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    • 33 minutes ago
      kristina blake likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Yes and it is really annoying especially when they "You shouldn't eat that - you're a diabetic" and it's even more annoying and irritating when it is being said by a person in a healthcare profession. I can honestly say from many years of experience as a PWTID and as a RN that hardly ANYONE in the general public or in the general medical field says "because you live with diabetes" when referring to a PWD or when they admonish someone for "being diabetic" . It is a label that doesn't acknowledge the person. As I have stated before in other posts, are people who live with cancer called "canceretics"?
    • 57 minutes ago
      Mary Coleman likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Yes. It’s f*ing annoying.
    • 59 minutes ago
      Mary Coleman likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Yes and it is really annoying especially when they "You shouldn't eat that - you're a diabetic" and it's even more annoying and irritating when it is being said by a person in a healthcare profession. I can honestly say from many years of experience as a PWTID and as a RN that hardly ANYONE in the general public or in the general medical field says "because you live with diabetes" when referring to a PWD or when they admonish someone for "being diabetic" . It is a label that doesn't acknowledge the person. As I have stated before in other posts, are people who live with cancer called "canceretics"?
    • 1 hour, 10 minutes ago
      John Barbuto likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Lol hell when haven't they. Lol
    • 1 hour, 10 minutes ago
      John Barbuto likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Yes and it is really annoying especially when they "You shouldn't eat that - you're a diabetic" and it's even more annoying and irritating when it is being said by a person in a healthcare profession. I can honestly say from many years of experience as a PWTID and as a RN that hardly ANYONE in the general public or in the general medical field says "because you live with diabetes" when referring to a PWD or when they admonish someone for "being diabetic" . It is a label that doesn't acknowledge the person. As I have stated before in other posts, are people who live with cancer called "canceretics"?
    • 1 hour, 10 minutes ago
      John Barbuto likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      This is actually one of my biggest pet peeves. People who say, "Are you sure you can/should eat that?" Excuse me, but I think I know how to take care of myself and my diabetes better than you ever could. Thankfully, this does not happen much anymore, but years ago, it was a common refrain...
    • 1 hour, 27 minutes ago
      Anthony Harder likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Like most of the above comments, it's more of a question. The statements have come in situations where I'm not actually eating something...like someone saying, "Oh, it must be hard to not be able to eat desserts!"
    • 1 hour, 28 minutes ago
      Anthony Harder likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Like others here, it's more of "Can you eat . . .?" than "You shouldn't eat . . .!" Nonetheless, it comes across the same way.
    • 1 hour, 29 minutes ago
      Anthony Harder likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      This is actually one of my biggest pet peeves. People who say, "Are you sure you can/should eat that?" Excuse me, but I think I know how to take care of myself and my diabetes better than you ever could. Thankfully, this does not happen much anymore, but years ago, it was a common refrain...
    • 2 hours, 39 minutes ago
      Steve Rumble likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Like others here, it's more of "Can you eat . . .?" than "You shouldn't eat . . .!" Nonetheless, it comes across the same way.
    • 2 hours, 40 minutes ago
      Steve Rumble likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      This is actually one of my biggest pet peeves. People who say, "Are you sure you can/should eat that?" Excuse me, but I think I know how to take care of myself and my diabetes better than you ever could. Thankfully, this does not happen much anymore, but years ago, it was a common refrain...
    • 4 hours, 4 minutes ago
      mojoseje likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      This is actually one of my biggest pet peeves. People who say, "Are you sure you can/should eat that?" Excuse me, but I think I know how to take care of myself and my diabetes better than you ever could. Thankfully, this does not happen much anymore, but years ago, it was a common refrain...
    • 16 hours ago
      Neha Shah likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      Long time ago - told there were certain occupations I would not be allowed to do because if T1D. Pilot, air traffic controller, military, etc.
    • 18 hours ago
      Amanda Ratliff likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      My grandma told me u could never have kid. I had two successful pregnancies.
    • 18 hours, 1 minute ago
      Amanda Ratliff likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      Oh my goodness… yes! As a child I was often reminded of my limitations because of diabetes. I’m hopeful that those misconceptions about T1D have changed over the decades.
    • 18 hours, 2 minutes ago
      Amanda Ratliff likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      Me too! 2kids and now soon to be 6 grandchildren. We just persevere, don’t we.
    • 18 hours, 2 minutes ago
      Amanda Ratliff likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      I was diagnosed with t1 41 years ago. I was told to NOT have children. But I did not listen and had two healthy children.
    • 18 hours, 53 minutes ago
      Sarah Berry likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      Long time ago - told there were certain occupations I would not be allowed to do because if T1D. Pilot, air traffic controller, military, etc.
    • 21 hours, 48 minutes ago
      René Wagner likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      Oh my goodness… yes! As a child I was often reminded of my limitations because of diabetes. I’m hopeful that those misconceptions about T1D have changed over the decades.
    • 21 hours, 53 minutes ago
      René Wagner likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      Long time ago - told there were certain occupations I would not be allowed to do because if T1D. Pilot, air traffic controller, military, etc.
    • 23 hours, 33 minutes ago
      Bonnie Lundblom likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      Is there a formula for how much more insulin to take when getting a steroid shot?
    • 23 hours, 33 minutes ago
      Bonnie Lundblom likes your comment at
      Between your regular T1D care visits, what questions tend to come up that you wish you could ask a diabetes expert? Share your thoughts in the comments.
      Dealing with wild bg swings.
    • 1 day ago
      Julianne likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      Long time ago - told there were certain occupations I would not be allowed to do because if T1D. Pilot, air traffic controller, military, etc.
    • 1 day ago
      lis be likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      Possess a Class A driver's license. Would allow u to drive a bus.
    • 1 day ago
      lis be likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      YES, DONATE PLASMA for the production of IGG. My wife is immune compromised with CVID. I was extremely disappointed when the technical support nurse basically said No you’re on insulin and it’s not filtered out during the washing process.
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    Do you currently feel like the financial costs associated with T1D require you to make sacrifices in other areas of your life?

