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    • 1 hour, 42 minutes ago
      Wanacure likes your comment at
      If you were to request the next available appointment with your T1D healthcare provider, when do you estimate the next available appointment would be?
      Being on Medicare and required to see my Endo. every three months, my next appointment is made prior to departure from my Endo's office.
    • 1 hour, 42 minutes ago
      Wanacure likes your comment at
      If you were to request the next available appointment with your T1D healthcare provider, when do you estimate the next available appointment would be?
      If I were not on Medicare, it would be difficult to get an appointment within 3 months, even in an emergency. In an emergency, they would assign me a nurse practitioner to see. It is possible to contact them through their "portal." Whether I get a timely response depends on whether there is a reliable nurse to respond.
    • 1 hour, 57 minutes ago
      Wanacure likes your comment at
      If you were to request the next available appointment with your T1D healthcare provider, when do you estimate the next available appointment would be?
      When I saw my endo a year ago, I wasn't able to make an appointment 6 months later because all available appointments were fully booked. I have to see her CDE who has more availability in order to meet Medicare requirements for quarterly visits. Many, many healthcare providers in my area burned out and quit during Covid. I injured my knee badly last June and can't get a consult with an orthopedic surgeon until May due to the backlog of people needing help. I'm on crutches until then. My sports medicine doctor stopped practicing medicine last month. Our healthcare system is in crisis with no solution in sight.
    • 1 hour, 58 minutes ago
      Wanacure likes your comment at
      If you were to request the next available appointment with your T1D healthcare provider, when do you estimate the next available appointment would be?
      On hold or actually talking about the issue and calling back to ensure someone follow's up as everyone seems to be over their head. Honestly, it varies. It can take considerable time just to raise the visibility of an issue, then the follow up can take weeks/months and patience to resolve. Another problem is patients without the cognitive skills for follow-up. These days i doubt anyone pays attention to them.
    • 4 hours, 19 minutes ago
      Wanacure likes your comment at
      If you were to request the next available appointment with your T1D healthcare provider, when do you estimate the next available appointment would be?
      I try to make my appointment for my next appointment when I check out. The scheduler always asks maki g it easier to remember. If I was to forget there would be a wait to get back int the rotation.
    • 11 hours, 28 minutes ago
      Greg Felton likes your comment at
      If you were to request the next available appointment with your T1D healthcare provider, when do you estimate the next available appointment would be?
      Before the onslaught of Type 2 Diabetes, I, as a T1D, could get an appointment almost anytime I needed one. Now, I cannot get an appointment within 3 months, which is the time within I must see rhe doctor for Medicare benefits. My doctor cancelled 2 (half ) of my sppointments last year. Caused ma a lot of problems. I live in Florida, a place where modern medicine does not seem to have reached yet.
    • 11 hours, 28 minutes ago
      Greg Felton likes your comment at
      If you were to request the next available appointment with your T1D healthcare provider, when do you estimate the next available appointment would be?
      I routinely see my Endo every three months. At the end of my appointment I schedule the next quarterly meeting date. But if I ever have to reschedule it, then it takes anywhere from two to four weeks to find a time that works for us.
    • 13 hours, 24 minutes ago
      Mike S likes your comment at
      If you were to request the next available appointment with your T1D healthcare provider, when do you estimate the next available appointment would be?
      It all depends on the urgency of my needs. I’ve gotten in the next day before, but those days may be gone! It also depends on who I see. But these days, even the PA is often booked. Of course, cancellations happen, so that can be a factor as well.
    • 13 hours, 40 minutes ago
      Jeff Marvel likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      The beginning of the year is always a bit iffy when you're on Medicare. Even though I've already paid my annual deductible, my pharmacy can't see that, so I must wait until it shows up on my Medicare account before I order new insulin. I always try to have plenty of insulin on hand at the end of December so it's not an issue. The organization I get my pump equipment from has a lot they must do because of Medicare, as well, and that can get time consuming. All-in-all, I'm lucky to have the time, energy and patience to deal with it, and I know up front these time-consuming moments are to be expected. If I wasn't retired, it'd be more of an issue.
