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    • 1 hour, 23 minutes ago
      Donna Owens likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Yes. It’s f*ing annoying.
    • 12 hours, 6 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.
    • 13 hours, 32 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!
    • 13 hours, 32 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.
    • 13 hours, 33 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.
    • 15 hours, 45 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.
    • 15 hours, 46 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
    • 15 hours, 46 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!
    • 16 hours, 29 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.
    • 17 hours, 52 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.
    • 19 hours, 49 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, 11 hours 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, 11 hours 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, 11 hours 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, 11 hours 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, 11 hours 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, 13 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, 13 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, 13 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, 17 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, 19 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, 20 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, 20 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, 20 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, 20 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.
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    For current or past insulin pump users: Have you ever changed your insulin delivery routine because of insulin absorption issues?

    Home > LC Polls > For current or past insulin pump users: Have you ever changed your insulin delivery routine because of insulin absorption issues?
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    If you could reach your health goals (e.g., A1c, time in range) equally well with any of these insulin delivery methods, which would you prefer to use?

    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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    35 Comments

    1. LizB

      For 16+ years I pretty much used my lower abdomen, manually inserting Silhouettes. In 2020-2021 I started having many alarms about insulin flow being blocked, no delivery. Last year I switched to Mio Advanced sets and I am able to reach all new areas I couldn’t before. I plan on giving my lower abdomen a good, long rest.

      1
      4 years ago Log in to Reply
    2. connie ker

      Insulin absorption issues can also happen to those of us doing the syringes and vials (MDI) too. It is important to change body spots and for me the best absorption is into the CORE.

      2
      4 years ago Log in to Reply
    3. Angela Naccari

      I answered that I changed to tru steel but a few more of the answers would have been correct. I wish there has been multiple choices. I have stopped using sites then went back to them and years ago I had to stop using a pump and used Afrezza because of poor absorption. Now using pump! 60 years TD2

      1
      4 years ago Log in to Reply
      1. AnitaS

        Unless I am misinterpreting your answer, there were multiple choices. I clicked on two of the choices.

        4 years ago Log in to Reply
    4. Annie Wall

      I took a two year pump vacation mainly due to infusion set site problems. I returned to pumping in June and am using TruSteel sets and that seems to make a big difference. It’s actually harder to vary sites as much as I’d like because your need extra space for the needle and for the second adhesive pad.

      1
      4 years ago Log in to Reply
    5. Louise Robinson

      Last June, I began having insulin absorption issues on Day 3 of my infusion site. (46 years w/Type 1 and pumping since 2011). I should have changed out my site early on Day 3 but, because I have been unable to obtain Medicare-approval for more frequent site changes, I am making my sites last the full 3 days and “supplementing” my insulin delivery on Day 3 with insulin injections via syringe. I have maintained good control by doing this with my A1c’s in the low 6’s. If I changed the sites early, I would run out of infusion sets and cartridges for my pump and have to resort back to MDI. Medicare allows 30 of each for a 90-day period. I did purchase out-of-pocket an extra box of each to prevent my running out. Even though I provided data about my glucose values on Day 3 and my syringe-delivered insulin on Day 3, my endo’s case notes of my office visits haven’t provided the info Medicare requires to approve site changes every 2.5 days vs every 3 days. I am in the process of changing endocrinologist and am more confident my new one will be able to navigate the Medicare requirements and get me what I need. So frustrating…all I’m trying to do is stay healthy.

      5
      4 years ago Log in to Reply
      1. KSannie

        The manufacturer recommends changing the Trusteel every 3 days, so Medicare has to approve that one for 2-day frequency of set changes. That solved my problems with high sugars on day 3. I am getting 45 sets every 90 days on Medicare.

        4 years ago Log in to Reply
    6. Chris Albright

      Beyond the choices that were provided, I have also changed infusion sets from a longer cannula (9mm) to (6mm) and visa versa.

      2
      4 years ago Log in to Reply
      1. Chris Albright

        In addition to my previous response, I have started to use the fatty area on my back (2-3 inches above belt line. I get really get good absorption from these areas since they have not been used prior. Little trickier to insert it but good spots for me

        4
        4 years ago Log in to Reply
      2. Jneticdiabetic

        Good reminder! Especially for those who have less padding or are noticing that they’re soft cannulas are bent at withdrawal.

