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    • 1 hour, 4 minutes ago
      alex likes your comment at
      Here’s What You Need to Know About the Dexcom G7
      This article explains the Dexcom G7 features in a clear and easy way, especially for people new to continuous glucose monitoring. Very informative and helpful. Sportzfy TV Download
    • 16 hours, 27 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.
    • 16 hours, 29 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.
    • 16 hours, 30 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.
    • 16 hours, 31 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
    • 16 hours, 39 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 ´ )⎠⎞
    • 18 hours, 31 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.
    • 18 hours, 32 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.
    • 18 hours, 34 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 ´ )⎠⎞
    • 22 hours, 35 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
    • 1 day 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, 1 hour 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, 1 hour 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, 1 hour 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, 1 hour 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, 1 hour 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, 1 hour 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, 1 hour 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, 1 hour 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, 2 hours 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, 2 hours 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, 2 hours 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, 14 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, 16 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, 16 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.
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    Do you currently use any of the following insulin pumps?

    Home > LC Polls > Do you currently use any of the following insulin pumps?
    Previous

    Do you currently use any of the following CGM systems?

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    Have you ever changed diabetes healthcare providers because you did not like their personality?

    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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    17 Comments

    1. Chip Brookes

      I have a Slim X2. Love the functions provided by Control IQ. I hate the method for installing the infusion set.

      5 years ago Log in to Reply
    2. Britni Steingard

      I answered both “Omnipod Dash” and “I do not wear an insulin delivery device” because I’m switching from Omnipod back to MDI later today. Gave it a year. Blood sugars didn’t improve and it’s often painful. Not worth the effort, but I will miss the food library and dose calculator.

      5 years ago Log in to Reply
    3. Gene Maggard

      Although the 670G was available when I upgraded my old Medtronic pump, I chose the 630G because it was covered under Medicare. I also hated the Medtronic CGM on my older pump, it was never accurate, gave me error alerts all night, and was constantly telling me to calibrate. Very happy with the 630G and Dexcom G6 combination.

      5 years ago Log in to Reply
    4. Kristen Clifford

      I still have a Medtronic 530G. The intention was to eventually switch me over to the 630G, but then before I knew it, the 670 was out. Now there’s the 770. I’m also contemplating an OmniPod or perhaps a T-slim.

      5 years ago Log in to Reply
    5. MARIE PEELER

      Husband is using the Tandem Tslim. Loves the Basal IQ function that keeps him from going too low during exercise. But we’ve deliberately not upgraded to Control IQ as it sets the target BG too high for people who already maintain tight control and can makes it impossible to achieve the same A1C and time in range.

      5 years ago Log in to Reply
    6. Thomas Hatton

      I just upgraded from 670G to a 770G, 3 weeks ago on the lift ticket program. I tried to trade in my 630G for the 770G but they objected to that. I wanted to keep my 670G as a back up. Looking forward the software upgrade to 780G with bolis capability.

      5 years ago Log in to Reply
    7. Nevin Bowman

      I’ve been using Medtronic for around 18 yrs, but I will be switching as soon as my insurance allows. They were innovative with pumps, but their CGMs have always been lacking in accuracy, and they are nowhere close to being reliable enough for me to trust it to give me insulin.

      5 years ago Log in to Reply
    8. Trina Blake

      I’m with Marie Peeler’s husband. Tandem X2 with Basal IQ. Same reasons he stayed with BIQ; Control IQ settings are higher than I want, I too have tight management. I’ve used Animas and the Cozmore in the past.

      5 years ago Log in to Reply
    9. William Bennett

      I switched from my Medt Paradigm 730 (the old pager-style pump) to the 670G when it came out, but after 6 months I gave up and went back to my 730. Hated the over-complicated and less accurate Guardian sensors, was getting much better results with my old Paradigm and Dexcom G6 CGM than the frustrating hybrid algorithm could produce, and it kind of soured me on the whole idea of AID pumps in general. Now I’m up for a new pump again, but the old Paradigm is still ticking along, and neither the 770/780G nor the Tandem system seems particularly attractive (I really dislike the fussy overcomplicated Tandem reservoir system).

      5 years ago Log in to Reply
    10. Sherolyn Newell

      I have Omnipod and Dexcom G6. I tried to switch to Dash, but the way they set it up for insurance purposes, BCBS wouldn’t cover it. I am looking forward to seeing what their closed loop system with Dexcom G6 is like.

      5 years ago Log in to Reply
    11. kamiandcrew

      I just started on the 770G 3 days ago. I was on the 670G. I like that it automatically downloads. The CGM transmitter was problematic when I first started but once I found a better way to secure it I’m happy with the results (no excessive calibrating, no uncontrolled highs , good correlation between fingerstick and reading, plus my A1C is the best it’s ever been)

      5 years ago Log in to Reply
    12. John McHenery

      I was on Paradigms for ~8 years and last year switched to Medtrum’s patch pump and sensor as I liked the idea of the sensor and pump coming from the same supplier. Bad idea and switched about 6 months later to the Ypso pump and Libre sensor.

      5 years ago Log in to Reply
    13. Molly Jones

      I currently use Tandem X2 with control IQ. I tried Medtronic 670G on a short trial almost three years ago after a decade of their other products, and a version of Omnipod in 2016. I like the idea of Omnipod the best. I use tandem as it partners with Dexcom.

      5 years ago Log in to Reply
    14. Patricia Maddix

      I have used Medtronic pumps since 1997 and currently have a model called the 723. This was actually a replacement for my 523 that died two years ago. Because of the timing of my warranties and Medicare regulations I have never been eligible for one of the more automated systems until now as my 723 is out of warranty. In the past I too struggled with in accurate readings from the Medtronic sensors and switch to Dexcom many years ago. I have been really on the fence as to which pump to choose next and I’m just staying with my current pump for now as it is working fine. I understand that tandem is going to be coming out with a new pump called the sport that is half the size of the current X2 and is operated either from a remote device or phone app. I am visually impaired and would really like a pump that could be controlled entirely or almost entirely from an accessible phone app. That feature seems to be on the near horizon so I am hanging tight.

      5 years ago Log in to Reply
    15. Leona Hanson

      I use medtronic 630 it works very well with high altitude

      5 years ago Log in to Reply
    16. Carlene Vaitones

      I prefer injection therapy. I have more control over my BGs, and no occlusions leading to lack of insulin coverage.

      5 years ago Log in to Reply
    17. Sally Numrich

      Tandem IQ and I love it! I spend so much less time thinking about my diabetes because the pump turns off if I am heading down! My glucose tablet usage has been reduced and my mental well-being has been great! I don’t test anymore and I can’t even tell you if the numbers are close because I don’t care. The pump just does its thing and I can go all day without looking at my pump if I’m not eating. Been pumping since 1990 and had 3 pumps in the first 20 years with Minimed/Medtronic. Never had any problems with them. I tried Omnipod during a trial, not my favorite due to kinking problems & only one length on length of needle & much bigger than I liked on my body parts. Made the switch to Tandem mainly due to how little Medtronic had made changes. The few times I upgraded, the changes were not that big a deal. And now with a pump that lets me not think, why change?! Of course my next trial is iLet pump and that is my dream because I won’t have to count carbs!

      5 years ago Log in to Reply

    Do you currently use any of the following insulin pumps? Cancel reply

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