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    • 15 hours, 2 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.
    • 15 hours, 4 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.
    • 15 hours, 5 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.
    • 15 hours, 6 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, 14 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 ´ )⎠⎞
    • 17 hours, 6 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.
    • 17 hours, 7 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.
    • 17 hours, 9 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 ´ )⎠⎞
    • 21 hours, 10 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, 12 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, 57 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, 13 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, is it an “automated insulin delivery” system?

    Home > LC Polls > If you use an insulin pump, is it an “automated insulin delivery” system?
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    When counting your carbs before bolusing, do you factor the amount of protein into your calculation at all? If so, share how in the comments!

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    Samantha Walsh

    Samantha Walsh has lived with type 1 diabetes for over five years since 2017. After her T1D diagnosis, she was eager to give back to the diabetes community. She is the Community and Partner Manager for T1D Exchange and helps to manage the Online Community and recruit for the T1D Exchange Registry. Prior to T1D Exchange, Samantha fundraised at Joslin Diabetes Center. She graduated from the University of Massachusetts with a Bachelors degree in sociology and early childhood education.

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    33 Comments

    1. PamK

      I use a Tandem pump, but I do not use the automated delivery. Why? Because I like tighter glucose control than it allows. If/when the FDA allows for tighter control I’d be willing to try it again.
      I did try it when it first came out, but my A1C went up, not down due to higher blood glucose than I normally ran on MDI. Without the automated delivery, I can get my A1C closer to where I want it. It’s still not perfect, but I’m working on it!

      4
      3 years ago Log in to Reply
    2. Janice Bohn

      I was using the Tandem x2 with Control IQ. In June I started the OmniPod 5.

      3 years ago Log in to Reply
    3. Carolann Hunt

      Loop is a hybrid closed loop system that still needs carb inputs

      2
      3 years ago Log in to Reply
    4. mbulzomi@optonline.net

      First thing you need to learn when using Tandem X2, Control IQ is let it run, don’t preempt it because it’s not correcting as fast as when you (Human) make the corrections. However, the pumps of today are set up for people that have not be persons with T1D for a long time. I almost have to change my Basels because of being a T1D for over 55 years and on a pump for over 39 years, along with using a CGM (Metronic and Dexcom) for over11 years. No Vergin sites left. AND when I do hit a relatively new site all hell breaks loose, dropping like a rock almost all day. Very hard to control, a least for three day make very drastic changes to my Basel settings.

      3
      3 years ago Log in to Reply
    5. GLORIA MILLER

      I got a Omnipod 5 and Dexcom G6 a few weeks ago. I am waiting until I return from international trip to set it up and to also get a supply of pods and sensors before switching. I know how unreliable delivery is too often with our medical supplies so I like to have a stock pile when I switch.

      1
      3 years ago Log in to Reply
    6. Lyn McQuaid

      I said “yes” but I only turn on Control IQ at night. It works best then when there is no food/activity, while I prefer to take care of things during the day. I like to have a lower target BG than it allows.

      2
      3 years ago Log in to Reply
      1. Bonnie Kruger

        I am sorry to hear Tricare doesn’t cover the cost of Omnipod 5 yet. I think of all people who get insurance to cover their insulin costs, former military personnel and their relatives deserve it FIRST. Speak with your congresspeople, particularly those who are constantly boasting about how they support the military. You deserve to have your insurance needs met and the political nitwits who run our government should be called out on this failure. It took old POTUS a little too long to reduce the cost of insulin to $35.00 a month, if you want my opinion…Big Pharma and lobbyists have a little too much power with both of the parties in our country.

        2
        3 years ago Log in to Reply
    7. Sondra Mangan

      Sadly, Tricare (insurance for military families) is not covering Omnipod 5 yet. Hoping to move to the Omnipod 5 as soon as possible—but could never afford paying out of pocket for it.

