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    • 1 hour, 8 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      I want a thumbs down icon!
    • 1 hour, 9 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      I seldom have any questions other than RX refill request which I submit through the patient portal. If I do have treatment questions, I typically do my own research, and if not satisfied with what I find out, I submit a question in the portal.
    • 1 hour, 9 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      When I come up with a question between visits, I usually just do some research.
    • 3 hours, 21 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      I keep my opened insulin in the refrigerator too. When traveling I use a FRIO evaporative pouch.
    • 3 hours, 22 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Sorry. Of course I store unopened in frig. Opened in my room as I use it up in 30 days
    • 3 hours, 23 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      No, I keep it in the oven! ;) Same answer as the last time they asked this ridiculous question!
    • 4 hours, 5 minutes ago
      Becky Hertz likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Unopened yes, and now even opened just in case. I am getting a new health [lan (thank goodness a much better one - with better doctors and hospitals in network!) so it's worth it. But I can't get any appt - even for a PCP until September. I've been occasionally buying out of pocket insulin, pump and CGM supplies (in my mind, hoarding is a character asset for T1D people). I need to have my enough stuff to see me through, Of course, I am hoping there''s an appt cancellation.
    • 5 hours, 28 minutes ago
      Bruce Schnitzler likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Unopened yes, and now even opened just in case. I am getting a new health [lan (thank goodness a much better one - with better doctors and hospitals in network!) so it's worth it. But I can't get any appt - even for a PCP until September. I've been occasionally buying out of pocket insulin, pump and CGM supplies (in my mind, hoarding is a character asset for T1D people). I need to have my enough stuff to see me through, Of course, I am hoping there''s an appt cancellation.
    • 7 hours, 25 minutes ago
      alex likes your comment at
      Here’s What You Need to Know About the Dexcom G7
      This article explains the Dexcom G7 features in a clear and easy way, especially for people new to continuous glucose monitoring. Very informative and helpful. Sportzfy TV Download
    • 22 hours, 48 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.
    • 22 hours, 50 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.
    • 22 hours, 51 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.
    • 22 hours, 52 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
    • 23 hours 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 ´ )⎠⎞
    • 1 day 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.
    • 1 day 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.
    • 1 day 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 ´ )⎠⎞
    • 1 day, 4 hours 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
    • 1 day, 6 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".
    • 1 day, 7 hours 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, 8 hours 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, 8 hours 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, 8 hours 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, 8 hours 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, 8 hours 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.
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    Do you approach strangers in public who have visible diabetes devices?

    Home > LC Polls > Do you approach strangers in public who have visible diabetes devices?
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    How much do you think your immediate family members know about T1D? Select all of the statements that you think are true for you.

    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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    27 Comments

    1. sweet charlie

      Yes… Because I hope by telling them that I have T1D from age 20 to 90 without any major problems, will help them on their outlook..

      18
      3 years ago Log in to Reply
    2. kilupx

      I answered “other” because so have never seen a stranger in public using diabetes devices. Perhaps some people around me have had devices and I just haven’t noticed.

      1
      3 years ago Log in to Reply
    3. Lawrence S.

      Yes, whenever possible. It’s rare to see someone’s diabetes devices because they are hidden in pockets and beneath their clothing. But, I am always eager to speak with other diabetics. I always tell them about the T1D Exchange website.

      3
      3 years ago Log in to Reply
    4. Robin Melen

      I think I would if I ever saw someone with a device. But I never have!

      2
      3 years ago Log in to Reply
    5. Liz Avery

      I answered no, but if I was having a low emergency, I might.

      1
      3 years ago Log in to Reply
    6. Nichole Pleisch

      I don’t usually approach people but I might point out my devices. People tend to approach me more

      3
      3 years ago Log in to Reply
    7. MARIE

      I said depends. Traveling, we approached an adult once who had the telltale plastic tubing from her pump sticking out of her pants pocket. She was very receptive. But we’ve seen kids with CGMs on the backs of their arms and we don’t say anything to kids.

      3 years ago Log in to Reply
    8. Ernie Richmann

      I often approach strangers with or without diabetes devices especially at the YMCA.

