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    • 3 hours, 38 minutes ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      The more important question is 'how well does the clip work'. For me, the Medtronic clip worked very well, but the Tandem clip is quite ineffective and the pump falls off my belt during things like yard work or other bending movements.
    • 3 hours, 39 minutes ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      I answered never. I always use a clip -- I wear my t:slim x2 on my belt -- but not the Tandem clip. I use the black t:Holster Rotating Belt Clip. Very pleased.
    • 3 hours, 40 minutes ago
      Lawrence S. likes your comment at
      If you use an insulin pump that comes with a clip, how often do you have your pump clip attached to your pump?
      I am rough on pumps and use a Tandem X2 but dont use the Tandem clip/holster. I use a neoprene case and a pouch with a metal clip. Thenmetal clip is uncomfortable while I sleep. Looking for a different solution for wearing my pump at night.
    • 23 hours, 56 minutes ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I answered that nobody wants to be screened, but I was answering based on my immediate family. I did let my deceased type-1 diabetic cousin's 35 year old son know he can be tested for his likelihood of becoming type-1 diabetic. He said he may be tested as he was always curious if he had a chance.
    • 1 day ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I have T1, and when my oldest grandson got T1, the other 3 grandkids got screened. The grandson who's the brother of the one with T1, showed a strong possibility of being a future T1 diabetic. It sadly came true about a year later.
    • 1 day ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I have LADA, and the idea of screening has not come up, either by me or my adult children. I guess I need to present the opportunity to them so they can make the decision.
    • 1 day ago
      Wanacure likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 1 day, 3 hours ago
      Samantha Walsh likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I was born in 1939 and had many childhood illnesses. Three different kinds of measles and tonsils removed before I was 5 years old, then mumps and chickenpox when I was 5. While recovering from the mumps and chickenpox, I began showing the symptoms of very high blood sugar. Three doctors examined me and they were not able to make a diagnosis. I had lost much weight, and I had stopped eating. I did not have an appetite. It was almost impossible for me to walk. A fourth doctor had my blood tested and he made the diagnosis. While receiving pork insulin I finally began to recover a few days after my sixth birthday. I did not have ant relatives with diabetes. I think the childhood diseases caused internal damage and that was the cause of my diabetes. At the present time there are still no type one diabetics among my relatives. I do not believe it is necessary for my children and grandchildren to be screened for T1D autoantibodies.
    • 1 day, 22 hours ago
      KarenM6 likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 2 days ago
      Katie Bennett likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 2 days, 1 hour ago
      Kate Kuhn likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 2 days, 1 hour ago
      Karen DeVeaux likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I was born in 1939 and had many childhood illnesses. Three different kinds of measles and tonsils removed before I was 5 years old, then mumps and chickenpox when I was 5. While recovering from the mumps and chickenpox, I began showing the symptoms of very high blood sugar. Three doctors examined me and they were not able to make a diagnosis. I had lost much weight, and I had stopped eating. I did not have an appetite. It was almost impossible for me to walk. A fourth doctor had my blood tested and he made the diagnosis. While receiving pork insulin I finally began to recover a few days after my sixth birthday. I did not have ant relatives with diabetes. I think the childhood diseases caused internal damage and that was the cause of my diabetes. At the present time there are still no type one diabetics among my relatives. I do not believe it is necessary for my children and grandchildren to be screened for T1D autoantibodies.
    • 2 days, 2 hours ago
      Kelly-Dayne likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 2 days, 3 hours ago
      William Bennett likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 2 days, 3 hours ago
      Jneticdiabetic likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I have led a team for the JDRF OneWalk annually since the late 1990's. We have been able to raise a lot of funds for JDRF...and I have enjoyed doing it. Good cause!
