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    • 14 hours, 50 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, 52 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, 53 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, 53 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
    • 15 hours, 2 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, 54 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, 55 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, 57 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, 57 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
    • 23 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".
    • 23 hours, 45 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 ´ )⎠⎞
    • 1 day 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 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 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 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 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, 1 hour 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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    Multiple daily injections (MDI) users: Do you use an app or other device to track your insulin dosing? Share the tools you use in the comments below!

    Home > LC Polls > Multiple daily injections (MDI) users: Do you use an app or other device to track your insulin dosing? Share the tools you use in the comments below!
    Previous

    Have you ever been stopped from entering a large event (concert, sports game, etc.) because you were carrying your T1D supplies or snacks in your bag? Share how you handled the situation in the comments!

    Next

    If you have a school-aged child with T1D, do you make any changes to their T1D care routine when they go on summer break? Share how you adjust to a summer schedule in the comments!

    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. Rob Smith

      Inpen for Fiasp, nothing for Tresiba.

      5 years ago Log in to Reply
    2. Bonnie kenney

      Diabetes M

      5 years ago Log in to Reply
    3. Richard Maingot

      When I was MDI I used the Jade Insulin Dose Calc app. I found it very useful

      5 years ago Log in to Reply
    4. Marcia Pulleyblank

      I used to use MDI but have just started on a pump and CGS Combo. When I used the Freestyle Libre, I would record doses in the comments section.

      5 years ago Log in to Reply
    5. victor.bautista@gmail.com

      SocialDiabetes.com

      With a FDA and CE Mark for medical device

      5 years ago Log in to Reply
    6. connie ker

      For years I kept a logbook with pen and paper notations. I took that book to my Dr. apts and he would highlight highs and lows with colored markers. Then it went to downloading the meter numbers and now it is downloading my Abbott Freestyle Libre reader. I have given up keeping a logbook so gave my extras books to my endo and they were so appreciative because many of their seniors still ask for them. Technology is replacing paper and pencil, newspapers, mail, and bill paying. I like technology until it doesn’t work and you have to call Comcast for help! You have to be so careful with technology too.

      5 years ago Log in to Reply
      1. Daniel Bestvater

        I use a pump most of the time, but I take a couple pump breaks per year. Tresiba & Apidra by pen without the use of technology. It’s a nice break.

        5 years ago Log in to Reply
    7. Natalie Daley

      We my older brother was also a T1d. He was a mathematician.

      5 years ago Log in to Reply
    8. Kim Rehtus

      InPen for Humalog is great for showing Insulin On Board. I also love the notification that appears once the last dose is no longer acting….that way I can check my BS and see if a correction dose is needed! I don’t use anything for my Tresiba.

      5 years ago Log in to Reply
    9. Natalie Daley

      Didn’t get to finish my comment. My older brother, a T1d from age 23 until he died at 67, was a mathematician, and designed a matrix for me for breakfast and dinner doses (I don’t eat lunch) and how much to take if I’m not eating but running higher than the norm. This was for short term insulin. Time release is one stable shot in the morning. This has worked for 25 years.

      5 years ago Log in to Reply
    10. Dave Akers

      Record my inhalations in the Dexcom app. Nothing for Tresiba other than a phone reminder that reminds me nightly to take long acting injection.

      5 years ago Log in to Reply
    11. CindyGoddard

      Oops I answered this question wrong because I am not MDI. I am on a pump. Sorry

      5 years ago Log in to Reply
    12. Yaffa Steubinger

      I use the Dexcom G6 app to enter my carbs and basal/bolus insulin dosages.

      5 years ago Log in to Reply
    13. Scott Rudolph

      I use xDrip+.

      5 years ago Log in to Reply
    14. Diane McEniry

      I use my Dexcom G6 iPhone app to record insulin doses but I also still write it on a formatted blank spreadsheet. I hate to admit it, but it’s still easier for me to look at my paper to quickly identify trends and see how best to dose (basal and bolus) depending on activity, meals, BS, …

      3
      5 years ago Log in to Reply
    15. Tod Herman

      I’ve been on a pump for over 8 years, but have recently been considering being able to switch to an MDI format to use when I go scuba diving (which I was actively doing before starting on the pump). The pump protocol had effectively killed my scuba diving options.

      For what it’s worth, I started scuba diving long after becoming a T1D in 1980. I’ve logged 100s of dives and even have a solo divers certificate.

      5 years ago Log in to Reply
    16. Becky Hertz

      I currently don’t use MDI, but I did use an app when I did. I don’t remember the name of it though. It was comparable with a Windows phone.

      5 years ago Log in to Reply
    17. Jenny Richardson

      I’ve been on MDI since diagnosis 37yrs ago. I now log my insulin doses in my Dexcom G6 app. Before that, good old hand written log book.

      5 years ago Log in to Reply
    18. Anthony Harder

      I’m a T1D for 55+ years doing multiple injections each day. I gave adjustments and slides based on current and past performance. All of these are recorded the same way they were when I started, in a log book/paper chart. The algorithms I use are much more complex, but I’ve advanced a bit since I was 7 years old, too. A big issue I have with electronic recoding is ad hoc notes are difficult to use.

      5 years ago Log in to Reply
      1. Britni

        I still use a log, too. I gave it up for a little while when I was using the Omnipod, but picked it up again when I gave up on the pump. I make a lot of typos on the phone and get frustrated so instead I make my own log in Excel and print it out each week. It has all the ratios for my corrections in the margin on the right and if I need more space for notes I can always write on the back.

        5 years ago Log in to Reply
    19. Marie Cardinell-Daldry

      I use the DexCom IPhone app for insulin doses, exercise, carbs. Information is automatically transmitted to my provider.

      5 years ago Log in to Reply
    20. P-O Heidling

      I’m a T1D and an MDI user since 1981. With the switch to lowcarb (LCHF) diet 11 years ago I basically take the same number of doses and insulin units every day. 24 U Lantus (at lunch) and 2 U of Humalog for the dinner, in total. I eat only 2 times a day, with total 20 grams of carb/day.

      If the bg, for some reason, gets over 8.5 mmol/l (153 mg/dL), I take 2 U extra Humalog. But that seldom happens.

      By eating low amount of carbs, and keep the E% of fat and protein the same for all meals, I don’t need to adjust my doses anymore. I’ve set my doses rather fixed and adjust my food intake based on the amount of insulin I use.

      A great freedom to not have to count carb and try to figure out the insulin doses for every meal and exercise.

      1
      5 years ago Log in to Reply
    21. Phyllis Lewis

      I keep a notebook with BG, injection amts, and food eaten. I also track BP and weight weekly.

      5 years ago Log in to Reply
    22. Steve Gold

      I use the Dexcom app (Dexcom Clarity is AMAZING!!! and Microsoft Excel and some Business Intelligence tools to supplement it.

      5 years ago Log in to Reply

    Multiple daily injections (MDI) users: Do you use an app or other device to track your insulin dosing? Share the tools you use in the comments below! Cancel reply

    You must be logged in to post a comment.




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