    • 1 day ago
      Gerald Oefelein likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      I selected 6 hours. So far, I have spent 6 weeks trying to get a new pump. I decided to look for a new pump in mid-December as my 770G warranty expired on January 3. I wanted to go hoseless with the Omnipod and the Dexcom 6. I contacted Dexcom and they sent me to the medical distribution company ASPN, and they could do the Omnipod but only with pharmacy part D with the Dexcom 6 sensor on DME My part D pharmacy plan had Omnipod as tier 6. $155.56 co pay and $150/month. The omnypod is not available as DME. I called INSULET the mfgr of omnipod. They told me they only supply via pharmacy plan to get more T2d's to sign up. Verses 100% DME coverage, part D coverage that was a non-starter. I contacted another supply company CCSmed. They could do both Dexcom 6 and tslim x2. Ineeded a Endo visit to get the notes and Rx. I had my Endo visit on Jan 20. Still waiting for CVSmed. Been waiting for 5 weeks now. Just called CCSmed and they got the endo notes and Rx but Medicare wanted to know who paid for my 770G 4 years ago. Fortunately, that was private/company. My new pump should now ship tomorrow. Finally.
    • 1 day, 4 hours ago
      Wanacure likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      Most of the 3-4 hours is way ting on a phone
    • 1 day, 4 hours ago
      Wanacure likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      I answered "No time," but I live in France, where we have a single provider. I receive a prescription from my doctor and go to the pharmacy monthly to have it filled. (Pump peripherals are provided by a separate supplier.) "Appeals" do not exist here since the doctor will only prescribe medicines that are reimbursed. And no, I have never needed a treatment that wasn't covered.
    • 1 day, 5 hours ago
      Wanacure likes your comment at
      When you experience an illness that makes your blood glucose levels more difficult to manage (whether because you are unable to eat, the stress of being sick, or any other reason), what resources do you refer to for help managing your blood glucose levels while sick? Please select all that apply to you.
      The resources I use in managing my glucose levels once sick is my own personal experience after living with t1d for 46 years
    • 1 day, 5 hours ago
      August Rossano likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      Switching to Medicare has created (seemingly) endless hours and day making this transition with all things diabetes related. We’re still in the midst of making this ā€˜delightful’ change. This week we learned that Medicare covers Either CGM stuff OR glucose test strips. Thank goodness that God is sovereign over all these details. He helps me walk through these challenges without despair.
    • 1 day, 5 hours ago
      August Rossano likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      The last 3 months have been filled with frustrating phone calls now that I switched back to traditional Medicare from a Medicare Advantage plan. I have been fighting to get strips authorized in addition to CGM- they did not authorize them because I had no proof that I had a meter!! Crazy making! I had to write an appeal letter in order to get them, but finally got it worked out. I also had some pump replacement issues, trouble getting insulin, etc.
    • 1 day, 5 hours ago
      August Rossano likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      I answered "No time," but I live in France, where we have a single provider. I receive a prescription from my doctor and go to the pharmacy monthly to have it filled. (Pump peripherals are provided by a separate supplier.) "Appeals" do not exist here since the doctor will only prescribe medicines that are reimbursed. And no, I have never needed a treatment that wasn't covered.
    • 1 day, 5 hours ago
      August Rossano likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      Much too much time! Part of it, I know, is my own fault, for not keeping anxiety at bay when I have to sort out which plan will work best, annually. But it is something I dread, every single year. When I call to get some help understanding, the people are almost always very nice, but I have had times when the information was incorrect or not explained clearly. I usually commiserate with the person on the phone for having such an annoying system, and agreement seems to rule the day. But I never chose to make sorting out insurance management a career!
    • 1 day, 5 hours ago
