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    • 11 hours, 56 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.
    • 11 hours, 56 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.
    • 11 hours, 57 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 - πŸ‘ immunosuppression needed - πŸ‘Ž
    • 17 hours, 44 minutes 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 β€œVery 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.
    • 17 hours, 44 minutes 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 - πŸ‘ immunosuppression needed - πŸ‘Ž
    • 18 hours, 44 minutes 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 - πŸ‘ immunosuppression needed - πŸ‘Ž
    • 18 hours, 54 minutes ago
      kristina blake likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I answered β€œVery 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.
    • 19 hours, 3 minutes ago
      Mike S likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - πŸ‘ immunosuppression needed - πŸ‘Ž
    • 19 hours, 23 minutes ago
      Eve Rabbiner likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I answered β€œVery 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.
    • 19 hours, 26 minutes ago
      Marty likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      no immunosuppression needed - πŸ‘ immunosuppression needed - πŸ‘Ž
    • 19 hours, 38 minutes ago
      John Barbuto likes your comment at
      How likely is it that you would participate in a clinical trial for islet cell transplantation?
      I answered β€œVery 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, 14 hours 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.
    • 1 day, 14 hours 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.
    • 1 day, 14 hours 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.
    • 1 day, 16 hours 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".
    • 1 day, 16 hours 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.
    • 1 day, 17 hours 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".
    • 1 day, 17 hours 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.
    • 1 day, 18 hours 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".
    • 1 day, 18 hours 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.
    • 1 day, 18 hours 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.
    • 1 day, 18 hours 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.
    • 1 day, 18 hours 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
    • 1 day, 18 hours 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?
    • 1 day, 18 hours 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.
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    How many appointments did you have in 2020 with your main diabetes healthcare provider?

    Home > LC Polls > How many appointments did you have in 2020 with your main diabetes healthcare provider?
    Previous

    For CGM users: How long have you had a CGM?

    Next

    Would you consider using a smart insulin pen such as InPen from Companion Medical/Medtronic?

    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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    15 Comments

    1. Britni Steingard

      I normally have 4/yr, but I started using a pump in February, so I’ve had at least twice that this year.

      5 years ago Log in to Reply
    2. Amanda Barras

      I only have 1x appt a year, each year. The only difference this year was it was a telemedicine appt instead of in person. Still had to go and get labs drawn at office a few days before tho.

      5 years ago Log in to Reply
    3. Mig Vascos

      For Medicare to cover my pump supplies, sensors and insulin, I’m required to see my endocrinologist every 3 months.

      5 years ago Log in to Reply
    4. Sherolyn Newell

      My doctor always says come back in three months, but usually it’s 4 months before she has an appointment open. That makes it 3 a year instead of 4.

      5 years ago Log in to Reply
    5. Stang777

      For the last 5 years or so, I have only been seeing my doc one time a year and this year was no different in that regard, but it was done as a video appointment instead of in person. I do go in twice a year for an A1c though and this year I only went in once, which was before the pandemic began. We skipped the one in I should have had in July and neither my doc or I cared about that at all. Both my doc and I are pretty sure we already know what my approximate A1c is as it has been very consistent all along, and I test often enough to know that there really would not have been much of a change.

      5 years ago Log in to Reply
    6. Jim Rogers

      I go 3 times a year as per my endocrinologist but after 37 years I kind of got it down now 😊

      5 years ago Log in to Reply
    7. Jana Foley

      I see my endo every three months. This year the last three visits have been telemedicine appointments. I would prefer them to be in person, but that’s not what they are doing right now. I still go in for labs prior to my appointments.

      5 years ago Log in to Reply
    8. John P McLaughlin

      I answered 5 times. Medicare requires a visit within 90 days in order to get supplies. Too much to manage, so I go every 10 weeks vs 12 weeks. All of those this year have been tele-med. Have A Sparkling Day! John P McLaughlin Sr

      5 years ago Log in to Reply
    9. Tim Lors

      For years I have been seeing my doc once a year to get lab work done and my prescriptions refilled. I will be going on Medicare soon, and don’t look forward to more frequent visits as they seem a waste of time & expense for someone whose TIR is 90%.

      5 years ago Log in to Reply
    10. Clare Fishman

      I have had 2 “visits” with my endo this year. 1 in person in early March and 1 via Telehealth in September. With Loop handling most of the insulin dosing decisions, basically the appointments are to make sure the prescriptions are written.

      5 years ago Log in to Reply
    11. Donna Condi

      I saw my endo twice and his NP the other two times.

      5 years ago Log in to Reply
    12. ANN GALLUZZO

      I went the 4 times per year required by Medicare for Type 1 diabetics on pumps.

      5 years ago Log in to Reply
    13. Bekki Weston

      Two, per usual, both in person. I’m not on Medicare yet, but looking to sign up in 2021. I’m curious, for all those on Medicare, who say they have to go every 3 months: is that because you only have Medicare? Or even if you have a Supplemental Insurance, do you still have to go every 3 months? Thanks for your input.

      5 years ago Log in to Reply
    14. Cheryl Seibert

      For decades, I saw my endo every 4 months (if I was doing well) and every 3 months if not. Now, as he approaches retirement and the number of diabetics are increasing, I see him every 4-6 months. He’s my lifeline.

      5 years ago Log in to Reply
    15. Ahh Life

      Four. All tele-medicine. Saves hours and hours of city traffic. The medicare requirement for every 90 days? Their committee of physicians and advisors recommends this, even though my secondary insurance does not. And many of us experienced veterans (long timers) find it risible at times. πŸ€·πŸ»β€β™‚β€ πŸ€·πŸ»β€β™‚β€ πŸ€·πŸ»β€β™‚β€

      5 years ago Log in to Reply

    How many appointments did you have in 2020 with your main diabetes healthcare provider? Cancel reply

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