    Home > LC Polls > Do you currently feel like the financial costs associated with T1D require you to make sacrifices in other areas of your life?
    Previous

    If you use a CGM, do you ever experience “compression lows”? These are inaccurate CGM readings that occur when there is pressure placed on the CGM transmitter and sensor. They typically look like a sudden and drastic drop on a CGM graph, and often occur when a person is lying on their sensor.

    Next

    For insulin pump users: Is your current pump still under warranty?

    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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    39 Comments

    1. Angela Naccari

      I answered yes which is incorrect. I thought I was answering a different question. Need to fix the percentages.

      2 years ago Log in to Reply
    2. Raj Gowin

      Since I have coverage as in Medical Insurance I no longer feel that way

      1
      2 years ago Log in to Reply
    3. Robert Wilson

      All the money I spend could have been invested or saved for something that would bring a long term value to myself or my family. In over 25 years I have spent, including my cost of insurance over $195,000. That’s what I have paid to stay alive for another 24 hours since I was diagnosed in 1997. If I could have put that in a retirement account instead…. even with the current downturn I would be in a way better retirement position since I am 9 years away from retirement today.

      3
      2 years ago Log in to Reply
    4. Lisa Sierra

      I’m currently disabled so I get full coverage for the first time in my life. In my 20’s and 30’s blood glucometer strips were super expensive. I couldn’t afford both strips and insulin so I’d only purchase insulin.

      1
      2 years ago Log in to Reply
    5. Nevin Bowman

      Absolutely, yes.

      2 years ago Log in to Reply
    6. Eve Rabbiner

      I am so sad to see how many people answered yes. I’m grateful that my Medicare Advantage plan covers most of my expenses.

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

      There are no financial costs associated with T1 Diabetes for myself as I live in the UK (United Kingdom of Great Britain and Northern Ireland) where all of financial costs are covered by our NHS (National Health Service), which is financed via direct taxation of all working people.

