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    • 1 hour, 1 minute ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      I want a thumbs down icon!
    • 1 hour, 1 minute ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      I seldom have any questions other than RX refill request which I submit through the patient portal. If I do have treatment questions, I typically do my own research, and if not satisfied with what I find out, I submit a question in the portal.
    • 1 hour, 1 minute ago
      Kathy Hanavan likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      When I come up with a question between visits, I usually just do some research.
    • 3 hours, 14 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      I keep my opened insulin in the refrigerator too. When traveling I use a FRIO evaporative pouch.
    • 3 hours, 15 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Sorry. Of course I store unopened in frig. Opened in my room as I use it up in 30 days
    • 3 hours, 15 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      No, I keep it in the oven! ;) Same answer as the last time they asked this ridiculous question!
    • 3 hours, 58 minutes ago
      Becky Hertz likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Unopened yes, and now even opened just in case. I am getting a new health [lan (thank goodness a much better one - with better doctors and hospitals in network!) so it's worth it. But I can't get any appt - even for a PCP until September. I've been occasionally buying out of pocket insulin, pump and CGM supplies (in my mind, hoarding is a character asset for T1D people). I need to have my enough stuff to see me through, Of course, I am hoping there''s an appt cancellation.
    • 5 hours, 21 minutes ago
      Bruce Schnitzler likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Unopened yes, and now even opened just in case. I am getting a new health [lan (thank goodness a much better one - with better doctors and hospitals in network!) so it's worth it. But I can't get any appt - even for a PCP until September. I've been occasionally buying out of pocket insulin, pump and CGM supplies (in my mind, hoarding is a character asset for T1D people). I need to have my enough stuff to see me through, Of course, I am hoping there''s an appt cancellation.
    • 7 hours, 18 minutes ago
      alex likes your comment at
      Here’s What You Need to Know About the Dexcom G7
      This article explains the Dexcom G7 features in a clear and easy way, especially for people new to continuous glucose monitoring. Very informative and helpful. Sportzfy TV Download
    • 22 hours, 41 minutes ago
      KarenM6 likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      Long time ago - told there were certain occupations I would not be allowed to do because if T1D. Pilot, air traffic controller, military, etc.
    • 22 hours, 43 minutes ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I have been told many times "YOU CAN'T EAT THAT!" ONLY to frustrate them and eat it anyway and then bolus accordingly.
    • 22 hours, 44 minutes ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I think it is a common experience for most people with T1D. People do not understand anything about it. I do not take it personally. I try to educate when appropriate.
    • 22 hours, 44 minutes ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Lol hell when haven't they. Lol
    • 22 hours, 53 minutes ago
      KarenM6 likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was only 2 when Diagnosed 70 years ago. My small town doctor admitted he didn't know much about T1D, and fortune for my parents and I he called what is now Joslin Clinic, and they told him how much insulin to give me. He taught my parents, who then traveled over 350 miles to Boston, to learn about how to manage T1D. My doctor learned more about T1D, and was able to help 2 other young men, that were later DX with T1D in our small town. I went to Joslin until I turned 18 and returned to become a Joslin Medalist and participated in the research study, 20 years ago. Still go there for some care.
    • 1 day ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was 7 when things changed in my home. My older brother was hospitalized for 2 weeks. When he came home, we no longer ate the way we had before. This was 1956. Dessert alternated between sugarless pudding or sugarless Jello. I learned that bread and potatoes had carbohydrates and that turned to sugar. There was a jar in the bathroom. It seemed my brother was testing his urine every time he went in there. There was a burner and pot on the stove designated for boiling syringes. I watched my brother give himself shots and I remember how hard it was to find someone to manage his care if my parents had to travel. Diabetic Forecast magazine came in the mail each month and there were meetings of the local diabetes association that my mother attended religiously. My brother got a kidney and pancreas transplant at age 60 and before he died lived for 5 years as a non-diabetic. A few years later I was diagnosed. Sorry he was not able to make use of today’s technology. I often wonder what he and my late parents would think about me, at age 66, being the only one in the family with type 1.
    • 1 day ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day, 4 hours ago
      kilupx likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      My brother was type 1 since an early age. I was only diagnosed in my late 40s
    • 1 day, 6 hours ago
      Phyllis Biederman likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Absolutely nothing. Diagnosed in late December 1962 at at the age of 8 years and was told I was going for a stay in hospital because I have "sugar diabetes".
    • 1 day, 7 hours ago
      Bill Williams likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day, 8 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was diagnosed in 1976 at the age of 18 while in college. One weekend, I was drinking a lot of water and peeing frequently. I remembered having read a Reader's Digest article on diabetes, and I told my friends I thought I might have it. Two days later, the diagnosis was confirmed.
    • 1 day, 8 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Absolutely nothing. Diagnosed in late December 1962 at at the age of 8 years and was told I was going for a stay in hospital because I have "sugar diabetes".
    • 1 day, 8 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I knew I couldn’t or shouldn’t have my two fav things in the world: Pepsi cola and chocolate. I was 42, and suspected very strongly that I had it, and ate a large piece of chocolate cake before my doctor’s appointment (sounds more like I was 12). Fast forward 25 years later: I never had a real cola again, but do occasionally have chocolate. I’m way healthier than I was back then in terms of diet. I no longer have irritable bowel, and I’m lucky to be able to afford what I need to combat the ill effects of this chronic disease. I’m blessed, and grateful for insulin.
    • 1 day, 8 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      It was 35 years ago for me. I had no experience with T1d. I was starting to show symptoms and my sister-in-law quickly researched T1d and told me what she found. I went to my GP a week or two later. My BG was over 600. He sent me to the hospital right away. Blood test confirmed it.
    • 1 day, 8 hours ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I only knew a little . That is why I give grace to others who do not know anything or have misconceptions.
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    If you have (or your child has) experienced diabetes burnout (feeling run down and not managing your diabetes in the way you normally would), how do you usually handle it? Select all that apply.

