Hi. I went thru the same process and my private tests for c-peptide also showed 1.1 and my GAD was negative like yours. The UK NICE says that GAD tests become unreliable the longer you wait after diagnosis and as in previous posts there are other causes for islet cell failure such as viruses and pancreatitis. I had a mysterious high white cell count just before diagnosis of 'T2' and had a constant mild abdominal ache for a year; could these highlight something?I was diagnosed with pre-diabetes almost four years by my GP. A few of my siblings are Type 2, but unlike them I am/was slim, ate pretty healthy and exercised daily. I've been struggling to get my HbA1c down from 6.5 since diagnosis despite radically changing my diet and losing a little weight. I'm 5'8 and weigh 58kgs. A mutual friend suggested I get tested for LADA as she was misdiagnosed as Type 2. I went to a private doctor/lab for testing (no insurance) and my c-peptide is low (1.1) according to the range. The doctor said he thinks my diabetes is an autoimmune issue and I'm not producing enough insulin to get my sugars down, but he said I need to work with an endo. However, I tested negative for ICAs and GAD antibodies. Has anyone else experienced this? I'm guessing I am a LADA and waiting to get insurance so I can get further testing done for free.
Hi. I went thru the same process and my private tests for c-peptide also showed 1.1 and my GAD was negative like yours. The UK NICE says that GAD tests become unreliable the longer you wait after diagnosis and as in previous posts there are other causes for islet cell failure such as viruses and pancreatitis. I had a mysterious high white cell count just before diagnosis of 'T2' and had a constant mild abdominal ache for a year; could these highlight something?
I'm sure I've seen info that says a greater number of patients are misdiagnosed as T2 than there are patients diagnosed as T1. It's just too easy for GPs to tell us to cut out the cakes and sweets and prescribe Metformin.
Hi again. I've no idea what my current c-peptide is as it's an expensive test and my NHS surgery refuse to accept I'm not a T2. They assume my 'T2' has progressed to insulin (well, it's progressive isn't it?). My Basal insulin has had to be increased from 10 units/day to a current 13 over 3 years which implies my c-peptide would now be lower (honeymoon period?). If you are a LADA then normally you would need at least tablets in the early years (not just Metformin) and almost certainly insulin in the longer term unless you very seriously low-carb which would delay these for a while.Thank you for the reply and it's reassuring. What's your C-peptide now and how often do you have it checked? That's good to know about the GAD tests. I'm not on any medication now because I thought I had Type 2 and could manage with diet alone, it's only been the past few weeks that I've learned about LADA. Unfortunately, I'm currently in Brasil with no insurance so can't do further testing at this time with an endo. Like you though I'm experimenting with a very low-carb high fat diet and daily fasting to get my blood sugars in the right range, but it's challenging.
I was previously diagnosed as type 2 and sent on a "DESMOND" course. Diagnosed with LADA in January and have been on insulin since then. The consultant refers to it as "Adult onset Type 1", which is more understandable. Waiting to do the type 1 course which is called "DAPHNE".I would like to hear the reason endo/ diabetes nurse have given to people that they are LADA rather than type 2?I am STILL struggling with this ..
I have never been told "Yes u are 100% type 1( lada) and this is why..."
My gp registered me for a course. It was for type 2 ,but organiserof the course told me on the phone to go along as it might help me. It was nice to meet other diabetics and there was some stuff relevant to me so I thought I would get something out if it .But basically I was put off the course by the facillitator as she said it would confuse me or others or some sort of thing... This made me a little upset and bothered as I dont know where I fit in...
Im not sure also whether I am down as a type 2 ,or 1.. I was initally 'wrongly'diagnosed as type 2!That bothers me because if there were trials or cure for a type 1( I know thats not coming anytime soon...) then I wouldnt be eligible .
I think I heard mentioned that there are other antibody tests besides GAD which I showed up negative for. Can I push to get other antibody tests if they exist?
Hi. To my knowledge there is no definition of LADA and as someone else has said the term doesn't exist within the medical community. Similarly there is no agreed age at which you are too old to be a T1 (is it 5 years old, 10 yrs old etc?). I would prefer the term LADA not to be used as not all Late onset T1s are due to antibodies. The term Late onset T1 covers a range of causes and timescales but implies the same outcome as an early age T1. No one can easily measure the honeymoon period and I bet even children have a honeymoon period but it may be months rather than years.Is Theresa May LADA? I've never seen her referred to as LADA before, just type 1. But obviously a type 1 diagnosed over 40 (as 1/5 type 1s are - I think that stat includes type 1 & 1.5). Is there an age of type 1 diagnosis when you are LADA? I thought it was more about the length of the honeymoon - so it would be possible to be diagnosed at 25 and be LADA if you had a really long honeymoon, possibly avoiding insulin for a time, and equally it would be possible to be diagnosed at 52 and be straight up type 1 no significant honeymoon?
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