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    • 1 hour, 20 minutes ago
      Lee Tincher likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      I disagree currently but the possible costs of all my medical conditions are a constant concern
    • 1 hour, 21 minutes ago
      Lee Tincher likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      Neither agree or disagree; the only thing that has changed for me is the cost of our Medicare Supplement Plan which when we started it almost 9 years ago the monthly cost for each of us was $220 and now is $330.
    • 1 hour, 21 minutes ago
      Lee Tincher likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      A financial burden? I said, "Neither agree nor disagree." But, even with Medicare and a secondary insurance, I still HAVE TO pay to see a doctor quarterly, pay for insulin, and deductibles. The cost is not strangling me, but it is a burden.
    • 1 hour, 22 minutes ago
      Lee Tincher likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      Neither agree or disagree. Over a lifetime of living with T1D It is what it is. The only time it gets to be a burden is if I have to replace something and/or pay out of pocket that isn't covered by insurance. I have always managed to get and have what I need on hand.
    • 1 hour, 22 minutes ago
      Lee Tincher likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      Although I can currently afford my medical costs, they are not cheap. Future expenses are always a concern. Insurance changes are always difficult. I can never feel truly secure in affordable diabetic care. Of course these expenses are taken away from other areas in my family's budget.
    • 3 hours, 12 minutes ago
      Daniel Bestvater likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      Although I can currently afford my medical costs, they are not cheap. Future expenses are always a concern. Insurance changes are always difficult. I can never feel truly secure in affordable diabetic care. Of course these expenses are taken away from other areas in my family's budget.
    • 6 hours, 21 minutes ago
      tpany likes your comment at
      If you could reimagine your diabetes technology, what’s the one thing you would change?
      The ideal is a cure like implantable cells to produce insulin without immunosuppressive drugs. Until then, smaller wearable pumps that last as long as the CGM needed to make it go along with true user control ala DIY systems.
    • 6 hours, 43 minutes ago
      Laurie B likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      A financial burden? I said, "Neither agree nor disagree." But, even with Medicare and a secondary insurance, I still HAVE TO pay to see a doctor quarterly, pay for insulin, and deductibles. The cost is not strangling me, but it is a burden.
    • 6 hours, 45 minutes ago
      Kenneth Gabby likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      the financial burden is huge but the solution is long term tech and that is why i am working on Re-Life which is a battery free and immune evasive bio interface to stop the need for constant sensor changes and reduce costs for everyone forever we need more than just tools we need a permanent breakthrough
    • 6 hours, 50 minutes ago
      Bonnie Lundblom likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      the financial burden is huge but the solution is long term tech and that is why i am working on Re-Life which is a battery free and immune evasive bio interface to stop the need for constant sensor changes and reduce costs for everyone forever we need more than just tools we need a permanent breakthrough
    • 6 hours, 52 minutes ago
      Kathy Hanavan likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      I disagree currently but the possible costs of all my medical conditions are a constant concern
    • 7 hours, 4 minutes ago
      ConnieT1D62 likes your comment at
      How often do you intentionally run your glucose slightly higher during certain activities (e.g., driving, public speaking, exercise)?
      when I am traveling, I will let it run a little higher because I don't know what I'll be doing at any given moment.
    • 7 hours, 13 minutes ago
      Mike S likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      A financial burden? I said, "Neither agree nor disagree." But, even with Medicare and a secondary insurance, I still HAVE TO pay to see a doctor quarterly, pay for insulin, and deductibles. The cost is not strangling me, but it is a burden.
