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    • 1 hour, 2 minutes ago
      alex likes your comment at
      Here’s What You Need to Know About the Dexcom G7
      This article explains the Dexcom G7 features in a clear and easy way, especially for people new to continuous glucose monitoring. Very informative and helpful. Sportzfy TV Download
    • 16 hours, 25 minutes ago
      KarenM6 likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      Long time ago - told there were certain occupations I would not be allowed to do because if T1D. Pilot, air traffic controller, military, etc.
    • 16 hours, 27 minutes ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I have been told many times "YOU CAN'T EAT THAT!" ONLY to frustrate them and eat it anyway and then bolus accordingly.
    • 16 hours, 28 minutes ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I think it is a common experience for most people with T1D. People do not understand anything about it. I do not take it personally. I try to educate when appropriate.
    • 16 hours, 29 minutes ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Lol hell when haven't they. Lol
    • 16 hours, 37 minutes ago
      KarenM6 likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 18 hours, 29 minutes ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was only 2 when Diagnosed 70 years ago. My small town doctor admitted he didn't know much about T1D, and fortune for my parents and I he called what is now Joslin Clinic, and they told him how much insulin to give me. He taught my parents, who then traveled over 350 miles to Boston, to learn about how to manage T1D. My doctor learned more about T1D, and was able to help 2 other young men, that were later DX with T1D in our small town. I went to Joslin until I turned 18 and returned to become a Joslin Medalist and participated in the research study, 20 years ago. Still go there for some care.
    • 18 hours, 30 minutes ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was 7 when things changed in my home. My older brother was hospitalized for 2 weeks. When he came home, we no longer ate the way we had before. This was 1956. Dessert alternated between sugarless pudding or sugarless Jello. I learned that bread and potatoes had carbohydrates and that turned to sugar. There was a jar in the bathroom. It seemed my brother was testing his urine every time he went in there. There was a burner and pot on the stove designated for boiling syringes. I watched my brother give himself shots and I remember how hard it was to find someone to manage his care if my parents had to travel. Diabetic Forecast magazine came in the mail each month and there were meetings of the local diabetes association that my mother attended religiously. My brother got a kidney and pancreas transplant at age 60 and before he died lived for 5 years as a non-diabetic. A few years later I was diagnosed. Sorry he was not able to make use of today’s technology. I often wonder what he and my late parents would think about me, at age 66, being the only one in the family with type 1.
    • 18 hours, 32 minutes ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 22 hours, 33 minutes ago
      kilupx likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      My brother was type 1 since an early age. I was only diagnosed in my late 40s
    • 1 day ago
      Phyllis Biederman likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Absolutely nothing. Diagnosed in late December 1962 at at the age of 8 years and was told I was going for a stay in hospital because I have "sugar diabetes".
    • 1 day, 1 hour ago
      Bill Williams likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day, 1 hour ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was diagnosed in 1976 at the age of 18 while in college. One weekend, I was drinking a lot of water and peeing frequently. I remembered having read a Reader's Digest article on diabetes, and I told my friends I thought I might have it. Two days later, the diagnosis was confirmed.
    • 1 day, 1 hour ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Absolutely nothing. Diagnosed in late December 1962 at at the age of 8 years and was told I was going for a stay in hospital because I have "sugar diabetes".
    • 1 day, 1 hour ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I knew I couldn’t or shouldn’t have my two fav things in the world: Pepsi cola and chocolate. I was 42, and suspected very strongly that I had it, and ate a large piece of chocolate cake before my doctor’s appointment (sounds more like I was 12). Fast forward 25 years later: I never had a real cola again, but do occasionally have chocolate. I’m way healthier than I was back then in terms of diet. I no longer have irritable bowel, and I’m lucky to be able to afford what I need to combat the ill effects of this chronic disease. I’m blessed, and grateful for insulin.
    • 1 day, 1 hour ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      It was 35 years ago for me. I had no experience with T1d. I was starting to show symptoms and my sister-in-law quickly researched T1d and told me what she found. I went to my GP a week or two later. My BG was over 600. He sent me to the hospital right away. Blood test confirmed it.
    • 1 day, 1 hour ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I only knew a little . That is why I give grace to others who do not know anything or have misconceptions.
    • 1 day, 1 hour ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day, 1 hour ago
      KCR likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I knew I couldn’t or shouldn’t have my two fav things in the world: Pepsi cola and chocolate. I was 42, and suspected very strongly that I had it, and ate a large piece of chocolate cake before my doctor’s appointment (sounds more like I was 12). Fast forward 25 years later: I never had a real cola again, but do occasionally have chocolate. I’m way healthier than I was back then in terms of diet. I no longer have irritable bowel, and I’m lucky to be able to afford what I need to combat the ill effects of this chronic disease. I’m blessed, and grateful for insulin.
    • 1 day, 2 hours ago
      Gary R. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day, 2 hours ago
      ConnieT1D62 likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day, 2 hours ago
      eherban1 likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day, 14 hours ago
      NANCY NECIA likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I think it is a common experience for most people with T1D. People do not understand anything about it. I do not take it personally. I try to educate when appropriate.
    • 1 day, 16 hours ago
      Anita Stokar likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I won't use the word "diabetic" as a noun. It's as simple as that, an adjective, yes. I didn't refer to a good friend with MS as a "sclerotic". When I was working with first responders, I tried to remember to say "schizophrenia is involved", or "there's alcoholism at play here".
    • 1 day, 16 hours ago
      Anita Stokar likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I think it is a common experience for most people with T1D. People do not understand anything about it. I do not take it personally. I try to educate when appropriate.
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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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