    • 2 days, 3 hours ago
      Lawrence S. likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      my siblings & parents are older (like me) and they've never expressed any interest in getting tested. my nieces and nephews have never said anything either
    • 2 days, 15 hours ago
      Karen Newe likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I participated in several ADA walks not long after being Dx with T1D. As Ahh Life points out large $ are rased, but where do they go? I stopped supporting ADA for that reason. I think JDF is much more open on where the funding goes.
    • 2 days, 15 hours ago
      Karen Newe likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      JDRF only. I like knowing that my contributions are going specifically to T1D.
    • 2 days, 15 hours ago
      Karen Newe likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I have led a team for the JDRF OneWalk annually since the late 1990's. We have been able to raise a lot of funds for JDRF...and I have enjoyed doing it. Good cause!
    • 2 days, 19 hours ago
      Joindy23 likes your comment at
      The last time you discussed adding a new device or medication to your T1D management routine with your health care provider, who initially suggested trying the new device or medication?
      Switched a long time ago to Tandem/Dexcom from Minimed because of improved and more automated control, and haven't looked back. Still wishing for a cure, but know it's not going to happen for dinosaurs like me. I'll just be glad when young people will will one day experience that magic word: cure. It's too easy to sit around and complain, but it's high time for a cure, and way past time having us depend on treatment that is pretty much a money maker for big Pharma when it seems as if there's a cure waiting in the wings. Filling up landfills with used pump supplies, etc., makes our society look nothing but incompetent and greedy. Sorry to rant.......
    • 2 days, 19 hours ago
      Joindy23 likes your comment at
      The last time you discussed adding a new device or medication to your T1D management routine with your health care provider, who initially suggested trying the new device or medication?
      They do too often. Why I ask? Well because it will help long term.... oh how do you know that it will help? It's a brand new medication, never been used by the D community, except for the shortest term study mandated in order to get it to market, and sell. Long term has never been achieved... its NEW. Let's revisit/wait a couple years... if its MAGIC medicine, sure I'll try it. But unless it's got magic properties, guarantees magic results why would I want it, until it's been used for a decent while??? Oh well... yeah, guess that does makes sense....
    • 3 days, 12 hours ago
      Wanacure likes your comment at
      Does your T1D health care provider currently offer the option to have virtual appointments (via phone or video call)?
      Yes and for the last year and a half that is exclusively what I have been offered so I am not getting all the usual checks an in person endo visit requires. ADA and others spent 10-20 years convincing endos they needed to check patients feet and that progress has evaporated.
    • 3 days, 12 hours ago
      Wanacure likes your comment at
      Does your T1D health care provider currently offer the option to have virtual appointments (via phone or video call)?
      I would rather see in person. He checks my feet, BP etc. we have a chance to catch up and for me to ask questions. To me so much better face to face. We did virtual during pandemic.
    • 3 days, 20 hours ago
      Phyllis Biederman likes your comment at
      If you use an insulin pump, do you currently have a protective case on your pump or PDM?
      I’ll occasionally use the holster with clip that came with my pump or a protective case of my own when I’m wearing something without pockets. However I find these quite bulky thus usually just slip my pump in a pocket.
    • 3 days, 20 hours ago
      KarenM6 likes your comment at
      Of the people in your life, who (if anyone) makes you feel judged or criticized for your T1D management (for example, what foods you eat, where or when you check your blood glucose, etc.)? Select all that apply to you.
      Hmmm... I'd almost welcome it, another challenge to enjoy?
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    If you use both an insulin pump and CGM, do you currently use any of the following automated insulin delivery (also known as “predictive low glucose suspend” or “hybrid closed loop”) algorithms to help keep your glucose in-range?

