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    • 3 minutes ago
      atr likes your comment at
      If a study required temporary changes to your usual diabetes routine, how willing would you be to participate?
      I participated in a 6 month study where I had to switch cgm (Dexcom g6 to g7) and go from omnipod 5 back to mdi (using tresiba, I had used lantus when I was mdi previously). I found it very enlightening. I had heard terrible things about the g7 and found I loved it. For me it is very accurate, love the 12 hour grace period (use it to presoak the next one). I was happy to switch to the g7 after the study. I also found I wasn’t so crazy about tresiba. The best part was I feel like I have a better understanding of my basal and bolus settings and I now feel very comfortable switching between the pump and mdi when I want to take a break😊
    • 21 minutes ago
      Gerald Oefelein likes your comment at
      If a study required temporary changes to your usual diabetes routine, how willing would you be to participate?
      I participated in a 6 month study where I had to switch cgm (Dexcom g6 to g7) and go from omnipod 5 back to mdi (using tresiba, I had used lantus when I was mdi previously). I found it very enlightening. I had heard terrible things about the g7 and found I loved it. For me it is very accurate, love the 12 hour grace period (use it to presoak the next one). I was happy to switch to the g7 after the study. I also found I wasn’t so crazy about tresiba. The best part was I feel like I have a better understanding of my basal and bolus settings and I now feel very comfortable switching between the pump and mdi when I want to take a break😊
    • 25 minutes ago
      Sarah Berry likes your comment at
      If a study required temporary changes to your usual diabetes routine, how willing would you be to participate?
      I participated in a 6 month study where I had to switch cgm (Dexcom g6 to g7) and go from omnipod 5 back to mdi (using tresiba, I had used lantus when I was mdi previously). I found it very enlightening. I had heard terrible things about the g7 and found I loved it. For me it is very accurate, love the 12 hour grace period (use it to presoak the next one). I was happy to switch to the g7 after the study. I also found I wasn’t so crazy about tresiba. The best part was I feel like I have a better understanding of my basal and bolus settings and I now feel very comfortable switching between the pump and mdi when I want to take a break😊
    • 9 hours, 29 minutes ago
      AmyM likes your comment at
      How confident do you feel understanding informed consent documents for research studies?
      I am unclear. Maybe you can explain what I am missing. The clinical studies I have done do not involve sharing data with social media. They are medical and are HIPAA protected.
    • 21 hours, 53 minutes ago
      Laurie B likes your comment at
      How often does cost influence your decision to try a new device or therapy?
      I guess it more an insurance restriction than a cost problem. But I don't want to be charged full price for a new pump.
    • 22 hours, 15 minutes ago
      ChrisW likes your comment at
      How often does cost influence your decision to try a new device or therapy?
      MDI and since FIASP is now covered under Medicare I wanted to try the inPen. They wanted over $600 for it so I said no thanks!
    • 23 hours, 4 minutes ago
      Lawrence S. likes your comment at
      How often does cost influence your decision to try a new device or therapy?
      Wish cost did not have to come into play but unfortunately it does.
    • 23 hours, 4 minutes ago
      Lawrence S. likes your comment at
      How often does cost influence your decision to try a new device or therapy?
      It isn’t that I can’t afford devices or meds, it’s more that I feel pharma is jacking up prices to see what the market will bare without conscience. Free enterprise does not work in most of the life sustaining medical community, particularly in the US.
    • 23 hours, 5 minutes ago
      Lawrence S. likes your comment at
      How often does cost influence your decision to try a new device or therapy?
      I guess it more an insurance restriction than a cost problem. But I don't want to be charged full price for a new pump.
    • 23 hours, 5 minutes ago
      Lawrence S. likes your comment at
      How often does cost influence your decision to try a new device or therapy?
      Having to wait for the warrantee period to run out before switching pump manufacturers is the biggest restraint. I had to wait to switch from Minimed 770 to T:slim X2 several months. I am now considering going back to Minimed because of the improvements in their sensor and the problems Tandem is having with infusion set manufacturing. So I have to wait a year.
    • 23 hours, 33 minutes ago
      Steve Rumble likes your comment at
      How often does cost influence your decision to try a new device or therapy?
