Hello all, another newbie here. Just wanted to stop by to give my story and to ask a few questions /waves
I've just been diagnosed with Type 2 after asking the doctor to check as I was concerned with some symptoms I have been having. I had previously done a free check at an Asda pharmacy and scored an 18.0 (this was essentially a fasting test as I hadn't eaten since dinner the night before) which made up my mind to get it checked. My offical fasting blood test was 15.5, which was better, but still very bad. I vaguely remember the dr showing me the three month test. It was 91, where it should be 43? (I see a lot of people on here put percentages, but I don't know what mine was or how I work it out).
The doctor has put me on Metformin, 1 tablet once a day, and I have already seen the DN who thoroughly scared the hell out of me by giving it to me straight. I just had no idea what I was truely dealing with. She recommended this forum and I'm glad she did
However, things are never straight forward are they? The nurse was concerned that I am having 'symptoms', like, a few hours after I eat breakfast or lunch, I have what I call a 'crash'. It's almost like I am hungry. I get lightheaded, shaky, nauseous, anxious; exactly how I when I'm hungry and haven't eaten yet. However, I don't get this after dinner when I've taken my Metformin and asked whether it would be better to take it at lunch, so I don't get that 'crash' in the afternoon. The nurse was rather shocked at hearing this. Apparent'y I'm not supposed to notice the effects Metformin is having on me and came out and said she thinks I am Type 1, or at least borderline Type 1. Now I am awaiting an appointment to revisit the dr and to get a BG monitor which she wants me to use before and after each meal for two weeks. She also informed me I need to stop trying for a baby for at least 6 months as to get pregnant right now would be dangerous to both me and a baby
As you can probably imagine, I left more confused and upset than when I went in! I've digested most of it since and I'm more at peace with the fact I now have diabetes and will have for the rest of my life. It just shocked me to learn it will only get worse as I get older, that I will need more tablets and it will be harder to manage. I had no idea.
Has anyone else been in the same boat with a confused diagnosis? I keep thinking that if I am Type 1 after all, how come they didn't pick this up when I had the tests? Do the dr's assume you'll be Type 2 and really only check for this? For now, I'm putting it down to an overly dramatic nurse and will assume I am Type 2 until I learn otherwise. But I was wondering, how will they check for Type 1? More fasting bloods? Urine samples. Both?
Anyway, I've rambled enough! It's nice to meet you all and I'm sure I'll be asking a load more questions as time goes on. I get the feeling I am barely scratching the surface on what's to come.
I've just been diagnosed with Type 2 after asking the doctor to check as I was concerned with some symptoms I have been having. I had previously done a free check at an Asda pharmacy and scored an 18.0 (this was essentially a fasting test as I hadn't eaten since dinner the night before) which made up my mind to get it checked. My offical fasting blood test was 15.5, which was better, but still very bad. I vaguely remember the dr showing me the three month test. It was 91, where it should be 43? (I see a lot of people on here put percentages, but I don't know what mine was or how I work it out).
The doctor has put me on Metformin, 1 tablet once a day, and I have already seen the DN who thoroughly scared the hell out of me by giving it to me straight. I just had no idea what I was truely dealing with. She recommended this forum and I'm glad she did
However, things are never straight forward are they? The nurse was concerned that I am having 'symptoms', like, a few hours after I eat breakfast or lunch, I have what I call a 'crash'. It's almost like I am hungry. I get lightheaded, shaky, nauseous, anxious; exactly how I when I'm hungry and haven't eaten yet. However, I don't get this after dinner when I've taken my Metformin and asked whether it would be better to take it at lunch, so I don't get that 'crash' in the afternoon. The nurse was rather shocked at hearing this. Apparent'y I'm not supposed to notice the effects Metformin is having on me and came out and said she thinks I am Type 1, or at least borderline Type 1. Now I am awaiting an appointment to revisit the dr and to get a BG monitor which she wants me to use before and after each meal for two weeks. She also informed me I need to stop trying for a baby for at least 6 months as to get pregnant right now would be dangerous to both me and a baby
As you can probably imagine, I left more confused and upset than when I went in! I've digested most of it since and I'm more at peace with the fact I now have diabetes and will have for the rest of my life. It just shocked me to learn it will only get worse as I get older, that I will need more tablets and it will be harder to manage. I had no idea.
Has anyone else been in the same boat with a confused diagnosis? I keep thinking that if I am Type 1 after all, how come they didn't pick this up when I had the tests? Do the dr's assume you'll be Type 2 and really only check for this? For now, I'm putting it down to an overly dramatic nurse and will assume I am Type 2 until I learn otherwise. But I was wondering, how will they check for Type 1? More fasting bloods? Urine samples. Both?
Anyway, I've rambled enough! It's nice to meet you all and I'm sure I'll be asking a load more questions as time goes on. I get the feeling I am barely scratching the surface on what's to come.