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    • 5 hours, 12 minutes ago
      KarenM6 likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      Moderately. My doctor and pharmacy are awesome, my insurance and durable medical equipment supplier, not so much. The excessive red tape of paper to get DME supplies shipped is almost always a nightmare!
    • 5 hours, 18 minutes ago
      KarenM6 likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      Run, don’t walk from Edgepark! Read my response to Nevin Bowman above! (Hint: the company I was referring to in that post was Edgepark)
    • 5 hours, 18 minutes ago
      KarenM6 likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I once had a supplier withhold old pump supplies while refusing to ship the order for a new pump and I was on a 3-way call with insurance and got to listen to DME lie directly to Insurance about it and then I had the pleasure of interjecting and getting to call them a liar! I would have been more vindicated if it actually accomplished anything, but after I finally got my shipment I fired that DME and never looked back. The red tape that insurance insists on for DME is excessive for chronically ill patients!
    • 5 hours, 27 minutes ago
      kristina blake likes your comment at
      How often do you guess or estimate carbohydrate amounts rather than calculating precisely?
      After doing this weighing and measurements you get pretty good at estimating
    • 6 hours, 48 minutes ago
      Patricia Dalrymple likes your comment at
      How often do you guess or estimate carbohydrate amounts rather than calculating precisely?
      I chose "Often". If I eat something packaged with a nutrition label, I'll use the carbs listed on the label. If I eat a plate of food, at home or at a restaurant, I estimate.
    • 7 hours, 59 minutes ago
      Kathy Hanavan likes your comment at
      How often do you guess or estimate carbohydrate amounts rather than calculating precisely?
      Been doing it for so long it's mostly estimation at this point. Every once in a while at home I'll measure out exact portions of rice, pasta, etc to remind myself just how SMALL portions should be as I tend to let them get a little bigger over time. (wishful thinking) Very helpful to have that image in mind at restaurants where portions tend to be way larger than a single serving.
    • 7 hours, 59 minutes ago
      Kathy Hanavan likes your comment at
      How often do you guess or estimate carbohydrate amounts rather than calculating precisely?
      Yes, for me never weighing or measuring but actively using the Calorie King book and app for several years I have most things memorized or I can make a decent assessment.
    • 7 hours, 59 minutes ago
      Kathy Hanavan likes your comment at
      How often do you guess or estimate carbohydrate amounts rather than calculating precisely?
      After doing this weighing and measurements you get pretty good at estimating
    • 7 hours, 59 minutes ago
      Kathy Hanavan likes your comment at
      How often do you guess or estimate carbohydrate amounts rather than calculating precisely?
      I chose "Often". If I eat something packaged with a nutrition label, I'll use the carbs listed on the label. If I eat a plate of food, at home or at a restaurant, I estimate.
    • 8 hours, 54 minutes ago
      Lawrence S. likes your comment at
      How often do you guess or estimate carbohydrate amounts rather than calculating precisely?
      I chose "Often". If I eat something packaged with a nutrition label, I'll use the carbs listed on the label. If I eat a plate of food, at home or at a restaurant, I estimate.
    • 9 hours, 34 minutes ago
      Amanda Barras likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      Well, since I'm waiting on pump supplies for 2 months now, my confidence is slipping.
    • 9 hours, 34 minutes ago
      Amanda Barras likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I am confident about access to my medical needs in the immediate future. I am not a fortune teller and have no idea what my access to medical supplies will be like in a year or longer. I don't take my spoiled lifestyle for granted.
    • 9 hours, 34 minutes ago
      Amanda Barras likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I've often said that "hoarding": is a character asset for T1D people. I try to purchase (paying out of pocket) a 60-90 day supply - just in case). I have a new health plan,. effective 1/1/26. AS we know, getting an appt with an HCP isn't easy. They have to be accepting new patients, they have to be in network etc. Once I knew what my new policy would be (nov 2025) I made an appt. The earliest appt I could get was in Sept 2026. Thank goodness for my stash of device supplies. I had to go to Urgent care to get an Rx for insulin (my old HMO plan "doesn't do bridge refills"). So yeah, I worry, and plan for hiccups in the supplies process.
    • 9 hours, 41 minutes ago
