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    • 8 hours, 40 minutes ago
      KarenM6 likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 9 hours, 31 minutes ago
      Mick Martin likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      First of all, I've said it before, and I'll say it again: stop asking questions about family screenings for antibodies!!!! This is seriously like the tenth time this question has come up. There are plenty of other questions about T1D you can ask. Second, there should be another option to the effect of "I have not discussed antibody screenings with my family," which is the category under which I fall.
    • 10 hours, 26 minutes ago
      Katie Bennett likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 11 hours, 9 minutes ago
      Kate Kuhn likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 11 hours, 29 minutes ago
      Karen DeVeaux likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      I was born in 1939 and had many childhood illnesses. Three different kinds of measles and tonsils removed before I was 5 years old, then mumps and chickenpox when I was 5. While recovering from the mumps and chickenpox, I began showing the symptoms of very high blood sugar. Three doctors examined me and they were not able to make a diagnosis. I had lost much weight, and I had stopped eating. I did not have an appetite. It was almost impossible for me to walk. A fourth doctor had my blood tested and he made the diagnosis. While receiving pork insulin I finally began to recover a few days after my sixth birthday. I did not have ant relatives with diabetes. I think the childhood diseases caused internal damage and that was the cause of my diabetes. At the present time there are still no type one diabetics among my relatives. I do not believe it is necessary for my children and grandchildren to be screened for T1D autoantibodies.
    • 12 hours ago
      Kelly-Dayne likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 12 hours, 5 minutes ago
      KCR likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      First of all, I've said it before, and I'll say it again: stop asking questions about family screenings for antibodies!!!! This is seriously like the tenth time this question has come up. There are plenty of other questions about T1D you can ask. Second, there should be another option to the effect of "I have not discussed antibody screenings with my family," which is the category under which I fall.
    • 12 hours, 59 minutes ago
      William Bennett likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      Hi Kristen, thanks so much for your feedback. We do plan to continue questions and education on T1D screening. The constantly evolving clinical trials and FDA-approved therapies that offer the potential to intervene, delay —— and hopefully some day prevent —— T1D are only effective if children are being screened for the earliest stages of T1D. Without screening, we cannot delay or prevent T1D. We do offer "No, my family members have no been screened" as an option. We appreciate your passion as a person affected by T1D and hope you enjoy our other daily questions. All the best, The T1D Exchange team
    • 13 hours, 1 minute ago
      Chrisanda likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      First of all, I've said it before, and I'll say it again: stop asking questions about family screenings for antibodies!!!! This is seriously like the tenth time this question has come up. There are plenty of other questions about T1D you can ask. Second, there should be another option to the effect of "I have not discussed antibody screenings with my family," which is the category under which I fall.
    • 13 hours, 30 minutes ago
      Gary Rind likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      First of all, I've said it before, and I'll say it again: stop asking questions about family screenings for antibodies!!!! This is seriously like the tenth time this question has come up. There are plenty of other questions about T1D you can ask. Second, there should be another option to the effect of "I have not discussed antibody screenings with my family," which is the category under which I fall.
    • 13 hours, 38 minutes ago
      Jneticdiabetic likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I have led a team for the JDRF OneWalk annually since the late 1990's. We have been able to raise a lot of funds for JDRF...and I have enjoyed doing it. Good cause!
    • 13 hours, 43 minutes ago
      Lawrence S. likes your comment at
      If you or someone in your family has T1D, have other members of your family been screened for T1D autoantibodies? If not, do you think your family would be willing to be screened for T1D autoantibodies?
      my siblings & parents are older (like me) and they've never expressed any interest in getting tested. my nieces and nephews have never said anything either
    • 1 day ago
      Karen Newe likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I participated in several ADA walks not long after being Dx with T1D. As Ahh Life points out large $ are rased, but where do they go? I stopped supporting ADA for that reason. I think JDF is much more open on where the funding goes.
    • 1 day ago
      Karen Newe likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      JDRF only. I like knowing that my contributions are going specifically to T1D.
    • 1 day ago
      Karen Newe likes your comment at
      Have you ever participated in a charity fundraising event that benefitted a diabetes organization (i.e., a walk, marathon, gala, etc.)?
      I have led a team for the JDRF OneWalk annually since the late 1990's. We have been able to raise a lot of funds for JDRF...and I have enjoyed doing it. Good cause!
