Subscribe Now

[hb-subscribe]

Trending News

T1D Exchange T1D Exchange T1D Exchange
  • Activity
    • 1 hour, 52 minutes ago
      KarenM6 likes your comment at
      Have you ever been told you couldn’t physically do something because you live with diabetes?
      Long time ago - told there were certain occupations I would not be allowed to do because if T1D. Pilot, air traffic controller, military, etc.
    • 1 hour, 54 minutes ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I have been told many times "YOU CAN'T EAT THAT!" ONLY to frustrate them and eat it anyway and then bolus accordingly.
    • 1 hour, 55 minutes ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I think it is a common experience for most people with T1D. People do not understand anything about it. I do not take it personally. I try to educate when appropriate.
    • 1 hour, 56 minutes ago
      KarenM6 likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      Lol hell when haven't they. Lol
    • 2 hours, 4 minutes ago
      KarenM6 likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 3 hours, 56 minutes ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was only 2 when Diagnosed 70 years ago. My small town doctor admitted he didn't know much about T1D, and fortune for my parents and I he called what is now Joslin Clinic, and they told him how much insulin to give me. He taught my parents, who then traveled over 350 miles to Boston, to learn about how to manage T1D. My doctor learned more about T1D, and was able to help 2 other young men, that were later DX with T1D in our small town. I went to Joslin until I turned 18 and returned to become a Joslin Medalist and participated in the research study, 20 years ago. Still go there for some care.
    • 3 hours, 57 minutes ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was 7 when things changed in my home. My older brother was hospitalized for 2 weeks. When he came home, we no longer ate the way we had before. This was 1956. Dessert alternated between sugarless pudding or sugarless Jello. I learned that bread and potatoes had carbohydrates and that turned to sugar. There was a jar in the bathroom. It seemed my brother was testing his urine every time he went in there. There was a burner and pot on the stove designated for boiling syringes. I watched my brother give himself shots and I remember how hard it was to find someone to manage his care if my parents had to travel. Diabetic Forecast magazine came in the mail each month and there were meetings of the local diabetes association that my mother attended religiously. My brother got a kidney and pancreas transplant at age 60 and before he died lived for 5 years as a non-diabetic. A few years later I was diagnosed. Sorry he was not able to make use of today’s technology. I often wonder what he and my late parents would think about me, at age 66, being the only one in the family with type 1.
    • 3 hours, 59 minutes ago
      lis be likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 8 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
    • 10 hours, 2 minutes ago
      Phyllis Biederman likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Absolutely nothing. Diagnosed in late December 1962 at at the age of 8 years and was told I was going for a stay in hospital because I have "sugar diabetes".
    • 10 hours, 44 minutes ago
      Anita Stokar likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Ironically, I was a 10 year old "before" my diagnosis. BUT, one day I was over my friend's house (on what they call a playdate in today's parlance) and we went to the pharmacy to by candy. I remember vividly a video playing on a loop on a little TV on the counter describing what diabetes was and insulin injections every day. I remember thinking to myself that those poor people must feel like pin cushions. Fast forward to two days after my 11th birthday and my doctor telling me that I had diabetes. I remember my mother being fully unaware of what it entailed. I remember telling her that it's ok, all I need to do is take shots every day. She looked at me puzzled, like how do you know this? The doctor was also a little perplexed but added, it's a little more than that, but correct. Then he explained it based on his two-three hours of training in medical school. It's funny how prompts trigger strange memories.
    • 10 hours, 47 minutes 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 ´ )⎠⎞
    • 11 hours, 11 minutes ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I was diagnosed in 1976 at the age of 18 while in college. One weekend, I was drinking a lot of water and peeing frequently. I remembered having read a Reader's Digest article on diabetes, and I told my friends I thought I might have it. Two days later, the diagnosis was confirmed.
    • 11 hours, 12 minutes ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Absolutely nothing. Diagnosed in late December 1962 at at the age of 8 years and was told I was going for a stay in hospital because I have "sugar diabetes".
    • 11 hours, 12 minutes ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I knew I couldn’t or shouldn’t have my two fav things in the world: Pepsi cola and chocolate. I was 42, and suspected very strongly that I had it, and ate a large piece of chocolate cake before my doctor’s appointment (sounds more like I was 12). Fast forward 25 years later: I never had a real cola again, but do occasionally have chocolate. I’m way healthier than I was back then in terms of diet. I no longer have irritable bowel, and I’m lucky to be able to afford what I need to combat the ill effects of this chronic disease. I’m blessed, and grateful for insulin.
