TakeItAway88
Well-Known Member
- Messages
- 74
- Type of diabetes
- Type 1
- Treatment type
- Insulin
Hello,
I'm a newly diagnosed diagnosed type 1 diabetic as of the 23rd of July 2015. My mother told me to get a blood test as she noticed I had increased hunger, thirst, frequent visits to the toilet and oral thrush. After the uncomfortable experience of having a needle pushed into my vein to extract blood, I suddenly get told the next day I had type 1 diabetes and had to visit the hospital immediately as my blood sugar was quite high (27.3 mm/gl)
At first I was in absolute shock. I cried and cried countlessly for days on end in the hospital wishing that this was some sort of bad dream I wished I could have woke up out of. Unfortunately, I realised I couldn't and was told I'd just have to live with it. The nurses and my family told me that there was a lot worse I could have been diagnosed with: however in my mind at that moment the only thing worse than what I had could have been death.
It's now been a few weeks and it feels like I'm managing a lot better, even though it's a major pain in the *** . Carb counting, injections and constant glucose monitoring are just a few examples of why this disease is so ****. Not to mention stone-cold food as it takes so darn long to do all the carb counting and injections yadayadayada
And to make matters worse, being diagnosed with this right in the middle of the summer after my GCSE's when I should be relaxing.
Eurgh, this just really sucks. I miss my pre-diabetic life where I didn't have to do all this annoying stuff.
Hi, I'm 19 and got recently diagnosed last year. It was a shock to me and my mum. I think she cried more than I did! I still struggle to this day with the constant things that you need to do. Although I don't carb count at the moment (it is something I'm wanting to learn) I'm always wary of the things I should eat and if I'm having enough insulin (on set doses). I'm going through a hard time at the minute after being in hospital a couple of months ago following a DKA. I may not be able to give the best advise to you at the moment as I am still stressing about it as well but if you ever want to drop me a message I'm always here for a chat
X
Hi, I'm 19 and got recently diagnosed last year. It was a shock to me and my mum. I think she cried more than I did! I still struggle to this day with the constant things that you need to do. Although I don't carb count at the moment (it is something I'm wanting to learn) I'm always wary of the things I should eat and if I'm having enough insulin (on set doses). I'm going through a hard time at the minute after being in hospital a couple of months ago following a DKA. I may not be able to give the best advise to you at the moment as I am still stressing about it as well but if you ever want to drop me a message I'm always here for a chat
X
Hey! I hate this disease too, we all do. But I hated wearing glasses when i first got them and now i wear them everyday without thought, so there is hope that, although you will not stop hating it, you will stop thinking about hating it and that means its essentially gone!
Its been just over 1 year since i was diagnosed, and it took me about 3 months to physically nail down treatment routines, and ease back into exercise etc, beyond the first 2 weeks though it never really effected my daily life, or social life. Its more of mental battle as you will find, so really take some time to level up your mental grip on diabetes. Don't let yourself get sad! Sadness breeds sadness, and that usually means poor management. So chin up robot, do what needs to be done and get on with your life.
The first tip i can give you to make things easier is simple - EAT LOW CARB.
The less carbs you eat means the less insulin you need means the less chance you have of screwing up the dose and going low or high.
The second tip is - LEARN. Learn everything you can possible learn about diabetes, management, what your readings mean, what your trending means, what foods do what and why. Once you start absorbing information it gets so so so much easier!
You got this.
Instead of hating it, just don't think about it. Nothing has changed from last month, or last year you are still you, sometimes you just stick yourself with a needle. Just know why, and when, and thats that!
Thanks. I'll take what you said in mind. I'm new to this forum so I don't know whether I should reply to every comment or what. Lol
What you said was really uplifting and I appreciate it.
Hello,
I'm a newly diagnosed diagnosed type 1 diabetic as of the 23rd of July 2015. My mother told me to get a blood test as she noticed I had increased hunger, thirst, frequent visits to the toilet and oral thrush. After the uncomfortable experience of having a needle pushed into my vein to extract blood, I suddenly get told the next day I had type 1 diabetes and had to visit the hospital immediately as my blood sugar was quite high (27.3 mm/gl)
At first I was in absolute shock. I cried and cried countlessly for days on end in the hospital wishing that this was some sort of bad dream I wished I could have woke up out of. Unfortunately, I realised I couldn't and was told I'd just have to live with it. The nurses and my family told me that there was a lot worse I could have been diagnosed with: however in my mind at that moment the only thing worse than what I had could have been death.
It's now been a few weeks and it feels like I'm managing a lot better, even though it's a major pain in the *** . Carb counting, injections and constant glucose monitoring are just a few examples of why this disease is so ****. Not to mention stone-cold food as it takes so darn long to do all the carb counting and injections yadayadayada
And to make matters worse, being diagnosed with this right in the middle of the summer after my GCSE's when I should be relaxing.
Eurgh, this just really sucks. I miss my pre-diabetic life where I didn't have to do all this annoying stuff.
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