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    • 7 hours, 39 minutes ago
      KarenM6 likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      There are many concerns, one being if I'll still be alive if it's ever offered :)
    • 7 hours, 39 minutes ago
      KarenM6 likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      At 78 I don't think islet transplantation will affect my life course. Big pharma sees biological treatments as the path to ever higher profits, not constrained by patent terms the way drugs are. Most diabetics would be better served by an improved standard of care from the ADA and the medical community.
    • 8 hours, 54 minutes ago
      Lawrence S. likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      Very, but more worried about it even making to the FDA and approved there first.
    • 8 hours, 55 minutes ago
      Lawrence S. likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      There are many concerns, one being if I'll still be alive if it's ever offered :)
    • 8 hours, 55 minutes ago
      Lawrence S. likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      At 78 I don't think islet transplantation will affect my life course. Big pharma sees biological treatments as the path to ever higher profits, not constrained by patent terms the way drugs are. Most diabetics would be better served by an improved standard of care from the ADA and the medical community.
    • 8 hours, 56 minutes ago
      Lawrence S. likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      Severe case of hardening of the “oughteries” here. Ought we be concerned with cost, insurance, coverage, hail storms, earthquakes? ▄█▀█● Why are we not homeschooled to enjoy the progress being made?
    • 8 hours, 57 minutes ago
      Lawrence S. likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      While those items are very much a concern, there are other factors that are more concerning ie immunosuppressant.
    • 8 hours, 58 minutes ago
      Amanda Barras likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      If they can transplant them such that we do not need immunosuppresants, we'd be fine. Otherwise, those meds are just one more thing that could become in short supply. But at least we could go through scanners at the airports and travel without huge bags of supplies.
    • 8 hours, 58 minutes ago
      Amanda Barras likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      General access to islet transplants is still years away. FDA has to deem it safe. Though, I am excited about the possibility.
    • 8 hours, 58 minutes ago
      Amanda Barras likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      At 78 I don't think islet transplantation will affect my life course. Big pharma sees biological treatments as the path to ever higher profits, not constrained by patent terms the way drugs are. Most diabetics would be better served by an improved standard of care from the ADA and the medical community.
    • 11 hours ago
      Patricia Dalrymple likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      If they can transplant them such that we do not need immunosuppresants, we'd be fine. Otherwise, those meds are just one more thing that could become in short supply. But at least we could go through scanners at the airports and travel without huge bags of supplies.
    • 11 hours, 38 minutes ago
      Gerald Oefelein likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      If they can transplant them such that we do not need immunosuppresants, we'd be fine. Otherwise, those meds are just one more thing that could become in short supply. But at least we could go through scanners at the airports and travel without huge bags of supplies.
    • 11 hours, 38 minutes ago
      Gerald Oefelein likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      While those items are very much a concern, there are other factors that are more concerning ie immunosuppressant.
    • 12 hours, 21 minutes ago
      Marty likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      much more concerned about my age (65) than anything else. 😉
    • 12 hours, 43 minutes ago
      dholl62@gmail.com likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      much more concerned about my age (65) than anything else. 😉
    • 13 hours, 7 minutes ago
      Steve Rumble likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      Severe case of hardening of the “oughteries” here. Ought we be concerned with cost, insurance, coverage, hail storms, earthquakes? ▄█▀█● Why are we not homeschooled to enjoy the progress being made?
    • 13 hours, 7 minutes ago
      Steve Rumble likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      While those items are very much a concern, there are other factors that are more concerning ie immunosuppressant.
    • 13 hours, 7 minutes ago
      atr likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      Severe case of hardening of the “oughteries” here. Ought we be concerned with cost, insurance, coverage, hail storms, earthquakes? ▄█▀█● Why are we not homeschooled to enjoy the progress being made?
    • 13 hours, 22 minutes ago
      Sarah Berry likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      much more concerned about my age (65) than anything else. 😉
    • 14 hours, 23 minutes ago
      Steve Rumble likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      Age 73 here. I'm in the same boat. I ogten am considered too old for consideration for "smaller" research projects. But - best of luck to them. I'll be rooting on the sidelines.
    • 14 hours, 24 minutes ago
      Steve Rumble likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - 👍 immunosuppression needed - 👎
    • 1 day, 5 hours ago
      Gerald Oefelein likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I've tried twice and was rejected both times because I control my diabetes as best I can. As others have already stated, if immunosuppressing drugs are involved, count me out. I'm not interested in something worse than what I already have.
    • 1 day, 5 hours ago
      Gerald Oefelein likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      Not if it requires immunosuppressant drugs. Been there done that time to move on to something much better.
    • 1 day, 5 hours ago
      Gerald Oefelein likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - 👍 immunosuppression needed - 👎
    • 1 day, 11 hours ago
      Natalie Daley likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I answered “Very Unlikely” not because I woud not want to participate but because, at age 75, I think it very unlikely that any researcher would want me in their patient panel.
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    If you use a CGM and share your real-time glucose levels with other people using an app (e.g., Dexcom Share, Carelink Connect, Nightscout, etc.), with whom have you shared your live CGM data? Select all that apply!

    Home > LC Polls > If you use a CGM and share your real-time glucose levels with other people using an app (e.g., Dexcom Share, Carelink Connect, Nightscout, etc.), with whom have you shared your live CGM data? Select all that apply!
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    A surprising number of employees living with T1D at T1D Exchange have a twin! For people with T1D, are you a twin (or a sibling of a multiple birth, such as a triplet)?

