krisjwoody
Member
- Messages
- 11
- Location
- Newcastle upon Tyne, UK
Hi,
I was diagnosed with type 1 on 23rd March 2012 (8 days ago), which was my Dad's birthday so had some great news to ruin his 59th! I am 25 and was very shocked when i thought i was going into the walk in centre to be told i had picked up some infection/virus/food poising from being in Thailand days before, but actually to have a glucose reading on 31.1.
Diabetes was the first word which was mumbled between the nurses but i wasn't too concerned as i didn't know anything about it and i was pretty much out of it with exhaustion and dehydration. Immediately i was put on an insulin drip and took in an ambulance to the diabetic ward at Newcastle's RVI hospital. The doctors were amazed how i was still walking around as they suspect i was high 20's throughout my time in Thailand and the days following. Maybe something to do with the 10l of water i was drinking everyday. My body must of been parched because i sucked up 3 bags of insulin and 5 bags of saline solution in the space of a few hours!
Spending the following 2 days after being diagnosed in hospital, i slowly began to come to terms with my condition. The more i spoke to friends, family and fellow diabetics the better i felt. Talking with the professionals let me understand my condition and allowed me to start figuring out how it would affect me day to day. At first everything seemed like it would change.
After several more meeting with various NHS professional i now fully understand what needs to be done, my diet doesn't have to change (maybe a bit healthier) and my lifestyle doesn't need to be affected. The only differences are i need to structure my eating more and understand what i am eating. I will also need to carry my insulin around with me all the time and be able to plan ahead a bit more.
I think the biggest thing i will miss is the spontaneous decisions i use to live my life by. Things will need more planning and thought. Being young i also can't help but think, big drinking sessions are a thing of the past now!!
Currently, i have been absolutely fine with dealing with my condition. It hasn't overwhelmed me or get me upset yet. However i am concerned that once real life gets going again (since i have been living with my parents for a week while i sort everything out) and move back to my house and start work i feel it might hit me more then. Mainly when i start to see the little things that diabetes might restrict me from doing. Has anyone else been the same?
All i can think for now is there are a lot of positives to take from this, one being that its the only chronic disease that is fully manageable. And if i do manage it then the chance of complications are reduced. Allowing me to life the same life as i intended.
Back to the NHS, can i say how excellent my care was throughout the whole process. I feel extremely lucky to have a public health service where care comes before insurance or cost.
Not to bore you too much with my story but i just wanted to put it out there for anyone who is in a similar situation or has been. It would be great to meet some people on here and hear their experiences and how they coped. Any advise or wisdom that anyone has would be much appreciated.
PM me if you want to chat.
Hope it helps. Kris
I was diagnosed with type 1 on 23rd March 2012 (8 days ago), which was my Dad's birthday so had some great news to ruin his 59th! I am 25 and was very shocked when i thought i was going into the walk in centre to be told i had picked up some infection/virus/food poising from being in Thailand days before, but actually to have a glucose reading on 31.1.
Diabetes was the first word which was mumbled between the nurses but i wasn't too concerned as i didn't know anything about it and i was pretty much out of it with exhaustion and dehydration. Immediately i was put on an insulin drip and took in an ambulance to the diabetic ward at Newcastle's RVI hospital. The doctors were amazed how i was still walking around as they suspect i was high 20's throughout my time in Thailand and the days following. Maybe something to do with the 10l of water i was drinking everyday. My body must of been parched because i sucked up 3 bags of insulin and 5 bags of saline solution in the space of a few hours!
Spending the following 2 days after being diagnosed in hospital, i slowly began to come to terms with my condition. The more i spoke to friends, family and fellow diabetics the better i felt. Talking with the professionals let me understand my condition and allowed me to start figuring out how it would affect me day to day. At first everything seemed like it would change.
After several more meeting with various NHS professional i now fully understand what needs to be done, my diet doesn't have to change (maybe a bit healthier) and my lifestyle doesn't need to be affected. The only differences are i need to structure my eating more and understand what i am eating. I will also need to carry my insulin around with me all the time and be able to plan ahead a bit more.
I think the biggest thing i will miss is the spontaneous decisions i use to live my life by. Things will need more planning and thought. Being young i also can't help but think, big drinking sessions are a thing of the past now!!

Currently, i have been absolutely fine with dealing with my condition. It hasn't overwhelmed me or get me upset yet. However i am concerned that once real life gets going again (since i have been living with my parents for a week while i sort everything out) and move back to my house and start work i feel it might hit me more then. Mainly when i start to see the little things that diabetes might restrict me from doing. Has anyone else been the same?
All i can think for now is there are a lot of positives to take from this, one being that its the only chronic disease that is fully manageable. And if i do manage it then the chance of complications are reduced. Allowing me to life the same life as i intended.
Back to the NHS, can i say how excellent my care was throughout the whole process. I feel extremely lucky to have a public health service where care comes before insurance or cost.
Not to bore you too much with my story but i just wanted to put it out there for anyone who is in a similar situation or has been. It would be great to meet some people on here and hear their experiences and how they coped. Any advise or wisdom that anyone has would be much appreciated.
PM me if you want to chat.
Hope it helps. Kris
