Subscribe Now

[hb-subscribe]

Trending News

T1D Exchange T1D Exchange T1D Exchange
  • Activity
    • 2 hours, 28 minutes ago
      Ahh Life likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      So far since Jan 1, ‘26, I’ve spent nearly 30 hours on the phone battling and trying to get Medicare covered diabetes supplies. Called 5 different suppliers t get what I need to use my pump.
    • 2 hours, 29 minutes ago
      Ahh Life likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      You are too modest. That hurdle is on fire and you have to juggle chainsaws as you jump over it. Congratulations and good luck making it over the next one in 90 days.
    • 16 hours, 10 minutes ago
      KarenM6 likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
    • 17 hours, 57 minutes ago
      Kristi Warmecke likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      Well, since I'm waiting on pump supplies for 2 months now, my confidence is slipping.
    • 17 hours, 58 minutes ago
      Laurie B likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I've often said that "hoarding": is a character asset for T1D people. I try to purchase (paying out of pocket) a 60-90 day supply - just in case). I have a new health plan,. effective 1/1/26. AS we know, getting an appt with an HCP isn't easy. They have to be accepting new patients, they have to be in network etc. Once I knew what my new policy would be (nov 2025) I made an appt. The earliest appt I could get was in Sept 2026. Thank goodness for my stash of device supplies. I had to go to Urgent care to get an Rx for insulin (my old HMO plan "doesn't do bridge refills"). So yeah, I worry, and plan for hiccups in the supplies process.
    • 17 hours, 59 minutes ago
      Kristi Warmecke likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I answered slightly. I'm absolutely certain supplies and medication will be available. However, I'm doubtful they will be affordable. If I can't afford them, I can't access them.
    • 18 hours, 57 minutes ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I am confident about access to my medical needs in the immediate future. I am not a fortune teller and have no idea what my access to medical supplies will be like in a year or longer. I don't take my spoiled lifestyle for granted.
    • 18 hours, 57 minutes ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I've often said that "hoarding": is a character asset for T1D people. I try to purchase (paying out of pocket) a 60-90 day supply - just in case). I have a new health plan,. effective 1/1/26. AS we know, getting an appt with an HCP isn't easy. They have to be accepting new patients, they have to be in network etc. Once I knew what my new policy would be (nov 2025) I made an appt. The earliest appt I could get was in Sept 2026. Thank goodness for my stash of device supplies. I had to go to Urgent care to get an Rx for insulin (my old HMO plan "doesn't do bridge refills"). So yeah, I worry, and plan for hiccups in the supplies process.
    • 18 hours, 58 minutes ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I answered slightly. I'm absolutely certain supplies and medication will be available. However, I'm doubtful they will be affordable. If I can't afford them, I can't access them.
    • 19 hours, 1 minute ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I am worried about the changes to Medicare making no provision for getting an immediate replacement if a pump fails. It sounds like we will have to get these from the suppliers instead of a warranty replacement from Tandem themselves (or whatever brand you use). Pumps will be rented and will have to be returned so they can verify the problem before replacing them, which is ridiculous. Meanwhile, Medicare would not pay for us to get long acting insulin as a temporary replacement for the basal.
    • 19 hours, 4 minutes ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I broke down for the first time in 25 years and bought a bottle of insulin because I think I may have thrown a bottle out with the box. Medicare wouldn’t fill the prescription because it was too early. I just didn’t want the fight and worry. I’m not sure that’s what happened but it’s the only explanation. Also, I live in Florida and the threat of losing power is always there. I should get a generator but I’m a little afraid of them and you still can’t be sure you have access to propane. If my insulin goes bad, I’m not sure I could get refills. My back up plan is to leave before hurricane or go to a hospital. But it is all just causes concern.
    • 19 hours, 17 minutes ago
      Derek West likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Very! However, I wish I could use Fiasp insulin in the Tandem pumps.
    • 21 hours, 52 minutes ago
      Bruce Schnitzler likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I broke down for the first time in 25 years and bought a bottle of insulin because I think I may have thrown a bottle out with the box. Medicare wouldn’t fill the prescription because it was too early. I just didn’t want the fight and worry. I’m not sure that’s what happened but it’s the only explanation. Also, I live in Florida and the threat of losing power is always there. I should get a generator but I’m a little afraid of them and you still can’t be sure you have access to propane. If my insulin goes bad, I’m not sure I could get refills. My back up plan is to leave before hurricane or go to a hospital. But it is all just causes concern.
    • 22 hours, 24 minutes ago