    • 1 day, 5 hours ago
      Joindy23 likes your comment at
      The last time you discussed adding a new device or medication to your T1D management routine with your health care provider, who initially suggested trying the new device or medication?
      Switched a long time ago to Tandem/Dexcom from Minimed because of improved and more automated control, and haven't looked back. Still wishing for a cure, but know it's not going to happen for dinosaurs like me. I'll just be glad when young people will will one day experience that magic word: cure. It's too easy to sit around and complain, but it's high time for a cure, and way past time having us depend on treatment that is pretty much a money maker for big Pharma when it seems as if there's a cure waiting in the wings. Filling up landfills with used pump supplies, etc., makes our society look nothing but incompetent and greedy. Sorry to rant.......
    • 1 day, 5 hours ago
      Joindy23 likes your comment at
      The last time you discussed adding a new device or medication to your T1D management routine with your health care provider, who initially suggested trying the new device or medication?
      They do too often. Why I ask? Well because it will help long term.... oh how do you know that it will help? It's a brand new medication, never been used by the D community, except for the shortest term study mandated in order to get it to market, and sell. Long term has never been achieved... its NEW. Let's revisit/wait a couple years... if its MAGIC medicine, sure I'll try it. But unless it's got magic properties, guarantees magic results why would I want it, until it's been used for a decent while??? Oh well... yeah, guess that does makes sense....
    • 1 day, 22 hours ago
      Wanacure likes your comment at
      Does your T1D health care provider currently offer the option to have virtual appointments (via phone or video call)?
      Yes and for the last year and a half that is exclusively what I have been offered so I am not getting all the usual checks an in person endo visit requires. ADA and others spent 10-20 years convincing endos they needed to check patients feet and that progress has evaporated.
    • 1 day, 22 hours ago
      Wanacure likes your comment at
      Does your T1D health care provider currently offer the option to have virtual appointments (via phone or video call)?
      I would rather see in person. He checks my feet, BP etc. we have a chance to catch up and for me to ask questions. To me so much better face to face. We did virtual during pandemic.
    • 2 days, 6 hours ago
      Phyllis Biederman likes your comment at
      If you use an insulin pump, do you currently have a protective case on your pump or PDM?
      I’ll occasionally use the holster with clip that came with my pump or a protective case of my own when I’m wearing something without pockets. However I find these quite bulky thus usually just slip my pump in a pocket.
    • 2 days, 6 hours ago
      KarenM6 likes your comment at
      Of the people in your life, who (if anyone) makes you feel judged or criticized for your T1D management (for example, what foods you eat, where or when you check your blood glucose, etc.)? Select all that apply to you.
      Hmmm... I'd almost welcome it, another challenge to enjoy?
    • 2 days, 6 hours ago
      KarenM6 likes your comment at
      If you use an insulin pump, do you currently have a protective case on your pump or PDM?
      I am rough on insulin pumps and cracked 2 minimed pump cases. I found the bare T:slim pump too slippery. I use the MEDmax silicone case. I put that in a AGOZ case with a belp clip. But I don't like the clip. It's too sharp and too stif. Looking for a belt for night time use.
    • 2 days, 6 hours ago
      KarenM6 likes your comment at
      If you use an insulin pump, do you currently have a protective case on your pump or PDM?
      I use the Tandem provided case and added a gorilla glass screen protector. I wear it on my belt in an pouch.
    • 2 days, 8 hours ago
      lis be likes your comment at
      Of the people in your life, who (if anyone) makes you feel judged or criticized for your T1D management (for example, what foods you eat, where or when you check your blood glucose, etc.)? Select all that apply to you.
      Insulin, meters, diabetic tech are not magic wands. Its usage does not guarantee only "positive" results. Negative events can and do occur, period. Non -D- typically (incorrectly) equate negative events as being total user failure, severe user errors. As diabetics we get blamed, despite having made zero mistakes on our part. We make seriously educated best guesses, despite that truth, we can and do fail anyway sometimes! Outsiders falsely need to believe inulin, our tech are complete-total cures, rather than tiny bandages at best. When confronted for using (sic. my) "drugs" in public, no matter how invisibly done... it is their self righteousness , poor assessment which is the issue. I gladly squash such insects...
    • 2 days, 9 hours ago
      Karen Tay likes your comment at
      If you use an insulin pump, do you currently have a protective case on your pump or PDM?
      No. I hate the clip on the case that came with my Tandem pump. I bought a couple of other cases, including Type 1 Tactical, and hate the bulk and the awful clips. I just stick the pump in my pocket and it's fine. At night I do use one of the other cases, from Type 1 Secura, because I can keep it clipped to my undies and easily slide the pump in/out if I have to look at it during the night.
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    Have you ever used nasal glucagon? This includes using it on yourself, using it to help someone else, or if someone else gave it to you.

