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    • 6 hours, 2 minutes 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. 😬
    • 7 hours, 49 minutes 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.
    • 7 hours, 50 minutes 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.
    • 7 hours, 50 minutes 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.
    • 8 hours, 48 minutes 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.
    • 8 hours, 49 minutes 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.
    • 8 hours, 50 minutes 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.
    • 8 hours, 53 minutes 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 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.
    • 8 hours, 55 minutes ago
      Lawrence S. likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I broke down for the first time in 25 years and bought a bottle of insulin because I think I may have thrown a bottle out with the box. Medicare wouldn’t fill the prescription because it was too early. I just didn’t want the fight and worry. I’m not sure that’s what happened but it’s the only explanation. Also, I live in Florida and the threat of losing power is always there. I should get a generator but I’m a little afraid of them and you still can’t be sure you have access to propane. If my insulin goes bad, I’m not sure I could get refills. My back up plan is to leave before hurricane or go to a hospital. But it is all just causes concern.
    • 9 hours, 9 minutes ago
      Derek West likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Very! However, I wish I could use Fiasp insulin in the Tandem pumps.
    • 11 hours, 43 minutes ago
      Bruce Schnitzler likes your comment at
      How confident are you about having consistent access to the diabetes supplies and medication you need?
      I broke down for the first time in 25 years and bought a bottle of insulin because I think I may have thrown a bottle out with the box. Medicare wouldn’t fill the prescription because it was too early. I just didn’t want the fight and worry. I’m not sure that’s what happened but it’s the only explanation. Also, I live in Florida and the threat of losing power is always there. I should get a generator but I’m a little afraid of them and you still can’t be sure you have access to propane. If my insulin goes bad, I’m not sure I could get refills. My back up plan is to leave before hurricane or go to a hospital. But it is all just causes concern.
    • 12 hours, 16 minutes ago
      Karen Newe likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      The most common comment: but you aren’t heavy. That’s when we get into the differences. A relative tried to tell me that insulin makes you lose weight. But when we last discussed this, one of you said it best: if it isn’t in their circle of experience, why would they know or care?
    • 12 hours, 33 minutes ago
      KSannie likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Very! However, I wish I could use Fiasp insulin in the Tandem pumps.
    • 12 hours, 34 minutes ago
      KSannie 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. 😬
    • 12 hours, 34 minutes ago
      KSannie likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      My first reaction was Very Satisfied but there is always room for improvement. I’d like a pump design that wasn’t meant to be worn on a belt just for men. To wear a dress, I have to only get those with pockets (and on both sides because opposite sides cause the CGM to lose contact) and put a button whole in each. The clip shows horribly on blouses worn out. I’ve tried the leg attachments and they never stay secure. I’m not big enough to wear it in my bra. All minor inconveniences. I’d like one that doesn’t keep alarming 20 minutes after I’ve eaten, although I get it that it is there to save my life. Again minor. Ask about CGMs (probably tomorrow’s question): lately I’ve had trouble removing the sensor from my arm without actually ripping off a strip of skin or very bad bruising. I’ve read about using baby oil for removal. That does help. I’m a rip it off fast person, but that didn’t work so well.
    • 14 hours, 1 minute ago
      Patricia Dalrymple likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      Try Uni-Solve Adhesive Remover (smith&nephew)- wipe it on wait a minute to let it work and it will come off easy. at least it works great for me and I've tried several different brands, I use it for CGM & Omnipod removal
    • 21 hours, 2 minutes ago
      Sandy Norman 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, 4 hours ago
      kristina blake likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      There are several conversations about this across social media. Many people chime in and vote for a new, more accurate name for type 1.. some of the popular alternatives- Pancreatic Autoimmune Disease, Beta Cell Destruction Disease, Autoimmune Diabetes, Autoimmune Insulin Failure, Autoimmune Absolute Insulin Deficiency (AAID)
    • 1 day, 4 hours ago
      kristina blake likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      The most common comment: but you aren’t heavy. That’s when we get into the differences. A relative tried to tell me that insulin makes you lose weight. But when we last discussed this, one of you said it best: if it isn’t in their circle of experience, why would they know or care?
    • 1 day, 4 hours ago
      kristina blake likes your comment at
      How often do people confuse type 1 and type 2 diabetes in your experience?
      In my experience the average person does not know the difference. It does not help that the commercials on TV just say diabetes and do not differentiate.
    • 1 day, 6 hours ago
      Kristi Warmecke 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, 9 hours ago
      Lee Tincher likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      If I could get a CGM that is consistent and predictable I'd be very happy with the Twiist or the Tandem. The weak point with pumps used to be infusion sites, but now that we are relying on poor performing technology to support potentially great algorithms itis quite frustrating.
    • 1 day, 11 hours ago
      Beckett Nelson likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      My first reaction was Very Satisfied but there is always room for improvement. I’d like a pump design that wasn’t meant to be worn on a belt just for men. To wear a dress, I have to only get those with pockets (and on both sides because opposite sides cause the CGM to lose contact) and put a button whole in each. The clip shows horribly on blouses worn out. I’ve tried the leg attachments and they never stay secure. I’m not big enough to wear it in my bra. All minor inconveniences. I’d like one that doesn’t keep alarming 20 minutes after I’ve eaten, although I get it that it is there to save my life. Again minor. Ask about CGMs (probably tomorrow’s question): lately I’ve had trouble removing the sensor from my arm without actually ripping off a strip of skin or very bad bruising. I’ve read about using baby oil for removal. That does help. I’m a rip it off fast person, but that didn’t work so well.
    • 1 day, 12 hours ago
      John Barbuto likes your comment at
      How satisfied are you with your current insulin pump brand/model?
      I have been using a insulin smart pen for the last 2 years; I find that it meets my current needs to ensure good management and results
    • 1 day, 13 hours ago
      Lawrence S. 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. 😬
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    Have you ever been an athlete with T1D? Tell us about your experience in the comments!

