--- In [email protected], "Dr. Patricia Maroudas" 
<[EMAIL PROTECTED]> wrote:
> Hello to Everyone,
>    I have recently as of Feb. 2005 been diagnosed with CML.  One 
week on Gleevac.  I am a mother of two active boys and Doctor of 
Chiropractic.  Not me I am healthy...  I have been told for many years 
to take care of myself, that others are always taking and I am always 
giving.  Well it is my turn now!  I have studied all the materials, 
listened to bunches of video tapes of trials and conferences, received 
about 10 new books in the mail, and now I want to know from others 
experiences.  Receiving slight stomach upset, other than that I think 
they got someones elses blood.  Maybe that is the denial part.  I have 
a positive attitude, eating healthy, no alcohol and praying.  I would 
love to hear from you all.  I have not met anyone as of yet with my 
diagnosis and would love to har from you.  
> Patty
____________________

Hi Patty,
For many of us the dx came out of the blue. I was dx over 6 years ago 
(9-98) and have been on Gleevec for 5 years, since an early trial. I 
am a recently retired physical therapist. The side effects with 
Gleevec (also abbreviated IM, for chem name) can vary....often fatigue 
is common, some nausea, maybe bone pain early on, etc. Take Gleevec 
with your largest meal and drink plenty of water...that might help. 

Your doctor should be monitoring you with regular blood work, CBCs and 
chemistries, to check esp. liver enzymes. Did you have a bmb at dx and 
do you know what % of cells were ph+? and how high was your white 
count? Information like this helps us with some suggestions. Your 
doctor should outline to you pretty clearly how he intends to monitor 
your disease and determine your response to IM......by repeated 
cytogenetics, FISH and/or pcr testing. Have you heard or read about 
all of this. 

2 good websites to check for additional information are:

www.cmlsupport.com
which list side effects and rememdies, glossary, etc. 

www.newcmldrug.com
tons of information and also a discussion list

One positive thing that I will share with you.....my cml specialist is 
Dr. Druker at OHSU/Portland who pioneered Gleevec. He told me about 6 
months ago that now (for the first time) when he sees a new patient 
who is in chronic phase cml, he can tell them that their disease will 
be a chronic disease (vs a previous often fatal disease) managed by 
medication. 

Let us know the questions you have. 
Also, you might contact your state Leu & Lymphoma Society and see if 
they have any support meetings near you....and they might have a 
telephone contact CMLer if you'd like.

Nancy C. 
Eugene, Oregon 





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