    • 7 hours, 14 minutes ago
      Mike S likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      I disagree currently but the possible costs of all my medical conditions are a constant concern
    • 7 hours, 17 minutes ago
      ConnieT1D62 likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      A financial burden? I said, "Neither agree nor disagree." But, even with Medicare and a secondary insurance, I still HAVE TO pay to see a doctor quarterly, pay for insulin, and deductibles. The cost is not strangling me, but it is a burden.
    • 7 hours, 17 minutes ago
      ConnieT1D62 likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      I disagree currently but the possible costs of all my medical conditions are a constant concern
    • 7 hours, 23 minutes ago
      Lawrence S. likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      the financial burden is huge but the solution is long term tech and that is why i am working on Re-Life which is a battery free and immune evasive bio interface to stop the need for constant sensor changes and reduce costs for everyone forever we need more than just tools we need a permanent breakthrough
    • 7 hours, 24 minutes ago
      mojoseje likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      the financial burden is huge but the solution is long term tech and that is why i am working on Re-Life which is a battery free and immune evasive bio interface to stop the need for constant sensor changes and reduce costs for everyone forever we need more than just tools we need a permanent breakthrough
    • 7 hours, 45 minutes ago
      John Barbuto likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      I disagree currently but the possible costs of all my medical conditions are a constant concern
    • 22 hours, 19 minutes ago
      Laurie B likes your comment at
      To what extent does diabetes technology reduce day-to-day stress for you?
      I use Tandem control-IQ. It works quite well at night, but during the day I often turn it off or I will become hypoglycaemic. My days are often somewhat physically erratic and the algorithm can’t predict what I’m going to do next. I think if a person’s days are very consistent automated insulin may be of use. With the use of CIQ my A1c seems to be directed towards ~6.5 when turned off I seem to fall into the high 5’s range. So at this point I’m neutral on automated insulin delivery. Not convinced automation can ever match the body’s islet cells….we a cellular treatment!
    • 22 hours, 19 minutes ago
      Laurie B likes your comment at
      To what extent does diabetes technology reduce day-to-day stress for you?
      I put somewhat since sometimes the technology adds stress (eg. Won’t connect, or alarms that tell me what I already know and am in the middle of treating)
    • 1 day ago
      lis be likes your comment at
      To what extent does diabetes technology reduce day-to-day stress for you?
      CGM is great, but sometimes too much data is stressful. All the pressure to be in range is a new numerical stress with statistical worries added on. The worries were always present, but nowadays they are front and center.
    • 1 day ago
      lis be likes your comment at
      To what extent does diabetes technology reduce day-to-day stress for you?
      The question is, which is better... "Ignorance is bliss" or "Knowledge is power" I'll take the Knowledge and deal with it. Automated insulin delivery and CGM have definitely improved my T1D management and reduced my emotional and mental workload.
    • 1 day ago
      lis be likes your comment at
      To what extent does diabetes technology reduce day-to-day stress for you?
      I selected “ somewhat” because sometimes when it works, it’s fantastic but sometimes when it doesn’t work is a nightmare. It is either your best friend or your worst enemy.
    • 1 day ago
      lis be likes your comment at
      To what extent does diabetes technology reduce day-to-day stress for you?
      I put somewhat since sometimes the technology adds stress (eg. Won’t connect, or alarms that tell me what I already know and am in the middle of treating)
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    If you use an insulin pump, which of these options best describes when you most often change your pump site?

