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

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what is a good book on sexual function post prostectomy

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gary.miller12@comcast.net - 14 Sep 2006 03:05 GMT
i was told by my urologist today that the intensity of orgasm can be
degraded after either radiation or surgery of the prostate. it is a
common side effect. Walsh's book states numerous times that there is no
degradation of orgasm intensity since the nerves that deal with it are
not close to the prostate.  my urologist states that the orgasm is
related to ejaculation and that the pelvic floor simulates sexual
excitement stimulation.  what does that mean?  Walsh claims that the
feeling is based in the brain and can be degraded by depression. if it
is purely depression, could a sex therapist or hypnotherapist help?
what is a good book that covers this topic?

gary
Bob Anthony - 14 Sep 2006 04:43 GMT
If you do find one, let us know.
I'm convinced that there are psychological as well as physiological
reasons for one's perceived diminished orgasms.
There have been others that report a greater intensity of orgasms after
treatment.
I, for one, am not of this camp at this juncture.

B.A.
gary.miller12@comcast.net - 14 Sep 2006 05:59 GMT
Scardino's book also agrees with Walch's that the orgasm is not
affected by the prostectomy.  they are either in denial or so far about
all 7 people i have heard from indicate a degradation in intensity of
orgasm.  could they all have depression?  is there anyone out there
that has a good result relating to orgasm?  it could be that Scardino
and Walch do not have honest feedback which is what my urologist
suggested.  he suggested they should have asked their wives for the
truth.  what can you say Beverly?

gary

> If you do find one, let us know.
> I'm convinced that there are psychological as well as physiological
[quoted text clipped - 4 lines]
>
> B.A.
mountainguy1958 - 14 Sep 2006 12:06 GMT
Dishonest responses to questions about sexual function is always a
possibility, but how would asking wives about the intensity of their
husbands' orgasms provide more valid information than asking the men
themselves? Would we expect men to be able knowledgably to answer
questions about the quality of their partners' orgasmic experiences?

My thought would be that anonymous data collection might be more likely
to yield meaningful replies than face-to-face interviews.

But, on the other hand, I also ask myself what would be the use of such
data? Naturally, it's a concern of my own as I'm on the road to radical
surgery myself. But if it were true that orgasms were diminished, or
even if they were non-existent after cancer removal, would that have
any bearing on treatment decision-making? Probably not for many. When
the choice comes down to "your orgasm or your life", most (though
perhaps not all), I should think would choose life.

But still, I'm interested in what others have to say on this issue.
It's obviously an important question.

Tom

> Scardino's book also agrees with Walch's that the orgasm is not
> affected by the prostectomy.  they are either in denial or so far about
[quoted text clipped - 4 lines]
> suggested.  he suggested they should have asked their wives for the
> truth.  what can you say Beverly?
tchtic@yahoo.com - 14 Sep 2006 12:18 GMT
> Scardino's book also agrees with Walch's that the orgasm is not
> affected by the prostectomy.  they are either in denial or so far about
[quoted text clipped - 3 lines]
> and Walch do not have honest feedback which is what my urologist
> suggested.

Your Uro is correct.  By the time we're through the treatment, we've
been battered and hammered.   No way anything is working like it used
to.

Think about the typical 60, 70-something geezer, libido on the wane,
Not really all there anyway.

Add in the slashing (RP) and burning (RT) and it's a wonder that
anything works.

I went ADT and rad, Lupron, IMRT and Pd seeds.  Beginning about 6
months after the Lupron, I managed a couple erections and orgasms a
week.  These were adequate but nothing like before the treatment.

My erection comes slow.  It takes visualization and stimulation and
without Vitamin-V, I'm just hard enough for penetration and fighting to
keep it up.  This was never a problem before.

I used to be good for 20 or 30 minutes of thrusting, well over the 5-10
minutes that gives the average woman a vaginal orgasm.  This was
satisfying for me and for her.  There's a lot of positive feedback and,
er, strokes that come from a woman moaning, gasping, shuddering, and
kicking her legs, not to mention the clawing and biting.

