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    • 4 hours, 12 minutes ago
      Laurie B likes your comment at
      How important is diabetes research to you?
      Diabetes research is why I'm still alive and healthy. Research is how we have CGMs and pumps that can modify doses based on CGM data. Current insulins are much better than previous versions, Even test strips are wildly more consistently accurate than when I was diagnosed in the 1990s. Personally the improvements to diabetes care made based on research have made a bigger impact on my life than medications and devices. Doctors were presented with evidence showing threatening patients leads to worse outcomes and doctors changed their behavior.
    • 6 hours, 51 minutes ago
      lis be likes your comment at
      How important is diabetes research to you?
      Due to age, etc, it probably won't benefit me personally but it's extremely important for the future! After all, isn't T1D going to be cured within 5 - 10 years? ;)
    • 7 hours, 9 minutes ago
      Phyllis Biederman likes your comment at
      In what ways has diabetes positively influenced your life?
      D.R.A.W. It’s a theme I’ve used in public speaking. D is for discipline; a concept some people have to join the army to learn. R is for reward. You must reward yourself for things well done. A is for awareness. Awareness of yourself and others keeps you alive. W is for wonderment. Believing or thinking about things bigger than yourself. ル˖ ♡ ₍ ᐢ..ᐢ ₎ 📍 ࣪ . >
    • 11 hours, 54 minutes ago
      Derek West likes your comment at
      How important is diabetes research to you?
      Strange question—all insulin development, medical devices — e.g. CGMS, pumps, etc are all research products. Would I rather go back to the starvation diet I was given and pills that didn’t work?
    • 11 hours, 54 minutes ago
      Derek West likes your comment at
      How important is diabetes research to you?
      Diabetes research is why I'm still alive and healthy. Research is how we have CGMs and pumps that can modify doses based on CGM data. Current insulins are much better than previous versions, Even test strips are wildly more consistently accurate than when I was diagnosed in the 1990s. Personally the improvements to diabetes care made based on research have made a bigger impact on my life than medications and devices. Doctors were presented with evidence showing threatening patients leads to worse outcomes and doctors changed their behavior.
    • 11 hours, 54 minutes ago
      Lawrence S. likes your comment at
      How important is diabetes research to you?
      Strange question—all insulin development, medical devices — e.g. CGMS, pumps, etc are all research products. Would I rather go back to the starvation diet I was given and pills that didn’t work?
    • 11 hours, 54 minutes ago
      Lawrence S. likes your comment at
      How important is diabetes research to you?
      I answered “very important,” but it very much depends on what the research is about. Genetic likelihood for family members? Not important for me. Possible stem cell treatment to regenerate a functioning pancreas? Extremely important. Possible connection between frequency of T1D low or high bg episodes and dementia? Extremely important! Impacts of different types of regular exercise on long term T1D management success? Very important. Etc.
    • 11 hours, 55 minutes ago
      Lawrence S. likes your comment at
      How important is diabetes research to you?
      All we are doing is treating the symptoms. We need a cure that doesn't require anti rejection inections.
    • 11 hours, 55 minutes ago
      Lawrence S. likes your comment at
      How important is diabetes research to you?
      Over the last 35 years, acure has been promised in 5 to 10 years. What is a real answer?
    • 14 hours, 59 minutes ago
      John Barbuto likes your comment at
      How important is diabetes research to you?
      Over the last 35 years, acure has been promised in 5 to 10 years. What is a real answer?
    • 14 hours, 59 minutes ago
      John Barbuto likes your comment at
      How important is diabetes research to you?
      Due to age, etc, it probably won't benefit me personally but it's extremely important for the future! After all, isn't T1D going to be cured within 5 - 10 years? ;)
    • 15 hours ago
      Patricia Dalrymple likes your comment at
      How important is diabetes research to you?
      It is important to me, not for me, but for the future
    • 15 hours, 17 minutes ago
      kristina blake likes your comment at
      How important is diabetes research to you?