    • 11 hours, 13 minutes ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      It was 35 years ago for me. I had no experience with T1d. I was starting to show symptoms and my sister-in-law quickly researched T1d and told me what she found. I went to my GP a week or two later. My BG was over 600. He sent me to the hospital right away. Blood test confirmed it.
    • 11 hours, 13 minutes ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I only knew a little . That is why I give grace to others who do not know anything or have misconceptions.
    • 11 hours, 16 minutes ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Ironically, I was a 10 year old "before" my diagnosis. BUT, one day I was over my friend's house (on what they call a playdate in today's parlance) and we went to the pharmacy to by candy. I remember vividly a video playing on a loop on a little TV on the counter describing what diabetes was and insulin injections every day. I remember thinking to myself that those poor people must feel like pin cushions. Fast forward to two days after my 11th birthday and my doctor telling me that I had diabetes. I remember my mother being fully unaware of what it entailed. I remember telling her that it's ok, all I need to do is take shots every day. She looked at me puzzled, like how do you know this? The doctor was also a little perplexed but added, it's a little more than that, but correct. Then he explained it based on his two-three hours of training in medical school. It's funny how prompts trigger strange memories.
    • 11 hours, 18 minutes ago
      Lawrence S. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 11 hours, 20 minutes ago
      KCR likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Ironically, I was a 10 year old "before" my diagnosis. BUT, one day I was over my friend's house (on what they call a playdate in today's parlance) and we went to the pharmacy to by candy. I remember vividly a video playing on a loop on a little TV on the counter describing what diabetes was and insulin injections every day. I remember thinking to myself that those poor people must feel like pin cushions. Fast forward to two days after my 11th birthday and my doctor telling me that I had diabetes. I remember my mother being fully unaware of what it entailed. I remember telling her that it's ok, all I need to do is take shots every day. She looked at me puzzled, like how do you know this? The doctor was also a little perplexed but added, it's a little more than that, but correct. Then he explained it based on his two-three hours of training in medical school. It's funny how prompts trigger strange memories.
    • 11 hours, 21 minutes ago
      KCR likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      I knew I couldn’t or shouldn’t have my two fav things in the world: Pepsi cola and chocolate. I was 42, and suspected very strongly that I had it, and ate a large piece of chocolate cake before my doctor’s appointment (sounds more like I was 12). Fast forward 25 years later: I never had a real cola again, but do occasionally have chocolate. I’m way healthier than I was back then in terms of diet. I no longer have irritable bowel, and I’m lucky to be able to afford what I need to combat the ill effects of this chronic disease. I’m blessed, and grateful for insulin.
    • 11 hours, 33 minutes ago
      Gary R. likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 11 hours, 46 minutes ago
      ConnieT1D62 likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 12 hours, 2 minutes ago
      eherban1 likes your comment at
      How much did you know about type 1 diabetes before you were diagnosed?
      Being 4 years of age, I think I can be forgiven for not knowing much of anything at all. That was 3 quarters of a century ago. ⎛⎝( ` ᢍ ´ )⎠⎞
    • 23 hours, 58 minutes ago
      NANCY NECIA likes your comment at
      Has someone ever told you that you can’t eat something because you live with diabetes?
      I think it is a common experience for most people with T1D. People do not understand anything about it. I do not take it personally. I try to educate when appropriate.
    Clear All
Pages
    • T1D Exchange T1D Exchange T1D Exchange
    • Articles
    • Community
      • About
      • Insights
      • T1D Screening
        • T1D Screening How-To
        • T1D Screening Results
        • T1D Screening Resources
      • Donate
      • Join the Community
    • Quality Improvement
      • About
      • Collaborative
        • Leadership
        • Committees
      • Centers
      • Meet the Experts
      • Learning Sessions
      • Resources
        • Change Packages
        • Sick Day Guide
        • FOH Screener
      • Portal
      • Health Equity
        • Heal Advisors
    • Registry
      • About
      • Recruit for the Registry
    • Research
      • About
      • Publications
      • COVID-19 Research
      • Our Initiatives
    • Partnerships
      • About
      • Previous Work
      • Academic Partnerships
      • Industry Partnerships
    • About
      • Team
      • Board of Directors
      • Culture & Careers
      • Annual Report
    • Join / Login
    • Search
    • Donate

