Hi Susan,

Thank you so very much for your encouragement and for your prayers.  I am sure 
that they help so much.  It's very early, but I intend on going back to bed.  I 
only sleep a couple of hours at a time.  I'm up taking my Tasigna now and then 
in another  hour I'll take my Thyroid meds. so I have it down to a system.  I 
don't sleep well because of the pain I have.  I think that the therapy is 
helping my pain some, but it's going to take a lot of time to get this right 
arm to move the way it should.  I am not giving up, never do. Once again, thank 
you so much for your caring.  I do hope that this finds you doing well.  I 
always keep you in my prayers, along with everyone suffering from this CML, and 
especially for those who have other issues with either side effects or other 
things.  I know that others are suffering as much or more then I am.  You take 
care of yourself and let me know how you're doing.

Hugs, Millie





----- Original Message -----
From: Susan Zimmerman <[email protected]>
To: [email protected]
Sent: Wed, 05 Mar 2014 22:11:34 -0500 (EST)
Subject: Re: [CMLHope] Marty

Dear Marty and Millie,


Thank you both for updating us on your status.  I am adding you both to my 
intercessors' list at my church.  We send out important prayer requests to 
interested prayer warriors from my church.  We will be praying for you both to 
improve as soon as possible.  My heart goes out to both of you in your battles. 
 I'm believing for your quick comebacks!!!


Love and prayers,

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: Marty Gartenberg <[email protected]>
To: cmlhope <[email protected]>
Sent: Wed, Mar 5, 2014 8:04 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]> 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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