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    • 52 minutes ago
      Ahh Life likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      So far since Jan 1, ‘26, I’ve spent nearly 30 hours on the phone battling and trying to get Medicare covered diabetes supplies. Called 5 different suppliers t get what I need to use my pump.
    • 53 minutes ago
      Ahh Life likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      You are too modest. That hurdle is on fire and you have to juggle chainsaws as you jump over it. Congratulations and good luck making it over the next one in 90 days.
    • 14 hours, 34 minutes ago
      KarenM6 likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
    • 16 hours, 21 minutes ago
      Kristi Warmecke likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      Well, since I'm waiting on pump supplies for 2 months now, my confidence is slipping.
    • 16 hours, 22 minutes ago
      Laurie B likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I've often said that "hoarding": is a character asset for T1D people. I try to purchase (paying out of pocket) a 60-90 day supply - just in case). I have a new health plan,. effective 1/1/26. AS we know, getting an appt with an HCP isn't easy. They have to be accepting new patients, they have to be in network etc. Once I knew what my new policy would be (nov 2025) I made an appt. The earliest appt I could get was in Sept 2026. Thank goodness for my stash of device supplies. I had to go to Urgent care to get an Rx for insulin (my old HMO plan "doesn't do bridge refills"). So yeah, I worry, and plan for hiccups in the supplies process.
    • 16 hours, 22 minutes ago
      Kristi Warmecke likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I answered slightly. I'm absolutely certain supplies and medication will be available. However, I'm doubtful they will be affordable. If I can't afford them, I can't access them.
    • 17 hours, 21 minutes ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I am confident about access to my medical needs in the immediate future. I am not a fortune teller and have no idea what my access to medical supplies will be like in a year or longer. I don't take my spoiled lifestyle for granted.
    • 17 hours, 21 minutes ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I've often said that "hoarding": is a character asset for T1D people. I try to purchase (paying out of pocket) a 60-90 day supply - just in case). I have a new health plan,. effective 1/1/26. AS we know, getting an appt with an HCP isn't easy. They have to be accepting new patients, they have to be in network etc. Once I knew what my new policy would be (nov 2025) I made an appt. The earliest appt I could get was in Sept 2026. Thank goodness for my stash of device supplies. I had to go to Urgent care to get an Rx for insulin (my old HMO plan "doesn't do bridge refills"). So yeah, I worry, and plan for hiccups in the supplies process.
    • 17 hours, 22 minutes ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I answered slightly. I'm absolutely certain supplies and medication will be available. However, I'm doubtful they will be affordable. If I can't afford them, I can't access them.
    • 17 hours, 25 minutes ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I am worried about the changes to Medicare making no provision for getting an immediate replacement if a pump fails. It sounds like we will have to get these from the suppliers instead of a warranty replacement from Tandem themselves (or whatever brand you use). Pumps will be rented and will have to be returned so they can verify the problem before replacing them, which is ridiculous. Meanwhile, Medicare would not pay for us to get long acting insulin as a temporary replacement for the basal.
    • 17 hours, 27 minutes ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I broke down for the first time in 25 years and bought a bottle of insulin because I think I may have thrown a bottle out with the box. Medicare wouldn’t fill the prescription because it was too early. I just didn’t want the fight and worry. I’m not sure that’s what happened but it’s the only explanation. Also, I live in Florida and the threat of losing power is always there. I should get a generator but I’m a little afraid of them and you still can’t be sure you have access to propane. If my insulin goes bad, I’m not sure I could get refills. My back up plan is to leave before hurricane or go to a hospital. But it is all just causes concern.
    • 17 hours, 41 minutes ago
      Derek West likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Very! However, I wish I could use Fiasp insulin in the Tandem pumps.
    • 20 hours, 16 minutes ago
      Bruce Schnitzler likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I broke down for the first time in 25 years and bought a bottle of insulin because I think I may have thrown a bottle out with the box. Medicare wouldn’t fill the prescription because it was too early. I just didn’t want the fight and worry. I’m not sure that’s what happened but it’s the only explanation. Also, I live in Florida and the threat of losing power is always there. I should get a generator but I’m a little afraid of them and you still can’t be sure you have access to propane. If my insulin goes bad, I’m not sure I could get refills. My back up plan is to leave before hurricane or go to a hospital. But it is all just causes concern.
