I will share my results when I get them. Seems like it might take an act of congress to get them.
I am not scheduled to go back to Hep DR. until August. I was told I could request a copy by calling a 1-800 #. I called that this morning and it was a recording that said I would have to go online and print some sort of release form off then mail or fax it to them..lol I just cracks me up to think that they would think ANYONE else might be wanting a copy of my biopsy results.
It seems like they could have had my sign the paper that day when I was there for the test.
Seems EVERYTHING has to have some red tape. Like we dont have enough to worry about!
I am feeling fine. I had a few little aches in the liver region for a few days but for the most part thats gone. I am just praying for good results
I tell ya this is not a cheap disease to have. I have good insurance but the expense it about to break us and I have not even been real sick like some of the people on here. I never knew that labs could cost $4500.00 for 1 visit. I am sure that when I see the bill for the biopsy I will be even more surprised. Just thankful for the Insurance and pray I can keep working as I am the holder of the policy..Thats something else to worry about....
I will stop babbling just wanted to get a few things off my chest.
You all take care and hope all is doing well!!!