After the treatment? 3 or 4 minutes is it.   Not quite in the premature
ejaculation range but too soon for a really good time.  We can adapt.
Tongues, lips, fingers, they all still work.

There is nothing like a good long, face-to-face session, tongues
probing lips, penis buried deep, making wet squishing sounds, ankles
against ears, hands on breasts, completely intertwined, joined, giving
and taking pleasure from each other, vulnerable and open to each other,
taking turns being dominating and demanding.with being submissive and
subserviant to her needs.  The give and take of a partnership of
pleasure.  Those were the old days before the cancer and the treatment.

Another disapointment is not "feeling" the tidal wave rush of semen at
orgasm.

There's some twitching, it feels good but the satisfaction of just
letting go and flooding into a woman is missing.  Semen that used to
squirt and make what one lady called, "an interesting mess, I like to
feel it oozing out afterward."  just dribbles.

Bottom line is that 2 years after rad, erections are serviceable,
orgasms are adequate, everything works but nothing is as good as
before.  The docs and books should be straight about this.

See the current movie, "Little Miss Sunshine", I used to imagine an old
age like the gramps, the retirement home lothario.  I'm not up to it.

-kh
Bob Anthony - 14 Sep 2006 14:25 GMT
kh:

I think I'll print out your post and tack it to the bed post! Maybe it
will help! ;) Good reply.

B.A.
rweigle@sbcglobal.net - 14 Sep 2006 15:15 GMT
kh

I absolutely agree.  My difference is I am only 59  Just finished ADT3
in June so still recovering from T recovery. My original Tx was IMRT,
HDR, and 2 years of ADT3 along with Taxotere at the begining.So while I
experience the same from you, I am unable to sort out damage from each
Tx modality from one another. Sigh....

Richard fr Monterey
Steve Kramer - 15 Sep 2006 01:58 GMT
Hi, Richard!  It's been over a year since you reported your PSA.  Still in
100ths?

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

> kh
>
[quoted text clipped - 5 lines]
>
> Richard fr Monterey
rweigle@sbcglobal.net - 16 Sep 2006 16:34 GMT
Steve,

Good that you remembered!!  Started Tx over 2 1/2 years ago.  PSA in
June was still <.001.  Get another workup at end of Sept.  I'll let you
know how that goes.  My biggest prblem now is the possibility of ONJ
from the pending tooth extraction I may need.  Going to talk with UCSF
Rad Oncl coming up in Oct.  Haven't had an Aredia infusion in almost a
year now.  QCT bone scan in May showed much improvement in density at
-1.25.

This string is turning into a "R" rating lol.  We got a budding author
among our membership.

Richard fr Monterey
bpsa 12, T2b,GS 8(4,4).
NICK - 16 Sep 2006 19:21 GMT
Richard wrote:

> QCT bone scan in May showed much improvement in density at
> -1.25.

Richard, was this a DEXA bone scan (without a coctail prior)?

My 2006 scan showed "no change" from 2 years ago at -2.00

That's what worries me about accepting any form of Tx for
PCa.  All rad and HRT involve some loss of bone density,
and I aready have the max loss I want to experience.
Steve Jordan - 16 Sep 2006 20:02 GMT
On September 16, NICK wrote, in pertinent part:
>  My 2006 scan showed "no change" from 2 years ago at -2.00
>
>  That's what worries me about accepting any form of Tx for
>  PCa.  All rad and HRT involve some loss of bone density,
>  and I aready have the max loss I want to experience.
>  
Haven't seen anything re: RT in and of itself causing loss of BMD (bone
mineral density), but ADT (androgen deprivation therapy, sometimes
called HT) certainly can.

It can be treated, reversed, or prevented by use of bisphosphonates such
as Aredia, Actonel and Zometa along with vitamin D3 and supplemental
calcium (citrate, no carbonate). See the authoritative website of the
Prostate Cancer Research Institute on side effects:
http://prostate-cancer.org/education/education.html#side_effects

The bisphosphonates themselves cause a small risk of osteonecrosis of
the jaw, so having any necessary invasive dental work done prior to
starting the therapy is prudent.

