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    • 11 hours, 12 minutes ago
      Gerald Oefelein likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I've tried twice and was rejected both times because I control my diabetes as best I can. As others have already stated, if immunosuppressing drugs are involved, count me out. I'm not interested in something worse than what I already have.
    • 11 hours, 13 minutes ago
      Gerald Oefelein likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      Not if it requires immunosuppressant drugs. Been there done that time to move on to something much better.
    • 11 hours, 13 minutes ago
      Gerald Oefelein likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - 👍 immunosuppression needed - 👎
    • 17 hours ago
      Natalie Daley likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I answered “Very Unlikely” not because I woud not want to participate but because, at age 75, I think it very unlikely that any researcher would want me in their patient panel.
    • 17 hours ago
      Natalie Daley likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - 👍 immunosuppression needed - 👎
    • 18 hours ago
      Marthaeg likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - 👍 immunosuppression needed - 👎
    • 18 hours, 11 minutes ago
      kristina blake likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I answered “Very Unlikely” not because I woud not want to participate but because, at age 75, I think it very unlikely that any researcher would want me in their patient panel.
    • 18 hours, 20 minutes ago
      Mike S likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - 👍 immunosuppression needed - 👎
    • 18 hours, 39 minutes ago
      Eve Rabbiner likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I answered “Very Unlikely” not because I woud not want to participate but because, at age 75, I think it very unlikely that any researcher would want me in their patient panel.
    • 18 hours, 42 minutes ago
      Marty likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - 👍 immunosuppression needed - 👎
    • 18 hours, 54 minutes ago
      John Barbuto likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I answered “Very Unlikely” not because I woud not want to participate but because, at age 75, I think it very unlikely that any researcher would want me in their patient panel.
    • 1 day, 14 hours 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.
    • 1 day, 14 hours 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.
    • 1 day, 14 hours 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.
    • 1 day, 15 hours 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".
    • 1 day, 15 hours 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.
    • 1 day, 16 hours 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".
    • 1 day, 17 hours 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.
    • 1 day, 17 hours 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".
    • 1 day, 17 hours 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.
    • 1 day, 17 hours 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.
    • 1 day, 18 hours 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.
    • 1 day, 18 hours 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
    • 1 day, 18 hours 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?
    • 1 day, 18 hours 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.
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    If you use an insulin pump or CGM, has anyone ever mistaken your device(s) for any of the following? Select all that apply!

    Home > LC Polls > If you use an insulin pump or CGM, has anyone ever mistaken your device(s) for any of the following? Select all that apply!
    Previous

    Have you been diagnosed with any of the following diabetes complications? Please select all that apply to you.

    Next

    If you eat or drink products containing sugar alcohols (erythritol, xylitol, sorbitol, etc.), do you notice any digestive side-effects in the hours or days after consumption?

    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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    29 Comments

    1. Maggie Morgan

      I have a friend who always asks if I need to feed my tomagotchi whenever we eat together 🙂

      3
      3 years ago Log in to Reply
      1. Annie Wall

        🤣

        2
        3 years ago Log in to Reply
    2. kilupx

      My pump has never been mistaken for anything but that doesn’t mean people haven’t commented. So I checked Something Else. I often get asked “What is that?”

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

      G7 Device

      3 years ago Log in to Reply
    4. Virginia Barndollar

      When golf course GPS systems first came out, I was playing in a tournament and was accused of using a GPS system, my pump was on my waistband and had to explain to the officials that it was an insulin pump.

      3 years ago Log in to Reply
    5. S Hernandez

      New to T1D, most of my experiences have been kids asking “What’s that?!?”

      3 years ago Log in to Reply
    6. terrih57@msn.com

      Mistaken more when I first started wearing. I think people are more aware of them now!

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

      I had someone ask if my Dexcom was birth control

      3 years ago Log in to Reply
      1. Claire Potocki

        Same

        3 years ago Log in to Reply
    8. Robin Melen

      Just a few people have asked, one actually knew what it was – she had one too! Mostly I keep it hidden but I think people look scared when they do see it – like I’m a robot! LOL

      1
      3 years ago Log in to Reply
    9. cynthia jaworski

      Dental hygienist assured my cgm is a pump

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

      Phone, pager, tape recorder, camera.

