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    • 6 hours, 15 minutes ago
      Kristi Warmecke likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      not for those of moderate income.
    • 6 hours, 16 minutes ago
      Kristi Warmecke likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I am hopeful- it may not be in my lifetime, but they have already made great strides in the research. The autoimmune response and need for immunosuppressants is still a pretty big sticking point.
    • 6 hours, 17 minutes ago
      Kristi Warmecke likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      But probably not in my lifetime.
    • 7 hours, 57 minutes ago
      dholl62@gmail.com likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I don't see how a cure will be possible without islet cells as they are what produce insulin. Using immunosuppressants or not is what will determine what the first "cure" will be like. If safe immunosuppresants are used, then it is actually a "functional cure". If they can infuse islet cells without needing immunosuppressants nor other meds, then I would call it a "cure".
    • 7 hours, 58 minutes ago
      dholl62@gmail.com likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I am hopeful- it may not be in my lifetime, but they have already made great strides in the research. The autoimmune response and need for immunosuppressants is still a pretty big sticking point.
    • 8 hours, 37 minutes ago
      Bruce Schnitzler likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I don't see how a cure will be possible without islet cells as they are what produce insulin. Using immunosuppressants or not is what will determine what the first "cure" will be like. If safe immunosuppresants are used, then it is actually a "functional cure". If they can infuse islet cells without needing immunosuppressants nor other meds, then I would call it a "cure".
    • 9 hours, 18 minutes ago
      Steve Rumble likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I think that a functional cure is the most viable scenario as far as a "cure" is concerned. It seems like the most progress is being made with islet cell therapies.
    • 9 hours, 26 minutes ago
      Natalie Daley likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I don't see how a cure will be possible without islet cells as they are what produce insulin. Using immunosuppressants or not is what will determine what the first "cure" will be like. If safe immunosuppresants are used, then it is actually a "functional cure". If they can infuse islet cells without needing immunosuppressants nor other meds, then I would call it a "cure".
    • 9 hours, 55 minutes ago
      Marty likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I am hopeful- it may not be in my lifetime, but they have already made great strides in the research. The autoimmune response and need for immunosuppressants is still a pretty big sticking point.
    • 9 hours, 55 minutes ago
      Marty likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      But probably not in my lifetime.
    • 10 hours, 5 minutes ago
      Kathy Hanavan likes your comment at
      If islet cell transplantation is proven safe and effective, how likely would you be to consider it a treatment option?
      Very likely provided immunosuppressants aren't required. Also younger people should receive the treatment first.
    • 10 hours, 6 minutes ago
      Kathy Hanavan likes your comment at
      If islet cell transplantation is proven safe and effective, how likely would you be to consider it a treatment option?
      as long as it doesn't require immunosuppression, I'm interested
    • 10 hours, 6 minutes ago
      Kathy Hanavan likes your comment at
      If islet cell transplantation is proven safe and effective, how likely would you be to consider it a treatment option?
      I was going to comment that there's always a trade off. Am I trading insulin replacement with some other daily treatment? If so, what's the difference? Is the new daily grind more harmful than the old?
    • 10 hours, 7 minutes ago
      Kathy Hanavan likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I am hopeful- it may not be in my lifetime, but they have already made great strides in the research. The autoimmune response and need for immunosuppressants is still a pretty big sticking point.
    • 10 hours, 37 minutes ago
      John Barbuto likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      But probably not in my lifetime.
    • 11 hours, 2 minutes ago
      KCR likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I am hopeful- it may not be in my lifetime, but they have already made great strides in the research. The autoimmune response and need for immunosuppressants is still a pretty big sticking point.
    • 11 hours, 3 minutes ago
      KCR likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I said, "Unsure." I do not have enough information to state an opinion.
    • 11 hours, 3 minutes ago
      KCR likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      But probably not in my lifetime.
    • 11 hours, 18 minutes ago
      Katrina Mundinger likes your comment at
      How willing would you be to take immunosuppressants if you were considering an islet cell transplant?
      Scylla and Charybdis being perhaps more apt.
    • 11 hours, 44 minutes ago
      TEH likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I think that a functional cure is the most viable scenario as far as a "cure" is concerned. It seems like the most progress is being made with islet cell therapies.
    • 14 hours, 26 minutes ago
      Ahh Life likes your comment at
      How willing would you be to take immunosuppressants if you were considering an islet cell transplant?
      After 70 years with T1d and some reduced kidney function and seeing my dad's poor recovery after a kidney transplant, I have no desire to be subjected to chemicals that would further accelerate the demise of my kidneys.
    • 1 day, 6 hours ago
      lis be likes your comment at
      How willing would you be to take immunosuppressants if you were considering an islet cell transplant?
      Nope, T1D is a manageable thing with today's technology. I'll keep the devil I know.
    • 1 day, 6 hours ago
      dako likes your comment at
      How easy is it for you to find research opportunities that feel relevant to you?
      Agreed, and there are plenty of issues aging with T1D.
    • 1 day, 12 hours ago
      eherban1 likes your comment at
      If islet cell transplantation is proven safe and effective, how likely would you be to consider it a treatment option?
      All depends on if anti rejection and immunosuppressive medications are needed. If so I would not be interested.
    • 1 day, 12 hours ago
      eherban1 likes your comment at
      If islet cell transplantation is proven safe and effective, how likely would you be to consider it a treatment option?
      Very likely provided immunosuppressants aren't required. Also younger people should receive the treatment first.
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    If you use a CGM and share your CGM data with any of your loved ones through an app, for which types of CGM alerts does your network receive notifications? Select all that apply!

