Thanks for the update Peg......I am glad that things sound a bit more stable 
for you...I do understand about not wanting to share with others if your road 
is hard so as to not scare us, ..but truly, each of us is unique, and our 
bodies respond very differently to treatments..so, please don't worry. Getting 
good support is also key to quality of life, as it's a lot less lonely...and 
together we can persevere... I am so sorry you have had to go through all that 
you did....I hope and pray that it somehow gets easier for you...wow...2 years 
at zero is marvelous, but the price you have paid........I don't have words for 
that..except you are so resilient, so amazing....take good care and know that 
you are cared for and loved here...


18's, love and hugs,
Beth



-----Original Message-----
From: Myvety2k via CMLHope <cmlhope@googlegroups.com>
To: cmlhope <cmlhope@googlegroups.com>
Sent: Tue, Feb 2, 2016 2:24 pm
Subject: Re: [CMLHope] Just wanted to check in with folks I remember



Peg, that was my Aunt's name.  Anyway, don't be a stranger.  All of us that 
have CML are in the same boat but taking different drugs.  I've been on Gleevec 
16 years 1 month, yes their are side effects but done that I can't handle.  
Cramps are the worse but I'm still here driving my wife crazy and she love's 
every second of it :)....
 
greenie
club member #48
 

In a message dated 2/2/2016 1:55:33 P.M. Eastern Standard Time, 
peg....@live.com writes:
  
Hi all,   
Thought I would check in today...it has been a while.  I see lots of   new 
names, but still a few that I remember.  I am now two years at zero   
detectable on only 100mg of Tasigna daily...1/4th of the recommended dosage.    
It got a bit rocky for a while, not from the CML, but along that course   they 
diagnosed me with five other, assume-ably unrelated, cancers including   skin, 
gastric, thyroid and lungs!  While I never lost my hope, I didn't   wanted to 
dim anyone else's hope by sharing news from my scary corner.   However, as of 
last month, all cancers are regressing, some we know for   certain are also due 
to Tasigna, and well, the others they are not sure why,   so I choose to 
believe it is also because of the Tasigna...and faith!  I   am battling some 
malnutrition issues that were from a severe reaction I had to   Gleevec when I 
was first diagnosed six years ago, but now knowing what those   are we are 
slowly making improvement towards gaining back a quality of life.    You can 
never underestimate the value of quality of life!  I hope   you are all finding 
your own quality, never give up on that.  You are   never far from my thoughts 
and prayers!  
  


  
Six years and still here! 
  
Fight on!!!
  
peg
  
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