      Insurance influences my decision to try a new device more than cost.
    • 23 hours, 36 minutes ago
      Kathy Hanavan likes your comment at
      How often does cost influence your decision to try a new device or therapy?
      Insurance influences my decision to try a new device more than cost.
    • 23 hours, 38 minutes ago
      Marty likes your comment at
      How often does cost influence your decision to try a new device or therapy?
      Insurance influences my decision to try a new device more than cost.
    • 1 day ago
      TEH likes your comment at
      How often does cost influence your decision to try a new device or therapy?
      Insurance influences my decision to try a new device more than cost.
    • 1 day, 17 hours ago
      ChrisW likes your comment at
      Have you ever declined a research opportunity? If so, what was the primary reason?
      I turned down a CGM study because the sponsors, a manufacturer, claimed the data would belong to them exclusively. While I may grant use of the data, its mine thank you!
    • 1 day, 22 hours ago
      Natalie Daley likes your comment at
      How confident do you feel understanding informed consent documents for research studies?
      My fear and concern with those who answer "very confident" and are non-lawyers is that you may be unaware of what Facebook, Google, Amazon, Nvidia, Apple, Microsoft, et al do with your data. As the old saying goes about the capitalist, "Here. Take it. How much money will you give me for this rope you are going to hang me by?"
    • 2 days, 23 hours ago
      Anita Stokar likes your comment at
      Have you ever declined a research opportunity? If so, what was the primary reason?
      While I'm not sure if I had a significant chance of being selected, I declined to further pursue the potential for being considered for the Vertex islet cell study, due to it preventing me from donating blood products for at least the duration of the trial. I'm a passionate platelet donor, and I am okay with living with diabetes in order to be able to continue doing so regularly.
    • 3 days, 10 hours ago
      kilupx likes your comment at
      How often do you experience device fatigue (feeling tired of wearing or managing devices)?
      My only fatigue is figuring out where to put my next pump site since pumping 28 years now
    • 3 days, 10 hours ago
      kilupx likes your comment at
      How often do you experience device fatigue (feeling tired of wearing or managing devices)?
      I get itchy rashes from the tandem canula adhesive, so that makes it more of a burden. I dislike having to report to dexcom when their devices fail. and i do feel tired of wearing a device when i see the double down or double up arrow.. they cause a lot of panic and over compensation (on my part). I'd say.. I'm weary, and honestly feel a little judged, every time I hear a beep or see a high or low number. but that's not the device's fault. I'm happy to use the devices though, they keep me closer to ok! especially during sleep.
    • 3 days, 17 hours ago
      lis be likes your comment at
      On average, how many hours per week do you spend actively thinking about or managing diabetes tasks?
      Actively thinking about things is only during pump,CGM changes, meals, activities. Which is not many hours in a day. However, it is always running in the back of mind.
    • 3 days, 17 hours ago
      lis be likes your comment at
      On average, how many hours per week do you spend actively thinking about or managing diabetes tasks?
      Probably just 1 hr most days. But better questions are: (1) how many times per day & (2) how taxing/draining is it?
    • 3 days, 17 hours ago
      lis be likes your comment at
      On average, how many hours per week do you spend actively thinking about or managing diabetes tasks?
      I'm not sure this is something that can be quantified in hours per week? 5 minutes here, 10 minutes there multiple times throughout every day, it adds up. But I don't keep track...it's just life
    • 3 days, 17 hours ago
      lis be likes your comment at
      On average, how many hours per week do you spend actively thinking about or managing diabetes tasks?
      For the last 52 years living with T1, my diabetes care is always on the forefront of everything I do.
    • 3 days, 22 hours ago
      Gerald Oefelein likes your comment at
      Have you ever declined a research opportunity? If so, what was the primary reason?
      I’m either too old or live too far away. I’m 72 and live in Arizona
    • 3 days, 22 hours ago
      Gerald Oefelein likes your comment at
      Have you ever declined a research opportunity? If so, what was the primary reason?
      Quite a few opportunities I would have considered I aged out.
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    Who in your family lives with T1D? Select all that apply. Please share more about your family’s experience with T1D in the comments!