    Home > LC Polls > Have you ever used nasal glucagon? This includes using it on yourself, using it to help someone else, or if someone else gave it to you.
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    In the past week, have you stayed up later than you planned to make sure your blood sugars are stable before going to sleep?

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    CGM users: Do your sensors typically last for their full approved session duration? If not, how many days early does your sensor fail or fall off, on average?

    Sarah Howard

    Sarah Howard (nee Tackett) has dedicated her career to supporting the T1D community 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 Manager of Marketing at T1D Exchange. Sarah and her husband live in NYC with their cat Gracie. In her spare time, she enjoys doing comedy, taking dance classes, visiting art museums, and exploring different neighborhoods in NYC.

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    25 Comments

    1. Rex Franklin

      I have nasal glucagon which I carry with me and have another at home.

      3 years ago Log in to Reply
    2. Jillmarie61

      I carry it in my purse and have some at home, but I’ve never used it yet. I haven’t given myself glucagon injects before.

      3 years ago Log in to Reply
    3. Britni Steingard

      Just got my first prescription for it. Seems much more user friendly than the injectable.

      3 years ago Log in to Reply
    4. Clare Fishman

      I used it on myself because my blood sugar was dropping so quickly I couldn’t bring it up and I was afraid I would pass out. It felt like a gun shot going off in my head but it worked well.

      3 years ago Log in to Reply
    5. Janet Wilson

      My kiddo HAS inhalable Glucagon. But, we’ve never had to use it, thank God. I feel better knowing we HAVE it, though. We have it at school, at home, and in her go-bag. PS – I HATE this new format so much I barely ever answer the questions anymore. This version is not AT ALL user-friendly. Please, consider changing it.

      3 years ago Log in to Reply
    6. Philip Bunsick

      I have it available but have never used it. Really this would be for sleep time emergency use. I do not carry it with me as my Lifesavers do the trick for this requirement.

      3 years ago Log in to Reply
    7. Dan Diehl

      I have one and haven’t had to use it. Rather expensive and not covered by my insurance. Much easier for anyone to administer.

      3 years ago Log in to Reply
    8. Patricia Dalrymple

      Agree Janet Wilson. It is not for users. Only the company. We used to be able to comment directly to people and encourage each other. This is company based pretty much totally. I am not learning from it as I did from GLU. And, on my phone anyway, it says there are all these comments that I haven’t figured out how to even see. If it doesn’t pertain directly to me, I hit delete.

      3 years ago Log in to Reply
    9. Jonathan Strait

      No, but that’s what’s on standby

      3 years ago Log in to Reply
    10. Steve Rumble

      No, but have some at home “just in case”

      3 years ago Log in to Reply
    11. Stacie G.

      My Dr. just prescribed it to me. I haven’t had an occasion to use it yet but next time I have a severer low, I will.

      3 years ago Log in to Reply
    12. Frederick Schulz

      I have used it once, when I was away from home ( I always carry one in my pocket when away). It gives quite a jolt in the nose, sort of like an intense tickle, but it does work, in a few minutes.

      3 years ago Log in to Reply
    13. connie ker

      Great for diabetics who play sports, or for children in school. Easy to use. How long before it expires? I remember throwing glucagon kits in the trash because they expired, and they cost $$$. Does insurance or Medicare cover nasal glucagon and does this spray get into the lungs? They have found anything that gets into the lungs can cause breathing problems.

