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    • 7 hours, 16 minutes ago
      KarenM6 likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      There are many concerns, one being if I'll still be alive if it's ever offered :)
    • 7 hours, 16 minutes ago
      KarenM6 likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      At 78 I don't think islet transplantation will affect my life course. Big pharma sees biological treatments as the path to ever higher profits, not constrained by patent terms the way drugs are. Most diabetics would be better served by an improved standard of care from the ADA and the medical community.
    • 8 hours, 32 minutes ago
      Lawrence S. likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      Very, but more worried about it even making to the FDA and approved there first.
    • 8 hours, 32 minutes ago
      Lawrence S. likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      There are many concerns, one being if I'll still be alive if it's ever offered :)
    • 8 hours, 32 minutes ago
      Lawrence S. likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      At 78 I don't think islet transplantation will affect my life course. Big pharma sees biological treatments as the path to ever higher profits, not constrained by patent terms the way drugs are. Most diabetics would be better served by an improved standard of care from the ADA and the medical community.
    • 8 hours, 33 minutes ago
      Lawrence S. likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      Severe case of hardening of the “oughteries” here. Ought we be concerned with cost, insurance, coverage, hail storms, earthquakes? ▄█▀█● Why are we not homeschooled to enjoy the progress being made?
    • 8 hours, 34 minutes ago
      Lawrence S. likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      While those items are very much a concern, there are other factors that are more concerning ie immunosuppressant.
    • 8 hours, 35 minutes ago
      Amanda Barras likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      If they can transplant them such that we do not need immunosuppresants, we'd be fine. Otherwise, those meds are just one more thing that could become in short supply. But at least we could go through scanners at the airports and travel without huge bags of supplies.
    • 8 hours, 35 minutes ago
      Amanda Barras likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      General access to islet transplants is still years away. FDA has to deem it safe. Though, I am excited about the possibility.
    • 8 hours, 36 minutes ago
      Amanda Barras likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      At 78 I don't think islet transplantation will affect my life course. Big pharma sees biological treatments as the path to ever higher profits, not constrained by patent terms the way drugs are. Most diabetics would be better served by an improved standard of care from the ADA and the medical community.
    • 10 hours, 37 minutes ago
      Patricia Dalrymple likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      If they can transplant them such that we do not need immunosuppresants, we'd be fine. Otherwise, those meds are just one more thing that could become in short supply. But at least we could go through scanners at the airports and travel without huge bags of supplies.
    • 11 hours, 15 minutes ago
      Gerald Oefelein likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      If they can transplant them such that we do not need immunosuppresants, we'd be fine. Otherwise, those meds are just one more thing that could become in short supply. But at least we could go through scanners at the airports and travel without huge bags of supplies.
    • 11 hours, 15 minutes ago
      Gerald Oefelein likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      While those items are very much a concern, there are other factors that are more concerning ie immunosuppressant.
    • 11 hours, 58 minutes ago
      Marty likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      much more concerned about my age (65) than anything else. 😉
    • 12 hours, 21 minutes ago
      dholl62@gmail.com likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      much more concerned about my age (65) than anything else. 😉
    • 12 hours, 44 minutes ago
      Steve Rumble likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      Severe case of hardening of the “oughteries” here. Ought we be concerned with cost, insurance, coverage, hail storms, earthquakes? ▄█▀█● Why are we not homeschooled to enjoy the progress being made?
    • 12 hours, 44 minutes ago
      Steve Rumble likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      While those items are very much a concern, there are other factors that are more concerning ie immunosuppressant.
    • 12 hours, 45 minutes ago
      atr likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      Severe case of hardening of the “oughteries” here. Ought we be concerned with cost, insurance, coverage, hail storms, earthquakes? ▄█▀█● Why are we not homeschooled to enjoy the progress being made?
    • 13 hours ago
      Sarah Berry likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      much more concerned about my age (65) than anything else. 😉
    • 14 hours, 1 minute ago
      Steve Rumble likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      Age 73 here. I'm in the same boat. I ogten am considered too old for consideration for "smaller" research projects. But - best of luck to them. I'll be rooting on the sidelines.
    • 14 hours, 1 minute ago
      Steve Rumble 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 - 👎
    • 1 day, 5 hours 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.
    • 1 day, 5 hours 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.
    • 1 day, 5 hours 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 - 👎
    • 1 day, 10 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.
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    If you wear a pump or sensor, how often do you put a site somewhere visible, such as on your arm or leg?

