in to Reply
      1. mbulzomi@optonline.net

        After reading some comments it evident that we use different Insulin pumps. and delivery systems. Most likely we cannot compare their action.

        4 years ago Log in to Reply
    23. PamK

      I chose 2-3 times/month because I only recently started doing this. I have found that when my BG is over 250mg/dl the calculator doesn’t deliver enough insulin to bring me down.

      4 years ago Log in to Reply
    24. Cheryl Seibert

      There are specific situations where I override a bolus calculation or enter a manual insulin-only bolus.
      1. My Tandem pump will occasionally ignore the IOB in the calculation. If my BG is NOT high, I will override the suggested bolus to the ‘correction calculation.
      2. Manual extended bolus if the site is getting bad and I cannot immediately change it. Extended bolus will act like an aggressive basal rate and absorb better.
      3. Intended exercise after a bolus….. I often reduce the meal bolus if the exercise will be moderate, heavy or of a long duration.

      4 years ago Log in to Reply

    If you use an insulin pump, on average, how often do you bolus an amount that is different from the suggested dose from the pump’s bolus calculator? (I.e., entering a number of insulin units without using the calculator at all, editing the bolus calculator’s suggested dose to be higher or lower, etc.) Cancel reply

    You must be logged in to post a comment.




    101 Federal Street, Suite 440
    Boston, MA 02110
    Phone: 617-892-6100
    Email: admin@t1dexchange.org

    Privacy Policy

    Terms of Use

    Follow Us

    • facebook
    • twitter
    • linkedin
    • instagram

    © 2024 T1D Exchange.
    All Rights Reserved.

    © 2023 T1D Exchange. All Rights Reserved.
    • Login
    • Register

    Forgot Password

    Registration confirmation will be emailed to you.

    Skip Next Finish

    Account successfully created.

    Please check your inbox and verify your email in the next 24 hours.

    Your Account Type

    Please select all that apply.

    I have type 1 diabetes

    I'm a parent/guardian of a person with type 1 diabetes

    I'm interested in the diabetes community or industry

    Select Topics

    We will customize your stories feed based on what you select here.

    [userselectcat]

    We're preparing your personalized page.

    This will only take a second...

    Search and filter

    [searchandfilter slug="sort-filter-post"]