Hello All,
Paul and I have had a very busy week with Dr.'s. We went to a surgeon
on Wednesday. He does the robotic surgery. We like him and he answered
most of our questions...only down fall he made us wait for 2 hours in
the waiting room. Nurse said he takes him time with patients and after
meeting him I believe it is true. So, while annoying I suppose knowing
when our turn comes around he will give his full attention and not be
in a hurry.
He has done roughly 400 surgeries on his own and over 600 where he
assisted. I realize assisting does not matter as he is not the one
controlling the robot. He also gave us his email address when we left
in the event we have any more questions. He told us Paul was a good
candiate for any treatment he chose.
This brings me to our next Dr. on Thursday we saw a radiologist
oncologist. I have to tell you on our way to the visit we were feeling
like we might be interested in brachtherapy. The Dr. was great. We
were with him for an hour and a half. He also talked about Paul being
a good candidate for any of the treatments. He was very detailed and
attentive.
First, we have felt exhausted with two days of DR's. The good thing,
all our reading and this group helped us know what both Dr.'swere
talking about. It was exhausting all the information coming at you but
I can only imagine what it would have felt like not being informed.
Our decision....Robotic surgery. I think it is done RLRP on the
site...is this correct? Can anyone tell me what further research we
might do on the surgeon and the hospital? There are only two Da
Vinci's in the DFW area. The hospital we will go to is a physcian
owned hospital. I am not familiar with it. It located some distance
from us. The oncology Dr. liked the group of uro were are using. I
worked in the business part of a hospital for 10 years. We knew the
best Doc's by way of nurses and word of mouth.
We feel relieved to have made our decision. I slept better last night
than I have in some time. We will plan for November.
Thanks to everyone for all your information and sharing your stories.
I hope as we go our experience will aid someone else just beginning
this journey. I know we still have the roughest part of the journey to
go but we are on our way.
Lisa
Paul & Lisa - 29 Sep 2006 13:31 GMT
Sorry it now posted 2 x's...crazy!
> Hello All,
>
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>
> Lisa
I.P. Freely - 29 Sep 2006 21:45 GMT
> Sorry it now posted 2 x's...crazy!
Correction: 4.
Please use the SNIP key generously, folks.
What a great example of the benefits of top posting when appropriate and
of the clutter that results from not using the SNIP key.
I.P.
>> Hello All,
>>
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>>
>> Lisa
I.P. Freely - 29 Sep 2006 21:39 GMT
> we still have the roughest part of the journey to go
Presuming treatment goes by the book, that may not be true. Successful
surgery and radiation are no big deal unless they lead to UNNECESSARY
side effects (i.e., bad side effects due to operator error rather than
necessity due to cancer stage). After all, you've already handled the
initial chock of joining the club, the realization of how complex this
stuff is, much of the research, and making a choice among the available
evils (treatments) available. Of the remainders -- treatment and
recovery -- the former is rote and out of your hands and the latter is
just weeks of soreness plus maybe months of impaired functions. Big
whoop! You're out of the woods until and unless SEs -- all of which beat
advanced cancer -- last too long and/or the tx ultimately fails and you
have to hit the books all over again and make some even tougher choices
among adjuvant treatments. You can worry about that if and when the time
comes due to recurrence or to your onc's recommendation for further tx.
I.P.
Steve Kramer - 29 Sep 2006 23:17 GMT
Making the first decision for treatment is probably the most difficult part
of prostate cancer. Don't look back -- and rest easy.
> Hello All,
>
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>
> Lisa