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    • 4 hours, 46 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.
    • 4 hours, 47 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.
    • 6 hours, 43 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.
    • 6 hours, 59 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.
    • 18 hours, 9 minutes 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.
    • 21 hours, 58 minutes 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
    • 22 hours, 1 minute 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.
    • 22 hours, 43 minutes 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
    • 22 hours, 43 minutes 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.
    • 22 hours, 45 minutes 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.
    • 22 hours, 50 minutes 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.
    • 22 hours, 51 minutes 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!
    • 22 hours, 52 minutes 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.
    • 22 hours, 53 minutes 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.
    • 22 hours, 53 minutes 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.
    • 23 hours, 29 minutes 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.
    • 23 hours, 40 minutes 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?)
    • 23 hours, 52 minutes 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.
    • 23 hours, 53 minutes 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, 1 hour 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.
    • 1 day, 2 hours ago
      ConnieT1D62 likes your comment at
      In your own words, how would you describe the feeling of a severe low?
      Nothing short of terrifying. I often go into seizures, having no idea where I am, who anybody, or even if I’m alive or dead. I’ll feel like I’m falling or hurtling toward something. At home I feel like my house is tilting. Im leaving a lot out but these are some of the scariest things.
    • 1 day, 3 hours ago
      Modee 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 Europe has the right idea! Is it a good health system for you overall? The US may be too large to implement a national system, but that doesn't hold states back (as long as there is federal money to help).
    • 1 day, 3 hours ago
      Modee 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, 3 hours ago
      Modee 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, 3 hours ago
      Modee 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.?
      PUMP USERS: Just in case nobody has told you, if you use a pump, Insulin is considered durable medical equipment, which can save a lot of money, even with the new price cap
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    Do you feel that your blood sugar patterns are different during times of the year when there are fewer hours of daylight, compared to when there are more hours of daylight? If yes, tell us how in the comments!

    Home > LC Polls > Do you feel that your blood sugar patterns are different during times of the year when there are fewer hours of daylight, compared to when there are more hours of daylight? If yes, tell us how in the comments!
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    21 Comments

    1. Ahh Life

      Back in the days when I was snow skiing, which uses gazillions of calories per hour, the BG patterns had to be re-managed. But at an older age now, nah, not much difference. ā‰§ā— ā€æā— ā‰¦āœŒ

      2 years ago Log in to Reply
    2. Clare Fishman

      More hours of daylight = summer when I am biking and playing tennis. Less hours of daylight = winter when I am hibernating except for the occasional foray out for food. So yes there is a noticeable difference in blood sugar and insulin use patterns.

      2 years ago Log in to Reply
    3. connie ker

      I answered slight difference because I am not exercising like I did in the summertime and could walk until 9:30pm. I am one who would not vote for daylight savings time because the change of the clocks brings change in the bio rhythms.

      2 years ago Log in to Reply
    4. Sherolyn Newell

      I think the difference comes from activity level as well. I tend to get sleepy soon after it gets dark. That means in the winter, I am not very active after dinner. I think that causes some night time high levels.

      2 years ago Log in to Reply
    5. Matt Trenton

      I get crushed by daylight changes as well as impending precipitation or large weather changes. Uber low as weather approaches, followed by highs once it because raining/snowing.

      2 years ago Log in to Reply
    6. Nevin Bowman

      Yes, there is a difference for me. I have to make a conscious effort to get exercise over winter when I’m cooped up inside most of the time.

      2 years ago Log in to Reply
    7. Pat Pitarra

      Everything effects me, temperature, driving in the rain (severe drops), time change…

      2 years ago Log in to Reply
    8. Ernie Richmann

      I’m not really sure. I am making an effort to control my blood sugar levels by adjusting diet and exercising through out the day. While it is true that I am slightly less active during the winter months, I have alternate ways of exercising like riding a bike on on stand in my basement, using resistance bands, walking the stairs. I want to get back to taking exercise classes at the Y but will wait for safer times. I wanted to make a presentation on diabetes at a Lions Winter retreat but I just cancelled- just to risky right now even with the lodge and participants taking precautions.

      2 years ago Log in to Reply
    9. Mary Ann Sayers

      I’ve always had no blood sugar pattern any time of the year! for 66 years!!! Actually, right now, I’m running very high bgs and I have no idea why! I’ve been quarantined for 10 months and live in a rest home. Meals are served by staff in our rooms, I choose my food and amounts, so I can’t blame the high bgs on that. Since the high bgs have happened only this last week, (my test for covid-19 was negative) I think my body’s metabolism is screwing up the works!!!

