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    • 7 hours, 30 minutes ago
      Amy Schneider 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.
    • 8 hours, 57 minutes 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!
    • 8 hours, 57 minutes 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.
    • 8 hours, 57 minutes 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.
    • 11 hours, 10 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.
    • 11 hours, 11 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
    • 11 hours, 11 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!
    • 11 hours, 53 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.
    • 13 hours, 16 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.
    • 15 hours, 14 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
    • 1 day, 6 hours 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.
    • 1 day, 6 hours 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.
    • 1 day, 6 hours 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.
    • 1 day, 6 hours 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
    • 1 day, 6 hours 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, 8 hours 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, 8 hours 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, 8 hours 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, 12 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, 14 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, 15 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, 15 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, 15 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, 15 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, 15 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.
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    On a scale of 1-5, how much do you think T1D impacts decisions you make in other areas of your life? (1 = the least possible impact, 5 = the most possible impact)

    Home > LC Polls > On a scale of 1-5, how much do you think T1D impacts decisions you make in other areas of your life? (1 = the least possible impact, 5 = the most possible impact)
    Previous

    If you wear a CGM, do you ever experience “compression lows” – false low blood glucose alerts that happen when there is pressure placed on the sensor, typically while you’re sleeping?

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    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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    23 Comments

    1. jeredb

      This is a tough one to answer. I answered it looking at does it lead me to not do things because of T1D and for the most part I don’t let it impact my life in that way. On the other hand, planning for T1D impacts nearly every aspect of life so when I do make the decision to do or not do something, the planning for diabetes certainly has an impact. So in this way, it’s major.

      7
      5 years ago Log in to Reply
    2. Patricia Dalrymple

      I had 4 and changed it to 5. Not to be overly dramatic, but it can be a matter of life or death, or at least a trip to the ER if you don’t think about it. I always go low when I change my pump site, I go low when I vacuum, I can go low for no reason I can detect, sometimes the insulin seems to be stronger. Highs are equally dangerous. When I travel it is the last thing I think about before I leave the house: do I have everything? Should I go boating? I live near the gulf. Waterproof does not include salt water. Am I gonna forget one day to take my pump off before I go in the water? Before I go anywhere: do I have food? Do I have my glucometer? Can I even take a purse into a sporting event or do I have to think about that (the answer is yes). It is constant, at least for me because I am a planner and don’t want to ruin other people’s experiences because I haven’t thought things through.

      4
      5 years ago Log in to Reply
    3. Jonathan Strait

      I put 2 because I often make the same decisions I would if I didn’t. However, HOW I do those things is completely affected by T1D. Such as: I will still go on a long run on Sundays as I would have if I wasn’t T1D – just not in the afternoon, not without bringing gels along, and not without telling someone and having my Dex connected and working!

      3
      5 years ago Log in to Reply
    4. Lawrence Stearns

      I try to live my day to day life a normally as possible. However, T1D impacts every decision I make, like it or not. What seems to impact my day to day life more than my T1D is my Celiac disease.

      2
      5 years ago Log in to Reply
    5. Daniel Bestvater

      I put 4.
      After 45 years of T1D I usually run on autopilot. But when I think about I take my T1D into account every time I walk out the door. How far will I walk, how long will l be gone, do I have glucose tabs with me, food …….

      5
      5 years ago Log in to Reply
    6. MARIE

      We live an active full life but diabetes is always there to affect our decisions. We still do most things that we used to, but not all and not the same way. For instance, diabetes has changed the way we travel. We used to go further, stay longer, and travel lighter. Now, two months is the max that we’ll go away and we have an entire piece of luggage devoted to diabetes supplies.

      4
      5 years ago Log in to Reply
    7. Dave Akers

      T1D factors into almost every decision I make. It does not restrict me from doing anything, I merely need to plan for it. Open Water Swimming, eating at restaurants, playing with my kids, waterpolo, gardening and doing the lawn, going for long hikes, etc… it doesn’t matter. Just need to know where your BG is, where it’s going, and know how to correct. After 17 years it’s like walking on river rocks and chewing gum. You’re gonna trip & fall a bit, but you can keep going.

      6
      5 years ago Log in to Reply
    8. connie ker

      I chose #1 because T1D is a full time job each and every day. I am a senior, widow, living alone; so I have to be mindfully present day and night with numbers and dosages of insulin.

