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    • 14 hours, 55 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, 57 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, 58 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, 58 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, 7 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 ´ )⎠⎞
    • 16 hours, 59 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 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, 2 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, 2 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, 4 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, 50 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, 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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    If you wear a CGM, what do you do when a sensor fails?

    Home > LC Polls > If you wear a CGM, what do you do when a sensor fails?
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    Have you ever used a digital health coaching app (ex: One Drop, mySugr, Livongo, etc.)? If so, share your experience in the comments!

    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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    25 Comments

    1. Bob Durstenfeld

      Dexcom is usually pretty good about replacements.

      5 years ago Log in to Reply
    2. Ahh Life

      Other. I call, but only after several have failed prematurely. I recently had 9 not meet their life expectancy. I suspect it was a bad batch. I called after several months. ( ͠° ͟ʖ ͡°)

      5 years ago Log in to Reply
    3. Thomas Hatton

      Minimed sensors fail often. I had one earlier this week. The medtronic diabetes store has a replacement link on the main menu. They will only replace 3 over a 3 month span. Because they cost so much i don’t hesitate ordering replacements. That’s how I know about the limit. If the sensors were more reliable, they wouldn’t have this problem.

      5 years ago Log in to Reply
    4. joan Fray

      I save it. Then call Dexcom and they are good about replacing them. I’ve only had two fail in three years. They always want me to send the old one back to them.

      5 years ago Log in to Reply
    5. connie ker

      I was having trouble with the Abbott Freestyle Libre staying on my arms, until I started using the clear tape that is worn over the entire sensor. It keeps the sensor on for the entire 2 weeks and my supplier does not charge extra for the tape, I just have to ask for it. So live and learn, but do what works best for you.

      5 years ago Log in to Reply
    6. Clare Fishman

      I recently found out that I can just go to Dexcom tech support online at https://www.dexcom.com/support You can put in your sensor problems or “chat” with a support person online. I have not had a sensor fail in more than a year, but when it does I always request a replacement.

      5 years ago Log in to Reply
    7. Gene Maggard

      I’ve only had one Dexcom G6 sensor fail in almost three years, so didn’t follow up. When I was using Minimed sensors I had a lot of problems and had several replaced. My situation now is that under my Medicare Advantage plan I don’t pay anything for the Dexcoms so an occasional one failing isn’t a big deal for me.

      5 years ago Log in to Reply
    8. William Bennett

      Website, because Dexcom offers a chat option on their contact page that is 20X faster and more responsive than calling and sitting on hold for hours. It’s limited to business hours Pacific time, but that’s not a huge problem even for an East Coaster like me.

      5 years ago Log in to Reply
    9. Lorri McLuckie

      I’ve had several sensor failures and always call for a replacement. Yesterday I had a transmitter fail and also called for a replacement for that.

      5 years ago Log in to Reply
    10. Amanda Barras

      A failed sensor happens so rarely that I throw it and just start anew with out worrying. I usually extend my sensors and get a an extra 4-5 days of wear beyond its life expectancy. So, with that I gain more time than I lose when one does fail.

      5 years ago Log in to Reply
    11. Kristen Clifford

      I throw out the one that failed and put on a new one. End of story.

      5 years ago Log in to Reply
    12. Kris Sykes-David

      Funny you should ask! Just last night my transmitter for my G6 failed after 20 days. I called Dexcom and they acted quickly, as always when I have a problem. After the warmup on the new sensor/transmitter combo, my readings were LOW. That’s not what my finger stick told me! Well, since it was late, I gave it overnight to “cook” to see if there would be any change in numbers. (I actually turned off my receiver and Bluetooth on my phone, no way to sleep with that racket!) This morning it is up a bit higher but over 50+ points off. Time to call Dexcom again ……

      5 years ago Log in to Reply
    13. Abigail Elias

      Not a common event but I call because they like defective products returned for quality control and troubleshooting.

