Subscribe Now

* You will receive the latest news and updates on your favorite celebrities!

Trending News

T1D Exchange T1D Exchange T1D Exchange
  • Activity
    • 8 hours, 31 minutes ago
      KarenM6 likes your comment at
      Of the people in your life, who (if anyone) makes you feel judged or criticized for your T1D management (for example, what foods you eat, where or when you check your blood glucose, etc.)? Select all that apply to you.
      Insulin, meters, diabetic tech are not magic wands. Its usage does not guarantee only "positive" results. Negative events can and do occur, period. Non -D- typically (incorrectly) equate negative events as being total user failure, severe user errors. As diabetics we get blamed, despite having made zero mistakes on our part. We make seriously educated best guesses, despite that truth, we can and do fail anyway sometimes! Outsiders falsely need to believe inulin, our tech are complete-total cures, rather than tiny bandages at best. When confronted for using (sic. my) "drugs" in public, no matter how invisibly done... it is their self righteousness , poor assessment which is the issue. I gladly squash such insects...
    • 13 hours, 31 minutes ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      The more important question is 'how well does the clip work'. For me, the Medtronic clip worked very well, but the Tandem clip is quite ineffective and the pump falls off my belt during things like yard work or other bending movements.
    • 13 hours, 32 minutes ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      I answered never. I always use a clip -- I wear my t:slim x2 on my belt -- but not the Tandem clip. I use the black t:Holster Rotating Belt Clip. Very pleased.
    • 13 hours, 33 minutes ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      I am rough on pumps and use a Tandem X2 but dont use the Tandem clip/holster. I use a neoprene case and a pouch with a metal clip. Thenmetal clip is uncomfortable while I sleep. Looking for a different solution for wearing my pump at night.
    • 1 day, 9 hours ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I answered that nobody wants to be screened, but I was answering based on my immediate family. I did let my deceased type-1 diabetic cousin's 35 year old son know he can be tested for his likelihood of becoming type-1 diabetic. He said he may be tested as he was always curious if he had a chance.
    • 1 day, 10 hours ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I have T1, and when my oldest grandson got T1, the other 3 grandkids got screened. The grandson who's the brother of the one with T1, showed a strong possibility of being a future T1 diabetic. It sadly came true about a year later.
    • 1 day, 10 hours ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I have LADA, and the idea of screening has not come up, either by me or my adult children. I guess I need to present the opportunity to them so they can make the decision.
    • 1 day, 10 hours ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 1 day, 13 hours ago
      Samantha Walsh likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I was born in 1939 and had many childhood illnesses. Three different kinds of measles and tonsils removed before I was 5 years old, then mumps and chickenpox when I was 5. While recovering from the mumps and chickenpox, I began showing the symptoms of very high blood sugar. Three doctors examined me and they were not able to make a diagnosis. I had lost much weight, and I had stopped eating. I did not have an appetite. It was almost impossible for me to walk. A fourth doctor had my blood tested and he made the diagnosis. While receiving pork insulin I finally began to recover a few days after my sixth birthday. I did not have ant relatives with diabetes. I think the childhood diseases caused internal damage and that was the cause of my diabetes. At the present time there are still no type one diabetics among my relatives. I do not believe it is necessary for my children and grandchildren to be screened for T1D autoantibodies.
    • 2 days, 8 hours ago
      KarenM6 likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 2 days, 10 hours ago
      Katie Bennett likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 2 days, 11 hours ago
      Kate Kuhn likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 2 days, 11 hours ago
      Karen DeVeaux likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I was born in 1939 and had many childhood illnesses. Three different kinds of measles and tonsils removed before I was 5 years old, then mumps and chickenpox when I was 5. While recovering from the mumps and chickenpox, I began showing the symptoms of very high blood sugar. Three doctors examined me and they were not able to make a diagnosis. I had lost much weight, and I had stopped eating. I did not have an appetite. It was almost impossible for me to walk. A fourth doctor had my blood tested and he made the diagnosis. While receiving pork insulin I finally began to recover a few days after my sixth birthday. I did not have ant relatives with diabetes. I think the childhood diseases caused internal damage and that was the cause of my diabetes. At the present time there are still no type one diabetics among my relatives. I do not believe it is necessary for my children and grandchildren to be screened for T1D autoantibodies.
