Thursday, August 2, 2012

Living With Type One Diabetes

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I have been living with an illness which over the last merge of years has become more and more common. This is called type One Diabetes. When habitancy hear these words they recognize the name but do not fully know or understand whatever about the illness. habitancy have a lot of ideas with what they have heard about the illness and how it affects habitancy straight through gossip or what they may have heard waiting in the doctors surgery. This can be a bad thing as there is clear misunderstanding what the illness is about, but the good thing is that the condition is not being ignored due to how more commonplace it is.

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How is Living With Type One Diabetes

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I have been diagnosed as having type one Diabetes since I was 10 and it came about when I was starting my last year of Junior School. I was experiencing a lot of symptoms before that such as having no energy, passing water, sleeping alot, drinking enduringly to quench my thirst which led to more visits to the bathroom. These symptoms where not as serious as i felt pain in my stomach and soreness underneath my underarm area which was a worry to my parents as well as me. At a young age I was used to having a bit of a cold and an earache as you normally get, so to be having these strange symptoms going on in my body was scary to me.

My parents made an appointment at the doctors and leading up to the appointment I became seriously ill. My energy had gone and i ended up being bed-ridden which meant my mum had to carry me to the doctors surgery. I waited with my mum drinking a big bottle of water as my thirst was so bad. I was called to the doctors room and my mum carried me in. The doctor took a water sample which was no question with all the water I was drinking. The doctor said it seemed like an additional one case of exhaustion as I had previously seen the doctor complaining of Tiredness and Lethargy. This time the doctor referred me to the diagnosis group at my local hospital as soon as possible.

We traveled to the hospital by taxi and the diagnosis group was at the top of the stairs. My mum had to physically drag me up as there were no lifts available. I was dumped on a chair and waited to have my blood tested. The test was a blur as I don't remember the needle going in. Afterwards we were told to go back to my doctors immediately as the results would be sent by fax as soon as they were completed. We traveled back by taxi and waited in the doctors surgery for the results and my condition got worse. No more than ten minutes had passed and I collapsed in the waiting room.

After my collapse my first memory i had was that it was still daytime and there was sunlight arrival straight through the window. I was in pain and my feeling was my body was aching all over and my thirst had gone. As I focused my eyes I had the best sight in the world, my mum and dad sat over me next to my bed. I looked around the room as best as i could and there were machines to my left and right with wires anywhere especially one in the back of my hand. I felt like crying as i was scared and i didn't know what was going on. Seconds later a nurse came to check to see if I was all right. After all the fussing the nurse said a doctor would be seeing us soon. I tried to use whatever energy I had to ask what was happening as I was a still unsure what was going on. My parents explained to me that I was at the hospital and I was taken poorly at the doctors and the ambulance brought me here. My head was hazy and like a jigsaw in pieces. I just didn't have the energy to put them together. My parents interpreted what the nurses where saying and said that my body had too much sugar in it and i needed to have medicine to get rid of it. That didn't sound too bad as I've had medicine before so what's there to worry about. After all this information was downloaded into my young brain I fell back asleep as I was physically gone.

A few hours later recovering in my sleep the doctor arrived and my parents woke me. The doctor basically tried to tell us with his trusted assistant (nurse) what type of Diabetes I had, what Diabetes was, how to treat Diabetes and all the information in one big chunk. It was a bit too involved for me as a child but a bit easier for my parents. We were told that I was to stay in hospital until I learned what insulin is and what it does, how to equilibrium my food intake with the units of medicine I was taking, daily dietary plans, learn food nutritional values such as carbohydrate, fat and also what effects corporeal activity had on my blood sugar levels. Also as leading was studying what is needed to equilibrium it out to stop hypoglycemia (high), hyperglycemia (low) events happening.

The list of studying about my illness was endless and then there was the scary part...how to administer my own medicine. That's when I found out I had to have injections for the rest of my life not just 1 but 2 types this scared me so much i nothing else but didn't understand the scope of what was happening. To be honest if it was not for my parents encouraging me, supporting me and willing me to learn everything I had too then I don't know where I could have found the strength after everything that had happened. At the end of the day its all about your condition you look after it and it looks after you. My real test was to come. The nurse brought a syringe with a dinky vial of water and an Orange. An Orange I bet your thinking why? Apparently an Orange skin is the closest thing that resembles human skin when administering an injection. The nurse showed me how to draw up the medicine and inject the water into the Orange. studying everything about my illness was made into a fun activity daily as that made the transition a whole lot easier and the preparing i needed when I nothing else but had to give myself my medicine once the drip was removed. seeing back it was mainly construction reliance for myself and the feeling of being scared, at last I tried and tried until I finally did it, I pressed the plunger and pow job done!

