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    • 9 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.
      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...
    • 14 hours, 1 minute 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.
    • 14 hours, 2 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.
    • 14 hours, 3 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, 10 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 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, 10 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 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, 10 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, 10 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, 14 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, 9 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, 11 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, 11 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, 12 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, 12 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, 13 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, 14 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, 14 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
    • 3 days, 1 hour 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.
    • 3 days, 1 hour 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.
    • 3 days, 1 hour 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!
    • 3 days, 6 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.......
    • 3 days, 6 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, 23 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, 23 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.
    • 4 days, 6 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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    How comfortable are you having open and honest conversations about your health and T1D management with your main T1D health care provider?

    Home > LC Polls > How comfortable are you having open and honest conversations about your health and T1D management with your main T1D health care provider?
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    For people who use multiply daily injections as their primary method of insulin dosing, how many injections do you typically administer in one day?

    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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    20 Comments

    1. Steven Gill

      I’m very confident with my knowledge, after 25 years I cutest a variety of studies, obtain both professor ups literature and those geared towards the diabetic. Likewise I’ve experienced less than par care and understand those concerns from them as well.

      3 months ago Log in to Reply
    2. Ahh Life

      Physicians are great at diagnosis. Me? I’m a 1% -er, even with Google scholar.

      Or as a urologist recently told my wife, “You describe. I diagnose..” My wife struggled with that considerably as she was convinced she knew what was wrong with her. C’est la vie. 🤷🏼‍♂️🤷🏼‍♂️🤷🏼‍♂️

      3 months ago Log in to Reply
    3. ConnieT1D62

      Very comfortable for the most part. The endocrine provider I worked with to co-manage my diabetes retired as of June 1st. We prepared for the transition to a new provider during the past year where I saw her every other visit and the new provider on the other every other visit. I was with her for 22 years … and I am very comfortable and compatible with the new endocrine provider who has taken over in her place.

      1
      3 months ago Log in to Reply
    4. Jeff Balbirnie

      Regardless of my “willingness”, they are NOT interested on any level. Not number, they are not interested, hard stop.

      1
      3 months ago Log in to Reply
    5. Jane Cerullo

      Have known my Endo for ten years and am comfortable discussing my diabetes and Graves’ disease with him. Also went to an NP for about four years and liked her also. She left after having a baby. I’m a nurse and I make a list of questions I may have before I my appointment. I keep up to date with new diabetes information and products and will bring to his attention. We will discuss what approach is right for me. The NO didn’t think I should go back to MDI because my A1c was so good but I said I would try for three months. Have been very happy with MDI for two years and my numbers are stable. I find it freeing. No tubes attached. Also would be nervous of the new pumps that make all of your decisions for you.

      3 months ago Log in to Reply
      1. Jian

        I was nervous also and am an RN CDE but I will say I did it in two steps basal iQ and then control IQ and to tell you the truth it does do a better job of my A1c and time in range than I ever had in 44 yrs. plus I can forget about it really when I am out and about. and I don’t carry my meter with me – just use it when I think there may be a difference, especially the first day of the sensor.

        3
        3 months ago Log in to Reply
    6. Lawrence S.

      I answered “moderately comfortable.” I am very open regarding my diabetes issues with my Endo (APRN). However, I know that she is very busy and on a tight schedule. So, I try to stay on point.
      In my case, unfortunately, I have a very long list of maladies; mostly related to my T1D. My Endo does not have the time for discuss my many health issues with me.

      2
      3 months ago Log in to Reply
    7. Louise Robinson

      After 46 years with Type 1 with the past 20 years in excellent control, I feel I know a great deal about managing my diabetes. But, aging with diabetes presents additional challenges. I see my endo every 3 months because Medicare mandates that in order to approve pump supplies. I saw my endo this week and expressed concern that during the past month my control had been slipping with more frequent and unexplainable highs and lows. Part of that may be caused by the beginnings of gastroparesis since I have been dropping to hypo after taking a meal time bolus and then rising precipitously an hour or more later. My A1c was 5.9 which was better than I had expected. Because my control showed 86% in range for the past month (where prior results were in the mid-90’s) she felt she couldn’t do anything to improve me results. I’ve been having insulin absorption site issues on Day. When I asked her about trying out a steel vs plastic cannula, she told me I should call the manufacturer to see if I could obtain sample to try. I’ve only been seeing her since January 2022 but may need to seek other alternatives. She also wasn’t very optimistic about obtaining Medicare re-approval for changing my sites every 2.5 days vs every 3 days. Medicare approval relies upon her clinical notes of my visits. Mid-year last year, we had obtained that approval but it has since lapsed and needs to be re-justified. Anyone else here who has maintained good to excellent control feel that they are not receiving the attention from their doctor that they should get?