      Karen Newe likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      The most common comment: but you aren’t heavy. That’s when we get into the differences. A relative tried to tell me that insulin makes you lose weight. But when we last discussed this, one of you said it best: if it isn’t in their circle of experience, why would they know or care?
    • 22 hours, 41 minutes ago
      KSannie likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Very! However, I wish I could use Fiasp insulin in the Tandem pumps.
    • 22 hours, 42 minutes ago
      KSannie likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
    • 22 hours, 43 minutes ago
      KSannie likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      My first reaction was Very Satisfied but there is always room for improvement. I’d like a pump design that wasn’t meant to be worn on a belt just for men. To wear a dress, I have to only get those with pockets (and on both sides because opposite sides cause the CGM to lose contact) and put a button whole in each. The clip shows horribly on blouses worn out. I’ve tried the leg attachments and they never stay secure. I’m not big enough to wear it in my bra. All minor inconveniences. I’d like one that doesn’t keep alarming 20 minutes after I’ve eaten, although I get it that it is there to save my life. Again minor. Ask about CGMs (probably tomorrow’s question): lately I’ve had trouble removing the sensor from my arm without actually ripping off a strip of skin or very bad bruising. I’ve read about using baby oil for removal. That does help. I’m a rip it off fast person, but that didn’t work so well.
    • 1 day ago
      Patricia Dalrymple likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Try Uni-Solve Adhesive Remover (smith&nephew)- wipe it on wait a minute to let it work and it will come off easy. at least it works great for me and I've tried several different brands, I use it for CGM & Omnipod removal
    • 1 day, 7 hours ago
      Sandy Norman likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
    • 1 day, 14 hours ago
      kristina blake likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      There are several conversations about this across social media. Many people chime in and vote for a new, more accurate name for type 1.. some of the popular alternatives- Pancreatic Autoimmune Disease, Beta Cell Destruction Disease, Autoimmune Diabetes, Autoimmune Insulin Failure, Autoimmune Absolute Insulin Deficiency (AAID)
    • 1 day, 14 hours ago
      kristina blake likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      The most common comment: but you aren’t heavy. That’s when we get into the differences. A relative tried to tell me that insulin makes you lose weight. But when we last discussed this, one of you said it best: if it isn’t in their circle of experience, why would they know or care?
    • 1 day, 14 hours ago
      kristina blake likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      In my experience the average person does not know the difference. It does not help that the commercials on TV just say diabetes and do not differentiate.
    • 1 day, 16 hours ago
      Kristi Warmecke likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
    • 1 day, 19 hours ago
      Lee Tincher likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      If I could get a CGM that is consistent and predictable I'd be very happy with the Twiist or the Tandem. The weak point with pumps used to be infusion sites, but now that we are relying on poor performing technology to support potentially great algorithms itis quite frustrating.
    • 1 day, 21 hours ago
      Beckett Nelson likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      My first reaction was Very Satisfied but there is always room for improvement. I’d like a pump design that wasn’t meant to be worn on a belt just for men. To wear a dress, I have to only get those with pockets (and on both sides because opposite sides cause the CGM to lose contact) and put a button whole in each. The clip shows horribly on blouses worn out. I’ve tried the leg attachments and they never stay secure. I’m not big enough to wear it in my bra. All minor inconveniences. I’d like one that doesn’t keep alarming 20 minutes after I’ve eaten, although I get it that it is there to save my life. Again minor. Ask about CGMs (probably tomorrow’s question): lately I’ve had trouble removing the sensor from my arm without actually ripping off a strip of skin or very bad bruising. I’ve read about using baby oil for removal. That does help. I’m a rip it off fast person, but that didn’t work so well.
    Clear All
Pages
    • T1D Exchange T1D Exchange T1D Exchange
    • Articles
    • Community
      • About
      • Insights
      • T1D Screening
        • T1D Screening How-To
        • T1D Screening Results
        • T1D Screening Resources
      • Donate
      • Join the Community
    • Quality Improvement
      • About
      • Collaborative
        • Leadership
        • Committees
      • Centers
      • Meet the Experts
      • Learning Sessions
      • Resources
        • Change Packages
        • Sick Day Guide
        • FOH Screener
        • T1D Care Plans
      • Portal
      • Health Equity
        • Heal Advisors
    • Registry
      • About
      • Recruit for the Registry
    • Research
      • About
      • Publications
      • COVID-19 Research
      • Our Initiatives
    • Partnerships
      • About
      • Industry Partnerships
      • Academic Partnerships
      • Previous Work
    • About
      • Team
      • Board of Directors
      • Culture & Careers
      • Annual Report
    • Join / Login
    • Search
    • Donate