    Home > LC Polls > If you use both an insulin pump and CGM, do you currently use any of the following automated insulin delivery (also known as “predictive low glucose suspend” or “hybrid closed loop”) algorithms to help keep your glucose in-range?
    Previous

    Do you have any flavors of glucose tabs that you prefer? Select all that apply!

    Next

    During which types of exercise and/or physical activities do you feel most confident in your ability to maintain comfortable blood glucose levels? Select all that apply!

    Sarah Howard

    Sarah Howard (nee Tackett) has dedicated her career to supporting the T1D community 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 Manager of Marketing at T1D Exchange. Sarah and her husband live in NYC with their cat Gracie. In her spare time, she enjoys doing comedy, taking dance classes, visiting art museums, and exploring different neighborhoods in NYC.

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    34 Comments

    1. MARIE

      My husband uses Tandem Basal-IQ but not the Control IQ because he can do a better job on his own of achieving low A1C and high time in range (with tightly controlled parameters) than the Control IQ can. His endo told him that the algorithm in the Control IQ is set much higher than what he targets and his stats would be no where near as good if he ‘upgraded’ to Control IQ.

      2
      1 year ago Log in to Reply
      1. kristina blake

        Same here – I could have written your post (but for me!). I am staying with BIQ (my decisions) for the same reasons your husband has.

        1
        1 year ago Log in to Reply
    2. Sherri Mason

      I use CIQ from evening til morning in sleep mode for the great overnight results. I use 50% of my basal insulin in the morning then inject for lunch and dinner. BAsically, I use 50% pump, 50% MDI. Works great for not going low during exercise.

      1
      1 year ago Log in to Reply
    3. Joan McGinnis

      I was very hesitant t get to Control IQ from basal IQ after years of doing my own methods but it was a leap and glad I did it. Now would not change unless something better comes along and easy to use .

      1 year ago Log in to Reply
    4. Nevin Bowman

      I’ve used Medtronic, and am now using Control IQ. They tech is getting better, but still does not keep me in range without my own input.

      1 year ago Log in to Reply
    5. lynn nelson

      The Tandem insulin pump is the best thing that has happened in my diabetic life. Been doing this for 47 years. I finally have my A12 below 7.0

      1
      1 year ago Log in to Reply
      1. Joan Fray

        Amen!

        1 year ago Log in to Reply
    6. Amy Jo

      I was using the Tandem Control IQ up until yesterday. Had to turn it off as I am pregnant, and the algorithm just doesn’t keep my BG in the tight range I need. It’s a little disappointing that the tandem product does not allow for customization (eg insulin duration of activity, target BG).

      2
      1 year ago Log in to Reply
    7. mojoseje

      I suspend mine manually depending upon how fast my bg is dropping.

      1 year ago Log in to Reply
    8. Sondra Mangan

      Omnipod for 14 years — but Tricare (for military families) is not currently covering Omnipod 5. Hoping that changes soon.

      1 year ago Log in to Reply
      1. ELYSSE HELLER

        That is so awful. I worked for the VA for almost 30 years (I had to retire earlier than I wanted to due to Covid-19), and I was amazed that the VA did not cover insulin pumps at all until a few years before I had to retire. I kept telling my patients to fight for insulin pump coverage. Such a shame that we need to do this.

        2
        1 year ago Log in to Reply
    9. ELYSSE HELLER

      I am anxiously awaiting my health insurance company (Blue Cross Blue Shield FEP federal employee program) to start covering the Omnipod 5 system. As soon as I am covered I will get the Omnipod 5. Why does it take so damn long for the USA to cover new medical products!

      1 year ago Log in to Reply
    10. Mike Plante

      Medtronic’s suspend was definitively beneficial over 100% manual mode, but when I moved to the 670G with AutoMode it was a nightmare.

      I have since moved to DIY with Omnipod & Dexcom and it’s been amazing and life-changing. I’m currently using Loop-Dev (Loop 3.0) on iOS and it’s my favorite system so far.

      1 year ago Log in to Reply
    11. john36m

      Currently on Omnipod 5 for 33 days. It is working quite well so far. It is improving my dawn phenomenon but very slowly. I was previously on Loop. I wish the Omnipod 5 gave me more usable data. If I ever abandon it, I will have no idea what it set as my basal rates.

      1 year ago Log in to Reply
    12. Janice Bohn

      I have been using OmniPod 5 dice June and previous using the Tandem IQ system. Like being tube free! Would like both systems to have more Robertson st algorithms

      1
      1 year ago Log in to Reply
      1. Janice Bohn

        Darn my phone – it does not like real words like robust systems

        2
        1 year ago Log in to Reply
    13. Ms Cris

      I want to use an algorithm, but the limits are set too high for me! I’d be in constant pain (muscle, joint, head especially). My Dr is hoping they allow more custom limits soon. Every T1D patient is different.

      2
      1 year ago Log in to Reply
    14. Jneticdiabetic

      I use Tandem Control IQ, but have been out of my Dexcom sensors for a few days (waiting for my next order). What I miss most is waking up in range every morning. Last 3 of 4 mornings I was 57 or > 200.

      1 year ago Log in to Reply
      1. AnitaS

        You possibly may need an adjustment in your overnight basal? Even if I don’t have on a CGM during the night which occasionally happens because of an MRI test which I occasionally need, I still wake up with good numbers. I do agree however that the night control feature does help on some nights.

