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    • 1 hour, 31 minutes ago
      Amy Schneider likes your comment at
      Do you store your unopened insulin in the refrigerator?
      I keep my opened insulin in the refrigerator too. When traveling I use a FRIO evaporative pouch.
    • 2 hours, 57 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      I want a thumbs down icon!
    • 2 hours, 57 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      I seldom have any questions other than RX refill request which I submit through the patient portal. If I do have treatment questions, I typically do my own research, and if not satisfied with what I find out, I submit a question in the portal.
    • 2 hours, 58 minutes ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      When I come up with a question between visits, I usually just do some research.
    • 5 hours, 10 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      I keep my opened insulin in the refrigerator too. When traveling I use a FRIO evaporative pouch.
    • 5 hours, 11 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Sorry. Of course I store unopened in frig. Opened in my room as I use it up in 30 days
    • 5 hours, 11 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      No, I keep it in the oven! ;) Same answer as the last time they asked this ridiculous question!
    • 5 hours, 54 minutes ago
      Becky Hertz likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Unopened yes, and now even opened just in case. I am getting a new health [lan (thank goodness a much better one - with better doctors and hospitals in network!) so it's worth it. But I can't get any appt - even for a PCP until September. I've been occasionally buying out of pocket insulin, pump and CGM supplies (in my mind, hoarding is a character asset for T1D people). I need to have my enough stuff to see me through, Of course, I am hoping there''s an appt cancellation.
    • 7 hours, 17 minutes ago
      Bruce Schnitzler likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Unopened yes, and now even opened just in case. I am getting a new health [lan (thank goodness a much better one - with better doctors and hospitals in network!) so it's worth it. But I can't get any appt - even for a PCP until September. I've been occasionally buying out of pocket insulin, pump and CGM supplies (in my mind, hoarding is a character asset for T1D people). I need to have my enough stuff to see me through, Of course, I am hoping there''s an appt cancellation.
    • 9 hours, 14 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
    • 1 day 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.
    • 1 day 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.
    • 1 day 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.
    • 1 day 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
    • 1 day 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 ´ )⎠⎞
    • 1 day, 2 hours 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.
    • 1 day, 2 hours 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.
    • 1 day, 2 hours 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 ´ )⎠⎞
    • 1 day, 6 hours 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, 8 hours 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, 9 hours 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, 9 hours 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, 9 hours 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, 9 hours 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, 9 hours 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.
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    If you use an insulin pump or CGM, how does your summer wardrobe impact where you insert your pump or CGM? Select all that apply.

    Home > LC Polls > If you use an insulin pump or CGM, how does your summer wardrobe impact where you insert your pump or CGM? Select all that apply.
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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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    29 Comments

    1. Molly Jones

      I don’t have much body fat and have to use the same rotated sites no matter what I wear.

      3
      3 years ago Log in to Reply
      1. KCR

        Me, too!

        3 years ago Log in to Reply
    2. Larry Martin

      It’s a medical device that keeps me alive!! Why should I hide it???? By the way, I am not a 14yo girl from California. Stop with these stupid questions!

      3
      3 years ago Log in to Reply
    3. TEH

      When we go to the beach I just wear a sleeveless t-shirt, and not show my abdomen. (Nobody wants to see it anyway!)

      3 years ago Log in to Reply
    4. Kelly Wilhelm

      Biggest issue in summer is the sweat factor! If I use my abdomen, I have issues with the devices sticking well.

      3 years ago Log in to Reply
    5. Jane Cerullo

      Just moved from upper buttock to arm. Was getting a compression low every night. My abdomen never worked for me. Use my thighs for basal MDI and abdomen/hips for bolus. Loving freedom of being pumpless.

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

      I wear my devices where they work, regard of time of the year. I don’t try to hide any of my devices. I just need to wear a belt, so I have a place to clip my pump. I wear my CGM on my upper buttocks, because that’s where it works the best for me. I do not wear my cannula on my arm because I cannot reach that area to place it there. I keep rubbing the cannula off when it is on my legs. So, mostly, I wear my cannulas somewhere on my abdomen; sun, rain or snow.

      3
      3 years ago Log in to Reply
      1. AnitaS

        I find that my insulin absorption is best on my stomach.

        3 years ago Log in to Reply
    7. Steve Rosenthal

      For my cgm it does not really matter where I place my cgm. For my infusion set is a different story. Because of sweat I need to use other parts in my sides or to spray antiperspirant down before inserting the infusion set. Hope everyone has a safe July 4th.

      1
      3 years ago Log in to Reply
    8. Abigail Elias

      No impact on placement but more likely to use an over-tape if I’m anticipating prolonged hot and sweaty activity.

      3 years ago Log in to Reply
    9. Sue Martin

      I always wear my CGM on my upper abdomen, where I don’t get compression lows. My clothes hide it well. Summer in my lattitude means not wearing a coat.