    Home > LC Polls > If you use a CGM and share your CGM data with any of your loved ones through an app, for which types of CGM alerts does your network receive notifications? Select all that apply!
    Previous

    Diabetes mellitus includes several types beyond type 1: there's type 2 diabetes mellitus, gestational diabetes mellitus, latent-autoimmune - and even more! Has anyone in your family been diagnosed with a type of diabetes mellitus other than type 1? Please select all that apply.

    Next

    Do you have different basal insulin rates for nights than for days?

    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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    15 Comments

    1. Mark Schweim

      I share my data on Sugarmate web app, it’s bookmarked on Mom’s computer, but the only time it shows on her computer is if I go down and load it onto her browser, but even when able to be monitored on her computer, the only times Mom has ever looked at the readings have been times when I’ve loaded it on her computer and left the Sugarmate page showing on her browser. But instead of using the data she can see, she usually just closes the tab after I leave the computer so it ends up wasted effort to bother to have it on her computer.

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

      I have been doing this for a long time, of course I share my low alerts with my wife.

      3 years ago Log in to Reply
    3. Joan Fray

      My diabetes educator can look at my results, but she hasn’t ever called me. I don’t share with anyone. If I ever have a bad low where I need outside assistance or pass out, I’ll start sharing. Been doing this sixty plus years, hasn’t happened yet…..

      2
      3 years ago Log in to Reply
      1. wyndare3

        Congrats on not having a bad low over that period of time!

        4
        3 years ago Log in to Reply
    4. wyndare3

      I use LIbre 2 reader and cannot share alerts. Actually neither of us can get the Libre 2 app on our cell phones. Would switch to Libre 3 and replace phones but Medicare doesn’t cover the Libre 3 sensor(claimed to be more accurate) at this time.

      3 years ago Log in to Reply
    5. Jen Farley

      My husband also receives rapid rise and rapid drop. I will sometimes get a text asking if I am ok. If I do not answer he will text one of my daughters to check on me. Sometimes it is a lifesaver when it is two arrows down and was running at 110. Helps me get the quick glucose I need. Love the new technology.

      3 years ago Log in to Reply
    6. Jneticdiabetic

      Use Dexcom/Clarity app. My husband was getting low alarms, not since we recently updated Android phones the app doesn’t seem to work. ☹️

      3 years ago Log in to Reply
    7. Lawrence S.

      I do not share my CGM data through an app with my wife. She hears my alerts going off, and says, “how are you doing honey?”

      3
      3 years ago Log in to Reply
    8. Mig Vascos

      I recently began sharing my data with my son. The idea was more for him to understand how the ups and downs of diabetes work than for him to help me since he lives two hours away from me, plus the fact that he’s busy on meetings on a daily base, and turns off his phone at night, so not following the app all the time.
      From time to time he’s called to make sure I’m ok or to ask what’s going on that my graphs show big ups and downs.
      I’ve been on insulin for 50
      Years and I don’t think my children are concerned about me dying from a low.

      1
      3 years ago Log in to Reply
    9. Tod Herman

      I use a G6 but I put down only the two I use and share. I’ve turned off all the other ones that are just annoying. By habit, I check my levels constantly throughout the day when I am working or doing things that might cause me to drop.

      3 years ago Log in to Reply
    10. Patricia Kilwein

      I use a guardian 3 sensor with a minimed 770g from medtronic. App is still not working and I get a notification that app is not compatible with my android system. So waiting on Medtronic to resolve this issue. Hope it’s soon.

      3 years ago Log in to Reply
    11. Kevin McCue

      I used to share with family but quit when they complained about the nuisance karma disturbing their work/school/life. They may come a day when I do it again but it will be out necessity not curiosity

      1
      3 years ago Log in to Reply
    12. Molly Jones

      I mistakenly chose “other” as I didn’t read the “loved ones”. I share my CGM data with my husband, my neurologist and endo.
      I should have chosen both high and low alerts, as my husband is the only one who receives the high and low alerts in case I need immediate help.
      The other two receive the data to help me with my ongoing health and treatment. They are appreciated, but not loved ones.

      3 years ago Log in to Reply
    13. Ahh Life

      The guy sitting next to me at the monthly diabetic meeting pulled out his Medtronic 630G and said, “Hmm, 196.”

      I then pulled out my tSlim X2 and said, “See you two and raise you two.”

      The room erupted in laughter. Guess they thought we were playing poker. 😵

      2
      3 years ago Log in to Reply
    14. Kristen Clifford

      I need to get CareLink set up on my husband’s phone.

      3 years ago Log in to Reply

    If you use a CGM and share your CGM data with any of your loved ones through an app, for which types of CGM alerts does your network receive notifications? Select all that apply! Cancel reply

    You must be logged in to post a comment.




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