    • 2 days, 12 hours ago
      Kelly-Dayne likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 2 days, 13 hours ago
      William Bennett likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 2 days, 13 hours ago
      Jneticdiabetic likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I have led a team for the JDRF OneWalk annually since the late 1990's. We have been able to raise a lot of funds for JDRF...and I have enjoyed doing it. Good cause!
    • 2 days, 13 hours ago
      Lawrence S. likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      my siblings & parents are older (like me) and they've never expressed any interest in getting tested. my nieces and nephews have never said anything either
    • 3 days, 1 hour ago
      Karen Newe likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I participated in several ADA walks not long after being Dx with T1D. As Ahh Life points out large $ are rased, but where do they go? I stopped supporting ADA for that reason. I think JDF is much more open on where the funding goes.
    • 3 days, 1 hour ago
      Karen Newe likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      JDRF only. I like knowing that my contributions are going specifically to T1D.
    • 3 days, 1 hour ago
      Karen Newe likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I have led a team for the JDRF OneWalk annually since the late 1990's. We have been able to raise a lot of funds for JDRF...and I have enjoyed doing it. Good cause!
    • 3 days, 5 hours ago
      Joindy23 likes your comment at
      The last time you discussed adding a new device or medication to your T1D management routine with your health care provider, who initially suggested trying the new device or medication?
      Switched a long time ago to Tandem/Dexcom from Minimed because of improved and more automated control, and haven't looked back. Still wishing for a cure, but know it's not going to happen for dinosaurs like me. I'll just be glad when young people will will one day experience that magic word: cure. It's too easy to sit around and complain, but it's high time for a cure, and way past time having us depend on treatment that is pretty much a money maker for big Pharma when it seems as if there's a cure waiting in the wings. Filling up landfills with used pump supplies, etc., makes our society look nothing but incompetent and greedy. Sorry to rant.......
    • 3 days, 5 hours ago
      Joindy23 likes your comment at
      The last time you discussed adding a new device or medication to your T1D management routine with your health care provider, who initially suggested trying the new device or medication?
      They do too often. Why I ask? Well because it will help long term.... oh how do you know that it will help? It's a brand new medication, never been used by the D community, except for the shortest term study mandated in order to get it to market, and sell. Long term has never been achieved... its NEW. Let's revisit/wait a couple years... if its MAGIC medicine, sure I'll try it. But unless it's got magic properties, guarantees magic results why would I want it, until it's been used for a decent while??? Oh well... yeah, guess that does makes sense....
    • 3 days, 22 hours ago
      Wanacure likes your comment at
      Does your T1D health care provider currently offer the option to have virtual appointments (via phone or video call)?
      Yes and for the last year and a half that is exclusively what I have been offered so I am not getting all the usual checks an in person endo visit requires. ADA and others spent 10-20 years convincing endos they needed to check patients feet and that progress has evaporated.
    • 3 days, 22 hours ago
      Wanacure likes your comment at
      Does your T1D health care provider currently offer the option to have virtual appointments (via phone or video call)?
      I would rather see in person. He checks my feet, BP etc. we have a chance to catch up and for me to ask questions. To me so much better face to face. We did virtual during pandemic.
    • 4 days, 6 hours ago
      Phyllis Biederman likes your comment at
      If you use an insulin pump, do you currently have a protective case on your pump or PDM?
      I’ll occasionally use the holster with clip that came with my pump or a protective case of my own when I’m wearing something without pockets. However I find these quite bulky thus usually just slip my pump in a pocket.
    Clear All
Pages
    • T1D Exchange T1D Exchange T1D Exchange
    • Articles
    • Community
      • About
      • Insights
      • Submit a Question
      • Donate
      • Join the Community
    • Quality Improvement
      • About
      • Collaborative
        • Leadership
        • Committees
      • Clinics
      • Meet the Experts
      • Learning Sessions
      • Resources
        • Change Packages
        • Sick Day Guide
      • Portal
      • Health Equity
        • Heal Advisors
      • Join Us
    • Registry
      • About
      • Recruit for the Registry
    • Research
      • About
      • Publications
      • COVID-19 Research
      • Our Initiatives
    • Partners
      • About
      • Previous Work
      • Academic Partnerships
      • Industry Partnerships
    • About
      • Team
      • Board of Directors
      • Culture & Careers
      • Annual Report
    • Join / Login
    • Donate