I fired a rad onc who prescribed ADT without any care for SEs.

Regards,

Steve J

"Empowerment: taking responsibility for and authority over one's own
outcomes based on education and knowledge of the consequences  and
contingencies involved in one's own decisions. This focus provides the
uplifting energy that can sustain in the face of crisis."
--Donna Pogliano, co-author of _A Primer on Prostate Cancer_, subtitled
"The Empowered Patient's Guide."
NICK - 17 Sep 2006 22:47 GMT
> Haven't seen anything re: RT in and of itself causing loss of BMD (bone
> mineral density), but ADT (androgen deprivation therapy, sometimes
[quoted text clipped - 3 lines]
> as Aredia, Actonel and Zometa along with vitamin D3 and supplemental
> calcium (citrate, no carbonate).

I was diagnosed with ankylosing spondylitis in 1977.  I had a joint
replacement in 2000 because of the damage already cause by the
disease.  Yet the damned uro never took into consideration my
fading bone density when he prescribed ADT.

> The bisphosphonates themselves cause a small risk of osteonecrosis
> of the jaw, so having any necessary invasive dental work done prior to
> starting the therapy is prudent.

Our local birdcage liner - the daily newpaper - has been running
display ads from law firms seeking clients who have taken
Fosamax and experienced jaw problems.

From one of the Fosamax package inserts:

"Severe bone, joint, and/or muscle pain, has been reported in patients
taking by mouth bisphosphonates drugs."  " Patients have had jaw
problems associated with delayed healing and infection, often
following tooth extraction."  "Abdoninal pain."  "Itching or eye
pain."
"A rash that may be made worse by sunlight."  "Allergic reactions
such as hives, swelling of face/lips/tongue/throat."

> I fired a rad onc who prescribed ADT without any care for SEs.

I should have done that in 2002 when the SOB uro did it to me.
Steve Jordan - 18 Sep 2006 00:06 GMT
On September 17, Nick replied to me:

(snip)
>  I was diagnosed with ankylosing spondylitis in 1977.  I had a joint
>  replacement in 2000 because of the damage already cause by the
>  disease.  Yet the damned uro never took into consideration my
>  fading bone density when he prescribed ADT.
>  
I wonder whether he even bothered to test for BMD. The usual test is the
DEXA scan, although some (e.g. Dr. Strum) say that the QCT scan is less
likely to be affected by pre-existent conditions.

I wrote:
>> The bisphosphonates themselves cause a small risk of osteonecrosis
>> of the jaw, so having any necessary invasive dental work done prior to
>> starting the therapy is prudent.
>>    
And Nick replied
>  Our local birdcage liner - the daily newpaper - has been running
>  display ads from law firms seeking clients who have taken
>  Fosamax and experienced jaw problems.
>  
Yes, they're all over the place. Thing is, Fosamax is essentially the
same as the other oral bisphosphonates. I understand that oral
bisphosphonates have substantially *less* risk of ONJ than the
injectables such as Zometa (which I'm on) or Aredia.

This is just a guess, but I suspect that whatever legal cause of action
Fosamax patients might have is based upon some sort of omission from the
instructions. And, of course, the imaginations of greedy lawyers. Peace,
counsel, there are genuine product-liability cases and also phony ones.
The objective is either to make the matter so expensive for the
manufacturer to litigate (successful plaintiffs recover costs, so it's a
good gamble) that it or its insurers will conclude that paying is better
than resisting, or to fool the ignorant boobs on the jury. I write this
based upon experience, not imagination.
>  From one of the Fosamax package inserts:
>
[quoted text clipped - 6 lines]
>  such as hives, swelling of face/lips/tongue/throat."
>  
Sounds awful, doesn't it? One of our number here would claim that such
things are inevitable, unavoidable, and the patient is guaranteed to
suffer, suffer, suffer. It ain't necessarily so. FWIW, my *anecdotal*
experience is that I have experienced none -- none -- of those SEs,
though I have very good fangs and have not had to undergo any invasive
dental procedures.
>> I fired a rad onc who prescribed ADT without any care for SEs.
>>    
>  I should have done that in 2002 when the SOB uro did it to me.
>  
Unfortunately, all too many of our brothers in adversity do indeed
suffer because of the ignorance of our medics.