      It is important to me, not for me, but for the future
    • 16 hours, 2 minutes ago
      Carol Meares likes your comment at
      What do you think is most important to your diabetes health? (Choose all that apply)
      The list is great. Medications need to be on the list too.
    • 16 hours, 27 minutes ago
      Kristi Warmecke likes your comment at
      How important is diabetes research to you?
      It is important to me, not for me, but for the future
    • 17 hours, 28 minutes ago
      Kathy Hanavan likes your comment at
      How important is diabetes research to you?
      I answered “very important,” but it very much depends on what the research is about. Genetic likelihood for family members? Not important for me. Possible stem cell treatment to regenerate a functioning pancreas? Extremely important. Possible connection between frequency of T1D low or high bg episodes and dementia? Extremely important! Impacts of different types of regular exercise on long term T1D management success? Very important. Etc.
    • 17 hours, 28 minutes ago
      Kathy Hanavan likes your comment at
      How important is diabetes research to you?
      Over the last 35 years, acure has been promised in 5 to 10 years. What is a real answer?
    • 1 day, 13 hours ago
      Lawrence S. likes your comment at
      What do you think is most important to your diabetes health? (Choose all that apply)
      I think access to healthcare - especially for those things we need to thrive (i.e. insulin, CGM's, pumps). I fear that things will go back to the pre-ACA days where people with pre-existing conditions can be refused coverage. Since the things we need (listed above) are Rx items and very expensive for paying out of pocket at retail prices, it will become close to impossible for us to live - not to mention thrive.
    • 1 day, 13 hours ago
      Lawrence S. likes your comment at
      What do you think is most important to your diabetes health? (Choose all that apply)
      Most all of the choices are important. My other health conditions/general health also affect my diabetes health.
    • 1 day, 14 hours ago
      Patricia Dalrymple likes your comment at
      What do you think is most important to your diabetes health? (Choose all that apply)
      In addition, to all the choices mentioned, Advocacy is important, given the fact that many in the healthcare field, think as we age, we have T2 Diabetes. This can be challenging when you are in a hospital as many don't understand what we have to do to maintain a reaonable BG, and many they lack knowledge of the devices we use to stay healthy.
    • 1 day, 14 hours ago
      Sarah Berry likes your comment at
      What do you think is most important to your diabetes health? (Choose all that apply)
      In addition, to all the choices mentioned, Advocacy is important, given the fact that many in the healthcare field, think as we age, we have T2 Diabetes. This can be challenging when you are in a hospital as many don't understand what we have to do to maintain a reaonable BG, and many they lack knowledge of the devices we use to stay healthy.
    • 1 day, 14 hours ago
      Sarah Berry likes your comment at
      What do you think is most important to your diabetes health? (Choose all that apply)
      Most all of the choices are important. My other health conditions/general health also affect my diabetes health.
    • 1 day, 14 hours ago
      Lozzy E likes your comment at
      What do you think is most important to your diabetes health? (Choose all that apply)
      Easiest way to stay in range is with physical activity. This is always true even before insulin was available. Tests and doctor appointments can cause mental stress. Physical activity does the opposite.
    • 1 day, 14 hours ago
      lis be likes your comment at
      What do you think is most important to your diabetes health? (Choose all that apply)
      I think access to healthcare - especially for those things we need to thrive (i.e. insulin, CGM's, pumps). I fear that things will go back to the pre-ACA days where people with pre-existing conditions can be refused coverage. Since the things we need (listed above) are Rx items and very expensive for paying out of pocket at retail prices, it will become close to impossible for us to live - not to mention thrive.
    • 1 day, 14 hours ago
      lis be likes your comment at
      What do you think is most important to your diabetes health? (Choose all that apply)
      In addition, to all the choices mentioned, Advocacy is important, given the fact that many in the healthcare field, think as we age, we have T2 Diabetes. This can be challenging when you are in a hospital as many don't understand what we have to do to maintain a reaonable BG, and many they lack knowledge of the devices we use to stay healthy.
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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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