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    • 3 hours, 3 minutes ago
      Greg Felton likes your comment at
      If you were to request the next available appointment with your T1D healthcare provider, when do you estimate the next available appointment would be?
      Before the onslaught of Type 2 Diabetes, I, as a T1D, could get an appointment almost anytime I needed one. Now, I cannot get an appointment within 3 months, which is the time within I must see rhe doctor for Medicare benefits. My doctor cancelled 2 (half ) of my sppointments last year. Caused ma a lot of problems. I live in Florida, a place where modern medicine does not seem to have reached yet.
    • 3 hours, 3 minutes ago
      Greg Felton likes your comment at
      If you were to request the next available appointment with your T1D healthcare provider, when do you estimate the next available appointment would be?
      I routinely see my Endo every three months. At the end of my appointment I schedule the next quarterly meeting date. But if I ever have to reschedule it, then it takes anywhere from two to four weeks to find a time that works for us.
    • 5 hours ago
      Mike S likes your comment at
      If you were to request the next available appointment with your T1D healthcare provider, when do you estimate the next available appointment would be?
      It all depends on the urgency of my needs. I’ve gotten in the next day before, but those days may be gone! It also depends on who I see. But these days, even the PA is often booked. Of course, cancellations happen, so that can be a factor as well.
    • 5 hours, 16 minutes ago
      Jeff Marvel likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      The beginning of the year is always a bit iffy when you're on Medicare. Even though I've already paid my annual deductible, my pharmacy can't see that, so I must wait until it shows up on my Medicare account before I order new insulin. I always try to have plenty of insulin on hand at the end of December so it's not an issue. The organization I get my pump equipment from has a lot they must do because of Medicare, as well, and that can get time consuming. All-in-all, I'm lucky to have the time, energy and patience to deal with it, and I know up front these time-consuming moments are to be expected. If I wasn't retired, it'd be more of an issue.
    • 16 hours, 26 minutes ago
      Gerald Oefelein likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      I selected 6 hours. So far, I have spent 6 weeks trying to get a new pump. I decided to look for a new pump in mid-December as my 770G warranty expired on January 3. I wanted to go hoseless with the Omnipod and the Dexcom 6. I contacted Dexcom and they sent me to the medical distribution company ASPN, and they could do the Omnipod but only with pharmacy part D with the Dexcom 6 sensor on DME My part D pharmacy plan had Omnipod as tier 6. $155.56 co pay and $150/month. The omnypod is not available as DME. I called INSULET the mfgr of omnipod. They told me they only supply via pharmacy plan to get more T2d's to sign up. Verses 100% DME coverage, part D coverage that was a non-starter. I contacted another supply company CCSmed. They could do both Dexcom 6 and tslim x2. Ineeded a Endo visit to get the notes and Rx. I had my Endo visit on Jan 20. Still waiting for CVSmed. Been waiting for 5 weeks now. Just called CCSmed and they got the endo notes and Rx but Medicare wanted to know who paid for my 770G 4 years ago. Fortunately, that was private/company. My new pump should now ship tomorrow. Finally.
    • 20 hours, 14 minutes ago
      Wanacure likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      Most of the 3-4 hours is way ting on a phone
    • 20 hours, 17 minutes ago
      Wanacure likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      I answered "No time," but I live in France, where we have a single provider. I receive a prescription from my doctor and go to the pharmacy monthly to have it filled. (Pump peripherals are provided by a separate supplier.) "Appeals" do not exist here since the doctor will only prescribe medicines that are reimbursed. And no, I have never needed a treatment that wasn't covered.
    • 20 hours, 59 minutes ago
      Wanacure likes your comment at
      When you experience an illness that makes your blood glucose levels more difficult to manage (whether because you are unable to eat, the stress of being sick, or any other reason), what resources do you refer to for help managing your blood glucose levels while sick? Please select all that apply to you.
      The resources I use in managing my glucose levels once sick is my own personal experience after living with t1d for 46 years
    • 20 hours, 59 minutes ago
      August Rossano likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      Switching to Medicare has created (seemingly) endless hours and day making this transition with all things diabetes related. We’re still in the midst of making this ā€˜delightful’ change. This week we learned that Medicare covers Either CGM stuff OR glucose test strips. Thank goodness that God is sovereign over all these details. He helps me walk through these challenges without despair.
    • 21 hours, 2 minutes ago
      August Rossano likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      The last 3 months have been filled with frustrating phone calls now that I switched back to traditional Medicare from a Medicare Advantage plan. I have been fighting to get strips authorized in addition to CGM- they did not authorize them because I had no proof that I had a meter!! Crazy making! I had to write an appeal letter in order to get them, but finally got it worked out. I also had some pump replacement issues, trouble getting insulin, etc.
    • 21 hours, 6 minutes ago
      August Rossano likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      I answered "No time," but I live in France, where we have a single provider. I receive a prescription from my doctor and go to the pharmacy monthly to have it filled. (Pump peripherals are provided by a separate supplier.) "Appeals" do not exist here since the doctor will only prescribe medicines that are reimbursed. And no, I have never needed a treatment that wasn't covered.
    • 21 hours, 7 minutes ago
      August Rossano likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      Much too much time! Part of it, I know, is my own fault, for not keeping anxiety at bay when I have to sort out which plan will work best, annually. But it is something I dread, every single year. When I call to get some help understanding, the people are almost always very nice, but I have had times when the information was incorrect or not explained clearly. I usually commiserate with the person on the phone for having such an annoying system, and agreement seems to rule the day. But I never chose to make sorting out insurance management a career!
    • 21 hours, 9 minutes ago
