I know what you mean.    dg
 
 
In a message dated 8/3/2011 7:51:00 P.M. Pacific Daylight Time,  
[email protected] writes:

Hi Greenie:


That is excellent news. I'm waiting for my three month results and if  they 
remain good, I'm having an eyelid lift in September. I'll let you know as  
soon as I have results. Can't wait to have peripheral vision!


Marcie

Sent from my iPhone

On Aug 3, 2011, at 10:24 PM, [email protected]_ (mailto:[email protected])  
wrote:





Thanks Marty
 
 
In a message dated 8/3/2011 11:13:50 A.M. Pacific Daylight Time, 
[email protected]_ (mailto:[email protected])  writes:

That's excellent Greenie!
 
18's to you
 
Marty


On Wed, Aug 3, 2011 at 2:05 PM, <[email protected]_ 
(mailto:[email protected]) >  wrote:


Hi just received my lab works and everything is O.K..  I'm low on some of 
the tests buts it's like that all the time.  I'm  good to go for another 3 
months.
 
greenie
 
 
In a message dated 8/3/2011 10:00:13 A.M. Pacific Daylight Time, 
[email protected]_ (mailto:[email protected])  writes:

Hi Draze,
 
Unfortunatly, I would like to welcome you to "the world of CML"  Fortunatly 
CML is now much more treatable then in years past.  Yes, as you mention it 
is cancer, however, if you have to have cancer  then this is probably the 
one to have because of all the new drugs and  treatments that are available 
now.
 
Your WBC being at 309 at your diagnosis wss quite high, but not  as high as 
mine when it was more then 23+ years ago. Mine was  486,000. 
 
Here is a website describing what PCR is and since you are newly  
diagnoised don't be disappointed if yours is not even close to PCRU.  Sometimes 
it 
takes many morths even years to get to PCRU but that is  what is really good 
about all of these drugs they usually help with  your disease and let you 
live your life. Your WBC going from 309 to 64  is a very good sign of this and 
your even able to go back to  work.
 
Check out what PCR is, at: 
_http://www.dna.gov/audiences/victim/know/interpreting_ 
(http://www.dna.gov/audiences/victim/know/interpreting) 
 
By the way, there is also another CML group you can post on. It  is 
[email protected]_ (mailto:[email protected])  
 
Both this, and that one are very good for information and there  are a lot 
of very friendly people on both of these lists. If you  should have any more 
questions or concerns just get on and post them.  By the way where do you 
live?
 
Now a little about myself.
 
I had an Allogeniec Bone Marrow transplant more then 22+ years  ago for 
CML. I am still here, and so are you. That is the way I look  at it...
 
I wish you good luck, and whenever I end an email I always end it  with a 
number, the number is 18's which means life. Stay in  touch.
 
18's to you!
 
Marty


On Wed, Aug 3, 2011 at 4:31 AM, Draz <[email protected]_ 
(mailto:[email protected]) >  wrote:

Hi all,

First time poster here, recently (3  weeks ago) I've been diagnosed
with CML at a chronic stage with  white bloodcell count 309. Treatment
started of with Glivec  (Imatinib) and almost 2 weeks ago they switched
it to Nilotinib  and I was placed in the researchgroup. Last week
Thursday my  count was 64 and the doctor said it was ok for me to  start
working a few hours a day and so on. All great news  considering it's
cancer, we're talking about.

Now  according to the Nilotinib research documentation I should  be
receiving PCR results but I have no idea when or what those  actually
are. Can someone shed some light for me when these  results start
coming in cause so far I've only been getting white  bloodcell  count.

Regards
Drazen

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