Hello Victoria and Marty
Guess I am one who is  just resting, There are, in the CML community, people
that say, "living so close to people who have CML, one becomes burnt out".
Not sure if this is the case here.  Some others are fighting health problems 
on many fronts, I do read all the posts but as you say "they are few and far
between".  In my case I have had CML for over 35 years, whenever I 
see a new case on here, I feel for them but let them know it is treatable.
Be safe all 
SkipD



________________________________
 From: Martin Gartenberg <[email protected]>
To: [email protected] 
Sent: Saturday, February 25, 2012 4:26:33 PM
Subject: Re: [CMLHope] Digest for [email protected] - 2 Messages in 2 
Topics
 

Hi Victoria,
 
Sometimes some among us just decides to take a break. Sometimes others become 
depressed at what they are reading about others. There could be a host of 
reasons that people are not posting as they once did. 
 
If your talking about the "pioneers" then that is probably what I am. I had CML 
more then 22 years ago. This May it will be my 23rd year. I had a bone marrow 
transplant 22 years ago when the procedure was relatively new and there wasn't 
a lot of information about it. At that time there were no TKI's available so I 
had no other choice of getting onto a blind trial of Alpha Interferon or the 
transplant. 
 
If I were to go into that trial basis I could not be guaranteed if I would be 
receiving it or just a placebo. Since my white blood count was over 486,000 at 
the time and I was about to go into blast chrises I opted for the transplant 
because I had a suitable donor, my sister.
 
So, there you have it, and just try to remember that sometimes people just like 
to keep to themselves unless that are comfortable about discussing their own 
problems with others, many of which are strangers to them.
 
I always end any of my posts with the numbers 18. Those numbers 18 symbolizes 
life.
 
18's to you,
 
Marty


On Sat, Feb 25, 2012 at 9:58 AM, Victoria Reiter <[email protected]> wrote:

It IS strange that no one, or very few, CMLers are posting.  Have we become 
fatigued with focusing on our chronic condition and its side-effects?  How many 
of us have decided just to get on with our lives and to live as fully as we 
can, trusting that Gleevec or the other inhibitors will keep us going?  I think 
we may have forgotten how dismayed (euphemism) each of us was when we were 
first diagnosed and how glad we were to find this website and the information 
and support we received from it.  Perhaps there are other, newer CML websites 
meant to provide information without demanding any personal, emotional 
involvement on the part of the reader.  No doubt pioneers eventually get 
tired.  Maybe that's what's at work here.   
>
>
>On Sat, Feb 25, 2012 at 5:50 AM, <[email protected]> wrote:
>
>  Today's Topic Summary
>>Group: http://groups.google.com/group/cmlhope/topics
>>      * FINALLY RELIEF FROM CRAMPS [1 Update]
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>> FINALLY RELIEF FROM CRAMPS 
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