      3 years ago Log in to Reply
    8. Tod Herman

      Today I am using my old Omnipod. I have the new Omnipod 5 next to me, but I haven’t gone through the training yet to start using it. Plus, I only have the 11 pods that came with it, the new prescription for the 5 pods hasn’t been filled yet. Mildly frustrating.

      3 years ago Log in to Reply
    9. dholl62@gmail.com

      On Medtronic 630G , awaiting training for tslim iq setting and dexcom 6 can hardly wait until I can use them

      3 years ago Log in to Reply
    10. Bonnie Kruger

      I am supposed to get an Omnipod 5 on Sept 2 but I am wondering if I want it. I was very interested in this last person’s comment regarding higher A1Cs. Mine right now is usually between 4.9 and 5.2 and I like it to be there since I feel that I can control my lows by eating when I need to and I just FEEL so much better when my blood sugar is around 80-120 like someone without T1 Diabetes feels. I am a former athlete and dancer and I, therefore, take less insulin and depend on exercise to reduce my need for constant carbs. Some days I rarely need to take much Fiasp at all because I don;t eat a diet super high in Carbs. I can often get away with only taking Tresiba and the tiniest bit of Fiasp (1-3 units when I eat something high in carbs. I am really, really worried about starting the Omnipod and don’t know if I am going to like it…

      2
      3 years ago Log in to Reply
      1. sweet charlie

        sounds like you are doing fine with what you are doing..!!!

        1
        3 years ago Log in to Reply
      2. LizB

        From everything I’ve read about the OmniPod 5, it’s algorithm is much like the one on the Medtronic pump I use (770g). The OmniPod 5 will also do automatic corrections for high BGs which my pump can’t do. But I believe that it aims for a higher target and doesn’t let you correct as aggressively as I’d like. My sister is afraid of lows and her BG runs high all the time. She is finally going to move from the original OmniPod to the 5 and for someone like her, with BGs and an A1c that are too high, the O5 sounds like it will be a huge help. For people like yourself & me, with A1cs in the low 5 range and tight control, it can be a big disappointment.

        1
        3 years ago Log in to Reply
      3. Wanacure

        Bonnie K, Thanks for your info. How many calories/day do you burn nowadays? Or how many minutes/day of exercise? With Covid risk, do you prefer exercise at home or gym or outdoors? Locally I notice one small gym has a HEPA filter system, another small gym just opens the windows and doors, and another very large gym recommends masks and social distancing. This fall I plan to start wearing N-95 mask whenever I’m in an enclosed space of any type for any reason. But for exercise in an even large gym when breathing hard on the elliptical or stationary bike…I’m perplexed.

        3 years ago Log in to Reply
    11. Carlos Gonzalez Perez

      Roche combo + Aaps
      DIY system

      1
      3 years ago Log in to Reply
    12. Nicholas Argento

      Yes. Game changer for nights….

      2
      3 years ago Log in to Reply
    13. Eva

      No. I dont have an automate pump. I am happy with the medtronic pump I have. My last A1c was 5.8 and very few hypos. Nothing less than 62.

      2
      3 years ago Log in to Reply
    14. Steven Gill

      Using the MEDTRONIC770G set-up it has the controlled loop capability but my days are so chaotic. I keep It in the “manual” except with my ranges for the CGM set for 65-130. Meaning I get warnings at 70 and 125 and react as needed. While the basal isn’t generally adjusted it suspends the basal at 60, I’ll be “alerted” if the systems senses I’ll reach 65 in 30 minutes (like yesterday morning woke me up with an alarm at 80 with 2 arrows down.

      My chaos at work? I’ll drive an hour to a job, than literally even setting the system into the “active” mode (allowing levels to rise to 150) 20 minutes early will go severely hypo~. Often I’ll need 1/3 a unit for that drive but 20 minutes before arriving to a job will reduce the basal to 50%, and often completely suspend it it there’s any drop.

