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  • Activity
    • 17 minutes 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.
      Insulin, meters, diabetic tech are not magic wands. Its usage does not guarantee only "positive" results. Negative events can and do occur, period. Non -D- typically (incorrectly) equate negative events as being total user failure, severe user errors. As diabetics we get blamed, despite having made zero mistakes on our part. We make seriously educated best guesses, despite that truth, we can and do fail anyway sometimes! Outsiders falsely need to believe inulin, our tech are complete-total cures, rather than tiny bandages at best. When confronted for using (sic. my) "drugs" in public, no matter how invisibly done... it is their self righteousness , poor assessment which is the issue. I gladly squash such insects...
    • 5 hours, 18 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.
    • 5 hours, 19 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.
    • 5 hours, 20 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.
    • 1 day, 1 hour 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, 1 hour 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, 2 hours 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, 2 hours 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, 5 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.
    • 2 days 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, 2 hours 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, 3 hours 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, 3 hours 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, 3 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, 4 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, 5 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, 5 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, 16 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, 16 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, 16 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, 21 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, 21 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, 14 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, 14 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, 21 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.
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    Do you currently use any of the following insulin pumps?

    Home > LC Polls > Do you currently use any of the following insulin pumps?
    Previous

    Do you currently use any of the following CGM systems?

    Next

    Have you ever changed diabetes healthcare providers because you did not like their personality?

    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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    17 Comments

    1. Chip Brookes

      I have a Slim X2. Love the functions provided by Control IQ. I hate the method for installing the infusion set.

      3 years ago Log in to Reply
    2. Britni Steingard

      I answered both “Omnipod Dash” and “I do not wear an insulin delivery device” because I’m switching from Omnipod back to MDI later today. Gave it a year. Blood sugars didn’t improve and it’s often painful. Not worth the effort, but I will miss the food library and dose calculator.

      3 years ago Log in to Reply
    3. Gene Maggard

      Although the 670G was available when I upgraded my old Medtronic pump, I chose the 630G because it was covered under Medicare. I also hated the Medtronic CGM on my older pump, it was never accurate, gave me error alerts all night, and was constantly telling me to calibrate. Very happy with the 630G and Dexcom G6 combination.

      3 years ago Log in to Reply
    4. Kristen Clifford

      I still have a Medtronic 530G. The intention was to eventually switch me over to the 630G, but then before I knew it, the 670 was out. Now there’s the 770. I’m also contemplating an OmniPod or perhaps a T-slim.

      3 years ago Log in to Reply
    5. MARIE PEELER

      Husband is using the Tandem Tslim. Loves the Basal IQ function that keeps him from going too low during exercise. But we’ve deliberately not upgraded to Control IQ as it sets the target BG too high for people who already maintain tight control and can makes it impossible to achieve the same A1C and time in range.

      3 years ago Log in to Reply
    6. Thomas Hatton

      I just upgraded from 670G to a 770G, 3 weeks ago on the lift ticket program. I tried to trade in my 630G for the 770G but they objected to that. I wanted to keep my 670G as a back up. Looking forward the software upgrade to 780G with bolis capability.

      3 years ago Log in to Reply
    7. Nevin Bowman

      I’ve been using Medtronic for around 18 yrs, but I will be switching as soon as my insurance allows. They were innovative with pumps, but their CGMs have always been lacking in accuracy, and they are nowhere close to being reliable enough for me to trust it to give me insulin.

      3 years ago Log in to Reply
    8. Trina Blake

      I’m with Marie Peeler’s husband. Tandem X2 with Basal IQ. Same reasons he stayed with BIQ; Control IQ settings are higher than I want, I too have tight management. I’ve used Animas and the Cozmore in the past.

      3 years ago Log in to Reply
    9. William Bennett

      I switched from my Medt Paradigm 730 (the old pager-style pump) to the 670G when it came out, but after 6 months I gave up and went back to my 730. Hated the over-complicated and less accurate Guardian sensors, was getting much better results with my old Paradigm and Dexcom G6 CGM than the frustrating hybrid algorithm could produce, and it kind of soured me on the whole idea of AID pumps in general. Now I’m up for a new pump again, but the old Paradigm is still ticking along, and neither the 770/780G nor the Tandem system seems particularly attractive (I really dislike the fussy overcomplicated Tandem reservoir system).

      3 years ago Log in to Reply
    10. Sherolyn Newell

      I have Omnipod and Dexcom G6. I tried to switch to Dash, but the way they set it up for insurance purposes, BCBS wouldn’t cover it. I am looking forward to seeing what their closed loop system with Dexcom G6 is like.

      3 years ago Log in to Reply
    11. kamiandcrew

      I just started on the 770G 3 days ago. I was on the 670G. I like that it automatically downloads. The CGM transmitter was problematic when I first started but once I found a better way to secure it I’m happy with the results (no excessive calibrating, no uncontrolled highs , good correlation between fingerstick and reading, plus my A1C is the best it’s ever been)

      3 years ago Log in to Reply
    12. John McHenery

      I was on Paradigms for ~8 years and last year switched to Medtrum’s patch pump and sensor as I liked the idea of the sensor and pump coming from the same supplier. Bad idea and switched about 6 months later to the Ypso pump and Libre sensor.

      3 years ago Log in to Reply
    13. Molly Jones

      I currently use Tandem X2 with control IQ. I tried Medtronic 670G on a short trial almost three years ago after a decade of their other products, and a version of Omnipod in 2016. I like the idea of Omnipod the best. I use tandem as it partners with Dexcom.

      3 years ago Log in to Reply
    14. Patricia Maddix

      I have used Medtronic pumps since 1997 and currently have a model called the 723. This was actually a replacement for my 523 that died two years ago. Because of the timing of my warranties and Medicare regulations I have never been eligible for one of the more automated systems until now as my 723 is out of warranty. In the past I too struggled with in accurate readings from the Medtronic sensors and switch to Dexcom many years ago. I have been really on the fence as to which pump to choose next and I’m just staying with my current pump for now as it is working fine. I understand that tandem is going to be coming out with a new pump called the sport that is half the size of the current X2 and is operated either from a remote device or phone app. I am visually impaired and would really like a pump that could be controlled entirely or almost entirely from an accessible phone app. That feature seems to be on the near horizon so I am hanging tight.

      3 years ago Log in to Reply
    15. Leona Hanson

      I use medtronic 630 it works very well with high altitude

      3 years ago Log in to Reply
    16. Carlene Vaitones

      I prefer injection therapy. I have more control over my BGs, and no occlusions leading to lack of insulin coverage.

      3 years ago Log in to Reply
    17. Sally Numrich

      Tandem IQ and I love it! I spend so much less time thinking about my diabetes because the pump turns off if I am heading down! My glucose tablet usage has been reduced and my mental well-being has been great! I don’t test anymore and I can’t even tell you if the numbers are close because I don’t care. The pump just does its thing and I can go all day without looking at my pump if I’m not eating. Been pumping since 1990 and had 3 pumps in the first 20 years with Minimed/Medtronic. Never had any problems with them. I tried Omnipod during a trial, not my favorite due to kinking problems & only one length on length of needle & much bigger than I liked on my body parts. Made the switch to Tandem mainly due to how little Medtronic had made changes. The few times I upgraded, the changes were not that big a deal. And now with a pump that lets me not think, why change?! Of course my next trial is iLet pump and that is my dream because I won’t have to count carbs!

      3 years ago Log in to Reply

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