Thank you so much, Greenie!!!  I've been so busy since Saturday I'm just now 
able to read these replies...you guys are the greatest!  I'll e-mail tomorrow, 
real sick with a chest cold...




Susan F. Zimmerman



-----Original Message-----
From: Myvety2k <myvet...@aol.com>
To: cmlhope <cmlhope@googlegroups.com>
Sent: Sat, May 18, 2013 2:00 pm
Subject: Re: [CMLHope] Re: posting my blood panel results today



Hi Susan, my daughter's name is Susan.  I live in South Fort Myers, minutes 
from the Golf, it's a 55 and older community .  I've been going to Northwestern 
University School of Medicine since 1999.  It's just 2 blocks south of the John 
Hancock building.  They call it the Robert H. Lurie Comprehensive Cancer Center 
of Northwestern University.  675 North St. Clair Street Suite 21 which is the 
21st floor.  Chicago, IL. 60611.  You can call 312-695-0990.  They have a team 
of Doctors that you would work with. My Doctors name is Jessica K. Altman MD., 
theirs Olga Frankfurt, MD,MS. theirs Dr. Leon C. Platanias, MD, PhD, just to 
name a few. How you would get in their I don't know unless you just call, or 
have your Doctor refer you to Northwestern.  I know one thing they are good and 
the area is very safe, easy parking right across the street.  Parking garage 10 
stories high.  I think they charge $10.00 for 7 hours and you get your receipt 
stamped at the desk before you leave.  Their pretty tight lipped and won't give 
out any information about other patients.  Which is O. K. by me.  And they have 
a great cafeteria to eat your lunch.  It's a big place, takes up a couple city 
blocks.  You should check it out and it's and easy drive.  If you want you can 
email me and give me your phone number and I'll call you and we can talk.   
myvet...@aol.com. 
 
Hope this helps,
 
greenie
 
In a message dated 5/18/2013 8:58:57 A.M. Eastern Daylight Time, 
rszim0...@aol.com writes:

Hi Greenie,   


  
I am from Indiana also, and looking for a good doctor in the Chicago area   
that knows a lot about CML.  Do you suggest someone at Northwestern or do   you 
know anyone at University of Chicago?  Dr. Druker's nurse told my   friend of a 
name, Dr. Larsen who is at U. of Chicago if he has not retired or   moved.  My 
latest FISH test showed 17.74 number, which gives me some   cause for alarm.  
Anyone have any opinion about that?  I'm the one   who hasn't had any medicine 
for six years and 2 months now.

  
I live in the South Bend/Granger area, and do not   have faith in any of these 
local doctors.  Where do you live,   Greenie?
  
Thanks and 18's,
  
Susan F. Zimmerman
  
"Look among the nations and watch; be utterly astounded!  For I will   work a 
work in your days which you would not believe, though it were told   you."  
Hab. 1:5


  
-----Original   Message-----
From: Myvety2k <myvet...@aol.com>
To: cmlhope   <cmlhope@googlegroups.com>
Sent: Thu, May 16, 2013 6:32   am
Subject: Re: [CMLHope] Re: posting my blood panel results today

  
  
  
Hi Beth, when I first started STI571 at Northwestern back in   Jan. of 2000 in 
a study sponsored by Novartis, Northwestern not Novartis   told me that as long 
as I stay alive they would supply me with the drug.    This new study is 
sponsored by Northwestern, I didn't mean to get Novartis   involved with my 
email I think they wanted someone that was of my age,   73 that's been on 
Gleevec for over 13 years.  I don't know   anything about the 2 other people 
involved in this study.  I asked one   time about the 7 other people that were 
in the first study back in 2000 and   they said they can't give out any 
information about them.  Seven of them   were from Chicago land and I was the 
only one from Indiana.  I don't even   know if any of them are still in any 
study or alive.
  
 
  
greenie 
  
 
  
  
In a message dated 5/15/2013 8:03:53 P.M. Eastern Daylight Time, 
bkbar...@aol.com writes:
  
OK. I     just got confused, You said you were in a new study with two others.  
   Always looking at options! Thanks. Feel good!! Beth


    
-----Original     Message-----
From: Myvety2k <myvet...@aol.com>
To: cmlhope     <cmlhope@googlegroups.com>
Sent:     Wed, May 15, 2013 6:33 pm
Subject: Re: [CMLHope] Re: posting my blood     panel results today

    
    
    
Hi Beth, I'm not taking anything put I am going to check     into it.
    
 
    
greenie
    
 
    
    
In a message dated 5/15/2013 6:11:22 P.M. Eastern Daylight Time, 
bkbar...@aol.com writes:
    
Greenie, are you on ponatinib? Let me       know. Beth


      
-----Original       Message-----
From: Myvety2k <myvet...@aol.com>
To: cmlhope       <cmlhope@googlegroups.com>
Sent:       Tue, May 14, 2013 6:36 pm
Subject: Re: [CMLHope] Re: posting my blood       panel results today

      
      
      
Hi Beth, Northwestern University and it's supported by       Novartis.  
      
 
      
Greenie
      
 
      
      
In a message dated 5/14/2013 6:15:54 P.M. Eastern Daylight Time, 
bkbar...@aol.com writes:
      
GReenie, glad your cml is         doing so well. What new study are you in? Beth


        
-----Original         Message-----
From: Myvety2k <myvet...@aol.com>
To: cmlhope         <cmlhope@googlegroups.com>
Sent:         Tue, May 14, 2013 3:56 pm
Subject: Re: [CMLHope] Re: posting my blood         panel results today

        
        
        
HI Suzieq,  I went to Chicago on May 1st to see         my Doctor, get my blood 
work and pickup my med's.  My son and is         wife and my 7 month old 
grandson picked me up at Midway.  Doctor         told me that I need not come 
back for (1) year only to pickup         same.   She said if I want to I could 
see a cancer Doctor here         in Fort Myers once a year that way I would be 
getting my month work         every 6 months instead of every 3 months.  It's 
up to me.  So         that's good news and they put me into another study with 
2 other people         plus some in other countries.  Good to here your doing 
O.         K.
        
 
        
Greenie
        
 
        
        
In a message dated 5/14/2013 4:43:53 P.M. Eastern Daylight Time, 
sheila.a.wat...@gmail.com         writes:
        
Jeanie:           


          
So glad to hear these test results.  Just awesome.  I           remember your 
past struggles.  
          


          
I go tomorrow for my sixth month Doctor visit.  Am curious           to see if 
mine are still stable being on 200mgs instead of           the 400. Will be 
hoping for these good blood counts as yours. :)
          


          
God Bless,
          
Suzieq
          
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