      August Rossano likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      I selected 6 hours. So far, I have spent 6 weeks trying to get a new pump. I decided to look for a new pump in mid-December as my 770G warranty expired on January 3. I wanted to go hoseless with the Omnipod and the Dexcom 6. I contacted Dexcom and they sent me to the medical distribution company ASPN, and they could do the Omnipod but only with pharmacy part D with the Dexcom 6 sensor on DME My part D pharmacy plan had Omnipod as tier 6. $155.56 co pay and $150/month. The omnypod is not available as DME. I called INSULET the mfgr of omnipod. They told me they only supply via pharmacy plan to get more T2d's to sign up. Verses 100% DME coverage, part D coverage that was a non-starter. I contacted another supply company CCSmed. They could do both Dexcom 6 and tslim x2. Ineeded a Endo visit to get the notes and Rx. I had my Endo visit on Jan 20. Still waiting for CVSmed. Been waiting for 5 weeks now. Just called CCSmed and they got the endo notes and Rx but Medicare wanted to know who paid for my 770G 4 years ago. Fortunately, that was private/company. My new pump should now ship tomorrow. Finally.
    • 21 hours, 9 minutes ago
      August Rossano likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      The beginning of the year is always a bit iffy when you're on Medicare. Even though I've already paid my annual deductible, my pharmacy can't see that, so I must wait until it shows up on my Medicare account before I order new insulin. I always try to have plenty of insulin on hand at the end of December so it's not an issue. The organization I get my pump equipment from has a lot they must do because of Medicare, as well, and that can get time consuming. All-in-all, I'm lucky to have the time, energy and patience to deal with it, and I know up front these time-consuming moments are to be expected. If I wasn't retired, it'd be more of an issue.
    • 21 hours, 9 minutes ago
      August Rossano likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      I said 8+ and the reason, as for so many others, can be summed up in a phrase: transitioning to Medicare.
    • 21 hours, 45 minutes ago
      Wanacure likes your comment at
      On a scale of 1-5, how satisfied are you with your current insulin delivery method (pump, pens, syringes, inhaler, etc.)? 5 = the most satisfied, 1 = the least satisfied
      I’m a reasonably satisfied MDI user with Lantus and Fiasp. I’ve looked into getting a pump but honestly, until I find one that does everything I want, I’ll probably hold off. My wish list for a pump: 1) no tubes 2) works well with Fiasp 3) controls that allow me to stay at my target of 70-90 mg/dl all night long.
    • 21 hours, 56 minutes ago
      Wanacure likes your comment at
      On a scale of 1-5, how satisfied are you with your current insulin delivery method (pump, pens, syringes, inhaler, etc.)? 5 = the most satisfied, 1 = the least satisfied
      MDI for the past 60 years and do not see any alternative that I would prefer. The needles for my pens are so thin and sharp that they are painless (a far cry from the lancets I once used). chiefly, I am glad not to have to deal with setting up a pump and. Although I love my libre, I am not good candidate for having devices affixed to me. If my insulin delivery got interrupted they way i have interrupted my cgm service, I would have been in trouble. Furthermore, I have a track record of having both mechanicall and electronic things malfunction. (Seriously, I sometimes act as a beta-tester for technology folks. Maybe I push to many buttons?)
    • 22 hours, 8 minutes ago
      Wanacure likes your comment at
      On a scale of 1-5, how satisfied are you with your current insulin delivery method (pump, pens, syringes, inhaler, etc.)? 5 = the most satisfied, 1 = the least satisfied
      I've had Tandem x2 and Dexcom since September. Previously on Medtronic for around 15 years. Grew to HATE the sensors and switched before the warranty on my last Medtronic was up. So far, I absolutely LOVE the Tandem and the Dexcom. I'm disappointed, however, in the amount of waste and plastic that this pair creates. Of course there will always be plastic waste from any pumps/sensors, but the amount of non-reusable stuff for insertions is ghastly.
    • 22 hours, 9 minutes ago
      Wanacure likes your comment at
      On a scale of 1-5, how satisfied are you with your current insulin delivery method (pump, pens, syringes, inhaler, etc.)? 5 = the most satisfied, 1 = the least satisfied
      Have your doctor prescribe the syringes with .5 unit increments instead of the 1 unit syringes. Not quite a .1 unit which you are hoping for, but .5 is better than 1 unit increments.
    • 23 hours, 25 minutes ago
      Ahh Life likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      I answered "No time," but I live in France, where we have a single provider. I receive a prescription from my doctor and go to the pharmacy monthly to have it filled. (Pump peripherals are provided by a separate supplier.) "Appeals" do not exist here since the doctor will only prescribe medicines that are reimbursed. And no, I have never needed a treatment that wasn't covered.
    • 1 day, 1 hour ago
      ConnieT1D62 likes your comment at
      In your own words, how would you describe the feeling of a severe low?
      Nothing short of terrifying. I often go into seizures, having no idea where I am, who anybody, or even if I’m alive or dead. I’ll feel like I’m falling or hurtling toward something. At home I feel like my house is tilting. Im leaving a lot out but these are some of the scariest things.
    • 1 day, 1 hour ago
      Modee likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      Most of Europe has the right idea! Is it a good health system for you overall? The US may be too large to implement a national system, but that doesn't hold states back (as long as there is federal money to help).
    • 1 day, 1 hour ago
      Modee likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      I answered "No time," but I live in France, where we have a single provider. I receive a prescription from my doctor and go to the pharmacy monthly to have it filled. (Pump peripherals are provided by a separate supplier.) "Appeals" do not exist here since the doctor will only prescribe medicines that are reimbursed. And no, I have never needed a treatment that wasn't covered.
    • 1 day, 1 hour ago
      Modee likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      I said 8+ and the reason, as for so many others, can be summed up in a phrase: transitioning to Medicare.
    • 1 day, 1 hour ago
      Modee likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      PUMP USERS: Just in case nobody has told you, if you use a pump, Insulin is considered durable medical equipment, which can save a lot of money, even with the new price cap
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    If you use an insulin pump, when changing your pump site, do your blood glucose (BG) levels rise afterwards? If so, please share in the comments if you take any steps to adjust for the rise when changing your site.

