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Long-term outlook/work

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Hi all -- I'm new to this group, and new to the world of AIH. I would

really appreciate your feedback on what may lie ahead with this disease. I

have a decision coming up as to whether or how much to cut back on work,

which is high-stress, deadline-driven and involves quite a bit of travel. I

have read up extensively on the disease and treatments, but now I need to

hear from the people who have been living with this condition so I might get

a better idea of what to expect over the long-term. I was really pleased to

find this group.

(FYI, I was diagnosed with AIH less than 3 months ago. My ALT/AST were

about 1800/900 and biopsy was Grade 4, stage 2 with fibrosis but not

cirrhosis. I have been on Prednisone (40/30/20) and am now reducing that to

10mg and have started Imuran; I am also taking Fosamax. The ALT/AST numbers

have come down and are now about double normal.)

I have always been the driven type that " pushes through " regardless of how

tired or crummy I might feel. I have always been fairly healthy and very

active. However, I dragged home from a recent trip with mono and a flare-up

of shingles that I had several years ago. This has forced me to rethink

working and traveling at the same level as in the past, especially with a

compromised immune system thanks to the meds.

I know everyone's situation is different with AIH, but I would greatly

appreciate hearing from any of you with feedback on how AIH - and dealing

with the meds and their consequences - has affected your life and what

adjustments you have had to make. I have to make some important decisions

about my future and really need some input as to what may lie ahead in

living with this disease. Thanks so much!

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