Hi Richard and all, I know you are on pins and needles waiting for your  
blood report; I always am and then so relieved when it comes back good.  I  
pray you have good results.  Glad you are settled in your new place and  hope 
you enjoy it.
I am still alive and kicking hehe.  I have some side effects but  learning 
to live with them.  Sinus headaches seem to be the worse.   The side pain I 
have could be as simple as IBS or ? Who knows?
I am trying a new blood pressure med, clonidine, but it is making me  so 
tired; probably won't be on it for long.
I am still on 100 mgs Sprycel daily; no telling what is doing to my body,  
but we don't have much choice it seems.
Going to Moffitt on the 11th of Aug.
Blessings
Jeanie<3
 
 
 
In a message dated 7/26/2014 11:36:24 P.M. Eastern Daylight Time,  
[email protected] writes:

I haven't seen any new messages for about a week. I hope everyone  is doing 
well.  We are settling into our new apartment but of have a lot  of little 
things to do.  I can't get used to this getting older bit, so  go harder 
than I should making recovery longer.  Fortunately, our  calendar shows no 
appointments for the next 5 weeks.  All the doctors I  have seen this month are 
putting me in a holding pattern until I get results  from the CML testing.  
That is great news, as that wll let all of them  helping to solve whatever 
is happening one priority at a time.  Most of  us how the TKI's side effects 
our livers, spleen, kidneys. Some of my Heart  Meds are also heavy duty that 
effect the same organs.  I also learned  this week that persons with 
Sjogrens Syndrome have to be watchful of the drugs  they take because those 
drugs 
neutralize the TKI's. The first round of testing  will begin in Oct. and I 
should have results by November.  


Wishing all Warriors the best health possible.  Please work on  finding the 
postive about your on situation.  


I will close with Marty's 18s  (life).


Richard H.





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