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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, 59 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, 3 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, 5 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 use a CGM, do you ever experience “compression lows”? These are inaccurate CGM readings that occur when there is pressure placed on the CGM transmitter and sensor. They typically look like a sudden and drastic drop on a CGM graph, and often occur when a person is lying on their sensor.

    Home > LC Polls > If you use a CGM, do you ever experience “compression lows”? These are inaccurate CGM readings that occur when there is pressure placed on the CGM transmitter and sensor. They typically look like a sudden and drastic drop on a CGM graph, and often occur when a person is lying on their sensor.
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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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    38 Comments

    1. Wanacure

      I didn’t know that I was having compression lows till I read about them months ago on this valuable website! Since then, I avoid them by not placing my Dexcom too far to left or to far to right of umbilicus. (Each night I alternate sleeping on my sides several times.) Alarms from compression lows used to drive me nuts!

      2
      3 years ago Log in to Reply
    2. Ahh Life

      Yes, but rarely. Most frequent errors are those of communication between pump & sensor. ☔

      3 years ago Log in to Reply
    3. lis be

      I never used to get them, with Libre or Libre 2, the systems were fantastic. Something seems to have changed in the product recently though, and I am getting false low alarms 2-3 times a night. I’m switching to Dexcom this week to see if it is any better. fingers crossed!

      2
      3 years ago Log in to Reply
    4. Amanda Barras

      Only remember 1-2x as usually where I wear it doesn’t cause a problem.

      3 years ago Log in to Reply
    5. Dale Norman

      Maybe? I have probably experienced it from time to time but didn’t realize that is what was happening

      1
      3 years ago Log in to Reply
    6. Yeissa Chabrier

      Compression lows are extremely frustrating and are the #1 reason we have regular sleepless nights! Wish something could be done about this, especially with little kids and their terrible sleeping positions. This is a big issue in our household…

      1
      3 years ago Log in to Reply
    7. mojoseje

      Not that I’m aware of. But, now that I know this is a thing, I’ll be watching out for them.

      3 years ago Log in to Reply
    8. stillarobyn

      I get these basically every night. I can see my habits of rolling on either side in my sleep in the dips on my sensor data graph. Nothing alleviates the issue.

      3 years ago Log in to Reply
    9. Amy Jo

      Like others, I mostly experience these overnight. I wear my Dexcom on my low back, so as long as I keep it more midline (I’m a side sleeper) I don’t have issues. Every now and then I will have them while I drive/sit for a long time if I have my sensor too low.

      1
      3 years ago Log in to Reply
    10. Jane Cerullo

      Wear Dexcom on upper arm. Very rarely get a compression low. Got more with FSL

      3 years ago Log in to Reply
    11. Marty

      Yes, I get them sometimes when I have my sensor between me and my mattress. I’m wondering if the new G7 sensors will alleviate the problem because of their lower profile.

      1
      3 years ago Log in to Reply
    12. dave hedeen

      i do get sudden cgm drops, yet usually on applying any pressure on cgm or pump. mostly g6

      3 years ago Log in to Reply
    13. Brian Vodehnal

      Only with the Libre 2 and it’s usually at night when I roll over on it. Then ina sleepy panic you eat something to correct it, only to launch you into a high…annoying.

      3 years ago Log in to Reply
    14. Chrisanda

      Just had one early this morning because I was sleeping on the arm that has the Dexcom G-6 sensor. It does not happen all the time. Since I can surmise it’s a “compression low,” I don’t get up to do any corrections. My alarm will go off again if I really am going low. So, back to sleep!

      1
      3 years ago Log in to Reply
    15. Drina Nicole Jewell

      I chose other. In the beginning I had them often. I figured out where to place them on my body to prevent them.

      3 years ago Log in to Reply
    16. Joan Plog

      No sure

      3 years ago Log in to Reply
    17. Sherrie Johnson

      Good to know

      3 years ago Log in to Reply
    18. TomH

      I think this is something new CGM wearers experience more regularly, longer-term users learn fairly quickly what sites work well and avoid the issue. I found out on my own; surprising that training videos don’t cover it better! It’s different for how you sleep, sit, rest, and if you have pets (yes, my cats like to be on my lap and effectively block or impact the signal). I use Dexcom G6 and am a side sleeper (mostly right side). For me the top/front of the left thigh works well, so does the belly as long as it’s fairly central (yes, outside the navel zone), the inside and backside of the left bicep, and back of the leftside “love handle.”

