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    • 6 hours, 14 minutes ago
      Kristi Warmecke likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      not for those of moderate income.
    • 6 hours, 15 minutes ago
      Kristi Warmecke likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I am hopeful- it may not be in my lifetime, but they have already made great strides in the research. The autoimmune response and need for immunosuppressants is still a pretty big sticking point.
    • 6 hours, 16 minutes ago
      Kristi Warmecke likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      But probably not in my lifetime.
    • 7 hours, 56 minutes ago
      dholl62@gmail.com likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I don't see how a cure will be possible without islet cells as they are what produce insulin. Using immunosuppressants or not is what will determine what the first "cure" will be like. If safe immunosuppresants are used, then it is actually a "functional cure". If they can infuse islet cells without needing immunosuppressants nor other meds, then I would call it a "cure".
    • 7 hours, 57 minutes ago
      dholl62@gmail.com likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I am hopeful- it may not be in my lifetime, but they have already made great strides in the research. The autoimmune response and need for immunosuppressants is still a pretty big sticking point.
    • 8 hours, 36 minutes ago
      Bruce Schnitzler likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I don't see how a cure will be possible without islet cells as they are what produce insulin. Using immunosuppressants or not is what will determine what the first "cure" will be like. If safe immunosuppresants are used, then it is actually a "functional cure". If they can infuse islet cells without needing immunosuppressants nor other meds, then I would call it a "cure".
    • 9 hours, 17 minutes ago
      Steve Rumble likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I think that a functional cure is the most viable scenario as far as a "cure" is concerned. It seems like the most progress is being made with islet cell therapies.
    • 9 hours, 24 minutes ago
      Natalie Daley likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I don't see how a cure will be possible without islet cells as they are what produce insulin. Using immunosuppressants or not is what will determine what the first "cure" will be like. If safe immunosuppresants are used, then it is actually a "functional cure". If they can infuse islet cells without needing immunosuppressants nor other meds, then I would call it a "cure".
    • 9 hours, 54 minutes ago
      Marty likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I am hopeful- it may not be in my lifetime, but they have already made great strides in the research. The autoimmune response and need for immunosuppressants is still a pretty big sticking point.
    • 9 hours, 54 minutes ago
      Marty likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      But probably not in my lifetime.
    • 10 hours, 4 minutes ago
      Kathy Hanavan likes your comment at
      If islet cell transplantation is proven safe and effective, how likely would you be to consider it a treatment option?
      Very likely provided immunosuppressants aren't required. Also younger people should receive the treatment first.
    • 10 hours, 4 minutes ago
      Kathy Hanavan likes your comment at
      If islet cell transplantation is proven safe and effective, how likely would you be to consider it a treatment option?
      as long as it doesn't require immunosuppression, I'm interested
    • 10 hours, 5 minutes ago
      Kathy Hanavan likes your comment at
      If islet cell transplantation is proven safe and effective, how likely would you be to consider it a treatment option?
      I was going to comment that there's always a trade off. Am I trading insulin replacement with some other daily treatment? If so, what's the difference? Is the new daily grind more harmful than the old?
    • 10 hours, 6 minutes ago
      Kathy Hanavan likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I am hopeful- it may not be in my lifetime, but they have already made great strides in the research. The autoimmune response and need for immunosuppressants is still a pretty big sticking point.
    • 10 hours, 36 minutes ago
      John Barbuto likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      But probably not in my lifetime.
    • 11 hours, 1 minute ago
      KCR likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I am hopeful- it may not be in my lifetime, but they have already made great strides in the research. The autoimmune response and need for immunosuppressants is still a pretty big sticking point.
    • 11 hours, 2 minutes ago
      KCR likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I said, "Unsure." I do not have enough information to state an opinion.
    • 11 hours, 2 minutes ago
      KCR likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      But probably not in my lifetime.
    • 11 hours, 17 minutes ago
      Katrina Mundinger likes your comment at
      How willing would you be to take immunosuppressants if you were considering an islet cell transplant?
      Scylla and Charybdis being perhaps more apt.
    • 11 hours, 43 minutes ago
      TEH likes your comment at
      How likely do you think islet cell therapies are to become a viable long-term treatment for T1D?
      I think that a functional cure is the most viable scenario as far as a "cure" is concerned. It seems like the most progress is being made with islet cell therapies.
    • 14 hours, 25 minutes ago
      Ahh Life likes your comment at
      How willing would you be to take immunosuppressants if you were considering an islet cell transplant?
      After 70 years with T1d and some reduced kidney function and seeing my dad's poor recovery after a kidney transplant, I have no desire to be subjected to chemicals that would further accelerate the demise of my kidneys.
    • 1 day, 6 hours ago
      lis be likes your comment at
      How willing would you be to take immunosuppressants if you were considering an islet cell transplant?
      Nope, T1D is a manageable thing with today's technology. I'll keep the devil I know.
    • 1 day, 6 hours ago
      dako likes your comment at
      How easy is it for you to find research opportunities that feel relevant to you?
      Agreed, and there are plenty of issues aging with T1D.
    • 1 day, 12 hours ago
      eherban1 likes your comment at
      If islet cell transplantation is proven safe and effective, how likely would you be to consider it a treatment option?
      All depends on if anti rejection and immunosuppressive medications are needed. If so I would not be interested.
    • 1 day, 12 hours ago
      eherban1 likes your comment at
      If islet cell transplantation is proven safe and effective, how likely would you be to consider it a treatment option?
      Very likely provided immunosuppressants aren't required. Also younger people should receive the treatment first.
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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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