    Home > LC Polls > If you use an insulin pump, when changing your pump site, do your blood glucose (BG) levels rise afterwards? If so, please share in the comments if you take any steps to adjust for the rise when changing your site.
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    46 Comments

    1. AnitaS

      I have on so few occasions that I don’t make any adjustments. If the sugar rise was noticeable, I could do a correction if needed.

      1
      1 month ago Log in to Reply
    2. Amanda Barras

      I notice a raise in bs when there is 20 U or less left in my pump, so an early site change actually helps correct that.

      1
      1 month ago Log in to Reply
      1. Derek West

        I found the same thing when I switched to the Tandem pump. Never had that problem with a Medtronic pump. I think the Tandem pump really does not know how much insulin is left, so I too change it out early.

        1 month ago Log in to Reply
    3. Lucia Maya

      I always give a bolus/prime when I change my site, even though I use tru-steel sets and they don’t recommend it. That really helps to saturate the site and mostly prevents BG rise after.

      2
      1 month ago Log in to Reply
      1. Becky Hertz

        I do that as well. 0.7 u.

        1 month ago Log in to Reply
    4. Mark Schweim

      Not since I started filling the cannula with 0.5 units more than the infusion set instructions say to use and leaving the old site inserted until at least 4 hours after starting to use the new site. If I remove the old site right away after starting the new site, my BG almost always rises, but leaving the old site in during the first 4 – 6 hours of new site use along with the extra 0.5 units used in the “Fill Cannula” step usually prevents the site change rises.

      1
      1 month ago Log in to Reply
    5. LizB

      I do often notice a rise and some sets seem to take awhile to start absorbing properly. I always fill the cannula with 1 unit instead of .3 and I try to change it shortly before lunch so I can push a larger bolus through.