    • 20 hours, 48 minutes ago
      Karen Newe likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      The most common comment: but you aren’t heavy. That’s when we get into the differences. A relative tried to tell me that insulin makes you lose weight. But when we last discussed this, one of you said it best: if it isn’t in their circle of experience, why would they know or care?
    • 21 hours, 5 minutes ago
      KSannie likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Very! However, I wish I could use Fiasp insulin in the Tandem pumps.
    • 21 hours, 6 minutes ago
      KSannie likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
    • 21 hours, 7 minutes ago
      KSannie likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      My first reaction was Very Satisfied but there is always room for improvement. I’d like a pump design that wasn’t meant to be worn on a belt just for men. To wear a dress, I have to only get those with pockets (and on both sides because opposite sides cause the CGM to lose contact) and put a button whole in each. The clip shows horribly on blouses worn out. I’ve tried the leg attachments and they never stay secure. I’m not big enough to wear it in my bra. All minor inconveniences. I’d like one that doesn’t keep alarming 20 minutes after I’ve eaten, although I get it that it is there to save my life. Again minor. Ask about CGMs (probably tomorrow’s question): lately I’ve had trouble removing the sensor from my arm without actually ripping off a strip of skin or very bad bruising. I’ve read about using baby oil for removal. That does help. I’m a rip it off fast person, but that didn’t work so well.
    • 22 hours, 34 minutes ago
      Patricia Dalrymple likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Try Uni-Solve Adhesive Remover (smith&nephew)- wipe it on wait a minute to let it work and it will come off easy. at least it works great for me and I've tried several different brands, I use it for CGM & Omnipod removal
    • 1 day, 5 hours ago
      Sandy Norman likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
    • 1 day, 13 hours ago
      kristina blake likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      There are several conversations about this across social media. Many people chime in and vote for a new, more accurate name for type 1.. some of the popular alternatives- Pancreatic Autoimmune Disease, Beta Cell Destruction Disease, Autoimmune Diabetes, Autoimmune Insulin Failure, Autoimmune Absolute Insulin Deficiency (AAID)
    • 1 day, 13 hours ago
      kristina blake likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      The most common comment: but you aren’t heavy. That’s when we get into the differences. A relative tried to tell me that insulin makes you lose weight. But when we last discussed this, one of you said it best: if it isn’t in their circle of experience, why would they know or care?
    • 1 day, 13 hours ago
      kristina blake likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      In my experience the average person does not know the difference. It does not help that the commercials on TV just say diabetes and do not differentiate.
    • 1 day, 15 hours ago
      Kristi Warmecke likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
    • 1 day, 17 hours ago
      Lee Tincher likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      If I could get a CGM that is consistent and predictable I'd be very happy with the Twiist or the Tandem. The weak point with pumps used to be infusion sites, but now that we are relying on poor performing technology to support potentially great algorithms itis quite frustrating.
    • 1 day, 19 hours ago
      Beckett Nelson likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      My first reaction was Very Satisfied but there is always room for improvement. I’d like a pump design that wasn’t meant to be worn on a belt just for men. To wear a dress, I have to only get those with pockets (and on both sides because opposite sides cause the CGM to lose contact) and put a button whole in each. The clip shows horribly on blouses worn out. I’ve tried the leg attachments and they never stay secure. I’m not big enough to wear it in my bra. All minor inconveniences. I’d like one that doesn’t keep alarming 20 minutes after I’ve eaten, although I get it that it is there to save my life. Again minor. Ask about CGMs (probably tomorrow’s question): lately I’ve had trouble removing the sensor from my arm without actually ripping off a strip of skin or very bad bruising. I’ve read about using baby oil for removal. That does help. I’m a rip it off fast person, but that didn’t work so well.
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    For CGM users: How long have you had a CGM?