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    New research found a gene that may put some people at higher risk for “long-COVID” (symptoms that persist after a COVID-19 infection, such as ongoing shortness of breath, fatigue, brain fog, or memory issues). What is your experience with long COVID? Share your experience in the comments.

    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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    23 Comments

    1. Jen Farley

      My husband and my daughter but only when watching the grandkids to help he know they are in good care.

      3 years ago Log in to Reply
    2. Gerald Oefelein

      I share with my diabetologist.

      3 years ago Log in to Reply
    3. Annie Wall

      Only my endocrinologist.

      3 years ago Log in to Reply
    4. KIMBERELY SMITH

      I share with my God son

      3 years ago Log in to Reply
    5. Sue Compo

      My endo has permission to view my cgm, but she rarely does except before my appt.

      2
      3 years ago Log in to Reply
    6. Mick Martin

      I selected “I use a CGM but do not share my real-time data” but the ONLY reason I don’t share my real-time data is because I don’t have the facility to do so.

      3 years ago Log in to Reply
    7. Ahh Life

      In the digital age, I take “real time” to mean minute-by-minute or hour-by-hour. That number is a big fat zero. The only “real time sharing” is when the wife asks, “What is it?” and I give her a verbal, not electronic, answer.

      I do aggregate data weekly to analyze it. I do have an endocrinologist download it every 3 or 4 months. But real time? That’s my baby and mine alone. 😏

      3
      3 years ago Log in to Reply
      1. Peter Richardson

        I also share with my wife verbally when she asks. I typically say things like “it’s perfectly balanced” which means somewhere between high and low or “it’s a bit low” which means anything below 65, or “a bit high” which typically means over 200.

        1
        3 years ago Log in to Reply
    8. Gary Rind

      Libre does not enable real-time sharing. Upload the info to my endo each time I change my sensor

      3 years ago Log in to Reply
    9. Carol Meares

      Whoops, I said I do not share my data, but I share with my doctor.

      1
      3 years ago Log in to Reply
      1. Carol Meares

        Doc who looks at it every 3-4 months. I do not share with anyone who gets alarms when I am going high or low. Yikes, couldn’t imagine doing that to someone.

        3
        3 years ago Log in to Reply
    10. Daniel Bestvater

      Shared my Dexcom data with my wife for about 48 hours once. The BG swings and alarms scared the pants off of her! So I do not share the real time data any longer. Unless the individual has T1D they really don’t understand the BG roller coaster we live on!!

      3
      3 years ago Log in to Reply
    11. Joan Benedetto

      We share Nightscout with our son’s teacher (no nurse), and our adult daughter who, also, has the Follow app on her phone. We download data, via Tidepool, to our son’s Endo prior to each appointment.

      3 years ago Log in to Reply
    12. Steve Rumble

      I share with my endocrinologist.

      3 years ago Log in to Reply
    13. Elle Hamann

      My child has had camp team members follow him and also occasionally my friends when I’ve had surgery (unable to reliably watch his numbers) or if he sleeps over at their house.

      3 years ago Log in to Reply
    14. William Bennett

      I chose “Someone else,” though it’s not a person. The Share channel is used by two add-on apps that I find very useful. Sugarmate, which displays my BG at the top control bar of my MacBook laptop, and Glance, which is a clock face for my Versa Two Fitbit. Only problem with the latter is that it’s especially handy for parties where you’re having to guesstimate boluses, but it can give people the impression that I’m rudely checking the time when I’m actually checking my BG!

      3 years ago Log in to Reply
    15. jo

      When I first got the G6 I shared with my husband and 2 sisters, sharing with my sisters lasted maybe 3 days. They drove me crazy. I told them that I had to pay for more than one person to have access to my real time numbers so now it’s just myself and my husband.

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

      I use t: connect so my healthcare could follow real time data, but I think only uses it if there’s an issue or when I have an appointment.

      0
      3 years ago Log in to Reply
    17. Russell Buckbee

      NO one seems to want that much data. They want A1c at most.

      3 years ago Log in to Reply
    18. Molly Jones

      The people who have access to this data are my husband, endocrinologist, and neurologist.

      3 years ago Log in to Reply
    19. Wanacure

      I deliberately chose an iPhone model capable of receiving Dexcom info. But So far I just use Dexcom receiver which I take twice a month to tech team for free paper download. I used to have an Epson color printer, but the frequency of ink refills annoyed me. Hmmm…🤔If I did use my iPhone, maybe I could download free printouts at public library with their fancy new color Wi-Fi printer.

      3 years ago Log in to Reply
    20. Kris van Bergen

      Our daughter’s data is shared real time with our school nurse, and with other family members (grandparents, aunts) who provide care for her.

      3 years ago Log in to Reply
    21. Jeff Balbirnie

      Readings every 5 minutes =12x/hour, = 288/day =2016/week. MY QUESTION, what the blazes does ANYBODY or can any normal human being DO with that much freaking raw BG data ?!?! Even pretending it was veinous, that’s obscene amount of information. How do you use THAT much information without drowning in it, or becoming OCD hyper vigilant because of it?

      3 years ago Log in to Reply

    If you use a CGM and share your real-time glucose levels with other people using an app (e.g., Dexcom Share, Carelink Connect, Nightscout, etc.), with whom have you shared your live CGM data? Select all that apply! Cancel reply

    You must be logged in to post a comment.




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