      Amanda Barras likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I am worried about the changes to Medicare making no provision for getting an immediate replacement if a pump fails. It sounds like we will have to get these from the suppliers instead of a warranty replacement from Tandem themselves (or whatever brand you use). Pumps will be rented and will have to be returned so they can verify the problem before replacing them, which is ridiculous. Meanwhile, Medicare would not pay for us to get long acting insulin as a temporary replacement for the basal.
    • 9 hours, 47 minutes ago
      Amanda Barras likes your comment at
      How often do you guess or estimate carbohydrate amounts rather than calculating precisely?
      After doing this weighing and measurements you get pretty good at estimating
    • 9 hours, 51 minutes ago
      Derek West likes your comment at
      How often do you guess or estimate carbohydrate amounts rather than calculating precisely?
      I chose "Often". If I eat something packaged with a nutrition label, I'll use the carbs listed on the label. If I eat a plate of food, at home or at a restaurant, I estimate.
    • 12 hours, 23 minutes ago
      Ahh Life likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      So far since Jan 1, ‘26, I’ve spent nearly 30 hours on the phone battling and trying to get Medicare covered diabetes supplies. Called 5 different suppliers t get what I need to use my pump.
    • 12 hours, 25 minutes ago
      Ahh Life likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      You are too modest. That hurdle is on fire and you have to juggle chainsaws as you jump over it. Congratulations and good luck making it over the next one in 90 days.
    • 1 day, 2 hours ago
      KarenM6 likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Somewhat satisfied with TSlimX2. Not because of pump shortcomings, but because of the sheer insanity of trying to get routine supplies through the American health care system. My current situation, to wit: "I am experiencing extreme frustration with Medicare that, 1) has an inoperable website, and 2) has an inoperable AI phone answering service. Consequently, I can no longer acquire needed supplies to operate the tSlimX2, particularly the T:Lock TruSteel 8mm 32.” This situation has persisted for 2 months. 😬
    • 1 day, 3 hours ago
      Kristi Warmecke likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      Well, since I'm waiting on pump supplies for 2 months now, my confidence is slipping.
    • 1 day, 3 hours ago
      Laurie B likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I've often said that "hoarding": is a character asset for T1D people. I try to purchase (paying out of pocket) a 60-90 day supply - just in case). I have a new health plan,. effective 1/1/26. AS we know, getting an appt with an HCP isn't easy. They have to be accepting new patients, they have to be in network etc. Once I knew what my new policy would be (nov 2025) I made an appt. The earliest appt I could get was in Sept 2026. Thank goodness for my stash of device supplies. I had to go to Urgent care to get an Rx for insulin (my old HMO plan "doesn't do bridge refills"). So yeah, I worry, and plan for hiccups in the supplies process.
    • 1 day, 3 hours ago
      Kristi Warmecke likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I answered slightly. I'm absolutely certain supplies and medication will be available. However, I'm doubtful they will be affordable. If I can't afford them, I can't access them.
    • 1 day, 4 hours ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I am confident about access to my medical needs in the immediate future. I am not a fortune teller and have no idea what my access to medical supplies will be like in a year or longer. I don't take my spoiled lifestyle for granted.
    • 1 day, 4 hours ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I've often said that "hoarding": is a character asset for T1D people. I try to purchase (paying out of pocket) a 60-90 day supply - just in case). I have a new health plan,. effective 1/1/26. AS we know, getting an appt with an HCP isn't easy. They have to be accepting new patients, they have to be in network etc. Once I knew what my new policy would be (nov 2025) I made an appt. The earliest appt I could get was in Sept 2026. Thank goodness for my stash of device supplies. I had to go to Urgent care to get an Rx for insulin (my old HMO plan "doesn't do bridge refills"). So yeah, I worry, and plan for hiccups in the supplies process.
    • 1 day, 4 hours ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I answered slightly. I'm absolutely certain supplies and medication will be available. However, I'm doubtful they will be affordable. If I can't afford them, I can't access them.
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    Talking about issues of discrimination because of a person’s race or ethnicity can be difficult and experiences based on one’s race and ethnicity are very personal. If you identify as a person of color, have you ever felt discriminated against in your T1D care because of your race or ethnicity?

