re:
Living with Liver Disease
message #:
2845.4 in response to 2845.3
Hi,
It has been a year since I found out I have auto immune hepatitis. In that year lots of things have changed for me. I discovered I had it when I went in for gallbadder surgery, my skin and eye whites were yellow. Was off from work for 6 weeks, which was a clue, usual recovery is 2 weeks. How I live my life and how I see the future is different. I am in the process of improving my health, with better diet and exercise. By exercise I am talking about walking and yoga. At this time don't think my body could take anything very strenuous. It has taken me this long to get some health issues taken care of, diabetes under control , so that my A1c is 6 (down from 7.5), going from 5 shots of insulin a day to one shot of lantus with metformin tabs twice daily. Also my doctor lowing my predisone and raising the imuran. The use of azathioprine allows for a lower dose of prednisone, which in turn reduces predisone’s side effects. They do this slowly so I don't have a flare, which could be very hard to get back under control. So now I take 12 pills in the am and 4 at night and one shot. In my future is a possible liver transplant, at this point I have stage 3 liver diease damage. I see signs that this is so, I have spider angiomas, or abnormal blood vessels, on the skin, bleeding easily, tiredness, gums that bleed easily -dental work is a major event now, abdominal discomfort - due to liver enlargement. I also have diabetes and thyroiditis, an inflammation of the thyroid gland , having other auto immune disorders is common with this diease. I am just doing the best I can with what I have. If anyone out there has auto immune hep. please write to me. I would be interested in how you cope and what treatments you are doing.