The solution, IMO, is (as I keep nagging) to Study, Learn, Take Charge!
The empowered patient is the one whose results will be optimal.

Regards,

Steve J

"Flagrantly, we docs ignore the declaration of biology. We do this out
of ignorance, greed or both. The prime directive of the physician, the
real physician, is patient outcome, & not physician income (or ego)."
-- Stephen B. Strum, MD
Steve Kramer - 19 Sep 2006 01:20 GMT
> Steve,
>
> Good that you remembered!!  Started Tx over 2 1/2 years ago.  PSA in
> June was still <.001.

Great news!

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

tchtic@yahoo.com - 15 Sep 2006 03:26 GMT
> I absolutely agree.  My difference is I am only 59  Just finished ADT3
> in June so still recovering from T recovery. My original Tx was IMRT,
> HDR, and 2 years of ADT3 along with Taxotere at the begining.So while I
> experience the same from you, I am unable to sort out damage from each
> Tx modality from one another. Sigh....

June, July, August, September, 1, 2, 3, 4.  Still early.  The ADT still
has you, uh, by the balls.

It was about 6 months after Lupron before my twitching and timid
stirring turned into something useable, that is, if you call
"stuffable" useable.

There was a very gradual improvement. Not really noticeable on a month
over month basis but looking over longer periods of time, there is
improvement and there is hope.

At 6 months, I noticed that women aren't funny looking guys and that
there was something interesting about that narrow waist and the way
long legged blondes walked.  I wasn't sure what was interesting about
them but if I thought about it while pullin' on the head, Jackson made
some action.  More than once or twice a week was too much work.

At one year,  I wrote down things that had happened when I was younger.
I had a girlfriend in my college years who was a much older woman, she
was 30!  She had worked for 10 years and decided to go back to school.
5'5" blonde, slim with smallish firm breasts, movie actress looks.

On our first overnight date, she asked if I could drag the bureau over
to the wall mirror so we could get on top of the bureau and watch
ourselves.  Unfortunately, the hotel had attached the furniture to the
wall.

Then she got on top, and just going at it with her hips, laughing and
hollaring about how it had been a year for her, "Women don't need sex
like guys do,  I didn't miss it.  Didn't even think about sex for a
year."

She stopped, looked down, pressed her tummy just below the navel, and
said, "I can feel you, you're right up there."  She taught me several
"new" things.  I was an eager student.

At one year, I began dredging up these old memories, only the most edgy
stories could firm things up.  At one year, orgasms had improved, there
was more firmness.  Frequency was increasing too.  Unfortunately at one
year, the grade was still "needs improvement, C+"

I'm about 18 months post Lupron now.   A lot of visualization AND
friction gives a B, B- erection, adequate for penetration, that is, if
care is taken to ensure wet, slippery, dewy,labia.

I think there are several problems.  The Lupron left my T at the low
range of normal.  250-300.  The radiation may have damaged the nerves
and the erectile valves.  Then there's the "dead" prostate.

What is it that actually propels semen in the normal,
squirt-squirt-squirt, of a good satisfying ejaculation? What fires a
couple tablespoons of cream a foot or two?   What muscle is that?

Whatever it was, it's not working.  I figure that the prostate itself
did that and without a healthy prostate, there's no satisfying
squirting.

Not that there's much left to squirt.

I'm hoping to improve to a B+ but I don't expect to make the Honor
Roll.  

