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Hi Mable,

I know what you mean about the 'supposedly' grown kids. I have two of my own

and we can't get them out of the house. They're single 25 and 26 years old - no

children.

How interesting that AIH was called CALD back in the 1980's. I wonder - do they

rename it every so often? It doesn't seem to me that they know much more about

it today than they did when I got sick in 1994. I was diagnosed by the process

of elimination. In other words, I didn't have anything else. It must be very

difficult trying to cope with AIH and Diabetes. How often do you go for labs?

I'm post transplant and have to go every 3 or 4 months, and I don't like it at

all.

It's great that you've been able to be off the Prednisone for that long,

---

Barbara Ann

AIH transplant recipient

On Sun, 16 May 1999 19:28:45 mable wrote:

>From: mable@...

>

>

>Hello everyone,I have been around a couple weeks now. I feel kinda like a

voyeur reading all your mail.

> this is my first real e-mail, I hope I do it right.

>I have AIH,cirrhosis, diabettes. I was diag in 1989

>I was very sick, they thought it was my GB and it

>was, partly. At that time they called it CALD,(chronic

>active liver disease) they have since renamed it.

>I have been completely off pred for over 3 yrs.

>They increased my imuran to 200mgs a day and I have done real well on that

although last yr I went to a

>diff dr and he wanted to drop it to 100 but I don`t

>think it`s working as well. I`ve been putting off

>getting my labs done cause I really don`t want to know

>I`m 52 yrs young, on ssd, div,, have 2 grown kids

>(supposedly).,and 4 grandkids.

> sorry this is so long, I`ve been saving up. Love

>reading your letters and hope to hear from you.

>I have lots more to say.

> mable@...

> THANKS

>

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