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    • 14 hours, 43 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, 45 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, 46 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, 46 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
    • 14 hours, 55 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, 47 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, 48 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, 50 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, 50 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
    • 22 hours, 52 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, 38 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 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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    If you use a CGM, where do you most prefer to view your sensor readings?

    Home > LC Polls > If you use a CGM, where do you most prefer to view your sensor readings?
    Previous

    For those who have gone through the process of getting a CGM: Last time you started using a new CGM, how easy or difficult was it for you to get the brand and model you most wanted to use?

    Next

    Did you have any diabetes-related achievements or milestones in 2022? Share what you’re proud of 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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    19 Comments

    1. Jen Farley

      I love Tandems new app that allows me to bolus from my phone. My Dexcom gives me the readings I can make corrections and carb bolus and not pull out my pump. Only trouble is I must clear warnings from my pump only. So I use my pump and smart device for all my readings.

      3 years ago Log in to Reply
      1. Lyn McQuaid

        I love the new bolus by phone too but wish they would include extended boluses!

        2
        3 years ago Log in to Reply
    2. William Bennett

      Had to click “other” because you didn’t include Sugarmate, which uses Dexcom Share to echo your data to lots of devices. In my case I get it on my (Fitbit) watch, which is covered here, but also in the status bar of my MacBook laptop, maybe the handiest place of all since I spend a LOT of time with that screen open. It’s nice to be able to just glance up and keep track that way. If you don’t know about Sugarmate, it’s worth checking out (and no, this is not a paid endorsement).

      2
      3 years ago Log in to Reply
      1. Sue Martin

        William, Thanks for the tip about SugarMate. It seems that it only works with Apple products at this time. I’ll keep an eye on it to see if they come out with other platforms.

        1
        3 years ago Log in to Reply
    3. Jane Cerullo

      On MDI so on phone and watch.

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

      I would say that I look at my pump 95% of the time because it is on my belt and I have it with me all of the time. I do not carry my phone everywhere with me, and I have to turn it on and password to get onto my phone. But, the phone app has some nice information, such as, time in range, or when I started my CGM. So, I do look at my phone from time-to-time.
      I do not have a smart watch.

      3 years ago Log in to Reply
    5. Mick Martin

      On my pump and as a downloaded PDF file from when I upload the data from my pump to the Medtronic/MiniMed website.

      3 years ago Log in to Reply
    6. Trina Blake

      On m y TandemX2 (with BIQ) pump only. Otherwise I gotta get out the old paramedic pants to carry all the devices. And my favorite times are when I can leave the phone at home.

      1
      3 years ago Log in to Reply
    7. Carol Meares

      I put all because on Omnipod. If I could operate everything from my phone that is what I would prefer. Please FDA, approve iOS operation of omnipod5 soon:)

      3 years ago Log in to Reply
    8. Linda Zottoli

      I carry both tandem pump and phone with me most of the time, so often I’m just looking at whichever I pull out of my pocket first. I do like having the TIR on the new tandem app, though (feels a bit like a game, keeping that number up, LOL), so maybe choosing the phone more often lately.

      3 years ago Log in to Reply
    9. Katrina Mundinger

      Don’t have a smartwatch. I use my phone and the pump only.

      1
      3 years ago Log in to Reply
    10. Becky Hertz

      When I switched to G6, I was told I couldn’t view Dexcom on the pump unless I had basal or continuous IQ which I preferred not to. Nice having only one thing going off with alarms.

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

        This sounds like a Medicare issue?

        3 years ago Log in to Reply
    11. Sue Martin

      The question was about CGM but the answers mostly included pumps. I don’t have a pump so it muddled the options for me. The questions and answer options should be streamlined. Thanks

      3 years ago Log in to Reply
    12. Britni

      Freestyle makes you pick either your phone or the receiver for each Libre 2 sensor. You can’t switch back and forth. I’ve stuck with the reader because the Libre app has gotten some really bad reviews and I don’t want to risk being at work and not being able to scan my sensor. Libre 3 only works with a phone, so if I switch sensors, my answer to this question will have to switch, too.

      3 years ago Log in to Reply
    13. Jeff Marvel

      Using Freestyle, and I’ve always had access to the app so didn’t want to pay up even *more* money for a separate reader device. Then I found DiaBox, a 3rd party app which is technically not supported but makes the Libre 2 work exactly like a CGM. It took some growing pains to figure some stuff out but I’m super happy with that setup now.

      3 years ago Log in to Reply
    14. AnitaS

      I probably use my pump the most to view sensor readings. 1) Because my phone is not always with me and 2) Because my wristwatch doesn’t always get readings so I am forced to look elsewhere. I many times confirm my readings on my phone or watch by double checking with my pump as sometimes the readings on my phone/watch aren’t the latest readings.

      3 years ago Log in to Reply
    15. Kristen Clifford

      I love having the MiniMed app on my phone. Sometimes I can see my phone before I do my pump, so it kickstarts me to keep an eye on things.

      3 years ago Log in to Reply
    16. Leona Hanson

      Medtronic pump only have cgm readings on pump only because phones and watches are to easy to hack

      3 years ago Log in to Reply

    If you use a CGM, where do you most prefer to view your sensor readings? Cancel reply

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