-kh
callalily - 15 Sep 2006 17:54 GMT
> > I absolutely agree.  My difference is I am only 59  Just finished ADT3
> > in June so still recovering from T recovery. My original Tx was IMRT,
[quoted text clipped - 63 lines]
> I'm hoping to improve to a B+ but I don't expect to make the Honor
> Roll.

jh

Dear JH
;

With all due respect:  20-30 minutes is just a flash in the pan.

'When my husband and I make love using Trimix I always put a large
pitcher of ice water and some Power Bars by the bedside just in case. I
find that after an hour you can get seriously dehydrated .The Power
Bars are for marathons.

Pardon me.  I have to go and take a cold shower.

Leah
callalily - 15 Sep 2006 17:54 GMT
> > I absolutely agree.  My difference is I am only 59  Just finished ADT3
> > in June so still recovering from T recovery. My original Tx was IMRT,
[quoted text clipped - 63 lines]
> I'm hoping to improve to a B+ but I don't expect to make the Honor
> Roll.

jh

Dear JH
;

With all due respect:  20-30 minutes is just a flash in the pan.

'When my husband and I make love using Trimix I always put a large
pitcher of ice water and some Power Bars by the bedside just in case. I
find that after an hour you can get seriously dehydrated .The Power
Bars are for marathons.

Pardon me.  I have to go and take a cold shower.

Leah
peter*pan - 14 Sep 2006 19:11 GMT
That was a great post!  4 years ago just reading it would have had me
raging!
Steve Jordan - 14 Sep 2006 19:54 GMT
> That was a great post!  4 years ago just reading it would have had me
> raging!
>  
Um, *what* was a great post?

Tnx.

Regards,

Steve J
Wayne - 14 Sep 2006 19:27 GMT
LOL
That would give most post rp's a hard on ;-)
Have you ever thought of writing a book?

Wayne
Beverley - 19 Sep 2006 21:43 GMT
I think that men have a macho self-image that would make it difficult for
many to admit that they have problems with erections, orgasm, etc. Take a
handful of men at the local hangout watching a favorite game on the big
screen. It's half time and the cheerleaders are strutting their stuff. The
cameraman is capturing the T&A show and the talk amoungst the guys has
turned from the game to what they'd like to do each cheerleader. Do you
really think that PC Survivor is going to admit he couldn't do anything even
if he wanted? Nope, he can still talk the talk. But on Monday morning PC
Survivor has a doc appt. The doc asks him if everything is fine and he
answers yes. So the doc asks him again if he's having any problems and PC
says no. This time the doc asks PC if he needs any help with erections and
maybe PC might manage to tell the doc that things aren't what they used to
be. So the doc hands him a scrip for Viagra. PC goes home and files the
scrip in the waste basket because he's too embarrassed to even take it to
the local drug store. How could he fill that scrip being the pharmacist is
the wife of another buddy and the tech is his game buddy's wife? Yes, ask
the wife if he has one. She'll tell you that sex is non-existent and she
hates that or that she could careless if it fell off and she was never
bothered again.

Women tend to be more honest about some things. Women will also be less than
honest and will not tell their partner that they are not satisfied. Do you
really think many wives going to tell their husbands that what they now get
for sex sucks? No. They will keep their mouth shut and say to themselves,
"oh, he tried". That leaves them three options actually four but the forth
would be to tell the husband and work to correct the situation so I'll stay
with the three. One finish off what he started by herself, resign herself to
less than optimal sex, or find satisfaction elsewhere.

Several years ago there was another guy on this group and he and his wife
had run up against the brick wall when it came to sex. She had some physical
problems due to aging that made intercourse unpleasant for her. He could not
get it up because of his age, RP, and ADT/chemo. But what they did still
have a closeness and they used that closeness wisely. They had snuggle
times. They'd get naked and do things like give each other massages,  and
they would do lots of kissing and touching. They tell each other how much
they loved one another, etc. It was like foreplay without the play. But for
them it was as special and intimate as full sexual intercourse.

