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Medical Forum / Diseases and Disorders / Prostate Cancer / August 2006

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limey - 24 Aug 2006 20:32 GMT
After a PSA reading of 66.5, my husband had a biopsy about two and a half
weeks ago and was  diagnosed with advanced prostate cancer which has spread
to the bones, even to the sternum and clavicle, so you can perhaps realize
how concerned we both are.

Actual details of the biopsy are not known, since the urologist is now on
vacation.  The next appointment with him is not until September 18.  In the
meantime, my husband was placed on 14 days
of Casodex.  He will get his first Lupron shot on Tuesday and one every four
months thereafter.  He has been told that surgery and radiation are out.

We know absolutely nothing about the intent of these drugs, nor their side
effects.   At this point, he feels flushed and sweaty quite often during the
day.   Can anyone tell me/him how he will feel after the Lupron shot, and
what the side effects will most likely be?  It's good to have a little
knowledge rather than going into this blind.

We know nothing of the "language" of prostate cancer, e.g., Gleason,
grading, etc., that I've read here so please bear in mind we're both
greenhorns.

Any information, help and support would be most appreciated.  Thank you.

Dora Crawford
for Henry Crawford

Signature

limey113@yahoo.com

Bob Anthony - 24 Aug 2006 21:35 GMT
Dora:

It would help the group if you can provide his age.

B.A.
limey - 24 Aug 2006 23:13 GMT
> Dora:
>
> It would help the group if you can provide his age.
>
> B.A.

He's 82.

Dora
Steve Jordan - 24 Aug 2006 21:47 GMT
On August 24, Dora wrote:
> After a PSA reading of 66.5, my husband had a biopsy about two and a
> half weeks ago and was  diagnosed with advanced prostate cancer which
> has spread to the bones, even to the sternum and clavicle, so you can
> perhaps realize how concerned we both are.
Seems to me that I've seen Dora's posts elsewhere, but I disremember
where. So if I repeat what I've previously written, I beg pardon.
> Actual details of the biopsy are not known, since the urologist is now
> on vacation.  The next appointment with him is not until September
> 18.  In the meantime, my husband was placed on 14 days
> of Casodex.  He will get his first Lupron shot on Tuesday and one
> every four months thereafter.  He has been told that surgery and
> radiation are out.
Surgery and radiation as primary treatments (txs) would likely not be
curative. Radiation can, however, be used sometimes for palliative tx of
bone metastases (mets).
> We know absolutely nothing about the intent of these drugs, nor their
> side effects.   At this point, he feels flushed and sweaty quite often
> during the day.   Can anyone tell me/him how he will feel after the
> Lupron shot, and what the side effects will most likely be?  It's good
> to have a little knowledge rather than going into this blind.
See the authoritative website of the Prostate Cancer Research Institute
(PCRI) at:
http://prostate-cancer.org/index.html
Search on "Androgen Deprivation Syndrome" (ADS) and on "High Risk PC."

No one can say with certainty what if any SEs (side effects) he will
experience. Virtually all of them can be alleviated at least so some
extent. The place to go for trustworthy information is the above website.

Having said that, I can say this: a very common but not inevitable SE of
ADT (androgen Deprivation Therapy) with Lupron and like meds is hot
flushes. These are normally controllable, and the above site on ADS will
provide very useful information. I controlled mine with an injection of
Depo-Provera in august, 2005. No hot flushes since then. But what helps
me might harm others and vice versa. Therein lies the risk of relying
upon anecdotes.

> We know nothing of the "language" of prostate cancer, e.g., Gleason,
> grading, etc., that I've read here so please bear in mind we're both
> greenhorns.
Everyone here was a greenhorn, and we still are to some extent.

The PCRI website also includes an extensive glossary. It also covers
every conceivable aspect of PCa.

