And a very good morning to you Jeannie,

I hope that your doing well.

As you probably already know I also have a home in Pennsylvania, it is in a
small town called Lackawaxen which is near Honesdale and Hawley. It is
located in a rustic community called Masthope which is a skiing community
on top of a 1,250 foot mountain.

Unfortunately I was not able to go there this past summer because I must
stay in Florida waiting for a call for a kidney transplant. We usually go
up there every summer but I also miss being up there because of the beauty
of the area.

I am looking to sell it but if I do get the kidney transplant I think I
will hold onto it to be able to enjoy our summers up there.

Check it out, here is a virtual tour to look at.

 http://tours.tourfactory.com/tours/tour.asp?t=894374


Jeannie, if your ever up that way when we are there you are always invited.


18's,

Marty



On Thu, Oct 9, 2014 at 7:57 AM, ICANDOALLTTC via CMLHope <
[email protected]> wrote:

>  Good morning Marty and great one to you I hope!
> I will pray for your kidney, and hope the best results for you daily.
> I am still hanging in there, and know you miss PA.
> That is one beautiful state.
> Cooler weather in FL and it is much welcomed.
> Love,
> Jeanie<3
>
>  In a message dated 9/22/2014 4:27:49 P.M. Eastern Daylight Time,
> [email protected] writes:
>
> I want to thank everyone for their thoughts and prayers. Hopefully
> soon I will finally be able to get a kidney transplant. Until then I
> will just have to hold on.
>
> To answer a question that was asked of me.
>
> I still have my house in Pennsylvania but I couldn't go there this
> summer because I have to wait in Florida for a call for my kidney
> transplant.
>
> 18's
>
> Marty
>
> On Mon, Sep 22, 2014 at 8:19 AM, Myvety2k via CMLHope
> <[email protected]> wrote:
> > Marty, I hoping all goes well for you on the second surgery I know this
> > can't be the must fun thing that you want to go through at this point.
> I'll
> > be thinking of you.  I have connections up above, I'm going to put a
> word in
> > for you so you can get that transplant soon.
> >
> > Take care,
> > greenie
> >
> >
> >
> > In a message dated 9/22/2014 7:00:16 A.M. Eastern Daylight Time,
> > [email protected] writes:
> >
> > Beth, I am very pleased to be hearing that your doing so well. May it
> > even get better fro you and everyone else.
> >
> > I just had another round of surgery on my arm to correct the narrowing
> > in my blood vessels for the fistula in order to get my dialysis. This
> > was done eleven days ago and it still isn't working right so I am now
> > scheduled for another round of surgery this tuesday. This will be the
> > tenth  and it seems that this has been going on every two months so I
> > really need that kidney transplant as soon as possible but I still
> > haven't heard anything as when.
> >
> > I can really use everyones prayers on this, and I thank you for them.
> >
> > 18's,
> >
> > Marty
> >
> > On Sun, Sep 21, 2014 at 11:17 PM, bkbarney via CMLHope
> > <[email protected]> wrote:
> >> HI all. Just wanted to offer my experiece to the mix. I have been on
> >> sprycel
> >> for 4 years in November, with some breaks for back/neck surgeries
> >> unrelated.
> >> In the beginning, I did get very mild PE which showed up on a chest xray
> >> that was done as a pre-surgery clearance test. It was not major. My doc
> >> did
> >> but me on furosimide 20 mgs plus potassium daily..and stated I needed to
> >> stay ahead of any possible swelling side effects if possible. I eat a
> low
> >> sodium diet and take this med religiously in the a.m....sprycel before
> >> bedtime. I am blessed to have no further issues with any PE for the last
> >> 3.5
> >> years. So, in my experience, I believe a daily diuretic with the sprycel
> >> has
> >> truly helped me. I am also on a low dose which maintains me at barely
> >> detectable to undetectable......40 mgs. I am truly blessed. Hope all is
> >> well
> >> with everyone. I miss you all. Still navigating back issues so not on
> line
> >> much at all these days...but keep everyone in my thoughts and prayers.
> My
> >> CML is in good control and I count my blessings....including all of
> >> you...take good care. warm regards, a 18
> >> s.....to all of you.... ( marty still prayng for a transplant..for
> you..)
> >> Beth
> >>
> >>
> >> -----Original Message-----
> >> From: LearnToBallroomDanceOnline.com <[email protected]>
> >> To: cmlhope <[email protected]>; pkshaub <[email protected]>
> >> Sent: Fri, Sep 19, 2014 11:23 am
> >> Subject: Re: [CMLHope] Re: Sprycel side effects
> >>
> >> Hi Peter,
> >>
> >> While it is true that many develop PE while on Sprycel; the upside is
> that
> >> the PE often coincides with PCRU!
> >>
> >> And unfortunately diuretics do not reduce the fluid that actually is in
> >> the
> >> sac that surrounds your lungs. For me it usually takes a break from
> >> Sprycel;
> >> I know that many people avoid Sprycel because of this risk, but to me,
> the
> >> risk of pleural effusion is less of a risk that the ones that come with
> >> Tasigna's Black Box Warning.
> >>
> >> My PE's have been more of an inconvenience at this point and fortunately
> >> clear quickly.
> >>
> >> Best to you all,
> >> Michele
> >>
> >> On Fri, Sep 19, 2014 at 4:54 AM, Peter <[email protected]> wrote:
> >>>
> >>> From what I have read here and elsewhere, it seems to me that Sprycel
> >>> will
> >>> definitely cause PE, it is only a question of WHEN, not IF.
> >>> For this reason, I have avoided this drug like the plague. Currently,
> >>> Tasigna is keeping at a 3.2 log reduction, which is a sub-optimal
> >>> response.
> >>> My doctor keeps telling me, that PE is "easily controlled with
> >>> diuretics".
> >>> However, I have not heard this from anybody else.
> >>> Does anyone here know anything about the use of diuretics to control
> PE?
> >>>
> >>> Peter
> >>>
> >>>
> >>> On Monday, September 8, 2014 11:33:33 PM UTC-4, grammie wrote:
> >>>>
> >>>> Have been reading the reports of various CMLers having side effects
> from
> >>>> the various TKIs.  Jut wanted to weigh in with my husband's latest
> >>>> experiences.  He was short-winded and family doc ordered a chest X-ray
> >>>> which
> >>>> revealed some effusion.  We reported this to Dr Talpaz (his CML
> >>>> specialist)
> >>>> and Dr T wanted him to have an echogram which we were able to do
> locally
> >>>> with his regular cardiologist.  Dr T said to quit taking Sprycel
> >>>> immediately
> >>>> and not to continue until he and the cardio conferred.  As of now, he
> >>>> will
> >>>> have another echo in a week to see if there is any change one way or
> the
> >>>> other.  He has an appointment with Dr Talpaz in Michigan the middle of
> >>>> October and it sounds like they are going to have him stay off Sprycel
> >>>> until
> >>>> at least then.  It's kind of scary being off the medication that you
> >>>> know is
> >>>> saving your life.  But Dr T is not concerned.  Don't know where this
> is
> >>>> going next.  All part of the journey.  Continue to pray for all the
> >>>> warriors
> >>>> out there.
> >>>> Thank you for your input.
> >>>>        Joyce in IL
> >>>
> >>> --
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