Looking back, 20 years ago now. I would say, get yourself a good team, that’s your credentialed diabetes educator, general practitioner and endocrinologist. If they are not encouraging and supportive, look for someone who is. This has made all the difference for me.

I have had Type 1 diabetes for 48 years. I urge any newly diagnosed Type 1s to save this video and come back to it often. I can tell you it will be a gem in your diabetic life. Can I add that despite living with this condition for so long, I have got to my 77 years of age with no complications and continue to live an enjoyable, active life. Another great contribution, Andrea. Well done!

I woke up with high blood sugar this morning. I've had Diabetes for 32 years. Though it's tough and it's tough to be perfect with levels all the time, the food far outweighs the bad. Thank you for this video!

Wish to God I'd seen this video a year ago when I was diagnosed as LADA! I'm very grateful I was diagnosed at a time when we have technology such as CGMs and ultra-rapid insulins, but it's still really tough, especially if you care about your health and are depended upon to earn a living. The hardest part remaining today for any newly- or recently-diagnosed Type-1 is the education. You're basically left to self-teach, and that's why people like you are so brilliant. Thank you so much 🙂

I was diagnosed last week and have not yet accepted this is a part of me and my life now. I am angry and sad... Thank you for telling me to be kind to myself and not to look for perfection. I hope I will be able to look on this from a positive point of view (like you are and I love it!) soon.

I am a newly diagnosed T1D. I was diagnosed March 3, 2022. It came out of left field. I am 54 years old and it has been a long six weeks. This video was what I needed today. Thank you!

I’m crying so hard right now. It’s been 8 days since my hospitalization and it’s Christmas. I just want to be alone and cry but I feel like I have to pretend to be happy around my husband’s family. I’m so so so sad and overwhelmed.

When I was diagnosed about 5 years ago I felt so lonely. I didn’t know anyone with type one and only 2 people with type 2. My educator wanted my to get a CGM and at the time I worked at an animal shelter and was afraid a dog would tear it off. I finally got a Freestyle Libre 2. I watched your video over and over and when I attached the sensor there was absolutely no pinch or pain!! Thanks for all you do!

I was diagnosed about 5 months ago, with LADA. I feel often like I don’t have a right to still be processing, like I should be better at managing the disorder, like no one but my bud with type 2 really can understand. I’ve watched 3 of your videos today. I came upon the exercise one because I need to figure out how to stay active as well as managing the diabetes safely, your video was tremendously helpful. This video made me cry like a silly baby because I feel like it’s okay to still be mourning and adjusting and also to be told that I don’t have to exist in a vacuum. I don’t know how to do it all yet and most likely there will be a day when I’ve gone entirely diabetic. But I might actually look forward to it so I don’t have to live in suspension, wondering when that will happen. Anyways… I am screaming into the KZfaq void right now, but my point was to thank you for the validation and encouragement. You already know how much it helps to have others that understand. 🙏🏼

My 1 year diagnosis is coming up in December. I was totally meant to see this video tonight, I’ve been struggling with high glucose levels the past two days and I’m not quite sure why lol. Being diagnosed during covid was very difficult, but your channel made/makes me feel less alone through it all. Thank you so much ❤️❤️

I've been a t1d 59 yrs and I agree with yon 100%. I wish there were support groups or family members I could have talked to about diabetes back in the day. You were so blessed to have your dad, brother and mom as your support team. New t1d's have the technology, social media and support groups, but some will still struggle with self-worth, sadness, depression, and a feeling of loneliness. I think your video will show them that it's okay to have these feelings, and that they are NOT alone. You have helped them to know that their CGM's will be up & down. There will be days/weeks that they just want to sit and cry. They need to know that their will be more good days than bad; and many good years to come. . After my first 5 years of being diagnosed. I found a Endo. that told me I could do and be anything that I wanted. I got married had 3 children, a career in nursing . Now I am happily retired enjoying life and 6 grandchildren it is possible. Do I still struggle with my diabetes... good days and bad yes I do, but that's life. Thanks so much for your videos I enjoy them keep them coming. ❤️❤️❤️

Was in a state of dka for 3 days thought I had a stomach virus/flu But when I was admitted my sugar was 570.....got diagnosed on the 2nd day and stayed in hospital for 10 days honestly it didn't hit me till I was released and had make everything apart of my 21 year old life..reassuring even though my wife and entire family is so supportive that there are people like you out there knowing exactly what it's like.