Regards,

Steve J

"Never -- never -- never give up!  Never go gently.  There will be plenty of
gentle after we die, so until then -- fight -- control the rhythms and tempo
of the dance, even when you have to let the PCa dancing bear lead for awhile
-- even when you have to wear the lead suit as you dance -- never let the
bear set the rhythm and tempo of your dance with life -- when the bear
finally takes control, it will be a very hollow feeling for him, because I
will be gone -- dancing in a better place."
--E. B. (Burns) Mixon, PCa survivor, June 14, 2005 on The Prostate
Problems Mailing List
Thank you, Burns. Live long and prosper.
limey - 24 Aug 2006 23:21 GMT
> On August 24, Dora wrote:
>> After a PSA reading of 66.5, my husband had a biopsy about two and a half
>> weeks ago and was  diagnosed with advanced prostate cancer which has
>> spread to the bones, even to the sternum and clavicle, so you can perhaps
>> realize how concerned we both are.

Yes, I originally posted (prior to Henry's biopsy) to
sci.med.prostate.cancer.  A poster there suggested I write to this group.

> Seems to me that I've seen Dora's posts elsewhere, but I disremember
> where. So if I repeat what I've previously written, I beg pardon.

blind.

> See the authoritative website of the Prostate Cancer Research Institute
> (PCRI) at:
[quoted text clipped - 23 lines]
> Regards,
> Steve J

Thanks, Steve.  I'll look it up.  The more knowledge, the better.

Dora
DrYew.com - 24 Aug 2006 21:51 GMT
Dora, Sorry about your struggles. Can I ask, Henry's age?

The casodex is an anti-androgen. It blocks the testosterone receptors
in the body.
Prostate cells (among many others) are sensitive and require
testosterone to live
and grow. Testosterone production by the testicles and adrenal glands
is complicated.
It is signaled and regulated in a very cyclical manner. Lupron or
Zoladex are LHRH
analogues (act like LHRH). Initial dose of LHRH will initially signal
your body to
STIMULATE testosterone, so you will have a surge. This means MORE
testosterone,
which in turn would STIMULATE the prostate cancer cells. This is why
you block
the receptors 2 weeks prior with casodex. Think of it like musical
chairs. If you
have a fixed number of chairs, and they are all filled with casodex, it
doesn't
matter if there are 10 testosterones looking for chairs or if there are
500.. all the
chairs (receptors) are filled. What if he didn't take casodex? Usually
nothing. But,
if he already has evidence of bone lesions, especially in
weight-bearing areas
(spine, legs), the Lupron will cause an initial flare and a spike in
testosterone
which in turn could, theoretically, increase his risk of pathological
fracture. Why
do we use Lupron if it stimulates testosterone? Because the way we give
lupron
is in a depot injection. It's steady and long-lasting, not cyclic like
"natural" LHRH.
After the initial spike, the ongoing presence of LHRH will then shut
down almost
all testosterone production, and hence slow prostate cancer growth.

Prostate cancer is very complex. It's easy to get overwhelmed with all
the info.
Henry's biopsy at this point, is probably of less importance compared
to his
findings on bone scan. If I had to guess, I'd predict he'll have
Gleason 8 or
higher. Gleason grade is a measure of how the cells look under a
microscope.
Think of it like "color". Red cells tend to be very aggressive, and
blue cells tend
to stay where they are and grow slowly. What's more important in
Henry's case
than biopsy grade is his stage. Stage means "where is it in my body
right now?"
Is it just in the prostate? fat just outside the prostate? lymph nodes?
bone?

I have some basic info on my website under "Prostate Cancer" at
www.DrYew.com

I agree with your docs. It seems Henry already has evidence of systemic
disease.
Therefore, there is likely not much benefit for a local treatment
(radiation or surgery),
unless he has local symptoms like bleeding in the urine, or urine
blockage.
He needs a systemic treatment. (hormones, chemo, or both).
Best wishes.

===
http://www.DrYew.com
http://www.SanDiegoRoboticProstatectomy.com
*IMPORTANT* Any comments by me are for general informational purposes
only, and should never be used to diagnose or recommend  treatments for
any condition without face-to-face consultation with a qualified
health-care provider. Thank you.
===
> After a PSA reading of 66.5, my husband had a biopsy about two and a half
> weeks ago and was  diagnosed with advanced prostate cancer which has spread
[quoted text clipped - 21 lines]
> Dora Crawford
> for Henry Crawford
limey - 25 Aug 2006 00:39 GMT
> Dora, Sorry about your struggles. Can I ask, Henry's age?