      That does NOT mean that we don’t have to make sacrifices in other areas of our lives. Having been retired on grounds of ill-health in 1990 and therefore requiring support from Government handouts, there are times when I’ve been admitted to hospital where it’s been found that I’ve been suffering with malnutrition. This is because we often have periods when we can’t even afford basic food necessities. (The only way that I’m able to use the internet is because one of our neighbours [neighbors] graciously allows me to ‘piggyback’ his internet connection.)

      I can’t remember how long it’s been since we last went out for a meal; visit a pub; visit a museum or art gallery, etc. but it’s been well over 25 years now.

      3
      2 years ago Log in to Reply
    8. Lisa Moir

      My insurance cover most of the costs, but the high cost of insurance premiums affect how I spend in other areas of my life.

      2
      2 years ago Log in to Reply
    9. Kathy Hanavan

      I am blessed that my answer is no due to insurance and a good job before retirement that keep me comfortable financially.

      2 years ago Log in to Reply
    10. TomH

      I don’t see how anyone with T1 can seriously answer “No” to this. My perception is just having to take insulin routinely, having to deal with injections, CGMs, pumps, insulin, and appointments, and meds forces “sacrifices” of some sort. That said, it’s how T1s “deal” or “handle” those impacts thats of consequence.

      5
      2 years ago Log in to Reply
      1. Katrina Mundinger

        The question is specifically about the financial sacrifices, not the emotional cost of having T1. I’ve had to stay in jobs (and my husband is currently staying in a job) that are not what I went to school for due to needing some type of coverage, no matter how slim.

        2 years ago Log in to Reply
    11. William Bennett

      Being in the Jardiance donut hole means I gotta pay $800 to cover me from August to the end of the year, and that kicks my bank account pretty hard. Yay for Tier 3 drugs. But it really helps level things out for me so I don’t want to go off it.

      2 years ago Log in to Reply
    12. Jane Cerullo

      Have said before I feel discriminated against by Medicare for choosing MDI over a pump. Have to pay monthly for two insulins, needles, InPen. The InPen lasts for a year and should be Part B as a pump is. May at some point have to go back to a pump for financial reasons

      1
      2 years ago Log in to Reply
      1. Karen DeVeaux

        I feel the same way.

        2 years ago Log in to Reply
    13. cynthia jaworski

      A few years ago when insulin prices first spiked, I was paying a co-pay for covered drugs. My box of pens for just one of my insulins was then listed as well over $1200 for 3 months. These expenses came out of the blue. I had to forgo retirements contributions and planning.

      2 years ago Log in to Reply
    14. Janice B

      In the past with different insurance yes. Now with Medicare and Medicare advantage no. However I have heard insurance rates are going to increase quite a bit next year- ouch. That may make a difference in how I answer.

      2 years ago Log in to Reply
    15. Jen Farley

      Just yesterday, my husband had retired, and my insurance was through his employer. When I called in my prescription for Novalog, I was told the cost was $317.00. My jaw dropped. I was paying $17 per bottle. My costs have increased, and it seems all of them have and it is not cool I am being punished for having diabetes. Thank you, insurance company.

      1
      2 years ago Log in to Reply
      1. Pauline M Reynolds

        You should not pay more than $35 a month no matter what insurance you have. New law.

        1
        2 years ago Log in to Reply
    16. Pauline M Reynolds

      No….not because I don’t have lots of medical expenses, but because I life rent free.

      2 years ago Log in to Reply
      1. Pauline M Reynolds

        *live

        2 years ago Log in to Reply
    17. KIMBERELY SMITH

      Inconvenient bladder products

      2 years ago Log in to Reply
    18. Jeremy Hanson

      I am self employed which means I pay through the nose for insurance premiums. Luckily, I can afford to pay for a good plan that covers most of my meds and supplies but I would certainly have a lower premium plan if I did not have T1D.