    Home > LC Polls > If you use an insulin pump, which of these options best describes when you most often change your pump site?
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    If you were diagnosed with T1D before age 26 or if you have a child with T1D who is now an adult, at what age did you or your child become financially responsible for the entire financial cost of diabetes supplies?

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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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    31 Comments

    1. Carol Evans

      My response was “other.” I only use 25 units of insulin a day, so I fill the reservoir (Tandem x-slim) with a week’s worth of insulin, but I change my infusion site every three days. I have been doing this for years with no issues. Medicare makes me get infusion sets and cartridges in the same quantity, even though I only need half the number of cartridges. I won’t enumerate the waste and cost of this system. Medtronic sells infusion sets without the tubing for exactly my situation, but Tandem has decreed that everyone must change out the cartridge every three days.

      1
      3 years ago Log in to Reply
      1. Marty

        I change my infusion set every 2-3 days after I exercise and shower, late morning or early afternoon. I fill my cartridge every 5-6 days at the same time as I switch sets. Somehow, I don’t have any problem getting the right number of sets and cartridges for my routine even though Medicare pays for them. Maybe it has to do with the way my endo writes my prescriptions.

        3 years ago Log in to Reply
    2. terrih57@msn.com

      No specific routine but I prefer earlier in the day when reservoir gets low

      1
      3 years ago Log in to Reply
    3. Greg Felton

      No routine – whenever the reservoir is low and the time is convenient. I used to have a set evening time but now that I can see an accurate number of insulin units left, I try to use it up. In fact, I’m so reluctant to waste insulin that before changing my site I will often eat something and bolus for it, even when I’m not hungry, just to use those last few units of insulin!

      2
      3 years ago Log in to Reply
      1. TEH

        💯
        Totally agree!

        3 years ago Log in to Reply
      2. Jennifer Bounds

        I’ve do the same thing if needed. Insulin is so expensive!

        3 years ago Log in to Reply
      3. ConnieT1D62

        We all have our quirks!

        3 years ago Log in to Reply
    4. Janice Bohn

      Start of my day which means I am woken up every 3 days at 3:30am by the reminder alarm around

      3 years ago Log in to Reply
    5. Daniel Bestvater

      I change my infusion set(steel) every 1-3days depending on how it is working. I change my insulin cartridge (Tandem X2) every 7-12 days. Depending on my activity level I use 15-25 units of insulin per day.

      2
      3 years ago Log in to Reply
    6. T1diabetic

      I don’t change sites until my reservoir is empty.

      3 years ago Log in to Reply
    7. stillarobyn

      Because I need to calibrate it so many times the first day, I do it as early in the day as possible.

      3 years ago Log in to Reply
    8. Joan Benedetto

      I answered end of day, but my son showers before dinner, and charges his pump then. After showering, he changes his pump site so that we know it’s working well before bed.

      1
      3 years ago Log in to Reply
    9. Jennifer Bounds

      No specific routine but also if I have any insulin left in the reservoir I’ll keep the pump on for the allotted up to 8hrs that my pump allows so not to waist the insulin.

      2
      3 years ago Log in to Reply
    10. Sherolyn Newell

      My pods expire every three days with several hours of grace period before they stop working. At the beginning, I picked a time of day when I am usually home, so around 5:30. Sometimes it’s later, but then I try to get back to my regular time.

      3 years ago Log in to Reply
    11. KIMBERELY SMITH

      On through the day

      3 years ago Log in to Reply
    12. Mig Vascos

      I don’t have a special time or a especial number of days. If it’s the site is working I might let it be up to the 4th day. If it’s not I might have to change it more often.
      After many years of injections I’m sure I have a lot of scar tissue even though not visible but many times the site just doesn’t absolve week enough to keep my BG where I want them.
      The tandem pump is great but it’s infusion sets really suck. All pumps give you a diagram of all the places you could input a set but in reality can you? No. The connection is not easy to hook up unless you can see and align the trident with the openings. So the back is out. If you’re a side sleeper can you lay on the site all night without getting bruises? can you use your arms if you do a lot of exercises and play sports? And so the list goes on.
      I visited my nurse practitioner who helps
      Me
      Manage the pump and she changed the correction feature on my settings and it seems to be working better. Now when the Control IQ is trying to keep my highs it’d be given more insulin and it’ll work faster. This way I might be able to avoid trying to do the corrections myself by bolusing and ended up with a low 2 or 3 hours later.
      Another problem as someone else mentioned is MEdicare and the rule that you have to get the same amount of infusion sets as of cartridges and syringes. It’s a complete absurdity.

      1
      3 years ago Log in to Reply
      1. Mig Vascos

        Meant to say “the site doesn’t absorb well.

        3 years ago Log in to Reply
      2. Marty

        I’m on Medicare but I get more sets than cartridges with no problem.

        3 years ago Log in to Reply
    13. Trina Blake

      I change my infusion set evrey 3 days – although the time of day varies with my schedule. I fill the cartrdge to the full 300 units, and change it when it is empty. Again, since my schedule is so varied I wouldn’t dare to try to come up with a 3-dyas-worth of insulin to change both out every 3 days. There are days when I don’t eat anythng but a small green salad for lunch and nothing else, days when I am very physically active, and dyas that my work requires sitting at the desk for 12+ hours. So insulin requirements vary greatly.