      5 years ago Log in to Reply
    14. Angela Naccari

      I use the Tandem X2 pump and Dexcom G6. The last time I had a problem with the transmitter failing early (just a few weeks after used), Tandem replaced the transmitter and the sensor that was lost

      5 years ago Log in to Reply
    15. Ceolmhor

      My answer isn’t as simple as the choices you provide. My Medtronic sensors are supposed to last a week. If the failure occurs in the last 2-3 days, I just throw it away. If it fails early, and my supply is low, I call for a replacement. If it fails early, and my supply is more than I need (that’s most of the time), I still call to see if they want the failed sensor returned for investigation. They request that less frequently these days, but sometimes it helps them discover the causes of their failures.

      5 years ago Log in to Reply
    16. Megan L

      Mine rarely fails, but when it does, I just get a replacement from the website (Medtronic). Much faster (and not having to deal with a frustrated representative), in my opinion.

      5 years ago Log in to Reply
    17. Elizabeth Thompson

      Medtronic always replace them but I didn’t know you could get a replacement sensor from the website. I thought you had to speak to a representative and answer all the questions etc! Takes a while for sure. Someone commented on getting more time from your sensor. How do you do that? Mine tells me to replace it after 7 days and the transmitter no longer receives readings. Thanks.

      5 years ago Log in to Reply
    18. KarenM6

      Mine fail about 55% of the time (and I have an Excel spreadsheet to prove it.) ;p One of the only times I’ve geeked out on data! ;p So, if a sensor fails on the 8th or 9th day, I just let it go. But, if it fails between 1 and 7 days, I _generally_ call for a replacement (especially if I’m low on sensors). Dexcom has always been fantastic with the customer service on this issue. I appreciate that about them so much. (I’m very excited to see what their G7 will be like!)

      5 years ago Log in to Reply
    19. Ann Taylor

      I very rarely have trouble – the last time I had a problem it was my transmitter that died Does anyone else have an issue with the Dexcom 6 being way off from the finger sticks? In the morning it can be right on or very close and by lunch it can be 30 or more off

      5 years ago Log in to Reply
    20. Cheryl Seibert

      Dexcom’s Live Chat feature on their support website is the easiest way to obtain a replacement. Plus everything discussed is documented. The tech support folks are extremely helpful and kind.

      5 years ago Log in to Reply
    21. Derek West

      This is for Elizabeth who questioned how to get her Medtronic sensor to last more than 7 days. I leave mime inserted but disconnect the transmitter and re-charge it. I then tell the pump it is a new sensor and it happily goes through the warm up procedure. To be able to remove the transmitter I use surgical tape to hold it in lace the first week, which comes off relatively easily. I only use the sensor for 2 weeks.

      5 years ago Log in to Reply
    22. Sasha Wooldridge

      I had no idea they would replace them now! I started with a Dexcom WAY back at the beginning for me, so 10 years ago or so. I argued so much with everyone about getting them replaced that I gave up and that’s when I started reusing them to create a stockpile just in case. I never revisited the issue in all this time. Good to know this is an option now!

      5 years ago Log in to Reply
    23. Molly Jones

      I chose other as my main goal was to call the company and report issues with the sensor, so cause could be found and prevented. I always receive a replacement, which is nice. I am curious if I have issues with my sensors about a quarter of the time due to quick fluctuations in BG. It can be difficult to find the right time to start a session when my BG will be stable.

      5 years ago Log in to Reply
    24. Bonnie Lundblom

      I’m on Medicare now and switched to the Dexcom CGM 6 in September. I’ve had multiple sensors fail since then and one transmitter that only lasted 4 weeks. When I call Dexcom tech support I’ve been told if the readings are off significantly from finger sticks and calibration doesn’t rectify this I’m to remove the sensor, apply a new one, and call for a replacement.

      5 years ago Log in to Reply
    25. Elizabeth Thompson

      Thanks, Derek! Appreciate you taking the time to explain.

      5 years ago Log in to Reply

    If you wear a CGM, what do you do when a sensor fails? Cancel reply

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