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    • 15 hours, 5 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, 8 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, 9 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, 9 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, 17 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, 10 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, 10 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, 13 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, 13 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, 15 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".
    • 1 day 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, 1 hour 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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    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

    How concerned are you right now about affording your next order of T1D supplies?

    Next

    If you’ve lived with type 1 diabetes for more than 10 years, what resources do you find most useful for your continued diabetes management education? Select all that apply!

    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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    20 Comments

    1. LizB

      I started using the original Medtronic sensors in 2007, when they introduced the 522/722 pumps that also acted as the receiver for the readings. Those old harpoon sensors worked very well for me.

      3 years ago Log in to Reply
    2. Lee Johnson

      A male nurse at a RWJ recommended a gm when I was in the ER. I started with a G4, then a G6 and now the G7 which seems to work the way they should. The arm location is a pain but my last two insertions are back to my abdomen. The accuracy of the G7 is very satisfying. I feel like a walking electric transmission machine with my fit bit, cgm and cell. My wife of 36 years is using the G6!

      3 years ago Log in to Reply
    3. Jane Cerullo

      Don’t remember exactly but as soon as available.

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

      My memory is foggy from time-to-time. It was either 2006 or 2008. My health insurance had not yet approved CGM financial coverage. After a 1 1/2 hour drive to work in the morning, I high a low blood glucose soon after arriving at work (I should note that I was doing 12 or more glucose blood tests daily) and collapsed. I broke my right ankle in the fall. While at home convalescing from my injury, I called the insurance company and said that if I had a continuous glucose monitoring (CGM) system, I probably would not be out of work, and they would not be paying money for my broken ankle. Soon afterward, I was approved for a CGM (Medtronic), and may have been the first approved by my insurance company for a CGM.

      1
      3 years ago Log in to Reply
    5. Steven Gill

      Used a CGM maybe 6 years ago with the Medtronic system, due to the costs stopped (my old dog’s meds were more expensive). Almost 2 years ago Medtronic offered the upgrade, added “patient assistance,” used the 770G in manual because the system wasn’t dosing aggressively enough. A year ago learned how to use the CGM correctly (and insulin), now retired/dropped health insurance and pay for the Libre3 (with insulin pens).

      3 years ago Log in to Reply
    6. Kathleen Juzenas

      It’s been at least 6 years but I don’t know exactly.

      3 years ago Log in to Reply
    7. Marty

      I started using the Medtronic CGM system with the harpoon sensors as soon as they were available to me, which probably was in 2006-2007. It was life changing, of course. I would probably give up my pump before I’d give up my Dexcom just for the peace of mind of knowing that I wasn’t on the verge an awful low.

      3 years ago Log in to Reply
    8. Nicholas Argento

      I did try the wrist watch system (Glucowatch) briefly but it was painful and inaccurate, so I did not count that. I started full time in 8-2006, which is when CGM became widely commercially available, It was the first Dexcom system, 3 days and not very accurate- but a game changer for me!

      1
      3 years ago Log in to Reply
    9. Leigh French

      Don’t know the date but I started when the first Dexcom was available. Stayed with them ever since.

      3 years ago Log in to Reply
    10. cynthia jaworski

      I waited until the libre was available. It seems that having competition spurred on development by dexcom with issues like calibration and warm-up times.

      3 years ago Log in to Reply
    11. Trina Blake

      15+ years. I had to look up when Dexcom first came on the market. It was the Seven. I’ve been dexcom’ing daily ever since. Sometimes with insurance coverage, otehr times without. But my 15+ fingersticks a day were more expensive because I had to pay retail for the strips (the meter covered by my insurance was proven – by the AACE, The Diabetes Tech Society et al – to read higher than actual for people with chronic anemia. That’s quite risky – directing patients to do a correction bolus when it’s the last thing they need (they are trending low)

      1
      3 years ago Log in to Reply
    12. Maureen Helinski

      I started with Medtronic’s first lolipop think that had to be taped on the arm. It gave some measurements. Then came the Enlites. I used them until people convinced me that the Dexcom was more accurate, and it was. Great movement foreword.

      1
      3 years ago Log in to Reply
    13. Kristine Warmecke

      I started in July 2007 with Medtronic’s sensor. I had just had an accident due to a very low BS that I tried to treat but everything I had with me, wasn’t enough, I totaled my SUV. I was trying to find an endocrinologist that was on my insurance and as good as the one I couldn’t see; after hearing of my accident he ordered the Medtronic sensor and had me start it without asking my opinion on it. I reluctantly used it. I hated the calibration and that it rarely was correct or even close to what meter said, thus I was STILL testing daily and more than before. I was FINIAlLLY able to go back to my endocrinologist with new insurance, her and her team convinced me that Dexcom would be worth the switch. Best decision, I’m so happy with mine now. 16 years of CGM and more to go!

      1
      3 years ago Log in to Reply
    14. Jneticdiabetic

      Can’t remember when I got my first CGM exactly (2004-2007-ish). I estimate off and on for roughly 15-17 years.

      1
      3 years ago Log in to Reply
    15. KarenM6

      I don’t remember precisely.
      I did have a Dexcom G4 for a short time, but I couldn’t handle it and stopped using it.
      I was convinced to try again (it may have been a G5), but, again, was not able to handle it.
      The next one was the keeper and the change in processing and thinking that was my game changer. I consider it the “beginning” even though I had a few false starts… but, I just don’t remember when that was. It was sometime between 2009 and 2012-ish… maybe?

      3 years ago Log in to Reply
    16. ConnieT1D62

      Started with Medtronic harpoon inserter whatever they were called, then the Enlite – was a start but hated them. In 2009 switched to Dexcom 4, then 5, then 6. Will upgrade to Dexcom 7 soon and stay with Dexcom for foreseeable present and future.

      1
      3 years ago Log in to Reply
    17. Wanacure

      I remember ads for the Glucowatch but was advised of its inaccuracy & unreliability. Affordability has been the main barrier for pumps and CGMs. So I didn’t get a CGM until a few years ago when insurance started covering them after accuracy and reliability had improved. I have no reservations about becoming a cyborg.😎

      3 years ago Log in to Reply
    18. sweetcharlie

      Been on Medicare Advantage insurance a LONG time and one injection per day, I did NOT qualify for free CGM… Started using finger sticks about 30 years ago, 3 per day… Then got aproval for 6 sticks per day…. Then about 2 years ago my Doctor wrote a letter to my insurance and they approved free CGM…. Now [ I think ] Medicare is approving CGM for all In sulin useres…

      3 years ago Log in to Reply
    19. Bruce Johnson

      I only use the Freestyle 2 CGM when I have enough money to afford it

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

      Started with the Medtronic Enlight, on to the Dexcom G4-G5 now on the G6 awaiting the G7.

      3 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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