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    • 22 minutes ago
      Steve Rumble 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, 10 minutes ago
      Donna Owens likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Yes. It’s f*ing annoying.
    • 13 hours, 53 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.
    • 15 hours, 19 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!
    • 15 hours, 20 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.
    • 15 hours, 20 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.
    • 17 hours, 32 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.
    • 17 hours, 33 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
    • 17 hours, 34 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!
    • 18 hours, 16 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.
    • 19 hours, 39 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.
    • 21 hours, 36 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, 12 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, 13 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, 13 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, 13 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, 13 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, 15 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, 15 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, 15 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, 19 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, 21 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, 21 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, 22 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, 22 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".
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    Have you recently experienced delays in receiving your T1D prescriptions or device supplies due to product shortages?

    Home > LC Polls > Have you recently experienced delays in receiving your T1D prescriptions or device supplies due to product shortages?
    Previous

    If you have a child with T1D (or at some point you were a child with T1D) who goes trick-or-treating, do you use any strategies to manage the amount of candy they consume? Share what works best for you in the comments!

    Next

    Which of these best describes how often you typically change your lancet?

    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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    28 Comments

    1. BARRY HUNSINGER

      My supply problem is due to MEDICARE’S REDICULOUS requirements of having the notes on my doctor visit.

      8
      4 years ago Log in to Reply
    2. Sahran Holiday

      Not product shortages, Severe delay Dexcom G6 from Express Scripts horrible incompetence and lying. And CIGNA Express Scripts owner. Horrible.

      2
      4 years ago Log in to Reply
    3. Lawrence Stearns

      I’ve had delays, but not because of supply shortages. My delays appear to be my supplier, Edgepark, and possibly Medicare.

      4 years ago Log in to Reply
    4. Mig Vascos

      None at all

      4 years ago Log in to Reply
    5. Alyne Branson

      I haven’t experienced delays because of product shortages, but the pharmacy I get things at is always behind. Even if I proactively call my refill in OR have it on auto-fill, I still have to make the phone call asking why it isn’t ready and they then move it to the front. If I didn’t call, who knows how long it would take.

      1
      4 years ago Log in to Reply
    6. TEH

      Yes I have. I switched from my previous employers health insurance to Meditcare with Gap (G) in August. My first Medtronic ordter has taken a month and they cut the number of boxs from 4 to 3 for 3 months. That is barley enough to to cover 90 days. It took over a month to get the Doctor visit, C peptide test and info to Medicare. But the good news is it is less than half the cost of what the health insurance was running me. The old story, less for less. 😞

      4 years ago Log in to Reply
      1. Miriam Gordon

        I had my endocrinologist write an RX for changing site every 2 days. So now i get enough sets.

        4 years ago Log in to Reply
    7. Janice B

      Not because of product shortages. But due to insurance rules I can only order my Dexcom supplies every 3 months. So I am out of sensors and the transmitter about 7 days while waiting for the new supplies.

      2
      4 years ago Log in to Reply
    8. Ahh Life

      Product shortages? No.

      Medicare and insurance issues? No.

      Postal service issues, lack of truck drivers for UPS and FEDEX? Yes.

      4
      4 years ago Log in to Reply
    9. cynthia jaworski

      I have had to change pharmacies because the distributor of my 1st pharmacy was having trouble supplying my FIASP. Similar problems have occurred with my blood pressuure medication.

      4 years ago Log in to Reply
    10. Louise Robinson

      No delays experienced but there have been substitutions of my preferred Tandem AutoSoft XC infusion sets with the Tandem AutoSoft 90’s which are very similar but more difficult to detach and reattach (e.g. for showering). We were advised several months back that this was being done because of product shortages.

      4 years ago Log in to Reply
      1. Henry Renn

        Ditto.

        4 years ago Log in to Reply
    11. Darlene Oller

      Three day delay on insulin because pharmacy was out of stock

      4 years ago Log in to Reply
    12. Henry Renn

      I have had a lot of problems with timely arrival from CCS. Idk if shortages were involved.

      4 years ago Log in to Reply
    13. Martin Fuhrer

      For some reason the Freestyle Libre 2 reader is not available for purchase from pharmacies in Canada (even from the Abbott Canada website). I had purchased Freestyle Libre 2 sensors in April, and the only way to scan them is by their smartphone app, but my iPhone 6 is not supported. After numerous phone calls to Abbott customer care over the course of several months, I finally was able to get them to send me a Libre 2 reader in October. Now I’m a happy camper. Not sure if this is a supply issue… but it does seem strange that the Libre 2 reader is not yet widely available in Canada.

