'A death sentence' in my own words!
Your posting has had 8 likes, 1 share and my son has sent me to message to say he read it and he is so proud of me for what we go through!! Oh and someone said how awful it must be for her dog who has diabetes and whose daily BS readings she posts on Facebook!! I have my own ideas of what should happen to the poor little fella if he is blind, cannot eat what he wants, has to fast before the vets, have injections daily, needles stuck in him.....can't be much of a life. Seriously it must have taken you ages to write and well done for raising awareness. The most I have ever shared is about a neighbour (type 1) who was unconscious and the other neighbour was rushed around to ours sceraming "He's diabetic, we'd better ´give him a shot of something´!" I posted that please, if I am ever found unconscious (and I have been) to leave my insulin alone, get some sugar into me and call an ambulance!!
I think the artificial pancreas algorithms are already here and can already do the job of handling food, based on my experience of using them. The far bigger issue is the insulins we have to use with them, that can't react fast enough, but even that's changing. Living with type 1 diabetes is going to get easier.Once the technology has been perfected, we will be very close to an artificial pancreas, where the Blood Glucose Measurement is virtually real time and an algorithm in a pump can adjust one's dose to ensure we stay between those two lines.
well im a type 1 diabetic , in my case , I was living with my partner and visited his family for a weekend break, I told them I was a diabetic , there have 8 grand children all who seemed to know what diabetes was, and didn't mind when I used to inject in the house.. what I used to do to break the ice, I took a blood BG test on most of them showing there readings on my meter. what I couldn't understand a child aged 7 said to me how long you had diabetes possibly his gran or a member of his family or school friend had it ? he wasn't frightened in any way.Hi There
I am hoping that the fabulous community here will post replies on this thread about the subject in the title.
or possibly provide links to people's blogs on the subject , or even copy a link to an old topic that covers this area
this topic could then hopefully be something that could be shown to gather support from family members, it could be helpful to newly diagnosed families as well as families with a D peep going through issues at the present time.
thanks so much for reading and for posting if you are able.
all the best !!
Hey @Stephen89Here Is My Honest Opinion
I've been Type One Diabetic since I was 3 (24 Years) Its been more of a Roller Coaster than an easy ride, I'm Not the best controlled or even considered a "Good Diabetic" I go for weeks being controlled and sticking to the book but the rest I spend sticking it to the man, I have Never ever missed an injection or Blood Test But my own issues lie solely with me being Lazy and "Giving up on myself and my health" << Bad, I Know!!
Recently (8 years ago Ha.) I was also diagnosed with Epilepsy Also.
I Began my Journey on 4 Potatoes, Spoonful of Carrots and Small Slice of this and that, Having to wear a "I Am Diabetic" Badge at school all day long and taken from class to go and fix my sugars, Mind you things haven't changed much today as the boss requires an email if I need to go and fix myself, Only thing that's missing is that badge Ha.
I enjoy playing football, always have and always will, Growing up was some what difficult with not only the football gear in the bag, but the BG Metre and bottle of lucozade and crisps Etc. Some of the team used to look at me funny (So would I) But after explaining they understood, It was more the times of being out young with friends kicking around the streets and park's and having to leave the fun to go do a test or eat a meal, But again I was getting used to all this after time.
High school again was no different, I had the badge and half of the kitchen in the bag going between classes. The older I got the lighter the bag got, when it was lucozade tablets and smaller bottles of juice.
I guess my quick story is the same as most people on here starting out young and having to go through bad times But life itself is not very easy and neither is the road ahead, But all you need is that one person behind you giving you a shove in the right direction, for me its my wife, who picks me back up and dusts me off every now and again.
Anyway this may be a pointless read or a not so bad one, who knows
Stephen,Here Is My Honest Opinion
I've been Type One Diabetic since I was 3 (24 Years) Its been more of a Roller Coaster than an easy ride, I'm Not the best controlled or even considered a "Good Diabetic" I go for weeks being controlled and sticking to the book but the rest I spend sticking it to the man, I have Never ever missed an injection or Blood Test But my own issues lie solely with me being Lazy and "Giving up on myself and my health" << Bad, I Know!!
Recently (8 years ago Ha.) I was also diagnosed with Epilepsy Also.
I Began my Journey on 4 Potatoes, Spoonful of Carrots and Small Slice of this and that, Having to wear a "I Am Diabetic" Badge at school all day long and taken from class to go and fix my sugars, Mind you things haven't changed much today as the boss requires an email if I need to go and fix myself, Only thing that's missing is that badge Ha.
I enjoy playing football, always have and always will, Growing up was some what difficult with not only the football gear in the bag, but the BG Metre and bottle of lucozade and crisps Etc. Some of the team used to look at me funny (So would I) But after explaining they understood, It was more the times of being out young with friends kicking around the streets and park's and having to leave the fun to go do a test or eat a meal, But again I was getting used to all this after time.