    Overall, how do you feel using a CGM affects your stress related to T1D management? If you’ve used one in the past, reflect on that experience to answer the question.

    Home > LC Polls > Overall, how do you feel using a CGM affects your stress related to T1D management? If you’ve used one in the past, reflect on that experience to answer the question.
    Previous

    If you have a child with T1D, have they ever gone to an overnight summer camp that is not specifically for kids with diabetes?

    Next

    Do you notice that different brands of the same type of insulin impact you differently?

    Sarah Howard

    Sarah Howard (nee Tackett) has dedicated her career to supporting the T1D community 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 Manager of Marketing at T1D Exchange. Sarah and her husband live in NYC with their cat Gracie. In her spare time, she enjoys doing comedy, taking dance classes, visiting art museums, and exploring different neighborhoods in NYC.

    Related Stories

    Blood Sugar

    How You Can Detect & Delay Type 1 Diabetes Before Symptoms Start 

    Ginger Vieira, 2 days ago 8 min read  
    T2D

    Why Your Heart Health Matters if You Live with Diabetes 

    Ginger Vieira, 1 week ago 5 min read  
    2023 Publications

    Association Between Health Insurance Type and Adverse Outcomes for Children and Young Adults With Type 1 Diabetes and Coronavirus Disease 2019 

    T1D Exchange, 1 week ago 1 min read  
    Meet the Expert

    Meet the Expert: Pursuing Beta-Cell Transplant with Temporary Immunosuppression  

    Jewels Doskicz, 3 weeks ago 6 min read  
    2023 Publications

    Institutional Barriers to the Successful Implementation of Telemedicine for Type 1 Diabetes Care 

    T1D Exchange, 3 weeks ago 1 min read  
    Insulin & Meds

    Perceptions About Nasal Glucagon in Young Adults and Caregivers 

    Caitlin Kelly, 3 weeks ago 6 min read  

    40 Comments

    1. Ahh Life

      Decreasing my stress is the wrong wording.

      Using a CGM (hopefully) keeps me from an immediate appointment with the grim reaper.

      4
      2 months ago Log in to Reply
    2. Steven Gill

      Definitely more at ease.

      2
      2 months ago Log in to Reply
    3. sweetcharlie

      I do not fully trust it , but it is a quick easy way to see how I am doing..

      3
      2 months ago Log in to Reply
    4. Lawrence S.

      Using a CGM makes my life easier. I don’t have to keep stopping to do blood tests. It automatically communicates with my insulin pump, and the pump makes adjustments, as needed. I used to have to do all of those things myself. Definitely less stressful.

      2
      2 months ago Log in to Reply
    5. cynthia jaworski

      Before blood testing existed, I simply ignored everyting and hoped for the best. CGM has gone beyond blood testing and makes it possible to do a decent job of managing. Of course, there is more worry than in the “ignore it” days because now there is responsibility coupled to having actual knowledge/data.
      I would probably not be here this long if it hadn’t come along.

      2
      2 months ago Log in to Reply
    6. Sue Herflicker

      It’s the arrows!! I raised 2 T1ds without the help of a CGM. They didn’t exist then. Being diagnosed myself at the age of 56, I find following the arrows can be stressful. It has so many good points don’t get me wrong. I do love it and don’t want to be without it, but being LADA, those 2 arrows down can be quite stressful. I can just imagine my poor boys, I can’t imagine following their arrows. However, at night time when they were sleeping or if they were sick, it would have been a gift.

