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    • 12 hours, 25 minutes ago
      KarenM6 likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
    • 14 hours, 12 minutes ago
      Kristi Warmecke likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      Well, since I'm waiting on pump supplies for 2 months now, my confidence is slipping.
    • 14 hours, 13 minutes ago
      Laurie B likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I've often said that "hoarding": is a character asset for T1D people. I try to purchase (paying out of pocket) a 60-90 day supply - just in case). I have a new health plan,. effective 1/1/26. AS we know, getting an appt with an HCP isn't easy. They have to be accepting new patients, they have to be in network etc. Once I knew what my new policy would be (nov 2025) I made an appt. The earliest appt I could get was in Sept 2026. Thank goodness for my stash of device supplies. I had to go to Urgent care to get an Rx for insulin (my old HMO plan "doesn't do bridge refills"). So yeah, I worry, and plan for hiccups in the supplies process.
    • 14 hours, 14 minutes ago
      Kristi Warmecke likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I answered slightly. I'm absolutely certain supplies and medication will be available. However, I'm doubtful they will be affordable. If I can't afford them, I can't access them.
    • 15 hours, 12 minutes ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I am confident about access to my medical needs in the immediate future. I am not a fortune teller and have no idea what my access to medical supplies will be like in a year or longer. I don't take my spoiled lifestyle for granted.
    • 15 hours, 12 minutes ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I've often said that "hoarding": is a character asset for T1D people. I try to purchase (paying out of pocket) a 60-90 day supply - just in case). I have a new health plan,. effective 1/1/26. AS we know, getting an appt with an HCP isn't easy. They have to be accepting new patients, they have to be in network etc. Once I knew what my new policy would be (nov 2025) I made an appt. The earliest appt I could get was in Sept 2026. Thank goodness for my stash of device supplies. I had to go to Urgent care to get an Rx for insulin (my old HMO plan "doesn't do bridge refills"). So yeah, I worry, and plan for hiccups in the supplies process.
    • 15 hours, 13 minutes ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I answered slightly. I'm absolutely certain supplies and medication will be available. However, I'm doubtful they will be affordable. If I can't afford them, I can't access them.
    • 15 hours, 16 minutes ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I am worried about the changes to Medicare making no provision for getting an immediate replacement if a pump fails. It sounds like we will have to get these from the suppliers instead of a warranty replacement from Tandem themselves (or whatever brand you use). Pumps will be rented and will have to be returned so they can verify the problem before replacing them, which is ridiculous. Meanwhile, Medicare would not pay for us to get long acting insulin as a temporary replacement for the basal.
    • 15 hours, 19 minutes ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I broke down for the first time in 25 years and bought a bottle of insulin because I think I may have thrown a bottle out with the box. Medicare wouldn’t fill the prescription because it was too early. I just didn’t want the fight and worry. I’m not sure that’s what happened but it’s the only explanation. Also, I live in Florida and the threat of losing power is always there. I should get a generator but I’m a little afraid of them and you still can’t be sure you have access to propane. If my insulin goes bad, I’m not sure I could get refills. My back up plan is to leave before hurricane or go to a hospital. But it is all just causes concern.
    • 15 hours, 32 minutes ago
      Derek West likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Very! However, I wish I could use Fiasp insulin in the Tandem pumps.
    • 18 hours, 7 minutes ago
      Bruce Schnitzler likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I broke down for the first time in 25 years and bought a bottle of insulin because I think I may have thrown a bottle out with the box. Medicare wouldn’t fill the prescription because it was too early. I just didn’t want the fight and worry. I’m not sure that’s what happened but it’s the only explanation. Also, I live in Florida and the threat of losing power is always there. I should get a generator but I’m a little afraid of them and you still can’t be sure you have access to propane. If my insulin goes bad, I’m not sure I could get refills. My back up plan is to leave before hurricane or go to a hospital. But it is all just causes concern.
    • 18 hours, 39 minutes ago
