Marty for President
 
greenie
 
 
In a message dated 11/12/2014 8:53:58 P.M. Eastern Standard Time,  
[email protected] writes:

Marty,


What a lovely email to Sue. We are traveling together and I feel like you  
are the Captain of our ship!


Thinking about you and keeping you in my prayers 


Love and 18s,


Marcie

Sent from my iPhone

On Nov 12, 2014, at 8:34 PM, Marty Gartenberg <[email protected]_ 
(mailto:[email protected]) > wrote:




Oh yes Sue, family. Well you know what they say? You can pick  your friends 
but your family is here to stay good or bad. No matter what you  can't 
change them.  


As my father used to say, "never argue with a moron, fool, idiot or  liar 
or someone that won't listen to what you have to say because no matter  what 
you try to tell them they will never change. 


But your focus shouldn't be on them but people that are willing to help  
you. That is what this site is all about as you can see.


When you travel on your journey all of us will be traveling along with  
you. I really mean that, and you will see that your not alone but with some  
very nice people that will be supporting you along.


18's,


Marty


On Wed, Nov 12, 2014 at 4:25 PM, smgedit <[email protected]_ 
(mailto:[email protected]) > wrote:


Hi,
First off, I love your terminology! (I'm a writer and editor by  trade). 
Secondly, thanks for your support. I'm limiting who knows and who  doesn't 
know what is going on for now but unfortunately one of the  ignorant statements 
was by a family member. Oh well. I'm happy to have  found this site and to 
be meeting nice people like you on  it.    Sue



Hi Sue,  


I read your post and just wanted to make some comments. Personally  I think 
that your hanging around with some people that I would classify  as Anal 
Orifices. And I only say that to be polite. Or even more  possible they suffer 
from Rectal Cranial Inversion (their head is up  their Azz.


I have to tell you that if one of them had CML or any other type of  cancer 
then they would certainly have a different attitude.


I hate to say this but sometimes you should keep some things to  yourself 
because of people like that. The less they know about you then  the better it 
will be for you.


Anyway, now that is off my chest let me go into something more  important. 
First, you have come to right place. All of those that are  here are very 
compassionate and really care about each other. They have  already gone 
through this and will be very happy to help you out with  any questions and 
anything else they can and will help you with  this.


CML is not what it used to be because it is not a "death sentence"  
anymore. There have been so many improvements in it's treatment,  not like in 
my 
day. I don't know what you may know about me but I am  here to help you out in 
any way that I can.


If you have read any of my posts you will see what I mean. Remember  any 
time that you would like to post anything please feel free to do so.  I would 
like to welcome you to this site.


Sue, whenever I end any of my posts I end it with two numbers 18  which is 
the symbol for life.


18's to you Sue.


Marty


On Wed, Nov 12, 2014 at 10:23 AM, smgedit  <[email protected]> wrote:


I was diagnosed with CML a little over a month ago and had a bone  marrow 
biopsy and started taking Gleevec last week.  I'm trying  to learn as much as 
I can about CML and my oncologist is great about  giving detailed 
explanations and answering questions. But I was  wondering if anyone else ever 
got 
what I consider a strange reaction  from others about my news. In the past 
week, I've had people say the  following things to me which upset me a lot.


"So what's the big deal? So you have to take a pill...I have to  take this 
antibiotic for my tooth infection this week too."


"There is so a cure for leukemia. Plenty of people are cancer  free. You 
don't know what you are talking about."
(This after explaining about the drugs and "response," vs.  "remission." 
etc.)


"Well I hope you have a speedy recovery. Good luck."


I know I can't put my energy into dealing with this right now but  it is 
weighing on my mind anyway. It made me happy to find this group  online where 
I know people can at least "get" it and where some of you  have been living 
with CML for quite a while.


Anyway, that's my first post. Nice to meet you.


Sue

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