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    • 1 hour, 35 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, 35 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, 36 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, 18 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, 41 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, 39 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, 1 minute 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, 4 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, 5 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, 5 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, 13 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, 6 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, 6 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, 9 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 wear a CGM, and share your data with your support team, have you ever shut off the sharing aspect when your numbers go out of range? 

    Home > LC Polls > If you wear a CGM, and share your data with your support team, have you ever shut off the sharing aspect when your numbers go out of range? 
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    If you had to pick one person, who is the person you turn to most for support with your diabetes?

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    Which of the following supplements or vitamins do you take on a regular basis? Select all that apply.

    Samantha Walsh

    Samantha Walsh has lived with type 1 diabetes for over five years since 2017. After her T1D diagnosis, she was eager to give back to the diabetes community. She is the Community and Partner Manager for T1D Exchange and helps to manage the Online Community and recruit for the T1D Exchange Registry. Prior to T1D Exchange, Samantha fundraised at Joslin Diabetes Center. She graduated from the University of Massachusetts with a Bachelors degree in sociology and early childhood education.

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    25 Comments

    1. Britni

      My values aren’t shared live. They get uploaded when I go in for my appointments. I don’t think I could hide when my numbers go out of range even if I wanted to.

      1
      3 years ago Log in to Reply
      1. Blormph

        I never share live either. I upload them

        2
        3 years ago Log in to Reply
    2. Joan McGinnis

      if you want help getting to your goal, why hide them
      if doctors dont see reality of living with diabetes as a challenge, they neds their wisdom and compassion, they won’t practice in endocrinology

      2
      3 years ago Log in to Reply
    3. TomH

      The purpose of sharing is to allow someone to help if I get in trouble and don’t realize it. If the “helper” is just being “judge” they wouldn’t be a helper for long!

      2
      3 years ago Log in to Reply
    4. Janice Bohn

      That would seem counter productive. How would my Drs team have the data they need to help make good decisions

      3
      3 years ago Log in to Reply
    5. Patricia Kilwein

      Why would you play games with your life like that?

      2
      3 years ago Log in to Reply
    6. Mary Dexter

      My endocrinologist can access my numbers through Clarity. I shared with my husband, but he wanted whatever caused the alarms to be fixed immediately, so for both our sanities, I stopped sharing with him.

      2
      3 years ago Log in to Reply
    7. Jeanne McMillan-Olson

      I don’t share with anyone, but I upload my numbers etc from my pump before I see my endo.

      1
      3 years ago Log in to Reply
    8. Lawrence S.

      No I do not “hide” my numbers from my Endocrinologist. It makes no sense to be dishonest. If I want help from my doctors, they need to know what is going on. Sending false information only hurts me.

      3
      3 years ago Log in to Reply
    9. Janis Senungetuk

      The only people who have any interest in my numbers are health care providers. I’m paying for their advise on managing those numbers and share that data only with them.

      2
      3 years ago Log in to Reply
    10. Kathy Morison

      I always let the nurse practitioner I see every 3 months for my type 1 diabetes to see my numbers and how much insulin I take but by no means does she provide any ongoing support for me and my daily challenges with my diabetes care

      1
      3 years ago Log in to Reply
    11. Natalie Daley

      My endocrinologist will download and study them at our visit. I drive 160 miles for his highly educated help. Why would I hide the info he needs to help me?

      4
      3 years ago Log in to Reply
    12. Andrew Stewart

      My endo has access through the Tandem pump portal and also provided a Glooko account that links with my G6. The advantage of the Glooko logger is that I can add meals, exercise and notes which add the needed context to help understand the CGM numbers. Context is king.
      #BeWell

      1
      3 years ago Log in to Reply
    13. Becky Hertz

      I’m sure they don’t have someone monitoring the shared data continuously. You share data for assistance. Now, if I were to be shamed for my numbers, I’d cut them off by leaving the practice.

      1
      3 years ago Log in to Reply
    14. kristina blake

      I upload (via T-Connect, it shows Dexcom and pump data) every month. I do it for me. Since T-Connect is a “pull” system – meaning the Endo goes to the system and pulls the data down (as opposed to a “push” system where it shows up automatically every month when I upload). I don’t share my data with anyone other than the Endo practice.

      3 years ago Log in to Reply
    15. Milly Bassett

      I don’t have a support team. My husband can see my numbers but he doesn’t really look at them. I’m ok with that. My doctor will download the numbers when I see him every 3 to 4 months. My adult children does not inquire, and although sometimes I share my stories, they have no clue what the concerns are.

      3 years ago Log in to Reply
    16. lis be

      this question is a bit odd.

      2
      3 years ago Log in to Reply
    17. Henry Renn

      Why not share? Feel no shame. Most of us lifers have had periods of poor control.

      1
      3 years ago Log in to Reply
    18. Angela Naccari

      I do not share with my care team on follow but I bring my endo hard copies of info from Connect app.

      1
      3 years ago Log in to Reply
    19. mbulzomi@optonline.net

      Share is for our safety. Why would you want to stop it???

      3 years ago Log in to Reply
    20. ConnieT1D62

      I don’t share and I manage quite well without sharing my CGM data – it’s nobody’s business except mine. I only upload prior to a visit with endo provider to look at TIR and trends and discuss any changes that need to be made.

      3 years ago Log in to Reply
    21. Jeff Balbirnie

      When I used one the sharing feature was not invented yet, it did not exist!

      3 years ago Log in to Reply
    22. T1D4LongTime

      No, never. There would be no point in doing that if I want a long life.

      3 years ago Log in to Reply
    23. Maurine Bowser

      I don’t think my endo ever looks at my “shared” data except at my regular visit and that is only the 14-day report.

      3 years ago Log in to Reply
    24. Kim Murphy

      I do turn it off while I am waiting for my blood sugar to come up after eating a snack. I don’t want to wake him up.

      3 years ago Log in to Reply

    If you wear a CGM, and share your data with your support team, have you ever shut off the sharing aspect when your numbers go out of range?  Cancel reply

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