      2 years ago Log in to Reply
    10. Lawrence Stearns

      My blood sugars change periodically, usually with the seasons. Normally, I have to increase my insulin in the winter time. When I notice a pattern change in my blood sugars, I adjust my basals or boluses. It’s an art.

      2 years ago Log in to Reply
    11. Abigail Elias

      My blood glucose patterns are highly dependent on physical activity level so shoveling snow affects insulin demand and calculations regardless of whether it’s midday in bright sun or before dawn in the dark.

      2 years ago Log in to Reply
    12. Beckie McCammitt

      More insulin resistant in the winter- not sure if it’s related more to the weather or daylight

      2 years ago Log in to Reply
    13. Kristine Warmecke

      Yea! Mine are much better this time of year. My body is intolerant of temps above 70 degrees, so I end to hibernate during summer. Right now I’m out enjoying my walks with my dogs. Just need some snow here!

      2 years ago Log in to Reply
    14. Sue Herflicker

      I always have to change my basils after daylight savings time is over. I am active most days during the summer, swimming in the pool, going to the beach, horseback riding, gardening, walking, as soon as it starts getting dark early that all stops and its time to up the basil … being LADA, exercise makes a huge difference in how much insulin I need. If I work in the yard all day raking leaves or am active I can usually get by with just my basil for the day and not even have to bolus for food, and I can eat anything!!! Love it!!

      2 years ago Log in to Reply
    15. ConnieT1D62

      I am more active for longer periods in the warmer months when daylight is the majority of a 24 hour time span. During the winter months my energy seems to dwindle when the sun goes down. I dislike daylight savings time. IMHO it is a waste of energy that really does not serve the greater good of the majority. It is inconvenient and wreaks havoc on the sleep schedules of people who work overnight shifts in healthcare and other businesses whose employees work from 11 pm to 7 am or 12 m to 8 am.

      2 years ago Log in to Reply
    16. Molly Jones

      My CGM reports do not show any different seasonal trends and I do not notice any myself. I am not fond of the sun and tend to stay indoors if it is above room temperature outside as my body’s thermostat doesn’t seem to work well, probably due to my thyroid issues.

      2 years ago Log in to Reply
    17. ANN GALLUZZO

      With me, it happens, and I am 100% sure that it does, because I eat the same breakfast and lunch every day of the year. But the blood sugar rise when there is less sun has nothing to do with daylight. It is entirely correlated with how warm or cold I am. When we have a cold day in October, I need more insulin. If we have a warm day in December, I need less. And if I visit someone who keeps their thermostat high in winter, I need far less insulin than I would at home. Someone needs to consider all factors, not just the number of daylight hours. Some people keep their home or work a constant 75 degrees year ’round, so they would not have the increased or decreased insulin requirement that I do.

      2 years ago Log in to Reply
    18. Donal Conway

      My BS reads in the last three months have become very erratic mainly going very high after breakfast in which carbs total is nearly always the same & I always take the same amount of Act Rapid. About 1.5-2hrs later my BGS jumps to 14-18mmols & I have to take more units of short acting along with jumping on to the Treadmill for 20 mins or so, if the weather is dry or good outsise in the garden where I would go & cut some firewood from the overgrown trees there, I did that same thing in the Summer but not as much, because we were preparing for the sale of the house which is happening right now. My diabetes Consultant would not allow me to increase the morning insulsin but I have to make the corrections anyway as I have been doing for the last thirty of the fifty years I have been a person with diabetes.

      2 years ago Log in to Reply
    19. RenƩ Wagner

      During DST, I tend to be outside working in the yard and enjoying the outdoors until dark. Standard time, it’s cold and dark early, so not out or active as much. I live in Florida and Houston areas.

      2 years ago Log in to Reply
    20. Mark Fuller

      It is a function of the time I can spend outside working on the house and yard.

      2 years ago Log in to Reply
    21. Debbie Kolterman

      I do gardening and am less active with less daylight.

      2 years ago Log in to Reply

    Do you feel that your blood sugar patterns are different during times of the year when there are fewer hours of daylight, compared to when there are more hours of daylight? If yes, tell us how in the comments! Cancel reply

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