        4 years ago Log in to Reply
    7. Hieromonk Alexis

      I do switch the site when absorption seems to be impaired, and that usually works. But it’s never a permanent change.

      4 years ago Log in to Reply
    8. Andrew Aronoff

      I’ve been a Type 1 for over 50 years. I’m currently on a 1 year pump vacation which will end in May. I’ll then resume use of my MiniMed 640G and the Quick-Set infusion sets. I’ve found that the biggest advantages of the pump are the ability to program different basal doses and use a square-wave bolus. FWIW, my A1C and time in range has not changed significantly since I went back to MDI (two shots per day of Levemir and Humalog before meals or snacks).

      4 years ago Log in to Reply
    9. Lawrence S.

      After years of rotating sites around the abdomen and butt, there are certain areas of my abdomen that just don’t allow insulin absorption. I’m also using my legs now. I cannot reach my arms to insert cannulas. I find that anywhere around the rib cage does not work, lower abdomen does not work, high up on my thigh does not work. I have lots of absorption issues on my legs. It seems that I’m running out of places to place my cannulas where I get decent absorption. I change sites early often.

      4 years ago Log in to Reply
    10. AnitaS

      I am always willing to tell people to give Tru-steel a try if they have issues with the soft cannulas. So many of my soft cannulas became bent with insertion which caused so many high blood glucose readings. Since starting the Tru-steel infusion sets a few months after starting to pump, I haven’t had those issues.

      1
      4 years ago Log in to Reply
    11. Sondra Mangan

      If I notice poor absorption, I will give a little more time for that spot in my Omnipod rotation.

      1
      4 years ago Log in to Reply
    12. Daniel Bestvater

      T1D ~ 45 years and have pumped for about 25 years. I use the steel needle canulas and find insulin absorption to be more consistent with them. I rotate all over my body and use different basal rates for different areas. I’m thin so to use some spots I gently bend the needle to ~ a 45 degree angle before insertion, this has worked well for me.

      4 years ago Log in to Reply
    13. George Lovelace

      23 yr Pumper started on Humalog then Mixed with Velosulin the Novolog and changed to Apidra. On Tandem so now with Novolog

      4 years ago Log in to Reply
    14. Amy Jo

      I answered “other” – I often need to change my site after only 2 days rather than 3. This was particularly true while pregnant/TTC – by day 3 I had much more frequency hyperglycemia (>200), which negatively impacted my A1c.

      4 years ago Log in to Reply
    15. Jim Gilligan

      I am getting better time in range and consistent glucose readings by changing injection areas. With Tandem AutoSoft 90 I had trouble disconnecting and reconnecting the tubing for a shower. So I had infusion sets only in my abdomen for well over a decade. The Tandem rep made me aware of AutoSoft XC infusion sets. I can disconnect the XC with one hand and this has allowed me to move to fresh real estate around my back and upper butt with significant absorption improvement.

      1
      4 years ago Log in to Reply
    16. Marty

      I had to change sites every 2 days when I was using Fiasp or increase my insulin by >30% on the 3rd day. When I switched to generic Humalog, that problem went away and I can now use the same site for 3 days. I speculate that the same ingredient that make Fiasp faster acting (niacinamide) also wore out my sites more quickly.

      4 years ago Log in to Reply
    17. Carol Meares

      I would also like to try inhaled insulin but my insurance won’t cover it.

      4 years ago Log in to Reply
      1. mentat

        Have you contacted Mannkind directly? They have some options for cases like this.

        4 years ago Log in to Reply
    18. M C

      As said before, I have gained much better control through the use of the insulin pump, however, I am running out of viable body ‘real estate’ due to scarring and hardening of the tissues under the skin. When this happens, absorption of the insulin gets more challenging, and uncomfortable. I would hate it, but it may come to the point where I will have to give up the use of the pump. (Solutions are welcome!)

