Thanks John. 
I was in remission a few months after being on Sprycel.  After a few months I 
was tested often. Then we changed it to every 3 months.  It was during these 3 
months that I lost my remission and my counts went way up.  A blood test was 
taken to see if I had a mutant against Sprycel--I did, therefore I was changed 
to Ponatinib.  No change to blood so far.   If you have no response by 3 months 
they will take me off.  
I pray it will work. 
Why so many tubes of blood?  They only take 2 from me. 

Prayers & Blessings Jeanie 18's 🐠🐠

> On Feb 3, 2015, at 10:49 AM, John Barrons <jl...@rogers.com> wrote:
> 
> I was philly 100% positive until I was on ponatinib. I did then have a 
> molecular change that reduced the Phillies to around 50%. I don't know where 
> they are now but I will try to find out tomorrow. I can't remember how long 
> it took to have the change, but it wasn't long, maybe three months???. How 
> did your platelet count get so high? I have check up every two to three 
> weeks, sometimes weekly.  Last Wednesday they took 11 tubes of blood (yikes). 
> I will find out the results tomorrow.  John
> 
> Sent from my iPad
> 
>> On Feb 3, 2015, at 9:49 AM, 'Icandoallttc' via CMLHope 
>> <cmlhope@googlegroups.com> wrote:
>> 
>> That's great john!!
>> Tkis are very expensive in the US.  My Sprycel was over$10,000 monthly. I 
>> haven't gotten the price of the ponatinib yet but I heard it was high. 
>> I have Medicare part D that pays most of the cost.  It hasn't worked for me 
>> yet--this is day 9--how long did it take for it to work for you?
>> 
>> Prayers & Blessings Jeanie 18's 🐠🐠
>> 
>>> On Feb 3, 2015, at 9:37 AM, John Barrons <jl...@rogers.com> wrote:
>>> 
>>> Hi all I get my ponatinib on compassionate considerations. How much does it 
>>> cost in the US? In Canada all the drugs are at no direct cost, but don't 
>>> ever think we don't pay for them some where along the line. John
>>> 
>>> Sent from my iPad
>>> 
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