Thank you so much for your insight into what diabetes is like after the diagnosis period. I will certainly be keeping all your advice in mind. I had my pancreas removed 3 weeks ago so I'm trying to get to grips with going from a type 2 diabetic to now being a type 3c (not too much different from a type 1) as well as trying to recover from the operation itself which is very much limiting what I am currently able to do. It's still very overwhelming for me at this point and I keep being told to stop obsessing over controlling the numbers but it's the only thing I've got control of in my life due to other medical conditions I have such as an unpredictable and unknown muscular condition. I'm sure I'll be watching this video many times to keep reminding myself of your wonderful advice and support. Thank you very much for making this video Andrea. I really appreciate it as I'm sure many others do as well.

Well said, Andrea! I've been a T1D for 20 years as well, and nothing is more exhausting than constantly being told by non-diabetic folk that you should 'take care of yourself better' or 'how could you let that happen!'. At the end of the day, we have to focus on the positive and accept that this condition is part of life, with its ups and downs. And we can definitely live happily with it (even if we don't do it right every single day).

Newly diagnosed type 1 and you Andrea are such a big inspiration. Having borderline personality with this diagnoses has massively impacted me and my mental health. So glad I came across this video its so deep and raw and appreciate you sharing the exact words I needed to hear as well as all you’re lovely comments, thank you❤

Just found your channel and watched a few videos Love how positive you are. I'm 52, and was just diagnosed last year with adult onset type 1. It's been crazy trying to adjust to worrying about carbs and sugar. I've found several KZfaq channels that have helped. I will definitely be watching more, and have subscribed.

I love that you are so encouraging and letting people know they are not alone and that it is ok to not be perfect and to be gentle with yourself. Thank you!

Wow! Thank you. You posted this 9 days after my diagnosis 💙 I so appreciate your channel, and especially this video!

Diagnosed 2 whole weeks now and I feel so overwhelmed by emotions, information and alone…. it’s definitely intimidating 🥲 This video helped A LOT! The comments help too! Thank you for posting 🩷

I remember finding your channel when looking for advice and information regarding the Libre2. When you attached the Libre2 to your underarm, and said that it wasn't painful, I decided to tell my doctor that I was ready to start using the device. Previously, she tried convincing me to use it, but I was too scared. Anyway, when I finally got the Libre2, it was that same video that gave me the courage to attach the sensor! And, of course, you were correct. . . it didn't hurt. I've been living with Type 1 / Type 2 Diabetes (I have half a pancreas to I eke out some insulin) for over 30 years and this is the only time where I have excellent A1Cs. Your videos make a difference in many lives. Thank you SO much! 😄

I need this right now. My blood sugar levels this past few days are going up and down and I get a little frustated about it. Thank you for the words of encouragement and reminding me that I am not alone. Thanks, Andrea💕 Take care always.💕💕

100% to all of this! Thank you, Andrea, for being a positive and educational place to go. You’re videos are so helpful for newly diagnosed T1Ds. ❤️

I've been T1 diabetic over 20 years also, and this video even helped me feel better! Thank you for doing these videos for us ❤️

Andrea I love the words “it’s like a dance” that you used! It’s so true! sometimes like yesterday for me the dance is incredibly frustrating and you feel like you’ve forgotten the steps or that some how they’ve changed on you. Like always you’ve shone light and positivity into T1D and any newly diagnosed person will be encouraged by your words. I know I was:)

Thank you Andrea for your authenticty. I find your videos not only informative but also reassuring. I was recently diagnosed this Easter weekend after ending up in the hospital in DKA and ended up in a diabetic coma for two and a half days. It came on suddenly and was quite scary. I find your videos helpful and in particular the one on type 1 on a sick day since i am now getting over a flu/cold. You are inspiring, motivational and I thank you.

Your videos are so inspirational! While I'm type 2 I still find your advice extremely useful!

I hope everything goes well for you, you've been really brave and you deserve health and hapiness.

Great video! So true, it took me over a year to get things back to some degree of normalcy. Such an important message!

Thank you for this Andrea! Even 3 years in, your words are a comfort. 💙

Beautifully said Andrea!