        1 year ago Log in to Reply
      2. Jneticdiabetic

        Thanks, Anita! I think my challenge overnight is I work late and often (but not always) eat right before bed. I tend to be more cautious with boluses before bed for fear of lows. The control IQ sleep mode helps to even me out if I over or under bolused for those midnight snacks.

        1 year ago Log in to Reply
    15. Katrina Mundinger

      Have been using Medtronic’s various products for years. Am currently in the process of switching to Dexcom, and then Tandem.

      FWIW I did like the 770G’s Auto Mode better than the 670’s. I am just DONE with the sensor’s annoying requests for either calibration or just “enter BG.” I know the Tandem has its own batch of challenging things but want a change!

      1
      1 year ago Log in to Reply
    16. Sharon Gerdik

      I’ve been on Control IQ for over 2 years now with my Tandem x2 and Dexcom G6. My Endo was quite impressed since he was a Medtronic fan. He said the Sleep Mode alone improved my A1C. Control IQ is not perfect but it has made my life easier. I’ve been on my Tandem x2 for 4 1/2 years now. I’m on Medicare and can get a new pump every five years. At this point, unless something majorly different comes along prior to next April, I would most likely stay with Tandem and Dexcom. I’m a T1D of 38 years and a pump user for 23 years.

      1 year ago Log in to Reply
    17. pru barry

      I use Tandem’s Control IQ, and am grateful for all it does to keep things in range. After so many years before this improvement, I had become used to doing lots of bolusing, and now find it somewhat difficult to rely on the algorithm enough to let it work its magic. Still learning, and trying :*)!

      1 year ago Log in to Reply
    18. Janis Senungetuk

      Tandem’s Control IQ app has created a more stable glucose level then previous Animas pump, but 6.3 A1c is higher than previous years. After 67 years of lots of guessing it’s a definite improvement. I’ll continue using it until something better is available.

      1
      1 year ago Log in to Reply
    19. Randell Cole

      I use Tandem with Basal IQ

      1 year ago Log in to Reply
    20. LizB

      I have a Medtronic 770g & Guardian 3 sensors. The pump works fine, the sensors work fine, but I hate the algorithm so I stay in manual mode.

      1 year ago Log in to Reply
    21. Randell Cole

      I use Tandem with Basal IQ. Don’t know if I should try Control IQ or not, since you can’t
      Go back if it doesn’t work out.

      1 year ago Log in to Reply
    22. William Bennett

      Tried Medt 679G when it came out and gave up after 6 months. I was getting better TIR and AIc on my own and I liked the Dexcom 6 CGM vastly better than the Medt Guardian. I’m still too skeptical toward AID systems at this point to try again. Just doesn’t seem like a good fit for me.

      1 year ago Log in to Reply
    23. Randell Cole

      Randell Cole
      I use Tandem with Basal IQ. Don’t know if I should try Control IQ or not, since you can’t
      Go back if it doesn’t work out.

      1 year ago Log in to Reply
    24. Bea Anderson

      16 years Medtronic. New to OmniPod 5, dexcom. Stayed in Automated for 4 pods. I was impatient with algorithms and today left Auto to lower bg numbers and fine tuned settings.

      1 year ago Log in to Reply
    25. csreineke

      Loop
      #SleepLikeNormal

      1 year ago Log in to Reply
    26. Mary Ann Sayers

      My closed loop system gives me info on how well I calculated insulin/glucose usage hours/day before and how well my basal is covering. I DO question the length of time insulin stays active in me— it’s set for 5 hours, but I think it should be less.

      1 year ago Log in to Reply
    27. PamK

      I tried both Basal IQ and Control IQ with my Tandem, but found I get better blood sugars doing it on my own.

      1 year ago Log in to Reply
    28. Patricia H

      I use the Omnipod5 and the Dexcom G6 closed loop system that was recently approved by the FDA.

      1 year ago Log in to Reply

    If you use both an insulin pump and CGM, do you currently use any of the following automated insulin delivery (also known as “predictive low glucose suspend” or “hybrid closed loop”) algorithms to help keep your glucose in-range? Cancel reply

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