      August Rossano likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      I selected 6 hours. So far, I have spent 6 weeks trying to get a new pump. I decided to look for a new pump in mid-December as my 770G warranty expired on January 3. I wanted to go hoseless with the Omnipod and the Dexcom 6. I contacted Dexcom and they sent me to the medical distribution company ASPN, and they could do the Omnipod but only with pharmacy part D with the Dexcom 6 sensor on DME My part D pharmacy plan had Omnipod as tier 6. $155.56 co pay and $150/month. The omnypod is not available as DME. I called INSULET the mfgr of omnipod. They told me they only supply via pharmacy plan to get more T2d's to sign up. Verses 100% DME coverage, part D coverage that was a non-starter. I contacted another supply company CCSmed. They could do both Dexcom 6 and tslim x2. Ineeded a Endo visit to get the notes and Rx. I had my Endo visit on Jan 20. Still waiting for CVSmed. Been waiting for 5 weeks now. Just called CCSmed and they got the endo notes and Rx but Medicare wanted to know who paid for my 770G 4 years ago. Fortunately, that was private/company. My new pump should now ship tomorrow. Finally.
    • 1 day, 5 hours ago
      August Rossano likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      The beginning of the year is always a bit iffy when you're on Medicare. Even though I've already paid my annual deductible, my pharmacy can't see that, so I must wait until it shows up on my Medicare account before I order new insulin. I always try to have plenty of insulin on hand at the end of December so it's not an issue. The organization I get my pump equipment from has a lot they must do because of Medicare, as well, and that can get time consuming. All-in-all, I'm lucky to have the time, energy and patience to deal with it, and I know up front these time-consuming moments are to be expected. If I wasn't retired, it'd be more of an issue.
    • 1 day, 5 hours ago
      August Rossano likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      I said 8+ and the reason, as for so many others, can be summed up in a phrase: transitioning to Medicare.
    • 1 day, 6 hours ago
      Wanacure likes your comment at
      On a scale of 1-5, how satisfied are you with your current insulin delivery method (pump, pens, syringes, inhaler, etc.)? 5 = the most satisfied, 1 = the least satisfied
      I’m a reasonably satisfied MDI user with Lantus and Fiasp. I’ve looked into getting a pump but honestly, until I find one that does everything I want, I’ll probably hold off. My wish list for a pump: 1) no tubes 2) works well with Fiasp 3) controls that allow me to stay at my target of 70-90 mg/dl all night long.
    • 1 day, 6 hours ago
      Wanacure likes your comment at
      On a scale of 1-5, how satisfied are you with your current insulin delivery method (pump, pens, syringes, inhaler, etc.)? 5 = the most satisfied, 1 = the least satisfied
      MDI for the past 60 years and do not see any alternative that I would prefer. The needles for my pens are so thin and sharp that they are painless (a far cry from the lancets I once used). chiefly, I am glad not to have to deal with setting up a pump and. Although I love my libre, I am not good candidate for having devices affixed to me. If my insulin delivery got interrupted they way i have interrupted my cgm service, I would have been in trouble. Furthermore, I have a track record of having both mechanicall and electronic things malfunction. (Seriously, I sometimes act as a beta-tester for technology folks. Maybe I push to many buttons?)
    • 1 day, 6 hours ago
      Wanacure likes your comment at
      On a scale of 1-5, how satisfied are you with your current insulin delivery method (pump, pens, syringes, inhaler, etc.)? 5 = the most satisfied, 1 = the least satisfied
      I've had Tandem x2 and Dexcom since September. Previously on Medtronic for around 15 years. Grew to HATE the sensors and switched before the warranty on my last Medtronic was up. So far, I absolutely LOVE the Tandem and the Dexcom. I'm disappointed, however, in the amount of waste and plastic that this pair creates. Of course there will always be plastic waste from any pumps/sensors, but the amount of non-reusable stuff for insertions is ghastly.
    • 1 day, 6 hours ago
      Wanacure likes your comment at
      On a scale of 1-5, how satisfied are you with your current insulin delivery method (pump, pens, syringes, inhaler, etc.)? 5 = the most satisfied, 1 = the least satisfied
      Have your doctor prescribe the syringes with .5 unit increments instead of the 1 unit syringes. Not quite a .1 unit which you are hoping for, but .5 is better than 1 unit increments.
    • 1 day, 7 hours ago
      Ahh Life likes your comment at
      Over the past 3 months, how much time would you estimate you have spent working through T1D prescription-related issues with pharmacies, insurance companies, durable medical equipment distributors, T1D device companies, health care providers, etc.?
      I answered "No time," but I live in France, where we have a single provider. I receive a prescription from my doctor and go to the pharmacy monthly to have it filled. (Pump peripherals are provided by a separate supplier.) "Appeals" do not exist here since the doctor will only prescribe medicines that are reimbursed. And no, I have never needed a treatment that wasn't covered.
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    If you wear a pump or sensor, how often do you put a site somewhere visible, such as on your arm or leg?

