Hello, I was diagnosed with type 2 hep c 8 months ago but for about a year I have felt so unwell. I think that it's probably come from a tattoo I got 5 years ago. In the past I've suffered from anxiety and depression but I've managed to keep it under control until being diagnosed. Since then, I've been off work in a state of being sick of tired of being sick and tired.
I was just wondering if anyone else has any symptoms? I'm so tired all of the time, I'll have say one good day of being able to do things but then it's like I've used up all my energy. I ache all over, I especially have a headache everyday when I wake up. My skin can get really itchy, so itchy that in my sleep I'm itching my skin off. I'm having great difficulty sleeping, I used to be so good at sleeping 😁 and I have this pain around my liver area, it's like a dull throb but put of nowhere there's a stabbing pain that takes the wind out of me. If I was lying down it never bothered me but it's gradually got worse.
My anxiety has obviously got worse as well, I've changed anti-depressants 3 times and have started going to therapy, which does help. The GPS in ,your village aren't very good.
I first got diagnosed by accident when having a blood test for meningitis. My local GP had to take more blood for more tests which they messed up by using the wrong tubes. Then they confused me by saying maybe I didn't have it maybe it's gallstones but I did have it.
I live in Orkney so I've had to travel down to Aberdeen a few times to see liver specialists. The first time I saw a specialist nurse who was really good and she agreed that it probably came from the tattoo 5 years ago. The second time down, I had to see a doctor, she thought that I only caught it a few months ago and didn't want to rush me onto treatment, due to my history of depression, as sometimes it can go away on its own. She wanted a blood test to be done 4 weeks later to check.
So anot her blood test was taken which was messed up again by my GP because of the wrong blood tubes. So finally after another blood test, it turns out I still have it. You can tell because it's your own body when you aren't well. Because of where I live and everything having to go to Aberdeen, I feelet it's just taking so long for anything to happen and nobody iso telling what's going on.
After everything that's happened, I feel like my GP just doesn't listen to me at all I'm at my wits end about what to do about the pain I'm in as the usual paracetamol and ibuprofen doesn't touch it at all.
Sorry for my life's story but I want to put my mind at ease. Does anyone else feel the same way? Or is it just me and my anxiety?
Thanks for reading, if you could bare it 😊