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  • Activity
    • 14 hours, 49 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.
    • 16 hours, 45 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.
    • 16 hours, 47 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.
    • 19 hours, 38 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.
    • 19 hours, 54 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.
    • 20 hours, 51 minutes 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.
    • 21 hours, 12 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, 16 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, 21 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, 21 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, 21 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, 17 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, 17 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, 18 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, 18 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, 21 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, 16 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, 18 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, 18 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, 19 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, 19 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, 20 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, 21 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, 21 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, 8 hours 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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    If you use an insulin pump, does your T1D healthcare provider typically examine your pump sites during your appointments?

    Home > LC Polls > If you use an insulin pump, does your T1D healthcare provider typically examine your pump sites during your appointments?
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    How many times in the past 12 months did you have your A1c measured by a healthcare provider?

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    Over the past 12 months, how many of your appointments with your diabetes health care provider were virtual visits?

    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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    26 Comments

    1. Lawrence S.

      With video appointments, that becomes more difficult. However, I don’t remember my current T1D provider ever looking at my pump sites. I don’t even remember raising my shirt. My feet get looked at about once a year.

      1
      8 months ago Log in to Reply
    2. Beckett Nelson

      I said sometimes because virtual visits they don’t, but in person they do

      8 months ago Log in to Reply
    3. Kim Davis

      50% of my apts are Telehealth ones

      8 months ago Log in to Reply
    4. Janice B

      None of my physicians have ever examined my pump sites.

      1
      8 months ago Log in to Reply
    5. Mig Vascos

      I have not seeing my endocrinologist or nurse practitioner in person since the pandemic began. Everything is telehealth.

      8 months ago Log in to Reply
    6. Katrina Mundinger

      When I first started on the pump, my endo did look at my sites. Then after a couple years he would ask about them. A couple of years after that he stopped asking. I think he trusts me to tell him if anything is unusual. 🙂

      1
      8 months ago Log in to Reply
    7. terrih57@msn.com

      I said no but he could have looked as a general check of abdomen. He did not check my cgm sites. I guess he expects endo to take care of it ….

      8 months ago Log in to Reply
    8. Eva

      I said sometimes. On my visit my endo review my numbers – at before/after meal time, during exercise, rest and sleep. If my blood sugar goes up and my data shows that I changed sites often, then she inspects my sites. Otherwise no – she doesn’t check.

      8 months ago Log in to Reply
    9. Georgina Sokol

      Examine your pump sites?? What’s that.? I’ve had a pump for twenty years and not once has an endo done that and I go every three months. I think overall most endos don’t really know much about pump use or TID. At least that’s been my 58 year experience.

      1
      8 months ago Log in to Reply
    10. Jen Farley

      My endocrinologist knows I have been on a pump for a very long time. He knows I rotate spots so I am guessing that’s why he does not check.

      8 months ago Log in to Reply
    11. cynthia jaworski

      What are they looking for? I imagine the patient would be the first to know if there were a problem. and if there is a problem, what can you do about it? Doesn’t everyone change sites all the time? Or do pump users run out of good spots? (Seriously, I don’t know. I am MDI)

      8 months ago Log in to Reply
      1. AnitaS

        Pump users can run out of good spots, just like MDI users. I am imagining people who use MDI change their locations just as often as pump users. Some people change often and some never change.

        1
        8 months ago Log in to Reply
    12. Henry Renn

      She would if I had anything to show her. I don’t have site issues.

      8 months ago Log in to Reply
    13. Tod Herman

      I selected “no” but thinking back, one of the first times I met with my (then new) Endo she checked the various areas where I have used for MDIs and pump sites, checking for scar tissue buildup. We discussed the topic of moving sites around but after that time she no longer checks them again.

      8 months ago Log in to Reply
    14. LizB

      I’ve been pumping for 18 years and the only time my site was checked was at my first or second appointment with my new endo 2 years ago. That was because I was experiencing so many “insulin flow blocked” alarms on my pump. I was manually inserting angled sets for 16 years exclusively in my abdomen. H ethought my abdomen felt okay but I did switch to a 90 degree set with an inserter so I can now use so many more areas. No “insulin flow blocked alarms” for the past 2 years, and my abdomen is getting a much needed rest.

      8 months ago Log in to Reply
    15. AnitaS

      I had a diabetes educator look at my stomach once because I told him that I had lost some fat at a few infusion sites. He was surprised as he said that most people he has seen get fat accumulation at infusion sites.

      8 months ago Log in to Reply
    16. Marty

      I remember being asked to show my site to my endo once, ~20 years ago. I’m not sure what he was looking for, but he never asked again. My endo’s NP commented that someone should look at my sites during our last telehealth visit. I’ve never actually seen her in person, but she’ll probably want to look if we ever do meet. I don’t have any issues with infections or fat build up although I might have some scarring after all these years.

      8 months ago Log in to Reply
    17. Carol Meares

      Never in all the years.

      1
      8 months ago Log in to Reply
    18. Stephen Woodward

      When I asked my endo to review data he stated he could not. Following up with the “why” I found it was a limit by the Med Group he was a part of, IT.

      As a result of asking him again I received a letter refusing to continue as a patient.

      8 months ago Log in to Reply
    19. Kristine Warmecke

      Only when I have a question about one.

      2
      8 months ago Log in to Reply
    20. KarenM6

      No and I wish they would!!! I have really bad lipoatrophy and I’ve begun to have to really be pushy about getting them to help me with this.

      1
      8 months ago Log in to Reply
    21. Joan McGinnis

      I HAD A NEW ENDO THIS PAST YEAR AND HE ASKED TO SEE MY SITES AND ONE TIME SINCE THEN

      8 months ago Log in to Reply
    22. Jneticdiabetic

      I was in between “Yes, sometimes” and “No,” so selected “Other.” Rarely would be a better fit. I’d guesstimate my endo/RN have asked to see my pump sites maybe 5 times in my 22 years of pump use. I also haven’t complained about my sites. Probably just a don’t ask, don’t bother to look situation.

      1
      8 months ago Log in to Reply
    23. ConnieT1D62

      Sometimes. However she always asks if I am having any insertion site issues. If the answer is “yes” she checks and we have a problem solving discussion.

      8 months ago Log in to Reply
    24. Mike Plante

      Pre-covid I’d have said “always” but I can’t seem to get an in-person appointment since 2019

      7 months ago Log in to Reply
    25. James Cheairs

      They don’t check because I stay on top of it and have a system of about 26 sites that I rotate through.

      7 months ago Log in to Reply

    If you use an insulin pump, does your T1D healthcare provider typically examine your pump sites during your appointments? Cancel reply

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