Hi Jeanie,

I would like to tell you and everyone else a story about me and what
recently happened to me.

As you know, I am on dialysis and am also on Warfrin, a blood thinner. In
order to get my dialysis they have to stick two large gauge needles #14
gauge into my arm and into my access point that is under the skin.

Once my dialysis is finished they remove the needles and I have to hold
several gauze pads over my access points for about five minutes in order to
stop the bleeding.

Well, this past Monday the bleeding could not be stopped from my arterial
part of the port called the fistula. I had to hold it on for more then an
hour but it still wouldn't stop bleeding so they put a special clamp over
the access points and left it there for another half hour. When they
removed it the blood just started spurting out again.

The clamp was put on once more and it finally stooped bleeding. I went home
with the clamp still on and had dinner. After I finished my dinner I
decided to remove the clamp and it again started spurting out again all
over the kitchen floor. I then put the clamp on again and went to the
hospital for further treatment.

I'm telling you this story for a reason that doesn't as yet make any sense
but you will understand more...

When I arrived at the hospital that took a CBC blood test and told me that
it would be ready in an hour. Now here is where my mind took over. Because
my bleeding was very severe I thought that my platelets may be low. This is
exactly what happened to me twenty three years ago and I was then diagnosed
with Leukemia.

So with this happening my mind started in with what if my Leukemia has
returned, and I started sweating until the results came back.

Now you all know me, but I am still human just like all of the rest of you
but I usually know how to control my mind and feelings and thoughts.
Emotions are very powerful if you can't or won't control them, but this
time it just brought back some terrible thoughts because of what I once
went through. I always try to discipline myself through most things but
sometimes just being human it is something that we must all try to deal
with.

So Jeanie and all of the rest of you, whenever your waiting for the results
of any tests I want you to try and remember that your all human and
sometimes your going to worry about the test results until you get them
back. It is only then that you will have to deal with them, and you will
whether good or bad.

In my case the bleeding was caused by to high an INR level was in my blood
(to thin from the doses of Warfren). The bleeding finally stoped by itself
after four more hours and I was discharged from the hospital after 1:30 AM
and we went home.

I started eating more dark greens and some Broccoli and asparagus and
lessened the dose of Warfren after speaking to my doctor.

When I went back on Wednesday for my four hour dialysis treatment and once
it was finished the bleeding stooped within five minutes, as it usually does

You all remember what I always say, your mind does control your body. CML
is a strange disease it does effect both your mind and body. Even after
these past twenty three years for me, and I have learned to be able to
control my mind.

I feel very close to all of you, or I wouldn't have told you this personal
story.

We must live with what we have, and the key word in that statement is live.

Remember that we are all human.

18's

Marty


On Sat, Aug 17, 2013 at 11:50 AM, <[email protected]> wrote:

> **
> Hi and I did almost the same on Tasi.  I never reached PCRU until I was
> put on Sprycel. This happened almost 6 years after I was dx.
> I saw so much of my doctor the  nurse told me I should put a bed in the
> office.
> I have scars in my arms where they took blood so often.
> I just reached the stage of going every 6 months about 6 months ago, but I
> do have my blood checked by my primary doctor often.
> It's funny about our blood test, we want to see them but we are afraid of
> the results.  I am still afraid after all these years.  I know how you can
> be going along well and then all of a sudden everything goes out of whack.
> Faith and pills get me through each day. Good luck and blessings everyone.
> Jeanie<3
>
>
>  In a message dated 8/15/2013 8:44:21 A.M. Pacific Daylight Time,
> [email protected] writes:
>
>
> I was on Tasignia until it stopped working and had blasts so they
> admitted me to hospital and started oral ponatanib 45mg daily.    Took 2
> solid months of hospitalization for my neutrophils to come down and
> platelets to go up.  Got a unit of blood almost every single day and
> sometimes two, and would get at least one bag platelets per day and often 3
> or more.   Finally my numbers started to pick up and they let me go home.
> I havn't felt what I would call "well" since being on this drug but at
> least they are saying I am in Hematological remission, not molecular but
> that is my goal.  I see my hematologist every week for labs to determine if
> I need another unit of red blood cells and usually my hemologin has been
> running around 8.5 which means I get a unit of blood.   So on Tuesdays i go
> for labs and then return on Wednesdays for blood if needed.    This sure
> beats the alternative - not being well.
>
> On Gleevac I experienced eye bleeds.
>
>   *From:* Susan Zimmerman <[email protected]>
> *To:* [email protected]
> *Sent:* Wednesday, August 14, 2013 4:49 PM
> *Subject:* Re: [CMLHope] Ponatinib
>
> Thanks Maggy for answering.  I'd like to hear more about how you are doing
> on this drug.  Not sure which one they will put me on after determining why
> I am having brain bleed tendencies.
> Was on gleevec for 2 yrs 3 mos, on nothing now for six years because of
> brain bleeds.  Numbers were going up upon last check, tried 15 days of
> tasigna and had an indication again of brain bleeding.  Sept. 4th going to
> Northwestern Univ. again to try to determine the cause.
>
> Blessings,
> Susan F. Zimmerman
>
> -----Original Message-----
> From: [email protected] <[email protected]>
> To: cmlhope <[email protected]>
> Sent: Tue, Aug 13, 2013 2:36 am
> Subject: Re: [CMLHope] Ponatinib
>
>
>
> Yes, been on this drug since around first week of June.  45 mg I
> believe.  Was hospitalized for almost two months while the drug did its
> thing.
>
>   *From:* John Barrons <[email protected]>
> *To:* CML Hope <[email protected]>
> *Sent:* Monday, August 12, 2013 10:53 AM
> *Subject:* [CMLHope] Ponatinib
>
> I have had CML for almost 14 years now. I failed gleevec and sprycel and
> am now on ponatinib. Is there anybody in this group who is on this drug?
>
> Sent from my iPad
>
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