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    • 30 minutes ago
      John Barbuto likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      I agree with Molly. I’m moderately concerned because if I were extremely or very concerned, I just wouldn’t participate. I’m concerned for others who are brave enough to risk their own health for the sake of research and helping others.
    • 30 minutes ago
      John Barbuto likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      Pinioned to youth, my comment may be difficult for some of you to understand. But at my age and experience level, long-term effects consists of what is going to happen in the next thirty to forty-five minutes. Sigh! 🎀 ྀིྀི
    • 4 hours, 28 minutes ago
      lis be likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      Our collective lack of concern about the long term ought to put us at the top of the transplant list.
    • 4 hours, 28 minutes ago
      lis be likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      For me, this is a hypothetical question. On the surface, I am not concerned, because it does not effect me . However, if I were seriously going to view this as a genuine therapy for me, I would be very seriously concerned about side effects and long-term effects or immune system response.
    • 4 hours, 28 minutes ago
      lis be likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      Long term effects are not a worry to me after 50 years of T1D…..not sure that I have a long runway ahead of me. If it helps advance a better life for young people with T1D sign me up.
    • 4 hours, 29 minutes ago
      lis be likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      Pinioned to youth, my comment may be difficult for some of you to understand. But at my age and experience level, long-term effects consists of what is going to happen in the next thirty to forty-five minutes. Sigh! 🎀 ྀིྀི
    • 4 hours, 43 minutes ago
      Natalie Daley likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      Pinioned to youth, my comment may be difficult for some of you to understand. But at my age and experience level, long-term effects consists of what is going to happen in the next thirty to forty-five minutes. Sigh! 🎀 ྀིྀི
    • 5 hours, 4 minutes ago
      ChrisW likes your comment at
      Have you heard about tegoprupart, an immunosuppressant alternative with fewer side effects than traditional immunosuppressants, now being used for islet cell transplantation?
      Well the first person in this trial has been insulin-free for over 1-1/2 years and has been feeling fine. All 12 participants in this trial so far are off of insulin. The trial is now going to include people with t-1 diabetes and some kidney damage as this immunosuppressant (tegoprubart) has shown no toxic effects to islet cells or to kidneys. I will keep watching as the trial progresses. This question only asked if we had heard about it. I didn't see the question as an advertisement.
    • 5 hours, 10 minutes ago
      ChrisW likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      Pinioned to youth, my comment may be difficult for some of you to understand. But at my age and experience level, long-term effects consists of what is going to happen in the next thirty to forty-five minutes. Sigh! 🎀 ྀིྀི
    • 5 hours, 11 minutes ago
      Brian Vodehnal likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      Concern is relative to outcome. Getting a five year reprieve on the daily management of T1D might be worth it.
    • 6 hours, 8 minutes ago
      Derek West likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      For me, this is a hypothetical question. On the surface, I am not concerned, because it does not effect me . However, if I were seriously going to view this as a genuine therapy for me, I would be very seriously concerned about side effects and long-term effects or immune system response.
    • 6 hours, 57 minutes ago
      Bonnie kenney likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      Pinioned to youth, my comment may be difficult for some of you to understand. But at my age and experience level, long-term effects consists of what is going to happen in the next thirty to forty-five minutes. Sigh! 🎀 ྀིྀི
    • 6 hours, 57 minutes ago
      Bonnie kenney likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      Moderately as this is for others. I don't imagine being offered this myself.
    • 6 hours, 58 minutes ago
      Bonnie kenney likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      For me, this is a hypothetical question. On the surface, I am not concerned, because it does not effect me . However, if I were seriously going to view this as a genuine therapy for me, I would be very seriously concerned about side effects and long-term effects or immune system response.
    • 6 hours, 58 minutes ago
      Bonnie kenney likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      Long term effects are not a worry to me after 50 years of T1D…..not sure that I have a long runway ahead of me. If it helps advance a better life for young people with T1D sign me up.
    • 7 hours, 1 minute ago
      atr likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      Our collective lack of concern about the long term ought to put us at the top of the transplant list.
    • 7 hours, 1 minute ago
      atr likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      For me, this is a hypothetical question. On the surface, I am not concerned, because it does not effect me . However, if I were seriously going to view this as a genuine therapy for me, I would be very seriously concerned about side effects and long-term effects or immune system response.
    • 7 hours, 2 minutes ago
      atr likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      Long term effects are not a worry to me after 50 years of T1D…..not sure that I have a long runway ahead of me. If it helps advance a better life for young people with T1D sign me up.
    • 7 hours, 3 minutes ago
      atr likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      I just love your comments. 😃
    • 7 hours, 4 minutes ago
      atr likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      Pinioned to youth, my comment may be difficult for some of you to understand. But at my age and experience level, long-term effects consists of what is going to happen in the next thirty to forty-five minutes. Sigh! 🎀 ྀིྀི
    • 7 hours, 4 minutes ago
      Gerald Oefelein likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      Pinioned to youth, my comment may be difficult for some of you to understand. But at my age and experience level, long-term effects consists of what is going to happen in the next thirty to forty-five minutes. Sigh! 🎀 ྀིྀི
    • 7 hours, 9 minutes ago
      Gary R. likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      Pinioned to youth, my comment may be difficult for some of you to understand. But at my age and experience level, long-term effects consists of what is going to happen in the next thirty to forty-five minutes. Sigh! 🎀 ྀིྀི
    • 7 hours, 9 minutes ago
      MT likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      Long term effects are not a worry to me after 50 years of T1D…..not sure that I have a long runway ahead of me. If it helps advance a better life for young people with T1D sign me up.
    • 7 hours, 26 minutes ago
      Meerkat likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      Long term effects are not a worry to me after 50 years of T1D…..not sure that I have a long runway ahead of me. If it helps advance a better life for young people with T1D sign me up.
    • 7 hours, 27 minutes ago
      Meerkat likes your comment at
      How concerned are you about the risks of islet cell transplantation such as unknown long-term effects or immune system response?
      Pinioned to youth, my comment may be difficult for some of you to understand. But at my age and experience level, long-term effects consists of what is going to happen in the next thirty to forty-five minutes. Sigh! 🎀 ྀིྀི
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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
      4 years ago Log in to Reply
      1. Blormph

        I never share live either. I upload them

        2
        4 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
      4 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
      4 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
      4 years ago Log in to Reply
    5. Patricia Kilwein

      Why would you play games with your life like that?

      2
      4 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
      4 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
      4 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
      4 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
      4 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
      4 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
      4 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
      4 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
      4 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.

      4 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.

      4 years ago Log in to Reply
    16. lis be

      this question is a bit odd.

      2
      4 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
      4 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
      4 years ago Log in to Reply
    19. mbulzomi@optonline.net

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

      4 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.

      4 years ago Log in to Reply
    21. Jeff Balbirnie

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

      4 years ago Log in to Reply
    22. T1D4LongTime

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

      4 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.

      4 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.

      4 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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