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    • 1 hour, 23 minutes ago
      Donna Owens 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.
    • 12 hours, 5 minutes ago
      Amy Schneider likes your comment at
      Do you store your unopened insulin in the refrigerator?
      I keep my opened insulin in the refrigerator too. When traveling I use a FRIO evaporative pouch.
    • 13 hours, 32 minutes ago
      Kathy Hanavan 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.
      I want a thumbs down icon!
    • 13 hours, 32 minutes ago
      Kathy Hanavan 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.
      I seldom have any questions other than RX refill request which I submit through the patient portal. If I do have treatment questions, I typically do my own research, and if not satisfied with what I find out, I submit a question in the portal.
    • 13 hours, 32 minutes ago
      Kathy Hanavan 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.
      When I come up with a question between visits, I usually just do some research.
    • 15 hours, 45 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      I keep my opened insulin in the refrigerator too. When traveling I use a FRIO evaporative pouch.
    • 15 hours, 46 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Sorry. Of course I store unopened in frig. Opened in my room as I use it up in 30 days
    • 15 hours, 46 minutes ago
      ConnieT1D62 likes your comment at
      Do you store your unopened insulin in the refrigerator?
      No, I keep it in the oven! ;) Same answer as the last time they asked this ridiculous question!
    • 16 hours, 28 minutes ago
      Becky Hertz likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Unopened yes, and now even opened just in case. I am getting a new health [lan (thank goodness a much better one - with better doctors and hospitals in network!) so it's worth it. But I can't get any appt - even for a PCP until September. I've been occasionally buying out of pocket insulin, pump and CGM supplies (in my mind, hoarding is a character asset for T1D people). I need to have my enough stuff to see me through, Of course, I am hoping there''s an appt cancellation.
    • 17 hours, 52 minutes ago
      Bruce Schnitzler likes your comment at
      Do you store your unopened insulin in the refrigerator?
      Unopened yes, and now even opened just in case. I am getting a new health [lan (thank goodness a much better one - with better doctors and hospitals in network!) so it's worth it. But I can't get any appt - even for a PCP until September. I've been occasionally buying out of pocket insulin, pump and CGM supplies (in my mind, hoarding is a character asset for T1D people). I need to have my enough stuff to see me through, Of course, I am hoping there''s an appt cancellation.
    • 19 hours, 49 minutes ago
      alex likes your comment at
      Here’s What You Need to Know About the Dexcom G7
      This article explains the Dexcom G7 features in a clear and easy way, especially for people new to continuous glucose monitoring. Very informative and helpful. Sportzfy TV Download
    • 1 day, 11 hours 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.
    • 1 day, 11 hours 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.
    • 1 day, 11 hours 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.
    • 1 day, 11 hours 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
    • 1 day, 11 hours 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 ´ )⎠⎞
    • 1 day, 13 hours 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.
    • 1 day, 13 hours 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.
    • 1 day, 13 hours 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 ´ )⎠⎞
    • 1 day, 17 hours 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
    • 1 day, 19 hours 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".
    • 1 day, 20 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 ´ )⎠⎞
    • 1 day, 20 hours 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.
    • 1 day, 20 hours 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".
    • 1 day, 20 hours 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.
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    Have you ever participated in a T1D charity fitness event (i.e., a walk, run, bike, etc.)? Share in the comments about your experience!

    Home > LC Polls > Have you ever participated in a T1D charity fitness event (i.e., a walk, run, bike, etc.)? Share in the comments about your experience!
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    Have you ever experienced other people acting fearful or otherwise negatively about you checking your BG levels or disposing of glucose strips because of the blood?

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    Have you had a virtual care appointment via phone or video call (sometimes called a telehealth or telemedicine visit) with your T1D health care provider?

