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    • 2 hours, 18 minutes ago
      lis be likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      Although I can currently afford my medical costs, they are not cheap. Future expenses are always a concern. Insurance changes are always difficult. I can never feel truly secure in affordable diabetic care. Of course these expenses are taken away from other areas in my family's budget.
    • 2 hours, 18 minutes ago
      lis be likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      the financial burden is huge but the solution is long term tech and that is why i am working on Re-Life which is a battery free and immune evasive bio interface to stop the need for constant sensor changes and reduce costs for everyone forever we need more than just tools we need a permanent breakthrough
    • 2 hours, 19 minutes ago
      lis be likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      I disagree currently but the possible costs of all my medical conditions are a constant concern
    • 3 hours, 43 minutes ago
      Lee Tincher likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      I disagree currently but the possible costs of all my medical conditions are a constant concern
    • 3 hours, 44 minutes ago
      Lee Tincher likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      Neither agree or disagree; the only thing that has changed for me is the cost of our Medicare Supplement Plan which when we started it almost 9 years ago the monthly cost for each of us was $220 and now is $330.
    • 3 hours, 44 minutes ago
      Lee Tincher likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      A financial burden? I said, "Neither agree nor disagree." But, even with Medicare and a secondary insurance, I still HAVE TO pay to see a doctor quarterly, pay for insulin, and deductibles. The cost is not strangling me, but it is a burden.
    • 3 hours, 44 minutes ago
      Lee Tincher likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      Neither agree or disagree. Over a lifetime of living with T1D It is what it is. The only time it gets to be a burden is if I have to replace something and/or pay out of pocket that isn't covered by insurance. I have always managed to get and have what I need on hand.
    • 3 hours, 45 minutes ago
      Lee Tincher likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      Although I can currently afford my medical costs, they are not cheap. Future expenses are always a concern. Insurance changes are always difficult. I can never feel truly secure in affordable diabetic care. Of course these expenses are taken away from other areas in my family's budget.
    • 5 hours, 35 minutes ago
      Daniel Bestvater likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      Although I can currently afford my medical costs, they are not cheap. Future expenses are always a concern. Insurance changes are always difficult. I can never feel truly secure in affordable diabetic care. Of course these expenses are taken away from other areas in my family's budget.
    • 8 hours, 44 minutes ago
      tpany likes your comment at
      If you could reimagine your diabetes technology, what’s the one thing you would change?
      The ideal is a cure like implantable cells to produce insulin without immunosuppressive drugs. Until then, smaller wearable pumps that last as long as the CGM needed to make it go along with true user control ala DIY systems.
    • 9 hours, 6 minutes ago
      Laurie B likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      A financial burden? I said, "Neither agree nor disagree." But, even with Medicare and a secondary insurance, I still HAVE TO pay to see a doctor quarterly, pay for insulin, and deductibles. The cost is not strangling me, but it is a burden.
    • 9 hours, 8 minutes ago
      Kenneth Gabby likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      the financial burden is huge but the solution is long term tech and that is why i am working on Re-Life which is a battery free and immune evasive bio interface to stop the need for constant sensor changes and reduce costs for everyone forever we need more than just tools we need a permanent breakthrough
    • 9 hours, 13 minutes ago
      Bonnie Lundblom likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      the financial burden is huge but the solution is long term tech and that is why i am working on Re-Life which is a battery free and immune evasive bio interface to stop the need for constant sensor changes and reduce costs for everyone forever we need more than just tools we need a permanent breakthrough