    How often does your T1D health care provider screen for neuropathy with a monofilament, tuning fork or pin prick on your bare feet?

    Home > LC Polls > How often does your T1D health care provider screen for neuropathy with a monofilament, tuning fork or pin prick on your bare feet?
    Previous

    If you use an insulin pump, on average, how often do you bolus an amount that is different from the suggested dose from the pump’s bolus calculator? (I.e., entering a number of insulin units without using the calculator at all, editing the bolus calculator’s suggested dose to be higher or lower, etc.)

    Next

    If you receive high alerts on your CGM, how frequently do your high alerts repeat after you acknowledge the alert? If you use different settings depending on time of day, please select the answer that corresponds to your alert setting at noon in your time zone.

    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.

    Related Stories

    Advocacy

    Blue Circle Health: A Free Virtual Program Expanding Support for Adults Living with Type 1 Diabetes 

    Michael Howerton, 2 days ago 4 min read  
    News

    Thyroid Eye Disease (TED): What You Need to Know 

    Jewels Doskicz, 4 days ago 4 min read  
    News

    Immunosuppressants in T1D Research: Expert Opinions from Diabetes Pharmacist Diana Isaacs 

    Jewels Doskicz, 1 week ago 5 min read  
    2025 Learning Session

    The 2025 T1DX-QI Learning Session: Driving Better Diabetes Care 

    Sarah Howard, 2 weeks ago 7 min read  
    Lifestyle

    Barriers to Care in Aging: Voices from the T1D Community 

    Jewels Doskicz, 3 weeks ago 7 min read  
    Lifestyle

    When T1D Becomes a Calling: Stories From our Team 

    Jewels Doskicz, 4 weeks ago 11 min read  

    43 Comments

    1. Randi Niemer

      She hasn’t since I’ve only seen her via teleheath since fall of 2020. My doc who I had before did it at every visit.

      4 years ago Log in to Reply
    2. Ahh Life

      Other. 4 or 5 years ago the answer would have been always. Then a diagnosis of peripheral neuropathy was rendered. So, currently, the answer is never.

      My question for those of you knowing more about this than me is: Is this standard medical practice to not use filament testing once diagnosis is determined?

      1
      4 years ago Log in to Reply
      1. Tom Caesar

        Don’t think I know any more, just my experience. Once it was determined I had severe neuropathy in my feet and started seeing podiatrist routinely for it, no more testing deemed necessary. I’ve got it and don’t expect it to go away, ha!

        1
        4 years ago Log in to Reply
      2. ConnieT1D62

        Yep – once the sensation/feeling is diminished and gone, the sensations of normal feeling is replaced with the altered sensations of weird numbness that comes with long duration neuropathy.

        4 years ago Log in to Reply
    3. Sherolyn Newell

      My old endo did it every time. The new one does it maybe every 6 months.