      1
      3 years ago Log in to Reply
      1. Trina Blake

        Adding, that since I am not qualified for Medicare, I can order just infusion sets which I do about every other order.

        3 years ago Log in to Reply
    14. Donald Cragun

      I change my infusion set just before I take a meal bolus (usually for breakfast).

      3 years ago Log in to Reply
    15. Becky Hertz

      No specific routine. When the site goes bad, after a certain amount in insulin has been infused, when the reservoir runs out, when I won’t make it through the night with what insulin is left, painful site.

      1
      3 years ago Log in to Reply
    16. Louise Robinson

      I’m retired. so have greater flexibility in my schedule. Because I have high insulin sensitivity and am required to load my Tandem t:slim X2 cartridge with more insulin than I will use in 3 days, I tend to change my cartridge when it runs out but will change my infusion site every 3 days or sooner rather than doing both at the same time. Otherwise, too much insulin is wasted.

      1
      3 years ago Log in to Reply
    17. William Bennett

      One thing I liked about my old dumb Paradigm pump was that you could choose to have the low reservoir alert go by time rather than units remaining. With an AID pump that’s more of a moving target, but with an old dumb pump it would just calculate out your basal rates. I found if I set it to 12 hrs I’d usually get warned during normal waking hours rather than the 3am pumps would just natural prefer. “Hey, if I’m not jerking you out of a deep sleep how do you know I care?”

      3 years ago Log in to Reply
    18. Chris Albright

      I found that it is never good to change anything (as it relates to diabetic medical devices late in the day…….. ) I like time to ensure everything is working right so earlier is better. I also leave my existing infusion set in place in the event that I need to go back to a known working site. Once the new site is verified, I remove the old set.

      1
      3 years ago Log in to Reply
    19. Stephen Woodward

      What does a resevoir amount have to do with site changes. There is no clinical reason I’ve found or studies to that say that you have to change site and resevour at the same time. Never done that in over 25 yrs of pump use. Why do T1Ds get told this, it’s not written in the pump guides.

      3 years ago Log in to Reply
    20. Carol Meares

      The pump runs me most of the time. I sometimes run it beyond the specified expiration if I am still getting good numbers. Sometimes I will change early if my daily plans will not coincide conveniently. Mostly I just change when it says to change, or close.

      1
      3 years ago Log in to Reply
    21. T1D4LongTime

      I chose: “No specific routine – whenever the site expires or the reservoir is too low”. However, I also look at my schedule for the next 24 hours. If I have an early morning, I will try to extend the site till later the next day or change it after supper. I don’t like to change right before bed nor when I need to leave home immediately after the change.

      3 years ago Log in to Reply
    22. Bill Kast

      I use an omnipod from Insulet. There is a hard failure wired into the electronics at the end of 3.00 days plus 8 hours. At that point the pump, and the injection point, stop working and the pump starts to squawk loudly. Because I am on medicare, I pay for my pump out of pocket. I usually try to utilize every moment of my allotted time with the pump. I end up being a slave to a sliding time-of-failure that is usually inconvenient for me.

      3 years ago Log in to Reply
      1. Teresa Schnoor

        Same here, I like to get every minute.

        3 years ago Log in to Reply
    23. KSannie

      I do it either 2 hours before lunch or supper, so I have a follow up period to make sure the set is working. (I am not up early enough before breakfast to do it 2 hours before.) And then a follow up period of a couple hours after the meal to make sure it handles the meal before going to bed. Which time I choose depends on where I am and what is scheduled. If I have a class two hours before lunch, I will do it 2 hours before supper. If I have a late afternoon dental appointment, I will do it before lunch. And so on.

      3 years ago Log in to Reply

    If you use an insulin pump, which of these options best describes when you most often change your pump site? Cancel reply

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