    Home > LC Polls > Who in your family lives with T1D? Select all that apply. Please share more about your family's experience with T1D in the comments!
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    Samantha Walsh

    Samantha Walsh has lived with type 1 diabetes for over five years since 2017. After her T1D diagnosis, she was eager to give back to the diabetes community. She is the Community and Partner Manager for T1D Exchange and helps to manage the Online Community and recruit for the T1D Exchange Registry. Prior to T1D Exchange, Samantha fundraised at Joslin Diabetes Center. She graduated from the University of Massachusetts with a Bachelors degree in sociology and early childhood education.

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    60 Comments

    1. kilupx

      I answered only myself. My late brother had type 1 from the age of 9. He was 64 when he died and I was diagnosed with LADA several years later. We had not lived in the same household since college and never had T1D at the same time.

      2 years ago Log in to Reply
    2. Jan Masty

      A nephew also has t1d.

      2 years ago Log in to Reply
    3. Bea Anderson

      Nephew, sister’s son diagnosed at 11 yrs after bout with influenza they think. In 50’s with complications.

      2 years ago Log in to Reply
    4. PamK

      To clarify: I live with T1D, my mother has LADA, and my maternal uncles – – one with T1D and one diagnosed T2D.

      2 years ago Log in to Reply
    5. mojoseje

      My sibling. 2/5 have T1.

      2 years ago Log in to Reply
    6. Tina Roberts

      Lots of type 2s in the family. I’m the only type 1.

      2 years ago Log in to Reply
    7. Lawrence S.

      I am the only living member of my family with T1D. I had a first cousin, on my father’s side of the family, who had a son who was T1D. Unfortunately, he did not take care of himself and died young, around 20 years old.

      2 years ago Log in to Reply
    8. Twinniepoo74

      Myself and my second youngest niece. I got diagnosed first and two years later she got diagnosed.

      2 years ago Log in to Reply
    9. JOAN ULMER

      Also have 2 nieces, 2 great nephews with TD1. Brother just dx with TD2.

      2 years ago Log in to Reply
    10. ConnieT1D62

      I am the only one still alive. My late father and his younger sister sister were diagnosed with LADA in their 30’s and a first cousin on my maternal side was diagnosed with LADA in her mid-20s. My father and his sister died in their early-50s of complications from another genetic disease processes other than T1D. My cousin tragically drowned during a cardiac arrest and episode of hypoglycemia whist going for a daily swim. At age 61 she was still navigating T1D in the dark with MDI and without a CGM.

      2 years ago Log in to Reply
    11. MDOberg

      My grandson who is 19 years old.
      My uncle on my mother’s side died with it at 12 years of age, and an uncle on my father’s side it at 41 years of age.

      2 years ago Log in to Reply
    12. Annie Wall

      I believe I answered this wrong! I answered “my spouse” because he lives with me and my diabetes! So I should have answered just me. In terms of blood relations, no one in my family on either side as long as anyone remembers has diabetes except me.

      2 years ago Log in to Reply
    13. Julie Blehm

      My sister also has Thpe 1 DM

      2 years ago Log in to Reply
    14. John McHenery

      In addition to my father and paternal grandfather, both deceased, two children on one cousin have T1D.

      2 years ago Log in to Reply
    15. Bruce Schnitzler

      Myself, my older brother (now deceased), and one of seven grandchildren.

      2 years ago Log in to Reply
    16. Daniel Bestvater

      I have had T1D myself for 45 years. My father also had T1D diagnosed in his mid 30’s. He did not live very long due to not accepting the diagnosis and turning to alcohol as his main treatment plan……this did not turn out very well!

      2 years ago Log in to Reply
    17. Jane Cerullo

      I have LADA. A first cousins diagnosed as a child. Father diagnosed as type 2 but I think may have been LADA

      2 years ago Log in to Reply
    18. Kathleen Juzenas

      My brother also has T1d.