      4 years ago Log in to Reply
    4. Cjfuge78

      My current endo checks once a year.

      4 years ago Log in to Reply
    5. Henry Renn

      I see a podiatrist every 3 months. My Endo referred me there.

      1
      4 years ago Log in to Reply
    6. George Hamilton

      My doctors did these tests regularly up to about 1985. At that time I was registering no reaction to either test. My peripheral neuropathy had progressed so far that there seemed to be nothing to measure. (Original diagnosis of diabetes was in 1963.) Doctors have tried again when we moved and engaged new health providers.

      3
      4 years ago Log in to Reply
    7. Don P

      due to Covid restrictions, haven’t seen anyone in over three years

      4 years ago Log in to Reply
    8. Jane Cerullo

      Used to be every appointment but my numbers are so stable with A1c always below 5.8 they have cut down. I always have a list of questions so they know I am involved and would mention any problems

      4 years ago Log in to Reply
    9. john36m

      2 Endo’s ago, he did it every time. Now 3 or 4 visits later with 2 different endo’s it has not been done. However, my PCP does it on my annual physical.

      4 years ago Log in to Reply
    10. Francisco Varea

      My endocrinologist does not check my feet. I see a podiatrist every year.

      4 years ago Log in to Reply
    11. Stephanie Cruickshank

      I used to get checked 1x a year. Haven’t been checked in 3

      4 years ago Log in to Reply
    12. cynthia jaworski

      My question is: what purpose does this test serve? Is there anything that can be d one if there is a loss of sensation? Or is this just another way to document our decline? Does it serve to motivate the patient? We already know about the value of good control…..

      5
      4 years ago Log in to Reply
      1. ConnieT1D62

        It is used and performed as an obligatory screening test to determine nerve peripheral nerve damage and how far it progresses over time. Does nothing to heal or change the condition. Serves as a tool for providers to check the feet, determine any progressive changes, document any subtle or significant changes, and check a box in your medical record that they did it. ADA Standards of Care recommend that it be done at least once a year, if not at every diabetes focused f/u visit.

        4 years ago Log in to Reply
    13. Mark Schweim

      It varies very highly… I moved back to Minnesota in November 2018 and started seeing my current Doctors in 2019.
      In 2019, it seemed like they were doing that foot test on every appointment.
      In 2020 my PCP and Endo each did that testing at only one appointment each.
      In 2021 neither of my doctors even glanced at my feet once over the year.
      This year my PCP did that test once when I went for the antibiotic-resistant bacterial/fungal infection I developed on April 3 and still haven’t fully recovered from, my Endo retired, but the person taking over for my Endo did that foot testing on my appointment in February..

      4 years ago Log in to Reply
    14. John Williamson

      Never but I see a podiatrist every 3 months.

      4 years ago Log in to Reply
    15. Lynn Smith

      We already know I have neuropathy in my feet, so there is not as much need to do it every time. The numbness/burning and tingling have been better since they started me on the Metanx supplement.

      4 years ago Log in to Reply
    16. Sue Martin

      When the appointments are inperson. It’s kind of hard to do via Zoom.

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

      I answered “At about 1/2 of my appointments.” But the truth is, almost all of my appointments since 2020 have been on Zoom. I went for an office visit 2 months ago, and she used a pin to check my feet, which was done often previously. I’ll probably do Zoom again in June with the uptick in Covid again.

      4 years ago Log in to Reply
    18. Mary Dexter

      The toes on both my feet are numb (tarsal tunnel syndrome) and I also have dyspareunia. But neuropathy reflects badly on the institution, so it is never identified. My feet are very sensitive. A small grain of cat litter feels like a stone, a hair like a sharp object, so I always feel the monofilament, so their concerns are alleviated.

      4 years ago Log in to Reply
      1. Ahh Life

        Cat litter and Legos were invented to impress people who insist on going barefoot in the middle of the night. Sigh!

