Hi Marty and so good to see you back on.  One of our problems with CML  is 
that we can't get our blood checked everyday to see how its reacting to the  
meds so we have to try something for a while and then get it checked.  I  
wish there was a machine that we could use to take our blood daily like a 
blood  glucose machine.  That would be great!
My onc doesn't want to talk about changing doses; he says if it isn't broke 
 don't fix it.
Good luck and blessings,
Jeanie<3
 
 
In a message dated 3/11/2014 8:54:10 P.M. Eastern Daylight Time,  
[email protected] writes:

 
 
 
 
Hi Peg, you seem to have brought up something that is very interesting.  
"Taking vinegar, lemon juice or even Coke with it first, before increasing  
it".


If that works and I have no reason to doubt it, then, I  think that 
everyone that is using it should discuss it with their Oncologist.  


So, you can see what a wonderful group this really is. People  that have 
CML all discussing very useful things to help out each  other.


18's,


Marty



On Tue, Mar 11, 2014 at 9:47 AM, peg <[email protected]_ 
(mailto:[email protected]) > wrote:

Hi Beth,

I know how scarey this is for you.  No one  should have to make choices 
only between bad and worse!  I don't have  much to offer on the problem of 
elevated CPK. That elevation, not a problem  in itself is actually a symptom of 
a bigger problem, myopathy, where the  muscles start breaking down, 
resulting not only in weakness, but damage to  the kidneys.  While I had a 
multitude 
of problems on Sprycel, including  an auto-immune reaction, Myopathy was 
not one of them.  However, I did  have a serious problem with that on Gleevec. 
 The answer for me was to  stop Gleevec and move on to another drug.  Since 
Gleevec was my first  back then, I still had options.   Being on the last 
one now, it  makes the potential for problems a bit more real and scarey.   

I can tell you for me that with all of  these drugs a little goes a long 
way.  Many of the serious side effects  could have been avoided by starting at 
a smaller dose and increasing only in  response to lagging PCR's.  In both 
cases with Gleevec and Sprycel we  started at the normal recommended dose, 
which in hind sight was far too much  for me!  When we started Tasigna in 
Nov, after a three month break, we  monitored my PCR monthly, and within two 
months I was down to trace  detectible, and in the third month I was zero 
detectible.  That was on  1/4th of the normal dose!  I do believe that less 
dose 
equals  less side effect risk.  I also think there is something to 
Michelle's  theory of using vinegar or lemon juice to increase stomach acid 
with  
Sprycel.  This has been confirmed to me by one of the Docs that helped  
develop Sprycel.  If a low dose is not working well over two  consecutive 
PCR's, I 
would try vinegar, lemon juice or even Coke with it  first, before 
increasing it.  That will increase the absorption of the  drug without 
increasing 
the dose itself.  Just something to think  about.

Keeping you in my prayers!

Fight  on,
peg




On Monday, March 10, 2014 10:36:59 AM UTC-7,  Beth wrote:  
Thank you Jeanie, Marty, Millie, and everyone else who send  
prayers...etc..I agree how unbelievably important it is to stay in  community 
and know 
others are there, thinking of you, listening and and  praying each in their own 
way for you and one another. I am still off  chemo...working on back 
pain....calming it down...getting ready to restart  up soon. Did BCR on 
Friday...will see results next week...and go from  there.  I can tell you for 
me that 
with all of these drugs a little  goes a long way.  
As I re uptake sprycel, I am wondering if anyone has had any success  
managing elevated CPK...with anything besides ongoing prednizone use?  Trying 
to 
keep that side effect under control from the get go this  time....thoughts??
 
Love to all of you,
 
Beth



-----Original  Message-----
From: houtz <[email protected]>
To: cmlhope  <[email protected]>
Sent: Sat, Mar 8, 2014 4:07  pm
Subject: Re: [CMLHope] Marty and Beth


Just want you to know that I'm thinking about you and hoping that each day 
you   will improve and get your numbers to where they should be.  I pray 
that you're 
 in remission soon and that you can get back to life and all it has to 
offer.  
 You've been through so very much, and I hope that you can listen to your 
surgeon 
 and not over do things to soon.  It does take a while to get past any 
surgery.  
 Time heals, so please take it  easy and let your recovery happen.  I'm 
dealing 
 with the pain, and having home care is helping as I don't have to leave 
the 
 house to get the blood work done.  They are getting me a meter to be able 
to 
 monitor my blood thinner from home.  I'm not sure if I'll be approved, but 
we 
 shall see.  I wasn't going to get one, but my nurse says I should have it. 
 If 
 it doesn't work for me, then I'll just have to go get the blood work done. 
 I'm 
 not going to think or worry about it. It will either work for me, or it 
won't.. 
 time will tell.
 
 Meanwhile, you take care and keep healing.  Keep us up on how things are 
going 
 for you.   You're always on my mind and in my heart and prayers.  I think 
that, 
 as a group, we do well in helping one another and as Marty says, that is 
what 
 we're here for.... to help one another. and I am a firm believer that it 
works.  
 I've improved so much in the  past few days and I know that it's because 
I've 
 had all of you to say prayers and encourage  me to get better.  Just know 
that 
 my prayers are being said for all of us.
 