Sex is going to be exactly what you make it be. I know that sounds weird but
it's true. If all you want to do is get it off then you'll make that happen.
If you want intimate then you can make that happen. If you worry about it
too much then you're going to have problems. Performance anxiety I think
does more harm to most men after PC. You can't worry about it. Chances are
you didn't have a rock hard, pressed against your bellybutton, erection
prior to treatment and you haven't had one of those since you were 30 years
old anyway! Slowly your body has been changing over the years but then PC
came along and accelerated that change by probably another 20 years. The
difference is that you noticed it!

Today there are a variety of options available to help an erection. What are
you willing to do to create an erection? There are a few guys that probably
still couldn't get an erection with caverject but that is probably very
rare.

Orgasms are still there. It is a different set of nerves and it is very tied
to the brain function. (We just had this discussion!) Personally, I think if
you worry too much about it you won't enjoy what you do have. So it's
different. Accept the differences and enjoy it. Let's face it sex at 45, 55,
65, and 75 is not what it was at 25 and 35.

At one point after treatment my husband just seemed incapable of having sex.
I think that he had some performance anxiety; he was so concerned about
trying to satisfy me and things just weren't working. So I turned the tables
on him and told him to just relax and expect nothing. I told him I wanted
nothing from him except to be able to give him the opportunity to just enjoy
the sensations. That was when he had his first orgasm without an erection.
It floored him! He didn't think that was possible. He has also discovered
that his orgasms are much more intense than ever before. He admits it is
still very different because there is no ejaculate so it has changed
considerably for him.

The whole sexual package is pretty depressing after PC. Rare are the guys
who get immediate sexual function going again and still they lack that ever
important sensation of ejaculate. For most the fun is gone because the
spontaneity is gone. They've got to work on it instead of it just happening.
A pretty girl walking by isn't going to send them in search of something to
hide the bulge. You are used to getting into the car turning the key and it
starts, now it is as if you have to push the car a block or two to get it
started and for some it is pushing it uphill the while way. So everybody
moans because they don't want to go push the car just to take a ride.
Bev

> Scardino's book also agrees with Walch's that the orgasm is not
> affected by the prostectomy.  they are either in denial or so far about
[quoted text clipped - 6 lines]
>
> gary
james_wv@hotmail.com - 14 Sep 2006 16:21 GMT
> i was told by my urologist today that the intensity of orgasm can be
> degraded after either radiation or surgery of the prostate. it is a
[quoted text clipped - 8 lines]
>
> gary

A year after traditional RRP with no further trearment and 2 months
before my 50th birthday:

My erections take a little longer to occur but are very sufficient once
they do.

My orgasms are definitely more intense and seem to last longer.
gary.miller12@comcast.net - 14 Sep 2006 18:06 GMT
James
were you depending on viagra before rrp like i do at the age of 66 yrs?
i suspect that you are a special case, being 50 yrs old.
the men that i have gotten feedback from are at least 10  yrs  older
than you.
does the lack of ejaculation affect your intensity of orgasm?
i remember having great orgasms starting around 7 yrs old without
ejaculation.
i wonder why that might be a problem today?
i wish i could find a good book or article to read on the subject.
gary

> > i was told by my urologist today that the intensity of orgasm can be
> > degraded after either radiation or surgery of the prostate. it is a
[quoted text clipped - 16 lines]
>
> My orgasms are definitely more intense and seem to last longer.
james_wv@hotmail.com - 14 Sep 2006 18:21 GMT
I never had any ED problem before surgery.  I was given some samples of
Cialis after the surgery (and a prescription to fill if I wanted).  I
took a few of the samples at about 5 months after surgery but stopped
because the nasal congestion made my snoring much worse.  The erections
came back on their own at about 9 months post-op.

I don't know if the lack of ejaculation causes the increased intensity
- there are very strong feelings of contractions.  The intensity of the
first post-op orgasm (which came as I was 'experimenting' before I
could have erections) REALLY shocked me.