        2
        4 years ago Log in to Reply
      2. AnitaS

        I had this happen twice. I had a dog with hair similar to a labs but a little shorter than that. Twice I got his hair in my feet which felt like slivers in my feet. Very strange to think hairs could be imbedded in skin in that manner.

        4 years ago Log in to Reply
    19. Mick Martin

      I selected “Rarely, less often than once per year”, but that’s because I have confirmed perpheral neuropathy as well as autonomic neuropathy. (I haven’t been able to feel my feet and lower legs for about the last 20 years.)

      I receive an annual “screening” by my podiatrist, though this is mostly not within the 12 months stipulated, and this also includes a test with a tuning fork to see if I can ‘pick up’ vibrations, as well as a doppler test to check blood flow to my extremities, as well as a review of my medications.

      4 years ago Log in to Reply
    20. Drina Nicole Jewell

      It was every appt, same with my primary doctor. Now, since I was diagnosed with Neuropathy, they both leave it with my Neurologist.

      4 years ago Log in to Reply
    21. Kristine Warmecke

      She does occasionally but I lost all feeling in my feet and hands in Sept. 2017 while on chemo for Stage 3 breast cancer.

      4 years ago Log in to Reply
    22. GiGi

      Once a year

      4 years ago Log in to Reply
    23. Jim Cobbe

      He does it every in-person appointment, but since COVID started most of my appointments with him have been telehealth.

      4 years ago Log in to Reply
    24. Becky Hertz

      At least once a year. In between endos currently.

      4 years ago Log in to Reply
    25. Amanda Barras

      I only see my Endo once a year. She usually checks at that appointment, but not always.

      4 years ago Log in to Reply
    26. Chris Wynn

      ADA Diabetes Care 2022;45:S188 recommendation is to check once per year. My current Endo hasn’t checked in 2.5 years since I have been seeing her. It is one of the many reasons her practice is substandard. However at this time I don’t need to spend the $8000/year required to access a better endo in my corner of the US. Part of the problem is Tenet Health’s 15 minute endo appointment standard. For those interested in what the minimum there doctor should be checking with regards to neuropathy in the US, this link is the ADA 2022 standards of care chapter 12
      https://watermark.silverchair.com/dc22s012.pdf?token=AQECAHi208BE49Ooan9kkhW_Ercy7Dm3ZL_9Cf3qfKAc485ysgAAAswwggLIBgkqhkiG9w0BBwagggK5MIICtQIBADCCAq4GCSqGSIb3DQEHATAeBglghkgBZQMEAS4wEQQM0-UYoFGkkDGftBpdAgEQgIICf23rv20tkOCd1oFoVgzVa-RAUG4xr_DxG6PsKadKiQ6VXG0Q-Lwqw4cu50gjuD3EtEffpwTHE3anA6XYf563lp3i1MQrpbPN8v4YmuxLZqPWM2OuKjeWYQ9bZ4R2LpXZWivk_FfXNB2MtmGsnFc4KiJHsly5h4k2e-1N3jJLKDNdK7A9Qm10UrNnZKRL4zTawHzH3RKYerJm5pYp_ldKCGJgPaUxDzFiRzNb1RDoJduA8FEJnX490KWb_leuos2fD_G6-X7bvxU47m6JuB8VGZax1aNCf2uAndl6UFN8rKdH05VfgCNZHHtrhKGSLcR7kJsmwlvGnizXfeaCtwllGnNyoqHCA_LQou3D-mzX-skLwzFDBE1HwL3I05lfM1SCUemW3Q16y8U8khZMyLc5aIsDfugzxT3LUGwZqPHs6XnBfcl1M6WpOiWBVhXBzLKdpLnQW8hNr2L9uxgzD6MKAutdgEg5_-PrRSLfUfRmmdgWHvoFmNohZToZruKIknCq45-pehq2OyaqrXOBFgnUSRYn1nZf7pZaVKLmCPiixmUs8-QONSTVWzYaYPwFi4fftmJarM5BBuD1MxyIYB_-KwypAiZBbOu9Te5aTL3B5svThQxQPlapfOcBBNXGDk36HljdAL-lmH4nK0PZdxSs194pD8j2mWbQYa3amUPcCzotSmBYXnkLilsgX0-aZtvqj370KShlgXKeOS3VIUzlPDgUXXINrlZ85AbnLJUr_QipfGZepwvvIXPureU_nquGDcN2m1XxjexfEDG5RTvn9VlS2u5sTbEGeM1Zmd3ChjGpzjFbNHRYfrvN4RUiotV-BiZGKfRpKU0yeQlUXU3zOw