      2 years ago Log in to Reply
    19. Steven Gill

      I’m single, working a true “lower-middle income” job meant cash consideration was always part of life. Along with plenty of overtime hours, I did yard work and other odd jobs for luxuries (to include the dogs I’ve rescued) like cable and yeah the insulin and other supplies. But my medical costs were always a consideration. Sacrifice? My vacations were to drive to visit family, in a vehicle I did all the maintenance. But my neighbors did similar to be sure their children had school items. Don’t know if my Saturday nights grilling hotdogs at a neighbor’s because steaks weren’t on sale is a sacrifice, but having diabetes for me is always a concern. I don’t know if I’d have a greater quality of life if not TYPE 1, more money.

      (Admitted last week I really feel lucky because I feel better at 63 than many much younger, that stress towards health might have offered a huge benefits. Even with a sore back and knees I really feel lucky, financially? Unsure)

      1
      2 years ago Log in to Reply
    20. Becky Lamont

      The cost of insulin and supplies is a major cost each month.

      1
      2 years ago Log in to Reply
    21. Sue Martin

      It used to be when I wasn’t employed. I’m now in a stable job and don’t worry about the costs so much.

      1
      2 years ago Log in to Reply
    22. Kristine Warmecke

      I answered yes; HOWEVER for many years it didn’t. Wasn’t until the drug companies, middle man, etc. wanted more money that it’s caused me to make sacrifices (food, electric, water, health and car insurance, rent, car payment) which one can I skip this month so I can pay for my Novolog since my Medicare Advantage plan STILL refuses to cover it even though I can’t use Humalog because I’m allergic to it. sigh

      1
      2 years ago Log in to Reply
      1. Kristine Warmecke

        I should also mention that my plan covers my pump & Dexcom supplies at 100%, thank goodness.

        2 years ago Log in to Reply
      2. Philip Bunsick

        I used Novolin R for a while to compare lower cost insulins to Humalog and it worked very well for me. Of course an older insulin and not as fast acting but my TIR was the same – but did have a few more lows – but for $30 per vial at Walmart and no prescription needed it worked well.

        2 years ago Log in to Reply
      3. Kristine Warmecke

        @Philip Bunsick I use Novolin R when I had to take a heavy duty steroid; that way my pump setting doesn’t have to be increased so much I’m changing it out daily.

        2 years ago Log in to Reply
    23. Bea Anderson

      Of course, but I was adult and remember the before and after. So perspective.

      2 years ago Log in to Reply
    24. T1D4LongTime

      I have good corporate insurance, however I still reach my out of pocket around September or October each year. I’m approaching Medicare now, so that may make expenses better with the sensors and insulin covered.

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

      YES definitely! For the past 68+ years the financial burden of increasing medical expenses has been a determining factor.

      2 years ago Log in to Reply
    26. Tb-well

      My sacrifices are more like staying in a job because of health insurance than deciding to use different things due to cost.

      1
      2 years ago Log in to Reply
    27. Jen Farley

      @Pauline M Reynolds
      I think their loop around is having me switch from one insulin to another and the one they have me switching to through another company is $35.00 per bottle. Still higher than $17.00 per bottle

      2 years ago Log in to Reply
    28. Jeff Balbirnie

      Money forced to buy mandatory D supplies, medications cannot be used elsewhere. 1,000% absolutely the costs require obscene tragic sacrifices.

      2
      2 years ago Log in to Reply
    29. Melinda Lipe

      I am used to dealing with insurance coverage as well as co-pays. It’s been a part of my life for 57 years. God has blessed, and helped me to afford what is needed.

      2 years ago Log in to Reply
    30. Dale Norman

      I answered no but I currently have employer provided insurance. As I approach retirement I am very concerned about keeping the same level of care at a reasonable cost.

      2 years ago Log in to Reply
    31. Katrina Mundinger

      I’ve not been able to do many things I’d like to do: purchase 2 more clarinets (ranging from 3,000 to 5,000 USD), travel to learn more music, and both of those things prevent me from getting more performances and income. 🙁

      2 years ago Log in to Reply
    32. jurgen vercauteren

      no, In Belgium we have fortunately a great health insurance system! All employees pay tax for that and we are not even in the Soviet Union 🙂 All medical costs are partial or fully re-imbursed.

      2 years ago Log in to Reply

    Do you currently feel like the financial costs associated with T1D require you to make sacrifices in other areas of your life? Cancel reply

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