He is 82.   I have saved and printed your message and thank you for such a
comprehensive reply.   If I may, I would like to be back in touch with the
group when we find out a little more.

Dora
limey113@yahoo.com
NICK - 24 Aug 2006 21:55 GMT
> After a PSA reading of 66.5, my husband

How old is he?

>  In the  meantime, my husband was placed on 14 days of Casodex.
> He will get his first Lupron shot on Tuesday and one every four
[quoted text clipped - 4 lines]
> what the side effects will most likely be?  It's good to have a little
> knowledge rather than going into this blind.

http://www.rxlist.com

http://www.fda.gov

The side effects will scare the life out of you.

Damned doctors don't tell patients half the story.

"This is chemical castration.  You'll lose libido.  You'll become
impotent."

But they won't mention "arthritis" and heart/lung problems, etc. etc.
etc.
limey - 25 Aug 2006 00:43 GMT
> limey wrote:
>
>> After a PSA reading of 66.5, my husband
>
> How old is he?


> http://www.rxlist.com
>
[quoted text clipped - 9 lines]
> But they won't mention "arthritis" and heart/lung problems, etc. etc.
> etc.

Henry is 82.   Many thanks for the links, Nick.  I will look up the info.

Dora
Beverley - 24 Aug 2006 22:32 GMT
Hi Dora, and welcome to the club that no one wants to join.

I'm sure right now you are spinning and just trying to get a grasp on what
you have been told. I'm not a doctor; I'm just a wife of a prostate cancer
(PC or PCa) survivor. Obviously your husband has PC which has metastasized
(mets). Gleason, grades and all the rest don't mean anything right now.
First this cancer is treatable. It has spread so there is no cure for it at
this time. I hope by now you have an appointment with a good radiation
oncologist (rad-onc) or an oncologist.

Take things one step at a time. There's lots to learn. Spend some quality
time together and learn together. When you are ready you can go to
http://www.phoenix5.org and look up end stage for prostate cancer. The thing
you have on your side right now is time. Use it wisely.
(HUGS)
Bev

> After a PSA reading of 66.5, my husband had a biopsy about two and a half
> weeks ago and was  diagnosed with advanced prostate cancer which has spread
[quoted text clipped - 21 lines]
> Dora Crawford
> for Henry Crawford
limey - 25 Aug 2006 00:44 GMT
> Hi Dora, and welcome to the club that no one wants to join.
>
[quoted text clipped - 14 lines]
> (HUGS)
> Bev

Thanks, Bev, for the support and the link. It means a lot.

Dora
Beverley - 25 Aug 2006 02:16 GMT
My father-in-law has had his cancer return. He is on Lupron and has done
very well now for several years. He's 84. Age is a big factor so the odds
are your husband will hopefully die with it rather than from it.

We are all here to help in any way that we can. Most of us have some
knowledge because we've been through so much. I know only a wee bit about
your husband's cancer at this stage. I do know that they can do some
radiation to the areas where they see mets but I'm not sure just what it
does. I also know they tend to give something to help retain bone density.

Bone mets can be serious. Mets to a leg can cause a fall because the leg
will break, not because the fall caused the break.

This is still very treatable cancer. I've seen PSA's in the 800's and more
on this group so a 66.5 is still high but probably within the parameters of
giving him several more good years. His PSA tests once he's on the Lupron
will be an indication as to the extent that the Lupron is keeping his cancer
controlled.

As I said before I know very little about this stage of prostate cancer. But
I'll do anything I can to help you or to help you find the information you
need. There are several guys here with advanced prostate cancer and I'm sure
they will chime in, too.

