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    • 4 hours, 6 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. 😬
    • 5 hours, 53 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.
    • 5 hours, 54 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.
    • 5 hours, 54 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.
    • 6 hours, 52 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.
    • 6 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'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.
    • 6 hours, 54 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.
    • 6 hours, 57 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.
    • 6 hours, 59 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.
    • 7 hours, 13 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.
    • 9 hours, 47 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.
    • 10 hours, 19 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?
    • 10 hours, 37 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.
    • 10 hours, 38 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. 😬
    • 10 hours, 38 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.
    • 12 hours, 5 minutes 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
    • 19 hours, 5 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, 2 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, 2 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, 2 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, 4 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, 7 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, 9 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, 10 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, 11 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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    Do you (or your loved one with T1D) take a Vitamin D supplement?

    Home > LC Polls > Do you (or your loved one with T1D) take a Vitamin D supplement?
    Previous

    How long does it typically take for your durable medical equipment or pharmacy supplier to obtain prior authorization or chart notes from your T1D health care provider’s office?

    Next

    Moving out on your own for the first time is exciting but extra challenging with T1D. If you’ve made it past the ‘moving out’ transition in your life, what is one piece of advice or something you wish you had known to give to young adults moving out today? If you are a young adult moving out on your own (or still finding your way!), do you have any questions for those who have successfully made the move from parent home to independent living?

    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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    46 Comments

    1. KarenM6

      Yup!
      I have been diagnosed in the past with Vitamin D deficiency, so have been on doctor ordered Vit. D for many years.
      I also have calcium issues and I know the two are connected. At one point, I was diagnosed with osteopenia, but I don’t know if that is still the case.
      Hoping all the calcium “horse pills” are doing their job! 🙂

      2
      4 years ago Log in to Reply
    2. Jillmarie61

      I have been on a prescription for Vitamin D for the last three years because m levels are so low.

      4 years ago Log in to Reply
    3. Ms Cris

      2500 IUs every day!

      4 years ago Log in to Reply
    4. Lyn McQuaid

      My answer is yes and my endo was the one who recommended it. He said vitamin D is more of a hormone than a vitamin and is crucial for health.

      4 years ago Log in to Reply
    5. kflying1@yahoo.com

      And as weather allows, I take my daily walks exposed as legally possible. I don’t give a S**t what people think about my flabby body or the CGM on my gut. I’ll get my natural Vitamin D production the way we were designed to.

      4 years ago Log in to Reply
      1. Wanacure

        Ha! Over 20 years ago California had a discrete public “clothing optional” beach. Even Seattle has a “Fraternity Snoqualmie” nudist club, again discrete. But my dermatologist told me to wear long sleeve shirts, full length pants, sunglasses and a broad brimmed hat, and SPF 50 sun blocker…even on wintry cloudy days. Every year she checks me for skin rashes and melanoma and so far has found a couple of small ones she removed in the office w/ just local anesthetic.

        1
        4 years ago Log in to Reply
    6. dave hedeen

      take D3 only during winter months

      2
      4 years ago Log in to Reply
    7. Henry Renn

      Only bc blood test showed a deficiency. Never took it before last year.

      1
      4 years ago Log in to Reply
    8. stillarobyn

      Seasonally – every day in the winter DST months

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

      My endo left the practice she was in, so my last appointment was with the nurse practitioner. It was annual lab time, and she added the vitamin D test. I had never had one before. My level was nearly 0. I saw the labs and bought a bottle of vitamin D. The nurse also sent in a prescription of super dosage D for once a week. I was already taking the others every, so I kept on doing that.

      1
      4 years ago Log in to Reply
    10. Melinda Lipe

      Not because I’m Type 1, but because my blood work showed a low Vit. D level.

      1
      4 years ago Log in to Reply
    11. Francisco Varea

      I take as part of a daily multi vitamin supplement

      4 years ago Log in to Reply
    12. TEH

      Just what’s in my multivitamin

      4 years ago Log in to Reply
    13. Gerald Oefelein

      My daily multivitamin contains 25 mcg of vitamin D.