      2 months ago Log in to Reply
    7. TEH

      I picked both. I am less stressed sleeping with CGM because it will catch lowes before they get too far. I get more stressed while driving. I can’t easily get to my pump with my seat belt on. I use a phone holder in one vehicle but checking SG is destracted driving hence more stressful. Still much better than pumping blind.

      1
      2 months ago Log in to Reply
    8. Jen Farley

      Using a CGM decreases my stress more by allowing me to see my low blood sugars coming on. It increases a slight bit because my husband can be on my case. -you going to take care of that-I did not see you eat anything-why is it to coming up.

      2 months ago Log in to Reply
    9. Kathleen Begbie

      Don’t have to carry my test kit everywhere

      1
      2 months ago Log in to Reply
    10. Jane Cerullo

      Makes T1D so much easier to manage. Prior to CGM I would be testing 10 times a day. Poor fingers. Only complaint I have with Dexcom G7 is that sometimes not accurate first day. Oh and the lousy adhesive. I use liquid SkinTac instead of patches. What’s the point of a smaller sensor if you have to add an over patch.

      1
      2 months ago Log in to Reply
      1. AnitaS

        I agree. I think the G7 should have a larger adhesive

        2 months ago Log in to Reply
    11. Kathy Hanavan

      Overall, I am more confident with CIQ, but the alarms can be stressful and annoying, especially the unnecessary ones that come repeatedly.

      1
      2 months ago Log in to Reply
    12. T1D4LongTime

      The CGM is one of the most beneficial devices for T1Ds. Knowing my glucose level in real-time decreases my stress in managing my brittle T1D. The downside is the alarms, but Dexcom app has adequate tools to eliminate alarm-overload.

      1
      2 months ago Log in to Reply
    13. Chris Albright

      Both. Enjoy the ability to see my bg at any time, but frustrated with frequent inaccurate values. With that said, it makes clossed loop pumping much easier and keeps me in my target A1c target range.

      1
      2 months ago Log in to Reply
    14. TomH

      Using a CGM is far and away better than finger sticks: better control, allows AID use with a pump, etc. It’s a life saver for those experiencing lows/severe lows. However, it can also be frustratingly stressful for unexplained highs and large swings if alarms go off if you’re not in the mindset of “Great! Now I can control it!” and more of “Damn! Now I have to control it!”

      2
      2 months ago Log in to Reply
    15. T1diabetic

      The convenience of being able to check blood sugar levels is so great!
      But the alerts that cannot be turned off is Not!

      4
      2 months ago Log in to Reply
    16. Jneticdiabetic

      Overall, CGM has made life much better. Reduces stress around worrying about unpredictable lows. The alarms and additional device management can also increase my stress at times. The last couple of days were associated with some CGM-stress. Sensor session ended just as I was getting into bed. Got up, replaced, comfortable that it would start reading in a couple of hours, but I failed to hit the last start CGM confirmation. Woke up in a rush for work with no readings. Started sensor, then about 1-2 later I get an alarm that my transmitter failed and needs to be replaced. Dang. Wasted a sensor. Then last night, with a brand new transmitter, I got multiple alarms of lost signal. I sleep so poorly as it is, such moments make me feel a little less appreciative. When it alarms that I’m heading down fast without symptoms, I quickly forgive it.

      2
      2 months ago Log in to Reply
    17. Nicholas Argento

      It has my back and protects me from severe hypoglycemia, a predator which has hunted me for 55 years. I know I can go to sleep and am extremely unlikely to be awakened by my wife frantically trying to revive me, or worse yet, a paramedic in my bedroom. I could be dead without CGM.

      2
      2 months ago Log in to Reply
    18. dave hedeen

      When CGM values are close to correct, stress disappears. Opposite, when values exceed acceptable variance, stress is magnified!

      1
      2 months ago Log in to Reply
      1. KCR

        Agree!

        2 months ago Log in to Reply
    19. Carol Meares

      On roller coaster days or on days when I have a stubborn high I watch my numbers too much and stress over them trying to stabilize but most of the time the CGM decreases stress. It would be extremely stressful to be without a CGM. I used to test 8-12 or more times per day before CGM and still unsure where my trend was going. I am so grateful for the CGM science and all it has done for my diabetes management.

