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    • 10 hours, 4 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.
    • 10 hours, 4 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.
    • 10 hours, 4 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 - 👎
    • 15 hours, 52 minutes 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.
    • 15 hours, 52 minutes 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 - 👎
    • 16 hours, 51 minutes 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 - 👎
    • 17 hours, 2 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.
    • 17 hours, 11 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 - 👎
    • 17 hours, 30 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.
    • 17 hours, 33 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 - 👎
    • 17 hours, 46 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, 13 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, 13 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, 13 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, 14 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, 14 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, 15 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, 16 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, 16 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, 16 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, 16 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, 16 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, 16 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, 16 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, 16 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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    When your pump or CGM sites feel irritated or uncomfortable on your skin, do you change your site or wait for the session to be over?

    Home > LC Polls > When your pump or CGM sites feel irritated or uncomfortable on your skin, do you change your site or wait for the session to be over?
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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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    19 Comments

    1. Ernie Richmann

      I change the site if my readings or BG does not seem right.

      5 years ago Log in to Reply
    2. Megan L

      If it’s my pump site, I’ll go ahead and change it if it’s actually bothering me because that’s rare. If it’s my sensor, I’ll try to hold off until it’s time to change it.

      5 years ago Log in to Reply
    3. connie ker

      Since I have been wearing a transparent medical tape over the sensor, some time the irritation is from the tape. So I just cut that piece of tape off the irritation and put cortizone cream on the irritation. So far, so good.

      5 years ago Log in to Reply
    4. Annie Wall

      When I was on the pump, I’d change my site right away. On Dexcom I’ve only once had the problem and I did change the sensor once it was obvious that the pain wasn’t going away. When I removedf it, there was a lot of blood so I called Dexcom and, after explaining the situation, they sent me a replacement.

      5 years ago Log in to Reply
    5. Mike S

      Only if the pump/cgm seems to be malfunctioning. Otherwise I do my best to wait it out.

      5 years ago Log in to Reply
    6. Grey Gray

      Tapes don’t bother my skin the only discomfort I have ever felt was the sure t site needle hitting muscle. I will usually change to avoid an unexpected blockage

      5 years ago Log in to Reply
    7. Dennis Dacey

      OTHET. Each instance of “iteration ” poses unique characteristics and need a reason. After analysis, i decide best option

      5 years ago Log in to Reply
    8. Kristine Warmecke

      I try to wait it out on my CGM, I have had Medtronic ones fall out because of my allergy to the actual sensor. For a pump site I change it out as soon as I can.

      5 years ago Log in to Reply
    9. cynthia jaworski

      I use the libre, and it seems to have fewer problems. I have never had any discomfort.

      5 years ago Log in to Reply
    10. casey shane

      Hello hope everybody is well. Ive used a medtronic mini med paradigm 720 since 2010, new one in 2015 never had an issue with the adhesive or site with pump site changes. Just got a sexy dexy g6, first three sensors no problem, the last 2 from the same lot# burned the skin on my arms. (Looks like i have a million red dots in the shape of a dexcom, itches, burns, is sore it actually hurts to be honest from the glue/adhesive) will start using all kare skin barrier too see if that helps. Also just received my new tandem tslim (eligible for a new pump every 5 years) and have had no site issues.

      5 years ago Log in to Reply
    11. Glenda Schuessler

      I currently use the Dexcom G5; I’ve used it 2 – 3 years. I usually re-start the sensor at the end of session and wear it 2 – 3 weeks (7 day sensor session with G5), I have not experienced skin irritations from the CGM sites. Occasionally I have an irritation with infusion sites, I use the Medtronic silhouette infusion sets with an Accu-Chek Spirit combo pump. I am very thankful that I have not had skin irritations with either!

      5 years ago Log in to Reply
    12. KarenM6

      As my sites (CGM and pump) are almost always uncomfortable, I wait it out (unless the pump and site are malfunctioning). The itchiness and/or pain (like a bruise being constantly pushed on and more) have to be endured… my insurance would never pay for the replacement devices… and, I would soon lose more real estate on my body for places to place the devices.

      5 years ago Log in to Reply
    13. Becky Hertz

      My skin has never gotten irritated, my sites yes, but not the skin. Assuming your talking more of an adhesive issue here.

      5 years ago Log in to Reply
    14. pioneir

      I do my best to wait it out.

      5 years ago Log in to Reply
    15. Leona Hanson

      Never had a skin problem with meditronic infusion sets but I have had a couple of them hurt because I put them in the wrong spot and they hurt I try too wait it out but usually change them out

      5 years ago Log in to Reply
    16. Donna Condi

      I have only had irritation one time wearing an Omnipod on my upper hip. It was 95 degrees in Minnesota and walking around outside all day while on vacation. We left are friends and drove a while until I couldn’t take the pain and asked husband to pull over so I could take a look. It looked bad enough that I removed it and put a new one on my stomach. When we got home I did research and began using a barrier wipe before attaching anything to my body. No problems since!

      5 years ago Log in to Reply
    17. Maria T

      I am in the same position as KarenM6- my insurance does not allow me any freedom to get 1 extra sensor or POD, so I just bite my lip and endure. The Dexcom adhesive used to be great, but in the past year has become more irritating.

      5 years ago Log in to Reply
    18. Sally Numrich

      I use metal infusion sets, so once in awhile it hurts a little.I usually just ride it out. It usually settles in after awhile. A few times, it hurts a lot and I just change it out. Sometimes I can just pull it out and put it in somewhere else. The joys of metal infusion sets.

      5 years ago Log in to Reply
    19. Cheryl Seibert

      I wait it out unless it gets more painful. Many times, the site irritation is because of clothing or large boluses with meals. A change of clothes or getting up and walking/exercising seems to make the irritation go away the majority of the time.

      5 years ago Log in to Reply

    When your pump or CGM sites feel irritated or uncomfortable on your skin, do you change your site or wait for the session to be over? Cancel reply

    You must be logged in to post a comment.




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