Oh Jeanie, I am on bosutinib now, not sprycel.  Anybody else out there on 
bosutinib?


18's,

Susan 




-----Original Message-----
From: 'Susan Zimmerman' via CMLHope <[email protected]>
To: cmlhope <[email protected]>
Sent: Tue, May 13, 2014 7:48 pm
Subject: Re: [CMLHope] how much sprycel susan


Thanks Jeanie,
All your adventures finally paid off.  I quit my onc locally because he had 
never heard of bosutinib or posatinib, said I was mixed up on my medications.  
That told me I was not getting the best care possible. Sure glad your nurse put 
in a good word for you.  We have to be pro-active!  I wrote an e-mail to Dr. 
Pinilla at Moffitt, my former onc.  He told me to please go to a university, 
whether it be Northwestern or Univ. of Michigan where he recommended docs at 
both.  So I went with the Chicago one, as it is a little closer.   So far been 
on 100 mg a day for a week now and no side effects yet.  I do take it at 
breakfast. Thanks for the well wishes from all about being able to tolerate 
this last one!



Wishing you all the best of 18's and good health,


Susan
"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: ICANDOALLTTC via CMLHope <[email protected]>
To: cmlhope <[email protected]>
Sent: Tue, May 13, 2014 6:34 pm
Subject: [CMLHope] how much sprycel susan



Hi Susan and so good to hear from you.  I remember I had to take my Gleevec 
with a large meal so I planned large breakfast and it worked for me.  When I 
started on Sprycel I was in the hospital as my platelets and wbc had gone way 
up.  I was having my blood cleaned daily, but it would to right back up after 
they cleansed it.  My onc at the time had me on a high dose of Gleevec (which 
had already quit working for me, and some other drugs.  I kept asking him for 
Sprycel, but he said he wasn't   familiar with it.  Finally a nurse came in 
that had worked for Moffitt Cancer Center and asked me why I wasn't on Sprycel; 
I told her and she must have talked to my onc because he came in and told me he 
was putting me on Sprycel.  
The hospital I was in acted like they couldn't get it so he gave my son a 
prescription and he filled it at Walgreens. He started me on 150 mgs daily in 
the beginning and sent me home.
After a few BMA I was put on 100 mgs daily and have been on that dose ever 
since, and yes it put me in remission after only a few months.
I use to have the EKG quite often but never had a problem so we stopped them.  
I do have them yearly.
I go to my onc now every 6 months, and so far so good.
Keep us informed on your journey with the new meds.
Blessings 
Jeanie<3
 

In a message dated 5/8/2014 6:49:45 P.M. Eastern Daylight Time, 
[email protected] writes:
Thanks Jeanie for your concern.  I must   take the med with food, which will 
change my eating habits, as I usually skip   breakfast.  So now, a breakfast, 
(which is good for me) with it, and no   problems so far at all.  With only 
taking 1/5 of the regular dose, I   shouldn't have any problems!  I forgot to 
tell you guys that the ekg   showed abnormality of my heart, (prolongation).  
I'm just a little over   the designated normal count, but over nonetheless.  
Now they must do an   ekg every time I go to make sure it doesn't change.  
(ugh)  Did the   sprycel put you in remission on the 100 mg a day?  What was 
your dosage   and what is it now?  I hope my numbers will go down without 
increasing   the dose.  

  
18's,
  
Susan F. Zimmerman
  



  
-----Original   Message-----
From: ICANDOALLTTC via CMLHope   <[email protected]>
To: cmlhope   <[email protected]>
Sent: Thu, May 8, 2014 6:19 pm
Subject:   Re: [CMLHope] No Updates?

  
  
  
Hi Susan, please let us know how you do on this new meds.  I am on   Sprycel 
and I remember when I started on it they put me on 3 50mgs   pills.  It wasn't 
long before they downed it to 2 pills daily.  Do   you have to take it with 
water or food?
  
Sprycel put me in remission and was the first drug to do so; I was on   Gleevec 
and Tasi.
  
My prayers are with you on your journey.
  
Blessings,
  
Jeanie<3
  
 
  
  
In a message dated 5/7/2014 9:50:52 P.M. Eastern Daylight Time, 
[email protected]   writes:
  
Hey everyone,     


    
I started on bosutinib yesterday at 100 mg.  Please keep me in     your prayers 
that this medicine will work and I can stay on it without any     stroke 
symptoms, like has happened with all the rest of the drugs.  I     am going to 
Chicago (Northwestern) at least once a month now, next again for     a two-week 
follow-up.  It's a one hour and forty minute drive with no     slow-downs.  I 
make it a fun day.  Last Wednesday my husband made     it a business trip and 
took me along, dropped me off and met again later.      It's easier on my 
nerves when driving downtown!  Dr. Altman wants     to check my reaction to the 
lowest dose in two weeks.  I'm sure it will     be fine......
    


    
They also did an EKG on me and it showed that I do have prolongation     
between heartbeats, just a tad above normal.  This could be why I'm so     
devastatingly tired all the time!  I do not want to develop anything     worse 
from the prolongation, so they will give me an EKG each time I go for     
awhile.  Got to do some homework on this.  Sure have     loved and enjoyed 
being off all medication for 7 whole years.  Dr.     Altman says I'm really 
"special" to have lasted this long.  Don't know     by that if she means 
"crazy" or idiotic, or what....it is what it     is!
    


    
Marty, I     am standing with everyone to pray you will receive a new kidney 
soon...and     Millie, keep pressing the docs about why all these pains are 
gripping you     and what can they do about it.  We have to be pro-active, 
although I     know just getting through the day sometimes is all the 
"pro-active" we can     be!!!  Beth, praying for you, too!
    

    
18's and hang in there,
    
Susan Zimmerman
    



    
-----Original     Message-----
From: C.M. Houtz <[email protected]>
To: cmlhope <[email protected]>
Sent:     Tue, May 6, 2014 11:54 pm
Subject: Re: [CMLHope] No Updates?

    
    
    
Hi     Richard,
    
 
    
I've been thinking     the same thing.  I hope that it means all if okay.  I 
have been     having a lot of Arthritis problems and can hardly move my arms.  
It     hurts to type a lot.  from the elbow down I'm fine, but from the elbow   
  up it's so painful to lift my arms or do anything that requires reaching,     
lifting, etc. What a mess I am..  I try to cope with it, and do some     
exercises that help, but if it hurts to do them, they tell me not to force     
it..  Say prayers for Marty, and Beth as I know they're having their     own 
set of problems.  If you have any left over, pray that my arms will     start 
working well enough for me to accomplish something.  Marty has a     weeks 
worth of tests, doctors, etc. to deal with, and Debbie has her back     issues. 
 I know that this is a CML site, but it seems like other things     get in the 
way that we deal with.  I do hope all is well with     you.  I'll keep watching 
for e-mails from the group, and hope that they     will all be good news.  
Jeanie got kicked off of the Goggle site, and I     can't remember why.  She 
was trying to change things and it took her     down.  I don't think she knows 
how to get back on.  I still e-mail     her and we talk that way, but she was a 
huge asset to our group.  I     forward her messages to you guys, but she needs 
to get hooked up     directly.  I sure don't want to loose touch with anyone.
    
 
    
Talk to you     soon.
    
Love, Hope, and     Prayers,
    
Millie
    
      
----- Original Message ----- 
      
From:       Richard H 
      
To: [email protected] 
      
Sent: Tuesday, May 06, 2014 11:40       PM
      
Subject: [CMLHope] No Updates?
      


      
I haven't seen any new or responses for almost a week.        I hope everyone 
is okay and just busy with life.       


      
Richard H.
      
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