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    • 1 hour, 26 minutes ago
      KarenM6 likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      There are many concerns, one being if I'll still be alive if it's ever offered :)
    • 1 hour, 26 minutes ago
      KarenM6 likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      At 78 I don't think islet transplantation will affect my life course. Big pharma sees biological treatments as the path to ever higher profits, not constrained by patent terms the way drugs are. Most diabetics would be better served by an improved standard of care from the ADA and the medical community.
    • 2 hours, 41 minutes ago
      Lawrence S. likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      Very, but more worried about it even making to the FDA and approved there first.
    • 2 hours, 42 minutes ago
      Lawrence S. likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      There are many concerns, one being if I'll still be alive if it's ever offered :)
    • 2 hours, 42 minutes ago
      Lawrence S. likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      At 78 I don't think islet transplantation will affect my life course. Big pharma sees biological treatments as the path to ever higher profits, not constrained by patent terms the way drugs are. Most diabetics would be better served by an improved standard of care from the ADA and the medical community.
    • 2 hours, 43 minutes ago
      Lawrence S. likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      Severe case of hardening of the “oughteries” here. Ought we be concerned with cost, insurance, coverage, hail storms, earthquakes? ▄█▀█● Why are we not homeschooled to enjoy the progress being made?
    • 2 hours, 44 minutes ago
      Lawrence S. likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      While those items are very much a concern, there are other factors that are more concerning ie immunosuppressant.
    • 2 hours, 45 minutes ago
      Amanda Barras likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      If they can transplant them such that we do not need immunosuppresants, we'd be fine. Otherwise, those meds are just one more thing that could become in short supply. But at least we could go through scanners at the airports and travel without huge bags of supplies.
    • 2 hours, 45 minutes ago
      Amanda Barras likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      General access to islet transplants is still years away. FDA has to deem it safe. Though, I am excited about the possibility.
    • 2 hours, 45 minutes ago
      Amanda Barras likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      At 78 I don't think islet transplantation will affect my life course. Big pharma sees biological treatments as the path to ever higher profits, not constrained by patent terms the way drugs are. Most diabetics would be better served by an improved standard of care from the ADA and the medical community.
    • 4 hours, 47 minutes ago
      Patricia Dalrymple likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      If they can transplant them such that we do not need immunosuppresants, we'd be fine. Otherwise, those meds are just one more thing that could become in short supply. But at least we could go through scanners at the airports and travel without huge bags of supplies.
    • 5 hours, 25 minutes ago
      Gerald Oefelein likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      If they can transplant them such that we do not need immunosuppresants, we'd be fine. Otherwise, those meds are just one more thing that could become in short supply. But at least we could go through scanners at the airports and travel without huge bags of supplies.
    • 5 hours, 25 minutes ago
      Gerald Oefelein likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      While those items are very much a concern, there are other factors that are more concerning ie immunosuppressant.
    • 6 hours, 8 minutes ago
      Marty likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      much more concerned about my age (65) than anything else. 😉
    • 6 hours, 30 minutes ago
      dholl62@gmail.com likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      much more concerned about my age (65) than anything else. 😉
    • 6 hours, 54 minutes ago
      Steve Rumble likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      Severe case of hardening of the “oughteries” here. Ought we be concerned with cost, insurance, coverage, hail storms, earthquakes? ▄█▀█● Why are we not homeschooled to enjoy the progress being made?
    • 6 hours, 54 minutes ago
      Steve Rumble likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      While those items are very much a concern, there are other factors that are more concerning ie immunosuppressant.
    • 6 hours, 54 minutes ago
      atr likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      Severe case of hardening of the “oughteries” here. Ought we be concerned with cost, insurance, coverage, hail storms, earthquakes? ▄█▀█● Why are we not homeschooled to enjoy the progress being made?
    • 7 hours, 9 minutes ago
      Sarah Berry likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      much more concerned about my age (65) than anything else. 😉
    • 8 hours, 10 minutes ago
      Steve Rumble likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      Age 73 here. I'm in the same boat. I ogten am considered too old for consideration for "smaller" research projects. But - best of luck to them. I'll be rooting on the sidelines.
    • 8 hours, 11 minutes ago
      Steve Rumble likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - 👍 immunosuppression needed - 👎
    • 23 hours, 11 minutes ago
      Gerald Oefelein likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I've tried twice and was rejected both times because I control my diabetes as best I can. As others have already stated, if immunosuppressing drugs are involved, count me out. I'm not interested in something worse than what I already have.
    • 23 hours, 11 minutes ago
      Gerald Oefelein likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      Not if it requires immunosuppressant drugs. Been there done that time to move on to something much better.
    • 23 hours, 12 minutes ago
      Gerald Oefelein likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - 👍 immunosuppression needed - 👎
    • 1 day, 4 hours ago
      Natalie Daley likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I answered “Very Unlikely” not because I woud not want to participate but because, at age 75, I think it very unlikely that any researcher would want me in their patient panel.
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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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