Hi there, this is my first post but have been a member for a couple of months.
I was diagnosed with a very fatty liver following a ultrasound last year + with Hep C last October + have completed a course of Maviret with no side effects other than fatigue which I have had for years anyway - though I was very Ill at week 7 of treatment when I caught the flu. At my very first appointment at the Liver Clinic/Hospital I asked if I could be kept up to date with all my test results + did indeed receive a detailed letter of my blood tests + what was going to happen next. After my diagnosis I was dealt with by the Hep C nurses at a satellite clinic. At my ‘end of treatment ‘ appointment I asked if I could have some information/copy of my records regarding my blood tests, a fibroscan + later ultrasound - but was told I didn’t need them as ‘I was fine’ After further discussion I asked about my Liver Function Test (not sure what I needed to ask for) + was told it was now 15, Fibroscan = 7 + my ultrasounds were ‘fine’. I also asked about drinking alcohol + was told it was ok to drink ??? + when I asked about when I would next see a Doctor regarding my very fatty liver I was told that I wouldn’t need to see a Doctor.
I realise that in the grand scheme of things I have been quite lucky + there are people on this site who are in a worse position than myself but I would still like to know what my results were so that can hopefully manage my health better in the future. Has anyone else has any problems getting info regarding their test results? Also should I be seeing a Doctor so that my fatty liver can be monitored - or am I worrying over nothing? For some reason I seem to be fretting over not getting my test results + being able to discuss them with someone + can’t understand why it should be such a big secret!
Please let me know what you think. X X X