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    • 4 hours, 7 minutes ago
      Lawrence S. likes your comment at
      On average, how often do you pre-bolus before eating?
      Yeah...The Pre-bolus...if I actually did this more often, I would be in much better control. It's my T1D Achilles' Heel.
    • 5 hours, 4 minutes ago
      Kathy Hanavan likes your comment at
      On average, how often do you pre-bolus before eating?
      Yeah...The Pre-bolus...if I actually did this more often, I would be in much better control. It's my T1D Achilles' Heel.
    • 21 hours, 58 minutes ago
      KCR likes your comment at
      How often do you feel informed about new therapies being studied for T1D?
      Only what is reported at conferences and covered by e-zines like DiaTribe.
    • 1 day, 1 hour ago
      Lawrence S. likes your comment at
      How often do you feel informed about new therapies being studied for T1D?
      It's sometimes difficult shift through. I get a lot of spam redirections. I'm also only really interested in autoimmune type diabetes. Right now GLP-1 interest is all the rage. I'm not a candidate for those type of drugs. Funny how these drugs which became so popular with the rich people mostly non diabetic have taken over by all the drug companies.
    • 1 day, 23 hours ago
      Anita Stokar likes your comment at
      Would you be willing to participate in long-term research (1 year or longer)?
      Hard to truly say without details. I said likely not, but really this is such an open ended question that has too many possibilities to answer.
    • 1 day, 23 hours ago
      Anita Stokar likes your comment at
      How often do you change infusion or sensor sites earlier than recommended?
      I use omnipod and dexcom G7. At 70 years old, I am fortunate to get the full 80 hours with each Omnipod which translates into three pump changes every 10 days. This works very well with the 10 day G7. I am also able to build up extra pods. I also use an open source AID algorithm so do not have to worry about having both CGM and pump on the same side of the body.
    • 2 days ago
      Anita Stokar likes your comment at
      If compensation were offered for research participation, what format would you prefer?
      It depends on the travel distance. The longer the distance the more important the reimbursement it is the total deal. If it's across the street keep the money. If it's across the country we need to talk.
    • 3 days, 18 hours ago
      lis be likes your comment at
      How often do you change infusion or sensor sites earlier than recommended?
      Every 9 days I have to have to change an infusion set after one day use to switch the sensor to the other side - come on deccom you can do better
    • 3 days, 18 hours ago
      lis be likes your comment at
      How often do you change infusion or sensor sites earlier than recommended?
      Starting in 1996, my midriff has received more pounding than the Gaza strip. Both look similar. Consequently, I change frequently, every 2.5 days or so. Whatever the landscape will tolerate. 📄🖍️o(≧o≦)o🧸
    • 3 days, 18 hours ago
      lis be likes your comment at
      How often do you change infusion or sensor sites earlier than recommended?
      I change infusion sites every other day rather than every 4th day. I’ve been doing this for years after I started to see my insulin requirements increase dramatically on the 3rd day. It’s not really “earlier than recommended” since my endo agrees with this schedule and writes my prescriptions to accommodate it.
    • 3 days, 18 hours ago
      Ahh Life likes your comment at
      How often do you change infusion or sensor sites earlier than recommended?
      I usually extend them rather than cut their longevity short. I am insulin resistant and if I don't refill pump at day 2 I can't get to day 3-4. So, I usually use it a day longer than instructed due to the refill. And before moving to G7 I would restart my CGM and get an average of 14 days with some rare, 21 day uses in the mix. Sadly, Dexcom has figured out how to make more money off us by forcing a restart every 10 days with a transmitter built in.
    • 3 days, 20 hours ago
      Molly Jones likes your comment at
      How often do you change infusion or sensor sites earlier than recommended?
      I change my infusion site early if it's ripped off (obviously) or if I'm running high for no reason I can detect. Changing the site can sometimes help. I only change my CGM early if 1) it's going haywire with my numbers (reading high or low without cause) or 2) sometimes it's just convienant due to scheduling. But that's usually one day early.
    • 4 days ago
      Lawrence S. likes your comment at
      How often do you change infusion or sensor sites earlier than recommended?
      Starting in 1996, my midriff has received more pounding than the Gaza strip. Both look similar. Consequently, I change frequently, every 2.5 days or so. Whatever the landscape will tolerate. 📄🖍️o(≧o≦)o🧸
    • 4 days, 1 hour ago
      Daniel Bestvater likes your comment at
      How often do you change infusion or sensor sites earlier than recommended?
      Starting in 1996, my midriff has received more pounding than the Gaza strip. Both look similar. Consequently, I change frequently, every 2.5 days or so. Whatever the landscape will tolerate. 📄🖍️o(≧o≦)o🧸
    • 4 days, 2 hours ago
      dholl62@gmail.com likes your comment at
      How often do you change infusion or sensor sites earlier than recommended?
      I change my infusion site early if it's ripped off (obviously) or if I'm running high for no reason I can detect. Changing the site can sometimes help. I only change my CGM early if 1) it's going haywire with my numbers (reading high or low without cause) or 2) sometimes it's just convienant due to scheduling. But that's usually one day early.
    • 4 days, 2 hours ago
      TEH likes your comment at
      How often do you change infusion or sensor sites earlier than recommended?
      Sites on my legs seem to get irritated with resultant higher glucoses by day 2, so I often change out these sites every 2 rather than 3 days.
    • 4 days, 3 hours ago
      atr likes your comment at
      Would you be willing to participate in long-term research (1 year or longer)?
      I answered "maybe" because I am house bound and can do survey's online, but not in person. Also, I am 86 and not eligible for most research.
    • 4 days, 3 hours ago
      atr likes your comment at
      Would you be willing to participate in long-term research (1 year or longer)?
      Assuming I would live long enough to complete it — I’m going to be 80, but I’m a healthy, active T1D.
    • 4 days, 3 hours ago
      atr likes your comment at
      Would you be willing to participate in long-term research (1 year or longer)?
      All depends on location and age requirements
    • 4 days, 3 hours ago
      atr likes your comment at
      Would you be willing to participate in long-term research (1 year or longer)?
      Yes. At my age (according to the social security life expectancy table) I have 8.6 years left. Whew! Thank heavens for that point-six. 🍄🦋
    • 4 days, 3 hours ago
      atr likes your comment at
      How often do you change infusion or sensor sites earlier than recommended?
      Starting in 1996, my midriff has received more pounding than the Gaza strip. Both look similar. Consequently, I change frequently, every 2.5 days or so. Whatever the landscape will tolerate. 📄🖍️o(≧o≦)o🧸
    • 4 days, 3 hours ago
      Chrisanda likes your comment at
      How often do you change infusion or sensor sites earlier than recommended?
      Starting in 1996, my midriff has received more pounding than the Gaza strip. Both look similar. Consequently, I change frequently, every 2.5 days or so. Whatever the landscape will tolerate. 📄🖍️o(≧o≦)o🧸
    • 4 days, 19 hours ago
      Ahh Life likes your comment at
      Would you be willing to participate in long-term research (1 year or longer)?
      I answered "maybe" because I am house bound and can do survey's online, but not in person. Also, I am 86 and not eligible for most research.
    • 4 days, 19 hours ago
      Ahh Life likes your comment at
      Would you be willing to participate in long-term research (1 year or longer)?
      Assuming I would live long enough to complete it — I’m going to be 80, but I’m a healthy, active T1D.
    • 4 days, 21 hours ago
      Mary Thomson likes your comment at
      Would you be willing to participate in long-term research (1 year or longer)?
      I answered "maybe" because I am house bound and can do survey's online, but not in person. Also, I am 86 and not eligible for most research.
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    Since your T1D diagnosis, have you ever been without health insurance? Please share any effects this had on your T1D management in the comments.