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

    For insulin pump users: How long have you worn an insulin pump?

    Next

    How many appointments did you have in 2020 with your main diabetes healthcare provider?

    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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    12 Comments

    1. Amanda Barras

      8+, would have been 13+ had my insurance not denied coverage for it when I first went on pump.

      5 years ago Log in to Reply
    2. Annie Wall

      Just over four years. I started Dexcom when I got the Tandem G4 pump. I couldn’t live without it now!

      5 years ago Log in to Reply
    3. Thomas Hatton

      I started CGM IN 2017. I am now dependent on CGM. Recently the charger for my Medtronic transmitter failed. I was off CGM for 36 hours. It was nerve wracking to not know where my BG was, but because of my experience with CGM I had a good guess…

      5 years ago Log in to Reply
    4. Jana Wardian

      CGM is a game-changer! Now I gave real time information about directionality to make better decisions about diet and activity. I think CGM needs to become standard of care for people with type 1 diabetes. And use in the hospital environment makes sense!

      5 years ago Log in to Reply
    5. Becky Buchanan

      I seriously don’t remember when I started on it. Pump has been 23 years, 50 years as a Type 1. I fought for one for years. It is a pain in the bottom but so worth it.

      5 years ago Log in to Reply
    6. David Smith

      I started with Medtronic probably 10-12 years ago, but at the time each insertion of a sensor was like harpooning yourself. My first insertion, during my training, was very dramatic and hurt like all get-out. So I was kind of on-again, off-again with Medtronic. Tried again in earnest maybe 4 years ago when Medtronic came out with their integrated pump and CGM system, but I had some issues with that, so once again, I stopped using CGM. Then DEXCOM came along. I decided to try it about a year ago, and I love it. Easy insertions, very reliable. And I agree with many of the other comments I’ve seen – now I can’t imagine not using CGM. The ease of use, instant feedback on my glucose levels and trends and detailed reports make my diabetes management so much easier and stress-free!

      5 years ago Log in to Reply
    7. Maureen Helinski

      I started with the first Medtronic sensor which was like a lolipop that I taped on my arm. I couldn’t believe in 1983 that was was nothing to measure the BG. Not even a meter for people. So I followed Medtronic through the Enlite 3 and then changed to Dexcom about 2014. How great now with Control IQ.

      5 years ago Log in to Reply
    8. Dorian Dowell

      Have been a Dexcom user since Dexcom Seven Plus was available. It made life a WHOLE Lot better. While I still had to finger stick for calibration and it wasn’t supposed to be for “dosing” decisions., It was very accurate and quite reliable. Sooooo! G4 and G5 were each better and better. Dosing decisions were actually even better. Now with G6 ——-. I was without sensors for a couple of days while waiting for the VA to send my next supply. Talk about near panic!!! My fingers still feel the “discomfort” after a long time without being stabbed. (psychosomatic)

      5 years ago Log in to Reply
    9. kristina blake

      Been with Dexcom since the Dexcom7. I was delighted when they G4 came out with the smaller receiver. And not with the G6 integrated with my TandemX2 pump – only 1 device!!!! I am NOT one of those people who HAS to have my phone with me at all times. I have been using my G6 to dose since I canot safely use the meter that is covered by my healthplan. I was a 12-15x a day fingersticks person. Problem was, the meter covered read higher than actual. Turns out that meter reads higher on people who are chronically anemic – been that way my entire life. So… I was correcting for high bg’s I wasn’t experiencing, I was dutiful, did a confirmation fingerstick when my CGM said I was was heading low. But…was told by the meter that I wasn’t low, and often that I was high. Lots of major scary lows. Several years ago I was added to the Endo CME list. One of the topics was issues with home mpnitoring systems. Lo and Bewhold! That’s where I learned about the problem with the system covered by my health plan. I grabbed copies of all the reports, read them and then purchased the system with the highest accuracy ratings. For two months I continued with my 12-15 fingersticks a day, comparing (on a spreadsheet) the two meters and my Dexcom. The accurate meter and my Dexcom were within 2-3 pts consistently. Couldn’t afford to pay out of pocket, so I started going with my Dexcom readings. No more scary lows for several years now. In order to avail myself of the patients assistance program of the accurate meter I had to have an Rx. When I called my endo to get the Rx, he told me he knew about the issue. Why didn’t he mention it to me? I was getting scolded for the lows. Dude! DexcomG6 is not only a game changer, it is a life saver.

      5 years ago Log in to Reply
    10. ANN GALLUZZO

      I started with a Medtronic CGM in 2008, but was allergic to the metal in it. That one had a 1-year warranty, so I had to wait a full year before getting my Dexcom G4. I’ve used Dexcoms ever since. I love them. The Medtronic one was not accurate the first 24 hours of 72 hours you would leave it inserted, which made it kind of useless. The Dexcom was accurate right away and lasted 7 days (now increased to 10).

      5 years ago Log in to Reply
    11. Molly Jones

      I started using Medtronic’s CGMs in 2007 off and on as it was not reliable in reporting my glucose. I tried Dexcom for the first in 2016 while using Medtronic’s pump and use it always as I am hooked to having reliable readings.

      5 years ago Log in to Reply
    12. Ahh Life

      Just do it📍 If you have to beg, borrow, or steal the things (yes, steal📍), the quickness and accuracy of down arrows and double down arrows can and will save your life. At least, if you take the amount of insulin I do, about 25 units per day. 🤷🏻‍♂‍

      5 years ago Log in to Reply

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

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