    Home > LC Polls > If you wear a pump or sensor, how often do you put a site somewhere visible, such as on your arm or leg?
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    23 Comments

    1. Anne Blayney

      I used to wear a Libre sensor, which was often visible (at least in warm weather). I now wear a Dexcom sensor and I get better results when it’s on my abdomen, so that’s less visible — but not because I’m trying to hide it. The pump sites are typically in covered areas because I want to avoid snagging the tubing!

      2 years ago Log in to Reply
    2. Mick Martin

      I used to wear a Freestyle Libre on one of my arms, which were visible, but now I’m using the Guardian Sensor 3 (MiniMed/Medtronic) I only occasionally use one of my thighs, which are generally not ‘visible’ unless you’re there to see me undress. šŸ˜‰

      2 years ago Log in to Reply
    3. Sean Gallagher

      I don’t put insets or sensors anywhere to specifically hide them but since I put them on my waist, they are not visible. I did wear the sensor on my upper arm for a while and that was visible at times.

      2 years ago Log in to Reply
    4. Gene Maggard

      I guess I’m just vain but I don’t like anything related to my diabetes care visible. Whenever I get a new pair of pants or shorts, my wife puts a slit in the inside of the right pocket with a velcro closure so I can hide the pump there along with the tubing. I used to clip my pump on my belt but it always brought up questions whenever anyone saw it and I’d rather not advertise the fact that I’m diabetic. My Dexcom G6 is placed on my abdomen. I tried it on my upper leg a couple of times but either due to circulation issues or other factors it was not comfortable.

      2 years ago Log in to Reply
    5. Dorian Dowell

      Mine is mixed. I wear the Dexcom G6 Sensor on my arm. Infusion sets are on leg, abdomen, Glute (Somewhat of a rotation). I find the CGM sensor works fine on my arm. Abdomen is a little inconvenient – especially with summer perspiration! I have tried the infusion set on my arm before. However, can’t get the tubing in the right length anymore – either too short or way too long!

      2 years ago Log in to Reply
    6. kristina blake

      Of course it depends on the season, if it is summer, short sleeves and shorts, more will be seen. But I do use my thighs and my upper arms. I did have one woman at a wedding insist I was beautiful, and to wish me luck when my Dexcom sensor was on my upper arm. (I was a guest). I guess she had seen one of those ads for the patch for chemo symptoms (Neulasta?). Anyway, I use patches that I turn into little paintings (my best is doing a sugar skull painting and a copy of Munch’s “The Scream” with the sensor as the face). Anyway, since I have ink anyway, it is barely noticeable.

      2 years ago Log in to Reply
    7. Sherolyn Newell

      Dexcom told me to put the sensor on my abdomen, so the pump is usually on the back of my arms or on my leg. If it shows, it shows. Doesn’t bother me. One day when it was showing, a mom with a newly-diagnosed 4-year-old saw it and asked me if I would talk to him. So sometimes it works out well if it shows.

      2 years ago Log in to Reply
    8. Jana Foley

      I use my upper arms and my forearms for my sensors and my upper arms for my infusion sets on a regular rotation. If they are seen, it does not bother me. If someone asks a question, I answer it and go on about my day. You just never know when your answer can help someone.

