Day 3- Take 27,478,347,356
That's how I feel. I keep having to start over. Always falling off the workout wagon. But hey!! Today's my 3rd day in a row of working out!!!!! (.....Again.)
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Day 3- Take 27,478,347,356
That's how I feel. I keep having to start over. Always falling off the workout wagon. But hey!! Today's my 3rd day in a row of working out!!!!! (.....Again.)
Goodbye to a great year
I’ve always loved the Albert Einstein quote- ‘Insanity is doing the same thing over and over again and expecting different results.’ This year I really put that quote to the test, personally and professionally. 2014 has been an amazing year of great changes for me. I took a couple leaps of faith that paid off more than I’d even hoped for.
I made a huge career move which required me to educate myself on a completely new world in which I am completely in love with, AND I did the most amazing thing for myself by having the gastric surgery. Because of both of these changes, I am a much happier, healthier, energized person and am in a much better place mentally and physically. Granted, I have a ways left to go, but in 2014 I took the big steps. I’m so excited to see how much farther I’m going to go in 2015.
2014 wasn’t without setbacks though. The biggest being Caleb getting sick and diagnosed with Type 1 diabetes. It’s been almost 3 months, and that first month was awful! Yes, I was obsessed. It’s all I thought about. Night and day. There was so much to learn, so many hard statistics to swallow, and a lifestyle change for all of us that hit us like a ton of bricks. Through this diagnosis, I found support in places I had no idea that existed. I’ve met amazing people I would have never met otherwise. And I learned to be grateful for the fact that his diagnosis is something we can manage. It is something he can live with. God Willing of course. So, even though it was rough, we’ve got the routine down, the shock has worn off, and I can reflect and be thankful again. I’m hopeful that in early 2015 he’ll get an insulin pump and our lives will become even easier. Thank God for today’s technology.
I am eternally grateful for so many things. All in all, 2014 was a great year, and God willing, 2015 will be just as great. I am so blessed to have an amazing, hardworking husband; responsible and warmhearted children; Healthy and vibrant parents; best friends for siblings; a huge loving family(both sides); and some of the most supportive loving friends that I don’t feel like I lose a day with no matter how much time or how many miles are between us. God Bless! And here’s to another great year!!
7 months post op- I've been beating myself up lately for my slowed progress so I decided to do a side by side of before and current. 60 pounds down-about 50 to go. I can do it!!!
Rut
I've been in a rut! I thought for sure I'd do well in November, but nope. I've not lost a pound!! It's so frustrating! I'm not eating a lot...agh!!! I hate plateaus!
Because it’s not caused by too much sugar.
Wearing blue for #worlddiabetesday in honor of my t1d photobombing warrior in the backseat!! 💙
November
I'm going to drop a ton of weight this month. That's all.
#iammorethandiabetes #projectbluenovember
#kissdgoodbye #kiss2cure #projectbluenovember #diabetesawarenessmonth diagnosed October 6, 2014
Love this!
My new life
Today is my 6 month Sleeviversary. Honestly, I feel like I should be a lot further along and I spend a lot of time beating myself up over my lack of good progress. I feel like I'm plateauing every time I turn around. But even if the progress is slow, it's still progress. I feel 100x better than I did before, I have tons more energy and I'm keeping up with my kids a lot better now too. I'm not taking naps-before I HAD to have them. I was so lethargic and blah. I'm not on bp meds anymore. And I can squeeze into a size 14, but 16 is really where I'm at. I was pushing a size 24 just 6 months ago. So, that's my progress, so I guess I'll take it.... My goal for the next 6 months is to get more serious about working out. No more excuses!
Love this! Funny AND True!!
My youngest son became really ill and was admitted into the hospital this past week with a diagnosis of Type 1 Diabetes. He’s only 12 years old. In a matter of hours we went from easy breezy to a now rigorous schedule of glucose testing and insulin shots every 3 hours around the clock with…
Hi there! I was diagnosed at 11 (10, technically; 3 days before my birthday). Been over a decade now. I see that you’re scared and hurting and overworked right now, so I wanted to share some stuff with you.