      2 years ago Log in to Reply
    19. CindyGoddard

      Myself at age 20, 50 years ago and my brother who was diagnosed at age 57 11 years ago

      2 years ago Log in to Reply
    20. Anne Blayney

      I’m the only one in my extended family to LIVE with T1D. My grandmother’s cousin died from it in that window between when insulin had been discovered and when insulin was actually available as a treatment. This family connection sure makes me appreciate my own treatment options, because I’m so aware that this used to be am automatic death sentence.

      1
      2 years ago Log in to Reply
    21. Kate Kuhn

      In order of diagnosis: paternal uncle, paternal aunt, father, myself, my sister, my paternal cousin, my son.

      2 years ago Log in to Reply
    22. Yaffa Steubinger

      I have T1 as do two of my grandsons. Autoimmune disease…the ‘gift’ that keeps on giving.

      2
      2 years ago Log in to Reply
    23. Ja'fr Yirka

      My sister

      2 years ago Log in to Reply
    24. Claire Potocki

      My sister

      2 years ago Log in to Reply
    25. KCR

      My dad was diagnosed T2 but as I look back I do wonder if he was really late-onset T1 like me.

      1
      2 years ago Log in to Reply
      1. jo

        I often think back and wonder the same thing about my Dad.

        2 years ago Log in to Reply
      2. Kristi Warmecke

        My Uncle was diagnosed as type 2; but needed insulin from the very start. Was in 40’s when he was. His endocrinologist refused to do a C- Peptide on him so when I was diagnosed in 1982 with 3 family members on insulin the endocrinologist my brother & I saw offered to do it for him, for their research and his knowledge. My Uncle’s endocrinologist refused to accept the fact that he was T1D; but he knew at least and could inform his other physicians.

        2 years ago Log in to Reply
    26. Kelly Steiner

      My brother

      2 years ago Log in to Reply
    27. KIMBERELY SMITH

      My step dad

      2 years ago Log in to Reply
    28. Dawn Konig

      My granddaughter

      2 years ago Log in to Reply
    29. Judith Marged

      My great-nephew was recently diagnosed.

      2 years ago Log in to Reply
    30. Carol Meares

      My sister and 2 paternal cousins once removed (son of one cousin and daughter of another cousin)

      2 years ago Log in to Reply
    31. Nevin Bowman

      Myself, niece, nephew, niece’s son(not the niece with diabetes)

      2 years ago Log in to Reply
    32. Scott Doerner

      Fascinating. I read that 60+% of T1D people, have it nowhere in the family. (Like me). But it seems so many do.

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

      On my dad’s side, his uncle had T1D. On my mom’s side, no T1D but lots of autoimmune: alopecia, RA, etc.

      2 years ago Log in to Reply
    34. Russell Buckbee

      I marked “only myself” but really my wife has to live thru hey highs and lows as well as all the time I spend managing it. She sometimes worries more than me. She may be right.

      4
      2 years ago Log in to Reply
      1. cynthia jaworski

        Anyone who lives with me could be considered a person living with type one.

        1
        2 years ago Log in to Reply
    35. Bob Durstenfeld

      My Dad was diagnosed In 1931 and died in 2000. I have 2 out of three younger brothers with T1D. My eldest son of three has T1D. His eldest daughter of two has T1D.
      I was dx”ed in 1956.

      2 years ago Log in to Reply
    36. Janis Senungetuk

      My maternal grandfather was dx in his 30’s, long before there was medical acceptance of types. He used beef/pork insulin until his death at 73 from a heart attack. My maternal grandmother had a first cousin who died before insulin was available and another cousin who died after rejectioning the use of insulin. After my dx as a child my paternal second cousin was dx at the age of three. We are the only two from our immediate families still living with Type 1.

      2 years ago Log in to Reply
    37. Natalie Daley

      Although I answered only myself that’s because my older brother already died of T1D complications at 67, and my maternal grandmother died in her mid-40s. She was misdiagnosed and given Diabinase. She died of gangarene. Both were late onset. My brother was 23. My grandmother was in her 40s.

      2 years ago Log in to Reply
    38. Anneyun

      Myself and one of my nephews.

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

      My maternal uncle, in 1929. My nephew, three months before me. However, the family is chock full of Type II’s.

      2 years ago Log in to Reply
    40. jo

      Myself, my older brother who passed and my nephew(brothers son).