      1
      2 months ago Log in to Reply
    20. NANCY NECIA

      Yes, the CGM is a major stress reducer. But I suffer from “alarm fatigue”. My biggest complaint is if my BG is going down but still above 180, the **** CGM keeps sending alarms. And it craves attention to actually tap “OK” to space out the alarm intervals. But still, the CGM is a major game changer for me and for so many other T1D! Therefore, a stress reducer across time.

      3
      2 months ago Log in to Reply
    21. Trina Blake

      Majlor decrease in the stress dept! Prior to CGM I was 15-0 fingersticks a day (why do many? Every time I got behind the steering wheel of my car I checked. I responded to too many accidents caused by impaired drivers to not check). I esp[ecially value the real time bg as well as the trend arrows and a day’s worth of flat-lining.

      I am very aggressive in my T1D mgt, I aim for normal labs, my settings reflect the range of non-D people. My CGM allows me to do that. It is also far more accurate than the meter covered by my health plan. The covered meter routinely read higher than actual (learned about that issue at an Endo CME). purchased the highest rated meter, ran my own experiment. The CGM and the highest-rated meter were very close. The covered meter often 100+ points higher than actual. That led me have an insulin correctio bolus when that was the last thing I needed. I am grateful for the alarms – and there are many since my range for alerts s 60-120.

      2 months ago Log in to Reply
    22. Janis Senungetuk

      Data overload and intermittent errors increase my stress while the ease of frequent use definitely decreases stress. Considering how often I experienced frequent, disabling lows in the past, use of a CGM now has reduced the burden of living with T1D.

      3
      2 months ago Log in to Reply
    23. AimmcG

      It’s the alarming that stresses me out

      2
      2 months ago Log in to Reply
    24. Stuart Pelcyger

      My stress decreases on days 2-7 of my G6 because it is pretty accurate then. My stress increases on the first and last 2-3 days of the session because at it time it proves totally inaccurate. Back to multiple finger sticks and eventually a call to Dexcom to replace the bad sensor.

      2 months ago Log in to Reply
    25. Sondra Mangan

      Dexcom user since 2007— less than a year after diagnosis. Before insurance covered Dex, I paid cash and made use of every bit of data I could get—charting what happened with different foods and modifying how I ate to minimize spikes. On MDI I had random overnight low lows and the Dexcom alarms kept me alive when I was awakened at 70 — not 38!

      2 months ago Log in to Reply
    26. Sue Martin

      Getting a CGM was also a great stress reducer for my husband. He didn’t have to wake me in the night to check my BG, he could just look at the CGM reader. The low alarm from DexCom really helped to wake me/us up if I really needed to make a correction.
      I had a couple of times that I didn’t get a new transmitter before the weekend and had to wait a couple of days. Being without it made me realize how much I depend on my CGM.

      1
      2 months ago Log in to Reply
    27. Amanda Barras

      Both.
      I’m more OCD about blood sugars and management but I also can live more carefree in terms of lows because I know I’ll be alerted before it becomes an issue.

      2
      2 months ago Log in to Reply
    28. KIMBERELY SMITH

      I feel much better

      2 months ago Log in to Reply
    29. Patricia Kilwein

      Using a CGM is great but it has definitely increased the stress levels. Lack of sleep is main factor. Fighting insurance and now medicare for supplies….. I could go on.

      2
      2 months ago Log in to Reply
    30. Maureen Helinski

      I love the CGM and wouldn’t do without it.

      2 months ago Log in to Reply
    31. ConnieT1D62

      The only time I stress using a CGM is when I have inserted the last one on hand from my diabetes supply closet and I await delivery of the next shipment from supplier. I am grateful and thank the powers of goodness that I have T1 diabetes sister friends nearby and we often borrow from one another to cover each other’s ass until the next shipment comes. Otherwise CGM makes T1D life so much better and less stress filled.

      2 months ago Log in to Reply
    32. Shelly Smith

      I love my CGM! I live with epilepsy as well, so knowing that my pump will take care of things on its own if I fall out is a real blessing.

