That's right Beth, I always say 18's. We must all help each other because
we are all in this together. Not so much me because I already traveled
through this journey. However, I always try to help others simply because
it is the right thing to do.

Times have changed so much since I fought my battle but I wish there was a
group such as this when I needed other peoples help but there wasn't then.
There is now!

18's to each and every one of you.

Marty


On Sat, Jul 13, 2013 at 4:22 PM, <myvet...@aol.com> wrote:

> **
> Well  Said,  Beth     from  greenie
>
>  In a message dated 7/13/2013 2:36:18 P.M. Eastern Daylight Time,
> bkbar...@aol.com writes:
>
> Dear Millie and Pat and Marcie and Norm and Tom and Greenie and Judi,
> Suziq, and Susan, and.....everybody! all our new combers, and our
> oldies...too tired today to list everyone..but just wanted to say that the
> past week, reading everyone's post, has been truly insipiring and helpful.
> We are all in this together. For those who do not have family or spouses,
> for younger or older folks, people of all ages, each of our circumstances
> is different....but what we all share, cml, and it's impact on our lives,
> fears,  , our capacities, our dreams...it's quite profound...sharing it
> means we are not alone and united, as witl the picture Pat sent from the
> conference she recently attended, it just breeds hope for improved futures,
> and more and more possibilities down the road...we need to buoy each other
> when we are down, and help each other to stay strong, manage side
> effects, share with each other whatever we have learned along the way....so
> we stay well held....in this world, and fighting this illness, there is
> strength in numbers.
> I wish everyone a good weekend. ..and Millie, those doctors are going to
> find out what exactly is causing what, get to the bottom of it, and
> hopefully you can get some relief...!!!
> 18's as Marty would say, Beth
>
> -----Original Message-----
> From: C.M. Houtz <ho...@ptd.net>
> To: cmlhope <cmlhope@googlegroups.com>
> Sent: Sat, Jul 13, 2013 11:41 am
> Subject: Re: [CMLHope]
>
>  *Hi Marcie,*
> **
> *I am trying to get myself going today.  I woke up with terrible back
> pain. It's always in the same area and my Onc. says that it's my gall on
> the left side and my liver on the right.  I couldn't get out of bed, so I
> took my pain meds and put some heat on it and was able to get up after an
> hour or so.  I'm still in some pain, but not to bad.*
> **
> *I was on Gleevec for years and it simply stopped working for me.  I was
> on 800 mg. at one point.  I did have a prescription which helped to control
> the diarrhea and for the life of me, can't remember the name.  I still had
> to watch everything that I ate.  I found that anything with tomatoes in it
> was a no-no and other things triggered it too.  On Tasigna, the worst I've
> had is constipation, and, of course, the liver problem.  My Onc. still
> thinks it's the gall causing the problem, and neither of us will know until
> the biopsy comes in.  I'm sure he'll do a lot of blood work on Monday to
> see if I'm still in remission, so I pray that I am.  As far as memory is
> concerned.  I don't feel I've lost any.  I always did have good recall, so
> I feel fortunate in that dept.*
> *I am a loss for a word every now and then, but think that's normal for
> 74.  It does frustrate me, but I find that if I just put it aside, it will
> come to me sooner or later.  Usually, it's such a simple word or name.  I
> do have good long and short term memory though, and that's a good thing.  I
> also feel that the drugs affect my bones and muscles.  I had arthritis
> before all of this, but the progression has been fast and now have
> polymialgia, which is a form of Arthritis.  They do a sed rate check when I
> get blood work, and have me on prednisone for that.  That can fluctuate
> from one blood check to another.  Right now it's bad and I can't lift my
> left arm very well.  It mainly affects me in my neck and arms...shoulders,
> etc.  It's quite painful, so I just deal with it the best way I can.*
> **
> *You are right that people don't understand.  There are times I could
> scream at them, but it wouldn't do any good.  I get told that I look good
> and must be feeling fine, but they haven't a clue.  It is a life time thing
> for us, and so we do the very best that we can.*
> **
> *It is so nice putting a face on you and the others.  I am going to print
> out the photo's and make a small album of all of my CML friends.  *
> **
> *You take care, and we'll talk again soon.  I find that in the past few
> days we've been able to open up more to one another and that's a great
> thing for everyone.*
> **
> *Love, prayers, and many hugs,*
> *Millie*
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