    Home > LC Polls > Talking about issues of discrimination because of a person's race or ethnicity can be difficult and experiences based on one's race and ethnicity are very personal. If you identify as a person of color, have you ever felt discriminated against in your T1D care because of your race or ethnicity?
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    Do you currently use any of the following insulin pumps?

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    If you have gone through menopause (or you expect to in your lifetime), what is one question you have about menopause and T1D? If you have already experienced menopause, what is one thing you wish you had known about menopause and T1D – or an unanswered question you still have? Please write your question in the comments!

    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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    11 Comments

    1. GLORIA MILLER

      I am a non-Hispanic white but I have two stepsons who are adopted from Ecuador (Hispanic) that I helped to raise. I’ve witnessed much discrimination against them.

      4 years ago Log in to Reply
    2. Mark Schweim

      Also not race related, but I was ruled by the EEOC as discriminated against by the same employer FOUR TIMES because of my T1D. Each time the EEOC fined the employer but kept the full amount of the fines with me getting absolutely none of it. Got my employment restored 3 of the 4 times, but absolutely no compensation for the income I’d lost due to the employment discrimination.

      Last time Pilgrim’s Pride was found guilty of employment discrimination against me, they told the EEOC that they’d agree to pay the added fines but I had already given them over 1.5 million “reasons to refuse to allow me to return to work for them” and when EEOC told me that, they never said how much I had ended up costing Pilgrim’s Pride in total, but the EEOC DID tell me that Pilgrim’s had paid over 1.5 million in fines for the previous 3 cases of employment discrimination they were found guilty of having committed against me!!!

      1
      4 years ago Log in to Reply
    3. Sherolyn Newell

      Interesting that 85% say non-Hispanic white. Is that because T1D hits a lot more non-Hispanic white people or because other ethnicities do not know about this website?

      1
      4 years ago Log in to Reply
      1. Samantha Robinson

        This is a great question! It is believed that T1D is more common in people who are non-Hispanic white, but the available research actually lumps together people with type 1 diabetes and type 2 diabetes. So, it’s unclear what the prevalence of T1D is by race/ethnicity on a national or international scale. But, we honestly don’t know too many details of the demographics of folks who make up our Online Community. It’s our goal to be a welcoming space for all people with T1D, so we were very interested to know more about these experiences – even if they represent a smaller portion of people in our community.

        2
        4 years ago Log in to Reply
    4. Linda Pease

      As a white person I only in encountered it in one place as a child not as an adult it was brutal experience but it shaped me to be inclusive of different races and abilities I think there are bad apples in all groups so to treat them like they are the bad apples before knowing them makes me a bad apple I have several races in my family and abilities and they are great ppl

      4 years ago Log in to Reply
    5. Mick Martin

      I am White European, but I AM a person of colour [color]. I have pinkish skin, blue-green eyes, brown hair, etc. and HAVE experienced discrimination because of my race/ethnicity. This was due to so-called “Positive Discrimination” which was proscribed in order to fill more positions, within the organisation [organization] with which I worked with more people of “ethnic minorities”.

      As for my Type Diabetes care, I don’t recall ever being discriminated against because of my race/ethnicity.