      1
      3 years ago Log in to Reply
    19. Janis Senungetuk

      Had more when I first started placing the Dexcom G6 sensor/transmitter on my upper arm. Didn’t have that problem with the G5. I’m a side sleeper so I try to place the transmitter/sensor facing my torso to lessen the possibility.

      3 years ago Log in to Reply
    20. Thomas Cline

      It was a serious problem when I did as Dexcom recommended and put the sensors on my belly. There is simply no belly location that doesn’t get compressed at some point at night because I turn around quite a bit. Lately I’ve switched to the inner part of my upper arm as a sensor location and have had no problem — even though that is not a recommended site (I suspect their recommendations are based solely on where they placed the sensors during their clinical trials, rather than on any more thoughtful consideration). Curiously, I seemed to have more trouble with compression early on in a session. The biggest problem I have with Dexcom is when a sensor site bleeds, something that seems to cause most problem early and late in a sensor session, but so far my inner upper arm location seems better than my belly in that respect as well.

      3
      3 years ago Log in to Reply
    21. Ms Cris

      Yes, and it’s why I also rarely use my arms anymore, since I need to sleep!

      3 years ago Log in to Reply
    22. Chris Albright

      I see them for the reason mentioned in the question, but also see what looks like a compression low with no pressure in the sensor. Also see spikes that return to normal for apparent reason. Not sure why I see these….

      3 years ago Log in to Reply
      1. AnitaS

        I had a spike recently about 2 hours before getting up in the morning. It jumped to about 150 and then came right down within 1/2 hour. Have no idea why that occurred. Sort of like a reverse compression low.

        3 years ago Log in to Reply
    23. Janice Bohn

      More trouble with no readings if I lay on my transmitter

      1
      3 years ago Log in to Reply
    24. Sharon Gerdik

      I have worn my sensors on my torso for a long time. If you wear sensors on your upper arms and sleep on that side, then you probably could get compression lows. I rotate between sites above and below my waistline and I love it.

      3 years ago Log in to Reply
    25. Jillmarie61

      I don’t know f. Have or not.

      3 years ago Log in to Reply
    26. Mary Ann Sayers

      I’ve seen fast rising and falling at different times not related to any reclining of my body on CGM or pump.

      3 years ago Log in to Reply
    27. Linda Pease

      Not lows but sensor offline occurs when I am laying on my sensor or my pump

      3 years ago Log in to Reply
    28. Melinda Lipe

      I had to learn not to insert the cgm on a place where I regularly sleep (on the outside of my arms or legs)

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

      You know, I’ve seen people mention “compression lows” on this site, but never knew what they were talking about. But, come to think of it, I seem to get them in bed. I wear the sensor on my buttocks. I Never realized what was happening.

      3 years ago Log in to Reply
    30. mbulzomi@optonline.net

      I have been on a CGM system for eleven (11) years, Medtronic ,Enlite and now Dexcom, G6. I have always taken precautions when I drive, sleep and relax to not be on the Sensor!

      3 years ago Log in to Reply
    31. Nicholas Argento

      I try to put the transmitter in a location where I don’t lay on top of it and that usually works to alleviate this which can otherwise be annoying

      3 years ago Log in to Reply
    32. Molly Jones

      I chose other as I don’t know.
      I wear my sensor on my lower inner arms and my inner abdomen.

      3 years ago Log in to Reply
    33. Bea Anderson

      Said no. Medtronic’s cgm seemed to have this. Haven’t noticed with Dexcom

      2
      3 years ago Log in to Reply
    34. Steve Rumble

      I have not noticed compression lows, but occasionally when pressure is placed on my sensor (Dexcom G6) it loses connection with my phone.

      3 years ago Log in to Reply
    35. Cheryl Seibert

      Very rarely. I keep sensor and infusion sites on the same side of the body for the CGM 10 day life and side-sleep on the ’empty side’ of my body. I have on a ‘new sensor’ day rolled onto the sensor and experienced the compression low

      3 years ago Log in to Reply
    36. martha Gruelle

      Not sure. I get these false lows, generally when the sensor is old (8th – 9th day), and I’ve never associated them with compression. They do happen during sleep but also other times.

      3 years ago Log in to Reply
    37. Jeff Balbirnie

      When I wore one, ABSOLU freakin-lutely

      Machine was inaccurate as hell, on a obscenely regular basis, sadly

      3 years ago Log in to Reply

    If you use a CGM, do you ever experience “compression lows”? These are inaccurate CGM readings that occur when there is pressure placed on the CGM transmitter and sensor. They typically look like a sudden and drastic drop on a CGM graph, and often occur when a person is lying on their sensor. Cancel reply

    You must be logged in to post a comment.




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