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    • 1 hour, 14 minutes ago
      Lawrence S. likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      Very, but more worried about it even making to the FDA and approved there first.
    • 1 hour, 14 minutes ago
      Lawrence S. likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      There are many concerns, one being if I'll still be alive if it's ever offered :)
    • 1 hour, 14 minutes ago
      Lawrence S. likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      At 78 I don't think islet transplantation will affect my life course. Big pharma sees biological treatments as the path to ever higher profits, not constrained by patent terms the way drugs are. Most diabetics would be better served by an improved standard of care from the ADA and the medical community.
    • 1 hour, 15 minutes ago
      Lawrence S. likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      Severe case of hardening of the “oughteries” here. Ought we be concerned with cost, insurance, coverage, hail storms, earthquakes? ▄█▀█● Why are we not homeschooled to enjoy the progress being made?
    • 1 hour, 16 minutes ago
      Lawrence S. likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      While those items are very much a concern, there are other factors that are more concerning ie immunosuppressant.
    • 1 hour, 17 minutes ago
      Amanda Barras likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      If they can transplant them such that we do not need immunosuppresants, we'd be fine. Otherwise, those meds are just one more thing that could become in short supply. But at least we could go through scanners at the airports and travel without huge bags of supplies.
    • 1 hour, 17 minutes ago
      Amanda Barras likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      General access to islet transplants is still years away. FDA has to deem it safe. Though, I am excited about the possibility.
    • 1 hour, 17 minutes ago
      Amanda Barras likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      At 78 I don't think islet transplantation will affect my life course. Big pharma sees biological treatments as the path to ever higher profits, not constrained by patent terms the way drugs are. Most diabetics would be better served by an improved standard of care from the ADA and the medical community.
    • 3 hours, 19 minutes ago
      Patricia Dalrymple likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      If they can transplant them such that we do not need immunosuppresants, we'd be fine. Otherwise, those meds are just one more thing that could become in short supply. But at least we could go through scanners at the airports and travel without huge bags of supplies.
    • 3 hours, 57 minutes ago
      Gerald Oefelein likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      If they can transplant them such that we do not need immunosuppresants, we'd be fine. Otherwise, those meds are just one more thing that could become in short supply. But at least we could go through scanners at the airports and travel without huge bags of supplies.
    • 3 hours, 57 minutes ago
      Gerald Oefelein likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      While those items are very much a concern, there are other factors that are more concerning ie immunosuppressant.
    • 4 hours, 40 minutes ago
      Marty likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      much more concerned about my age (65) than anything else. 😉
    • 5 hours, 2 minutes ago
      dholl62@gmail.com likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      much more concerned about my age (65) than anything else. 😉
    • 5 hours, 26 minutes ago
      Steve Rumble likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      Severe case of hardening of the “oughteries” here. Ought we be concerned with cost, insurance, coverage, hail storms, earthquakes? ▄█▀█● Why are we not homeschooled to enjoy the progress being made?
    • 5 hours, 26 minutes ago
      Steve Rumble likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      While those items are very much a concern, there are other factors that are more concerning ie immunosuppressant.
    • 5 hours, 27 minutes ago
      atr likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      Severe case of hardening of the “oughteries” here. Ought we be concerned with cost, insurance, coverage, hail storms, earthquakes? ▄█▀█● Why are we not homeschooled to enjoy the progress being made?
    • 5 hours, 42 minutes ago
      Sarah Berry likes your comment at
      How concerned are you about potential barriers to islet cell transplantation, such as cost, access, eligibility, or insurance approval?
      much more concerned about my age (65) than anything else. 😉
    • 6 hours, 42 minutes ago
      Steve Rumble likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      Age 73 here. I'm in the same boat. I ogten am considered too old for consideration for "smaller" research projects. But - best of luck to them. I'll be rooting on the sidelines.
    • 6 hours, 43 minutes ago
      Steve Rumble likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - 👍 immunosuppression needed - 👎
    • 21 hours, 43 minutes ago
      Gerald Oefelein likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I've tried twice and was rejected both times because I control my diabetes as best I can. As others have already stated, if immunosuppressing drugs are involved, count me out. I'm not interested in something worse than what I already have.
    • 21 hours, 44 minutes ago
      Gerald Oefelein likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      Not if it requires immunosuppressant drugs. Been there done that time to move on to something much better.
    • 21 hours, 44 minutes ago
      Gerald Oefelein likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - 👍 immunosuppression needed - 👎
    • 1 day, 3 hours ago
      Natalie Daley likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I answered “Very Unlikely” not because I woud not want to participate but because, at age 75, I think it very unlikely that any researcher would want me in their patient panel.
    • 1 day, 3 hours ago
      Natalie Daley likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - 👍 immunosuppression needed - 👎
    • 1 day, 4 hours ago
      Marthaeg likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - 👍 immunosuppression needed - 👎
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    At your most recent (or current) job, did you tell your coworkers that you live with T1D?