First of all, it is really weird that they’re asking you to give him insulin every 3 hours. Did they not prescribe long acting insulin? When I was first diagnosed, I was given a long acting insulin immediately. Asking the family/patient to deal with that is kind of extreme, and I’m very much so questioning the doctor. Was s/he a family doctor? If so, I highly recommend you get your son in to see an endocrinologist ASAP. At any rate, yes, managing the insulin dosages will become much easier, and not just because you’ll “get used to it.” The schedule itself will become significantly more reasonable once long acting insulin is introduced to the routine.
You are Super Mom. Your son might not understand everything that you’re doing for him right now, but when he’s older he’ll come to appreciate what you’re going through, which is a lot. Maybe more than even he is right now, depending on his understanding of what “chronic” means. I certainly didn’t at that age. On his behalf, thank you so much. You’re amazing.
There is definitely hope for a cure. Apparently research at Harvard has had a major breakthrough recently; however, do not expect a cure within the next few years. I wouldn’t even tell your son about the Harvard thing, if I were you. It is heartbreaking to be told over and over that there will be a cure soon, and then have nothing happen. When they cross the finish line and a cure is found/becomes available, then shout it from the rooftops!
Finally, some advice. Do not manage your son’s diabetes for him, as much as you might want to. He NEEDS those skills later in life. Measuring meals for him is one thing, but make sure he knows how to carb count and calculate insulin doses and all that fun stuff. I’ve had doctors tell me horror stories about college kids who didn’t know how to give themselves a shot.
Don’t let his fears (or your’s) hold him back. All through school, I shied away from sports because I was too afraid of going low. It took me until after I graduated high school to try martial arts, which is honestly now one of my passions. He will learn how to best prevent lows and handle them when they do happen.
Managing diabetes is like a very, very long marathon, and after a while he will get tired and stumble. Please do your best not to be judgmental when his sugars are out of whack. It’s just information to help him choose what to do next, not a grade. As one of my old doctors used to say, “it’s just a number.” That kind of pass/fail thinking messes up a lot of diabetics, discouraging testing sugars regularly, or sometimes leading to overly controlling/obsessive behavior. Imagine having someone look over your shoulder when you stand on a scale and then grade you on whether your weight is “good” or not. That’s a lot like how it feels.
Lastly, feel free to turn to the diabetic community. :) People don’t always realize this, but support-givers need support too! If you have any questions, I’m always happy to help out.
I love all the advice. It’s great hearing from people who’ve lived and survive this every day. He actually is being seen by the Diabetic Center at Children’s Hospital. He is on the long lasting insulin as well as the bolus. I’m under the understanding the every 3 hr checks through the night is only temporary while they get his dosages figured out. Maybe a month or so. He is already testing his sugar and has even given himself a couple shots. I am doing the calculations for now, but he’s definitely conscious of the carb factor and asking all the right questions. I’m truly amazed at how well he’s adjusting with it just being one week out. I’ll tell you though- I am terrified of the complications. It will be hard not to scrutinize when he’s doing his own care but I think you are right. It’s something I’m going to try to stay aware of when and if that time comes. Thank you for kind words and advice.
My youngest son became really ill and was admitted into the hospital this past week with a diagnosis of Type 1 Diabetes. He’s only 12 years old. In a matter of hours we went from easy breezy to a now rigorous schedule of glucose testing and insulin shots every 3...
I completely see what your saying and yes since he's a new onset they have me testing every 3-4 hrs with 3 being the primary target now. When he was admitted and diagnosed this past week he had high ketones plus we still haven't gotten his numbers completely under control enough yet. So, at this point we're testing for ketones every time he's over 240 which is most of the time. They just made a significant number change and they have improved tremendously, so hopefully those days will be behind us soon. Then I think we'll be able to slack off a little at night and on ketones testing. I'm new to this life and simply following the instructions from Children's hospital. They also suggested I not burn him out by making him responsible for his own care at this point, and suggested I wait awhile before making him take it all on. He is learning to do it all. None of this is 'hard' per se, it's just learning a new way to live. You sound like a an old pro, and I'm very optimistic that all that you say will happen for us too in no time which is very reassuring.