    • 9 hours, 15 minutes ago
      Kathy Hanavan likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      I disagree currently but the possible costs of all my medical conditions are a constant concern
    • 9 hours, 26 minutes ago
      ConnieT1D62 likes your comment at
      How often do you intentionally run your glucose slightly higher during certain activities (e.g., driving, public speaking, exercise)?
      when I am traveling, I will let it run a little higher because I don't know what I'll be doing at any given moment.
    • 9 hours, 36 minutes ago
      Mike S likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      A financial burden? I said, "Neither agree nor disagree." But, even with Medicare and a secondary insurance, I still HAVE TO pay to see a doctor quarterly, pay for insulin, and deductibles. The cost is not strangling me, but it is a burden.
    • 9 hours, 37 minutes ago
      Mike S likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      I disagree currently but the possible costs of all my medical conditions are a constant concern
    • 9 hours, 40 minutes ago
      ConnieT1D62 likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      A financial burden? I said, "Neither agree nor disagree." But, even with Medicare and a secondary insurance, I still HAVE TO pay to see a doctor quarterly, pay for insulin, and deductibles. The cost is not strangling me, but it is a burden.
    • 9 hours, 40 minutes ago
      ConnieT1D62 likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      I disagree currently but the possible costs of all my medical conditions are a constant concern
    • 9 hours, 46 minutes ago
      Lawrence S. likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      the financial burden is huge but the solution is long term tech and that is why i am working on Re-Life which is a battery free and immune evasive bio interface to stop the need for constant sensor changes and reduce costs for everyone forever we need more than just tools we need a permanent breakthrough
    • 9 hours, 47 minutes ago
      mojoseje likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      the financial burden is huge but the solution is long term tech and that is why i am working on Re-Life which is a battery free and immune evasive bio interface to stop the need for constant sensor changes and reduce costs for everyone forever we need more than just tools we need a permanent breakthrough
    • 10 hours, 8 minutes ago
      John Barbuto likes your comment at
      How much do you agree with the following statement: “The financial costs of diabetes are a burden for me (or my family).”
      I disagree currently but the possible costs of all my medical conditions are a constant concern
    • 1 day ago
      Laurie B likes your comment at
      To what extent does diabetes technology reduce day-to-day stress for you?
      I use Tandem control-IQ. It works quite well at night, but during the day I often turn it off or I will become hypoglycaemic. My days are often somewhat physically erratic and the algorithm can’t predict what I’m going to do next. I think if a person’s days are very consistent automated insulin may be of use. With the use of CIQ my A1c seems to be directed towards ~6.5 when turned off I seem to fall into the high 5’s range. So at this point I’m neutral on automated insulin delivery. Not convinced automation can ever match the body’s islet cells….we a cellular treatment!
    • 1 day ago
      Laurie B likes your comment at
      To what extent does diabetes technology reduce day-to-day stress for you?
      I put somewhat since sometimes the technology adds stress (eg. Won’t connect, or alarms that tell me what I already know and am in the middle of treating)
    • 1 day, 2 hours ago
      lis be likes your comment at
      To what extent does diabetes technology reduce day-to-day stress for you?
      CGM is great, but sometimes too much data is stressful. All the pressure to be in range is a new numerical stress with statistical worries added on. The worries were always present, but nowadays they are front and center.
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    For how many years have you been going to the health care practice where you currently receive your T1D care?