      3
      4 years ago Log in to Reply
      1. KarenM6

        I’m with you, M C!
        I don’t know that there is a solution involving injections or pumps. No educated individual that I have asked has come up with a working solution. The most common answer is “move your site.” But, that’s not workable for me. Also, I’ve not used my abdomen in _years_, yet the lipoatrophy is still there and quite visible. So, it’s a big bummer that I can’t use the abdomen anymore.
        Carol Meares’ answer may be the only one that comes close to working: inhaled insulin.
        I need a lot more education on inhaled insulins before I could say for sure, though.
        I hope we both find a solution!!!! 🙂

        1
        4 years ago Log in to Reply
      2. Kim Murphy

        Try the tubeless OmniPod it can go in at least 10 different sanctioned areas which gives you twenty or thirty spots and I get great absorption. I use much less insulin than I used to just because my absorption has improved with so many areas where you can put it.

        4 years ago Log in to Reply
    19. Russell Buckbee

      I had reactions to all insulin types and processes for a while. It went away after many trials to get my insulin into me. (This includes injections)

      4 years ago Log in to Reply
    20. Bonnie Lundblom

      I had to give my abdomen a several years vacation after MDI there for almost 30 years. Now using the Tslim pump and rotating sites every 3 days using a chart I made showing rotation order to ensure I leave sites alone for as long as possible, so far so good.

      4 years ago Log in to Reply
    21. Christina Trudo

      No, not in over 30 years. Now that I think of it, I did change to metal needles but hadn’t had a huge amount of trouble first, just the educator’s hunch it might help.

      4 years ago Log in to Reply
    22. Mig Vascos

      A couple of years into using the Tandem t:slim 2x i was having bad problems with absorption. I asked both Tandem and my NP to meet with me and go over the training. After some back and forth they agreed. I found that I was not holding the cap containing the infusion set correctly and consequently when I pull it back it didn’t catch well enough. They also suggested the metal needle which I tried and didn’t like at all. I also changed to the AutoSoft XC.
      Anyway, to make the story shorter, the training helped me do things correctly. Eventually I decided to tape the back end of the incision set and also the tube right where it begins. I only need to retape the tube after I shower. Now I get a better absorption and they last 4 days and even 5 without problems.
      Still Tandem infusion sets are not that easy to connect and disconnect unless I can see it and because I’m a side sleeper I”m only able to use the front of my abdomen.
      I still at times have absorption problems but now I know that when my BGs are not working correctly is not my fault. So, i just found a new place and replace it with a new one.
      Taping my sound like another hassle, but it really helps.

      1
      4 years ago Log in to Reply
    23. Jneticdiabetic

      I found absorption from my abdomen didn’t work as well after my two pregnancies. I’ve had good luck with the area at the top back of my hip just above our below the beltline. I have more padding there.
      I always had trouble with the infusion sets that get inserted straight in (e.g. Quickset). They would frequently kink/bend and fail within a day or 2. I’ve had much better luck with infusion sites that are inserted at an angle (Medtronic Silhouette, Tandem Vari-Soft).

      4 years ago Log in to Reply
    24. Kim Murphy

      I was having absorption issues so I switched from a tubed pump which only worked in my stomach to the Omnipod which I can put in 10 different locations.

      4 years ago Log in to Reply
    25. Linda Zottoli

      After 67 years of injected/pumped insulin, I’ve many times given the lower abdomen a rest, once for about 3 years. Being pretty thin, I began, years ago, using the silhouette/varisoft type set in order to use the area in front of my lower rib cage just below the skin, and I guess it would also work on the lower back. This was uncomfortable sometimes at first, but it seemed the insulin built up more fat, there, pretty quickly, and it’s been years since I had any discomfort with it. But the scars from heart surgery have limited that area. A steel set might be easier to put in the back above the waist, though I used to do fine with varisoft below waist — maybe work harder on that stretch first before I try putting in a set.

      4 years ago Log in to Reply
    26. Twinniepoo74

      I stopped my meditronic after someone hacked my pump but years later I am back on the omnipod

      4 years ago Log in to Reply
      1. mentat

        Wow!! Do you know who/why??

        4 years ago Log in to Reply
    27. Molly Jones

      Other was my answer as I changed my sites, but….
      My BG is quite variable. Who knows why. Bodily stress comes in infinite forms. In the early years of pump use I would try new sites to see if this was the cause.

      4 years ago Log in to Reply

    For current or past insulin pump users: Have you ever changed your insulin delivery routine because of insulin absorption issues? Cancel reply

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