You have no idea how much I needed this today. This video is an absolute gift from the universe. I have been so frustrated, so desperate to get my numbers right, I just want to show everyone that I can do it. I was giving up on myself. I was being so hard on myself. Thank you so much for this video.

Thank you, you’re an inspiration 😊

I would love to hear you sing, because you have a great voice and you speak very well and speak clearly and pronounce out your words understandably which is awesome.

I have just hit my 2 years since diagnosis - this video would have been perfect for me at that time. It’s great to see a video that talks about the human/realistic side of the condition and dealing with it, as I think it’s just as much a challenge mentally as it if physically - I don’t struggle with the physical side, it more the mental part for me. It great to have the reassurance that what you are thinking is ‘normal’ and rationale. This is a great video for the newly diagnosed! x

So much power to you dear❣️newly diagnosed with TD1..still figuring out

Thank you, thank you, thank you. I was dx type 1 almost a month ago and of all the advice I've been told and read, you video has been the most helpful when I needed it it most. Thank you.

Excellent video that will help so many. Wish I would've had this when I was first diagnosed!

I think reaching out to resources on social media and youtube is such excellent advice! Seeing how other people are able to cope with their conditions and hearing their stories is always so positive and inspiring! ❤️❤️❤️

Im very glad that I found this channel because Andrea is very inspiring person and make people feel less alone and thank you 😊

Hi andrea I was recently diagnosed this year and your videos have been so helpful..its a rough road but you have really helped me thank you so much and ps you look abs great ..I hope to do as well as you much love

Hi Andrea! I've been following you since my son, who is now 11yo, was diagnosed 2 years ago on Halloween (of all the days right!?). This video hit home, he's been having such a rough time coping and dealing with it all. I hope your words reach him, and help him in ways mine can't. Stay healthy and I truly wish you the best on luck with everything you do!

Your channel has been such a huge help to me. I was diagnosed about 6 weeks ago, at age 38. It was a huge surprise, as we don't have any diabetes in the family. Your videos were the first T1D resource I found and they helped me wrap my head around what it would mean to me. I was in mourning; I cried with you, and I cried for myself. Eventually I was ready to come out of mourning and figure out how to live with diabetes, and your empathetic and optimistic attitude helped me accept that fact that I would continue to have a good life, if a more complicated one. So thank you again, and from one T1D to another, I wish you great blood sugars, straight CGM lines, and a happy mind ;)

Thank you so much for this video. I was diagnosed with LADA 8 months ago. Wow. 8 months! Seems like it has been a constant overwhelming learning process. Found your videos as I was trying to research options for a pump because I am injecting 4-5 times a day and still don’t seem to be getting it right. I just want to say thank you for reassuring us that we can’t be diabetic perfectionists and that is ok. My mom can’t seem to understand that some days there is just no rhyme or reason to the highs. And I just can’t seem to explain it to her. I can eat “perfectly” and do everything my doctor says to a tee and research and analyze and try to limit stress (however you can control that) and sometimes you just have an off day. Accepting that it just happens that way has actually been the hardest adjustment. You just have to say I’m going to do everything I can to maintain a good blood sugar, and if the day is just all over place, well, tomorrow is another day.

Thank you so much for this! My 10 year old daughter was just diagnosed September 2. It’s definitely a very overwhelming disease. All your videos are very helpful to us. Thank you ❤️

Last week was my tenth Diaversary, and this video was still so reassuring. For any diabetics who are in a rough patch, just know that you can do this. Diabetes is a difficult, but beautiful journey!

I woke up almost low low not newly diagnosed but when I was I found your channel and it was very very helpful keep it up!

Hi Andrea ,Thankyou again for great advice not just for the newly diagnosed, but even when you have had type 1 for years. Except for your channel, there is no one I am in contact with that has type 1. I was blessed at work, a very rare thing I use to have lunch with two colleagues who both were type 1, that was special. I like the dance analogy , every day a different dance. God Bless, Rex ❤

Andrea, you aren't an inspire only to people who have the challenge of managing a chronic disease, you are an inspiration to everyone ❤ There is immense energy in your positivity and motivation to live life to the fullest you can ❤