      Karen Newe likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      The most common comment: but you aren’t heavy. That’s when we get into the differences. A relative tried to tell me that insulin makes you lose weight. But when we last discussed this, one of you said it best: if it isn’t in their circle of experience, why would they know or care?
    • 18 hours, 56 minutes ago
      KSannie likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Very! However, I wish I could use Fiasp insulin in the Tandem pumps.
    • 18 hours, 57 minutes ago
      KSannie likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
    • 18 hours, 58 minutes ago
      KSannie likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      My first reaction was Very Satisfied but there is always room for improvement. I’d like a pump design that wasn’t meant to be worn on a belt just for men. To wear a dress, I have to only get those with pockets (and on both sides because opposite sides cause the CGM to lose contact) and put a button whole in each. The clip shows horribly on blouses worn out. I’ve tried the leg attachments and they never stay secure. I’m not big enough to wear it in my bra. All minor inconveniences. I’d like one that doesn’t keep alarming 20 minutes after I’ve eaten, although I get it that it is there to save my life. Again minor. Ask about CGMs (probably tomorrow’s question): lately I’ve had trouble removing the sensor from my arm without actually ripping off a strip of skin or very bad bruising. I’ve read about using baby oil for removal. That does help. I’m a rip it off fast person, but that didn’t work so well.
    • 20 hours, 25 minutes ago
      Patricia Dalrymple likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Try Uni-Solve Adhesive Remover (smith&nephew)- wipe it on wait a minute to let it work and it will come off easy. at least it works great for me and I've tried several different brands, I use it for CGM & Omnipod removal
    • 1 day, 3 hours ago
      Sandy Norman likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
    • 1 day, 10 hours ago
      kristina blake likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      There are several conversations about this across social media. Many people chime in and vote for a new, more accurate name for type 1.. some of the popular alternatives- Pancreatic Autoimmune Disease, Beta Cell Destruction Disease, Autoimmune Diabetes, Autoimmune Insulin Failure, Autoimmune Absolute Insulin Deficiency (AAID)
    • 1 day, 10 hours ago
      kristina blake likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      The most common comment: but you aren’t heavy. That’s when we get into the differences. A relative tried to tell me that insulin makes you lose weight. But when we last discussed this, one of you said it best: if it isn’t in their circle of experience, why would they know or care?
    • 1 day, 10 hours ago
      kristina blake likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      In my experience the average person does not know the difference. It does not help that the commercials on TV just say diabetes and do not differentiate.
    • 1 day, 13 hours ago
      Kristi Warmecke likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
    • 1 day, 15 hours ago
      Lee Tincher likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      If I could get a CGM that is consistent and predictable I'd be very happy with the Twiist or the Tandem. The weak point with pumps used to be infusion sites, but now that we are relying on poor performing technology to support potentially great algorithms itis quite frustrating.
    • 1 day, 17 hours ago
      Beckett Nelson likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      My first reaction was Very Satisfied but there is always room for improvement. I’d like a pump design that wasn’t meant to be worn on a belt just for men. To wear a dress, I have to only get those with pockets (and on both sides because opposite sides cause the CGM to lose contact) and put a button whole in each. The clip shows horribly on blouses worn out. I’ve tried the leg attachments and they never stay secure. I’m not big enough to wear it in my bra. All minor inconveniences. I’d like one that doesn’t keep alarming 20 minutes after I’ve eaten, although I get it that it is there to save my life. Again minor. Ask about CGMs (probably tomorrow’s question): lately I’ve had trouble removing the sensor from my arm without actually ripping off a strip of skin or very bad bruising. I’ve read about using baby oil for removal. That does help. I’m a rip it off fast person, but that didn’t work so well.
    • 1 day, 18 hours ago
      John Barbuto likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      I have been using a insulin smart pen for the last 2 years; I find that it meets my current needs to ensure good management and results
    • 1 day, 19 hours ago
      Lawrence S. likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
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    For insulin pump/CGM users who wear dresses and skirts: How often do devices get in the way of your ability to comfortably wear dresses and skirts?