    Home > LC Polls > Since your T1D diagnosis, have you ever been without health insurance? Please share any effects this had on your T1D management in the comments.
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    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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    23 Comments

    1. Steve Rumble

      I was diagnosed T1D while in the USAF, once discharged I had no health insurance but my T1D needs were covered by the Veterans Administration.

      2 years ago Log in to Reply
    2. Mick Martin

      I don’t have personal insurance, in fact, I’ve never had personal insurance, but I live in the UK (United Kingdom of Great Britain and Northern Ireland) where our medical needs are taken care of via our NHS (National Health System) which is financed via direct taxation of all people who earn more than a ‘given amount’. i.e. that would be most working people. This covers treatment costs and prescription costs.

      1
      2 years ago Log in to Reply
      1. Lawrence S.

        No one should be denied health care. Kudos to the UK for taking care of it’s citizens.

        1
        2 years ago Log in to Reply
      2. Gustavo Avitabile

        Same for me, in Italy.

        1
        2 years ago Log in to Reply
      3. Mick Martin

        @Lawrence S. I ‘hear’ what you say, sir, but SOME people do resent the taxes they pay being put forward to taking care of those that aren’t as fit as themself/ves. 😉

        2 years ago Log in to Reply
      4. Mick Martin

        @Gustavo Avitabile. I’m pleased that Spain also offers coverage for people, sir.