    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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    28 Comments

    1. Britni

      My JDRF One Walk team walked in two different cities every year for over a decade (we started back when it was the Juvenile Diabetes Foundation “Walk for the Cure”). My sister and I were co-captains in our hometown and my paternal grandparents captained the other half of the team in Florida. My sister and I would visit during spring break and walk with all our grandparents’ friends. For the one in our hometown, our whole family and all our friends participated in some way. My maternal grandfather couldn’t walk so he would volunteer to help tally the donations. And all my cousins, on both sides, would come to visit for the weekend. It felt like a big party, even better than my birthday, and as a kid I used to tell people it was the one day of the year having diabetes was fun.

      2
      3 years ago Log in to Reply
      1. Jneticdiabetic

        What a great support network! 💙

        3 years ago Log in to Reply
    2. Ernie Richmann

      I have participated in many running/walking events for charity. The last one was Outrun 24- I did not make the 24 hours this time but I managed 27 miles on a rocky trail with elevation. I raises about $1000 for a camp for diabetic children.

      2
      3 years ago Log in to Reply
    3. Greg Felton

      Several ADA rides, JDRF running ents, and 5-6 JDRF century rides in different locations in the US. I never see the number of T1 participants that I hope to see, but it is nice to see so many people out to support a T1 cause.

      3 years ago Log in to Reply
    4. Danele Smith

      Yes- but only in the first few years after diagnosis. We stopped. Felt it was too much to ask of others.

      3 years ago Log in to Reply
    5. Kristen Clifford

      Not yet, but I really want to do the JDRF One Walk! Something is just always going on when the Chicago one comes about. I believe last year’s was the same weekend of my wedding.

      3 years ago Log in to Reply
    6. Joan Fray

      JDRF Walkathons

      3 years ago Log in to Reply
    7. Mick Martin

      I ran a marathon, wearing a backpack filled with housebricks, in the early 1980s. (The housebricks were my inane idea at showing how ‘hard’ I was after I’ve just come out of the British Army. lol)

      3 years ago Log in to Reply
    8. Bea Anderson

      No, not sure why. Love these events. Daughter and grandkids have for years walked with t1 friends. Great tshirts too. I ran for head injury event in past.

      3 years ago Log in to Reply
    9. Mary Dexter

      I participated in a biking event. Riding alone in a crowd with no one to talk to pointed up the difference in experiences of those diagnosed T1 as children, who are surrounded by supporters, and those diagnosed T1 as adults, who are expected to just get on without bothering or imposing on anyone else. We are invisible.

      3 years ago Log in to Reply
      1. Jneticdiabetic

        🙁 I’m sorry you’ve felt isolated. Agree that walks are better than the biking events in terms of interacting.
        I was also diagnosed as an adult-ish (18) and I do wish my first endocrinologist would have thought to refer me to a T1D support group. Pediatric endos/nurses seem to be better at referring newly diagnosed kids and their parents to these important resources they need. I went years without knowing anyone else with T1D.
        Local JDRF chapters sometimes host education events and coffee meet-ups for adults. You can look for a chapter near you here. Good luck!
        https://www.jdrf.org/chapter-finder/

        3 years ago Log in to Reply
      2. PamK

        Sorry to hear about your experience. I did a JDRF bike ride several years ago with my husband. He rides faster than I do, so I told him to go on ahead. There was another woman who also rode slower, so I paced myself with her and we talked while we rode. All it took was my saying, “Hi.”

        I’d say, give it another try! Remember that everyone there is connected to someone with T1D in some way. So, saying hello and asking if they have T1D is the best way that I’ve found to start the conversation. If they say yes, ask how long or when they were diagnosed. If they say no, they’ll usually say their child/sister/spouse/friend has it. Either way, the conversation has been started!

        3 years ago Log in to Reply
    10. TEH

      I have done 3 ADA walks 15 years ago. Modest turn out for 2 of the 3. It seems like they were more about gathering $$$ than helping T1d’s. Haven’t done another since.

      3 years ago Log in to Reply
    11. Sherolyn Newell

      I haven’t ever heard about any, so I’ve never thought about it.

      3 years ago Log in to Reply
      1. PamK

        Check with your local JDRF and ADA websites to see when they are holding events in your area. It’s a great way to meet people!