    Home > LC Polls > For insulin pump/CGM users who wear dresses and skirts: How often do devices get in the way of your ability to comfortably wear dresses and skirts?
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    Have you supported T1D Exchange through our Express Feedback for Good Campaign? This program allows people to create donations just by giving their opinions in 1 minute or less on brands and products. Learn more at bit.ly/t1dXEFG

    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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    26 Comments

    1. Sondra Mangan

      Omnipods make it easy to wear what I want.

      5 years ago Log in to Reply
    2. Tina Roberts

      Always. I don’t even buy or wear dresses and skirts any longer. Not since 2007.

      5 years ago Log in to Reply
    3. Kristine Warmecke

      I no longer wear dresses, due to my pump, a skirt is much more manageable. I attempted to continue to wear dresses when I first started on my very first pump in February 1997 but soon found it too much of a hassle. With a skirt I can clip it on the waist and have access to it.

      5 years ago Log in to Reply
    4. Annie Maley

      If I use a thigh band, I still have to pull up my dress or skirt to do anything with the pump. Not an ideal situation. I like to wear dresses and this is problem when there’s no place to put the pump with easy access. I have a Medtronic 670G.

      5 years ago Log in to Reply
    5. Sherolyn Newell

      That’s one of the things I thought about before getting a pump. Just one of the reasons I selected Omnipod.

      5 years ago Log in to Reply
    6. connie ker

      The Abbott Freestyle Libre is worn on the arm, so not a problem with dresses or skirts. The reader can read through long sleeve dresses, but this year there are no occassions to go to wearing a dress or skirt. The most popular women’s wear for 2020 was sweat clothes.

      5 years ago Log in to Reply
    7. Mig Vascos

      During the 10 years I’ve been on the pump I’ve only worn a dress once, to my son’s wedding. Spent months tryin to find an adequate outfit. I finally wore a dress and just had to go to the bathroom when I needed to bolus. The CGM was no problem since I read it on my phone app.

      5 years ago Log in to Reply
    8. Catherine Davis

      I try to find dresses and skirts with pockets — they are rare. Then I can cut a small hole in the back of the pocket for the tubing to go through. Mostly I don’t bother, just wear jeans.

      5 years ago Log in to Reply
    9. ConnieT1D62

      Sometimes. With a skirt I usually adapt and clip to waist band or an outside pocket. I do the same when wearing jeans, pants, or leggings. It’s a bit more cumbersome wearing a dress but I usually find a way to adapt by clipping pump on the inside or outside, or cutting a small hole for tubing in a pocket or side seam and hemming the edges so the fabric doesn’t unravel. It challenges one’s creativity to find practical, discrete & clever ways to wear a dress and a pump at the same time!

      5 years ago Log in to Reply
    10. Kim Detwiler

      I rarely wear dresses because of it. Nightgowns either. I pretty much always wear pants or shorts or pajamas so I can clip my pump into the waistband.

      5 years ago Log in to Reply
    11. Caitlin St. Jean

      Non-issue with Omnipod for a pump (I love my pods!)

      5 years ago Log in to Reply
    12. Maureen Helinski

      I had three children marry while on a pump and had to cut holes in each mother of the bride/groom dress so I could get to my pump. At those times I had the medtronic pump and enlite CGM and had to see the readings on the pump to know what my BG was. Otherwise I hung the pump from my bra strap and reached under blouse to do bolus etc. Now I am on the Tandem/Dexcom with Control IQ. So-so much easier. I also have an apple watch to see numbers.

      5 years ago Log in to Reply
    13. Germaine Sarda

      I wear skirts and dresses all the time and only buy them if they have pockets which means I have to shop online. I tried every other way to work it but pockets are the easiest way for me. I also only buy men’s PJ bottoms because they usually have pockets. It’s a hassle and I didn’t care for the Omnipod aside from its tubelessness.