      1 month ago Log in to Reply
    6. Mick Martin

      On the contrary, I always notice a fall in BG levels after infusion site changes. I guess my antibodies are good at determining when a ‘foreign body’ is in place and it does its best to ‘reject’ that foreign body … i.e. the cannula. I already need to change my sites every 2 days due to the effects of my blood glucose levels rising within the period that I have an infusion set inserted. (Sometimes, when changing the site, I notice a ‘build-up’ of ‘gunge’ surrounding the end of the cannula which, I guess, limits the amount of insulin that’s being infused, even though my pump advises that the insulin is being delivered.

      1 month ago Log in to Reply
    7. Ron Pierce

      My BG #’s go down when it is time to change an infusion site because of clotting around the old site makes it harder for insulin to get where it needs to go, hence higher #’s. No clotting around the new site, so lower #’s.

      1
      1 month ago Log in to Reply
    8. Debra Nance

      I do a 1 unit bolus to help

      2
      1 month ago Log in to Reply
    9. Kerry Rubio

      I increase my basal rate to 200% for 2 hrs and do a .5 unit bolus after changing my site. This helps with the typical rise I get.

      1 month ago Log in to Reply
    10. Lyn McQuaid

      I answered “other” because, like others have commented, I offset the rise by giving an extra 0.5 unit bolus, which stops the rise I used to see.

      1 month ago Log in to Reply
    11. Virginia Barndollar

      For years my endo has had me filling with a little more than the priming tube amount. It has worked great.

      1 month ago Log in to Reply
    12. Joan Fray

      I cange sites every three days unless there’s a problem. My
      Bg usually dips a bit after a site change. A figurred it was because the insulin was newer. Good lord, what do I know?! I just do it and adjust……hope for the best, deal with the rest…..

      6
      1 month ago Log in to Reply
      1. MT

        ā€œHope for the best…deal with the restā€. ā¤ļø

        4
        1 month ago Log in to Reply
    13. KSannie

      My blood sugar plummets about 4 hours after inserting a new infusion set. This has happened to me for the entire time I have used a pump, and through 3 different pump manufacturers. I try to change the infusion set two hours before a large meal and then decrease the insulin suggested by the pump by one unit. This sometimes works, but sometimes I still go low.

      1 month ago Log in to Reply
    14. kylekk@gmail.com

      I almost always see a slight rise while the new pump is acclimating. I generally run a 35% basal increase for 2 hours and give myself 2-3 units of a bolus (depending upon what is going on when I’m changing my pump).

      1
      1 month ago Log in to Reply
    15. Lawrence S.

      Generally, my BG levels do not change when I change a pump site around my belly area. I prime with .7 units in the cannula (as directed).

      However, when I put the site in my thigh, my blood glucose levels almost always go up. I usually have bad luck with putting the sites in my legs. But, I don’t have many other options, so I keep using my legs.

      1
      1 month ago Log in to Reply
    16. Eva

      When changing my site, i check various things. First, i check for kinks in the cannula. Then, i check my blood sugar often as it maybe due to more fatty tissue at the site.

      1 month ago Log in to Reply
    17. beth nelson

      When I move from a very insulin-friendly site to a less fatty location, I often see a rise in BS, and it remains fairly constant, though not as much an increase as when the site is initially changed. Of course, the opposite is true when I move from lean to fatty tissue. I’m thinking I should create a separate profile on my t:slim, one named “fatty” the other “lean” and raise the basil a bit on the lean. Any thoughts on that?

      3
      1 month ago Log in to Reply
    18. Bruce Schnitzler

      I rarely notice a rise unless the new site port fails for some reason, notably an undetected bent needle. A sharp rise in BG is then observed and another port installed.

      1
      1 month ago Log in to Reply
    19. Drina Nicole Jewell

      I do a .25-.5 bolus before I change my pump site so no rise after a site change.

      1 month ago Log in to Reply
    20. Jeannie Hickey

      I gradually raised the cannula fill amount from 0.3 to 1.7u until I no longer saw the rise after changing sites. I also leave the old site in for several hours.

      2
      1 month ago Log in to Reply
      1. Becky Hertz

        Maybe we can talk about leaving the old site in at the next Pump and Sensors zoom call.

        1
        1 month ago Log in to Reply
    21. John McHenery

      I use corrective boluses and sometimes increase basal rates till the situation stabilises.

      1 month ago Log in to Reply
    22. Patricia Kilwein

      Sometimes I have a rise in bg because hitting some scar tissue. It drops after moving it again. Socks on supplies tho.

      1
      1 month ago Log in to Reply
      1. Patricia Kilwein

        Sucks on supplies. Sorry was up all night with new sensor issues….

