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    • 14 hours, 1 minute ago
      ConnieT1D62 likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I usually bolus for breakfast right at the time I start eating. But I prefer to bolus 15 minutes before. Better results. But I always forget.
    • 15 hours, 57 minutes ago
      KarenM6 likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I said 15-30, but it may have been more than 30. I wasn't watching the clock this morning. I just checked my pump bolus history. It was about 30 minutes. I need to bolus early in the morning because my blood sugars shoot up high after breakfast. Bolusing sooner seems to help keep my BG from going off the charts. But, if I bolus too soon, I have serious low BG's. It's all an art ... and luck.
    • 15 hours, 59 minutes ago
      KarenM6 likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I am able to pr bolus for Breakfast and dinner as I am at home. I never know when I am going to eat at work so bolus is at start of meal.
    • 18 hours, 50 minutes ago
      Mick Martin likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      Question is misleading until type of insulin is understood. I said 15 because I use Fiasp insulin.
    • 19 hours, 6 minutes ago
      Kris Sykes-David likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I said 15-30, but it may have been more than 30. I wasn't watching the clock this morning. I just checked my pump bolus history. It was about 30 minutes. I need to bolus early in the morning because my blood sugars shoot up high after breakfast. Bolusing sooner seems to help keep my BG from going off the charts. But, if I bolus too soon, I have serious low BG's. It's all an art ... and luck.
    • 20 hours, 3 minutes ago
      Ernie Richmann likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      I said 15-30, but it may have been more than 30. I wasn't watching the clock this morning. I just checked my pump bolus history. It was about 30 minutes. I need to bolus early in the morning because my blood sugars shoot up high after breakfast. Bolusing sooner seems to help keep my BG from going off the charts. But, if I bolus too soon, I have serious low BG's. It's all an art ... and luck.
    • 20 hours, 25 minutes ago
      Robin Melen likes your comment at
      When did you bolus for your most recent meal? If you bolused multiple times for your last meal, please select all that apply.
      My most recent meal was breakfast and, during the work week, I am far better at bolusing ahead of time. The rest of my meals in the day though end up receiving the bolus as I start eating or part at the start and more later on (depending on what I am eating and whether I know how much I'll eat.)
    • 1 day, 15 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...
    • 1 day, 20 hours 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.
    • 1 day, 20 hours 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.
    • 1 day, 20 hours 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.
    • 2 days, 16 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.
    • 2 days, 16 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.
    • 2 days, 17 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.
    • 2 days, 17 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
    • 2 days, 20 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.
    • 3 days, 15 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
    • 3 days, 17 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
    • 3 days, 18 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
    • 3 days, 18 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.
    • 3 days, 18 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
    • 3 days, 19 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
    • 3 days, 20 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!
    • 3 days, 20 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
    • 4 days, 7 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.
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    From which healthcare provider do you receive the majority of your diabetes care?

    Home > LC Polls > From which healthcare provider do you receive the majority of your diabetes care?
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    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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    32 Comments

    1. AnitaS

      A physician’s assistant who specializes in diabetes.

      3
      8 months ago Log in to Reply
      1. Gary Taylor

        Same here. There is no endocrinologist in my area.

        8 months ago Log in to Reply
    2. Jane Cerullo

      I answered NP because I usually see my Endo’s NP. This month see the doctor as his NPs keep leaving. I rally liked the NP I had for years but she left after having second baby. Saw her replacement once but he is gone now. Been going to this office for over ten years so too complicated to change now. Truthfully I take care of own diabetes. Need them for scripts mostly and labs.

      4
      8 months ago Log in to Reply
    3. Robin Melen

      I answered endocrinologist, but honestly most of my questions and concerns are answered in my every-other-month calls with my diabetes educator! She’s terrific!

      8 months ago Log in to Reply
    4. GLORIA MILLER

      I marked endo but I mainly go only because my insurance demands twice yearly visits in order to fill my prescriptions. I would not go otherwise since, after 66 years, I feel I can take care of myself regarding diabetes. When I was younger I stopped going to doctors for about ten years and I did just fine.