    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.
    Previous

    If you (or your loved one) were diagnosed with T1D as a child, at what age were you diagnosed?

    Next

    Do you currently have a kit containing the T1D supplies you would need in case of a natural disaster or emergency?

    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.

    Related Stories

    News

    What’s Keeping Glucagon Out of Reach for Many with T1D? 

    Jewels Doskicz, 2 days ago 6 min read  
    News

    Thinking About Type 1 Diabetes Autoantibody Screening? Here’s What to Consider 

    Jewels Doskicz, 1 week ago 9 min read  
    2025 Learning Session

    T1DX-QI 2025 November Learning Session Abstracts 

    QI Team at T1D Exchange, 2 weeks ago 1 min read  
    Advocacy

    The Language of Type 1 Diabetes: Why Words Matter 

    Jewels Doskicz, 2 weeks ago 6 min read  
    News

    Understanding Time in Range, GMI, and A1C in Type 1 Diabetes 

    Jewels Doskicz, 3 weeks ago 4 min read  
    News

    Out of Insulin? Expert Tips from Diana Isaacs, PharmD 

    Jewels Doskicz, 4 weeks ago 9 min read  

    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
      4 years ago Log in to Reply
    2. Ahh Life

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

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

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

      4 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
      4 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
      4 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.

      4 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.

      4 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
      4 years ago Log in to Reply
    10. Jane Cerullo

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

      4 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
      4 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

      4 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.

      4 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
      4 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.

      4 years ago Log in to Reply
    16. Joan Plog

      No sure

      4 years ago Log in to Reply
    17. Sherrie Johnson

      Good to know

      4 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
      4 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.

      4 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
      4 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!

      4 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….

      4 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.

        4 years ago Log in to Reply
    23. Janice Bohn

      More trouble with no readings if I lay on my transmitter

      1
      4 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.

      4 years ago Log in to Reply
    25. Jillmarie61

      I don’t know f. Have or not.

      4 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.

      4 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

      4 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)

      4 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.

      4 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!

      4 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

      4 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.

      4 years ago Log in to Reply
    33. Bea Anderson

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

      2
      4 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.

      4 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

      4 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.

      4 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

      4 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.




    101 Federal Street, Suite 440
    Boston, MA 02110
    Phone: 617-892-6100
    Email: admin@t1dexchange.org

    Privacy Policy

    Terms of Use

    Follow Us

    • facebook
    • twitter
    • linkedin
    • instagram

    © 2024 T1D Exchange.
    All Rights Reserved.

    © 2023 T1D Exchange. All Rights Reserved.
    • Login
    • Register

    Forgot Password

    Registration confirmation will be emailed to you.

    Skip Next Finish

    Account successfully created.

    Please check your inbox and verify your email in the next 24 hours.

    Your Account Type

    Please select all that apply.

    I have type 1 diabetes

    I'm a parent/guardian of a person with type 1 diabetes

    I'm interested in the diabetes community or industry

    Select Topics

    We will customize your stories feed based on what you select here.

    [userselectcat]

    We're preparing your personalized page.

    This will only take a second...

    Search and filter

    [searchandfilter slug="sort-filter-post"]