I stayed in hospital for two weeks, the first week was the rescue from my collapse and sorting my bodies theory out. The second week was to learn about diabetes and managing it straight through diet and medicine intake. It seemed like I was there for a long time as I was enduringly busy studying more and more, conspiratorially I just wanted to get out of there and get back home and feel safe again.

Adjusting to home life and managing my new friend for life (diabetes) wasn't as hard as I first concept it would be. Lucky for me I had the help and reserve of my house which seeing back I comprehend the point of them and what they did for me. I at last went back to school after about a month off straight through my doctors say so, i didn't nothing else but know what to expect when i went back but my teachers were very helpful and normally asked me how I was after my extended summer holiday. To be honest Junior School went without a hitch to my surprise and my diabetes was well controlled as I was having 3 monthly reviews at my diabetic clinic and doctor so everything was in good hands.

During High School myself and my diabetes started to turn I started having more and more problems with my diabetes. I found it hard to operate my blood sugar levels and could not understand why even though i was doing everything i was taught. This also started to affect my weight and I began to put more weight on and found myself being overweight in my first 2 years by at least a stone. I was becoming increasingly worried by this and yet no reasons for it. This carried on, even after trying new techniques with my diabetes it didn't seem to help me deal with my uncontrollable blood sugars and the weight changes. As I hit the 3rd year of High School I started to moderately lose weight and this coincided with my blood sugar operate improving. The reasons for this as was explained by my doctor was that when I hit puberty and my hormones changing this had an adverse affect on my blood sugar control. This was a great relief as i was very worried for so long with enduringly battling this question and even happier as it started to ease its way out and back to normality.

Over the years i have found that every day a diabetic man might have to turn their routine of blood sugar operate depending on what they have planned for that day. Lets say exercise. You may have to whether eat more food and keep your insulin intake the same or eat a normal meal and sell out your insulin intake by a unit or 2. Practice is a sugar or glucose burning activity so if you over do it and you do not have adequate sugar in your blood then you will have a hypo straight through low sugar levels. The opposite to this is the reverse reaction, having high blood sugar which is down to not burning adequate glucose during Practice activities and getting your food or medicine intake all wrong at the same time. Basically what I'm trying to say is that daily and every activity is a balancing act which isn't easy at first but in time and with experience you know what your body reacts to what you do to it.

I recall that i have suffered from an extreme case of low blood sugar. It happened whilst watching television and even though in most cases you can feel the effects of a hypo but the degree it can hit you means you may need man else to help get some sugar into your body. This one time I was on my own and my parents where out for the night. I didn't feel the onset of the hypo at all and then all of a sudden wham and i hardly remember what happened. When they arrived home they found me semi-conscious on the floor and gave me some lucozade. Lucozade is one of the best things to give yourself when you have a hypo because liquids take less time for your body to discharge into the bloodstream and push your sugar levels up again. My dad had to feed the lucozade to me like you do when feeding a baby, hold and tilt the head back and let your throat glands do the job whilst your in a hypo state. The ambulance was called and by the time the rapid response arrived the lucozade had done its job and I was sat up and talking. The paramedics checked me over and made sure I was fine they checked my blood sugar and my blood pressure. Some habitancy are lucky and they never have any severe episodes of hypo but they do happen no matter how good your sugar operate has been.

Now I am the grand age of 30 I have 20 years of living side by side with my friend (Diabetes) and to be honest it's had its ups and downs with blood sugars and I am still going strong. Every day is still the usual balancing act and after a long period of time it becomes an commonplace part of life. Diabetes is an illness not a disease as some habitancy call it. I have all the time concept to myself that just because you have it for life, it does not mean that its the end of the world it could just be the start.

I hope to the many habitancy who have read this that they have found some attractive and beneficial information on how it has been for me coping with my new friend (Diabetes). I would like the opening to say never let it put your life on hold. Thank you for reading my story and I will be back with more soon.

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