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  • Activity
    • 6 hours, 59 minutes ago
      ConnieT1D62 likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I usually bolus for breakfast right at the time I start eating. But I prefer to bolus 15 minutes before. Better results. But I always forget.
    • 8 hours, 55 minutes ago
      KarenM6 likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I said 15-30, but it may have been more than 30. I wasn't watching the clock this morning. I just checked my pump bolus history. It was about 30 minutes. I need to bolus early in the morning because my blood sugars shoot up high after breakfast. Bolusing sooner seems to help keep my BG from going off the charts. But, if I bolus too soon, I have serious low BG's. It's all an art ... and luck.
    • 8 hours, 57 minutes ago
      KarenM6 likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I am able to pr bolus for Breakfast and dinner as I am at home. I never know when I am going to eat at work so bolus is at start of meal.
    • 11 hours, 48 minutes ago
      Mick Martin likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      Question is misleading until type of insulin is understood. I said 15 because I use Fiasp insulin.
    • 12 hours, 4 minutes ago
      Kris Sykes-David likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I said 15-30, but it may have been more than 30. I wasn't watching the clock this morning. I just checked my pump bolus history. It was about 30 minutes. I need to bolus early in the morning because my blood sugars shoot up high after breakfast. Bolusing sooner seems to help keep my BG from going off the charts. But, if I bolus too soon, I have serious low BG's. It's all an art ... and luck.
    • 13 hours, 1 minute ago
      Ernie Richmann likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I said 15-30, but it may have been more than 30. I wasn't watching the clock this morning. I just checked my pump bolus history. It was about 30 minutes. I need to bolus early in the morning because my blood sugars shoot up high after breakfast. Bolusing sooner seems to help keep my BG from going off the charts. But, if I bolus too soon, I have serious low BG's. It's all an art ... and luck.
    • 13 hours, 23 minutes ago
      Robin Melen likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      My most recent meal was breakfast and, during the work week, I am far better at bolusing ahead of time. The rest of my meals in the day though end up receiving the bolus as I start eating or part at the start and more later on (depending on what I am eating and whether I know how much I'll eat.)
    • 1 day, 8 hours ago
      KarenM6 likes your comment at
      Of the people in your life, who (if anyone) makes you feel judged or criticized for your T1D management (for example, what foods you eat, where or when you check your blood glucose, etc.)? Select all that apply to you.
      Insulin, meters, diabetic tech are not magic wands. Its usage does not guarantee only "positive" results. Negative events can and do occur, period. Non -D- typically (incorrectly) equate negative events as being total user failure, severe user errors. As diabetics we get blamed, despite having made zero mistakes on our part. We make seriously educated best guesses, despite that truth, we can and do fail anyway sometimes! Outsiders falsely need to believe inulin, our tech are complete-total cures, rather than tiny bandages at best. When confronted for using (sic. my) "drugs" in public, no matter how invisibly done... it is their self righteousness , poor assessment which is the issue. I gladly squash such insects...
    • 1 day, 13 hours ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      The more important question is 'how well does the clip work'. For me, the Medtronic clip worked very well, but the Tandem clip is quite ineffective and the pump falls off my belt during things like yard work or other bending movements.
    • 1 day, 13 hours ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      I answered never. I always use a clip -- I wear my t:slim x2 on my belt -- but not the Tandem clip. I use the black t:Holster Rotating Belt Clip. Very pleased.
    • 1 day, 13 hours ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      I am rough on pumps and use a Tandem X2 but dont use the Tandem clip/holster. I use a neoprene case and a pouch with a metal clip. Thenmetal clip is uncomfortable while I sleep. Looking for a different solution for wearing my pump at night.
