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]> 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]> 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
>>>> -- 
>>>> -- 
>>>> [CMLHope]
>>>> A support group of http://cmlhope.com
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