Even though my circumstances and diagnosis are different from someone who has T1, I greatly appreciate you making this video, Andrea. I feel like my T2 diabetes is something I hardly think about now compared to when I first started down this journey, but I still have days where I'll forget to check my blood sugar or struggle to remain consistent with my eating habits. Everything really is done best in moderation, and it's definitely okay to not be perfect like you said. Thank you again for the encouragement! ❤

So generous for you to share you are such a sweet Soul.💗 My story is quite the opposite as I was diagnosed very late in life at the age of 60. Unfortunately due to my age I was wrongly diagnosed as a Type 2. Prior to that at my yearly physical my PCM told me, “Your blood sugar is higher than I’d like it to be,” not telling me at the time that I was pre diabetic. She put me on a low carb diet of which I was very strict about and we would check my A1C in three months. After the 3 months were up I was very upset to find out that my A1C got worse and that I was officially a Type 2 Diabetic! I started taking my blood sugar and recording everything I was eating to no avail as I continued to have high numbers. She finally said I had to start taking Metformin. During this time I was the sickest I have ever been. I was so nauseous I could barely get of the couch or eat anything. She continued to raise the dose of the Metformin because it wasn’t working. Over the course of nine months I lost 45 pounds and was basically a shell of my former self. At last she said I needed insulin that she could prescribe it or I could go to an Endocrinologist. Omg yes go to an Endocrinologist please!!! I had to take a class on carb counting before I could have an appointment with the doctor and I was booked out over a month. At the end of this day long class before I left I spoke to the nurse who ran the class and I told her “My appointment isn’t for another month and I’m going to die before then” I was so very sick and frail. She she they talked about me during the break and that they new exactly what was wrong with me and that they would get me in asap! Turns out I was not a Type 2 I was a Type 1 and was immediately was put on insulin and by that time my A1C had risen to 10.7. I felt like you overwhelmed, but I also felt violated to know I would have to wear something stuck to me for the rest of my life. But over time the CGM and my pump has been a game changer and a life saver and I’m so very grateful for such advanced technology. Being diagnosed during this time of great advancement makes me very grateful indeed. I wanted to share my story so that it may help someone else who is struggling. Late onset Type 1 is a very real thing and I’m also so grateful for the Endocrinologist who saved my life and for KZfaq and folks like you who have carried me through some very difficult times. 💗

I was diagnosed in February I wish I had this! Thank you so much, I love you!

Hi! You have been a breath of fresh air to me. I am 56 and was diagnosed a year ago, very late in life for this diagnosis. I have throughout the year gone through a study programme for over 50s so the Diabetes Team can gain an understanding as to why someone of my age group can get type 1. You are my comfort blanket, when I feel overwhelmed I listen to you, thank you so much, take care xx

I love your channel. You are so soothing and calm. In my mind we're friends 😂 I wish, not only because you're so cool and kind, but because I need a mentor. I cut out every part of my life after I was diagnosed. 🙁

Hi Andrea!🙂 It was very impressive that you shared your diabetes story with us (your first diagnosis) . It is also helpful to create a positive perspective for newly diagnosed ones. Thank you Andrea for your heartfelt shares.... And waiting a new live stream. Maybe a new Q&A? I wish you happy and health week.

Lovely, supportive video. :) We’re just over a year past my son’s diagnosis. I would add that as you’re reaching out and making connections, one thing you’ll notice immediately is the strong and conflicting opinions on diet. There isn’t a right or wrong diet for Tyoe 1s, just as there isn’t for the general population. Tune that out for now, focus on a generally healthy balance, and you’ll soon learn what works best for your body.

Thank you for all the tips and helpful information that you put on KZfaq page it’s been a process to help my mother with her Diabets I help her declutter a lot of her meds and brought her a myabeties purse she loves it ❤️ and got her a backpack with all the essentials she needs and I love how organized you are I look up to you thank you soo much for everything Sincerely melissa

I just watched ya newly diagnosed video, am still getting the grips of mine, was diagnosed a week before the first coved lockdown(uk) , sure is a rollercoaster ride of blood sugar levels, I did stop eating wat I like at first, now I eat wat I like , I take more nova rapid wen I need to, of course am stilll learning about my condition, suppose I always will just like you and everybody, your videos really do help me

I was diagnosed with T2 last year but none of the medications were working. I switched doctors a couple weeks ago and yesterday I was told I was misdiagnosed and it’s actually T1.

