I was diagnosed with IgAN back in September. My doctor was very nonchallant about the diagnosis and basically said that there was really nothing I could do about it until the disease progressed. I researched like mad and found out that there is a ton that I can do. For instance, get a biopsy!!!
You need to get one done for several reasons. One, to verify the diagnosis. Two, the progression. Three, state of mind.
Besides all that, you are seeing a nephrologist right? And also, you need to know your Creatitine level. That determines your kidney function. B/c if it is high you need to look into meds to help. And your BP? Is it low or high? I could go all day but the best piece of advice I can give is to go to this site and join the group. Very informative, friendly people who all have teh same disease in different stages. Best of luck. [url="http://www.egroups.com"]www.egroups.com[/url]