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    • 20 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.
    • 21 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
    • 22 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!
    • 1 hour, 4 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.
    • 2 hours, 27 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.
    • 4 hours, 24 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
    • 19 hours, 47 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.
    • 19 hours, 49 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.
    • 19 hours, 50 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.
    • 19 hours, 51 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
    • 19 hours, 59 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 ´ )⎠⎞
    • 21 hours, 51 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.
    • 21 hours, 52 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.
    • 21 hours, 54 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 ´ )⎠⎞
    • 1 day, 1 hour 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, 3 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, 4 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, 5 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, 5 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, 5 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, 5 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, 5 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.
    • 1 day, 5 hours 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, 5 hours 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, 5 hours 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 ´ )⎠⎞
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    What areas of T1D research do you currently find most important? Select all that apply.

    Home > LC Polls > What areas of T1D research do you currently find most important? Select all that apply.
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    Do you ever purchase sugar-free candy instead of full-sugar candy for yourself?

    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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    18 Comments

    1. Bob Durstenfeld

      How about a cure? I have only been waiting 65 years. I have been told all of my life that a cure is only a few years away. Now I think it would be lovely for my almost-three-year-old granddaughter with T1D.

      5 years ago Log in to Reply
    2. Pat Reynolds

      My “other” are two things: 1) Research into prevention and treatment of associated health conditions such as diabulrmia and diabetes axiety 2) research into the cost and effectiveness and models for sustainability of peer learning and support in t1d communities (including looking at how such learning and support can be fostered in communities where doctor/specialist nurse lead teaching and support is known to be less effective, or generic advice is known to be insufficient (eg elite sports, comorbidities).

      5 years ago Log in to Reply
    3. jeredb

      I put automated systems. While some of the other items would be better and more of a true cure, I’ve been waiting over 30 years for that. It seems technology advancements with cgm and pumps using those readings to deliver insulin is the one thing that’s becoming reality. Price needs to come down so they’re more affordable to all people but that technology holds real promise to improve the ease of living with diabetes.

      5 years ago Log in to Reply
    4. Sherolyn Newell

      My son told me a research group, I think at UAB, cured mice with altered insulin-producing cells. They changed them enough that the mice’s immune system didn’t recognize them and kill them off. I believe his exact words were “so they might have a cure before you die”. I am hopeful, but I haven’t heard any more about the study.

      5 years ago Log in to Reply
    5. Nevin Bowman

      Any that are taking care of the root cause. All the others are bandaids that do nothing to stop diabetes.

      5 years ago Log in to Reply
    6. Katy Giebenhain

      Faster-acting insulin!

      5 years ago Log in to Reply
    7. joan Fray

      Now thatI am a LT T1d, long term t1d, i am beginning to notice that my memory is failing, and I don’t know whether it’s just old age(71) or 60 years with T1d. No glucometer for the first 25 years, just pee strips, and they were mostly 4+. Yes, I got religion when my T1d dad died a long slow death at 67, when I was forty. But I’d like to see more studies of us old timers.

      5 years ago Log in to Reply
    8. Ernie Richmann

      Checked all the choices and other. The other would be understanding how to better manage and cope with diabetes.

      5 years ago Log in to Reply
    9. Steven Gill

      A cure for TYPE 1 would be priceless, the ability to cure one autoimmune disease would open doors for other autoimmune diseases as well (to include graves, rheumatoid arthritis, lupus as well as diabetes). But preventing this “over active” part of our body seems just put of reach of research. My insulin pump has really improved my day to day control, and quicker acting insulin (more closely acting like our natural insulin) allowing a deceased risk of hypoglycemia and lowering after meal spikes. Combining both tools with a continuous looped system adding a glucose/glucagon side could completely remove the risks of human error. There are studies towards this, more readily allowing a more normal life.

      5 years ago Log in to Reply
    10. Donna Young

      Outside of cure being the most important research priority, glucose responsive insulin would be the greatest improvement to daily living. If you could just take one shot a day or similar, it would greatly reduce the burden in managing the disease. Pump/cgm systems are not only expensive but are uncomfortable, sometimes unreliable/inaccurate, and require frequent manual intervention. There is little truth to the idea that automated systems make diabetes management effortless or foolproof.

      5 years ago Log in to Reply
    11. Melinda Lipe

      I marked the first 2 because they are currently benefiting all Type 1 s today. The next 4 are the gold standard for finding a relevant cure, but are not as close – we’ve been hearing about some of them for years. How sad.

      5 years ago Log in to Reply
    12. connie ker

      How about turning Type 1 into Type None

      5 years ago Log in to Reply
    13. Gene Maggard

      Forgive me for being cynical, but I fear the billions being made by manufacturers of insulin, pumps, supplies, meters strips, and all the other cash-generating products, not to mention doctors, clinics, and the rest, have made it unlikely we will ever see a cure. Getting better technology is much more possible since it won’t negatively affect their cashflow.

      5 years ago Log in to Reply
    14. Kristine Warmecke

      We have a stable premixed glucagon, I’m long past ready for a tire “artificial” pancreas pump. Being able to make my own islet cells work again, wow! I’ll believe it when I see it.

      5 years ago Log in to Reply
    15. ConnieT1D62

      I selected all of them because each one contributes something worthwhile to make life with T1 diabetes easier, safer, longer, and more aligned with healthy outcomes. The only “cure” for those who have developed full scale beta cell demise would be to reintroduce functional living beta cells into the body, or to prevent the ones that are still active in early stages of disease progression from dying before they totally wear out and self-destruct. Keeping beta cells alive in susceptible humans, especially in the early stages of disease progression is a key factor to prevent total beta cell destruction.

      5 years ago Log in to Reply
    16. Molly Jones

      I chose Treatments that re-program the immune system, Beta cell implantation, Restoring insulin-producing cells in the body and Preventing onset of T1D and because all together they would prevent or restore our islet cells to work properly. My GAD antibodies are incredibly high and I assume they are the cause of both epilepsy and T1D. I also have some nonexistent numbers of other necessary antibodies. If I had beta cells implanted I would need to make sure my immune system was in good working order first. Besides this site, PubMed and ClinicalTrials are good places to see what research and hypotheses are out there, being worked on and if you can participate.

      5 years ago Log in to Reply
    17. Sally Numrich

      I have been involved with automatic insulin pumps and starting another hopefully this week. I have also been in a Viactye stem cell study. I do believe stem cell will be the answer but it is a long way off. In the meantime, it is automatic pumps and much faster, much faster insulins to make live much, much easier. Things are happening. Just think back in the 70’s using one shot and testing urine. And now think of the last 10 years, how much has happened and how fast.

      5 years ago Log in to Reply
    18. Cheryl Seibert

      I selected all the categories. It is important to find a cure and preventative (beta cell transplants, auto-immune solutions, vaccines, reactivating the islet cells), but until that time, the advancement of insulin delivery technology is equally important.

      5 years ago Log in to Reply

    What areas of T1D research do you currently find most important? Select all that apply. Cancel reply

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