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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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    If you use an automated insulin delivery system (also sometimes known as a hybrid closed-loop system), how do you feel like your sleep changed when you started using your current device? Share more about your experiences with sleep and automated insulin delivery in the comments!

    Home > LC Polls > If you use an automated insulin delivery system (also sometimes known as a hybrid closed-loop system), how do you feel like your sleep changed when you started using your current device? Share more about your experiences with sleep and automated insulin delivery in the comments!
    Previous

    If you are an adult with T1D, how much has type 1 diabetes affected your thought-process and decision to have/not have children?

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    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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    27 Comments

    1. Kevin Stephani

      I rested better because my overnight bg was much more in control. My A1c improved by .5 and I was already doing well (consistently under 6)

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

      Alarms, what can I say other than life of a diabetic?

      5
      3 years ago Log in to Reply
    3. terrih57@msn.com

      Other than the alarms, I think my sleep has improved because my bgs are better controlled. I wish the alarms would stop after first – I have usually eaten carbs after first alarm – second time is just annoying

      2
      3 years ago Log in to Reply
    4. GLORIA MILLER

      I rest much better now since I no longer have to worry about severe lows when asleep. If only the day time hours were as good!

      3
      3 years ago Log in to Reply
    5. Lawrence S.

      I said improved a little because my blood glucose levels stay within range better. However, I still have highs and lows, but not quite as often. The alarms keep going off all night to keep me awake. It is very annoying! Especially the dumb alarm that tells me that I had a high or low blood glucose 2, 3, or 4 hours ago. TOTALLY USELESS INFORMATION!!!!!!!!! YOUR ARE KEEPING ME AWAKE!

      4
      3 years ago Log in to Reply
      1. AnitaS

        Look at the response from Marty above. He described a way to keep those useless alarms from going off.

        1
        3 years ago Log in to Reply
    6. Marty

      I used to have mid-night alarms several times a week and now I’m woken by an alarm less than once per month. Huge improvement! It also helps that I turned off every alarm except for the severe low alarm on my pump and rely on my watch/phone for other alarms. If I use the “Do not disturb” setting on my phone while I sleep, I’m not woken by the other annoying/useless alarms like the complaint that my blood sugar was high three hours ago.

      2
      3 years ago Log in to Reply
    7. Hark87

      Literally the BEST thing to ever happen to me!! I am so thankful for my insulin pump!!!

      2
      3 years ago Log in to Reply
    8. Tere North

      While I said decreaseda little, it is because it is in conjunction with a CGM. I’ll get alarms that my BSG is too low. While waking me up, I’ll take that over the alternative of not waking up, even in the morning. That had happened before and paramedics were called as I was comatose. A little sleep is not much to give up to be alive.

      3
      3 years ago Log in to Reply
    9. Dennis Dacey

      Mmmmmm, my sleep may have improved a little bit since I’ve been using an iAIDs, but not much difference since I began using a pump a couple of decades ago.
      Like everything else, “improved / worsened” is relative to how lousy management had bEen in prior era.

      3 years ago Log in to Reply
    10. Janis Senungetuk

      Quality of sleep has decreased a bit because of CGM alarms. I especially find the 3 AM reminder alarm that 3 hours ago I had a high or low bg level very useless and annoying.

      5
      3 years ago Log in to Reply
      1. AnitaS

        Look at the response from Marty. He described a way to stop those useless alarms.

        3 years ago Log in to Reply
    11. Ron Pierce

      Quality of sleep has decreased alot because of CGM alarms.

      1
      3 years ago Log in to Reply
    12. Shelly Smith

      I answered that my sleep has improved a little. My experience will sound a lot like some of the rest of y’alls . I sleep better because I’m not as worried about going low, but at the same time this good sleep is interrupted by useless alarms! Nonetheless, I wouldn’t want to give up my closed-loop system, so…..there’s the info for whatever its worth!

      1
      3 years ago Log in to Reply
    13. Amanda Barras

      A lot!
      Switching from 670 to TSlim the overnight alarms completely stopped and I have a flat line hovering around 100 all night!

      1
      3 years ago Log in to Reply
    14. Nicholas Argento

      For me, much less sleep disturbance w HCL-CGM compared to open loop pump and CGM. Far fewer night lows. I had fewer sleep disturbances prior to CGM, but occasional very severe hypoglycemic reactions, many requiring 911 calls, or my wife bailing me out. My life was in danger as a result. I’ll never not use CGM again.

      1
      3 years ago Log in to Reply
    15. Bob Durstenfeld

      My sleep improved, but the bedtime improvement was my morning BG being consistently between 90 and 110. It is so much easier to manage T1D whe you start the day in range.

      1
      3 years ago Log in to Reply
    16. Jillmarie61

      I just switched to the OmniPod5, so it’s literally stuck to you. I try to place it in an area on my body where I’m not laying on it in my sleep, but so far it’s been a trying time to find that perfect spot or area.

      3 years ago Log in to Reply
      1. AnitaS

        My warranty on my Tandem Slim x2 is expiring this coming summer. I would like to try a tubeless system but the problem you are describing is a reason I may just stay with a tubed pump. Having tubing really doesn’t bother me.

        3 years ago Log in to Reply
    17. August Rossano

      Alarms are annoying. but with AID, I experience a a lot fewer of them.

      3 years ago Log in to Reply
    18. kenneth brooks

      The main reason I switched from a separated pump and CGM system to the Tandem Control IQ was because I hoped that I would get fewer CGM alarms during the night. Now I almost never get an alarm after bedtime. A1c is great and time in range well over 90%

      1
      3 years ago Log in to Reply
    19. Carol Meares

      O5 has worsened my overnight numbers whereas I have finally reached some better numbers during the day. I have been on O5 since early November. I have found it difficult to work with an algorithm based on total daily insulin vs basal insulin.

      3 years ago Log in to Reply
    20. Donna Condi

      Knowing that if I do go low that my Pump will stop delivering insulin and alarms will sound to wake me and my husband gives me mental peace of mind. But I do wake up more often because of the alarms but I have never had a problem going back to sleep immediately.

      3 years ago Log in to Reply
    21. Ben Galindo

      Have been on Control IQ about a year, it wakes me up a lot. Why wake me up, if the algorithm indicates to DO NOTHING?

      3 years ago Log in to Reply
    22. AnitaS

      I am not sure if my sleep improved a lot or not, but waking up to blood sugars not much above 100 every day is definitely something that didn’t happen often like it does since having a pump with A.I.D.

      3 years ago Log in to Reply
    23. Rex Franklin

      I switched from Med. 670G to Tandem with Dexcom 6, hourly nightly alarms are no more. Changing to Tandem was a live changing event for me.

      3 years ago Log in to Reply
    24. T1D4LongTime

      I would say it worsened a little. NOT because of the pump, but rather because of the CGM. Alarms, while necessary, disturb my sleep. As a child and pre-pump adult, I slept very sound. 3am extreme lows were a problem, but found eating popcorn or complex carb snack before bed took care of the lows. Oh, to sleep and not keep the phone on! Those days are gone!

      3 years ago Log in to Reply

    If you use an automated insulin delivery system (also sometimes known as a hybrid closed-loop system), how do you feel like your sleep changed when you started using your current device? Share more about your experiences with sleep and automated insulin delivery in the comments! Cancel reply

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