    Home > LC Polls > At your most recent (or current) job, did you tell your coworkers that you live with T1D?
    Previous

    CGM sensors are only approved for specific areas of the body, but many people use other locations. If you use a CGM, do you have an area of your body where you feel you get the most accurate sensor readings? Select all that apply!

    Next

    How does drinking caffeinated drinks impact your blood glucose levels? Share more about your experience with caffeine in the comments.

    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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    35 Comments

    1. Ceolmhor

      I said “Other”, as I was diagnosed after I retired (age 72).

      1
      2 years ago Log in to Reply
    2. Steven Gill

      Diagnosed 26 years ago, recruited to 4 different jobs afterwards with health insurance as a carrot (less payments for insurance). I’m not bashful, made a point to not be handicapped in anyway, and “forgiving” if someone was foolish enough to try. Carried sweetened drinks into crawlspaces and attics (I imagined going low in confined spaces made me nervous), and joked with a co-worker to drag me out by my feet as I was in a hole if I yelled weirdly.

      With a pump/CGM people know something’s up.

      3
      2 years ago Log in to Reply
    3. Jeff Balbirnie

      NEVER!!! Under no circumstance would I EVER reveal my health status to them. I would never reveal something so intimate, so personal to them. Their psychiatric/sexual health is none of my business, why would trust or share something this personal with total strangers, people never worthy of my trust.

      1
      2 years ago Log in to Reply
      1. Jane Cerullo

        Wow sorry you seem to work in a hostile workplace. I always felt someone should know in case of a serious low.

        3
        2 years ago Log in to Reply
    4. Kristen Clifford

      Nearly everyone I work with knows I’m diabetic. Half of them have seen either my pump or my meter at one point or another. If they walk in on me checking my sugar, they let me have a minute or so to finish, and then we go about our business. No one looks twice at it. I don’t hide it anymore, and if something were to happen on the job, I don’t want to be surrounded by people panicking because they don’t know what to do.

      1
      2 years ago Log in to Reply
    5. AimmcG

      Yes and at two of them I had coworkers who were Type 1 Diabetes and diagnosed as adults just like me!

      2 years ago Log in to Reply
    6. William Bennett

      I started my last job in 2000, back when I was still on R/NPH MDI. With that regimen you absolutely had to eat to the clock, and even at that it wasn’t super predictable. So having people I worked with know about it was a safety thing, as well as practical stuff like not scheduling meetings at noon if I could avoid it. By the time I went on to better regimens where it might have been less critical it was already embedded as part of my work identity.

      1
      2 years ago Log in to Reply
    7. Kate Kuhn

      Yes and when one of them became T1D, I became a resource for him.

      2
      2 years ago Log in to Reply
    8. Chrisanda

      I told them when they asked about seeing my pump. Back in the day the kids at the school I taught thought it was a pager! I would just say it’s not. I prefer to “reveal” my status only when necessary, or with close friends. I’ve never run into any issues once revealed. Everyone in my experience has been very respectful, and never made any big deal about it.

      1
      2 years ago Log in to Reply
    9. Justin

      I work from home and work via email and Zoom; my T1D doesn’t come up during those conversations. None of my clients know, but my partner and my only co-worker who live/ work in the same house as me, they do know. Only one board member knows because we are close friends.

      2 years ago Log in to Reply
    10. Jane Cerullo

      I do not hide my T1D and try to educate people on the disease. Most have no concept of the different types of diabetes. Then they tell me not to eat certain things lol

      2
      2 years ago Log in to Reply
    11. Ernie Richmann

      I’m retired now but I let the fitness instructors at the YMCA, the bike club leaders, race directors, and friends know that I am type 1 diabetic.

      2 years ago Log in to Reply
    12. Rex Franklin

      Yes, all my coworkers know. I don’t hide my T1D life. I was told by management that I could not test my BG at work unless I was in the restroom stall. Testing isn’t an issue now with my pump.

      2 years ago Log in to Reply
      1. Trina Blake

        Oh yeah, the fingerstick prohibit! I had one department head who thought I would be spreading blood-borne diseases. Fortunately, one of his favorite employees (a young man who was “gonna go far, fast) overheard the dept head scolding me. The young man piped in askig if employees should limit their papercuts to the restroom. Loved that young man.

        1
        2 years ago Log in to Reply
    13. TomH

      At my last job, I didn’t know I had T1 LADA.