So off topic but just wanted to say. You are such a great example. You look sooooo healthy and adorable. Inspiring. I am the mother of the type 1 so thank you for the encouragement for the life my son can still have.

Hi Andrea, great videos for encouraging newcomers. I`m reaching 50 y of diabetes t1 after a long time with poor tech availability. What I have realized over those years is that Information and togetherness are what bring comfort to them. We can say we have a tech cure with these pumps and the CGM loop connection. Take care.

I think this video will be incredibly helpful for the newly diagnosed folks & their families too. I have been living with Type 1 for forty-six years now, & Andera, I wish I had known someone then with your reality contact. It was a very different world then, on so many levels, I was doing urine testing - which showed where I might have been two hours earlier. Besides the medical people, we also need cheerleaders like you. Thanks, Andrea!

Being connected to other diabetic's is a big help. Been T1D since 1970 and had pretty much been doing it alone. Endo suggested going to the Tandem pump a year and a half ago. That's when I came across Andrea and other channels researching pumps and CGMs. And then realized I wasn't as bad a diabetic as I thought I was. Everyone had good and disappointing parts of even a day. So many variables effect diabetes that what works for a few days in a row doesn't work as well for the next day. Look on the plus side that when you do have those decent days caring for yourself you are way better off than not taking care of yourself at all for those days. Take the bad, learn from it if you can, and start doing it over again. Just two days ago I started fighting lows in the evening. Had some carbs. CGM still going down. Check with a finger stick, CGM is accurate. Some more carbs. Sort of leveled off. Went to bed. Low glucose alerts. More carbs. My wife wasn't home and is connected to my CGM so I know she was getting alerts as well. 2:00 am still low alerts. Tired and frustrated I "ate the kitchen". 4:00 am high alert with double arrows up! Went from mid 40's to 321 within nine hours. Finally got back to normal ranges by early afternoon. Been fine since. I did change my infusion set that I had changed the previous morning. Whether that was the problem or not I'll never know. Lucky me with an endo appointment tomorrow. But knowing others have things like this happen was a lot of consolation. Off my soapbox.

WELL PUT

God is speaking through you. Thank you for being a great advocate. Drs are truly unrealistic the numbers fluctuate and I just started learning that it's perfectly normal. I am 18 years into this thing ,the journey gets tough I appreciate your input and insights.❤

I was diagnosed with LADA on April 21, 2020 and was started on MDI. Being diagnosed during a world wide pandemic was a very tough pill to swallow and I felt that there was a huge lack of support. In May of this year I switched from MDI to the Tandem T:Slim X2 and for some reason it felt like being diagnosed all over again. Being part of the DOC and doing some events with Connected in Motion had been extremely helpful this time around.

The Waiting is Over!!!!!!Thank You ❤️ For Uploading This Video Andrea...💘 I was Diagnosed 8 Months Ago!!!! Found this Video Really Helpful 😃❤️!!! Lots Of Love 🤩❤️

This is just the perfect video for new diabetics in terms of reassurance that you will get a handle on this and life goes on. Like many people i love food and _worship_ carbs so one of the hardest things for me was thinking about all the foods i wasn't going to be able to eat anymore. They will absolutely send my BG on a roller coaster. But then you just have to think " Am i _never_ going to eat Chinese food and honest to god, white flour crust pizza again to avoid a bad blood sugar day?" I said hell no so let's rip this band aid off lol. So i get them once in a while. Not as much as my carb-craving ass wants, but i didn't have to give it up entirely. Like Erika said: "Perfection and Diabetes don't go together".

My beautiful 6 year old daughter got diagnosed almost 3 weeks ago. It’s been so difficult for us. I am hoping and praying it gets better

Diagnosed last summer as LADA - type 1.5 - at age 59. Life has changed...and not for the better.

Anyone who was newly diagnosed here I hear you andrea I have had myself in a vacuum as I am scared to live my normal life but I'm gonna do my best ...its I think more a mental disease and I agree with you it can take over your life if you let it good luck to anyone newly diagnosed xx

I was diagnosed with diabetes on the 4th of January of this year and I fell in to DKA

You are so beautiful ! I'm recently diagnosed with T1D almost 3.5 months.. and in December i have covid.. my dr endocrinologist told me that because of covid i i have now T1D.. and she told me that it's having this problem with alot of children who's was infected with covid .. after that they made T1D.. and some other dr that i have speak told me that covid it's the guilty that now on 39 years old i have developed T1D.. 😪

I had a hard time at first with my diagnosis since it blended in with Covid lock downs. I was freaked out about getting Covid and having problems with going low on my meds. Lockdown helped me really look at what I had to do for my Type 2 and try to get out of the mind set of being scared about getting covid.