      (Historically doctors seemed comfortable with a1C’s in lower 7’s because of my glucose drops, but since I’ve learned to pre-bolus and to decrease my bolus prior, by the equations “mg/dL” to a1C looking at 5.5 with a lot fewer hypo~ reactions. Up to the lab work next month.

      3 years ago Log in to Reply
    15. Pauline M Reynolds

      Not sure what that is, but put “Yes”. My pump does bolus automatically if I’m too high and lower the insulin if too low.

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

      Nope. Tried the 670G Guardian 3 system for 6 months and gave up, went back to my old pager-style Paradigm, and Dexcom. One of the odd things about these systems is that, in the name of doing everything for you they lock away the kinds of controls you need to individualize them. To me it felt very much like a “Doctor knows best!” system that slapped my hands away whenever I tried to make adjustments that would conform to my own body and how I experience and deal with T1.

      4
      3 years ago Log in to Reply
      1. sweet charlie

        I like your sentence !!!!

        3 years ago Log in to Reply
      2. sweet charlie

        Last sentencee,I ment..

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

      I’m not sure what you mean by “automated insulin delivery” system. I wish you’d have defined it. But, I said “yes” anyway. I use the Tandem X2 Control IQ, with a Dexcom G6. (oooh, sounds very esoteric) (Allow me a little humor 😉

      1
      3 years ago Log in to Reply
      1. Lawrence S.

        By the way, Yesterday, I updated my Tandem Control IQ system to the 7.6 software. What an exciting jump forward! Now, I can see my glucose levels on my phone, which I could not do with the old app. The details are amazing! And, Tandem finally put the boluses onto the timeline, which is very helpful. I used to get the boluses on the timeline years ago with my Medtronic pump, but Tandem never did it until now. Kudos Tandem! Great job. Oh, by the way, it now allows you to give boluses through your phone. However, I do not have that feature on my phone.

        3 years ago Log in to Reply
    18. Mick Martin

      I answered “Yes”, but that REALLY depends on what YOU mean by “automated insulin delivery” system.

      I still have to ‘tell’ the pump the amount of carbohydrates that I’ve imbibed. It will then work out, based on the information that I’ve already input, such as my insulin sensitivity factor, how many units of insulin are required to bring down my glucose level by a given amount, and the range at which I’m aiming to keep my blood glucose level. i.e. Time in Range.

      Coupled with my CGM, the pump makes micro-adjustments to ensure that Time in Range is adhered to. If my blood glucose level falls outside of that ‘Time in Range’ (TIR), the pump alerts me to check my blood glucose level, recalibrate the reading(s) it gets from my CGM, and to take remedial action.

      1
      3 years ago Log in to Reply
    19. Tim Kirchgessner

      My pump has the ability to automate the delivery but I can’t afford the suppies to use it.

      3 years ago Log in to Reply
      1. AnitaS

        So sorry to hear that. Insurance should have to cover most, if not all of the cost, to use the pump to its full ability. I know that I am assuming you have insurance for your pump

        3 years ago Log in to Reply
    20. LizB

      I said Yes because I have the Medtronic 770g which will automate the basal rates. I don’t use that feature because it keeps my BG in a much higher range than I like.

      3 years ago Log in to Reply
    21. TomH

      Using Loop-Dev with Dash and an AID.

      3 years ago Log in to Reply
    22. JuJuB

      Isn’t “automated insulin delivery” system the same thing as “insulin pump?” I answered Yes, but the question is oddly written (as others have pointed out).

      1
      3 years ago Log in to Reply
    23. Magnus Hiis

      FreeAPS X (Oref1) w G6 and Eros

      3 years ago Log in to Reply
    24. Donna Condi

      Yes I use Tandem X2 with Control IQ.

      3 years ago Log in to Reply
    25. csreineke

      I use Loop – a DIY system with auto-basal and auto-bolus dosing strategies.

      3 years ago Log in to Reply

    If you use an insulin pump, is it an “automated insulin delivery” system? Cancel reply

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