 Love and Hugs,
 Millie
 
 
 From: [email protected]
 To: [email protected]
 Sent: Sat, 08 Mar 2014 16:45:15 -0500 (EST)
 Subject: Re: [CMLHope] Marty and Beth
 
 Thanks Beth, I hope everything is good.  Sprycel will get them back  into 
a 
 good place, at least it has worked good for me.
 Keep healing,
 Blessings,
 Jeanie<3
  
  
 In a message dated 3/6/2014 7:39:17 P.M. Eastern Standard Time,  
 [email protected] writes:
 
 hi Jeanie! Glad to hear from you...I don't know what my counts  
are...going 
 tomorrow for BCR, will let you know once I get results   back...I was not 
 in remission when I had to go off for surgery....so I know  without the 
meds 
 and not in remission that my numbers will be up...so going  back on is a 
 priority....
 take care,
  
 Beth
 
 
 
 -----Original  Message-----
 From: ICANDOALLTTC <[email protected]>
 To: cmlhope  <[email protected]>
 Sent: Thu, Mar 6, 2014 4:53 pm
 Subject:  Re: [CMLHope] Marty
 
 
  
 Thanks Beth,
 Hang in there; time will heal.  What are your counts since you have  been 
 off the drug?
 Yes, it's scary off and scary on the drugs.
 Hope everyone gets better, and we will all have a block party.
 Blessings,
 Jeanie<3
  
  
 In a message dated 3/6/2014 5:30:30 P.M. Eastern Standard Time, 
 [email protected]_ (mailto:[email protected])  writes:
 
 Dear Marty and Millie and all my other  CML family,
  
 Just a note to say I am thinking about you, praying for you, holding  you 
 close. I am slowly healing as well...back surgery taking much longer to  
heal 
 than anyone could predict...nerves and wound healing.... somewhat  
 compromised from long term use of our meds...will re-uptake sprycel next  
 week....not what surgeon wants..but too long off becomes too  scary to  
 me....must get 
 numbers back in control.....always a balancing act..for most  I know....my 
 woes seem far lighter than many here, so today I am praying  that MIllie's 
 pain eases and Marty, - the the new fistula  ripens quickly so it can be 
used 
 as soon as possible....hoping a donor  will come any day......
  
 and Pat E...wherever you are, I am praying for you as well....
 take care to all,
  
 love and light,
  
 Beth  
 
 
 
 -----Original  Message-----
 From: Marty Gartenberg <[email protected]_ ([email protected]) >
 To: cmlhope  <[email protected]_ (mailto:[email protected]) >
 Sent:  Wed, Mar 5, 2014 7:04 pm
 Subject: Re: [CMLHope] Marty
 
 
  
  
  
  
 Dear Millie and everyone else,
 
 
 Thank you for your concern.  I am slowly getting back to myself. Dialysis 
 is becoming more difficult and  I am in need of a kidney transplant soon. 
A 
 new fistula was put into my  other arm but it has to mature for another 
month 
 and a half in order to be  used. 
 
 
 Millie, I'm so sorry to hear that you have to go through  all of that. As 
 you pray for me so do I for you and everyone  else.
 
 
 I have to get going now. I'm really tired. Until next time...
 
 
 
 18's,
 
 
 Marty
 
 
 
 On Wed, Mar 5, 2014 at 2:21 PM, houtz <[email protected]_ 
 ([email protected]) > wrote:
 
 I  am so concerned about Marty.  Has anyone heard from him besides me.  
The 
 last I heard was days ago and he was having trouble with his  dialysis and 
 sounded really bad.  If anyone has heard, would you  please put it on our 
 site.  I will write again today and he has  always answered my e-mails, 
even 
 not feeling well.  They were short,  but I knew that he was not doing 
well.  
 If I hear any more, I'll let  you know.  I know that dialysis wasn't going 
 well and don't know if  they were able to use his new port or not.  
Actually, 
 it's not a  port, but has another name that I forget.  I haven't heard 
from 
 any  of you, so if you are checking your e-mails, please let me know 
what's 
  going on with each one of you.
 
 My latest is that, even on 1/2 dose  of the Tasigna, I'm still in 
 remission.  The bad news is that every  muscle and joint in my body is 
screaming 
 and 
 they put me back on Home  Care.  I can hardly do anything.  I did manage 
to 
 go downstairs  for a while today.  My physical therapist came and had me 
go 
 down..  This after noon my occupational therapist is coming to work on my  
 upper body strength.  She made it worse a year ago when she worked on  it, 
so 
 if that happens this time, I'll tell her that I don't want any.  The gal 
 that worked on my legs today was very good, and I want to  keep her.  The 
 other one doesn't listen to anything you tell her. Oh  well, others have 
thrown 
 her out of their house, and I just might do the  same thing.  I have an 
aid 
 that comes every couple of days to bathe  me as I can't get into the 
shower 
 right now.  I'd fall if I tried.  I can't use my walker very well, and 
just 
 getting from my bedroom to  the bathroom is horrible, causing me so much 
 pain.  I have to have  someone with me when I attempt that.  My aid and 
the 
 nurse that comes  a couple of times a week are wonderful.  I had them the 
last 
 two  times I was under home care.  I know that the nurse is going to take  
 blood tomorrow.  That's always fun. :>)  I'm trying hard to  do what I 
have 
 to do.  My wonderful son is doing everything for me  right now and I want 
to 
 get back to the point where I can do things for  myself. Enough about me.  
I 
 just wanted to catch up on these things  with all of you.  I hope that 
 you're all doing as well as you can.  Write and tell me how it's going.  
Thank 
 God for my television,  phone, and computer in my room.  It's nice to be 
able 
 to connect with  the world.  It keeps me out of trouble.
 
 Again, if anyone knows  anything about Marty, please let us all know.  If 
I 
 hear anything,  I'll let you know. Marty has become a good friend to me 
and 
 to others on  our site.
 
 Hugs,
 Millie
 
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