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    • 16 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.
    • 1 hour, 42 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!
    • 1 hour, 42 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.
    • 1 hour, 43 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.
    • 3 hours, 55 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.
    • 3 hours, 56 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
    • 3 hours, 57 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!
    • 4 hours, 39 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.
    • 6 hours, 2 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.
    • 7 hours, 59 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
    • 23 hours, 22 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.
    • 23 hours, 24 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.
    • 23 hours, 25 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.
    • 23 hours, 26 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
    • 23 hours, 34 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 ´ )⎠⎞
    • 1 day, 1 hour 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, 1 hour 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, 1 hour 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, 5 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, 7 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, 8 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, 8 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, 8 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, 8 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, 8 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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    Have you ever altered your clothing to accommodate T1D devices?

    Home > LC Polls > Have you ever altered your clothing to accommodate T1D devices?
    Previous

    If you wear a device, how many times in the past month have you accidentally ripped out a sensor or pump site?

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    Which of these best describes how often you typically change your lancet?

    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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    34 Comments

    1. Patricia Dalrymple

      For a wedding, I wore a dress with pockets. I normally don’t wear dresses because of the pump but I deliberately wanted one with pockets to put a hole in the pocket so I could put my pump in it. It worked great.

      5 years ago Log in to Reply
    2. Bob Durstenfeld

      I like a pocket for my pump in my pajama top

      5 years ago Log in to Reply
    3. Janis Senungetuk

      I had an inside pocket added to a suit jacket to hold my pump.

      5 years ago Log in to Reply
    4. Ahh Life

      ❥ Starting on a pump in 1996, I put a small 1/4″ hole in every right pants pocket, since I invariably carried the pump in my right pocket. I suppose my clothes will be given to a thrift store after I die. Wonder what the recipients will think about each right pocket having the same hole in the same place in them? ❥

      5 years ago Log in to Reply
    5. Gene Maggard

      Every time I buy a new pair of pants, my wife slices the inside of the right pocket and sews on velcro. to enable it to be closed after I put my pump in. My night shirts are all pocket tees to accommodate the pump while I’m sleeping.

      5 years ago Log in to Reply
    6. joan Fray

      I stopped wearing dresses after I got the pump. Which is fine because now I only wear 👖. Warmer, easier, go with anything. Of course I wear tops too!

      5 years ago Log in to Reply
    7. connie ker

      I donated all of my sleeveless dresses and tops because of the Abbott Freestyle Libre sensors worn on the upper arms. I have seen Theresa May of England in a sleeveless top, and her Freestyle sensor showed on TV. So I know she is wearing one and I could identify with this lady. She probably is public with her takng of insulin too, and we need to get over being secretive with our condition and treatments.

      5 years ago Log in to Reply
    8. Beckie McCammitt

      I’ve cut small holes in the pockets of dresses/rompers for the tubing of my pump

      5 years ago Log in to Reply
    9. AimmcG

      I have altered little but I choose certain clothing to accommodate my insulting pump. I have to admit I have considered changing my pump to a pod due to the tubing issue and clothing with the pump but the continuous loop is not an option with the pod yet.

      5 years ago Log in to Reply
    10. Ernie Richmann

      No- alterations are beyond my pay grade. Just use the belt clip.

      5 years ago Log in to Reply
    11. Deb Souther

      I try to choose clothing with pockets. I will often cut a hole in the pocket to accommodate tubing. I sometimes sow a pocket in a bra or leggings to accommodate my pump.

      5 years ago Log in to Reply
    12. Annie Wall

      I answered “other”. When I was on the pump, I stopped wearing dresses. But a year and a half ago, I went off the pump (after 24 years, scarring prevented infusion sets from working properly) so I can wear anything now. I wear my Dexcom pretty much anywhere including my bare arms and have actually met others wearing CGMs and I’ve enjoyed that. I don’t mind being “public” with my T1D.

      5 years ago Log in to Reply
    13. Sherolyn Newell

      I have pods and I don’t care if they show, so my answer was no. Clothes were one of the reasons I chose the pods. I know you can strap the pumps to your leg for dresses, but then what? You lift up your dress to give a bolus? I didn’t care for that idea.

      5 years ago Log in to Reply
    14. Kathleen Amper

      I started my first pump in 1986 and they were so large that my grandmother sewed pockets in all my pants custom made for the pump.

      5 years ago Log in to Reply
    15. Clare Fishman

      I wear pods. Their tubeless design is one of the main reasons I chose them over a tubed pump. I use a DIY Loop which allows my iphone to collect my Dexcom readings and use a RileyLink to send instructions to my pod. It is pretty sweet. I have been Looping almost 2 years and have never experienced such ease of blood sugar management.