    Home > LC Polls > Have you ever been an athlete with T1D? Tell us about your experience in the comments!
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    If you were diagnosed with T1D as an adult, for how long did you notice symptoms of T1D before getting a proper diagnosis?

    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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    32 Comments

    1. Bob Durstenfeld

      I played water polo in high school and a bit in college in the days before pumps, cgm, or blood test strips

      5 years ago Log in to Reply
    2. Kimberly Green

      I was a cheerleader for 3 years of high school

      5 years ago Log in to Reply
    3. jeredb

      Played high school football and bareback bronc riding in rodeo in college and a while after college. Quit at age 30. Of course before pumps and cgm’s! Lots of finger pricks and I had trainers in football that would bring out juice for me to drink during timeouts when others were drinking water. In rodeo, just made sure blood sugars were good before the ride and monitored for a couple hours after because the activity and adrenaline really played with them.

      5 years ago Log in to Reply
    4. Anthony Harder

      HS football, wrestling, track. College football. All before CGM. Coaches had boxes of sugar cubes with the training equipment. One of the difficulties was predetermining extreme bursts of energy. Another was basic instability during my teens & 20’s. Things have stabilized as I’ve aged.

      5 years ago Log in to Reply
    5. Ken Raiche

      I’ve been extremely fortunate to have had the opportunities to participate in numerous sports over the years. I was diagnosed 47 years ago and I found that T1D never ever interfered with my ability to participate in any sport(s) that my mind on. Preparation is of the utmost importance for me especially due to my hypoglycemic unawareness. Admittedly the advancements and combination of a pump and CGM sure helps life potentially alot easier if well prepared. Love sports all sports…….

      5 years ago Log in to Reply
    6. Ernie Richmann

      I continued to run competitively after my diagnoses at 57. At age 61 I won my age group at the Akron Ohio marathon. I broke my neck in 5 places in 2011 and although I ran after recovering it took the edge off. Today I bike, hike, walk- all for enjoyment and fitness. I use a tandem pump and dexcom G6 cgm.

      5 years ago Log in to Reply
    7. Chester Oby

      Played tennis in high school and college. Could not tell if blood sugar was low then. No cgm or blood test meters. Used to notice that the ball I hit did not have the penatration that it did when blood sugar was normal. Coach would ask if I wanted some Pepsi.

      5 years ago Log in to Reply
    8. Rose Lentzke

      When I was diagnosed 64 years ago, things were a lot different. My father always encouraged me to be active, but it was rough at times with out a CGM. OJ traveled with me everywhere. Now when I cycle, I use my exercise basal rate and all is good.

      5 years ago Log in to Reply
    9. Jordan Mooty

      I played soccer my whole life until college. I also got into other sports here and there. I would usually suspend my pump and take it off while playing. The exercise was enough to keep blood sugars good, even while replenishing water and electrolytes. I also didn’t like risking falling on my pump. I would test and reconnect when on the sideline. Now, most of my activity is biking working out. I usually do a temporary basal for biking. I start it a little before the ride and carry it on through the ride. I do try to have minimal insulin-on-board when I start riding. CGM’s help a lot, but I don’t have good success with them staying on me. My strength training workouts are usually short, less than an hour. I just keep my pump in my pocket and don’t make any changes. I have always used Medtronic. I have a 670G now.