      4 years ago Log in to Reply
    14. cynthia jaworski

      i believe that it is common for people with ti to have low Vitamin D levels.

      3
      4 years ago Log in to Reply
    15. Eva

      I get my vitamin d level checked every year so if I dont get sun for an extended period of time, I take a supplement.

      4 years ago Log in to Reply
    16. Jennifer Wilson

      Yes, high dose D2 weekly.

      4 years ago Log in to Reply
    17. P-O Heidling

      Yes, 5000 IE of D3 vitamins daily, during the fall/winter months (Oct-March).

      4 years ago Log in to Reply
    18. HMW

      My doctor recommended I take my full weekly dose once per week.

      4 years ago Log in to Reply
    19. Kim J

      Yes, once a week.

      4 years ago Log in to Reply
    20. Moe Giguere

      Have been for 20 years when diagnosed with Low D. Large % of population is low. Had read that people with normal D less likely to get COVID and other diseases. My wife, brother and I have not gotten it even though we’ve been exposed many times. We’ve all had our shots as well, but that only affects severity. Who knows. Have been and continue to be a believer in D.

      4 years ago Log in to Reply
    21. Carole Ludwig

      I was deficient in Vit D so I take 1000 units daily. Am just having blood work to see if it is more normal. Have osteoporosis so I take Calcium pills and also get a Prolia shot twice a year. Nine months ago I tripped and dislocated my shoulder. My doc said the fall could have been a lot worse if I hadn’t been taking supplements.

      4 years ago Log in to Reply
    22. Bonnie Lundblom

      Yes, 2000 IU (50 mcg) D3 daily due to low levels many years ago. My PCP and endocrinologist both monitor my blood levels I think because of problems those with low levels have when ill with COVID. I’m fully immunized and boosted, as is my husband, but he’s got COVID right now.

      4 years ago Log in to Reply
    23. Janis Senungetuk

      Have been taking a daily D3 25 mcg supplement for many years.

      4 years ago Log in to Reply
    24. Trisha Oldenkamp

      2000 units every day. I also have just crossed into osteoporosis so it matters.

      4 years ago Log in to Reply
    25. mbulzomi@optonline.net

      I have been taking Vitamin D3, 250 MCG (10,000 IU) twice a day for over twenty years.

      4 years ago Log in to Reply
    26. Lynn Smith

      D3, 2000 mg. I’m old and old people need more vitamin D. 😂

      1
      4 years ago Log in to Reply
      1. Lynn Smith

        Actually that should say 2000 units, not mg. And I also have osteoporosis.

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

      To my surprise, last year I had a blood test that showed low vitamin D. I don’t remember being tested to vitamin D before. Since then, I’ve been taking a daily dose of D3, 25mcg, 1000IU.

      4 years ago Log in to Reply
    28. Anneyun

      Yes I do, but not because I’m diabetic, because I live in the Pacific Northwest and don’t get much sun. I didn’t know there was any correlation with diabetes and vitamin D deficiency.

      4 years ago Log in to Reply
    29. trisha moynihan

      i have been prescribed large amounts 2x a month…which i put as “other,” but the answer is YES

      4 years ago Log in to Reply
    30. M C

      I now only get what the daily multi-vitamin provides. At one point I had been taking additional Vit D, only to finally make the connection between doing that and an increasing severe pain and weakness in my hands. It was the only thing new I had added in my life over the previous year – so I stopped taking the additional Vit D, and my hands, quite quickly, reverted back to ‘normal’! For whatever reason, my body can’t handle the additional boost of Vit D.

