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    • 14 hours, 5 minutes ago
      KarenM6 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.
    • 14 hours, 7 minutes ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I have been told many times "YOU CAN'T EAT THAT!" ONLY to frustrate them and eat it anyway and then bolus accordingly.
    • 14 hours, 8 minutes ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I think it is a common experience for most people with T1D. People do not understand anything about it. I do not take it personally. I try to educate when appropriate.
    • 14 hours, 8 minutes ago
      KarenM6 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
    • 14 hours, 17 minutes ago
      KarenM6 likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 16 hours, 9 minutes ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was only 2 when Diagnosed 70 years ago. My small town doctor admitted he didn't know much about T1D, and fortune for my parents and I he called what is now Joslin Clinic, and they told him how much insulin to give me. He taught my parents, who then traveled over 350 miles to Boston, to learn about how to manage T1D. My doctor learned more about T1D, and was able to help 2 other young men, that were later DX with T1D in our small town. I went to Joslin until I turned 18 and returned to become a Joslin Medalist and participated in the research study, 20 years ago. Still go there for some care.
    • 16 hours, 10 minutes ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was 7 when things changed in my home. My older brother was hospitalized for 2 weeks. When he came home, we no longer ate the way we had before. This was 1956. Dessert alternated between sugarless pudding or sugarless Jello. I learned that bread and potatoes had carbohydrates and that turned to sugar. There was a jar in the bathroom. It seemed my brother was testing his urine every time he went in there. There was a burner and pot on the stove designated for boiling syringes. I watched my brother give himself shots and I remember how hard it was to find someone to manage his care if my parents had to travel. Diabetic Forecast magazine came in the mail each month and there were meetings of the local diabetes association that my mother attended religiously. My brother got a kidney and pancreas transplant at age 60 and before he died lived for 5 years as a non-diabetic. A few years later I was diagnosed. Sorry he was not able to make use of today’s technology. I often wonder what he and my late parents would think about me, at age 66, being the only one in the family with type 1.
    • 16 hours, 12 minutes ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 20 hours, 12 minutes ago
      kilupx likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      My brother was type 1 since an early age. I was only diagnosed in my late 40s
    • 22 hours, 15 minutes ago
      Phyllis Biederman likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Absolutely nothing. Diagnosed in late December 1962 at at the age of 8 years and was told I was going for a stay in hospital because I have "sugar diabetes".
    • 22 hours, 56 minutes ago
      Anita Stokar likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Ironically, I was a 10 year old "before" my diagnosis. BUT, one day I was over my friend's house (on what they call a playdate in today's parlance) and we went to the pharmacy to by candy. I remember vividly a video playing on a loop on a little TV on the counter describing what diabetes was and insulin injections every day. I remember thinking to myself that those poor people must feel like pin cushions. Fast forward to two days after my 11th birthday and my doctor telling me that I had diabetes. I remember my mother being fully unaware of what it entailed. I remember telling her that it's ok, all I need to do is take shots every day. She looked at me puzzled, like how do you know this? The doctor was also a little perplexed but added, it's a little more than that, but correct. Then he explained it based on his two-three hours of training in medical school. It's funny how prompts trigger strange memories.
    • 23 hours ago
      Bill Williams likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 23 hours, 24 minutes ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was diagnosed in 1976 at the age of 18 while in college. One weekend, I was drinking a lot of water and peeing frequently. I remembered having read a Reader's Digest article on diabetes, and I told my friends I thought I might have it. Two days later, the diagnosis was confirmed.
    • 23 hours, 24 minutes ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Absolutely nothing. Diagnosed in late December 1962 at at the age of 8 years and was told I was going for a stay in hospital because I have "sugar diabetes".
    • 23 hours, 25 minutes ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I knew I couldn’t or shouldn’t have my two fav things in the world: Pepsi cola and chocolate. I was 42, and suspected very strongly that I had it, and ate a large piece of chocolate cake before my doctor’s appointment (sounds more like I was 12). Fast forward 25 years later: I never had a real cola again, but do occasionally have chocolate. I’m way healthier than I was back then in terms of diet. I no longer have irritable bowel, and I’m lucky to be able to afford what I need to combat the ill effects of this chronic disease. I’m blessed, and grateful for insulin.
    • 23 hours, 26 minutes ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      It was 35 years ago for me. I had no experience with T1d. I was starting to show symptoms and my sister-in-law quickly researched T1d and told me what she found. I went to my GP a week or two later. My BG was over 600. He sent me to the hospital right away. Blood test confirmed it.
    • 23 hours, 26 minutes ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I only knew a little . That is why I give grace to others who do not know anything or have misconceptions.
    • 23 hours, 29 minutes ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Ironically, I was a 10 year old "before" my diagnosis. BUT, one day I was over my friend's house (on what they call a playdate in today's parlance) and we went to the pharmacy to by candy. I remember vividly a video playing on a loop on a little TV on the counter describing what diabetes was and insulin injections every day. I remember thinking to myself that those poor people must feel like pin cushions. Fast forward to two days after my 11th birthday and my doctor telling me that I had diabetes. I remember my mother being fully unaware of what it entailed. I remember telling her that it's ok, all I need to do is take shots every day. She looked at me puzzled, like how do you know this? The doctor was also a little perplexed but added, it's a little more than that, but correct. Then he explained it based on his two-three hours of training in medical school. It's funny how prompts trigger strange memories.
    • 23 hours, 31 minutes ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 23 hours, 33 minutes ago
      KCR likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Ironically, I was a 10 year old "before" my diagnosis. BUT, one day I was over my friend's house (on what they call a playdate in today's parlance) and we went to the pharmacy to by candy. I remember vividly a video playing on a loop on a little TV on the counter describing what diabetes was and insulin injections every day. I remember thinking to myself that those poor people must feel like pin cushions. Fast forward to two days after my 11th birthday and my doctor telling me that I had diabetes. I remember my mother being fully unaware of what it entailed. I remember telling her that it's ok, all I need to do is take shots every day. She looked at me puzzled, like how do you know this? The doctor was also a little perplexed but added, it's a little more than that, but correct. Then he explained it based on his two-three hours of training in medical school. It's funny how prompts trigger strange memories.
    • 23 hours, 34 minutes ago
      KCR likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I knew I couldn’t or shouldn’t have my two fav things in the world: Pepsi cola and chocolate. I was 42, and suspected very strongly that I had it, and ate a large piece of chocolate cake before my doctor’s appointment (sounds more like I was 12). Fast forward 25 years later: I never had a real cola again, but do occasionally have chocolate. I’m way healthier than I was back then in terms of diet. I no longer have irritable bowel, and I’m lucky to be able to afford what I need to combat the ill effects of this chronic disease. I’m blessed, and grateful for insulin.
    • 23 hours, 46 minutes ago
      Gary R. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 23 hours, 59 minutes ago
      ConnieT1D62 likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day ago
      eherban1 likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 1 day, 12 hours ago
      NANCY NECIA likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I think it is a common experience for most people with T1D. People do not understand anything about it. I do not take it personally. I try to educate when appropriate.
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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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    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.

      3 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
      3 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
      3 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
        3 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

      3 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.

      3 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.

      3 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
      3 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
      3 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.

        3 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!

      3 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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