    Home > LC Polls > If you have (or your child has) experienced diabetes burnout (feeling run down and not managing your diabetes in the way you normally would), how do you usually handle it? Select all that apply.
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    Have you ever asked a stranger in public for help with hypoglycemia or hyperglycemia (for example, asking someone for a snack, to stay with you, or help in some other way)?

    Sarah Howard

    Sarah Howard has worked in the diabetes research field 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 Marketing Manager at T1D Exchange.

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    22 Comments

    1. Tina Roberts

      This is and has been a real problem for me. I haven’t figured it out yet and the damage it will do seems to not deter it.

      2
      2 years ago Log in to Reply
    2. Lawrence S.

      I do feel overwhelmed at times about the continuous 24/7/265 relentless care of my T1D, Celiac disease, Asthma, etc. etc. ; especially when my blood glucose is all over the place. Mentally, high blood glucoses bother me more than lows. What works for me is to push myself through. I know it’s not going to change, so, if I want to live, I have to do what is necessary. I don’t take “breaks” or “vacations” from my diabetes. That’s just denial, in my eyes, and does not resolve anything. I work on correcting my blood glucoses, and keep myself busy. The feeling goes away because I’m focused on a task.

      2
      2 years ago Log in to Reply
    3. Jeff Marvel

      Issues with highs are much more frustrating, in which case rather than ignoring/not treating the high with insulin, I’ll “treat” it instead by fasting or skipping my next meal. Immediate relief in that I don’t have to think through all the things that could be messing up (bad infusion site, stress reactions, just an “off day”), though disordered eating isn’t a great option in the long run. It can take the pressure off without feeling too irresponsible, though.

      2
      2 years ago Log in to Reply
    4. KIMBERELY SMITH

      I will let different people know

      1
      2 years ago Log in to Reply
    5. Ahh Life

      Rather than “burnout”, how about as one definitive dictionary indicated the attributes of:

      1. Heavy workload
      2. Lack of control
      3. Unrealistic expectations
      4. Lack of support
      5. Unhealthy lifestyle

      We all experience all of these. Each is addressed differently. Unrealistic expectations is the one I handle best. 100 BG? Meh. 80% TIR? Meh. Life and accidents happen with unmitigated regularity. 😁

      4
      2 years ago Log in to Reply
      1. Edward Geary

        I agree that “burnout” is an overused term. As a former HR professional, I dealt with “job” burnout frequently and the options available such as training, transfer, severance, etc. Diabetics can’t walk away from their. Diabetes, however, I’ve found many Type 1s incredibly resilient and bounce back. Thanks for sharing.

        2
        2 years ago Log in to Reply
    6. KCR

      I don’t think I have experienced diabetes burnout, when I am really not taking care of myself, but definitely have felt diabetes distress (frustration, fatigue, and low mood). Talking with family and friends, posting concerns or questions in the online D forums, and mindful breath practice all help relieve my stress.