      2 years ago Log in to Reply
    9. Ernie Richmann

      I wear the cgm on my abdomen. I have had a few sensors not work and when I call Dexcom, I am always asked where I was wearing the sensor. I got the idea they will not replace a sensor unless I follow the directions.

      2 years ago Log in to Reply
    10. George Lovelace

      I use abdomen and arm and Love Handle areas BUT usually have pump in a Shirt or pants pocket, sometimes with tubing exposed. After 56 years I have no modesty about my Dm.

      2 years ago Log in to Reply
    11. Candace Jackson

      Our 1 year old loves my pump & sensor so I do my best to hide both of them.

      2 years ago Log in to Reply
    12. Janis Senungetuk

      Both are always visible, that’s not an issue for me. I’ve found wearing the CGM on my upper arm the most comfortable location. The pump inset is on my abdomen with the pump clipped to my waistband or pants pocket. When I was using MDI and a meter I’d check my bg and inject in public. I’ve always tried to go ahead and do what I needed to do without making a big production out of it.

      2 years ago Log in to Reply
    13. Kimberly Starkey

      Both the pump infusion set and cgm are on my abdomen. Having clothing cover them adds some protection from being bumped or pulled out. My pump, however, is in a zippered, padded case that I sewed a hole in and slipped a carbiner through to hook to my beltloop. The pump and tubing are visible, but the pump won’t fall off as it occasionally did when I used a clip. I tuck the tubing into my pants to minimize it getting caught on things.

      2 years ago Log in to Reply
    14. Donald Cragun

      I insert infusion sets in my leg (usually covered by pants) and CGM sensors in my abdomen (usually covered by a shirt). I sometimes remove my shirt if it is hot. I sometimes remove my shirt and/or pants for medical exams. I don’t care who sees my infusion sets or CGM sensors as long as I’m not exposing private parts.

      2 years ago Log in to Reply
    15. Nancy Taylor

      I use Omnipod Dash pump (pods) with no tubing to deal with. A much more flexible option! I wear both CGM and Omnipod on my abdomen (opposite sides). Like another user mentioned, I have had a number of Dexcom G6 sensors fail. Dexcom has sent me replacements for every single sensor. They do always ask where you placed it but that has never affected the replacements. They have aslo included an extra sensor in each of my last two replacement shipments when I had to return 2 or 3 sensors at a time. If you do have Dexcom failures be sure to call them. They have always been very helpful to me.

      2 years ago Log in to Reply
    16. Ely Kozminsky

      Pump – belly Sensor – Arms

      2 years ago Log in to Reply
    17. Jennifer Wilson

      My arm is most comfortable but has the greatest risk of being accidentally hit or bumped off. In the extreme warm and cold months, I tend to not wear it exposed to protect it from the harsh sun or weather elements. Clothing over the pod does add another cushion of protection. I only really intentionally do not want it visible if I am dressed in evening or formal wear.

      2 years ago Log in to Reply
    18. Clare Fishman

      Since I use Omnipod my site options are limitless and I use them all. Generally my Dexcom is on the back of my arm. It is the most comfortable spot for long term use and I use each sensor for at least a couple of sessions.

      2 years ago Log in to Reply
    19. Steven Gill

      Wearing a pump folks see my tubing, which I often have to work hard to protect (pulled the insert loose before)..

      2 years ago Log in to Reply
    20. Lenora Ventura

      With my Dexcom, I use my arm 90% of the time. With my pump, never.

      2 years ago Log in to Reply
    21. Bonnie Lundblom

      I use my arms a lot for my Dexcom and it depends on sleeve length whether or not it shows. My insulin pump does have tubing but the insertion site doesn’t show.

      2 years ago Log in to Reply
    22. Leona Hanson

      I wear my pump set so everyone can see it but also wear it so no one can see it because of rotation of sites but when visible the kids love it because they know that there not alone that there is someone else who has diabetes isn’t it great

      2 years ago Log in to Reply
    23. Sally Numrich

      I use all areas equally. I rotate sites so arms and legs get used as much as hips, buttocks and upper/ lower stomach. All areas are possibilities for site locations.

      2 years ago Log in to Reply

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