      3
      5 years ago Log in to Reply
    9. Amy Schwinghammer

      I put 4. People without T1 will never fully understand the incessant multi-tasking our brains are required to do every moment of every day in order to keep our bodies functioning as best they can. Yes we get used to it (humans are resilient like that) and yes we don’t let us hold us back, but I don’t even remember what it was like to live without T1. Stay strong, everyone!

      13
      5 years ago Log in to Reply
    10. Grey Gray

      I put a 5 since my T1D affects pretty much every decision I make.

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

      Eudaimonia is the only thing that would get a 5. ( ◡́.◡̀)(^◡^ )

      However, the T1D being so ubiquitous does come in at a 4. I fully embrace the “fix it & forget it” philosophy, but equipment failures, biological failures, man-made insurance failures, to name a few, make this a much bigger challenge than it ought to be. (っ^▿^)💨

      1
      5 years ago Log in to Reply
    12. Ken Raiche

      I guess it really comes down to the individual and hire they are controlling the disease. Honestly I really don’t think there’s anything that a diabetes can’t do if you set your mind to it. For me it’s not to much of a problem being properly prepared for whatever it is that your going to embark on is a good first step. All that to say 2 is the number I selected I’m pretty thorough about everything involving my condition and my needs.

      1
      5 years ago Log in to Reply
    13. cynthia jaworski

      It depends on how you mean impact. It does not change WHAT I choose to do, but it impacts HOW I do things: timing, preparation, etc. Therefore, I answered with a 3.

      8
      5 years ago Log in to Reply
    14. Carol Meares

      24/7, I pack T1D with me wherever I go, whatever I do. T1D is not who I am but it is definitely a part of who I am plain and simple. When I plan for it, my life is so much better, every activity, every inactivity and everything in in between.

      7
      5 years ago Log in to Reply
    15. ConnieT1D62

      5 – T1D impacts planning and decision making 24/7/365. It is a constant underlying thread that is intricately woven into the fabric and design of the magic carpet journey that is my life.

      11
      5 years ago Log in to Reply
    16. Janis Senungetuk

      Life with T1D has had a definite impact on my journey over the past 66 years. Plans have been derailed and choices limited, but I have pursued and persisted in achieving my goals.

      4
      5 years ago Log in to Reply
    17. Bonnie Lundblom

      I said 4 since my T1D factors into so many decisions every single day. I’m very grateful for the technology that at least helps guide so many of my decisions.

      4
      5 years ago Log in to Reply
    18. Sahran Holiday

      Also grateful for the technology. Have always been careful about nutrition and always been active. Subject to serious lows so always carry snacks, enough for everyone.

      1
      5 years ago Log in to Reply
    19. Becky Hertz

      I said 3 but have lived with it for 47 years so probably it affects my decision making more than I’m aware.

      3
      5 years ago Log in to Reply
    20. Germaine Sarda

      I wavered between saying 4 and 5. I said 4 because I overthought it and figured it doesn’t affect small things like what I decide to watch on TV, but then again I watch a lot of T1 stuff, so 5 it is! I can relate to everyone’s comments here. Wishing all of us good health filled with easy blood sugar days.

      1
      5 years ago Log in to Reply
    21. Velika Peterson

      This question doesn’t capture the perspective of T1D caretakers. Which school a child go to in order to accommodate the medical needs, can a parent work and what work hours, is it wise to go on vacation to a location without a hospital for hours, etc

      1
      5 years ago Log in to Reply
    22. Cheryl Seibert

      I answered “3” because it depends on the decision being made. T1D had little impact on daily decisions and tasks. However it has a big impact (5), any kind of long term travel decisions (air vs car, I avoid overseas travel due to potential issues with customs). Travel has the biggest impact and, in the past, the decision to have children also had a big impact.

      5 years ago Log in to Reply
    23. Molly Jones

      I chose 2, as epilepsy impacts my decisions more than any other medical concern I have. I have all I need for diabetes to be fairly well controlled, and it is part of my daily life.

      5 years ago Log in to Reply

    On a scale of 1-5, how much do you think T1D impacts decisions you make in other areas of your life? (1 = the least possible impact, 5 = the most possible impact) Cancel reply

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