    • 2 days, 9 hours ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I answered that nobody wants to be screened, but I was answering based on my immediate family. I did let my deceased type-1 diabetic cousin's 35 year old son know he can be tested for his likelihood of becoming type-1 diabetic. He said he may be tested as he was always curious if he had a chance.
    • 2 days, 9 hours ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I have T1, and when my oldest grandson got T1, the other 3 grandkids got screened. The grandson who's the brother of the one with T1, showed a strong possibility of being a future T1 diabetic. It sadly came true about a year later.
    • 2 days, 10 hours ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I have LADA, and the idea of screening has not come up, either by me or my adult children. I guess I need to present the opportunity to them so they can make the decision.
    • 2 days, 10 hours ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 2 days, 13 hours ago
      Samantha Walsh likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I was born in 1939 and had many childhood illnesses. Three different kinds of measles and tonsils removed before I was 5 years old, then mumps and chickenpox when I was 5. While recovering from the mumps and chickenpox, I began showing the symptoms of very high blood sugar. Three doctors examined me and they were not able to make a diagnosis. I had lost much weight, and I had stopped eating. I did not have an appetite. It was almost impossible for me to walk. A fourth doctor had my blood tested and he made the diagnosis. While receiving pork insulin I finally began to recover a few days after my sixth birthday. I did not have ant relatives with diabetes. I think the childhood diseases caused internal damage and that was the cause of my diabetes. At the present time there are still no type one diabetics among my relatives. I do not believe it is necessary for my children and grandchildren to be screened for T1D autoantibodies.
    • 3 days, 8 hours ago
      KarenM6 likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 3 days, 10 hours ago
      Katie Bennett likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 3 days, 11 hours ago
      Kate Kuhn likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 3 days, 11 hours ago
      Karen DeVeaux likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I was born in 1939 and had many childhood illnesses. Three different kinds of measles and tonsils removed before I was 5 years old, then mumps and chickenpox when I was 5. While recovering from the mumps and chickenpox, I began showing the symptoms of very high blood sugar. Three doctors examined me and they were not able to make a diagnosis. I had lost much weight, and I had stopped eating. I did not have an appetite. It was almost impossible for me to walk. A fourth doctor had my blood tested and he made the diagnosis. While receiving pork insulin I finally began to recover a few days after my sixth birthday. I did not have ant relatives with diabetes. I think the childhood diseases caused internal damage and that was the cause of my diabetes. At the present time there are still no type one diabetics among my relatives. I do not believe it is necessary for my children and grandchildren to be screened for T1D autoantibodies.
    • 3 days, 11 hours ago
      Kelly-Dayne likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 3 days, 12 hours ago
      William Bennett likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 3 days, 13 hours ago
      Jneticdiabetic likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I have led a team for the JDRF OneWalk annually since the late 1990's. We have been able to raise a lot of funds for JDRF...and I have enjoyed doing it. Good cause!
    • 3 days, 13 hours ago
      Lawrence S. likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      my siblings & parents are older (like me) and they've never expressed any interest in getting tested. my nieces and nephews have never said anything either
    • 4 days ago
      Karen Newe likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I participated in several ADA walks not long after being Dx with T1D. As Ahh Life points out large $ are rased, but where do they go? I stopped supporting ADA for that reason. I think JDF is much more open on where the funding goes.
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    Has a stranger ever approached you to talk about your visible diabetes device(s)?