      2 months ago Log in to Reply
      1. Wanacure

        I think my seizure disorder developed AFTER having severe hypoglycemic episodes with increasing frequency. No seizures since taking relatively new anti seizure oral med w/o side-effect of brain-fogging liver-taxing Dilantin.

        2 months ago Log in to Reply
    33. Wanacure

      After the initial stress of learning how to apply a CGM & then learning how to avoid “compression lows” from commentators on this website, it’s more time in range, better control, better understanding and much less stress than ever. Cherry on top: last week’s grand jury conspiracy indictment for a prominent US Mussolini/Franco wanabe.

      2 months ago Log in to Reply
    34. AnitaS

      I was hoping for a choice of not increasing or decreasing my stress. I do worry less about going low, but I don’t know if my worry was enough to be called stressful.

      2 months ago Log in to Reply
    35. mbulzomi@optonline.net

      I have been a person with Diabetes for 55 years, on an Insulin pump for over 40 years, along with using a CGM for over 11 (Medtronic and Dexcom) years. The best thing so far to maintain my overall health, including Diabetes.

      2 months ago Log in to Reply
    36. Jeff Balbirnie

      I do not NEED to know what is now available every waking second of every day. The approach induces severe hyper-vigilance, dangerous obsessiveness that has zero tangible improvement to the quality of our lives. Evert five minutes is excessive data… I was never afraid before the technology existed. Too many are now solely because of it. If you do not immediately (and instantly) know your BG soooo what! I will not be taught fear because of this technology. A good and positive life is very possible without dependance on any tech, much less this tech. Maintenance is never cure.

      2 months ago Log in to Reply
    37. lis be

      the arrow that says that my blood sugar is increasing or decreasing quickly often causes me to take a little too much insulin or too much glucose.

      2 months ago Log in to Reply

    Overall, how do you feel using a CGM affects your stress related to T1D management? If you’ve used one in the past, reflect on that experience to answer the question. Cancel reply

    You must be logged in to post a comment.

    This site uses Akismet to reduce spam. Learn how your comment data is processed.




    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

    © 2023 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.

    2019 Publications

    0 Stories Related

    2020 ADA

    12 Stories Related

    2020 ADCES

    0 Stories Related

    2020 ATTD

    0 Stories Related

    2020 EASD

    0 Stories Related

    2020 ISPAD

    7 Stories Related

    2020 Publications

    0 Stories Related

    2021 ADA

    11 Stories Related

    2021 ADCES

    0 Stories Related

    2021 ATTD

    4 Stories Related

    2021 ISPAD

    8 Stories Related

    2021 Publications

    21 Stories Related

    2022 ADA

    11 Stories Related

    2022 ADCES

    4 Stories Related

    2022 ATTD

    10 Stories Related

    2022 ISPAD

    0 Stories Related

    2023 ADA

    12 Stories Related

    2023 ADCES

    2 Stories Related

    2023 ATTD

    7 Stories Related

    2023 Publications

    16 Stories Related

    ADA

    17 Stories Related

    ADCES

    2 Stories Related

    Advocacy

    23 Stories Related

    ATTD

    17 Stories Related

    Blood Sugar

    2 Stories Related

    Conditions

    8 Stories Related

    COVID-19

    6 Stories Related

    EASD

    0 Stories Related

    General Publications

    25 Stories Related

    Get Involved

    11 Stories Related

    Insulin & Meds

    17 Stories Related

    ISPAD

    1 Stories Related

    Journal of Diabetes

    21 Stories Related

    Lifestyle

    15 Stories Related

    Lifestyles

    1 Stories Related

    Meet the Expert

    28 Stories Related

    Mental Health

    12 Stories Related

    News

    35 Stories Related

    Our team

    23 Stories Related

    Partner Content

    7 Stories Related

    Press Release

    7 Stories Related

    Question of the Day

    28 Stories Related

    Research

    73 Stories Related

    Stories

    18 Stories Related

    T2D

    3 Stories Related

    Technology

    26 Stories Related

    Uncategorized

    0 Stories Related

    We're preparing your personalized page.

    This will only take a second...

    Search and filter

    • Clear All
    • Sort By

    • Select Category