Brenda,
Yes, I remember well how anxious I was to read posts from those who 
were surviving with CML.  The longer - the better!  Actually, I was 
scared to death when diagnosed because my father had been diagnosed 
with CML in 1988 and died within a year after going into blast 
crisis.  Don't let this scare you though.  After doing my own 
research, reviewing his medical records, and  a lot of thought - I 
don't think it was the CML but basically, poor treatment decisions 
that led to his death. Since I was diagnosed in Jan. 1998, many new 
options have been introduced and available.  Interferon, Ara-C, 
Gleevec, and now the new "hopefuls".  I have always found comfort in 
knowing that all things happen for a reason.   I have not learned 
those reasons but am confident that it's all part of a larger plan.

Hang in there.  Things are really looking up.  Take each day at a 
time and make the most of it.  Nothing in life is certain!
Dianne



--- In [EMAIL PROTECTED], "Brenda Morelli" <[EMAIL PROTECTED]> wrote:
> 
> Wow 7th year, I'm a newbie and folks like you give me hope and 
> optimism where might otherwise be fear and sadness.  Thanks to all 
of 
> you for your courage, persiverness and knowledge. It has made the 
> journey a little easier for the rest of us who have had to follow.
> 
> Brenda
> dx 5/04
> Gleevec 6/04
> 6mth bmb, pending results 
> 
> 
> 
> --- In [EMAIL PROTECTED], [EMAIL PROTECTED] wrote:
> > Greetings friends!
> > 
> > For those of my friends and those of you who are new, I'm writing 
> to let you know that I'm actually approaching the "7th" year since 
> diagnosis in January.
> > 
> > Tracey,
> > I think of you often and am wishing you the best.  Perhaps one of 
> the newer drugs will be available sooner than expected.  I know 
that 
> those in accelerated and blast have access sooner than anyone in 
> chronic. You've certainly been a trooper!
> > 
> > Nanc,
> > I'me still a turtle who doesn't know what direction to go!  I 
> increased back to 600 mg. in hopes of getting rid of some of those 
> PH+.  I'll be travelling to MDACC in January to see Dr. Talpaz.  
> AI'll be meeting a friend who has been dealing with CML 15+ years!  
> She's been through it all.
> > 
> > Wishing everyone a very happy holiday season.
> > Dianne
> > Ohio
> > DX 1/98





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