      5 years ago Log in to Reply
    14. Patricia Dalrymple

      I have always said that pumps must be designed by men. I am thin and at 62 am pretty proud of my body shape and the bulges produced by the pump I feel are a necessary evil. I know this sounds vain, and believe me I am grateful for both insulin and pumps, but I’m hoping they will get thinner. I can wear skirts but don’t wear dresses unless they have pockets and do the hole thing. When I first started on the pump, my educator said just hide it in your bra. The only problem with that is she was about 4 sizes larger than me. 😀

      5 years ago Log in to Reply
    15. Sasha Wooldridge

      I avoid wearing skirts and dresses except for very special occasions because it’s such a pain to deal with pump/site placement. I have a hard enough time with pants.

      5 years ago Log in to Reply
    16. NAK Marshall

      I just don’t care anymore things can show or not. I’ve found locations that don’t get knocked off & don’t care if they show. I’m proud to be a 60 year type 1 & have the devices I never dreamed of as a kid !!!!!

      5 years ago Log in to Reply
    17. Angela Naccari

      I am on my 3rd week with Tandem. I expect to have difficulty when I do want to wear a dress or a skirt because it is hard enough to keep it on when wearing leggings. The pump pulls the waist down on me!

      5 years ago Log in to Reply
    18. Linda Murphy

      When I did wear dresses, I tried to avoid wearing them because of the access problem. Sometimes put in my bra, if tube was long enough. Skirts were easier.

      5 years ago Log in to Reply
    19. Janis Senungetuk

      Yes, even with the small Tandem pump finding a place to clip it on a dress is very much an issue.Now I very rarely wear dresses, prefer suits with jackets or wear nice slacks with pockets.

      5 years ago Log in to Reply
    20. ANN GALLUZZO

      I used to use a pocket on my leg under a skirt, but I no longer wear skirts as I get too cold even in the warmest weather, and I need to see the pump to see what my BG is. I have never used my bras, as it shows under my clothes there. So I use pockets of shorts and slacks, and that is it. The pump is very accessible that way, and does not show, since I use a tSlim. The Dexcom shows under my sleeves, though, unfortunately. I would never use an Omnipod because it would look even worse than a Dexcom sensor.

      5 years ago Log in to Reply
    21. Molly Jones

      Skirts and dresses are the most comfortable clothing for me as long as I am wearing long johns in the winter. I have learned to use the longest available tubing so that all insertion sites can be used with my clothing. Skirts are the easiest, but dresses usually work just as well. Belts can help. I just clip my pump at the top with the dresses without button fronts unless they have too high of a neck.

      5 years ago Log in to Reply
    22. Jana Foley

      I wear both dresses and skirts weekly and never have a problem because I always keep my pump in bra.

      5 years ago Log in to Reply
    23. Chris Deutsch

      I have a couple of dresses that I like to wear, but that doesn’t make it easy. You have to jerry-rig the dress – either sew o new pocket into a side-seam or cut o hole into a pocket inside the dress. I haven’t yet figured out how to conceal the hole I accidentally snipped in the patch pocket I was amending….drat. From this pump-wearers POV, making a dress or pants without pockets is HEARTLESS.

      5 years ago Log in to Reply
    24. Janice B

      I have had pockets added to dresses and skirts, and holes for the tubing. My bra is convenient with a dress until you need to pull the pump our to bolus then not so much. I have tried to wear thigh length spanx to hold the pump but that is not comfortable – so the struggle continues.

      5 years ago Log in to Reply
    25. Robby Doyle

      I highly recommend using Spanx or similar, (panties with midzethigh shorts). I run my pump tubing down to the thigh area where I can simply reach under my skirt or dress to access. I’ve also used in between my breasts, which also works well if you’re not wearing a low-cut top.

      5 years ago Log in to Reply
    26. T1D5/1971

      Since starting with pump/CGM 16 years ago, my wardrobe has changed to include mostly pants – as I wear my device(s) on the waistband. Skirts are easier than dresses for that same reason. It can be hard to find a dress with pockets or a button front. I’ve tried the thigh and belly bands, but they just don’r cut it for me. As others have noted, access to the screen is critically important, so reaching up under a dress/skirt in public or while driving just isn’t OK – especially when an alarm demands attention.

      5 years ago Log in to Reply

    For insulin pump/CGM users who wear dresses and skirts: How often do devices get in the way of your ability to comfortably wear dresses and skirts? Cancel reply

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