      4 years ago Log in to Reply
    27. Beckett Nelson

      My doc used to check at every appointment, but then when COVID hit, appointments were done by phone, so not done. So I guess, every appointment that is in-person?

      4 years ago Log in to Reply
    28. Carol Meares

      At my in person appts

      2
      4 years ago Log in to Reply
    29. PamK

      I just started with a new endo and he said something like, “Let’s check your feet,” in a tone that implied this is something he does regularly. So, I am guessing that it will be every appointment.
      My old endo never checked in the 4 years I was seeing him. In fact, when this new endo brought it up, I hadn’t realized how long it had been since someone checked!

      4 years ago Log in to Reply
    30. KarenM6

      Even before covid, it had been years and years since anyone had tested my feet… I don’t have a podiatrist who is checking… just me and the weird stuff my cats leave around the house!

      4 years ago Log in to Reply
    31. Chris Albright

      My previous endo did it on every visit , ,current endo has never done it

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

      Not only my Endo., but my Podiatrist also screen for neuropathy with a monofilament at every visit.

      1
      4 years ago Log in to Reply
    33. Marcia Pulleyblank

      I am advised to see a chiropodist at least once a year. I finally broke down and made an appointment where my feet were examined with filament and with tuning fork. I was given a very thorough examination and given a copy of the results to share with my endocrinologist and my GP. I was asked to return in two months.

      4 years ago Log in to Reply
    34. jamesmpii

      I’ve only had one appointment with an endocrinologist and he did not check for neuropathy. He recommended I start seeing a podiatrist and ophthalmologist.

      4 years ago Log in to Reply
    35. persevereT1D52

      Neuropathy is advanced and documented way beyond the monofilament.

      4 years ago Log in to Reply
    36. Mary Thomson

      He checks the pulses in my feet.

      4 years ago Log in to Reply
    37. Elisabeth Raskopf

      Once a year

      4 years ago Log in to Reply
    38. Wanacure

      Once per year at annual checkup. But some years I may have more than that one appt w/ primary care physician.

      4 years ago Log in to Reply

    How often does your T1D health care provider screen for neuropathy with a monofilament, tuning fork or pin prick on your bare feet? Cancel reply

    You must be logged in to post a comment.




    101 Federal Street, Suite 440
    Boston, MA 02110
    Phone: 617-892-6100
    Email: admin@t1dexchange.org

    Privacy Policy

    Terms of Use

    Follow Us

    • facebook
    • twitter
    • linkedin
    • instagram

    © 2024 T1D Exchange.
    All Rights Reserved.

    © 2023 T1D Exchange. All Rights Reserved.
    • Login
    • Register

    Forgot Password

    Registration confirmation will be emailed to you.

    Skip Next Finish

    Account successfully created.

    Please check your inbox and verify your email in the next 24 hours.

    Your Account Type

    Please select all that apply.

    I have type 1 diabetes

    I'm a parent/guardian of a person with type 1 diabetes

    I'm interested in the diabetes community or industry

    Select Topics

    We will customize your stories feed based on what you select here.

    [userselectcat]

    We're preparing your personalized page.

    This will only take a second...

    Search and filter

    [searchandfilter slug="sort-filter-post"]