      1
      2 years ago Log in to Reply
    7. Jane Cerullo

      Was just on a cruise and my new Dexcom’s failed. Used finger sticks and was somewhat liberating. Didn’t check until InPen said 0 insulin on board. And of course ate things I usually don’t. Diabetes type 1 is a pain to deal with

      6
      2 years ago Log in to Reply
    8. Edward Geary

      I call it a diabetes reboot. Essentially, getting back to basics. Outside help is always welcome, however, after 49 years it’s up to me to take charge and solve the problems. Peer support is emotionally helpful as my fellow T1Ds will attest because there is no substitute for personal experience.

      3
      2 years ago Log in to Reply
    9. Bill Williams

      I don’t do much of anything. After 63 years of it, I know that the situation/mindset/whatever will improve shortly. If I’m higher than I’d like for a couple of days, it’s just not a big deal. After all, I’ve been playing with house money for a very long time.

      6
      2 years ago Log in to Reply
    10. Trina Blake

      I guess it’s my personality – I like being responsible for things, I’m detail oriented, take pride in my T1D mgt (I take get great joy in proving healthcare providers wrong (their low opinion of patients with D of any kind). Chances are, my “Spouse with Bipolar1 and Anger Mgt issues burnout” that shows up more often. Could that be a perfect distraction?

      2 years ago Log in to Reply
    11. Amanda Barras

      Be more intentional.
      But, also, I had a period where I had no insurance and the stress of that, and not having the insulin and supplies I needed made life a huge challenge.

      1
      2 years ago Log in to Reply
    12. TEH

      I just deal with it for the majority of the time. Infrequently, I can have a down day. When that happens, as others have noted, I review what happend and consider what I could have done better. I make notes in my phone and look them over and see what I can change. Over the following days I consider what theae changes.

      1
      2 years ago Log in to Reply
    13. Audrey Coleman

      I am going through that now. I “forget” to bolts for meals. I am trying to find a counselor to speak with but everybody is booked solid and tell me they will get back to me. My control is usually pretty tight. Husband dislocated his shoulder so more is falling on me and I have a bunch of my own physical limitations. We are both 78 years old. Live rural and cannot find people to help. Can someone recommend one of the Diabetes chat groups. Husband has no idea what one goes through to manage this disease. I am almost at the 50 year mark living with T1D.

      2 years ago Log in to Reply
      1. jamesmpii

        There are many groups on Facebook. I am a member of several. Join a few and check them out. All at least offer support and a multitude of answers to questions.

        2 years ago Log in to Reply
    14. Gordon Jones

      Isaiah 26:3 Tells me, “Thou will keep him in perfect peace whose mind is stayed on Thee because he trusteth in Thee.”

      2 years ago Log in to Reply
    15. jamesmpii

      like several who have posted comments, I am gong through it now. I don’t have any answers. Reading the comments is a start.

      1
      2 years ago Log in to Reply
    16. Chris Albright

      I feel sorry for myself for a few hours/day and suck it up and get back to my goals and diabetic health plan.

      2 years ago Log in to Reply
    17. ConnieT1D62

      Focus on other things in my life that bring me joy WHILST handling my diabetes self-care obligations with self-compassion and gratitude that I have so many resources that make living with T1D so much easier these days than when I was first diagnosed in 1962. When BGs get out of control, I problem solve to figure out why, and pick myself up, dust myself off and start all over again.

      2 years ago Log in to Reply
    18. T1D4LongTime

      My first step is to analyze all available data on Dexcom and Tandem to determine a logical reason for the problem, especially if I see patterns in the data. 98% of the time, stress is the problem for highs. I have high stress due to caregiving 2 older people as well as myself. I do a lot of research on Mayo Clinic, Cleveland Clinic and Joslin sites as well as some of the other medical sources. My husband has also been a gem in listening to me talk out the problem (he does a lot of “yeah…. ok…. I see” and nodding LOL!). He is having health problems now too, so I’ve had to turn to yoga, walking, and mindfulness exercises to keep stress under control. I will admit….. severe burnout causes me to indulge too much, bolus appropriately and ignore the alarms for a few hours….. 😉

      2 years ago Log in to Reply
    19. Jeff Balbirnie

      Grim bitterness?! Whatever usually handling means (by your definition) apparently does not work or is not working. I have zero honed or effective tools for this diabetes “Groundhog Day” routine. A cycle which never ends…

      2 years ago Log in to Reply
    20. Anita Stokar

      There may be days where I don’t track my sugar levels as closely as other days, but I never really considered myself having burnout.

      2 years ago Log in to Reply

    If you have (or your child has) experienced diabetes burnout (feeling run down and not managing your diabetes in the way you normally would), how do you usually handle it? Select all that apply. Cancel reply

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