Where are you located? (State/Providence/Country)

I'll keep you in my thoughts.
Bev (posted and emailed)
limey - 25 Aug 2006 20:04 GMT
> Where are you located? (State/Providence/Country)
>
> I'll keep you in my thoughts.
> Bev (posted and emailed)

You have no idea what all this support means to me right now.   My husband
is still dealing with this himself and doesn't want it mentioned to anyone.
I feel like I'm leading a double life.
Your words were a big encouragement and are very comforting.  Thanks, Bev.

He gets his first Lupron shot on Tuesday and sees the urologist again on
September 18.

We live on the Eastern Shore of Maryland.

Dora
Steve Jordan - 25 Aug 2006 20:18 GMT
On August 25, Dora wrote:
> You have no idea what all this support means to me right now.   My
> husband is still dealing with this himself and doesn't want it
> mentioned to anyone. I feel like I'm leading a double life.
It is sometimes difficult for a man to admit that he needs help. Let's
hope that the light will soon dawn.

(snip)
> He gets his first Lupron shot on Tuesday and sees the urologist again
> on September 18.
I wonder what a uro, who is a surgeon, can effectively do in this case
when surgery is, I understand, not an option. I hope that the Lupron is
prescribed by a cancer specialist, an oncologist.

Regards,

Steve J
limey - 26 Aug 2006 19:56 GMT
> On August 25, Dora wrote:
>> He gets his first Lupron shot on Tuesday and sees the urologist again on
>> September 18.

> I wonder what a uro, who is a surgeon, can effectively do in this case
> when surgery is, I understand, not an option. I hope that the Lupron is
> prescribed by a cancer specialist, an oncologist.
>
> Regards,
> Steve J

There are a lot of questions we need answered.  I have wondered about the
exact point you raised - I don't know who is on their staff or whether Henry
gets sent elsewhere to an oncologist.  The urologist felt that speed was of
the essence in starting him on Casodex, followed by Tuesday's Lupron shot.
The dr. is  still on vacation but we're compiling a list of questions.  This
has all been such a rush that we don't even know what options there are, as
far as treatments and specialists.

Dora
Steve Kramer - 25 Aug 2006 20:52 GMT
> You have no idea what all this support means to me right now.

I've not had an opportunity to answer any of your questions before you got
great answers from others.  But, rest assured, we know the importance of
this newsgroup.  99% of us were diagnosed with cancer.  Probably more than
half have advanced cancer.  You and Henry are among friends.

> My husband is still dealing with this himself and doesn't want it
> mentioned to anyone.

I was the same way.  My wife finally convinced me to tell people other than
her an my children.  I was finally convinced when I realized how hard it was
on her to know and have no one to talk to.

> We live on the Eastern Shore of Maryland.

Hey Bev!  Just a short jaunt up I-95.
Beverley - 25 Aug 2006 21:59 GMT
Nope that would be out of the way, she's up RT 13.

The Eastern Shore is a very beautiful, lush farm area surrounded by lots of
fishing villages, and a few summer resort towns against the Atlantic Ocean
on one side and the Chesapeake Bay on the other. Rt 13 used to be a little
two lane highway now it is a big 4 lane divided one with McD's and other
fast food restaurants, Walmarts, and just about every gas station you can
imagine. I remember when we had to take the children to see their
grandparents and there was almost nothing between here and Salisbury MD (the
only big town) on the ES. We used to put the little child potty in the car
because the kids could never make it. There were only 2 gas stations before
Salisbury and they had horrible bathrooms in fact one barely had a door on
it. (Be thankful it flushed?)  I also learned never to make peanut butter
crackers ahead of time, they get soggy - just take the crackers and the jar
of peanut butter. It is still a deadly stretch of road and over the years
I've seen the most horrific accidents on Rt 13. I still hate the drive but
the landscape is beautiful!
Bev

> > You have no idea what all this support means to me right now.
>
[quoted text clipped - 13 lines]
>
> Hey Bev!  Just a short jaunt up I-95.
limey - 26 Aug 2006 20:01 GMT
> Nope that would be out of the way, she's up RT 13.

No!  We're not up Route 13.  That's a long way from us.   We're off Route 50
(on the way to Ocean City), about 15 miles east of the Chesapeake Bay
Bridge.  A really long way for you, Bev.

