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    • 1 hour, 36 minutes ago
      Amy Schneider likes your comment at
      Do you store your unopened insulin in the refrigerator?
      I keep my opened insulin in the refrigerator too. When traveling I use a FRIO evaporative pouch.
    • 3 hours, 3 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      I want a thumbs down icon!
    • 3 hours, 3 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      I seldom have any questions other than RX refill request which I submit through the patient portal. If I do have treatment questions, I typically do my own research, and if not satisfied with what I find out, I submit a question in the portal.
    • 3 hours, 3 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      When I come up with a question between visits, I usually just do some research.
    • 5 hours, 16 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      I keep my opened insulin in the refrigerator too. When traveling I use a FRIO evaporative pouch.
    • 5 hours, 17 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Sorry. Of course I store unopened in frig. Opened in my room as I use it up in 30 days
    • 5 hours, 17 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      No, I keep it in the oven! ;) Same answer as the last time they asked this ridiculous question!
    • 6 hours ago
      Becky Hertz likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Unopened yes, and now even opened just in case. I am getting a new health [lan (thank goodness a much better one - with better doctors and hospitals in network!) so it's worth it. But I can't get any appt - even for a PCP until September. I've been occasionally buying out of pocket insulin, pump and CGM supplies (in my mind, hoarding is a character asset for T1D people). I need to have my enough stuff to see me through, Of course, I am hoping there''s an appt cancellation.
    • 7 hours, 23 minutes ago
      Bruce Schnitzler likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Unopened yes, and now even opened just in case. I am getting a new health [lan (thank goodness a much better one - with better doctors and hospitals in network!) so it's worth it. But I can't get any appt - even for a PCP until September. I've been occasionally buying out of pocket insulin, pump and CGM supplies (in my mind, hoarding is a character asset for T1D people). I need to have my enough stuff to see me through, Of course, I am hoping there''s an appt cancellation.
    • 9 hours, 20 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
    • 1 day 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.
    • 1 day 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.
    • 1 day 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.
    • 1 day 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
    • 1 day 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 ´ )⎠⎞
    • 1 day, 2 hours 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.
    • 1 day, 2 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.
    • 1 day, 2 hours 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 ´ )⎠⎞
    • 1 day, 6 hours 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, 8 hours 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, 9 hours 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, 10 hours 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, 10 hours 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, 10 hours 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, 10 hours 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.
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    In a typical week, how often are you woken up by your CGM or other diabetes-related alarms (such as, for a low or a high alert)?

    Home > LC Polls > In a typical week, how often are you woken up by your CGM or other diabetes-related alarms (such as, for a low or a high alert)?
    Previous

    On a scale of 1-5, how much are your personal relationships (social and intimate) affected by living with T1D? (5 = the most affected, 1 = the least affected)

    Next

    If you’re a caregiver of a child living with type 1, how often do you wake your child up when they need a low snack in the middle of the night?

    Samantha Walsh

    Samantha Walsh has lived with type 1 diabetes for over five years since 2017. After her T1D diagnosis, she was eager to give back to the diabetes community. She is the Community and Partner Manager for T1D Exchange and helps to manage the Online Community and recruit for the T1D Exchange Registry. Prior to T1D Exchange, Samantha fundraised at Joslin Diabetes Center. She graduated from the University of Massachusetts with a Bachelors degree in sociology and early childhood education.

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    26 Comments

    1. Trina Blake

      Every “night” – sometimes I sleep during the day, other times my schedule allows me to be a regular person and sleep at night. I also have my alarms set to a very narrow range – 60 for low alerts and 120 for high alerts (I like to nip highs in the bud)

      2 years ago Log in to Reply
    2. A Montalbano

      Used to be almost every night, multiple hours of management even on closed loop. Most common was compression lows that led to turning off basal and subsequent highs OR poor communication between devices putting it in limited mode.

      2 years ago Log in to Reply
    3. Janice B

      For highs or lows rarely woken up.
      However I am woken up every 3 days at 2:00am by OmiPod telling me my pod is about to expire. Wish this was an alarm that could be disabled!

      2
      2 years ago Log in to Reply
      1. Kathy Hanavan

        You can change how far ahead the alarm will beep you I think

        2 years ago Log in to Reply
    4. Jane Cerullo

      Can’t win. On MDI. Was injecting long acting in the morning but kept waking up with rising glucose. So switched to night time. Now having lows. Working on it. In process of switching to a tandem pump. Lots of paperwork. Even want a c peptide.

      2 years ago Log in to Reply
      1. cynthia jaworski

        Before tresiba, I would split my long-acting dose to a morning plus an evening dose. That worked pretty well, but tresiba is better. Good luck with the pump.

        2 years ago Log in to Reply
    5. TEH

      I have gotten into the habit of checking my BG at bedtime. If it is approaching low I will eat a snack before going to bed. This has helped avoid night time lows for me.

      2
      2 years ago Log in to Reply
    6. Carol Evans

      I use Medtronic 770G with Guardian 4 and over 90% of my nights are very stable between 95-115.