    Home > LC Polls > Has a stranger ever approached you to talk about your visible diabetes device(s)?
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    Sarah Howard

    Sarah Howard (nee Tackett) has dedicated her career to supporting the T1D community 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 Manager of Marketing at T1D Exchange. Sarah and her husband live in NYC with their cat Gracie. In her spare time, she enjoys doing comedy, taking dance classes, visiting art museums, and exploring different neighborhoods in NYC.

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    38 Comments

    1. Wanacure

      Before anyone complains about question repetition, just remember that there are always new participants (hopefully) in QOTD at T1D.

      5
      2 weeks ago Log in to Reply
    2. Lawrence S.

      I always keep my insulin pump visible on my belt, which is around my waste. Very rarely does someone ask me about it. Usually, it’s a question about my phone, pager, tape recorder, etc. On approximately two or three occasions, I’ve been asked if it was an insulin pump. No matter what I am asked, I respond that it is an insulin pump. If the person knows it is a pump, I usually ask, “are you a diabetic also?”. I am happy to discuss details about what kind of pump I use, what kind of insulin, or any other related subject matter.
      But, I’ve noticed, even with other diabetics, that most people don’t care to discuss details. They just want to know what it is that is on my belt.

      2
      2 weeks ago Log in to Reply
    3. KIMBERELY SMITH

      No stranger I use one

      2 weeks ago Log in to Reply
    4. Carol Evans

      I often get asked about the CGM on my upper arm (when I’m wearing short sleeves or a tank top). Occasionally if I whip out my pump to bolus or turn off an alert, someone will ask about it. Almost always because they know someone who also has a pump. They usually ask me how I like it, and I tell them it’s better than five shots a day! (That’s my short elevator speech; otherwise I would have to say, “you got an hour or so to talk?” 😉)

      7
      2 weeks ago Log in to Reply
    5. stillarobyn

      No but I once complimented someone’s dexcom!

      2
      2 weeks ago Log in to Reply
    6. Tina Roberts

      Yes. A man in his 70’s approached me while I was shopping. He saw my sensor and asked how I was able and o keep it on because his always fell off too soon. I asked him if he used Amazon. He said yes so I showed him skintac on Amazon from my phone. He said oh great. Now I can wear my sensors! No one had told him about it. Very sad.

      5
      2 weeks ago Log in to Reply
    7. Annie Wall

      Sure and it’s usually when my sensor can be seen. People have always been very interested and I have had some good conversations.

      4
      2 weeks ago Log in to Reply
    8. Sondra Mangan

      Yes, lots of times—always positive interactions. Most recently in grocery checkout line, the Dad approached and asked if I would talk to his daughter—a darling 10-year old who whipped out her Omnipod 5 Controller to show me. We both are anxiously awaiting IOS FDA approval. She was happy to see somebody “just like her” — I’m 74!

      8
      2 weeks ago Log in to Reply
    9. Dennis Dacey

      Yes, several times – and years after persons mistaking a pump to be an outdated pager.
      Notable times were when I accompanied z neighbor to the hospital ER and the nurse noticed and we compared my t-Slim with her 630G. Another time the security agent at the airport asked me if I had spare time to step out of line and speak with her – her husband was considering pumps and she wanted my input, pros vs. cons.

      4
      2 weeks ago Log in to Reply
    10. Twinniepoo74

      Just yesterday lol I was talking about my omnipod and dexcom g7. She was a diabetic also who had omnipod dash and dexcom g6. I was very happy to talk to her. I never mind strangers asking better asking than staring.

      2
      2 weeks ago Log in to Reply
    11. Annie Simon

      Absolutely as my sensor is generally seen on my upper arm. What I do enjoy is meeting fellow diabetics as we identify ourselves from our sensors. Was recently in a cruise and another woman was wearing the exact same Freestyle Libre sensor and gave each other a high 5. This is the future of technology and making managing diabetes so much easier👍

      3
      2 weeks ago Log in to Reply
    12. Amanda Barras

      Yes, and I have also accosted others I spot in the wild myself. LOL

      2
      2 weeks ago Log in to Reply
    13. Kris Sykes-David

      I answered no, however, I have approached other T1D’s in the wild! One being my neighbor and now friend with LADA like me!

      2
      2 weeks ago Log in to Reply
    14. mlettinga

      All the time. I look at it as an opportunity to educate people about type 1 diabetes and difference from type 2

      3
      2 weeks ago Log in to Reply
    15. Ahh Life

      Ancient history, but in the late 1990’s while touring Buckingham Palace in an area with multiple “NO PHOTOGRAPHY” signs, I whipped out my Medtronic to bolus a bit.

      Female guard came unglued. She was ready to banish me from the kingdom for taking pictures. And even when provided an explanation, her eldritch manner did not allow for a smile. Must be a requirement of the job. 💂‍♀️

      4
      2 weeks ago Log in to Reply
      1. Mick Martin

        @Ahh Life, that ‘tickles’ me, sir. I’m from the UK and I KNOW how obstreperous SOME people can be over here. 😉

        2
        2 weeks ago Log in to Reply
    16. dgmarrero

      I sometimes get questions about my CGM when working out at the gym

      2
      2 weeks ago Log in to Reply
    17. Carrolyn Barloco

      I’m very eager to share with any other CGM buddies see around. Just to ask how it’s going and do they like their device!😃

      2
      2 weeks ago Log in to Reply
    18. Jim Andrews

      Got asked recently why I was still wearing a pager

      2
      2 weeks ago Log in to Reply
    19. Mick Martin

      Presumably, when you mention “visible diabetes device(s)” that could include ALL diabetes devices. If so, I was once approached by the landlord of a public house and requested to leave as someone had reported me ‘shooting up’.