        2 years ago Log in to Reply
    3. Jane Cerullo

      Thankfully have always had insurance. Bit as a nurse have seen how devastating not having insurance does to diabetes care.

      1
      2 years ago Log in to Reply
    4. Daniel Bestvater

      I live in Canada and owned my own business. So I have never had any type of medical/drug coverage. I live in Ontario so once I hit 65 I will have some drug coverage. Ironic that insulin was discovered in Toronto Canada, but many people here struggle to pay for it.

      2 years ago Log in to Reply
    5. GLORIA MILLER

      In late 1980s after a divorce, I had a few years without health insurance. The cost of insulin and syringes at that time was not expensive so I paid it myself. It was not a problem to not have coverage at that point but it would be today.

      1
      2 years ago Log in to Reply
    6. cynthia jaworski

      Paying for insulin and day to day maintenance is not my main reason for wanting insurance. I am more concerned about the increased likelihood we all have of major health complications: kidney disease, cardiovascular issues, retinopathy, etc. Any of these could be impossible to afford in the US.

      1
      2 years ago Log in to Reply
    7. Gary Taylor

      I was diagnosed in 1976 while in college. Insulin, syringes, and urine test strips were inexpensive and could be purchased without a prescription. My first insurance came five years later when I was hired by a school district that provided it.

      1
      2 years ago Log in to Reply
      1. Tom Caesar

        Very similar story, diagnosed in 1969. Sporadic insurance until my early 40’s, then was blessed with a job teaching with benefits. Now retired with medicare.

        2 years ago Log in to Reply
    8. Anneyun

      I only got on a health plan as an adult about 5 years ago. Before that I couldn’t consider getting a pump or CGM because of the costs. My control is so much better now.

      2 years ago Log in to Reply
    9. Sue Martin

      I was without insurance for about 3 years. I didn’t get the annual exams I needed, like eyes, or timely doctor visits. I had to pay for insulin and CGM supplies out of pocket. I rationed other things to afford my insulin. It was about $450 a vial. I was grateful to get a job and have insurance coverage again.

      2 years ago Log in to Reply
    10. Anthony Harder

      A few months before Medicare, insurance botched my coverage and cancelled my insurance. Fortunately, I had a small surplus of supplies and medications to bridge this gap.

      2 years ago Log in to Reply
    11. Bob Durstenfeld

      Yes, both as an adult and as a child with T1D. It was both disruptive and expensive.

      2 years ago Log in to Reply
    12. KSannie

      I was diagnosed in college. I went to the UK about 8 months later, where the national health system covered me. I married an American, but was not covered while home the 3 months before our wedding and the 3 months before my husband’s insurance kicked in from his new job. Insulin, syringes and test strips were not expensive. Later my husband was sent to work abroad and we had coverage, but it was in the UK again, and they did not provide pumps. So when we returned to the U.S. I finally got a pump. Around that time the UK started covering pumps for kids, and later for adults.

      2 years ago Log in to Reply
    13. Jennifer Wilson

      Recently laid off and public insurance is very expensive. I have to ration my medication and might have to go back to syringes and vials… old school.

      2 years ago Log in to Reply
    14. mbulzomi@optonline.net

      My answer was NO. I have been employed since I was 1 discharged from the USN at 21 years old, now 79, retired and covered my last employer the Federal Aviation Administration.

      2 years ago Log in to Reply
      1. mbulzomi@optonline.net

        I forgot Medicare parts A and B.

        2 years ago Log in to Reply
    15. Steven Gill

      Retired last year, went without insurance until December when I entered the VA health system. From February until December purchased all prescriptions through Amazon, the Libre3 through Wal-Mart and GoodRX. Insulin pens with Glargine and initially Lispro through Amazon, until I found Aspart was so inexpensive in vial form at Wal-Mart (again GoodRX). My a1C dropped from 6.0 to 5.2, more time? able to do what I wanted? (a lot of volunteering, gardening, and yeah worked part-time).

      2 years ago Log in to Reply
    16. Vicki Andersen

      I had to switch to Medicare this year and getting my supplies was very difficult. I was really stressed out for about a month while fighting the battles. It was a very disappointing experience!

      2 years ago Log in to Reply
    17. PamK

      This happened to me once. I called the manufacturers of my supplies. I was able to get some discounts, which really helped!

      2 years ago Log in to Reply

    Since your T1D diagnosis, have you ever been without health insurance? Please share any effects this had on your T1D management in the comments. Cancel reply

    You must be logged in to post a comment.




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