I remember that phone call, on my birthday of all days, they said I'm diabetic and needed insulin shots. I was extremely upset. I was turning 19 and it felt like the sky was falling. Fast forward 6 years and life is pretty good. Having a good medical team and support made all the difference. Tho, I still hate feeling kind of like a pincushion with all the shots and finger sticks. 😅 Those things were overwhelming in the beginning then its just my normal now. It's almost like autopilot now.

Diagnosed with hypoglycemia 30 years ago, diabetes (assumed T2) about 12 yrs ago, currently awaiting lab results to confirm whether Type 1 or Type 2, because new Dr doesn't feel I fit the "stereotype" for Type 2 (he's not the first one to mention this, but is the first to recommend the blood test to confirm)

Hi Andrea ,you are amazing .

Hey there. I was diagnosed 5 months ago. It is really tough for me ,I hope this could be a platform where I have that support. In my country we don't have the best of health care. Yes, thankfully I get my insulin. But there was no one to explain to me the procedure, what to do or how to be better. All I can say is the internet was really helpful. My story is too long to tell of how I found out, but if it wasn't for myself that asked if they can take my blood sugar levels, they would have never known. NEVER. That is scary. I had the signs such as constantly thirsty ,frequently urinating, I lost an incredible amount of weight. I started to weigh 35kg, I got infections almost every month,and my skin is so dry, it is still dry. I just can't get it to become moist. And I am only 19. I was in matric(senior year) writing my final papers. Yet, I was sooooo tired. It was beyond me. They said I was lazy and never want to do chores, but honestly they also did not know. I was crying for weeks when I had to inject myself, because I thought why me? Just whoever you are, just educate yourself, you won't be perfect from the start, I am myself still struggling. Thanks you for reading.

I was diagnosed with T1 about 4 years ago (aged 27). I have been managing it pretty well just by using insulin pens - quick acting for when I eat and for doses to bring my sugars down when required, and long acting for sleep. My control isn't bad with my hba1c averaging at around 7-7.5%. I use the Libre freestyle 2 sensor which has been great for me. My doctor has talked to me about the possibility of moving onto a pump. I have heard good things about it lowering my hba1c but I don't really like the idea of having something always connected to my body, and having to carry the pump with/on my person at all times. Do you have any advice/recommendation? Btw I really love this channel. Keep up the good work. It's a great resource for T1 diabetics (the invisible and little understood disease!)

Hi Andrea. I’m a little off topic but do you ever have a problem with the clip on your pump digging into your stomach? Do you know if there’s a softer clip available? 💙

I like you happy talk greetings from Belgium

I was diagnozed a week ago. came a bit as a shock but to be honest, its not bad at all. sure you have to pen yourself several times a day but that will become your daily bread and will be no problem. doesn't matter where you are. Plus it is a very good reason for you (us) to live a healthier life. this doesn't hurt anyone :) keep injecting until research comes up with a cure. And they will. :) Much love to y'all

Great to see you smile The hair looks great I got in a accident the bus i was on got into a crash LOL CITY BUS I am banged up whiplashed achy

my 3 year old daughter was diagnosed 3 weeks ago... I wish It would have been me... It is so hard for me to digest that my little girl need to go through all this. I'm so afraid for her, for complications if I will not manage well her glucose. How to live my life now? I'm all afraid and stressed

During your first 8 years of being a T1D how did you know how much insulin to take when you Weren’t carbs counting? This question is driving me nuts; I’ve been watching T1D videos for over the last 3.5 years and all I know is the carb counting

I see that this your last video on youtube which was filmed 2 years ago. I hope you are doing well.

Insulin prices for pumps , almost can’t afford anymore

Hi, Andrea, how are you doing? I like the more elegant style you have now.

❤️

I was lucky because at a very young age my mom had t1d and I learned a lot about it. So when I was diagnosed I just jumped right in telling my doctor to put me on insulin because he put me on Glyburide and metformin I was a t1d so that wouldn't work lol.