      2
      2 years ago Log in to Reply
    7. spencercarter1

      I have used Dexcom for years and every night I get woken up from alarms, usually 1-3 times. A few months ago, I removed Dexcom and went back to finger pokes, ~20-30 times a day. My sleep has significantly improved. Perhaps the cost of this is a high in the night that I don’t correct for and we’ll see how my HbA1c has changed. I have a feeling it will be slightly higher, but not by much. I’m wondering if it’s better to get a good night’s sleep or better glucose control. I’m in a sleep study right now for T1Ds and I have come to appreciate the value and benefits that come from better quality sleep. A few months ago I would have never considered not using Dexcom and thought that was crazy. But, I’m really starting to like not using it because my sleep has improved significantly and as a result my health should too. I would be interested in what other’s thoughts are on this and whether you think I should go back to using Dexcom.

      1
      2 years ago Log in to Reply
      1. MT

        I stopped using Guardian sensor for this very same reason. Also gave up the pump and now use Libre 3 with MDI. Way better sleep, way less expensive and still good control. 86% in range after some trial/error.

        1
        2 years ago Log in to Reply
      2. Bob Durstenfeld

        Tim in range matters and the
        cgm is better for that. Seems you need to have some help adjusting your basal rates so you alarm less.

        2 years ago Log in to Reply
      3. Marty

        I also value a good night’s sleep. Cognitive behavioral therapy and a CPAP machine helped me overcome sleep apnea and chronic insomnia. On my endo’s advice, I turned off the high and low alarms on my pump (Tandem with Control IQ). I rely exclusively on my phone alarms, which are set to vibrate. Unless something unusual is going on, my BGs stay within range through the night and CGM alarms almost never wake me up. The benefit has been lower blood pressure, higher energy, and a general sense of well being.

        1
        2 years ago Log in to Reply
    8. Patricia Kilwein

      Didn’t have an option for how many times a night….

      2
      2 years ago Log in to Reply
      1. mojoseje

        Yes, some nights are bad.

        1
        2 years ago Log in to Reply
    9. Steve Rumble

      I answered 5 or 6 times, but that is not exclusively glucose level alerts, many are “loss of signal” alerts from my G7 sensor.

      1
      2 years ago Log in to Reply
    10. Lawrence S.

      I answered “3 or 4 nights per week,” but could have easily been “5 or 6 nights per week.” Recently, I’ve been making adjustments to my basal rates after having lots of lows. But, when my alarms go off during the night, it usually doesn’t even measure in my mind unless I’m going very low or very high.

      2 years ago Log in to Reply
    11. Katherine Kettig

      I do not have alarms on my CGM but do keep it beside me at night and check myself during the night.

      2 years ago Log in to Reply
    12. John McHenery

      Most common wake up is due to loss of contact with sensor.

      1
      2 years ago Log in to Reply
    13. Janis Senungetuk

      I have the alarms set on vibrate because they were disturbing my spouse and our cat. When they wake me it’s rarely because of a high or low alert.My bg level 3 hours ago is not of any value in the middle of the night. Fortunately CIQ works well to keep me around 110 most of the night. I check CGM before going to bed and either take a correction bolus or eat a small snack to prevent a low while sleeping.

      2
      2 years ago Log in to Reply
    14. KCR

      I answered 3-4 times a week but 2-3 times is more typical. I love those weeks with no alarms at all so I sleep better!

      2 years ago Log in to Reply
    15. Chris Albright

      If I go to bed without a bunch of Basel insulin on board, the Tandem algorithm will stop/decrease my Basel insulin so I stay between 90 and 110(ish) all night

      2 years ago Log in to Reply
    16. Dylan Sutton

      Typically for compression lows rather than real low BG. Depending on sensor placement, this may happen once or twice a week or 5 times in the one night.

      1
      2 years ago Log in to Reply
    17. Russell Buckbee

      When I take my hearing aids out I can’t hear them.

      2 years ago Log in to Reply
    18. Steven Gill

      I’m an extremely light sleeper (wake when my cat comes in the pet door across the house), so waking comes easily. My alarms are set 70-130, kind of tight and while Medtronic’s algorithm does great one thing consistent with diabetes is change…

      I clicked 3-4 times a weekly, sometimes for a low (lemonade is on the nightstand), or a trending rise (count the “autobolus, do an easy correction with a pump and roll over).

      2 years ago Log in to Reply
    19. Jian

      maybe there is something wrong with me but my CGM alarm goes off more than 6 times a week, I think

      2 years ago Log in to Reply
    20. Elizabeth T.

      Of course there’s no such thing as a typical week living with T1D! I can have weeks with no alarms waking me now I’m using Guardian 4s but
      occasionally I’ll have a bad night with 5 or 6 alarms.

      1
      2 years ago Log in to Reply

    In a typical week, how often are you woken up by your CGM or other diabetes-related alarms (such as, for a low or a high alert)? Cancel reply

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