Marty....You and I were diagnosed in the same year.  I had my sisters tested 
but there wasn't a good match.  I then decided that I'd take the 5 years that 
they gave me rather then hunt for a match....I also was reaching the age where 
they wouldn't do a transplant, so it was a choice I made.  They started giving 
me shots of Interferon and I thought I'd die on that.  It got so bad that at 
times I had to have the nurse come out of the clinic to give me my shot in my 
car because I couldn't make it in.  In PA they wouldn't let me give the shots 
to myself and so for 5 days a week I got the shots.  On Monday, Tues. and Wed. 
I wish I were dead.  I ran high fevers and couldn't get out of bed most days 
with the exception of going to the clinic for my shot.  By Thurs. I was feeling 
better and then Friday thru Sunday were okay.  Monday it started all over again 
because they wouldn't give me the shots on the weekends...No one was there that 
could do it.  After wishing for death...and I'm not exaggerating...They put me 
on a medication I believe was called Hydroxeria, but that would never put me 
into remission.  Gleevec came a little later and I never got into remission 
with that either.  After that stopped working, they put me on Tasigna.  I've 
been on that for 6 years and it did put me into remission.  It has always been 
a struggle of some sort, and now the liver issue, but I'm still alive, and 
still here.  I did tell everyone that he is putting me on a liver transplant 
list...so we shall see.  I never give up...I'm just happy that I've had the 
time I've had.  Much longer then the 5 years they gave me in the beginning.  I 
can't imagine being in a small bubble for 7 mo.  I am sure that you had to 
fight to adjust to that.  You are such a strong person, and that probably 
helped you towards being one.

I am not giving in to this thing and will  live as long as I can as I have many 
things to accomplish.

Many hugs and 18's,
Millie

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