    Home > LC Polls > If you wear a pump or sensor, how often do you put a site somewhere visible, such as on your arm or leg?
    Previous

    Were you already connected to anyone with T1D before your/your loved one's diagnosis? If not, tell us in the comments how you first found others with T1D.

    Next

    Today is the start of National Diabetes Awareness Month! Based on your experience, what percentage of the general population do you think knows the difference between type 1 diabetes and type 2 diabetes?

    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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    23 Comments

    1. Anne Blayney

      I used to wear a Libre sensor, which was often visible (at least in warm weather). I now wear a Dexcom sensor and I get better results when it’s on my abdomen, so that’s less visible — but not because I’m trying to hide it. The pump sites are typically in covered areas because I want to avoid snagging the tubing!

      5 years ago Log in to Reply
    2. Mick Martin

      I used to wear a Freestyle Libre on one of my arms, which were visible, but now I’m using the Guardian Sensor 3 (MiniMed/Medtronic) I only occasionally use one of my thighs, which are generally not ‘visible’ unless you’re there to see me undress. 😉

      5 years ago Log in to Reply
    3. Sean Gallagher

      I don’t put insets or sensors anywhere to specifically hide them but since I put them on my waist, they are not visible. I did wear the sensor on my upper arm for a while and that was visible at times.

      5 years ago Log in to Reply
    4. Gene Maggard

      I guess I’m just vain but I don’t like anything related to my diabetes care visible. Whenever I get a new pair of pants or shorts, my wife puts a slit in the inside of the right pocket with a velcro closure so I can hide the pump there along with the tubing. I used to clip my pump on my belt but it always brought up questions whenever anyone saw it and I’d rather not advertise the fact that I’m diabetic. My Dexcom G6 is placed on my abdomen. I tried it on my upper leg a couple of times but either due to circulation issues or other factors it was not comfortable.

      5 years ago Log in to Reply
    5. Dorian Dowell

      Mine is mixed. I wear the Dexcom G6 Sensor on my arm. Infusion sets are on leg, abdomen, Glute (Somewhat of a rotation). I find the CGM sensor works fine on my arm. Abdomen is a little inconvenient – especially with summer perspiration! I have tried the infusion set on my arm before. However, can’t get the tubing in the right length anymore – either too short or way too long!

      5 years ago Log in to Reply
    6. kristina blake

      Of course it depends on the season, if it is summer, short sleeves and shorts, more will be seen. But I do use my thighs and my upper arms. I did have one woman at a wedding insist I was beautiful, and to wish me luck when my Dexcom sensor was on my upper arm. (I was a guest). I guess she had seen one of those ads for the patch for chemo symptoms (Neulasta?). Anyway, I use patches that I turn into little paintings (my best is doing a sugar skull painting and a copy of Munch’s “The Scream” with the sensor as the face). Anyway, since I have ink anyway, it is barely noticeable.

      5 years ago Log in to Reply
    7. Sherolyn Newell

      Dexcom told me to put the sensor on my abdomen, so the pump is usually on the back of my arms or on my leg. If it shows, it shows. Doesn’t bother me. One day when it was showing, a mom with a newly-diagnosed 4-year-old saw it and asked me if I would talk to him. So sometimes it works out well if it shows.

      5 years ago Log in to Reply
    8. Jana Foley

      I use my upper arms and my forearms for my sensors and my upper arms for my infusion sets on a regular rotation. If they are seen, it does not bother me. If someone asks a question, I answer it and go on about my day. You just never know when your answer can help someone.

      5 years ago Log in to Reply
    9. Ernie Richmann

      I wear the cgm on my abdomen. I have had a few sensors not work and when I call Dexcom, I am always asked where I was wearing the sensor. I got the idea they will not replace a sensor unless I follow the directions.