      3 years ago Log in to Reply
    11. TEH

      TSA always asked me to take my cell phone off. Then when I told them it was an insulin pump I won bonus screening.

      1
      3 years ago Log in to Reply
    12. Ehamilton0722

      I’ve had my pump mistaken for a microphone, like the ones people wear on TV when being interviewed.

      3 years ago Log in to Reply
    13. kim bullock

      I have been asked if my cgm is a pain patch.

      3 years ago Log in to Reply
    14. Bob Durstenfeld

      I have a funny mistaken ID of my pump. I had a nuclear medicine test and I was mildly radio active a day later. I was chaperone for some middle school students to the White House and the Secret Service thought I was a walking nuke and my pump was the detonator. This was during the Clinton administration. I was strip searched at gun point.

      3 years ago Log in to Reply
      1. KarenM6

        =:o
        Oh my, Bob!
        That is one for the “You’d never think this could happen…” files.

        3 years ago Log in to Reply
    15. Brent Boyd

      Mine has been mistaken for a “secret camera”

      3 years ago Log in to Reply
    16. Sue Martin

      When I had a DexCom G3 someone thought the PDM was a cell phone. It was larger than the subsequent versions.

      3 years ago Log in to Reply
    17. lis be

      No one has mistaken it, but I have had several people recognize it and say they have a sister/ friend/ brother etc. with one!

      1
      3 years ago Log in to Reply
      1. KSannie

        Ditto

        3 years ago Log in to Reply
    18. KarenM6

      I’ve had most of the ones listed.
      I had the nicest child… about 7 years old… ask me what my pump was because I had to use it.
      I said that I had an illness called diabetes and that my pancreas didn’t work right, so it was to help it.
      She then asked, “what’s a pancreas?”
      It was quite the “oh yeah! non-diabetics (especially when they’re _7_) don’t usually know about these things” moment.
      So, we had a wonderful conversation about diabetes! I really enjoyed answering her questions.

      2
      3 years ago Log in to Reply
    19. McKenzie H

      I have had people think that my CGM is a tattoo

      3 years ago Log in to Reply
    20. JuJuB

      LOL! I am Jewishly observant, and was sitting in Yom Kippur services — a day of reflection an FASTING (which I partake in, thanks to my Tandem x2 and Dexcom G6) — when my pump alerted to a low bG, on vibrate. I took the pump out of my bra (where it was discretely tucked away) to silence the buzzing, and got a dirty look from the bitty sitting next to me, and then a sour “who brings their phone to yom kipper?”

      Sigh. I smiled sweetly and said, “It’s a medical device. I am sorry it interrupted your prayer.”

      (If you get it, you get it.)

      3 years ago Log in to Reply
    21. Steve Rumble

      I use my phone to communicate with my CGM, and my censors are typically covered by my clothing, so there’s nothing much to observe.

      3 years ago Log in to Reply
    22. PamK

      I had someone ask me once if my infusion set was birth control.

      3 years ago Log in to Reply
    23. Jeff Balbirnie

      The CAT thought the tubing was invisible STRING. Stalked it, pounced on it, and attacked the snot out of it in the middle of the night WHILE I was sleeping. Ripped it clean out [sic. hard] she thought it was a KITTY toy!!! Baaaaad kitty….

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

      We still have some who think Pagers/Beepers are still in use?

      3 years ago Log in to Reply
      1. KarenM6

        LOL! There may be some people who still use pagers… maybe? I wonder if doctors still do? Now I’m curious how ER doctors get notified that they need to help someone. I’m going to go do some googlin’!

        But, in my case, the beeper comments happened when beepers WERE still around!

        3 years ago Log in to Reply

    If you use an insulin pump or CGM, has anyone ever mistaken your device(s) for any of the following? Select all that apply! Cancel reply

    You must be logged in to post a comment.




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