      1
      4 years ago Log in to Reply
    14. Kathleen Juzenas

      Three day delay in getting CGMs due to 2 week power outage in New Orleans. Maybe a distribution problem rather than production shortage.

      1
      4 years ago Log in to Reply
    15. M Fedor

      No delays over product shortages, but I have experienced delays in getting pump supplies, Dexcom sensors and insulin due to confusion/miscommunication about Medicare requirements.

      4 years ago Log in to Reply
      1. Miriam Gordon

        I had lots of issues with Edgepark getting pump and Dexcom supplies since i went on Medicare. Long waits on the phone too. I switched to CCS medical and have had zero problems. Also they pick up the phone right away. .

        4 years ago Log in to Reply
    16. Donald Cragun

      I haven’t had supply chain issues, but I have had delays caused by Solara. After multiple cases of being without infusion sets, sensors, and/or a transmitter I finally switched to ADS and haven’t had any problem since (so far).

      1
      4 years ago Log in to Reply
      1. Kristine Warmecke

        I had issues with Byram, they never sent the correct infusion set’s. EdgePark has never gotten my supplies wrong, thank heavens. The Tandem rep. knew me by first name because she saved me when Byram refused to send the correct ones – every single time.

        4 years ago Log in to Reply
    17. Natalie Daley

      I take Tresiba and Humologue and Costco pharmacy has had delay issues in getting either or both.

      4 years ago Log in to Reply
    18. PamK

      I was unable to get the infusion sets that I normally use and had to settle for different ones that I do not like.

      4 years ago Log in to Reply
    19. Stacia Wohlford

      Dexcom through diabetes Supply Is taking longer than it used to. By backup supply is seriously dwindling.

      4 years ago Log in to Reply
    20. Kristine Warmecke

      No, not due to supply shortages. Just because of shipping delays, once they’ve been shipped.

      4 years ago Log in to Reply
    21. William Bennett

      MIO Advance infusions sets have been unavailable for months due to supply chain problems. I vastly prefer the over the previous model but I’m told they won’t be available until after the turn of the year.

      4 years ago Log in to Reply
    22. Bea Anderson

      Novolog 100 vial. 3 weeks late from Walmart. With recent availability of generic and according to Medicare guidelines to substitute without patient’s consent or knowledge to generic I was really waiting for generic. I was told back ordered. Insurance delays. Dr delays. Finally pharmacist said it was generic delayed. I asked what my prescription was actually written for and they said Novolog, but they were bound by law to sub generic. I was desperate to get my insulin and asked for Novolog I had always previously received because I was filling reservoirs with last vial and had been waiting 3 weeks and needed some insulin. Finally a fill in part time pharmacist said my Dr did not check the box for “no substitutions” on that prescription. Call Dr who wrote new prescription and finally got Novolog 3 of 4 vials that day. Horrible experience and treatment from pharmacy I’d gone to for 16 years. I checked websites that list drug delays and never found Novolog or it’s generic on a shortage list. I asked for any explanation how this could happen. Real shortage? Medicare coverage? A guideline does exist that says pharmacist are to sub generic for medicare customers. Running up to last reservoir fill was frightening. I made appointment to talk to walgreen pharm manager to better understand what really happened. I wanted them to see how desperate my situation was and know I was a real person who needed better help. I called/emailed every 5 days. Showed printouts of their Response emails said back order, then shortage, then insurance, then dr delay. I verified insurance and dr were not problem. Furthermore my dr office said they knew if no shortage. Walgreens didn’t know if others were having delays with insulin. My husband suspected since Medicare pays so poorly that Walgreens didn’t see me as a customer they wanted any longer. Wherever this perfect storm came from, I had never been so frightened. The Walgreens meeting ended with them admitting their explanations seemed like excuses and getting me at least one vial was always possible. Just not provided. Long, odd story.

      3
      4 years ago Log in to Reply
    23. Henry Renn

      My father bought all the candy from me. I kept non-candy food items to eat as appropriate.

      4 years ago Log in to Reply
    24. Kim Murphy

      When omnipod and dexcom stopped letting customers order directly from them and I had to start getting my supplies from a pharmacy it was a nightmare. The pharmacy got my omnipods a couple of times then told me they couldn’t get them anymore. I finally found a mail order pharmacy that would send me my omnipods but you have to pay for 3 months at a time and that is a couple thousand dollars because marketplace health insurance doesn’t cover diabetic supplies until you spend $6,000.00.

      1
      4 years ago Log in to Reply

    Have you recently experienced delays in receiving your T1D prescriptions or device supplies due to product shortages? Cancel reply

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