      2 years ago Log in to Reply
    14. Janice B

      All of my coworkers know, and they also know where my supplies are to treat lows. I have never needed any outside interventions in the 30 years of having T1D

      1
      2 years ago Log in to Reply
    15. Kristi Warmecke

      As a bedside RN, I let those on my shift and that I worked most with, know. Not only for myself but my patients. I wouldn’t have been able to live with myself if I unintentionally harmed someone because of a low sugar.

      2 years ago Log in to Reply
    16. Richard Condi

      Not me, but a coworker let me know she was hypoglycemic. I asked her what her preferred treatment was and always kept a stock in my desk. My wife is Type 1 and I am comfortable in treating her lows.

      2
      2 years ago Log in to Reply
    17. Michael Fishman

      I tell everyone, but only after I’m on the insurance.

      2 years ago Log in to Reply
    18. William Ervin

      I have always been very open about being a T1D. I’m not ashamed, embarrassed or feel less than because of this dumb disease. I have educated 100’s of people over the years. Many are very appreciative to learn about the difference between T1D and T2D.

      2
      2 years ago Log in to Reply
    19. Glenda Schuessler

      I am retired. I have not kept my T1D secret from employers, family, friends. . . .it has led to interesting and educational interactions.

      1
      2 years ago Log in to Reply
    20. Janis Senungetuk

      I notified my supervisor and the Department Manager.

      2 years ago Log in to Reply
    21. Edward Geary

      I wore my pump and, if asked, I told them what it was.

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

      Even as a pre-teen, I reasoned that it was better to broach the subject, rather than wait until I needed help, since trying to explain it when lo would probably be garbled and confusing. I never needed that kind of help, but I was much more comfortable knowing that my friends understood what I was up to with my snacks, etc.

      2 years ago Log in to Reply
    23. Yaffa Steubinger

      I’m a fitness instructor who wears her Dexcom on her arm. They know and sometimes will ask about it.

      1
      2 years ago Log in to Reply
    24. kim bullock

      I am unable to work currently but when I did I told all my co-workers

      1
      2 years ago Log in to Reply
    25. Trina Blake

      My last job was with a large city Fire-Rescue and EMS dept. With my colleagues being EMT’s and paramedics, I was open about it. I eventually was able to have impact on their training (such has how to turn pumps off, keep them clipped securely to the clothing so it doesn’t fall off the gurney during transport, not pulling the infusion set off – the patient can’t resume insulin delivery when they are able to – hospitals don’t have infusion sets to share). One of my fondest work-related/T1D memories was on a response where the patient was newly Dx’d with T1D and his wife was overwhelmed with worry and fear. My colleague pointed at me and said “she has T1D, and it hasn’t stopped her”.

      4
      2 years ago Log in to Reply
    26. Richard Vaughn

      I retired from my teaching job in 1997. My coworkers knew much less about diabetes then than they would now.
      I left the pig in the poke. No reason to reveal my diabetes then, except for people I was with every day.

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

      YES! Always. I told all of my immediate coworkers, including my supervisor. Because I worked in a large facility with over 500 employees, and I was one of the top administrators of the facility. I walked around the facility everyday, and shared my information about T1D with as many employees as possible. I’ve never been shy about sharing information about T1D with others. I go out of my way to talk with others.

      1
      2 years ago Log in to Reply
    28. Anita Stokar

      I worked with hundreds of people so even if I told 20 people, I considered that a few. I wish I had mentioned my diabetes to one coworker as he died from which I believe was a diabetic coma due to low blood sugar. If I had known he was diabetic and living alone, I would have told him to call me every day just so I could keep an eye on him to make sure he was okay. Maybe I could have saved his life. 🙁

      1
      2 years ago Log in to Reply
    29. KarenM6

      I talk about it all the time.
      In fact, just last Thursday, I had to leave work early because my pump occluded and I didn’t have a spare infusion set on me.
      When I talk about it, though, I mostly just get blank looks.

      1
      2 years ago Log in to Reply
    30. Nicholas Argento

      I wear a pump. It is not exactly a secret, and never has been since I started a pump in 1982…

      1
      2 years ago Log in to Reply
    31. George Lovelace

      I Worked Tech Support from home so I Notified HR of the possibilities and I’ve Shared with Coworkers during slow times

      1
      2 years ago Log in to Reply
    32. Jennifer Farley

      I claim a disability and have (at my current position) had to get a Reasonable Accommodation (due to not giving out FMLA or intermittent short leave) for my first year of employment. I had a question about a disability code and the trainer had let me know she had diabetes also. So, I guess it was just sharing information on a common health issue.

      2 years ago Log in to Reply
    33. qachemist

      I did not have LADA when I was working.

      2 years ago Log in to Reply

    At your most recent (or current) job, did you tell your coworkers that you live with T1D? Cancel reply

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