On the tasigna my molecular level was 
0.04. Since I changed to gleevec that level has risen to 3.98. So that's where 
I'm at
Sent from my iPhone

> On May 30, 2016, at 10:18 PM, Marty Gartenberg <wa2...@gmail.com> wrote:
> 
> Hi Kate,
> 
> First of all if you have CML then you have the Philadelphia Chromosome. What 
> bothers me is if the oncologist told you about you never reaching remission, 
> then what level was he talking about? Have you taken any PCR tests yet? And 
> if you did then what were the results? But since you are a " newbie" you may 
> have not taken any, and also is your doctor a CML specialist?
> 
> There is a lot to think about, trust me you will learn to ask questions. 
> Remember the more ask the more that you will learn.
> 
> Glad to see that your sporting the 18's
> 
> 18's to you as well.
> 
> Marty 
> 
>> On Mon, May 30, 2016 at 9:27 PM, kathy walls <cand...@originalsbykate.com> 
>> wrote:
>> I'm still a newbie was diagnosed 1/9 and started tasigna on the 23rd, oh 
>> yeah I'm lucky enough to have the ph chromosome to boot.  I stopped tasigna 
>> in December because of horrible side effects, I got an awful rash and cysts. 
>> Switched to Gleevev and I feel much better, but did dr said at this level i 
>> will never see remission.  I'm ok with that.  Quality of like is much 
>> important to me than quantity.  I'm 56 I have  a 4 yr old grandson and  3 
>> month old grandson. I'd much rather a little pep in my step than being in 
>> remission but to sick to anything!  Just my thoughts. We all are fighting 
>> the same fight each in our way
>> BEST TO ALL. -18's
>> Kate
>> 
>> Sent from my iPhone
>> 
>>> On May 30, 2016, at 8:55 PM, Marty Gartenberg <wa2...@gmail.com> wrote:
>>> 
>>> Yes Jeanie,
>>> 
>>> we are still all kicking! Jeanie what happened in the past according to 
>>> your oncologist about you being to old should remain in the past and I will 
>>> tell you why. I also want you to think about something called BASHERT, 
>>> which I have already mentioned many times. It's meaning is it was meant to 
>>> be. Sound familiar? I believe that things that are meant to be are 
>>> predestined.
>>> 
>>> For instance this site, and everyone that reads it or posts on it are meant 
>>> to be because all of us are still kicking (as you said) and we all share 
>>> this disease called CML and let's not forget that.
>>> 
>>> There are so many stories that surrounds us and every one of them are meant 
>>> to be. We all stand here and try help each other. Why? it's because it is 
>>> meant to be. We give of each other, and also to each other, and you know 
>>> what I am talking about. It is all about trying to live our lives the best 
>>> way that we can.
>>> 
>>> Also, all of these new TKI's weren't they all predestined or if you like, 
>>> meant to be?  That is how I look at things, how about you? And how about 
>>> everyone else here? 
>>> 
>>> Why do you think I always end any of my posts with those two numbers? 18's, 
>>> because it stands for life, and isn't that we have now.
>>> 
>>> 18's,
>>> 
>>> Marty
>>> 
>>>> On Mon, May 30, 2016 at 5:41 PM, 'Jeanie' via CMLHope 
>>>> <cmlhope@googlegroups.com> wrote:
>>>>   Thank you so very much Marty. 
>>>> If I knew then what I knew today I think I would have
>>>> Had the transplant.  My onc at that time thought I
>>>> Was too old.  However I'm still alive and kicking 
>>>> After 4 tkis.   I am sick; I can't seem to kick this flu. 
>>>> Just resting after my vacation. 
>>>> I sure had a good time with family. 
>>>> Thanks for all as usual. 
>>>> 
>>>> Sent from my iPhone
>>>> 
>>>>> On May 30, 2016, at 4:57 PM, Marty Gartenberg <wa2...@gmail.com> wrote:
>>>>> 
>>>>> 
>>>>> Hi again Jeanie,
>>>>> 
>>>>> I just spoke with my good friend Gloria today and I asked her if she 
>>>>> wouldn't mind for me to send you and the rest of the group three of her 
>>>>> pictures. One before her BMT, one during her BMT and one about one year 
>>>>> after her BMT. She thought it was a very good idea. She also mentioned 
>>>>> that she would like to try getting onto this CML site and introduce 
>>>>> herself so please be on the lookout for her.
>>>>> 
>>>>> The main thing here is those pictures which proves that there is life 
>>>>> after a bone marrow transplant. Think about something else... What about 
>>>>> those 1,286 people, including myself which now makes it 1,287.
>>>>> 
>>>>> 18's,
>>>>> 
>>>>> Marty
>>>>> 
>>>>> Scroll down please...
>>>>> 
>>>>> 
>>>>>                                                            GLORIA
>>>>> 
>>>>> Forward
>>>>> Edit subject
>>>>> Pop out reply
>>>>> 
>>>>> 
>>>>> To
>>>>> 
>>>>> cmlhope@googlegroups.com
>>>>> 
>>>>> CcBcc
>>>>> Cc        
>>>>> 
>>>>> Bcc       
>>>>> 
>>>>> 
>>>>> 
>>>>> Replies will be sent from wa2...@gmail.com
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>>>>>  
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>>>>> 
>>>>> 
>>>>> Sans Serif
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