      3 years ago Log in to Reply
    14. connie ker

      Can somebody answer my questions about the lungs, and about the insurance coverage.

      3 years ago Log in to Reply
    15. Ken Raiche

      It would be great to get more information on this product from all of those individuals who have actually used it. At this point I haven’t ordered it but may consider doing so in the not too distant future.

      3 years ago Log in to Reply
    16. KarenM6

      Hi Connie – The nasal glucagon I have called Baqsimi lasts 18 months to two years. My insurance covered it, but I don’t know that ALL insurances would… and, I don’t know about Medicare. I don’t know if it gets into the lungs. From my experience with nasal sprays for allergies, it doesn’t seem likely, but I couldn’t say for sure. The spray is intended to be absorbed in the nose… seems the spray would stay focused in the nose… BUT, there are all kinds of procedural type issues by the user which might mean it _could_ get into the lungs. (Like accidentally inhaling a drink and then coughing badly for the next hour.) Although it’s not much, I hope that helps! I agree that this new format is not as good as the old GLU. Agree with the others that the old format was better for talking with other diabetics and getting good info or encouraging, etc. People may need to ask a question and we can’t do that now. We can’t message people privately when more and detailed info is needed that is not necessary to share with ALL the users.

      3 years ago Log in to Reply
    17. Patricia Maddix

      I have always kept glucagon on hand in case of an emergency for my family to use but have never had to use it. Just switched to having the nasal on hand instead of the injectable as it seemed easier for someone to use in an emergency situation. My Medicare insurance did not pay for it. When my husband was working and we had employer-based insurance, then insurance was paying for it my nasal glucagon prescription does have an expiration date on it. For those of you who indicated you had used the nasal glucagon, did you have any after effects like nausea, vomiting, very high blood sugars?

      3 years ago Log in to Reply
    18. Alison Neumann

      Yes I have, it stung my nose like crazy. I was drippy and snotty for a good few hours after and was even a little nauseous. I had to sleep the nausea off afterwards. But it really worked well in getting my glucose numbers back up!!! I think it’s the best option out there, and would recommend ONLY using it in an emergency since the side effects are not fun.

      3 years ago Log in to Reply
    19. Marie Seymour-Green

      I have Baqsimi on hand, but have never had to use it.

      3 years ago Log in to Reply
    20. Janice B

      I have Baqsimi at home but have never had to use it. In 27 years with T1D I have only used glucagon once, so hoping that it will remain just a back up item in my arsenal that never gets used.

      3 years ago Log in to Reply
    21. Jan Masty

      I agree with others about the new format. Don not like it and “answer” it much less frequently

      3 years ago Log in to Reply
    22. Sally Numrich

      I haven’t had to use glucagon since I was a child. Do I have regular glucagon? Yes but the reality is, with a CGM there really isn’t a need for it.

      3 years ago Log in to Reply
    23. ConnieT1D62

      Tickles my nose a bit – a brief and temporary side effect. I like that it works quickly within minutes to elevate BG. I have it on hand to use instead of glucagon to treat a severe low. Unfortunately it’s not covered on my insurance formulary and I have to pay out of pocket, so I only use when BG is trending <50 – which is rare these days because of Tandem Control IQ.

      3 years ago Log in to Reply
    24. Nicholas Argento

      I have it available but have not needed it. The 2 choices now for easier to use glucagon- Baqsimi nasal glucagon and an epi-pen like device with premixed glucagon, Gvoke Hypopen, are both big advances in making glucagon easier and more reliable for use in emergency. They also both are good for at least 2 years from date of manufacture, also an improvement.

      3 years ago Log in to Reply
    25. Stang777

      I have it but haven’t used it. I am actually more afraid to have this one used on me than I am the old glucagon kit that has to be injected due to some of the comments I have seen in other places from those who have had it used on them. I also hate this new format and do not answer questions on it nearly as much as I use to, and I answer the questions less and less as time goes by, which I never did on the old format.

      2 years ago Log in to Reply

    Have you ever used nasal glucagon? This includes using it on yourself, using it to help someone else, or if someone else gave it to you. Cancel reply

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