      5 years ago Log in to Reply
    16. Kelly Steiner

      My wedding dress! They added a pocket for my pump!

      5 years ago Log in to Reply
    17. Trina Blake

      For some dresses I simply wear lightweight men’s boxers underneath – nice waistband. I have also taken the side bands from worn out bras, cut them off the old bra and use them to make pockets in the sidebands of new bras. Easy access to the pump via my neckline. Of course most of the time, I wear pants so I use the clip.

      5 years ago Log in to Reply
    18. Kristine Warmecke

      Yes, I no longer wear one piece clothing like dresses, jumpsuits, etc. unless I have to. Then I have to have it altered so that it works for me & still lays correctly.

      5 years ago Log in to Reply
    19. Ceolmhor

      After the 30-lb weight loss that was one of the symptoms that caused me to self-diagnose as diabetic at age 72, I don’t have enough real estate around my waist to support a system of rotating sites for sensors and infusion sets (Medtronic). So I use my thighs for those placements, and I’ve had button-hole style openings made inside all my front pants pockets to allow the pump in my pocket to connect with the infusion set internally.

      5 years ago Log in to Reply
    20. Nicholas Argento

      No. Most men do not have to for a simple reason: pockets. I use a belt clip most of the time but pockets other times. I feel for women on this, because it is far more of a challenge, esp with more formal attire.

      5 years ago Log in to Reply
    21. Donald Stitt

      I have cut holes in pockets to run the infusion set through… sometimes I like to have my pump in my pocket without the line going out of my waistband….

      5 years ago Log in to Reply
    22. Thomas Brady

      Hated the pump line coming out of my pocket routed to the infusion site! I had a tailor put button hole style pockets in my suit pants so it did not show.

      5 years ago Log in to Reply
    23. Janice B

      I have had pockets added clothing and holes on pockets for tubing. I have had pouches made for bras for my pump. I have also added a slim clip attached directly to my pump so the pump sits closer to my clothing so the pump does not protrude as much.

      5 years ago Log in to Reply
    24. Carol Meares

      No but I buy clothing to accommodate my pump and supplies. All clothing must have pockets. Many times multiple pockets.

      5 years ago Log in to Reply
    25. Stacie G.

      Yes, I’ve cut slits into pockets so my pump can fit through and my inset line won’t be hanging out so much. It tends to get caught on door handles, cabinets and my purse if I don’t.

      5 years ago Log in to Reply
    26. Molly Jones

      Dresses now have to have buttons up the front or not have a high neck in order to be worn. This would be the only alteration in my clothing I can think of.

      5 years ago Log in to Reply
    27. Pat Reynolds

      Al the time! I make holes so that I can feed the cannula from apimp in a pocket Tomy flesh.

      5 years ago Log in to Reply
    28. Pat Reynolds

      A pump!

      5 years ago Log in to Reply
    29. Pat Reynolds

      To my!

      5 years ago Log in to Reply
    30. Nevin Bowman

      Every pair of pants has a hole in the top of the right pocket to run my pump tubing through.

      5 years ago Log in to Reply
    31. ConnieT1D62

      Occasionally. I mostly adapt and make due with whatever I choose to wear. I often just slip the pump into a pocket or clip it to the waistband of whatever I am wearing. T-slim has a pretty slim profile. If wearing a one piece dress sometimes I just stick it into my bra.

      5 years ago Log in to Reply
    32. Joanne Bohm

      Oh my gosh, I almost laughed at this question. Only because of the daily modifications I go through for all of my attachments. Not for looks but for convenience. Judging from the results of the answers, it is not that way for half of us. I have other T1 complications that also have attachments so I’m sure that adds to the ordeal.

      5 years ago Log in to Reply
    33. Anita Galliher

      When I was wearing a pump with tubing I would cut a hole in the pocket to run the tubing through. I even thought about starting a clothing line with a hole already there and call it something like “Hole In My Pocket.” Then I started wearing an Omnipod which is tubeless -YES!!! So in the winter I wear Jeanne Pierre sweaters that many times have 2 small pockets at the bottom of the sweater (I ONLY buy the ones with pockets) and in the summer I wear dresses and skorts and shorts with pockets. I need the pockets for my CGM and PDM. Oh how I’d love a cure!!! (57 years and counting)

      5 years ago Log in to Reply
    34. abir albazian

      Fitted dresses rly bother me with the pump on my waist so I try to use the thigh pump band but so far they slip. Let me say that while that’s annoying it’s nothing compared to how angry I get trying to wear a jumper. Nowhere for the tubing to come out! Unless I’m wearing my set on my arm but then the tubing is running down my body on the outside of my clothes which rly irritates me!

      5 years ago Log in to Reply

    Have you ever altered your clothing to accommodate T1D devices? Cancel reply

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