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    • 15 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.
    • 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
    • 16 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!
    • 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.
    • 2 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.
    • 4 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
    • 19 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.
    • 19 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.
    • 19 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.
    • 19 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
    • 19 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 ´ )⎠⎞
    • 21 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.
    • 21 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 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, 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 ´ )⎠⎞
    • 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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    Have you ever run out of insulin and had issues getting more because of insurance? Share in the comments what you did.

    Home > LC Polls > Have you ever run out of insulin and had issues getting more because of insurance? Share in the comments what you did.
    Previous

    How many extra (unopened) insulin vials/pens do you have on-hand?

    Next

    If you’re at an event that asks guests to “silence devices,” do you adjust the alarms on your CGM and/or insulin pump?

    Samantha Walsh

    Samantha Walsh has lived with type 1 diabetes for over five years since 2017. After her T1D diagnosis, she was eager to give back to the diabetes community. She is the Community and Partner Manager for T1D Exchange and helps to manage the Online Community and recruit for the T1D Exchange Registry. Prior to T1D Exchange, Samantha fundraised at Joslin Diabetes Center. She graduated from the University of Massachusetts with a Bachelors degree in sociology and early childhood education.

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    21 Comments

    1. Mark Cosiano

      I paid out of pocket to get the insulin.

      2 years ago Log in to Reply
    2. Janice B

      I once was out of town – dropped and broke my insulin vial. Went to pharmacy and had to pay retail. Then found the silicone vial protector online – what a blessing that has been.

      2 years ago Log in to Reply
      1. Sherolyn Newell

        I am going to look that up. Thanks.

        2 years ago Log in to Reply
    3. Sherolyn Newell

      My original prescription was one vial a month, and I always was afraid of running out. Now it’s two vials, and I have insulin to spare because I only use about 1.5. I keep the vials in the refrigerator all the time so I don’t have to worry about the 28 day limit.

      1
      2 years ago Log in to Reply
      1. Bret Itskowitch

        Good for you. I don’t understand why absolutely everyone doesn’t do this!

        2 years ago Log in to Reply
    4. lenglish@cimginc.com

      I was in another state and my insulin was put into the freezer by mistake. I ended up in the hospital – the only time I’ve been in hospital due to my diabetes – for the entire day, waiting for the doctor in that state to order the insulin…then my insurance declined the order because it was “too early”. Literally begged the insurance person at the company who got managerial permission to allow one vial to cover the rest of my trip. This was prior to being able to pay $35.00 over the counter.

      2 years ago Log in to Reply
    5. Justin

      Never ran out, but had issues with insurance. For example, they covered insulin pens, but I had to pay out of pocket for the needles and test strips.

      2 years ago Log in to Reply
    6. Amber Dietz

      I’ve not had issues with insurance, but doctors have been a huge issue. I’ve had doctors who would not write me new Rx until I came to see them regardless of the fact that I still have diabetes and need insulin.

      2 years ago Log in to Reply
    7. Kristi Warmecke

      At one time my brother and niece were using Novolog, too, and we would loan to each other; then their insurance made them start using Humalog and I couldn’t loan from them due to my allergy to Humalog. So when I saw I was getting close to running out out I began rationing it.

      2 years ago Log in to Reply
    8. LuckyPineapple

      One time, somehow, an insurance payment was 10 cents short..they never told us. One day I went to pick up my insulin and they wanted like $600 for it and I was like uhhh no? So I called my insurance right then and there and they said our payment was past due for 6 months so they shut our coverage off. She said we were behind 10 cents. 10 measly pennies. It was a Friday and I didn’t have enough insulin to get me through the weekend. The callous lady was all “you can pay it, and then we’ll reinstate your coverage in 3-5 business days after we receive it” and I said to her..”it’s Friday, so it won’t go through till Monday, then 3-5 days after that?? I’m going to die by then. I will drive to your office and hand you the ten cent piece right now if you just let me get my insulin now. Wouldn’t you rather me be alive and paying you for years than me dying and you never getting money from me again?!” She didn’t care. Thankfully the pharmacist….chemist? Is that what you call them there? lol was kind and lent me some insulin from my prescription from when it was caught up. I couldn’t believe that ten cents was worth more to that insurance company than my *life*.

      2
      2 years ago Log in to Reply
    9. Joan Benedetto

      Thankfully, no. Our son was diagnosed at 18 mos of age. His Endo encouraged us to use a vial beyond 28 days as he was using less than ten units per day. She also wrote the script to allow for an extra vial in case of breakage. Our son now uses about 25 units per day, but we have somewhat of a stockpile built up.

      2 years ago Log in to Reply
    10. Brian Vodehnal

      My original endo used to leave town and not tell his patients. Helped him communicate better by finding the mass text function on his software. But it did result in several of us running low and out in some cases. Not sure he still uses it as I’m on with a new Endo.

      2 years ago Log in to Reply
    11. BOldfield

      Had to change the brand of insulin that the insurance company approved of

      2 years ago Log in to Reply
    12. PatC

      Purchased Novolin-R (no prescription needed) and filled my pump with it.

      2 years ago Log in to Reply
    13. Donna Condi

      Because I use one and one half vials a month I keep lots of backup insulin. I’m not sure what I would do if I ran out.

      2 years ago Log in to Reply
    14. KarenM6

      Yes.
      I was at a time when I had to order more through a mail order pharmacy. So I ordered there. But, the insulin didn’t show up soon enough even though I paid the extra “expedite” fee.
      So, my doctor gave me a physical Rx and I went to a pharmacy but they wouldn’t give me more and said that the system showed that I had enough already.
      No matter how hard I tried to explain that I _didn’t_ have any, they wouldn’t accept it.
      So, I had to call my doctor (and, I think it was after hours and/or on a Saturday) and he gave me an Rx for a different type of insulin, which did the trick.
      I was panicking hard for awhile there, though!
      It was about another week before the mail order stuff showed up.

      2 years ago Log in to Reply
    15. Anita Stokar

      I accidentally forgot an extra bottle of insulin when I went on a vacation. I paid out of pocket at a pharmacy while on the vacation so I didn’t use my insurance. However, when I got home, I was able to be reimbursed for the purchase by my insurance. So my answer was “no”.

      2 years ago Log in to Reply
    16. KSannie

      I just waited an extra day before getting a new supply. My sugars were a little high.

      2 years ago Log in to Reply
    17. Jeff Balbirnie

      Absolutely, yes. Pen went bad (insulin became wonky), vials have broken many times. The WORST is when you call to get a literal emergency refill from your medical doctor, but they REFUSE until you have a MANDATORY in person appointment, but cannot get you on the schedule for weeks/months. NOT EXCUSABLE.

      2 years ago Log in to Reply
    18. Rex Franklin

      When I had KP insurance, I would run out all the time. the worst was when I was fooled to had KP send my insulin by mail order and it was sent in a bag during 100 degree weather. Couldn’t get it replaced to during Open Enrollment I changed insurance.

      2 years ago Log in to Reply
    19. Vicki Andersen

      When switching to Medicare I ran out of FIASP and they wouldn’t approve my script due to insurance issues. It was a battle and very stressful.

      2 years ago Log in to Reply

    Have you ever run out of insulin and had issues getting more because of insurance? Share in the comments what you did. Cancel reply

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