Andrea, I'm am asking Ms Anne this same question. Wondering what you think. I am a nurse in mid-TN, not a diabetic but have taken care of a ton of people with both T-1 and T-2; apparently I haven't been as supported as I should have been, not sure. What would you tell a new nurse about what really is needed from us to better care for diabetes; beside wash your hands and use a small needle? Old dog needs to learn new tricks, thanks

Got these through Google, doctors are hiding Will be helpful in future. For trigger finger n other diabetic related problems , Advanced glycation end products (AGEs) are proteins or lipids that become glycated as a result of exposure to sugars AGEs are the main culprits for Diabetic Complications also. Better to control blood sugar tightly. Thanks. 😁😁

Dr. James Shapiro from University of Edmonton, Alberta Canada has apparently cured type 1 diabetes in mice. He is currently trying to raise funds to get to a stage where he could go to human trials with government approval & peer reviews. There are video & internet posts as well as news coverage posted online. Maybe , just maybe we might see progress in our lifetime.

The reason you got to finish your singing competitions is because you had family with the condition who had some idea what you could get away with. People who don't have that will be rushed into hospital and subjected to several days of being yelled at about how important it is to follow the medical advice. I have seen someone be diagnosed and go through that (I was there) and she stopped doing basically everything except treat the condition. I couldn't blame her. Given that advice, I'd have done the same. The result was that her dreams really were dead. Most people will not have the experience you had, because, as you rightly say, most people do not have the support group you had and the medical people are beyond useless.

Hi. My daughter was diagnosed in 2020 at age 13. Wish I could have seen this then. It was definetly a shot to the gut, and as a parent, I just wanted to make it better, but I couldn't. We have learned so much since and are doing well now. We had CGM pretty much from the get-go, which was a huge help, and after about a year we tried a tubed pump, and that was a fail for us. We kept having infusion site problems and she ended up not liking the tube. We now are on Omnipod and she likes that so much more. Site incertions are almost always flawless, and no tube. Almost immediately after diagnosis though we struggled with weight gain. We have since learned that insulin is the body's gatekeeper hormone to energy storage, and we all know how the body stores energy. We did everything to try and help, (extreme low carb to minimize insulin needs, watching calories - only after we learned that she was trying to do so all on her own in private to try to address the issue - and we are always promoting all of us to getting out and being active). It was tough for awhile though. She almost instantly saw a different person in the mirror, and that was hard for her to accept on top of also having to accept her diagnosis. I was really concerned that she might have been heading down a dark path.... We are fortunately doing much better with that now too. She is indeed very healthy, but the struggle with insulin and its affect on the body to make for quick weight gain is still 'there'. We remain fairly low carb, (we buy special bread, we've pretty much cut rice and potato out of all our diets, I make special low carb tortillas and pizza dough for her, & we track everything on an app), but again, we still struggle with this issue. I am explain all this to get to a question. Hopefully one not too personal. Because here you are talking about not taking things away. I assume therefore that you enjoy what you want to enjoy for food. (Within reason, same as anyone else wanting to be healthy). And you clearly are not experiencing - (how shall I put this...?), insulin causing your body to easily and quickly store energy... Which is great. You look great - and very healthy! My question therefore is: how have you avoided this issue? Do you have a special food plan? Or do you truly just eat normal healthy food and avoid nothing? (Within reason.) Or do you just run a marathon a day... ? I don't mean to get too personal, but I'm just wondering what you do, and how different it may be from what we are doing. Because sometimes I can't help but wonder if some of the things we are doing to minimize insulin use may actually be part of the problem. And I know everyone's diabetes is different, and I also know that genetics plays a part too as well as family habits. For what it's worth though, both her mother and I are lean, we are health conscious, active, and we eat healthy home prepared foods 95% of the time. And prior to T1D, our daughter too was all that. But like a light switch, her body went into energy storage immediately after diagnosis and starting insulin therapy. Hormones and puberty probably were, and are, playing a role too. But again, we have struggled, and your words encouraged me to take a shot and reach out to see what advice you might have on this, because clearly you have not experienced this issue, (or at least are not now experiencing this issue.) I hope is is not too forward of me to ask you for input & advice on this based largely on your physical appearance in your videos.... . Thanks - Cheers!