      2 years ago Log in to Reply
    41. mlettinga

      My brother who got type one at age 5 and myself at age 8. Didn’t see a sibling box.

      2 years ago Log in to Reply
    42. Jian

      3 brothers with type 1, 1 cousin 2 nieces, 2 daughters. We sure got an unusual family

      1
      2 years ago Log in to Reply
    43. Tanya Levchuk

      My half brother is also a type 1 diabetic

      2 years ago Log in to Reply
    44. Steven Gill

      Besides a maternal grandmother, paternal cousin, and myself a younger adult brother (didn’t see a sibling listed).

      2 years ago Log in to Reply
    45. Bekki Weston

      My older brother (by 3 years) was dx in his mid-40s, about 20 years ago. I’m coming up on 10 years.

      1
      2 years ago Log in to Reply
    46. LizB

      One of my sisters also has Type 1.

      2 years ago Log in to Reply
    47. Molly Jones

      I’m the only one with T1D, but many others on my maternal side have autoimmune conditions.

      2 years ago Log in to Reply
    48. William Bennett

      My 1st cousin’s daughter (“2nd cousin”) is the only one we know about in my extended family, which comprises about 50 people in all. Type 2 not a thing for my family either.

      2 years ago Log in to Reply
    49. mbulzomi@optonline.net

      Only me, and no other person with T1D or T2D.

      2 years ago Log in to Reply
    50. T1D Dadvocate

      When our son was diagnosed with Type 1 Diabetes just over four months ago, at the age of 7, I was overwhelmed with various emotions. Initially, I felt a sense of guilt, wondering if I could have detected it earlier or if it was somehow connected to the autoimmune diseases prevalent in my family. I shed tears and mourned the life I had envisioned for him.

      Fast forward to today, my perspective has drastically shifted. I immersed myself in learning everything about diabetes and continue to do so. I began sharing our journey on Instagram (@xanderst1djourney) to spread awareness about Type 1 Diabetes. I proudly embrace my role as a stay-at-home #T1dDadvocate 🦸🏻‍♂️🩸💙.

      I no longer grieve over the life I thought he would miss. Instead, we have discovered the incredible love and support within the T1D community. Recently, I hosted a JDRF Meetup at a local park and we just returned from the JDRF One Walk in San Diego, an exhilarating experience for Xander. He donned a cool blue cape and even met professional baseball player Adam Duvall! These experiences are ones many children only dream of. Xander is not just living his life; he’s inspiring newly diagnosed T1D warriors. I hope that by sharing our struggles and triumphs in parenting a child with T1D, I can resonate with other caregivers and reassure them that they are not alone.

      2
      2 years ago Log in to Reply
    51. Kristi Warmecke

      First T1D was my maternal great-Grandmother, then my brother, then a maternal Uncle, then myself, & my oldest niece. My youngest niece showed antibodies at brith in her cord blood and has been a part of a prevention trial since.

      2 years ago Log in to Reply
    52. Sue Herflicker

      My brother has T1D, diagnosed at 4 years old. He wasn’t a choice above. I was diagnosed at 56. My 2 sons were diagnosed at 23 months and 3 years old.

      2 years ago Log in to Reply
    53. Anita Stokar

      I used to have a type-1 cousin but unfortunately she passed away a few years ago due to complications from diabetes. I am the only one left that I know of who is type-1.

      2 years ago Log in to Reply
    54. Kim Murphy

      My Sister has it. I was diagnosed at age 19 and she was diagnosed at age 8 just two years after I was diagnosed.

      2 years ago Log in to Reply
    55. Sparklee

      Besides myself, my sister who was diagnosed at age 41, and her daughter, my niece, who was diagnosed at age 4.

      2 years ago Log in to Reply
    56. Mary Berube

      “Other” as none of the options applied. My sibling (identical twin), one of our nieces, and me.

      2 years ago Log in to Reply
    57. Steve Rumble

      There was no response for myself and someone else so I answered only myself and my spouse/domestic partner

      2 years ago Log in to Reply

    Who in your family lives with T1D? Select all that apply. Please share more about your family's experience with T1D in the comments! Cancel reply

    You must be logged in to post a comment.




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