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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, 2 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.
    • 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, 45 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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    Would you be willing to use a bio-similar insulin if it were available at a lower cost than your current insulin?

    Home > LC Polls > Would you be willing to use a bio-similar insulin if it were available at a lower cost than your current insulin?
    Previous

    On average, how many adjustment boluses would you estimate you manually give yourself in a day, excluding the times you are also bolusing for food?

    Next

    If you were to go on a 7-day trip away from home, which of the following supplies would you bring, in addition to what you would normally use in 7 days? Select all that apply to you.

    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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    15 Comments

    1. Mick Martin

      I selected “Other”, but it’s really N/A (Not Applicable) as I don’t have to pay for my insulin. I live in the United Kingdom of Great Britain and Northern Ireland where our NHS (National Health Service) pays for insulin … and every other medical prescription for Type 1 diabetes sufferers. (The NHS is funded via direct taxation of all working people.)

      Having said that, if I did have to pay for my insulin I’d have been dead by now. Believe me, I can empathise [empathize] with my American cousins … as well as cousins elsewhere around the World. (I’ve exchanged emails with people, in the United States, who are sadly no longer on this Earthly plane, due to the fact that they simply could not afford the insulin that had been prescribed to treat their diabetes. )

      4
      4 years ago Log in to Reply
    2. Christina Trudo

      I said “maybe” but I could just as easily said “don’t know”, not sure if there is a difference there? In my case “maybe” because of what I currently don’t know about this hypothesized insulin. That being said, as a pump user my insulin is covered on Part B Medicare rather than Part D and I have a supplement which means I pay nothing for the insulin (though the supplement is a bit pricey). Ah, Nick, I envy your situation! Your American cousins can be so stubborn about universal care.

      4 years ago Log in to Reply
    3. George Lovelace

      I said “Maybe”, there are differences in insulins and the differences in bio-similars have yet to be discovered.

      2
      4 years ago Log in to Reply
    4. LizB

      I said “maybe” because I have no experience with biosimilar drugs. I don’t pay much for my Humalog right now, $35 for a 3 month supply, so it would pretty much have to be free to get me to switch if I had a choice.

      4 years ago Log in to Reply
    5. Heather Sharp-Keys

      I’m not sure what a bio-similar insulin is. I use Tresiba and Novolog and I pay $5 each.

      2
      4 years ago Log in to Reply
    6. Sherolyn Newell

      I don’t know what it is. I would have to know a lot more to answer this question or switch to it.

      1
      4 years ago Log in to Reply
    7. KarenM6

      I don’t know anything about bio-similar insulins.

      4 years ago Log in to Reply
    8. Wanacure

      I already use bio-similar insulins: lispro and glargine which are generated by genetically altered organisms (GMOs) to be identical or almost identical to human insulin. If you use brand names Novolog and Lantus, you are too. T1Ds like me who earlier had no choice but beef and beef-pork insulins are not supposed to donate or sell blood or plasma, due to risk of our transmitting mad cow disease.

      4 years ago Log in to Reply
    9. Mark Schweim

      Aren’t ALL the currently available Insulin varieties already “bio-similar Insulin” products??? If it worked in my pump and was less expensive, and worked at least as rapidly as the bio-similar Insulin I’m already using, I’d gladly switch… But the ONLY way any bio-similar Insulin could possibly be at a lower cost than my current Insulin is with my current insurance would be if the manufacturer was willing to PAY ME TO USE IT since my current insurance is providing EXCLUSIVELY Novolog for me at $0 cost to me!!!

      4 years ago Log in to Reply
    10. Lawrence S.

      I didn’t understand the question.

      4 years ago Log in to Reply
    11. Marcia Pulleyblank

      I would want to test it out to make sure that I reacted to it appropriately

      4 years ago Log in to Reply
    12. Kristine Warmecke

      If it is exactly like Novolog, which I’m not allergic to, I’d be willing to try it.

      1
      4 years ago Log in to Reply
    13. Becky Hertz

      As long as it worked similarly and I want allergic to it.

      4 years ago Log in to Reply
    14. PamK

      I already use a “bio similar” – – Humalog!

      4 years ago Log in to Reply
    15. Cheryl Seibert

      I answered ‘maybe’. It would depend on my local reaction to the bio-similar and its rate of effectiveness (how fast it lowers BG).

      4 years ago Log in to Reply

    Would you be willing to use a bio-similar insulin if it were available at a lower cost than your current insulin? Cancel reply

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