      2
      3 years ago Log in to Reply
    9. Jneticdiabetic

      I often do. Always nice to meet someone else with T1D. This past year I met a fellow Dexcom user while hiking in Zion, the Dad of a newly diagnosed boy at a kiddie birthday party, a man with an alarming Tandem on a garden walk who jokingly told me “is not you, it’s me” when I checked my own pump in response. Sometimes just a flash of the a nod or smile of recognition.
      #DiabetesInTheWild

      6
      3 years ago Log in to Reply
    10. Carole Ludwig

      I would but I have not had the opportunity. I live in a small town and there are not that many type 1’s

      1
      3 years ago Log in to Reply
    11. Linda Zottoli

      Like sweet charlie above, I figure my almost 68 years of diabetes is sometimes encouraging to people with newer diagnoses, and I’ve also become friends with people I’ve met.

      2
      3 years ago Log in to Reply
    12. KCR

      But several times people have approached me and I am happy to answer questions when the situation allows.

      3
      3 years ago Log in to Reply
    13. Sue Martin

      No, I haven’t seen any strangers with visible diabetes devices.

      3 years ago Log in to Reply
    14. cynthia jaworski

      My answer was “always.” However, I approach differently, depending onn the circumstances. Many times I simply point to my libre and nod.

      1
      3 years ago Log in to Reply
    15. George Lovelace

      I keep my Pump in a shirt Pocket and take it out to show with a Big Thumbs Up!

      1
      3 years ago Log in to Reply
    16. Mary Dexter

      I don’t. If someone approaches me, I try to be polite, but really it’s none of their business. I talk to strangers about other, less personal things: the weather, groceries (have you ever tried this and does it taste good, do you know where they keep…). Probably why so many keep their devices hidden.
      When I was 14,I wore a Milwaukee Brace. Strangers would come up to me wanting to know the details of the car accident and I just wanted to be as invisible as any adolescent, but my mother would walk away, leaving me to politely explain scoliosis. Yes, I’m deformed. We hide to avoid rude, ignorant, opinionated people.

      1
      3 years ago Log in to Reply
    17. Janis Senungetuk

      Definitely depends on the circumstance. If I notice a pump or CGM on someone in a grocery,
      farmers market or park I’ve approached and simply gestured to my pump and CGM, saying “me, too”. Sometimes there’s a positive response.

      3
      3 years ago Log in to Reply
    18. Wanacure

      If I see a stranger with something on their hip or wearing any device, I cannot assume it’s diabetes related. It might be a pacemaker, it might be a device using small electric shocks for pain, it could be a cellphone. Like Ernie I have no qualms talking to strangers.
      BTW I noticed a CGM on the arm of S. Epatha Merkerson on NBC TV’s Chicago Med where she plays chief administrator. In real life she was diagnosed as T2D in 2002. (Looper.com)

      3
      3 years ago Log in to Reply
    19. Jillmarie61

      I should of put sometimes, but most of the time it’s them approaching me.

      3 years ago Log in to Reply
    20. Jan Masty

      I never notice anyone wearing a pump or cgm. I have met other type 1’s because they have mentioned it during a conversation. Then I share my experience if appropriate.

      3 years ago Log in to Reply
    21. Bekki Weston

      Yes! Last year, I was in the zig-zag line at the airport, awaiting security check-in, and I spoke with a man in the next lane over, who had an Omnipod on his arm. Agree with others, that devices are often hidden, and we don’t even realize a fellow T1D is right beside us.

      1
      3 years ago Log in to Reply
    22. Cheryl Weaver

      Not if I don’t know them.

      3 years ago Log in to Reply
    23. Jen Farley

      Always good to understand how someone else thinks about and handles situation’s and always a moment to learn from another pumper. I am a lifelong learner and always willing to make a new friend.

      2
      3 years ago Log in to Reply
    24. LizB

      I have never noticed a device on anyone in public but if I did I might say something, depending on the situation.

      1
      3 years ago Log in to Reply
    25. Mike Plante

      I don’t because I’m an introvert, but I’m happy to talk with t1d strangers if they initiate it.

      2
      3 years ago Log in to Reply
    26. Bea Anderson

      Only if device is really noticeable!! Have had some great chats. And people have all different ways to achieve their goals!! Lots of questions. back and forth. I’m semi-private, but have had only good experiences.

      2
      3 years ago Log in to Reply
    27. Michael Andrews

      Is this annoying or not?

      3 years ago Log in to Reply

    Do you approach strangers in public who have visible diabetes devices? Cancel reply

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