Hi Angie, and what a wonderful story.  I hope your kidney gets better  
congrats on your 13 years of hope and fight.
I too, have high potassium, but it only went really  high once.   I had to 
have special treatment, but everything you eat is high in potassium so  it's 
the quantity that is really important.  It's like a weight watchers  diet 
really.
Good luck and keep on going on.
Jeanie<3
 
 
In a message dated 3/13/2014 3:59:16 P.M. Eastern Daylight Time,  
[email protected] writes:

18's to you Marty. You are such a loving wonderful human being...I am  
thankful you are able to be here with us. Thank you for your prayers for all  
of 
us..they are returned to you...May the light you shine on all of us,  
continue to shine over you as well. Still praying for that kidney....
 
Beth



-----Original  Message-----
From: ANGELYN ESDERS <[email protected]>
To: cmlhope  <[email protected]>
Sent: Thu, Mar 13, 2014 8:24  am
Subject: Re: [CMLHope] Aniversary 13


 
 


Good luck to you, Marty....
I passed 13 years with CML this past December. I have  complications in the 
kidney also. I gave my brother a kidney in 1979. Sadly,  my remaining one, 
that has been working solo for those 35 years, is  starting to decline. I am 
on a special diet of low potassium and trying hard  to control my blood 
sugar
in order to preserve the kidney. Nobody promised us that Life would be  
easy.
We must take JOY in all that we do, concentrate on the positive and let  go 
of the negative as well as we can. I firmly believe that if we are not  
happy then our meds are not working to their full capacity.
18's to you...
Angie


What lies behind us and what lies before us are tiny matters compared to  
what lies within us....
Angie



 
 

From: Marty Gartenberg <[email protected]_ (mailto:[email protected]) >
To: [email protected]_ (mailto:[email protected])   
Sent: Thursday, March 13,  2014 9:00:12 AM
Subject: Re:  [CMLHope] Aniversery 13



 
 
 
Hi Dawn,


You are a shining example of what 18's means. You  are also an example for 
everyone to see that no matter how it effects them  they are still alive 
because of something that was not around when I had CML.  I had no other viable 
choice but to have gone through a bone marrow transplant  almost 24 years 
ago. Everyone that is reading this is a survivor and should  keep that in 
mind. 


I would like to bring someone up. His name is Skip, and he has had CML  for 
over 36 years, I believe now going on 37 years, and is currently not on  
any TKI's but is still alive. I know him personally and I know that his mind  
is what is controlling his body. This man has such a great attitude that we  
should all take an example from him, I know that I do.


I truly love each and every one of you because you are fighters which  few 
can understand because they don't know what we all go through and still  
keep on "ticking". I am proud to call you my extended family.


Just one more thing to say: When I read about someone being PCRU I am  over 
joyed because of all the advances that have been maid because of all the  
ways CML is now being treated. Mark my words, before to long CML will be a  
disease that will be no more, just like Polio was once. A simple vaccine took 
 care of that and so it will be for CML. For those that are not PCRU, then 
so  what, because it is only a bunch of numbers and you are all still alive. 
 


Before my bone marrow transplant I was given only a fifteen percent  chance 
of survival. I went into this but said to myself, "hey, this is only a  
number" and I am still here and alive. It is like the doctor telling his  
patient you have only six months to live, and the doctor died shortly  after.


Remember what I have said many times. It is your mind that can help to  
control your body. Try and live by that and you will be a much happier person.  
I am not here to preach to any of you but simply trying to help in any way  
that I can. As I previously mentioned, your all part of my extended family. 
 


As most of you know, I have been going through some difficult times and I  
have been getting so many prayers and good wishes that I just want to return 
 it to all of you. My mind is truly helping me through every day that I  
live.


Now you know why I end each and every post with those two numbers 18's  
(the symbol for life) to all of you. 


Marty





18's to each and every one of you.


Marty



On Wed, Mar 12, 2014 at 11:02 PM, DAWN  RODEGHIER 
<[email protected]_ (mailto:[email protected]) > wrote:


 
17 for me, been on Gleevec since it was approved in the US, I  also go 
Monday to my Onc. I still get the cramps in different parts of the  body but 
that's better than the alternative. 



 
 

From:  Richard H <[email protected]_ 
(mailto:[email protected]) >
To: [email protected]_ (mailto:[email protected])  

Sent: Tuesday, March 11, 2014 11:13  PM
Subject: [CMLHope]  Aniversery 13


 


I have passed my 13th year with CML.  Monday I will meet  with my ONC for 
the results on my blood tests.  My CBC was eactly where  it should be so I am 
praying for good results.  About a month ago I  noticed a spring in my 
steps to coffee club and increased energy. I will  report the findings after I 
get them.  


I am praying for all, and so glad Marty is feeling better and able to  join 
on line.


Richard H.   

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