        1
        1 month ago Log in to Reply
    23. Kayci Marr

      I only noticed this occurring this past time. Otherwise, they stay pretty steady, thankfully! šŸ™‚

      1
      1 month ago Log in to Reply
    24. Sherrie Johnson

      I answered occasionally but most of the time it goes low that’s why I never change my pump in the evening hours always in the a.m.

      1 month ago Log in to Reply
    25. Jillmarie61

      I try to bolus before removing the old site/pod to cover me while I’m off. I used to do that when I wore a pump that couldn’t get wet too, but since switching to the OmniPod I no longer need to do that.

      1 month ago Log in to Reply
    26. Don (Lucky) Copps

      Only when I hit scar tissue.

      1 month ago Log in to Reply
    27. Becky Hertz

      My body is not an insulin absorption machine. Usually if there is a rise in bg’s after a site change, it’s due to a poor site.

      1 month ago Log in to Reply
    28. Jeanne McMillan-Olson

      Since I have been using my Tandem T slim X2 pump I have rises after site changes. Never noticed this with my older Medtronic Paradigm pump.

      1 month ago Log in to Reply
    29. csreineke

      I set Loop to my custom ā€œsite changeā€ override, telling the AID system that I need 130% insulin for 3 hours.

      1 month ago Log in to Reply
    30. Stephen Woodward

      Whenever a new site is put in the old site should stay in for a few hours to absorb the insulin, the cannula should be filled, and the site should be primed to get the insulin to start being used as soon as possible. The priming is done to get the infusion site to absorb insulin asap, the insulin needs to break up the clumps, the form that keeps it stable in the vial, and then the insulin comes in contact with more fatty tissue sooner than if no priming is done. Yes it is a hack never taught, and that’s a shame.

      For me for the last 30 yrs I’ve used 1u to fill my cannula and 1u to prime the site, using soft XC sets.

      The exact amount will vary from person to person and from site set to site set.

      This should be taught to everyone who uses a pump, as I was 31 yrs ago.

      1 month ago Log in to Reply
    31. George Lovelace

      I use a Teflon Cannula Set so instead of the Standard Prime of 0.7 U I always Prime a Full Unit, it all evens out

      1
      1 month ago Log in to Reply
    32. ELYSSE HELLER

      I often go low after a pod change, not high.

      1 month ago Log in to Reply
    33. Adam Heath

      We often give Adam a corrective SQ injection while waiting for the new site to work completely. The endocrinologist suggested trying inhaled insulin for these corrections, saying there would be less risk of rebound lows/stacked doses. Adam has Down syndrome and he is not great with the inhaler despite practice so I’m never sure how much insulin he’s getting. Other suggestions?

      1 month ago Log in to Reply
    34. C B

      I always bolus for a site/pod change to avoid the rise

      1 month ago Log in to Reply
    35. Linda Zottoli

      I use 0.8 instead of the directed 0.7 for the cannula fill, and also bolus in the next few minutes — for food (or occasionally correction), whether I had intended to eat or not (usually I’m changing the site before breakfast, so it isn’t an issue). In the past, when I’ve noticed a problem with a rise after putting in a new set, it’s always been when I didn’t bolus for a while.

      1 month ago Log in to Reply
    36. PamK

      I have noticed a slight rise in my blood sugar levels an hour or two after a site change. I adjusted my cannula fill setting from 0.5 to 0.7 units. This seems to take care of it!

      1 month ago Log in to Reply
    37. Kristen Clifford

      More often, I have a drop in my BGs after changing sites.

      1 month ago Log in to Reply
    38. Leona Hanson

      I’ve never noticed a big rose when changing my tubing it takes me only maybe 2 min. To change my tubing really not much of aa rise there is

      1 month ago Log in to Reply
    39. Katie Craft

      I always experience a rise after a site change, and have started using Afrezza inhaled insulin to combat this once my bg reaches 200 after a site change. Brings it right down. Cannot take it before reaching 200 or I go low.

      4 weeks ago Log in to Reply
    40. Andrea Hultman

      Usually experience a decline in sensor glucose after a site change. If it rises, that most often indicates a bad site, and lo and behold, a bent cannula.

      3 weeks ago Log in to Reply
    41. James Cheairs

      With the release of DIY Loop 3.0, I can customize how much insulin is injected as part of the Omnipod pod change.

      2 weeks ago Log in to Reply

    If you use an insulin pump, when changing your pump site, do your blood glucose (BG) levels rise afterwards? If so, please share in the comments if you take any steps to adjust for the rise when changing your site. Cancel reply

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