      5 years ago Log in to Reply
    10. connie ker

      I was diagnosed with LADA, so was beyond athletic competition. However when our son was diagnosed and was playing on the golf team, I kept encouraging him to stay active and physical. One of the One of themost famous T1D atheletes is Gary Hall who was diagnosed before going to the Olympics. He found a Dr. who was willing to travel with him to Australia for competition, and he returned home with a couple Gold, Silver and Bronze medals. JayCutler was the quarter back for the Chicago Bears football team, Catfish Hunter played for the Yankees, Mark Andrews played for the Baltimore Ravens, Ryan Reed competed in Nascar, Kendall Simons played on the Steelers, and the list goes on. I don’t know how they do it; the attitude of never giving up!!!

      5 years ago Log in to Reply
    11. Stacey Rose

      I was dxd 43 years ago. I was always active growing up – swimming, ballet, etc. I started running at age 37 and have since run many, many races including 3 marathons. Using a pump and CGM have helped me keep my blood sugar stable while running for hours.

      5 years ago Log in to Reply
    12. Virginia Barndollar

      I have been diabetic for 56 years, since I was 6 yo. I swam all summer, participated in school sports: track and basketball in junior and high school. I even went to states 3 times. I skied and golfed through college. Now, I’m in my 60’s, I run, hike, backpack and mountaineer. I climb high peaks all over the world. I usually wear a pump and CGM but many times, due to temperatures and difficult climbs I’ll switch to pens and a Libre sensor. Only to switch back when I’m on easier turf.

      5 years ago Log in to Reply
    13. Lisa Shandalov

      I was a swimmer and a runner before the advent of pumps and cgm. I kept glucose tablets handy, and I ran cross country and 5K races; I swam with my college team. Now, I bike and do Zumba!

      5 years ago Log in to Reply
    14. Mark Fuller

      I have continued to play competitive sports for the 34 years I have had T1D. I deal with it by wearing my CGM and always having orange juice or a coke or pepsi with me should it be necessary to add some sugar to my system. I rarely if ever have a serious low. It is all about monitoring and awareness.

      5 years ago Log in to Reply
    15. Ginger Vieira

      Yup, and when I asked my endo for helping in learning how to juggle my insulin doses around competitive powerlifting, he basically laughed at me. I went on to set 15 records in two years — without his help! It was very disappointing but I forged ahead without him.

      5 years ago Log in to Reply
    16. AimmcG

      Not sure what you mean exactly. I go on hikes, ski, play tennis but not competitively. When I do this things I change my pump to exercise mode or turn it off and have juice handy.

      5 years ago Log in to Reply
    17. jorie P

      I was active in gymnastics when I was diagnosed 49 years ago at age 14. I don’t recall many problems (though, at that time, I only tested at home with unwieldy test tubes and tablets.) I usually felt low at the end of a practice and it was a great treat to buy a Fanta Orange soda for the ride home. these days I walk, so yoga, and dance.

      5 years ago Log in to Reply
    18. Germaine Sarda

      Dxd in 1974 at the age of 8 when I was a competitive swimmer and gymnast through 1979. We only had pee tests back then and my mom always had OJ for me to treat lows. I did find gymnastics more difficult when dealing with my BGs just because it varied so much. I do believe my BGs ran much higher than they should have been back then. I started brisk walking as a teen and it’s still my favorite for staying healthy.

      5 years ago Log in to Reply
    19. William Sheldon

      Enjoy staying fit! Although I no longer will do them, I completed a few marathons and triathlons before “retiring”. Still enjoy, swimming, hiking, and the gym, among other healthy exercise, 😉

      5 years ago Log in to Reply
    20. William Sheldon

      Btw, low bs naturally was/is the challenge. Cgm use and appropriate sugar supplements are the key!

      5 years ago Log in to Reply
    21. Yaffa Steubinger

      I was never an athlete but I am a group fitness instructor. Wearing a Dexcom is important to me. I always have to start my classes with a high blood sugar (around 180) because the workout will drop it 50-60 points. Of course, I have glucose shots right next to my water should my blood sugar go low.

      5 years ago Log in to Reply
    22. Greg Felton

      I was diagnosed at age 5, then played team sports through high school. When I was very young my parents signed me up for rec soccer and had to fight to allow me to play after my T1D was disclosed during registration. Little League and city basketball were easier to deal with, and after getting on a team I might let the coaches know that I was going to keep snacks with me on the sideline just in case. Or I only revealed T1D if a coach asked why I was eating a granola bar during a timeout. I made excuses and skipped the postgame trips to Dairy Queen. It was best to keep a low profile. This was the early 80’s before pumps and CGMs. think I got a BG meter when I was in about 9th grade but I kept it at home because it wasn’t portable or fast. Likewise, I didn’t carry supplemental insulin back then. I would play sports, and if I felt low I would secretly eat something and continue. I probably misdiagnosed myself several times when the sweating, exhaustion, and anxiety from a competitive high school game felt like hypoglycemia. In the dark ages of diabetes, it was best to stay hidden. I was no pioneer like Ron Santo, but it was very different then.

