Wendy's email. 
caligirlny...@aol.com

Sent from my iPhone

> On May 30, 2016, at 8:48 AM, 'Jeanie' via CMLHope <cmlhope@googlegroups.com> 
> wrote:
> 
> I was wondering if you could give her some advice.  She is set up for a BMT 
> but can't decide.  Thanks
> 
> Sent from my iPhoneI love to see people get on this page and talk about 
> living with CML rather than dying from CML... I believe if you truly want to 
> see the face of cancer walk into a transplant doctor's office... Amazing 
> thing is they too are living! From those without masks on their fave they 
> smile, others chuckling in conversation... Funny part is now that I'm typed 
> and ready to go for stem cell transplant I'm dragging my feet... My CML has 
> presented signs of acute and waiting to see if more meds will work is playing 
> with fire but here on a higher dose I wait because now I'm finally scared of 
> dying... Maybe it's because I was just in a hospital in long term care vented 
> and traked and I remember like it was yesterday my youngest on the phone 
> crying in my ear as they held it there when was I going to come home and me 
> looking out the window wondering if I was ever gonna leave or dye trying,.. 
> There are photos of me in a coma machines covering me but the one that hurts 
> me the most that I still cannot bear to look at is of my teenage daughter 
> asleep in a hospital chair at the foot of my bed... If the doctors had it 
> their way I would be into my pre 30 day transplant mode but instead they wait 
> for me to say go... I believe I truly can't until I feel in my heart I will 
> survive... I'm supposed to be the strong one! Can any stem cell transplant 
> survivors tell me what is going to happen because right now the uncertainty 
> is what's killing me and the internet doesn't help! I'm going to start a blog 
> documenting my life through this process hoping it will help others... Lord 
> knows I will have plenty of time on my hands when I do say Go... Thanks for 
> reading if you made it YaY! LoL
> 
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