Dora
limey - 26 Aug 2006 19:58 GMT
"Steve Kramer"  wrote >
> "limey"  wrote >
>> You have no idea what all this support means to me right now.
[quoted text clipped - 10 lines]
> than her an my children.  I was finally convinced when I realized how hard
> it was on her to know and have no one to talk to.

I hope my husband soon realizes that but here's where it really helps to
have this group.

>> We live on the Eastern Shore of Maryland.
>
> Hey Bev!  Just a short jaunt up I-95.
No - we're a long way from Bev.

Dora
Steve Kramer - 27 Aug 2006 02:30 GMT
> "Steve Kramer"  wrote >
>> "limey"  wrote >
[quoted text clipped - 19 lines]
>> Hey Bev!  Just a short jaunt up I-95.
> No - we're a long way from Bev.

Dora,

If you stick around, you'll see people from Canada, UK and Australia on a
regular basis.  200 miles is real close!
Roy - 25 Aug 2006 21:39 GMT
> You have no idea what all this support means to me right now.   My husband
> is still dealing with this himself and doesn't want it mentioned to
[quoted text clipped - 3 lines]
> He gets his first Lupron shot on Tuesday and sees the urologist again on
> September 18.

Talking about it is a very good thing. I was just diagnosed this month.
Surgury is scheduled for 9/18. And one of the things that I have been able
to determine is that communicating with others allows one to learn that
prostate cancer is a very large club - meaning that many men will
unfortunately get to join. But knowing how common this is has helped me put
my head back on straight. And finding from others that everyone knows
someone that has this, actually brought me comfort. One of the things about
civilization is the knowledge that we are not alone. Sharing brings comfort.
Is this a life changing event? I'm sure it will be. But we adapt. One thing
I read from the info at the Mayo's web site on prostate cancer is to make
each day include something that makes you happy.
limey - 26 Aug 2006 20:05 GMT
"Roy"  wrote > >>

> Talking about it is a very good thing. I was just diagnosed this month.
> Surgury is scheduled for 9/18. And one of the things that I have been able
[quoted text clipped - 7 lines]
> One thing I read from the info at the Mayo's web site on prostate cancer
> is to make each day include something that makes you happy.
Very true, Roy.  By nature I am a pretty darned happy person and love to
laugh and joke.  I'm getting ready to put that hat back on.

Dora
MAS - 26 Aug 2006 00:02 GMT
Dora,

I have APCa (advanced prostate cancer) and have had for 4 1/2 years. I am
currently 59 years of age. Two years ago I had 2 spots in my spine that
indicated metatasis. Today I have none and the bone is completely healed.
PSA is an undetectable level. Now that could change next month, and will
probably change within two years. But such with PCa.

A Urologist diagnosed and I sought out two Radiation Ocologists for primary
treatment. After it was obvious that primary treatment failed, BOTH
recommended that I see a Medical Oncologist who specializes in Prostate
Cancer. Although both offered to treat, both said if they were in my shoes
it is what they would do. They were very careful to say that a Medical
Oncologist would not do me any good; it had to be one that specializes in
PCa.

I selected one that has researched the disease for 25 years in a research
hospital. He sees no patients on the outside, only in the Geniurological
Clinic. All of his patients are enrolled in clinical trials.

At 82 and with treatment your husband has plenty of years left!

Some excellent comments have been offered by this group. It is a wonder
support group. Keep us informed and find a person that specializes in
Prostate Cancer.

Take Care.

Gourd Dancer

> My father-in-law has had his cancer return. He is on Lupron and has done
> very well now for several years. He's 84. Age is a big factor so the odds
[quoted text clipped - 28 lines]
> I'll keep you in my thoughts.
> Bev (posted and emailed)
limey - 26 Aug 2006 20:11 GMT
> Dora,
> I have APCa (advanced prostate cancer) and have had for 4 1/2 years. I am
[quoted text clipped - 14 lines]
> hospital. He sees no patients on the outside, only in the Geniurological
> Clinic. All of his patients are enrolled in clinical trials.

