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    • 14 hours, 51 minutes 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.
    • 14 hours, 53 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.
    • 14 hours, 54 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.
    • 14 hours, 54 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
    • 15 hours, 3 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 ´ )⎠⎞
    • 16 hours, 55 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.
    • 16 hours, 56 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.
    • 16 hours, 58 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 ´ )⎠⎞
    • 20 hours, 58 minutes 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
    • 23 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".
    • 23 hours, 46 minutes 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 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 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 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 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 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 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 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 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 ´ )⎠⎞
    • 1 day ago
      ConnieT1D62 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, 1 hour ago
      eherban1 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, 12 hours ago
      NANCY NECIA 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.
    • 1 day, 15 hours ago
      Anita Stokar likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I won't use the word "diabetic" as a noun. It's as simple as that, an adjective, yes. I didn't refer to a good friend with MS as a "sclerotic". When I was working with first responders, I tried to remember to say "schizophrenia is involved", or "there's alcoholism at play here".
    • 1 day, 15 hours ago
      Anita Stokar 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.
    • 1 day, 15 hours ago
      Anita Stokar likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      No one has said (in seriousness) you can't eat that, but I have gotten the question "Can you eat that?"
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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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    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.

      2 years ago Log in to Reply
    2. Gerald Oefelein

      I share with my diabetologist.

      2 years ago Log in to Reply
    3. Annie Wall

      Only my endocrinologist.

      2 years ago Log in to Reply
    4. KIMBERELY SMITH

      I share with my God son

      2 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
      2 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.

      2 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
      2 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
        2 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

      2 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
      2 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
        2 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
      2 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.

      2 years ago Log in to Reply
    12. Steve Rumble

      I share with my endocrinologist.

      2 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.

      2 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!

      2 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
      2 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
      2 years ago Log in to Reply
    17. Russell Buckbee

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

      2 years ago Log in to Reply
    18. Molly Jones

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

      2 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.

      2 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.

      2 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?

      2 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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