High school again was no different, I had the badge and half of the kitchen in the bag going between classes. The older I got the lighter the bag got, when it was lucozade tablets and smaller bottles of juice.
I guess my quick story is the same as most people on here starting out young and having to go through bad times But life itself is not very easy and neither is the road ahead, But all you need is that one person behind you giving you a shove in the right direction, for me its my wife, who picks me back up and dusts me off every now and again.
Anyway this may be a pointless read or a not so bad one, who knows
BRILLIANT!Today is the start on a new chapter in my life now that I am going to work to get a pump!
I was diagnosed with type 1 diabetes in early April of 2015; My whole life I struggled with food, not what I'm eating but more of feeling like I get nothing from it. Ever since I was little I remember after breakfast every single day, whether I ate 400 calories or 1400, I still didn't feel full, not the feeling that I was hungry but like I got zero energy from it and completely lethargic. I also randomly would experience severe cold sweats and shakes, it would happen a few times in a week and then would disappear for weeks.
I remember one time before hockey having a big plate of whole wheat pasta, only to find I had no energy to skate when I hit the ice! I would constantly tell my doctor at checkups I don't feel right and the answer was always the same, have a snack of nuts between meals, eat small meals, etc.. Of course this never changed anything, I was having 6 small balanced meals a day since the time I was 16 till I finished playing hockey around 23; this changed nothing. I had blood samples taken once a year and my family physician would always say "nothing abnormal, you're a healthy young male". This was hella frustrating considering I ALWAYS felt off!
So fast forward closer to my diagnosis, I had symptoms for 12+ months, predominantly fatigue and constant sensation to want to urinate but when in the bathroom couldn't. I would say around 4 months pre diagnoses I started to feel extreme symptoms such as thirst, falling asleep uncontrollably, zero energy, muscle spasms, and UTI's. Finally one day my dad who is a type 2 diabetic decided to check my sugar on his meter which read >30 mmol/L. He freaked out and I rushed to the hospital, where they did a blood test reading a BS of 46 mmol/L. That day being told I was a type 1 diabetic received an initial reaction of a blessing and sense of relief "Finally I know what has been going on with my body all this time, and there is a way to feel better now" I thought to myself. That feeling did not last long, and shortly after faded.
It took a few weeks to get myself back to normal, I had a hard time balancing and running felt completely abnormal. I got right back into the gym, I felt a massive increase in my strength, I was eating food and feeling great and on top of the world for about 3 months, then I got sick. Everything changed that week, my sugars were high, I couldn't exercise properly I felt like a bag of ****. Following weeks I started to get low blood sugars randomly and at different times causing such a disruption in my routine, destroying my motivation to do anything. Then following was nagging injuries from hockey coming back up keeping me from doing any intense form of activity, my sugars regularly became higher and unpredictable more so.
I consulted with my diabetic team at the hospital and decided to try the OMNI pod for 4 months or was it 5, I forget. This did nothing but further stress me out and failed to make my sugars any lower, I had to constantly change the formula ratio for how much insulin to carbs I needed, my basal rate, it would come off if I did play hockey or when climbing the latter at work. Overall it was a stressful experience which made me feel less normal which I despised. So, I decided to go back to the pen. At this point now I'm in a worked up frenzy, completely frustrated that things aren't working, constantly having to adapt, feeling like a slave to diabetes. Work became a complete nightmare and I became and anxiety case not knowing what was happening from day to day being unable to plan from hour to hour, my diabetes fell to the wayside and I felt like complete garbage for a good 3 months failing to sleep more than 3 hours a night 5 days a week. It got to the point I took a sickness leave this October trying to get a routine down and things back on track.
So far I have been unsuccessful in doing so, finding the correct balance of exercise and intensity, not to much, not to little, doing it at the right time, knowing how my body reacts to this type of food and at this time of day, correcting my insulin dose according to the time of day and what I did, all of it seems impossible to deal with. My brain is so exhausted I can't even begin to list of all the stressors diabetes has brought to my life. Every minute of every day feels as if it has to be thought out and planned precisely, I do not enjoy life this way, I thrive off the unexpected yet as a type one fear that anything can happen for unknown reasons as my blood sugars have proved in the past. All of the things you stated @Snapsy is exactly how I feel! I needed to rant and let things out before I explode, I feel like nobody except for my girlfriend is understanding of my diabetes and expects me to just carry on as a normal person. I can barely get through a day just trying to survive, how am I supposed to function in society, work and live a normal life and not feel the symptoms of a high and low blood sugar.
With all this said I haven't given up I'm still trying things, I've just downloaded an APP mysugr which is helping me log more advanced details throughout my day and I am testing between 10-14 times in a day to figure out whats going wrong and where and I am hopeful despite the frustration and anger diabetes brings to my well-being. There has to be an answer out there, something I'm missing and I am determined to figure it out! This is my experience with diabetes, thus far.
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