    Home > LC Polls > For how many years have you been going to the health care practice where you currently receive your T1D care?
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    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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    34 Comments

    1. Melissa Childers

      I have been seeing the same provider for 20-30 years, but in that time she has been with 3 practice/ hospital systtems, the most recent change about 3 years ago.

      4 years ago Log in to Reply
    2. Ahh Life

      Over 30 years. It is incumbent upon practices or hospitals to accumulate data and improve patients’ experiences.

      Physicians, like patients, come and go. But an organization that generates, accumulates, and aggregates data and continually improves patient outcomes, is an aspired reference group. ᕙ(の_の)ᕗ

      2
      4 years ago Log in to Reply
    3. Lori Lehnen

      I was diagnosed about a year ago but already switched endocrinologists. I believe my current doctor is a good fit and anticipate staying with her for a long time.

      4 years ago Log in to Reply
    4. Steve Rumble

      Not the same physician, but the same practice (an HMO).

      1
      4 years ago Log in to Reply
    5. Greg Felton

      Hmmm…T1 has probably taught me to value routine and consistency, so I have been with my endo practice for 20+ years.

      4 years ago Log in to Reply
    6. Lawrence S.

      I moved here just over 10 years ago. I’ve been going to the same hospital/dr’s office since I moved here. Then the During that time, they have assigned me 4 different practitioners. The first 2 were Endocrinologists (doctors), the last 2 have been ARNP’s. I only saw the 2nd Endo/dr. one time. The vast majority of the time, I have seen the ARNP’s. I felt that the ARNP’s were both better at helping me than the doctors were.

      4 years ago Log in to Reply
    7. Karen Taylor

      I moved 3 1/2 years ago. I’ve had the same Endocrinologist since being here. Prior to my move I wasn’t seeing one even though I had T1D for over 55 years.

      4 years ago Log in to Reply
    8. mojoseje

      I started going to my current practice when I was 18. My doctor has since retired but I continue to see the DA who became more knowledgeable than him in the most recent years. I also took a break in my mid-twenties when my insurance required me to stay in network. That doctor knew so little about diabetes that he was reading how to manage diabetes from a medical volume as I was sitting in the room. He put me on an insulin that made me break out in boils. Horrible experience.

      4 years ago Log in to Reply
    9. Mary Dexter

      Madison has 3 HMOs, two of which are loosely joined. I have been bouncing between them, hoping to find a doctor willing to deal with my reality for the last 18 years. Start a new endocrinologist next week. If this doesn’t work, I may need to go out of Wisconsin. Scoliosis and LADA

      4 years ago Log in to Reply
    10. Kim Davis

      Way back in 1979, my PCP told me to go to several endocrinologists & then determine which one was the best for me. At that time, I knew that a medical center near my home would allow me to see any different specialist that I might need in the future. Also continuity of care would work so they could read the same information in the days before computers!

      4 years ago Log in to Reply
    11. Natalie Daley

      Oregon Health and Science University, OHSU, is, as the name implies, a teaching hospital. I was referred to my current endo by a local doctor over 25 years ago when he said he had no idea how to treat me. My endo is now the head of endocrinology and an excellent doctor.

      4 years ago Log in to Reply
    12. Cheryl Seibert

      My endo is one of the top diabetes endos in the region. I started going to him when I moved to my current city.

      4 years ago Log in to Reply
    13. Karen Mason

      38 years and have moved away and back here finally after retirement. I like the then modern things they did and now still do as advances have been made in caring fir the diabetic.

      4 years ago Log in to Reply
    14. Gary Taylor

      Less than one year because the endo that I saw for 15 years retired.

      4 years ago Log in to Reply
    15. Jane Cerullo

      Have had our ups and downs. Have had to be an advocate for myself. In a good place now

      4 years ago Log in to Reply
    16. Patricia Dalrymple

      Moved or I would still be with my original Endo I took myself to a year after being diagnosed and treated as a T2. I was really LADA T1. Only with this one because convenient. When I retire, I might look for one who is a better communicator.

      4 years ago Log in to Reply
    17. LizB

      Even though I’ve had Type 1 for 35 years I only saw an endo for the first time (since diagnosis) in 2005. I was very happy going to that hospital but in 2021 they went out of network with my insurance I had to go somewhere new. In 2022 they’re back in network but my endo retired! The NP is still there so I will continue to see her. The endo I saw in 2021 is good but I prefer my original practice/location more.

      4 years ago Log in to Reply
    18. Deb Loyola

      Same doctor but he changed clinics so I moved with him. Been seeing him almost 10 years.

      4 years ago Log in to Reply
    19. Louise Robinson

      After having been 13 years with my old endo, I switched to a new one this spring. Last June, I began having issues with my Day 3 insulin absorption. Specifically, the last half of Day 3 yielded higher glucose levels despite using up to 33% more insulin with no appreciable changes in carbohydrate intake or illness or stress. I’ve always rotated my sites among different body areas but have been Type 1 since 1976 and pumping since 2011. My old endo’s case notes were insufficient for Medicare to authorize site changes more frequently than every 3 days, despite repeated attempts. If I were to change earlier than every 3 days, I would run out of cartridges and infusion sets due to Medicare’s “rationing” approach and failure to consider that some sites may need to be changed earlier.. I took to supplementing my pumped insulin with injections during the last half of Day 3. I am currently in the process of trying to get Medicare -approval for site changes every 2.5 days via my new endo. (Believe me, if I could make the site last the full 3 days, I’d be jumping for joy!)