> James
> were you depending on viagra before rrp like i do at the age of 66 yrs?
[quoted text clipped - 28 lines]
> >
> > My orgasms are definitely more intense and seem to last longer.
Leonard Evens - 14 Sep 2006 23:56 GMT
> i was told by my urologist today that the intensity of orgasm can be
> degraded after either radiation or surgery of the prostate. it is a
[quoted text clipped - 6 lines]
> is purely depression, could a sex therapist or hypnotherapist help?
> what is a good book that covers this topic?

Keep in mind that most of the men who are having no problems whatsoever
after their treatment are probably not taking part in this or any
support group in the first place.   So remember that your sample may be
biased.

> gary
Steve Kramer - 15 Sep 2006 01:44 GMT
>i was told by my urologist today that the intensity of orgasm can be
> degraded after either radiation or surgery of the prostate. it is a
[quoted text clipped - 6 lines]
> is purely depression, could a sex therapist or hypnotherapist help?
> what is a good book that covers this topic?

Many here have complained of lack of intensity.  Many here have reported
increased intensity.

I think it's the brain.

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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
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tchtic@yahoo.com - 15 Sep 2006 19:31 GMT
> if it
> is purely depression, could a sex therapist or hypnotherapist help?
> what is a good book that covers this topic?

I thought a bit more about this and, nah, I don't think it's all in our
heads.  Either RP or RT is a big deal, physical hammering.  Add in some
ADT and the bad news is that we are damaged goods.

My vote is with the "use it or lose it" side.

Look at it this way, suppose you were a dancer, runner, basketball
player or whatever.  You're in an accident, the doc's set or immobilize
your leg.  You're not going to perform even at a rookie level.

It's going to take dedication, motivation, physical therapy, and a
willingness to go the distance, push through.

I'm not saying that everyone will be fine and recover fully.

If you've lost a leg, no way you'll win the New York Marathon.   You
might be able to finish a 10K though, balancing on one leg and a
prosthesis.

My opinion is that's where we are.   Set high goals with a realistic
chance of success and go for it.

You guys who are limp and short? My tongue goes, um, less than an inch.
My longest finger is 3.25 inches.  A backrub with 30 cents of olive
oil while telling her how incredibly desireable she is. Work her
shoulders.  How much you crave her body. Run your fingers along her
spine and knead the muscles of her lower back.  How her scent gets the
blood pounding in your temples. A half hour backrub is a minimum.  It
strengthens your hands and arms.

Yeah, the disease and treatment was rough but it left you aching for
her, so bad that you taste electricity in your mouth.  That's when you
turn her over and use the tip of your tongue on her nipples.  These are
so beautiful.  Bite them with your lips.  Run your hands down the front
of her thighs and press her thighs apart.

She might be shy, it's been a while after all.  Too long.  A year, two?
 Stroke her inner thighs and apply a gentle but firm pressure.

Don't rush.  As eager as you might be.  Don't rush.  Bend forward and
kiss her inner thighs.  Part her lips and kiss both sides.   As the
Lupron wore off, I missed this. Even when things were still not
working, I missed hearing a woman's breathing and sighing.

If it's been a while, she might quickly come to orgasm.   Slow down but
don't stop.  Give her another.   After the Lupron and the treatment,
it's good for her and for you.

If you can muster an erection, slide in as deep as you can.  If it
takes Vitamin-V or a shot, the quality time is good for both of you.
Even better if you can time the entrance to her orgasm and give her
something to squeeze and clinch.

When you are joined together, looking into the eyes of an orgasming
woman or even during her afterglow, that helps the healing.   When you
are inside, even if it's only stuffable, tell her that's where you
belong.  Inside her.   Move your hips slowly and smoothly.  "I'm inside
you. That's where I belong."

I hate this disease and what it takes from us.  We can beat it.

If you can't manage an erection, women have told me that as much as
they like being penetrated by a firm penis, they really like being
licked, long, slow, smooth.  

-kh
Beverley - 19 Sep 2006 21:47 GMT
You're a good lover!
Bev

> > if it
> > is purely depression, could a sex therapist or hypnotherapist help?
[quoted text clipped - 66 lines]
>
> -kh
 
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