Recently had my first nephrologist appointment and he has basically told me he believes I have IgAN. He has ordered an ultrasound and blood tests. He took 7 vials of blood, and I didn’t ask what for. Does anybody know what he may be ruling out before I’m offered a biopsy. I had a CT scan 4 weeks ago because of flank pain. Thanks.
So, I finally have my nephrologist consultation tomorrow after 9 years of permanent blood +++ and protein +++. My eGFR is 96. Urine is typically coffee coloured when poorly. Crazy kidney flare ups once every couple of years at least.
Had all the usual test, CT scan etc.
What to expect? Will I finally be taken seriously. Thanks.
***UPDATE***
For anybody curious. Saw my nephrologist this evening, he’s 75% certain I have IgAN waiting on some blood results and an ultrasound before a biopsy to confirm. This will all take place over the next few weeks.