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    • 1 hour, 37 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.
    • 1 hour, 37 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
    • 1 hour, 38 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!
    • 2 hours, 20 minutes 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.
    • 3 hours, 43 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.
    • 5 hours, 40 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
    • 21 hours, 3 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.
    • 21 hours, 6 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.
    • 21 hours, 6 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.
    • 21 hours, 7 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
    • 21 hours, 15 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 ´ )⎠⎞
    • 23 hours, 8 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.
    • 23 hours, 8 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.
    • 23 hours, 10 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 ´ )⎠⎞
    • 1 day, 3 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, 5 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, 5 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, 6 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, 6 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, 6 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, 6 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.
    • 1 day, 6 hours 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, 6 hours 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, 6 hours 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, 6 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 ´ )⎠⎞
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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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    30 Comments

    1. Molly Jones

      “Other” as I don’t know.
      This will be something good to test.

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

      For a long time I wasn’t sure what you all were talking about when you referred to “compression lows.” However, I recently experienced several compression lows while I was sleeping. I found that relocating my CGM from areas where my body meets the mattress appears to have resolved the problem.

      2
      2 years ago Log in to Reply
    3. Gary Rind

      Keep my Libre (now 3) on my left arm so I try to make sure that I sleep on my right side. Don’t want the alarm going due to compression lows.

      2 years ago Log in to Reply
    4. BARRY HUNSINGER

      I have not noticed this, and I did not know that this was possible. I will be aware of it now.

      1
      2 years ago Log in to Reply
    5. KIMBERELY SMITH

      It stops

      2 years ago Log in to Reply
    6. Brian Vodehnal

      Not with Dexcom….Libre? Constantly. One of the many reasons I don’t use Libre.

      1
      2 years ago Log in to Reply
    7. Jen Farley

      I have never heard of that being something that happens. I will now pay attention, I will have a conversation with my endocrinologist about this.

      2 years ago Log in to Reply
    8. Jane Cerullo

      When I had a G6 it happened rarely. Happens more frequently with the G7. For me it’s more difficult to place on arm. Always had G6 on arm but didn’t seemed to compress like the G7. Also happens more in the beginning of sensor placement. Then not so much. Annoying

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

      I have a hard time finding a spot that is not my abdomen to place the sensor so I don’t get compression lows. So annoying in the middle of the night!

      2 years ago Log in to Reply
    10. T1D4LongTime

      I’ve had only 1 in 3 years that I can attribute to laying on the sensor in the night. I put the pump infusion set and the sensor on the same side of my body, so I’m used to sleeping 10 days on my right side and 10 days on my left side! LOL! No compression lows!

      2 years ago Log in to Reply
    11. Sherolyn Newell

      I don’t think so. If I get a low alarm at night, I eat sugar and go back to sleep. I don’t get up and double-check with a finger stick.

      1
      2 years ago Log in to Reply
    12. mojoseje

      Not that I’m aware of.

      2 years ago Log in to Reply
    13. marge slater

      I am not know

      2 years ago Log in to Reply
    14. Janice B

      While I have experienced compression lows they have been infrequent. I have a bigger problem with loss of connection to my pump if I lay on the Dexcom transmitter

      2 years ago Log in to Reply
    15. cynthia jaworski

      I had compression lows only if I had been dehydrated as well. This is more likely to happen after traveling.

      2 years ago Log in to Reply
    16. Kris Sykes-David

      I answered “no”, however, I am very aware of where my G7 is located when sleeping on that side.

      2 years ago Log in to Reply
    17. Mark Schweim

      Regularly if sensor is inserted in my abdomen or arms, but only rarely when inserted on my inner thighs.

      I said Yes, but rarely because I almost always insert my sensor rotating from one leg to the other on my inner thighs.

      I tried a sensor on my calf but in the calf, it sometimes hurt and frequently gave sensor out of range errors on my pump.

      2 years ago Log in to Reply
    18. Anneyun

      I get them when I have my G6 on my arm, so I don’t put it there anymore. I only put it on my abdomen. So far so good.

      2 years ago Log in to Reply
    19. cmangels

      Any pressure results in not getting readings at all.

      2 years ago Log in to Reply
    20. Mig Vascos

      I do occasionally during the night

      2 years ago Log in to Reply
    21. KarenM6

      On the G6, I got them all the time.
      I am now on the Eversense which does not have compression lows (no matter how I sleep.) I believe this has to do with the sensor being inside the body and being “compressed all the time”, so to speak.

      2 years ago Log in to Reply
    22. Ceolmhor

      I said “other”. I get inexplicable rapid drops (not instantaneous, but sloping down significantly over 3-5 5-minute test periods. I had never considered this as a possible cause. When it happens, I go and do a calibration, usually finding that my true BG level is 30 or more points higher than the indicated SG. I had never considered this as a possible cause. I’ll pay attention to that now. Thanks.

      2 years ago Log in to Reply
    23. Beckett Nelson

      No, I’ve learned where sites are bad for this and don’t use them there. Been 12-15years without a compression low now

      2 years ago Log in to Reply
    24. Joan Benedetto

      Not too often, but when they happen, we usually have multiple alarms in a night. It’s always after a sensor change when we, of course, switch arms.

      2 years ago Log in to Reply
    25. Maureen Helinski

      Yes and that prevents me from putting the sensors on my arms because I sleep on my sides. Now I have the sensors on my thighs nearer the inside where I won’t sleep on them.

      1
      2 years ago Log in to Reply
    26. Diane

      Every time I lay on it, I either lose the signal or go low.

      2 years ago Log in to Reply
    27. Jeff Balbirnie

      Fascinating, was unaware there was a term for this specific nightmare(s)

      2 years ago Log in to Reply
    28. Melinda Lipe

      Yes, often within just the first 24 hours after inserting a new sensor!

      2 years ago Log in to Reply
    29. Bonnie Lundblom

      Yes, but with the CGM 6 not as frequent as the CGM 5. I was thinking about what CGM to use next and after reading all the comments I’m not sure what to use, so for now sticking with the Dexcom CGM 6 because in our area there’s only 1 endocrinologist who does the Eversense and sadly it’s not my endocrinologist.

      2 years ago Log in to Reply
    30. Andrea Hultman

      I’m a side and stomach sleeper, so I used to get compression lows all the time in Manual Mode on the 670G and 770G pumps (Medtronic). Now I run Auto Mode and have very few compression lows.

      2 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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