Great advice.  Our son has also ecommended checking on clinical trials.

> At 82 and with treatment your husband has plenty of years left!
>
[quoted text clipped - 4 lines]
> Take Care.
> Gourd Dancer

The group is a godsend and one I really need right now.   I'm passing all
the info along to Henry (who can't type worth a darn).

Dora
ron - 25 Aug 2006 21:05 GMT
Hi Dora...I'm sorry to read that your husband has been diagnosed with
advanced prostate cancer (PCa).  Given your husband's age, I suspect
that quality of life (QOL) is important to him (and you).  The androgen
deprivation therapy (ADT) route that you are embarking upon is
practiced at some point by most men with advanced PCa.  Many of the
other posters have discussed the effects it can produce.  For some men
it hardly has an effect, for others it can be devastating.  Effects can
include bone density deterioration, mental acuity, lethary, hot
flashes, predisposition towards other diseases, etc..  Prior to the
discovery of the Casodex - Lupron (Avodart/Finasteride) approach, men
used estrogen to suppress testosterone levels.  From what I read in the
various newsgroups and in the press, some men are beginning to use this
old approach once again.  Estrogen therapy has potential drawbacks
(breast enlargement), but the former concerns involving blood clots and
DVTs seem to have been addressed by using the trans-dermal application
route rather than oral administration.  As opposed to drawbacks,
estrogen seems to have a beneficial effect upon overall well-being
(QOL).  I'm not advocating estrogen therapy in your case, but just
wanted to make you aware that it is an available option.  You should
discuss estrogen therapy vis-a-vis ADT with an oncologist who
specializes in prostate cancer so that you can make an informed
decision.  BTW once you start ADT or estrogen therapy, it doesn't
preclude switching to the other therapy.

In terms of PCa oncologists, one of the best lives back your way in
Virginia, Dr. Charles "Snuffy" Myers, he himself is a prostate cancer
survivor.  You can Google his name or use this link to get contact
information

http://www.healthsystem.virginia.edu/internet/news/experts/myers.cfm

He is widely respected and used by many...Best wishes and good health,
ron
limey - 26 Aug 2006 20:19 GMT
> Hi Dora...I'm sorry to read that your husband has been diagnosed with
> advanced prostate cancer (PCa).  Given your husband's age, I suspect
[quoted text clipped - 29 lines]
> He is widely respected and used by many...Best wishes and good health,
> ron

Many thanks for all the info.
I'm afraid that Charlottesville is a long way from us and therefore not
practical.   We do, however, have Johns Hopkins some 60 plus miles or so in
Baltimore.   My son has strong connections there and could probably follow
through if my husband wanted him to get referrals.
We'll have to see where this is heading and what the urologist has in mind,
so my husband can make an educated decision.

Dora
Steve Kramer - 27 Aug 2006 02:42 GMT
> practical.   We do, however, have Johns Hopkins some 60 plus miles or so
> in Baltimore.   My son has strong connections there and could probably
> follow through if my husband wanted him to get referrals.

Johns Hopkins....  Johns Hopkins...

Seems like I should know that name.

Just kidding.  The book that was "the bible" for prostate cancer when I
first got it was Dr. Patrick Walsh's "Guide to Surviving Prostate Cancer."
Dr. Walsh is a Johns Hopkins doc.
tchtic@yahoo.com - 25 Aug 2006 22:32 GMT
> After a PSA reading of 66.5, my husband had a biopsy about two and a half
> weeks ago and was  diagnosed with advanced prostate cancer which has spread
[quoted text clipped - 4 lines]
> vacation.  The next appointment with him is not until September 18.  In the
> meantime, my husband was placed on 14 days

Hello Dora,

Everyone here understands your situation very well.

Here's the bad news. Your husband has cancer and barring a miracle,
it's incurable.

That's about it for the bad news.   The good news is that the treatment
that you mentioned will very likely surpress the cancer for a long,
long time.   Possibly beyond his expected life span.