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

      I was not going to respond to this question, because I am white, non-hispanic. But I am deeply discouraged by some of the responses that I have read. Some people openly ignore the facts that our country (and the world) have always discriminated against others because of their race, ethnicity, religion, etc. We are the country that had hundreds of years of slavery, committed genocide against the Native American people, hated the Irish, Italians, Middle Easterners, Hispanics, Jews, Catholics, etc. etc. Yes, racial and ethnic discrimination does occur, and we cannot stick our head in the sand, and say that it does not happen.
      Discrimination happens against people because of their diseases as well.

      4 years ago Log in to Reply
    7. Samantha Robinson

      As we stated in the post and in a previous comment, we understand that issues of discrimination are personal experiences. We do not diminish anyone’s personal feelings or experiences that they have had in their lifetimes about discrimination. However, we want to remind members of our community that sharing their own experiences can be accomplished without minimizing others’ experiences. We want comments to remain on the topic of health care discrimination. And regardless of anyone’s personal experiences, research supports that people in communities of color have faced systemic discrimination because of their race or ethnicity – and that healthcare settings are no exception to a context in which this discrimination can happen.

      We use the term “people of color” as a shorthand to ask about racial and ethnic identity. This comment section is not the appropriate space to argue about the semantics of an imperfect but widely accepted shorthand term. Comments that include arguments about semantics (that is, the meaning of the word ‘color’ and who it applies to) will be removed.

      Diminishing the experiences of others in historically marginalized communities because it is different from your personal lived experiences or arguing about the semantics of a term to put the focus back onto a historically non-marginalized group makes this comment section an unwelcoming place and takes the focus away from our goal of understanding and improving the lives of everyone with T1D.

      3
      4 years ago Log in to Reply
    8. Bea Anderson

      I understand the question, but discrimination as it pertains to a medical setting has far more heads than just our racial backgrounds. A more inclusive question for this group’s interests may have been: Have you ever felt discriminated against for any reason while obtaining your T1 care? Race, sex, age, income, and more. What everyone DOES with their feelings and T1 experiences is the beauty of this place. And I can only imagine some embarrassment to be singled out or excluded on this forum in this way. You have your statistics in hand already. And everyone is personally sensitive for good or bad to our melting pot’s situation. This is only one person’s take on today’s question. I most often love answering these daily questions and appreciate our hosts.

      3
      4 years ago Log in to Reply
      1. Samantha Robinson

        Bea, thank you for your thoughtful comment. We agree that discrimination in healthcare can occur for many reasons and not only race/ethnicity and that it’s important to explore those other areas as well. We have had some similar questions about other areas in the past and we do anticipate having more in the future. Even though these can be sensitive topics, we believe the best way to learn about how specific issues affect our community is to ask.
        We’ve had past questions specifically only apply to some members of our community and not others. Thus we were not expecting to receive the reaction that we did by asking another specific question that only applies to some members with regards to race/ethnicity.

        To your point about statistics, we actually do not have any numbers on the demographic make-up of our Online Community. When people sign up for the Online Community, they have the option to fill out profile details which include their personal connection to T1D, their gender, and their age; however, only about 50% of community members include these details on their profile. So, much of the information we have on our community is gleaned from the community’s response to previous Questions of the Day. There is nothing that we collect in any systematic way that allows us to know the representation of any group – whether that is race/ethnicity, educational attainment, socioeconomic status, or anything else within our Online Community.

        4 years ago Log in to Reply
    9. PamK

      Although I am “White,” I would like to note that I live in an area with a lot of Native Americans and have been mistaken for Native American or Hispanic. My level of care definitely changed in these instances and not for the better. I wish I could do more to change this!

      4 years ago Log in to Reply

    Talking about issues of discrimination because of a person's race or ethnicity can be difficult and experiences based on one's race and ethnicity are very personal. If you identify as a person of color, have you ever felt discriminated against in your T1D care because of your race or ethnicity? Cancel reply

    You must be logged in to post a comment.




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