        3 years ago Log in to Reply
    12. Jordan Mooty

      I’ve done a few ADA Tour de Cure rides and loved them, but Alabama hasn’t had one for the last 3-4 years, very unfortunately. I also did a walk a few years ago for a local diabetes camp (Seale Harris).

      3 years ago Log in to Reply
    13. Carol Meares

      Used to do bike events many years ago. Great fun.

      3 years ago Log in to Reply
    14. Jneticdiabetic

      I’ve done multiple JDRF One Walks in Southern California. As one person cook commented they are focused on raising money for research, but also have informational booths for welcoming newly diagnosed families, where you explore the latest diabetes pump/CGMs devices, fun stuff for the little T1Ds, etc. I find them inspiring.
      If interested, you can search for a JDRF walk near you here:
      https://www2.jdrf.org/site/SPageServer?pagename=walk_homepage

      3 years ago Log in to Reply
    15. Virginia Barndollar

      Three years ago I signed up for the Western PA Tour de Cure. While I am very active, I never really rode a bike except when I was a kid. I went back and forth between the metric century and the half. The metric century won out. Needed a bike, found a vintage Cannondale mountain bike, rode it a few times, bought new tires for the ride, and never thought about the Pittsburgh hills that would be on the course.
      I can honestly say I had the time/ride of my life. The support staff was awesome, the group I rode with were so much fun, and the finish line festivities were a welcome site.
      Would encourage anyone that thinks they want to do a ride, walk or run for diabetes…do it!

      3 years ago Log in to Reply
    16. Becky Hertz

      Yes! Year 2 for JDRF Ride for the Cure. Want to donate? http://Www.ride.JDRF.org, search for Becky Hertz. Thanks!

      3 years ago Log in to Reply
    17. Kristine Warmecke

      Yes, my brother and I used to ride in the Bike-a-thon by the ADA in the 70’s & early 80’s, it later turned into a walk, which I walked in and was on the committee for it.

      3 years ago Log in to Reply
    18. PamK

      I have done the walks for many years and have done one bike ride. I also volunteered at a run after walking that morning. That was the best day of all! I got to participate in two ways, so I gave and gave back.

      I love doing the walks for several reasons:
      1) It’s great exercise
      2) It’s a great reminder that I’m not the only one living with T1D
      3) The support is amazing – – from the vendors to the juice/water stations, everyone is wonderful!
      4) The vendors – I love getting free stuff and learning about the latest improvements in diabetes management. Reps from all the companies are there to answer questions and explain what they have to offer. So, if you haven’t done a walk/run/bike ride come early so you have time to visit all of the booths!

      3 years ago Log in to Reply
    19. Patricia Dalrymple

      The first year I was diagnosed at age 40 I went to a set up event. It was held at a restaurant and they offered pizza and real coke. I never went back because I felt they didn’t get it. I should try again.

      3 years ago Log in to Reply
    20. ConnieT1D62

      Participated in a Diabetes Sisters Orange Will Walk in Raleigh, NC a few years back to raise money and awareness for furthering the cause of support for women living with diabetes. I wish they had continued with their efforts – it was great fun and helped to fund a noble cause.
      http://www.diabetessisters.org

      3 years ago Log in to Reply
    21. Molly Jones

      I chose other as I don’t remember

      3 years ago Log in to Reply
    22. Christine Gran

      It was a corn hole toss out diabetes event.

      3 years ago Log in to Reply
    23. Cheryl Seibert

      Years ago, my son and I rode our bikes in a ADA fundraising event. It was very well organized and a good experience. Our local ADA/JDF group dissolved after the organizer passed away, so I have not participated in any out of town events.

      3 years ago Log in to Reply
    24. Chris Deutsch

      I have helped keep the event running, but have never exercised in one.

      3 years ago Log in to Reply

    Have you ever participated in a T1D charity fitness event (i.e., a walk, run, bike, etc.)? Share in the comments about your experience! Cancel reply

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