Hello everyone. 
So glad everyone is checking in.  Thanks for all the updates. 
This is my 16 th day on ponatinib.   No major side effects so far. Going to 
doctor tomorrow to get blood done.  Also getting a cat scan done. Pray that my 
counts are on the way down.  


Prayers & Blessings Jeanie 18's 🐠🐠

> On Feb 11, 2015, at 2:00 PM, "'Marcie Goodman' via CMLHope" 
> <cmlhope@googlegroups.com> wrote:
> 
> Hi SusieQ,
> 
> Good to catch up with you. I know that same worry when you go from undetected 
> to a positive reading. And you are correct that we aren't cured even if 
> undetected, just cells hiding due to our TKIs.  Hang in there and please let 
> us know the results in March
> 
> Marcie
> 
> Sent from my iPhone
> 
>> On Feb 11, 2015, at 9:44 AM, Suzieq <sheila.a.wat...@gmail.com> wrote:
>> 
>> Hello CML Survivors:
>> 
>> It's been some time since I stopped by and left word.  Thought that I should 
>> check on ya'll.....sorry to hear of the troubles you are having Marty.  I do 
>> hope you receive your Kidney and all goes well.  Jeanie...I see you are 
>> having a few problems once again and I hope that the doctors can get you 
>> back on track. So many newer drugs now than when we all started our journey 
>> with Gleevec.  
>> 
>> My last doctor visit was December 31st.  Had really good blood work results 
>> and all looked good until I got my BCR-ABL results back.  They did not tell 
>> me that they were going to use a new lab.....instead of sending it to where 
>> they always did,  they (Sitemen Cancer Center) are now doing the testing 
>> in-house.  I knew that the results had come back a lot quicker.   Nothing 
>> like what I was use to, no graph, nothing.  Just said "Positive"  & 0.02%.  
>> I fell apart.  Course this was around 7:00 at night when I had picked up the 
>> mail after going to the movies. My husband was out of town.   The next 
>> morning (Friday), I called and left a message for the doctor to call me 
>> back. It was around 4 that afternoon when the NP called me back and we had a 
>> nice chat. That's when she told me that "we really can't go by these results 
>> since we are using a new lab.  And,  it was a "more sensitive" test."  I 
>> asked her if I should up my dosage (remember I have gone from 400mgs. down 
>> to 200, & now to 100mgs. since I've been "non-detected" since July '09.  She 
>> told me no, to stay doing what I've always done and that if I wanted to come 
>> back in earlier than the ever six months as normally, I could.  So, we set 
>> that up where I will go back next month (March) the 25th and be retested.   
>> 
>> I guess I was so use to seeing that "non-detected" over a long period of 
>> time, that it gives one that false belief that we are in total remission and 
>> the CML is gone.  It's like my husband & I discussed......a few of the 
>> leukemic cells are still there all along,  just do not show up unless they 
>> use deeper tests.  This positive test brought me back to reality and 
>> reminded me exactly what Dr. Khoury told me in the beginning of my journey, 
>> "There is no cure for CML yet."   
>> 
>> So, there's my story. I guess we will always be in this fight for the rest 
>> of our lives.  I'm hoping to continue on just the 100mgs.,  but if I need to 
>> go back to the higher dosage, I will.  
>> 
>> Keep Looking Up,
>> Suzieq
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