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    • 14 hours, 48 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, 50 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, 51 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, 51 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 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, 52 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, 53 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, 55 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, 55 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, 57 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, 43 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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    For CGM users: How long have you been using a CGM?

    Home > LC Polls > For CGM users: How long have you been using a CGM?
    Previous

    If you use an insulin pump or CGM, do you use additional overlay patches to help your device(s) stick?

    Next

    Do you have a medical ID set up on your phone?

    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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    30 Comments

    1. Ahh Life

      2006, starting with the hellspawn Medtronic harpoon.

      2
      4 years ago Log in to Reply
      1. ConnieT1D62

        Great description of the barbaric Medtronic harpoon device! I started using CGM back then with Enlite and the harpoon as well. Have been on Dexcom since 2011.

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

      Started with Medtronic Enlite then switched to Dexcom G5, G6 for a total of 11 years.

      2
      4 years ago Log in to Reply
    3. connie ker

      I waited for the Abbott Freestyle 14 day Libre to come out and was one of the first owners in 2018. Before that it was a 10day sensor . I am still using the same CGM and my fingers thank me each and every day.

      4 years ago Log in to Reply
    4. ELYSSE HELLER

      I am anxiously waiting for Insulet’s Omnipod 5 system to be approved, when it’s approved, I’m in!

      1
      4 years ago Log in to Reply
      1. GLORIA MILLER

        Omnipod 5 got FDA approval January 28, 2022 but it has not be released for the general public yet. Only a select group has received it to date. I’m also eager for the general public to get it. But I also am waiting for the Dxcom G7 to get FDA approval. I want the smaller size of the G7.

        2
        4 years ago Log in to Reply
    5. RoseMary Deininger

      Technology advancements have been great. When will the cure come?

      2
      4 years ago Log in to Reply
    6. Jane Cerullo

      Started with old Medtronic one. Was awful. Thick needle and large shell like device. Then got Dexcom 4-6 over the years. Then insurance would only cover freestyle Libre so have been on FSL 2 Changed insurance but will stay on the FSL. Good and bad with both. FSL3 should be approved soon and will be able to see on Apple Watch. Only thing I really miss.

      4 years ago Log in to Reply
    7. gary rind

      used the Libre 14 day to start but was always for readings to catch up to reality. like the Libre2 much better although the 12 hour warmup drives me crazy. we’ll see what the Libre3 has in store.

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

      I answered 15 to 20 years, but I really don’t remember. I wore a Medtronic CGM for many year, several different versions. All of them were inaccurate and not useful to me. I switched to Dexcom G4, then G5 and now G6. All of the Dexcom CGM’s were far superior to the Medtronic CGM’s.

      1
      4 years ago Log in to Reply
    9. Becky Cain

      I started in 2011 with the Dexcom SEVEN and then with G4, G5 and now G6 with the Tslim integration. Wonderful advancements!

      4
      4 years ago Log in to Reply
    10. Natalie Daley

      I’m 75, and I started using a CGM in April because the latest version came out with an alarm system that is programmable and works reliably. My hands have carpal tunnel, and this use air to use. My 85 tea told husband is no help, and while he never was, this can be an issue at my age. I font love being tethered to my illness, but I appreciate the steady reliability.

      4 years ago Log in to Reply
    11. Gary Taylor

      I may be one of the very few who still uses Medtronic sensors. I started using sensors in 2008, initially Medtronic 3-day sensors (stretched to 7) which were fair. Then upgraded to their 7-day Enlite which were awful. Switch to Dexcom G4 for a couple of years. I then went back to Medtronic’s current version. Approved for 7 day use, I try to stretch them out to 10-14 days.

      1
      4 years ago Log in to Reply
      1. TEH

        I have gone down a similar path but I had not switched form Medtronic.

        4 years ago Log in to Reply
      2. LizB

        I have only ever used Medtronic as well, starting as soon as they integrated the receiver into the pump, the 522/722 Paradigm models. Those original sensors worked great for me although insertion was not fun! I always extended them and often got several weeks with great results. The longest I went was 56 days and it was accurate the entire time until it died suddenly. I hated to see it go. Moved to the Enlite when I got a new pump and they sucked. Every single one would only read low no matter what. I tried for months and gave up. I should have gotten a Dexcom then but didn’t, went without a sensor for years. Got the 670 in 2018 (now 770) and the Guardian sensors work great for me.

