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    • 1 hour, 54 minutes 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.
    • 4 hours, 13 minutes 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".
    • 4 hours, 15 minutes 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.
    • 4 hours, 16 minutes 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?"
    • 5 hours, 19 minutes ago
      ConnieT1D62 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I get the 'you can't eat that, can you?' comments when friends see me eat a lot of carbs or have a nice dessert. I remind them that as long as I have insulin, I can eat whatever I want.
    • 5 hours, 20 minutes ago
      ConnieT1D62 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.
    • 5 hours, 22 minutes ago
      ConnieT1D62 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".
    • 8 hours, 48 minutes ago
      Lenora Ventura likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Like most of the above comments, it's more of a question. The statements have come in situations where I'm not actually eating something...like someone saying, "Oh, it must be hard to not be able to eat desserts!"
    • 8 hours, 48 minutes ago
      Lenora Ventura 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.
    • 8 hours, 49 minutes ago
      Lenora Ventura 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?"
    • 10 hours, 1 minute ago
      kristina blake likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Yes and it is really annoying especially when they "You shouldn't eat that - you're a diabetic" and it's even more annoying and irritating when it is being said by a person in a healthcare profession. I can honestly say from many years of experience as a PWTID and as a RN that hardly ANYONE in the general public or in the general medical field says "because you live with diabetes" when referring to a PWD or when they admonish someone for "being diabetic" . It is a label that doesn't acknowledge the person. As I have stated before in other posts, are people who live with cancer called "canceretics"?
    • 10 hours, 25 minutes ago
      Mary Coleman likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Yes. It’s f*ing annoying.
    • 10 hours, 27 minutes ago
      Mary Coleman likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Yes and it is really annoying especially when they "You shouldn't eat that - you're a diabetic" and it's even more annoying and irritating when it is being said by a person in a healthcare profession. I can honestly say from many years of experience as a PWTID and as a RN that hardly ANYONE in the general public or in the general medical field says "because you live with diabetes" when referring to a PWD or when they admonish someone for "being diabetic" . It is a label that doesn't acknowledge the person. As I have stated before in other posts, are people who live with cancer called "canceretics"?
    • 10 hours, 38 minutes ago
      John Barbuto 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
    • 10 hours, 38 minutes ago
      John Barbuto likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Yes and it is really annoying especially when they "You shouldn't eat that - you're a diabetic" and it's even more annoying and irritating when it is being said by a person in a healthcare profession. I can honestly say from many years of experience as a PWTID and as a RN that hardly ANYONE in the general public or in the general medical field says "because you live with diabetes" when referring to a PWD or when they admonish someone for "being diabetic" . It is a label that doesn't acknowledge the person. As I have stated before in other posts, are people who live with cancer called "canceretics"?
    • 10 hours, 39 minutes ago
      John Barbuto likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      This is actually one of my biggest pet peeves. People who say, "Are you sure you can/should eat that?" Excuse me, but I think I know how to take care of myself and my diabetes better than you ever could. Thankfully, this does not happen much anymore, but years ago, it was a common refrain...
    • 10 hours, 55 minutes ago
      Anthony Harder likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Like most of the above comments, it's more of a question. The statements have come in situations where I'm not actually eating something...like someone saying, "Oh, it must be hard to not be able to eat desserts!"
    • 10 hours, 56 minutes ago
      Anthony Harder likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Like others here, it's more of "Can you eat . . .?" than "You shouldn't eat . . .!" Nonetheless, it comes across the same way.
    • 10 hours, 57 minutes ago
      Anthony Harder likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      This is actually one of my biggest pet peeves. People who say, "Are you sure you can/should eat that?" Excuse me, but I think I know how to take care of myself and my diabetes better than you ever could. Thankfully, this does not happen much anymore, but years ago, it was a common refrain...
    • 12 hours, 8 minutes ago
      Steve Rumble likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Like others here, it's more of "Can you eat . . .?" than "You shouldn't eat . . .!" Nonetheless, it comes across the same way.
    • 12 hours, 8 minutes ago
      Steve Rumble likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      This is actually one of my biggest pet peeves. People who say, "Are you sure you can/should eat that?" Excuse me, but I think I know how to take care of myself and my diabetes better than you ever could. Thankfully, this does not happen much anymore, but years ago, it was a common refrain...
    • 13 hours, 32 minutes ago
      mojoseje likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      This is actually one of my biggest pet peeves. People who say, "Are you sure you can/should eat that?" Excuse me, but I think I know how to take care of myself and my diabetes better than you ever could. Thankfully, this does not happen much anymore, but years ago, it was a common refrain...
    • 1 day, 1 hour ago
      Neha Shah 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.
    • 1 day, 3 hours ago
      Amanda Ratliff likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      My grandma told me u could never have kid. I had two successful pregnancies.
    • 1 day, 3 hours ago
      Amanda Ratliff likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      Oh my goodness… yes! As a child I was often reminded of my limitations because of diabetes. I’m hopeful that those misconceptions about T1D have changed over the decades.
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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.

      4 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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