The question then is, aside from the cancer, how's his health?  Blood
pressure, cholesterol, how's he feeling?   Is he a young 84 or is he
ailing?    Does he get out and around, active in hobbies, sports?  The
good news is that he can continue these activities.  In fact, he should
make an effort to get more exercise.

The Lupron will surpress his testosterone, drive it to zero.  With zero
testosterone, the cancer will get very lazy, even start to shrink.  It
will probably come back but a Lupron and other treatments, such as spot
application of radiation, the docs may keep it at bay for 5, 10, or 20
years.

The Lupron has many, many side effects.  These include the hot flashes,
he can get by that by keeping the temperature down and there are
medications that help.

Lupron can aggrevate joint pain, cause memory loss, induce
irritability, and so on.  Type Lupron Depot Side Effects into google.

He should monitor his blood chemistry, not just cholesterol, everything
that they commonly test for including blood sugar.

The other side effect is that Lupron zero's out libido and erections
and orgasms are a thing of the past.  I'm mad about this one.  Some
fellows report that they can "perform" while on Lupron but wasn't my
experience.

Good luck to you and your husband.  Take him to "the Fisherman's Inn"
on Kent Island, I like to have lunch there.
limey - 26 Aug 2006 20:29 GMT
<tchtic@yahoo.com> wrote >

> Hello Dora,
>
[quoted text clipped - 6 lines]
> good news is that he can continue these activities.  In fact, he should
> make an effort to get more exercise.

Other than the big C,  he's in great shape, exercises a lot in the yard
(which is big, with the usual grass and flowers plus vegetables) and stays
as active as possible.  He's a "man's man" and fights being babied!

                   <snipped and saved>

> Good luck to you and your husband.  Take him to "the Fisherman's Inn"
> on Kent Island, I like to have lunch there.

Hey - our favorite place!  We had dinner there last night and are there
frequently.    It's only about 10 - 12 miles from our house, which is in the
wilds of nowhere.

Thanks for writing.  I really appreciate it.

Dora
I.P. Freely - 26 Aug 2006 21:34 GMT
> He's a "man's man" and fights being babied!

Bollix! Tell 'im it takes a REAL man to admit it when he needs help.

I.P.
Beverley - 26 Aug 2006 22:28 GMT
I figure that the restaurant is probably only about 35 miles as the crow
flies from hubby's parent's home in DE. I think my husband's sister used to
keep her boat over in that area. We'll have to check it out some day.

It would be something of a fishhook off of Rt 13.
Bev

> <tchtic@yahoo.com> wrote >
> >
[quoted text clipped - 25 lines]
>
> Dora
limey - 26 Aug 2006 20:32 GMT
To everyone who has been kind enough to write me, I can't express my thanks
enough.  You have done a great deal to put us back on an even keel.

I'm embarrassed that this thread is so long but felt I had to respond
personally to every person who wrote.   If I may, I'll keep you posted as we
go along.

Dora
I.P. Freely - 26 Aug 2006 21:29 GMT
> I'm embarrassed that this thread is so long
This is a short thread.

> but felt I had to respond personally to every person who wrote.
Not necessary, not the norm, and sometimes impairs further responses by
providing apparent closure. It's more efficient for both you and us to
lump comments in one post and not post similar comments to similar posts.

>  If I may, I'll keep you posted as we go along.
That's what we're here for.

I.P.
Steve Kramer - 27 Aug 2006 02:49 GMT
> To everyone who has been kind enough to write me, I can't express my
> thanks enough.  You have done a great deal to put us back on an even keel.
>
> I'm embarrassed that this thread is so long but felt I had to respond
> personally to every person who wrote.   If I may, I'll keep you posted as
> we go along.