      Fortunately, work colleagues that were with me immediately jumped to my defence, indicating that what I was ‘shooting up’ was insulin as we’d ordered food to eat-in.

      The landlord accepted this after I showed him indication that I am, in fact, a Type 1 diabetic.

      3
      2 weeks ago Log in to Reply
    20. Jane Cerullo

      Happens a lot and ends in a good conversation.

      2
      2 weeks ago Log in to Reply
    21. Janis Senungetuk

      Yes, while waiting in line at the grocery checkout was asked about my sensor on my upper arm. The person asking recognized it from the almost constant Dexcom TV commercials. They asked if it was worth the cost. I explained that it had made a tremendous difference over testing 10 times a day, especially since it paired with my pump.

      3
      2 weeks ago Log in to Reply
    22. TEH

      I have quite a few times. I have approached others wearing a pump or Dexcom 6 or 7. Most recently a young lady wearing an Omni pod.

      1
      2 weeks ago Log in to Reply
    23. Nicholas Argento

      Not as often now that they are so common. I started a pump in 1982 and CGM in 2006, few had them then, more questions.

      2 weeks ago Log in to Reply
    24. Jneticdiabetic

      Yes! I love meeting fellow T1Ds is the wild! Most recently in the seat next to me on a flight. The gal next to me noticed my pump in my pocket and showed me her pod. Had a nice chat. What odd luck that two T1D strangers are assigned seats next to each other. I should have bought a lottery ticket that day.

      3
      2 weeks ago Log in to Reply
    25. KarenM6

      It happens all the time and I am happy to chat with anyone who asks.
      Most recently, two women in line waiting to get onto a plane asked if I was type 2 and asked about my CGM. They were very nice.
      I explained I have had type 1 for nearly 52 years and just blabbered for a bit about diabetes in general… they started to seem slightly dazed, so I stopped… and, in any case, the line started to move again.

      1
      2 weeks ago Log in to Reply
    26. Karen Mielish-Clausell

      No, but I have spoken to people with devices and showed them mine

      1
      2 weeks ago Log in to Reply
    27. lis be

      I said yes, but never to have a conversation, it’s always more like a “Cool, I have one too” kind of moment. It’s a club!

      3
      2 weeks ago Log in to Reply
    28. kim bullock

      I have been asked if it is a pain pump, a pager. Asked whst that pink or purple tape on my arm is. I use over the counter tape to secure my cgm

      2 weeks ago Log in to Reply
    29. Steven Gill

      Just last week was asked about my “medic alert bracelet,” and our discussion veered to her being a newly diagnosed TYPE 2.

      2 weeks ago Log in to Reply
    30. KC

      They asked if it was a nicotine patch…ya know…to quit smoking. Man, if my patch is THAT big, I have a serious problem!

      1 week ago Log in to Reply
      1. KC

        Also, many people think my OG omnipod PDM is a BlackBerry hahaha they’re like “How are your text bubbles blue if THAT’s your phone?!” (Iphone’s text bubbles are blue).

        1 week ago Log in to Reply
    31. Brad Larson

      Rarely as my CGM sensor is hidden. Will go back on the pump in October, we’ll see. I do approach people with visible pumps or CGM sensors on their arms. It is like approaching a stranger with a dog- it is okay to ask about the dog, right? Once I say I am a T1D, all is well.

      1 week ago Log in to Reply
      1. Brad Larson

        One time, entering London by flight, the immigration official asked if that was a “pain pump.” Have never heard that term.

        1 week ago Log in to Reply
      2. AnitaS

        Sometimes people who need morphine for pain control have devises that give them the medication just as an insulin pump gives insulin. Hence the term “pain pump”.

        1 week ago Log in to Reply
    32. AnitaS

      I don’t believe anyone has that I can remember as most of the time, the devises can’t be seen. However once while on the beach while on vacation, someone saw me with a waterproof devise hanging from my neck which I used to put glucose tabs in if I ever needed them while out in the water. They asked me what I had in that necklace.

      1 week ago Log in to Reply
    33. PamK

      I love it when this happens!

      1 week ago Log in to Reply
    34. Fay Jacobsohn

      Usually kids!

      6 days ago Log in to Reply

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