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    • 14 hours, 56 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, 58 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, 59 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, 59 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
    • 15 hours, 8 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 ´ )⎠⎞
    • 17 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.
    • 17 hours, 1 minute 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.
    • 17 hours, 3 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 ´ )⎠⎞
    • 21 hours, 3 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
    • 23 hours, 5 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, 51 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, 1 hour 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, 13 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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    Do you have extra insulin in addition to what you received in your most recent prescription re-fill? If so, how long would that additional insulin last you if needed?

    Home > LC Polls > Do you have extra insulin in addition to what you received in your most recent prescription re-fill? If so, how long would that additional insulin last you if needed?
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    On average, how satisfied are you with the general customer service provided by T1D supply companies?

    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. Chris Deutsch

      I do not understand what you are asking…. I have 2

      5 years ago Log in to Reply
    2. Chris Deutsch

      I do not understand what you are asking about “extra insulin”…. Are you asking whether I keep extra (i.e., more than 3 months supply) of my usual insulin on hand as backup or Are you asking whether I have alternate forms of insulin to use if I had none of the usual insulin?? I keep Lantus and Humalog pens on hand as might be needed for pump failure, but don’t consider those are “extra”.

      5 years ago Log in to Reply
    3. LizB

      It is always good to have extra insulin. This past year I have used more insulin in my pump than ever before due to being home almost all the time.

      5 years ago Log in to Reply
    4. Britni Steingard

      I wind up with extra Humalog because of the way the math works out (how many units I need each month plus the fact I can’t get half a bottle from the pharmacy). Lantus, though, I only wind up with extra if I use up the whole bottle instead of discarding it after 28 days.

      5 years ago Log in to Reply
    5. ConnieT1D62

      I always keep extra on hand. I have a 3 to 4 month supply of Novolog on hand for what I use in my pump and to use for bolus injection (w/30cc syringes) when off the pump. I also have Basaglar and Fiasp pens to use as back-up when off pump.

      5 years ago Log in to Reply
    6. Clare Fishman

      My endocrinologist wrote my rx to use up to 100 units per day in my pump. I get 3 vials a month and use a little more 1 so I have what is left in the fridge. I just have to arrange it so the “oldest” is on top. If a friend needs some I am happy to share.

      5 years ago Log in to Reply
    7. Robert Brooks

      I agree with Chris that the question needs clarification. My source of insulin is the refill. the refill carries me for three months. There is no extra insulin.

      5 years ago Log in to Reply
    8. Ken Raiche

      I usually have 1 to 2 spare vials of Humalog in the fridge which in worst case scenarios would last me approximately 1 to 2 months. To top things off I also keep a pen set of Humalog and Tresiba just in case a issue would present itself with my current pump setup. Better safe then sorry as they say.

      5 years ago Log in to Reply
    9. Kathryn Keller

      Trying Fiasp out now, so have extra humalog left over

      5 years ago Log in to Reply
    10. carol Huhn

      I refill my prescription. I don’t know how I could have a back up supply. That would be nice.

      5 years ago Log in to Reply
    11. Gene Maggard

      Because of my changing insurance companies and then going on Medicare, I have been able to hoard about an extra two-month supply. This comes in handy if, pandemic allowing, I go on an extended cruise or other type of vacation when I have to carry extra.

      5 years ago Log in to Reply
    12. Sherolyn Newell

      I build up extra because I use over 1 vial per month, so my prescription is for 2 vials. Since I don’t use a full 2 vials, the extra builds up. Someone else had the same comment.

      5 years ago Log in to Reply
    13. Pat Reynolds

      I don’t understand how people can be prescribed precisely 3 months insulin. Exercise more, you’ll use less. Get sock, you’ll probably use more. And what if you needed 1043 units bu some calculation? Do you ge5 a part-vial/pen for the odd units??? So you will gradually build up a little stock. I have prefilled pens as back ups for my pump (prefer the short acting to be vials, but Dan disagrees. So I have lots of pens that have _technically_ been out of the fridge for too long. Now it seems that Brexit+Covid has not seriously disrupted the supplies, it will be going to a charity to distribute in a developing country.

      5 years ago Log in to Reply
    14. Sarah Austin

      Just ask your Endo to prescribe a little extra for you to have in hand in case of emergency. Most will gladly do so

      5 years ago Log in to Reply
    15. Kristine Warmecke

      When I wet on Medicare I thought my need to ration my Novolog would end. I couldn’t have been more wrong. The cost of my Novolog just rises every year, making it even harder to afford on disability. I REALLY wish I wasn’t allergic to Humalog, the formulary one.

      5 years ago Log in to Reply
    16. Sasha Wooldridge

      I consider this question to be asking if you have a stockpile or safety supply that’s over and above your normal prescription “allowance” so to speak. I had a decent stockpile and then my endo retired and I spent it all during the 1+ year I was looking for a new endo. Almost ran out three times in the last few months, but finally have a new endo and a new script, so I’m working on my stockpile again. Ditto on the comment about asking your endo for a little extra. We’ll never hit the nail on the head and if their any good they’ll know that. Add in all the cannulas, tubing, needles, etc. and you can’t ever be completely exact. My script is for a bit more than my total daily dose and if I need to “save up” I just don’t eat the heavy carb stuff for a while until I’m comfortable with my stockpile size. Nothing major, I just don’t have a piece of cake after dinner, don’t eat out a ton, stay away from potato chips and other snacky items. Stuff like that. It adds up and poof! Extra vials of insulin in the fridge.

      5 years ago Log in to Reply
    17. Chester Oby

      I have about a 4 month supply in my fridge. Living in California my endo told me to keep a earthquake supply on hand.

      5 years ago Log in to Reply
    18. Sally Numrich

      About 3-4 months. Prescription is written with a comfort zone for each bottle. I just feel like I have to have extra in case of natural disaster (earthquake, wildfires) or losing my job. Need that back stock always!

      5 years ago Log in to Reply
    19. Anthony Harder

      Doctors are always willing to prescribe a bit more. They understand the situation and the predicament of running out. Then there is insurance and pharmacy benefit managers. They are a totally different story.

      5 years ago Log in to Reply
    20. Patricia Maddix

      My Endo always writes my prescription of insulin for my pump with a much larger amount than I actually use as he wants me to be prepared for any disaster or problem that might delay prescription orders.

      5 years ago Log in to Reply
    21. Ginger Vieira

      Knowing you cannot live even 24 hours without that liquid gold means T1s practically become hoarding squirrels preparing for winter!

      5 years ago Log in to Reply
    22. Beth Franz

      It’s a shame we need to stockpile in the first place or convince a doctor to write a script on time. How about we make all insulins over the counter with no prescription like many other countries do??

      5 years ago Log in to Reply
    23. Cheryl Seibert

      I have a terrible time with my PBM mail order services unless I sign up with the AutoRefill. A year or so ago, I had just received a refill, then my doctor sent in a new prescription for the year, so I had some on hand. However, now the PBM sends the refills about every 75 days (thus increasing their revenue for the year with the copay). If I try to put it on hold, then it seems to trigger their system to keep reviewing the order, so I just let the refills continue.

      5 years ago Log in to Reply

    Do you have extra insulin in addition to what you received in your most recent prescription re-fill? If so, how long would that additional insulin last you if needed? Cancel reply

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