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    • 14 hours, 42 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.
    • 14 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 have been told many times "YOU CAN'T EAT THAT!" ONLY to frustrate them and eat it anyway and then bolus accordingly.
    • 14 hours, 45 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.
    • 14 hours, 46 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
    • 14 hours, 54 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 ´ )⎠⎞
    • 16 hours, 46 minutes 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.
    • 16 hours, 47 minutes 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.
    • 16 hours, 49 minutes 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 ´ )⎠⎞
    • 20 hours, 49 minutes 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
    • 22 hours, 52 minutes 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".
    • 23 hours, 37 minutes 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 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 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 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 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 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.
    • 1 day ago
      Lawrence S. 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
      KCR 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 ago
      Gary R. 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
      ConnieT1D62 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
      eherban1 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, 12 hours ago
      NANCY NECIA 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.
    • 1 day, 15 hours ago
      Anita Stokar likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I won't use the word "diabetic" as a noun. It's as simple as that, an adjective, yes. I didn't refer to a good friend with MS as a "sclerotic". When I was working with first responders, I tried to remember to say "schizophrenia is involved", or "there's alcoholism at play here".
    • 1 day, 15 hours ago
      Anita Stokar 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.
    • 1 day, 15 hours ago
      Anita Stokar likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      No one has said (in seriousness) you can't eat that, but I have gotten the question "Can you eat that?"
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    Did you learn anything new about T1D in 2020? Share what you learned in the comments!

    Home > LC Polls > Did you learn anything new about T1D in 2020? Share what you learned in the comments!
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    Do you (or your loved one with T1D) have seasonal affective disorder (SAD)?

    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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    29 Comments

    1. Bob Durstenfeld

      Using overnight insulin control to set basal rates and how to use time in range.

      5 years ago Log in to Reply
    2. Gustavo Avitabile

      Steps forward in research about suppressing the autoimmune process

      5 years ago Log in to Reply
    3. Elissa Macher

      I learned that I can keep my blood sugars normal by avoiding carbs as much as possible. I also have lost weight as a result and use very little insulin.

      5 years ago Log in to Reply
    4. Jana Wardian

      I learned that about 60% of people with T1D are diagnosed in adulthood.

      5 years ago Log in to Reply
    5. Jonathan Strait

      I learned getting excited/stressed by simply watching your kid’s football game releases cortisol and adrenaline which can spike sugar levels!! I kept spiking during games and couldn’t figure it out 😂

      5 years ago Log in to Reply
    6. connie ker

      I learned that time in range was just as important as the A1C number. They are both important but before cgms, we couldn’t see time in range as well. Happy New Year to all of the type 1s from a 72 year old woman with LADA for the past 23 years. Husband was a juvenile type 1 and one adult child is also a juvenile. 3 under the same roof for awhile; now my grand dog is a diabetic on insulin, wore a freestyle libre at first, and has had cataract surgery! I learned vets treat diabetes too and vet opthamologists are expensive and hard to find!

      5 years ago Log in to Reply
    7. Kathy Hanavan

      I learned about Control IQ and how to make work arounds when it does not work the way I want.

      5 years ago Log in to Reply
    8. Gene Maggard

      I learned two things: (1) As others have said, Time in Range is more important than A1C, since the latter can be affected more from the lows and I always seemed to go low a lot, even with my CGM. And (2) It’s ok to be out of the 80-120 range as long as I’m keeping in the >80% TIR value. In the past trying to keep within that tight range pretty much ensured I would always gravitate to lows.

      5 years ago Log in to Reply
    9. Mara Pentlarge

      I started using Afrezza, the fast acting insulin that I inhale. The last doctor visit I had before the March shut down was to the pulmonologist to have the test to see that my lungs work well enough to use this insulin (no problem). I only use it when my blood sugar won’t come down after a few boluses from my pump. But then I need to pay attention because sometimes the numbers come down really quickly.

      5 years ago Log in to Reply
    10. Bill Marston

      I learned of a wider range of even just Type 1 diabetes sub-types and the several different varieties of broken gene pieces(!) in the context of T1D-social media. For example a couple of Facebook T1D group surveys of “will you take the COVID-19 vaccine”, revealed a minority whose reluctance and/or concerns were the range of comorbidities beyond ‘merely’ pregnancy – allergies, Lupus, etc. Hooray for bioscience research!

      5 years ago Log in to Reply
    11. Patricia Dalrymple

      I learned a lot from other subscribers on glu. I’m not learning as much from others on this site and on my phone can no longer read ALL the comments. It only shows me the last few. I too learned TIR is more important and don’t know why meters don’t calculate those like they do averages. Should be pretty easy to program.

      5 years ago Log in to Reply
    12. Patricia Dalrymple

      Says are 11 comments but I can only view the last 6 on my XR iPhone that is only a couple of years old. What’s up with that? How can I learn from others if I can’t see the comments? I am on my laptop 55 hours a week for work. Don’t feel like seeing if I can get to more comments on the laptop. I’m done with that in off hours.

      5 years ago Log in to Reply
    13. keith johnson

      Alarm fatigue is a real thing relating to medical decides ( GGM/PUMPS). I thought I was being overly sensitive.

      5 years ago Log in to Reply
    14. Jose Almodovar

      If COVID-19 hits you, confirmation is uncontrolled high blood glucose levels. Even before the results are back.

