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    • 1 hour, 26 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      I want a thumbs down icon!
    • 1 hour, 26 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      I seldom have any questions other than RX refill request which I submit through the patient portal. If I do have treatment questions, I typically do my own research, and if not satisfied with what I find out, I submit a question in the portal.
    • 1 hour, 26 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      When I come up with a question between visits, I usually just do some research.
    • 3 hours, 39 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.
    • 3 hours, 40 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
    • 3 hours, 40 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!
    • 4 hours, 22 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.
    • 5 hours, 45 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.
    • 7 hours, 43 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
    • 23 hours, 6 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.
    • 23 hours, 8 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.
    • 23 hours, 9 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.
    • 23 hours, 9 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
    • 23 hours, 18 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 ´ )⎠⎞
    • 1 day, 1 hour 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.
    • 1 day, 1 hour 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.
    • 1 day, 1 hour 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, 5 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, 7 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, 8 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, 8 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, 8 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, 8 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, 8 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, 8 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.
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    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

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

    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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    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 years ago Log in to Reply
    2. Steven Gill

      Definitely more at ease.

      2
      2 years 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 years 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 years 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 years 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 years 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 years 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 years ago Log in to Reply
    9. Kathleen Begbie

      Don’t have to carry my test kit everywhere

      1
      2 years 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 years ago Log in to Reply
      1. AnitaS

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

        2 years 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 years 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 years 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 years 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 years 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 years 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 years 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 years 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 years ago Log in to Reply
      1. KCR

        Agree!

        2 years 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 years 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 years 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 years 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 years ago Log in to Reply
    23. AimmcG

      It’s the alarming that stresses me out

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

      I feel much better

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

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

      2 years 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 years 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 years 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 years 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 years 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 years 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 years 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 years 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 years 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

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