      5 years ago Log in to Reply
    10. George Lovelace

      I use abdomen and arm and Love Handle areas BUT usually have pump in a Shirt or pants pocket, sometimes with tubing exposed. After 56 years I have no modesty about my Dm.

      5 years ago Log in to Reply
    11. Candace Jackson

      Our 1 year old loves my pump & sensor so I do my best to hide both of them.

      5 years ago Log in to Reply
    12. Janis Senungetuk

      Both are always visible, that’s not an issue for me. I’ve found wearing the CGM on my upper arm the most comfortable location. The pump inset is on my abdomen with the pump clipped to my waistband or pants pocket. When I was using MDI and a meter I’d check my bg and inject in public. I’ve always tried to go ahead and do what I needed to do without making a big production out of it.

      5 years ago Log in to Reply
    13. Kimberly Starkey

      Both the pump infusion set and cgm are on my abdomen. Having clothing cover them adds some protection from being bumped or pulled out. My pump, however, is in a zippered, padded case that I sewed a hole in and slipped a carbiner through to hook to my beltloop. The pump and tubing are visible, but the pump won’t fall off as it occasionally did when I used a clip. I tuck the tubing into my pants to minimize it getting caught on things.

      5 years ago Log in to Reply
    14. Donald Cragun

      I insert infusion sets in my leg (usually covered by pants) and CGM sensors in my abdomen (usually covered by a shirt). I sometimes remove my shirt if it is hot. I sometimes remove my shirt and/or pants for medical exams. I don’t care who sees my infusion sets or CGM sensors as long as I’m not exposing private parts.

      5 years ago Log in to Reply
    15. Nancy Taylor

      I use Omnipod Dash pump (pods) with no tubing to deal with. A much more flexible option! I wear both CGM and Omnipod on my abdomen (opposite sides). Like another user mentioned, I have had a number of Dexcom G6 sensors fail. Dexcom has sent me replacements for every single sensor. They do always ask where you placed it but that has never affected the replacements. They have aslo included an extra sensor in each of my last two replacement shipments when I had to return 2 or 3 sensors at a time. If you do have Dexcom failures be sure to call them. They have always been very helpful to me.

      5 years ago Log in to Reply
    16. Ely Kozminsky

      Pump – belly Sensor – Arms

      5 years ago Log in to Reply
    17. Jennifer Wilson

      My arm is most comfortable but has the greatest risk of being accidentally hit or bumped off. In the extreme warm and cold months, I tend to not wear it exposed to protect it from the harsh sun or weather elements. Clothing over the pod does add another cushion of protection. I only really intentionally do not want it visible if I am dressed in evening or formal wear.

      5 years ago Log in to Reply
    18. Clare Fishman

      Since I use Omnipod my site options are limitless and I use them all. Generally my Dexcom is on the back of my arm. It is the most comfortable spot for long term use and I use each sensor for at least a couple of sessions.

      5 years ago Log in to Reply
    19. Steven Gill

      Wearing a pump folks see my tubing, which I often have to work hard to protect (pulled the insert loose before)..

      5 years ago Log in to Reply
    20. Lenora Ventura

      With my Dexcom, I use my arm 90% of the time. With my pump, never.

      5 years ago Log in to Reply
    21. Bonnie Lundblom

      I use my arms a lot for my Dexcom and it depends on sleeve length whether or not it shows. My insulin pump does have tubing but the insertion site doesn’t show.

      5 years ago Log in to Reply
    22. Leona Hanson

      I wear my pump set so everyone can see it but also wear it so no one can see it because of rotation of sites but when visible the kids love it because they know that there not alone that there is someone else who has diabetes isn’t it great

      5 years ago Log in to Reply
    23. Sally Numrich

      I use all areas equally. I rotate sites so arms and legs get used as much as hips, buttocks and upper/ lower stomach. All areas are possibilities for site locations.

      5 years ago Log in to Reply

    If you wear a pump or sensor, how often do you put a site somewhere visible, such as on your arm or leg? Cancel reply

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