      4 years ago Log in to Reply
    31. Wanacure

      As prescribed I take 40 mcg/day Vit D3 (200% daily value) in caplets w/ calcium citrate 2520 mg/day (192% daily value) since diagnosis of osteopenia and possible SAD (Seasonal Affect Disorder). Up here at meridian 47 degrees north w/ 9 months of
      overcast/year and/or drizzle SAD is frequently diagnosed in Seattle residents. Despite 3 glasses of milk/day & weightlifting, etc since age 15 T1D onset, diabetes and genetics resulted in
      osteopenia diagnosis in my 50’s. I went from 6’4” to today’s 6’1”. COULD OSTEOPENIA HAVE BEEN PREVENTED IF I’D STARTING SUPPLEMENTING IN MY MID-40S AFTER 30 YEAR TID ONSET? This is the only dietary supplement I take.

      4 years ago Log in to Reply
    32. Jneticdiabetic

      I answered “Sometimes”. Aka (when I remember).
      I actually do notice a difference in how I feel when I take Vit D regularly. I don’t know if this is related to my T1D, thyroid function (I also have Hashimoto’s), independent factors, all of the above?
      Risking TMI… I have noticed that I find my spouse more irristible when I’m taking my Vit D. 😘
      Lots of interesting articles in the medical literature about Vit D level correlations with immune function, cardiovascular disease, sex drive, mental health, etc.
      Okay I talked to myself into it – just said a daily alarm. 🙂

      1
      4 years ago Log in to Reply
    33. Patricia Dalrymple

      I live in FLA and ride my bike at lunch for 20 5 out of 7 days usually. I sometimes take it, especially when a little constipated (sorry probably TMI) and it seems to help. I take red yeast rice on advice of Endo because my cholesterol is only slightly elevated and liver enzymes are good. I also take turmeric for joint pain and that DOES work for me.

      1
      4 years ago Log in to Reply
      1. Ahh Life

        Patricia–hey! This is a health research web site. There is definitionally no such thing as TMI. Even for psychopathy (ala Doc Martin)

        1
        4 years ago Log in to Reply
      2. Patricia Dalrymple

        Good to know! I’m pretty sure I’ve shared other personal info on here. I find you all incredibly kind and supportive.

        4 years ago Log in to Reply
    34. LL

      Yes, daily especially because was found to be deficient. Has more than one autoimmune condition, as does a sibling and parent.

      4 years ago Log in to Reply
    35. Robert Brooks

      Daily does prescribed by my nephrologist. Vitamin D3 plays a crucial role in kidney function.

      4 years ago Log in to Reply
      1. Becky Hertz

        Interesting cause my nephrologist took me off of mine!!! I’ll have to revisit this with her.

        4 years ago Log in to Reply
    36. Becky Hertz

      I used to everyday because of where I live (Seattle Area) and because my levels were low, but my nephrologist took my off all my silent except fish oil. My non-D sister also has low levels (lower than I ever did and she lives in southern Oregon) and also supplements daily.

      4 years ago Log in to Reply
    37. Lenora Ventura

      My Endo prescribed once weekly 50,000 iu supplement. Been taking it for over 5 years.

      4 years ago Log in to Reply
    38. Cheryl Seibert

      I do not take Vit D supplement. My endo says I eat a balanced enough nutrition-laden meal to not need supplements. My OB-GYN has been pushing Vitamin D. I won’t take the supplements without my endo’s approval.

      3 years ago Log in to Reply
    39. PamK

      I answered “Yes” but I do not take it for my diabetes. My mother has Osteoporosis so I was told to take vitamin D with calcium to protect myself. I started this when I was 30 years old.

      3 years ago Log in to Reply
    40. Stang777

      I was diagnosed with type 1 almost 9 years ago and other than the amount of vitamin d that is in the multi-vitamin I have taken daily, I did not take vitamin d until I had a bone density scan last month which revealed I have osteoporosis. At that time, after doing some research on osteoporosis, I started taking a vitamin d pill each day in addition to the multi-vitamin.

      3 years ago Log in to Reply
    41. Cmore

      My Endo prescribed twice weekly 50,000 iu (prescription)in 2000. It was switched to once weekly in 2020.

      3 years ago Log in to Reply

    Do you (or your loved one with T1D) take a Vitamin D supplement? Cancel reply

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