Warning: veeeery long post!!
I was properly diagnosed in December 2021, tho I was pretty sure I was diabetic since October from a blood test. Still, I was shocked to find out it was type 1 and I needed insulin for life.
How did I feel? Really upset and scared about the needles. It was hard to accept I had a chronic condition when I had always been pretty healthy. I was lucky in that I was allowed to start on only basal, and it worked for me for a while, so it was only one injection per day at the time, in the morning. For at least a week it was my first waking thought and I dreaded getting out of bed because it meant doing the finger prick and injection. I had a few good cries in the shower thinking how much this would limit my life in terms of food, activities, travel...Spoiler alert, it doesn't! Sure, it takes some extra thought and carrying supplies around, but it hasn't stopped me from doing anything important to me. I am generally a positive person. The first few months I was in a dark mind place, eventually I came to terms with it and focused on managing as best as I can. The forum really helped
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How did I find out? It was my first summer working in the hotel restaurant. It greatly disturbed my eating and sleeping routines, and I did a lot more hours than I had in my previous job. So I didn't give much importance to the first symptoms or tiredness and feeling "off". Later they got worse and I also felt the extreme thirst, blurred vision and the worst one for me: peeing for England. It was very disruptive, I woke up multiple times per night, couldn't stay far from a toilet for long and sometimes got to the point where I barely made it to the toilet. I remember thinking "I'm 25, that's too young for incontinence!". It was particularly bad at work, where I was supposed to let my manager know when I went to the toilet but I was embarrassed to say it every time so I sneaked out. At times I tried not to drink anything during the shift, but it felt like torture and I STILL had to pee every 30 minutes.
Coincidentally my period disappeared around that time (to this day I am not sure why, but it lasted 8 months!) so I feared I was pregnant. Once that was ruled out I thought it might be a hormonal problem that was causing all of my issues. In October I went on holiday to my home country, where I was more familiar with the health system and got a full set of blood tests. I also had a very long check at the opticians, since I was struggling to read, and the man clearly saw something was wrong but couldn't figure out what. They made me a pair of glasses that didn't help much and have been sitting in a drawer since I got on insulin and my eyesight recovered
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The blood test results came when I was already back to England. My fasting BG was 280 mg/ml (15 mmol/ml) and it clicked. I googled "diabetes" and found out I ticked all the boxes. The doctor told me to get tested to confirm it, which was a long and stressful wait: almost 4 weeks for a phone appointment (NHS was still very strained with COVID) and another few to actually get my blood taken. It just so happens that my dad had been diagnosed with Type 2 the same year and had very good results with diet and Metformin, and I assumed that would be the case for me. So I cut carbs down while I waited for diagnosis and it did help my symptoms. I got a call soon after the test saying my HbA1c was 84 and if I could go to the hospital the next morning for further tests, as they feared I was Type 1. I didn't know you could get that type as an adult!
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They were not completely sure about the type as my age and weight didn't suggest T2, but the symptoms were not as drastic and quick to appear as they are usually in T1, and I have family history of both. But they wanted me to start insulin ASAP because they were concerned about my levels. As I mentioned, I was not happy about the injections and it took me a while to get used to it, but I didn't have a choice! The antibodies test came back strongly positive so I've been treated as Type 1 since then. It seemed to be a slow progressing case though, because I've not needed a full basal-bolus regime until recently, so 3 years later! Before I went through seasons of only basal, only bolus and even no insulin. I spoke about it with the consultant and he said that autoimmunity is different for each individual, and as long as my BG was good I didn't need to change my system. Oh, and I got Libre one year after diagnosis, so I had plenty of time to practice my finger pricks! Libre is the best thing that's happened for me as a diabetic
Song in my head: Espresso, by Sabrina Carpenter.