Yes, Richard, just waking up for another day of life gives us  hope to 
fight on.  I think having a goal to reach each day will keep us on  track;  
sometimes mine is just taking a walk or reading a good book or  seeing a good 
movie.  I'm retired but work as long as you can is my  advice.  Keep family 
support if you can and don't be afraid to ask for  help.  My daughter and 
granddaughter take me to my doctor's appointments,  and this uplifts me greatly.
Blessings,
Jeanie<3
 
 
 
In a message dated 12/14/2013 12:23:43 A.M. Eastern Standard Time,  
[email protected] writes:

Yes due to other problems as well as CML I still have mountains  to climb.  
Every day I wake up and see the sun shining over that mountain  top I 
rejoyce that I can climb another foothill.  I continued working  after I was 
diagnosed and it was a struggle as many others do.  


Richard H. 

On Friday, December 13, 2013 1:14:59 AM UTC-6,  Mar wrote:  
Thank you everyone for responding. Feels less like you are on  an isolated 
island... there are no support groups in my area... so, I do  appreciate 
your emails with encouragement and support.   


I was glad to hear there are other medications. I gather this is a long  
journey... to figure out which drug and at what level... not one that can be  
answered quickly. I find the side effects difficult to deal with as I  
continue to work. Not sure if it is possible to work while all of this is  
being 
figured out.  Do most people continue working?    


Richard, diagnosed in 2003 and there are still mountains?  I guess  I am 
expecting to much to soon. 


Beth,  My hematologist specialist didn't put me on the 100mg I was  on at 
the beginning because of the first toxicity. I have been on 20 mg  which 
doesn't seem to be much but, I can't believe my body doesn't even like  the 20 
mg... I just learned today I am back into the toxicity and  cytopenias.   I 
have side effects to Diasanatib I didn't have on the  Gleevec as well. I 
found the 100 mg gave me insomnia, medically induced  depression and rash... I 
only have the rash at 20mg.  But, seem to have  a lot of bone pain lately.


I am giving you all a big hug and thank you for your emails as it is  nice 
to know there are people who understand much more than I do (being such  a 
newbie).  I look forward to hearing from all and learning from you. I  hope 
all of you are doing well in your own journey :) 


Ididn't know that 1and 8 meant life.. will post this in front of me for  
inspiration!


Cheers,
Mar

On Thursday, December 12, 2013 8:25:25 PM UTC-8, Richard H  wrote:  
Welcome to this group.  Almost every one has had  problems adjusting to the 
meds.  Try your best to remain positive as  that seems to help most of us. 
We are here to listen and in return we give  back what we have learned to 
get over this little hill at this  moment.  I was diagnosed in 2003 and the 
mountain I have to climb is  still on the horizon.    


Richard H.

On Thursday, December 12, 2013 8:42:51 AM UTC-6,  Mar wrote:  
Hi, I am new to the group. I was diagnosed January 10 2013.  Since then I 
have been on Gleevec, failed (due to toxicity twice) and  was switched to 
Dasatinib which I have toxicity to as well and had to  stop taking the 
medication. Each time I have had the toxicity my blood  levels are so low that 
it 
takes 4-5 weeks for them (neutrophils,  platelets and wbc's) to go back to 
even the lower range of normal. Thus,  I have not yet had any cytogenic or 
molecular recovery.. if anything, my  last result was going backward. I have 
another appointment on December  19th to see if there is any recovery at all... 
I am keeping my fingers  crossed. It has been quite the roller coaster... I 
am not sure if others  have had the same type of roller coaster in the 
first year.   


I just ran into this group tonight and I appreciated reading others  emails 
about their recovery... thank- you.. Hope to be able to post one  of my own 
recovery stories one of these days.


Mar











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