        4 years ago Log in to Reply
    12. Melinda Lipe

      I started on an Enlite from Medtronic in 2008 when insurance started covering them, but fingersticks were absolutely necessary – sensor was not reliable! 5 years on G5-G6.

      2
      4 years ago Log in to Reply
    13. connie ker

      I waited to order the Abbott Freestyle Libre when the system went to 14 day instead of 10 days before a sensor change needed. I have had this system for 4.5 years and have to keep until 5 years before making any changes with Medicare coverage. I am very pleased with this Abbott system except for the accuracy component. My fingers thank me 10 times every day!!

      2
      4 years ago Log in to Reply
    14. George Lovelace

      2009 Started on Dexcom System 7+ and upgraded G4, G5 and G6. Looking Forward to the G7 to integrate with Tandem X2

      1
      4 years ago Log in to Reply
    15. Mig Vascos

      I don’t know how we were able to survive before CGMs. I began using a Dexcom 7+ in 2/2011. My life and control have been transformed for the better with CGMs and all the apps available these days.

      2
      4 years ago Log in to Reply
    16. Mig Vascos

      I had a horrible experience with the Enlite. The results were all over but never close to reality. It drove me crazy.

      3
      4 years ago Log in to Reply
    17. Jeanne McMillan-Olson

      I first used the Dexcom CGM in a research study at the University of Washington in 2009. It was wonderful but not as accurate as the G6 is now. Tried the Medtronic sensor first but had a hard time putting it in correctly. My insurance would not cover a CGM after the study. Many years later Medicare approved the Freestyle Libre, which was not that accurate for me. Medicare finally approved the Dexcom G6 and I love it. My fingers look like real fingers again! Looking forward to the G7.

      1
      4 years ago Log in to Reply
    18. Keith LeMar

      I started using the Abbott Navigator in 2008. I have also used Medtronic and Dexcom. Currently using the Dexcom G6 with my Tandem X2 pump

      4 years ago Log in to Reply
    19. lis be

      started as soon as my insurance helped lower the price. it’s still about $100 a month though.

      4 years ago Log in to Reply
    20. Marty

      I started with the first Medtronic CGM (known as the “harpoon”) as soon as it was available. I’m not sure when that was exactly. I use a Dexcom G6 now and will upgrade to the G7 as soon as I can.

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

      I’ve been using Dexcom G5, G6 for not quite 6 years. When I first started using the G5 I really struggled trying to get the transformer to fit correctly. Now with the G6 I have few problems because it’s much easier to insert the sensor/transmitter on my upper arm instead of my abdomen. Using the CGM/Tandem combo with Control-IQ has made a tremendously positive difference in my quality of life. I’m now very concerned that increased DME cost in addition to insurance coverage changes will force me to return to MDI without the use of the CGM.

      4 years ago Log in to Reply
    22. pru barry

      From test tubes and tablets like a mini chem lab, to a Dexcom with a Tandem hanging out in its pretty blue case until I will get the newest version when my warranty runs out. What a trip it’s been! My 15 year old Labradoodle wears a Libre sensor. Are we all tricked out? Can’t say any of this has been a choice, but I’m old and healthy, and loving every minute!

      4 years ago Log in to Reply
    23. Jneticdiabetic

      Off and on for about 14 years I think?? Starting with the early iterations of the Medtronic CGMs then long break, the Dexcom 4, then Medtronic with 670G pump, now Dexcom 6 with Tandem pump.

      2
      4 years ago Log in to Reply
    24. Nicholas Argento

      Not sure how someone could be using more than 20 years. Personal CGM has only been widely available commercially since Spring of 2006. Maybe they were in studies. I started in 8-2006, have been on it continuously since, and am likely only alive today as a result. Before CGM, hypoglycemia was trying to kill me.

      1
      4 years ago Log in to Reply
    25. Bonnie Lundblom

      I’ve been using CGM’s for over 8 years now, all have been Dexcom. I’m really looking forward to the Dexcom 7, but I’m not sure when Medicare will allow the change from 6 to 7.

      4 years ago Log in to Reply
    26. jamesmpii

      Since diagnosis 4 months ago. I have never known T1D life without one.

      4 years ago Log in to Reply

    For CGM users: How long have you been using a CGM? Cancel reply

    You must be logged in to post a comment.




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