      3 months ago Log in to Reply
      1. Lawrence S.

        For what it’s worth. I deal with gastroparesis. I find that using extended boluses helps a lot. I don’t get the lows after I take my insulin.

        3 months ago Log in to Reply
    8. Modee

      The question is how comfortable is she at HEARING it!!!!!

      3
      3 months ago Log in to Reply
      1. Jeff Balbirnie

        Hearing “it” pre-supposes they actually LISTEN…. ; )

        3 months ago Log in to Reply
    9. Jillkdubois

      I have a hard time communicating with endocrinologists, I have been through 5 since diagnosed 8 years ago (4 through Kaiser) I don’t think they listen to what you’re struggling with, and they definitely are not equipped to deal with the mental side of T1D. I left appointments in tears when first diagnosed. The formulas for carb to insulin were not working for me, I was going low all the time and figured they knew best, but they are guessing the same as I was. I was told by a nurse in one of the offices that the doctor I was seeing was a good doctor, but with a focus on thyroid issues, not diabetes.
      When I have appointments now I just tell them what they want to hear, I’ve learned to control my blood sugar pretty much on my own, through lots of trial & error. I just need them for the prescription.
      I know what I’m saying is harsh, but at least in Denver, I haven’t found a good endo who will listen.

      4
      3 months ago Log in to Reply
      1. Jeff Balbirnie

        Brief grim smile. Not harsh in the least. They have zero training nor any interest in the mental aspects (Medicine is far more art than science). If they helped us with the mental pieces the physical would be very easy because we had the mental tools, skills, techniques to deal with whatever the physical issues might be/become. Just saying….

        1
        3 months ago Log in to Reply
      2. Lawrence S.

        I once saw an Endo who told me that he specializes in Thyroid, not Diabetes. I only saw him once. But, I hear your frustration. You need someone who will spend time with you and do followup on the phone or video. Perhaps, a Diabetes Educator, and or Diabetes Nutritionist might be helpful. You also need to find the doctor who fits your needs. Don’t give up.

        1
        3 months ago Log in to Reply
    10. Eva

      Absolutely, I feel comfortable talking about my overall health and T1D management with my endo. I have seen him for the last 25 years. I’m so well controlled that he has his PA see me 3 times a year and I only see him once (usually) just to get an overall review of how I am doing. I just feel that because he treats endocrinological diseases, he only has a very specialized, narrow perspective about “health.” So, if need to talk about women’s health, I go to my OBGYN. If I need to talk about my muscles, ligaments ect.. I go see my exercise physiologist. For my eye health, I see a ophthalmologist. But if any issues arise with any of my other body parts, my endocrinologist is first to know.

      1
      3 months ago Log in to Reply
    11. Janis Senungetuk

      Until very recently, I was very comfortable discussing glucose management with my endo of 8 years. My appointment last month was not as comfortable for a variety of reasons. She was very rushed, which put constraints on discussing concerns I had. I was not pleased with an insurance decision that moved coverage of my CGM from DME to pharmacy benefit, only to learn that endo physicians had recommended it. I also wasn’t thrilled regarding an HMO sudden change that limited the use of MyChart to message healthcare staff. Charges are now applied for all staff time in replying. She defended that change and that’s how the appointment ended.

      3 months ago Log in to Reply
    12. Molly Jones

      I am comfortable talking about my concerns and hearing them openly discuss possible issues and be honest with me about not knowing what the definite causes are.
      I like going to a University hospital and trying to stay up to date with current medical hypotheses.

      3 months ago Log in to Reply
    13. Jneticdiabetic

      I’m extremely comfortable having frank discussions with my doctor. I figure I will get better advice if I’m transparent. I admittedly approach my visits a bit like a confessional… Recapping my BG mgmt challenges and what I think I can do better to improve them (e.g., I get busy at work and often forget to bolus before eating, this results in hours above range). It’s not forgiveness I’m seeking, but sound medical advice. At my last visit, my doctor mentioned some recently released and upcoming pump technology that might help and sounds promising.

      3 months ago Log in to Reply
    14. sweetcharlie

      VERY comfortable !!!!!

      3 months ago Log in to Reply
    15. Glenda Schuessler

      I am grateful to have had the same Endo since 1996. What a blessing to have this long term care relationship. He challenges me, teaches me, keeps me moving forward with the best care for me.

      3 months ago Log in to Reply

    How comfortable are you having open and honest conversations about your health and T1D management with your main T1D health care provider? Cancel reply

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