      2
      8 months ago Log in to Reply
    5. TEH

      My answer is really both. I see my Endo once a year and the other 3 times I see my PA. My Endo knows the physiological and the PA knows how to tweak the pump.

      1
      8 months ago Log in to Reply
    6. Merry Woolsey

      I answered Endo, however, if I don’t have one my primary care provider always “provides”.

      8 months ago Log in to Reply
    7. Steven Gill

      I’ve seen 5 endocrinologists (their specialty is the endocrine system/hormones, not necessarily diabetes) one said I was too old to need insulin and lose more weight. Another just ran tests and sent me on the way, at least the last got me on a pump/CGM. The only efficient one was at those medical trials, he taught me a good bit. For now I’ve been seeing a general practitioner although that may change.

      Am now retired and entering the VA health system, up to what’s required to follow up my care.

      2
      8 months ago Log in to Reply
    8. Liz Avery

      I answered NP as I see the nurse practitioner at my Endocrinologist practice.

      1
      8 months ago Log in to Reply
    9. Marsha Miller

      I see a Nurse Practitioner, but she specializes in Type 1 Diabetes.

      1
      8 months ago Log in to Reply
    10. Georgina Sokol

      Endo, but no longer. I have been TID FOR 58 years, and waiting for his majesty the endo for three hours in the office only to gave him cancel 2 out of 4 appointments a year is ridiculous ver. At this point, there is nothing the endo can tell me. This kast year I had a new pump that turned out to be faulty and was replaced. The whole time, the endo told me it was my imagination. I have had 5 endos in my life and they are not worth the frustration, lack of knowledge and waste of time driving an hour to get there, wait 3 hours to see him and then drive home for an hour. I am sooo disappointed in the general lack of attention and knowledge on the oart of endos concerning T1D’s. I have no faith left and will just rely on my GP for insulin prescriptions and reports to Medicare. My hA1C is consistently around 5.7. I do this myself with great control.

      1
      8 months ago Log in to Reply
    11. Lawrence S.

      I clicked “other” because I’m not sure what the person I see is. I go to the Endocrinology unit of a large hospital for quarterly visits. I always see a person who is an APRN, DNP. I have no idea what APRN means, but I believe the RN part means registered nurse. This hospital does not allow patients to select doctors or practitioners, the patient is assigned their health care providers. (This is a world renowned hospital).

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

        Advanced Practice Registered Nurse.

        8 months ago Log in to Reply
      2. Lawrence S.

        A DNP, Doctor of Nursing Practice, is a higher-education degree. Those who earn a DNP have completed the highest level of training in nursing practice. A DNP-prepared nurse has a deep knowledge of evidence-based care and the ability to apply this knowledge in practice. A nurse with a DNP degree can influence healthcare policies, take on administrative roles and provide clinical education for nursing programs. .

        8 months ago Log in to Reply
    12. Lee Johnson

      I have not found a competent endo doc for the last 15 years. Current one has a terrible staff which jeopardizes her reputation!

      8 months ago Log in to Reply
    13. spencercarter1

      Although I see my endo regularly, I also use Your Diabetes Insider consultant Ben Tzeel. He is amazing and provided so much insight. I’ve had T1D for 45 years and thought I knew it all, but once I started working with Ben, I realized I didn’t.

      1
      8 months ago Log in to Reply
    14. Katrina Mundinger

      I’ve been seeing the same endo for almost 30 years. There was one visit I had with a different endo when my insurance changed but then my insurance changed back. My endo is fabulous. He knows the pumps, knows their ins and outs, and ALWAYS talks to me like I’m a person.

