Hey Bill,
Things have really started moving since you were dx'd, I can see your 
treatments have moved right along with the research and discoveries, 
your an inspiration to us newbies.  For the new ones (I was dx'd 
5/04) it shows that this disease does not need to be and really is no 
longer a death sentence.  Thank goodness for trials and the brave 
warriors who volunteer for them.  There are so many options now I 
hope you'll find one that suits you.  Take Care
Brenda
dx 5/04
pcru 5/05


--- In [email protected], <[EMAIL PROTECTED]> wrote:
> Dear list,
>       I have been "listening" to all of the positive things that 
are happening
> for so many of you and your loved ones.   It is heartening indeed!  
I was dx
> with CML in 6/93 (Philidelphia +) at age 46.  My first reaction was 
to be
> scared witless!  Been through the angry and the depressive stages 
as well.
>      I was told in '93 that an unrelated donor BMT was a high risk 
option and
> have since been on a veriety of meds including Hydrea, 15 months 
Intron-A
> (interferon) / Ara-C (cytarabine), 12 months HHT 
(homoherringtonine) / Ara-C
> and currently taking Topotecan / Ara-C (just started).  To date no 
chromosomal
> response has occurred and the WBC / platelet rollercoaster ride has 
been
> something else.
>      Don't know what the future holds but I thank the Almighty for 
the last 5
> years, my family (high school sweetheart / mother-in-law of 33+ 
years (they
> came as a matched set), daughter 24, son 21) and the support of so 
many good
> and dear friends.  Also praying that a cure can be found for us all 
(amazing
> amount of research going on?!!).  I cannot accept that this thing 
will get the
> best of us!
>                                         Bill Henderson 
([EMAIL PROTECTED])
>                                          Stafford, TX
>      
> 
> 
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