Hi all and yes we each have other health issues but fighting our blood cancers 
us a battle we all share.  I'm glad you are winning your battle. Fight on 
warrior. 

My Motto: Faith and Pills❤️
With 💗Jeanie 🐟🐟18,s 
Dx 1/2004. CML Leukemia
Started Gleevec 2/2004
Started Tasigna  9/2009
Started Sprycel 11/2009
Started Ponatinib January 2015
Dr Balducci Moffitt Cancer Center

> On Feb 3, 2016, at 11:41 AM, 'Susan Zimmerman' via CMLHope 
> <cmlhope@googlegroups.com> wrote:
> 
> Hello Peg,
> So glad to hear from you!  We are tough, us CML bunch.  We can take it if you 
> want to share with us the additional battles that have gone along with your 
> CML.   We are here to encourage!  You don't need to suffer alone, (altho I'm 
> hoping you have a good family, etc.)  Your battle could have involved fear, 
> as most people would let it in.  But just to remind, fear is False Evidence 
> Appearing Real, put there by the enemy.  Can you think of one thing that is 
> good about fear?  Same goes for worry.  No, they are only destructive.  Many 
> of us have come to the place where we know our bodies are only one third of 
> our whole being, and probably the least important of the three. (body, soul 
> and spirit).  So we try to let the other two rule our thinking, our outward 
> actions, and so on.  I know because of your faith you walk by faith, not by 
> sight!
> 
> I just thought of a good joke that came from facebook.  A big picture of a 
> huge grisly bear roaring.  The caption read, "Fear NOTHING!  Except a grisly 
> bear, because they will kill you."
> 
> Anyway, so glad your reports are getting better all the time. I hope you 
> enjoy your days and come back to share a word with us often!  We have missed 
> you!
> 
> 18's and blessings,
> Susan F. Zimmerman
> "Look among the nations and watch; be utterly astounded!  For I will work a 
> work in your days which you would not believe, though it were told you."  
> Hab. 1:5
> 
> 
> -----Original Message-----
> From: bkbarney via CMLHope <cmlhope@googlegroups.com>
> To: cmlhope <cmlhope@googlegroups.com>
> Sent: Tue, Feb 2, 2016 3:36 pm
> Subject: Re: [CMLHope] Just wanted to check in with folks I remember
> 
> 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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