      5 years ago Log in to Reply
    23. Kristine Warmecke

      My brother and I played in Kory league baseball/softball; my niece does the same softball along with school basketball & volleyball.

      5 years ago Log in to Reply
    24. Nick Trubov

      I was diagnosed in 1963. I have always liked to eat so I started cycling in 1971. Soon I started racing and learned that I could eat a LOT. It was often difficult to eat enough, but I tried. I remember buying Baskin and Robbins ice cream by the tub! I always carried orange juice in my water bottles and frequently stopped at little stores on the road to purchase cookies (they were a lot more convenient to carry in my jersey pockets). Eventually Boehringer Mannheim produced chemstrips that allowed me to monitor my CBG while riding. I often found that I would actually become HYPERglycemic on long rides (these were often rides of several hours in length) so I actually carried regular insulin and an insulin syringe and would take insulin while I rode. Now I’m old and decrepit and no longer ride, but I no longer have the desire to eat as much as I did when I was much younger. I also now wear an Abbott freestyle CGM. My most recent hgb a1c was 4.7.

      5 years ago Log in to Reply
    25. Becky Hertz

      I played competitive sports in high school but never considered myself an “athlete”. I guess it depends on your definition.

      5 years ago Log in to Reply
    26. Guy Hornsby

      I played football and ran track as a scholarship athlete at the University of South Carolina. After graduating, I competed in road racing and ran one marathon. I next competed in the sport of Olympic weightlifting. I still compete at the age of 69 in USA Masters Weightlifting.

      5 years ago Log in to Reply
    27. Pat Reynolds

      I was diagnosed aged 6 and feel that I have always had “sugar and salt” in my blood. I was fortunate enough to go to a school where dinghy sailing was an option (just a normal state school). At 17 I was part of the top all-girl crew in that class. Not just young women, not just working class, but one Black, one disabled. In the 1970s UK … I returned to sailing a decade ago, and have a fondness for traditional vessels and warm waters.

      5 years ago Log in to Reply
    28. cynthia jaworski

      i have participated in many sports, but was never very good. Has nothing to do with diabetes, though.

      5 years ago Log in to Reply
    29. Molly Jones

      My answer was no, as I am athletic enough to get out of bed after usually ten hours of sleep. If friends are involved physical sports/ activities are fun but less than monthly. Didn’t deal with diabetes until I was thirty.

      5 years ago Log in to Reply
    30. ConnieT1D62

      I have been active in dance activities since my early childhood before and after diabetes diagnosis. Through my teens – ballet, jazz, tap, international folk dance, Irish clogging, and musical comedy performance dance. In my 20s and 30s I was a semi-professional dancer and choreographer in musical comedy productions and dance collective performances; in my late 30s to mid-50s I taught creative movement dance classes for women and girls of all ages and abilities, performed and choreographed dances for spiritual gatherings, and was part of a tribal style belly dance troupe for several years Throughout my adult years I have been active as a student and teacher of creative movement and modern dance styles, belly dance, yoga, tai chi, and folk dancing. In my youth I always sucked at athletic sports activities – I did not have the speed, coordination and was always the last one picked for a team in gym classes. But I was dedicated to intense dancing for most of my life and it has given me inner discipline strength and stamina that has helped me to live well after all these years with diabetes. Now I do Sliver Sneakers movement and fitness classes on Zoom – as a participant, not as a teacher.

      5 years ago Log in to Reply
    31. Henry Renn

      Played soccer in college. Coach required note from doctor. Team trainer was aware of my condition & I gave him hard candy to hold for me & I think he kept can of coke & an orange for me in his supplies. I don’t recall needing glucose very often. I was not a starter so need would have most likely been at practice.

      5 years ago Log in to Reply
    32. Ed

      A few years after I was diagnosed I finally managed to quit smoking and then decided to buy a serious bicycle for long distance riding. I had always loved riding bicycles but never really rode that far. I decided on a road bike and single track off road bike spending near $2500 on 2 bicycles, mainly the road bike costing me 3/4 of that price.I got up with a group of people and over the period of a few months I was riding daily 25 to 30 miles after work and sometimes as much as 100+ miles each day on the weekends. I got married and my mileage tapered off. My daily work routine took a toll on me as it was a hard daily grind on the body physically with very heavy manual labor. Surgery started happening regularly on my joints and then was forced into retirement from injuries sustained from military service required cervical and lumbar fusion causing some serious stiffness and really slowing down my daily bike riding. 35+ years later I’m now a weekend rider when the weather is good. Onward I go many surgeries later still fighting the Big T1D

      5 years ago Log in to Reply

    Have you ever been an athlete with T1D? Tell us about your experience in the comments! Cancel reply

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