Nonsense, Dora.  We are not offended if you respond to each of us
personally.  However, we might be if you didn't keep us posted..  :-)

Signature

PSA 16 10/17/2000 @ 46
Biopsy 11/01/2000 G7 (3+4), T2c
RRP 12/15/2000 G7 (3+4), T3cN0M0 Neg margins
PSA  .1  .1  .1  .27  .37  .75
EBRT 05-07/2002 @ 47
PSA  .34 .22 .15 .21 .32
Lupron 07/03 (1 mo) 8/03 (4 mo), 12/03, 4/04, 09/04, 01/05, 5/05, 10/05,
2/06, 6/06
PSA  .07 .05 .06 .09 .08 .132 .145
Casodex added daily 07/06
Non Illegitimi Carborundum

Peter Headland - 30 Aug 2006 02:13 GMT
> After a PSA reading of 66.5, my husband had a biopsy about two and a half
> weeks ago and was  diagnosed with advanced prostate cancer which has spread
> to the bones, even to the sternum and clavicle, so you can perhaps realize
> how concerned we both are.

It's at times like this that I wish I were religious, because then I
would be able to pray for you both. As it is, you are in my thoughts
and I hope things go well for you and Henry. Everything happens slower
as we age, including the spread of cancer, and PCa is generally a slow
moving beast anyway, so the ADT should keep you going for a good while
with any luck at all. Fingers crossed, stay positive, and post here any
time you feel down and need a little sympathy.

One note I didn't see from others - ADT can cause osteoporosis, so be
on the watch for that. Treatments exist if needed, some oncologists may
prescribe them preemptively.

Signature

Peter Headland

NICK - 30 Aug 2006 04:54 GMT
Dora Crawford wrote:

> The next appointment with him is not until September 18.  In the
> meantime, my husband was placed on 14 days of Casodex.  He
> will get his first Lupron shot on Tuesday and one every four
> months thereafter.
> Can anyone tell me/him how he will feel after the Lupron shot,
> and what the side effects will most likely be?

You can locate some side effects at   http://www.fda.gov
and search for LUPRON.  The data below is from another site.

Lupron Side Effects and Drug Interactions

Body as a whole - Asthenia, General pain, Headache/Migraine (65%)

Cardiovascular System - Hot flashes/sweats 98%, shortness of breath

Gastrointestional System - Nausea/vomiting

Metabolic and Nutritional Disorders - Edema, Weight gain/loss

Musculoskeletal System - Joint disorder - osteoarthritis, ankylosing
spondylitis

Nervouse System - Decreased libido, depression/emothion lability
(22%),
                                Dissiness, Nervousness, Neuromuscular
disorders,
                                Paresthesias

Urogenital System - Breast changes (enlargement)/tenderness/pain

Hemic and Lymphatic system - Decreased WBC

Central/Peripheral Nervous System - Peripheral neuropathy, Spinal
         fracture/paralysis

Urogenital Syem - Prostate pain

Body odor, flue syndrome, palpitations, appetite changes, dry mouth,
thirst, ecchymosis, lymphadenopathy, anxiety, insomnia/sleep disorder,
delusions, membor disorder, personality disorder, hair disorder, nail
disorder,
conjunctivitis, ophthalmologic disorders, taste perversion.

Changes in Bone Density
In controlled clinical studies, when LUPRON DEPOT 3.75mg was
administered for 6 months, vertebral bone density as measured by
dual energy x-ray absorptiometry (DEXA) decreased by an average
of 3.2% compared with the pretreatment value.
When LUPRON DEPORT 3.76 was administered for 3 months,
bertebral trabecular bone mineral density as assessed by
quantitative digital radiography (QDR) revealed a mean decrease
of 2.7% compared with baseline.
        Use of LUPRON DEPOT for longer than 3 months in the
       presense of other know rish factors for decreased bone
       mineral content may cause additional bone loss and is not
       recommended.

Lipids - Triglycerides were increase above the upper limitn of normal
in 12% of the patients who received LUPRON DEPOT 3.75mg.
HDL (good) cholesterol fractions decrease below the lower limit.
LDL (bad) cholesterol fractions increased above the upper limit.

Postmarketing
  Like other drugs in this class, mood swings, including depression,
have been reported.  There have been reports of suicidal ideation
and attempts.
Patients should be counseled on the possiblity of development or
worsening of depression during tratment with LUPRON.

03/06/2006
 
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