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

        I also have problems with the third day of a pump site but it isn’t every time. I sympathize with your frustration and wish you good outcomes in reaching out to Medicare.

        4 years ago Log in to Reply
    20. gary rind

      have been with mine for all 19 years as a T1D. within the last year, I asked him if he planned on retiring anytime soon and he told me that he didn’t! very happy about that.

      4 years ago Log in to Reply
    21. KarenM6

      I’ve been with mine for 26 years of my 50 years of diabetes. (I’m telling everyone about my 50 year anniversary… even strangers in parking lots… I get odd looks sometimes.) ;p
      Although, my doctor is retiring this year, so things are about to change… eep! I have gotten a few names, so I can choose and I anticipate I will get a great new doctor and PA soon. 😀

      6
      4 years ago Log in to Reply
      1. sweet charlie

        See my note to Lynda !!

        4 years ago Log in to Reply
      2. Ahh Life

        50 is a biggie. No matter whether it’s age, marriage longevity, or diagnosis. Celebrate. You’re worth it. \(T∇T )/

        4 years ago Log in to Reply
    22. lynda meyer

      I will be “celebrating” my 69th anniversary on a few days. I have retired 5 endo’s but have been with the same clinic for the past 30 years.

      4
      4 years ago Log in to Reply
      1. sweet charlie

        WOW, Lynda !!! 69 years for me also !!! I just turned 90 years OLD !!!! NO T1D problems !!! I like to say this to make the newbies feel hopeful !!!

        1
        4 years ago Log in to Reply
    23. JoAnn Pinkowitz

      I have been going to my same diabetes specialist for over 42 years. I get excellent care there. He is also my primary doctor so I have one stop shopping. Unfortunately he will be retiring in a year. I will look for a younger doctor in his practice which he stared and hope I get as good care.

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

      I have been with my current endocrinologist for 32 years now. I’ve had to try other’s due to insurance with different job’s, but I’ve never found another one that I work with so well. I’ve always come back after a visit or two and paid out of pocket if I had too. Before being to see her, I saw the same attending pediatric endocrinologist since 6 months after my diagnosis in Jan. 1982; I only left because they said I was too old to be seen there any more.

      4 years ago Log in to Reply
    25. Kathleen Juzenas

      I think 24 yrs. My first endo unfortunately stopped seeing patients but remains on consult. My new endo as of several years is at same practice. So far so good. The same great nurse practitioner has helped with the transition.

      4 years ago Log in to Reply
      1. Kathleen Juzenas

        Oops! Huge math error. It’s 44 yrs!

        4 years ago Log in to Reply
    26. Cheryl Weaver

      I began seeing my Endo since around 2005, when my primary physician referred me to him for diabetes and thyroid care. He is an excellent Dr. and his staff and nurse practitioners and PAs are awesome. I have been a pump patient since around 2006, and I am going to begin using the t slim x2 pump in just a few days. I’m really looking for a pump that will communicate with my Dexcom 6. I like the fact that my blood sugar is read automatically with that every 5 minutes, and am hoping to have much better control of this monster with this new pump. I’ve had type 1 diabetes since I was 14 years old, and am now 77.

      4 years ago Log in to Reply
    27. M C

      It took a number of years to find the ‘right fit’, and I did this by asking others, I knew to be diabetic, who their endocrinologist was, and whether they liked them or not. Then got a referral, and have been with this same doctor for over 11 years now.

      4 years ago Log in to Reply
    28. Antsy

      My END just left her practice (to do research), so I’m without one until I establish care with my new one in August. I was with this last one for 4 years this time, but she was my 1st END when I was diagnosed in ’93 (so roughly 9yrs overall). In between, I was with my prior doc for 10+ years. My two endocrinologists were pretty great, they just moved on to other things, or out-of-network practices. Hopefully my new one will stay put – and that I like her!

      4 years ago Log in to Reply
    29. PamK

      I recently got a new insurance plan and had to change doctors. So far, I like my new endo and will probably stay with him.

      4 years ago Log in to Reply

    For how many years have you been going to the health care practice where you currently receive your T1D care? Cancel reply

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