      3 years ago Log in to Reply
    10. Patricia Dalrymple

      I’m with everybody else. These devices no matter how the insulin is delivered save our lives. That’s much more important than where we wear them. Having said that, I would love for a woman to design a pump for women. The Medtronic was clearly designed to be worn on a belt. Most women my age (64) wear over blouses so that hides a lot. But I can’t wear a dress unless it has pockets and I put holes in the pocket. But the pump weighs down the pocket. Good news is a lot of clothing now has a place for cell phones, so that gives us a cleaner line with less bumps when women wear them. But I’m mainly just grateful for insulin.

      1
      3 years ago Log in to Reply
      1. AnitaS

        I know there are clothing lines that make places to hold pumps while wearing a dress. Sorry I can’t remember the brand or lady who designed these dresses, but diabetes-connections.com recently had an interview with the lady. I very rarely wear dresses, but if I do, I generally wear my pump on my thigh (using an insulin belt made for thighs) and just discreetly give myself a bolus while seated at a table. I use Tandem2x so with the bolusing from my phone which should be out soon will make it that much easier to bolus

        1
        3 years ago Log in to Reply
      2. Patricia Dalrymple

        Anita,

        Thank you. Yes, I have a thigh holder but I am pretty tall and always felt I had to go to the bathroom to bolus which defeats the purpose of the pump. And I never felt very secure with the thigh holder. I will look into the clothing line, though. Thank you!!

        3 years ago Log in to Reply
    11. Natalie Daley

      Freestyle Libre 2 is only supposed to be placed in the back of the upper arm. Season is irrelevant. I called the company and they said that’s where research placed the sensors, so don’t change it if you want them to work. Sleeping on them hurts. I don’t care what they look like. They are better than jabbing my fingers 2-6 times a day.

      1
      3 years ago Log in to Reply
      1. AnitaS

        I switch wearing my cgm between my arm and my stomach. I seem to get more compression lows when I wear it on my arm than on my stomach even though I don’t normally sleep on my side which is where my compression lows come from when wearing it on my arm.

        3 years ago Log in to Reply
    12. cynthia jaworski

      Libre is only to be worn on the upper arm. So that is what I do. Much more attractive than all the tattoos I see these days.

      3 years ago Log in to Reply
    13. Steven Gill

      My pump and CGM on my abdomen, pretty much all the time.

      2
      3 years ago Log in to Reply
    14. Tina Roberts

      Other: nothing changes for me in the summer. I wear everything the same. Pump on abdomen, cgm on arm.

      3
      3 years ago Log in to Reply
    15. Karen Mason

      More affected by where to carry my pump and senser I need pockets all year long.

      1
      3 years ago Log in to Reply
    16. Becky Hertz

      My cgm goes on lower 1/3 off thighs, I routinely rotate sides between arms, back fat, buttocks, legs, occasionally stomach. Guess I got tired of reading the given answers and didn’t see “no impact on placement”

      3 years ago Log in to Reply
    17. Melinda Lipe

      Duh – my entire placement of sites is directed at getting the best adhesion, absorption, and keeping the things in. Appearance in summer clothes is very much secondary.

      5
      3 years ago Log in to Reply
    18. TomH

      The devices I use (Omni Dash/G5) have minimal impact and if they matter to others then I don’t need their opinions or involvement in my life. If I was younger, seeking friends and a mate, it would probably be of more concern, though I hope I’d realize if it made that much difference to a potential friend or mate that I they weren’t that much of a need in my life.

      3 years ago Log in to Reply
    19. GLORIA MILLER

      If I am flying I will put the Omnipod and Libre where it is easy to show security if I am asked. I have Global Entry so I am not asked very often what I have on my body. Also I have to remove the pump before the plane departs (or I get severe lows below 30) and then put it back on when we reach 35,000 feet so I need to be able to do that without much trouble.

      1
      3 years ago Log in to Reply
      1. ConnieT1D62

        Thank you for sharing such good practical points for air travel with a pump!

        1
        3 years ago Log in to Reply
    20. mbulzomi@optonline.net

      I’m not a Female/woman/girl/ opposite sex. (At least I know what a woman is contrary to the next Supreme Court Justice.) No big deal, I’ve worn my pump it in the same place for the last 39 years. On my belt.

      3 years ago Log in to Reply
    21. Bonnie Lundblom

      I now rotate my pump sites every 3-4 days using my outer thighs, inner thighs, buttocks, areas above my waist, and my upper chest. I know this may sound weird but after developing lipodystrophy on my abdomen, after years of abdominal MDI’s. I feel that this type of rotation may help prevent problems in other pump sites. I do occasionally use my abdomen maybe once every 6 weeks or so, my Dexcom CGM is always on my upper arms since that’s the only spot where I get accurate readings most of the time. I don’t change my device placement based on seasons!

      3 years ago Log in to Reply
    22. ConnieT1D62

      Not at all. I wear it all year round where I have pliable integumentary real estate w/o a build-up of scar tissue where (1) it will penetrate and deliver insulin, and (2) where it will stay in place w/o sweating the adhesive off – usually on my lower abdomen below the waist line, or outer upper thighs.

      3 years ago Log in to Reply
    23. Sherolyn Newell

      Like everyone else, I put them where they work.

      3 years ago Log in to Reply

    If you use an insulin pump or CGM, how does your summer wardrobe impact where you insert your pump or CGM? Select all that apply. Cancel reply

    You must be logged in to post a comment.




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