      5 years ago Log in to Reply
    15. George Hamilton

      I have to new discoveries: 1. Control-IQ works better to produce stable BG levelsthan anything I have tried before. 2. For me, as I grow older I find that very small changes in activity level (it does not have to be even light exercise) produces quick changes in BG level. I started using Control-IQ in May, 2020 with good results. My biggest challenge is to be patient with it so that I receive full benefits. I have spent years trying to manage my own insulin and carb interaction to adjust for ups and downs. Control-IQ provides a more finely tuned result than I can, but I have to wait for the adjustments to take effect, Then it is great. On the activity level question, I find that shifting from desk work to even 10 or 15 minutes of food prep or other household activities will trigger a drop in BG level. (I am 78 years old. Diagnosed at age 20. I did not have such swings in BG from light activity even 5 years ago.

      5 years ago Log in to Reply
    16. Kristine Warmecke

      Nothing about T1D. A lot about how to control T1D. Which is what the question ask.

      5 years ago Log in to Reply
    17. Mig Vascos

      I learned to use Control IQ. It’s fantastic for night time. During the day it helps, but waiting for adjustments to work takes forever. I keep my pump on sleep mode, that way it strives to keep the glucose at a lower level than when it is at the standard setting. It has also help me determine that if my glucose levels are not as they’re supposed to by my food intake and insulin on board, it has nothing to do with the insulin going bad in the cartridge, it has to do with the infusion site not absorbing the insulin well. So now all I do is get a new infusion set but do not replace the cartridge if it still has more than half the insulin I originally put in. I also agree with another contributor that the way this site is set up now, it doesn’t allow us to see all the answers. It’s also more complicated to sign in. Why do all the sites push us to sign up thru Facebook or Google when we can sign up directly to the site. It takes longer.

      5 years ago Log in to Reply
    18. Maureen Helinski

      I have been using Control IQ and love it but as others said it takes getting used to. A tiny bit of activity-putting out trash etc.-can send me low. A correction doesn’t show up immediately so I put in a fake BG-85-to not have another alarm. All other alarms are turned off.

      5 years ago Log in to Reply
    19. Becky Hertz

      Strategies for bg management from TCOYD web conferences. In particular how to bolts for the different arrow configurations going up. Very helpful.

      5 years ago Log in to Reply
    20. Bekki Weston

      Added Afrezza to my tool box. Helpful with stubborn highs. Also, I’ve had a Dexcom for about four years, and just started using its Clarity program. Really like ability to see Time in Range. Keep learning, everyone!

      5 years ago Log in to Reply
    21. Jeff Perzan

      Consistently, Medtronic Guardian sensors glucose readings have a bias towards numbers lower than blood glucose readings.

      5 years ago Log in to Reply
    22. Stephen Woodward

      This year I’ve joined several d product and T1D Facebook groups. The thing that seems to have never changed, even with the new technology, is that the lack of direct support and education about managing T1D is still causing a lot of suffering and killing us. Facebook can be very helpful, however, the abundance of misinformation and negativity comes from those who think they’re right or know the facts.

      5 years ago Log in to Reply
    23. Patricia Maddix

      I have learned that with even more accurate blood glucose information I’m able to greatly decrease my hemoglobin A-1 C and improve my time in range. A year ago Medicare allowed us to get the Dexcom G6 which gives much more accurate information and when you are using more accurate information to make dosing decisions you’re going to get a lot better results. I also started using a More accurate blood glucose meter for win I need to double check the Dexcom This year I also researched all of the major insulin pumps and continuous glucose monitor systems on the market to understand them more completely as I am going to have to be getting a new insulin pump soon. Although all the new technologies for type one diabetes are fantastic, I learned that all of the alarms and alerts and hands on things that you have to do are very stressful. I am involved in a number of diabetes related social media sites and there is never an end to learning. I have had diabetes for 60 years.

      5 years ago Log in to Reply
    24. Skye Greer

      High Intensity Interval Training (HIIT) is a great long-term BG lowering ‘tool’.

      5 years ago Log in to Reply
    25. Leona Hanson

      I learn when to take my insulin before meals and the new insulins I could use.

      5 years ago Log in to Reply
    26. Molly Jones

      It is interesting to read pubmed.gov and see headway being made on knowledge of and vaccinations for T1D.

      5 years ago Log in to Reply
    27. Bonnie Lundblom

      I learned that I enjoyed the previous “glu” online site more than this revised one, my apologies to those who revamped it! The previous version was so much easier to navigate and I got so much more from it. I also learned that recovering from major surgery while hospitalized was difficult when an endocrinologist picked up my Tslimx2 pump and tried to make changes to my settings. T1D is always teaching us each and every year. Hoping 2021 will bring happiness and good (or at least improved) health and stable blood sugars to everyone!

      5 years ago Log in to Reply
    28. Melva Church

      I changed from Humalog to lyumjev to help with BS spikes I have not experienced any stinging or pain on insulin delivery Wearing Omnipod and G6 and looper for 2 1/2 years T1D 55 years T1D for

      5 years ago Log in to Reply
    29. Jneticdiabetic

      After 25 years with T1D, I still learning about how my body responds to different carbs, exercise, insulin, and other life happenings. Also, involved in diabetes research and encouraged by discoveries and advances being made.

      5 years ago Log in to Reply

    Did you learn anything new about T1D in 2020? Share what you learned in the comments! Cancel reply

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