      2
      8 months ago Log in to Reply
    15. Eva

      I’m not sure the question really captures all the different types of “diabetes” care that some type 1’s require. In terms of how insulin is absorbed relative to what I eat and how much, my endo provides most information. In terms of exercise, how much cardio and strength training I need for my organs to stay healthy given that I take insulin, my trainer would be the provider of that information. Examining the minerals, vitamins and how my body processes the food that I need (macros, sensitivities etc…) given the exercise that I preform, my functional physician is my go to provider. Each has a role to play in my diabetes care.

      8 months ago Log in to Reply
    16. Tom Rintelmann

      I’ve seen an Endocrinologist off and on my whole adult life but now I see only my knowledgeable Primary Care Physician. I study many aspects of my T1D and only see an Endocrinologist when a specific test needs to be run. My last three A1C tests have been 5.7 to 6.1.
      Tom R

      8 months ago Log in to Reply
    17. Thomas Cline

      I use my GP because I’ve found (from experience) that endo’s seem to be useful only for those who can’t or won’t manage their diabetes well. I get better/more information from the web. If I could find a knowledgeable endo who was a Type I diabetic themselves I might consider it — I truly believe it takes one to know one with this medical problem.

      1
      8 months ago Log in to Reply
    18. Jneticdiabetic

      The majority of my care comes from my certified diabetes educator who n is bc also a nurse practitioner at my local endocrinology office. I’ve found my diabetes nurses are often a bit more tech savvy and better able to give helpful advice on pump/CGM adjustments..

      8 months ago Log in to Reply
    19. Janis Senungetuk

      Since 2006 I’ve been under the care of an endocrinologist. The first one for 10 years until insurance coverage changed. The current one for the past 9 years. For the quarterly Medicare required appointments I alternate between the endo and the diabetes educator. They’re both very knowledgeable about all of the tech devices and treat me as a whole person, not just a disease with a number.

      1
      8 months ago Log in to Reply
    20. fletchina

      I see my endo more than my CDE, but my CDE provides the most valuable care/ recommendations/ suggestions for optimizing my BG control

      8 months ago Log in to Reply
    21. Daniel Bestvater

      My diabetes care has mainly been self inflicted. I’ve been a pharmacist-CDE for about 35 years. In Canada insulin, pumps and most diabetic products are nonprescription so it is very easy to try new insulins, cgms and pumps.

      8 months ago Log in to Reply
    22. Patricia Kilwein

      My Endocrinologist actually has a team. I receive care from Dr, educators, nursed and dietitian. Very awesome care!

      8 months ago Log in to Reply
      1. Patricia Kilwein

        Nurse

        8 months ago Log in to Reply
    23. George Lovelace

      My Endo and I “just click”, I am her “Pump Poster Boy” and she Fine Tunes my Numbers, last A1c’s were 5.4 and 5.6

      1
      8 months ago Log in to Reply
    24. Wanacure

      I don’t actually see her. We have phone appts.

      8 months ago Log in to Reply
    25. Lauren Carey

      I see my assigned endocrinologists PA. He is more knowledgeable and understanding about trying to live a normal life with T1D. The one and only time I actually saw my endo, he tried to make me change everything about myself, instead of working with me. I will keep seeing the PA as long as I can.

      8 months ago Log in to Reply
    26. Liadona

      I was originally diagnosed as T2 because I was over 40 and still produced _some_ insulin. I received care from my GP then. It was, however, a misdiagnosis and I am now properly diagnosed as T1 and receiving care from an Endo.

      8 months ago Log in to Reply
    27. mbulzomi@optonline.net

      I have been using an Endo. for many years, but he has a CDE staff that I see at least 3 hour’s a year. (Medicare)

      8 months ago Log in to Reply
    28. James Cheairs

      I do not use an endo though I am in good shape. I was finally able to find an Internal Medicine MD (with a focus on diabetes) that was willing to be both my PCP and Diabetes doc. I see her annually for T1D and general health. Otherwise we communicate via My Chart. She follows my lead on how to write my prescriptions for pump and insulin supplies which is simply fabulous and has made life easier.

      7 months ago Log in to Reply

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