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RP on Monday 12/29

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Good morning! My name is Liz & my husband is having RP

tomorrow, 12/29/08 for PCa. His Gleason score is 6 (3+3), age 50,

stage b1 per urologist. PSA doubled in a year to 4.47 in October

2008. Biopsy showed cancer in only one side of prostate, 12 samples

taken, think cancer was in 4-6 of them - I wrote it down somewhere

but can't find it now.

We are both scared but cannot imagine living knowing the cancer is

growing (no matter how slowly) inside him. So with the blessing of

both his GP (a close friend who lost his first wife to cancer) and

his urologist (another longtime friend), we are off to surgery

tomorrow.

I have read all I can on the internet. I want to know everything that

I can.

If anyone has tips for surviving the next few weeks including

suggestions for living with 's new friend " Mr Catheter " , please

let me know!

What a way to start the New Year!! But I have to know that God is in

charge and has given us this challenge for a reason - I hope I can be

still and listen to Him as we travel this path.

Hugs - Liz

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Where to start. Is this the open type surgery? First I'd suggest

trying to be there at night with him in the hospital. Place is full of

people in the daytime, not bad in the evening, desolate at night. Be a

comfort and probably a real help to have someone to keep an eye on

things for him as he'll be helpless. The catheter is not that big of a

deal after getting used to it for a day or two. Leg bag is handy.

Drink plenty of water with it. He'll be on his feet Tuesday, not real

strong or steady for sure. And be assured, these operations have been

performed for about a hundred years now, surgeons know what they're

doing. Best of luck and hoping for a full cure with the surgery.

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Where to start. Is this the open type surgery? First I'd suggest

trying to be there at night with him in the hospital. Place is full of

people in the daytime, not bad in the evening, desolate at night. Be a

comfort and probably a real help to have someone to keep an eye on

things for him as he'll be helpless. The catheter is not that big of a

deal after getting used to it for a day or two. Leg bag is handy.

Drink plenty of water with it. He'll be on his feet Tuesday, not real

strong or steady for sure. And be assured, these operations have been

performed for about a hundred years now, surgeons know what they're

doing. Best of luck and hoping for a full cure with the surgery.

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Hi Liz:I am 53, 23 months out from LRRP. The catheter is manageable, but there may be irritation at the tip of his penis. K-Y jelly can be used to lessen the irritation. Also, there are several bags that can be used. I used a 500 cc leg bag after the surgery for during the day. At night, you can go to a surgical supply/drug store and purchase a large "drainage bag", that he can use at night. I had to drain mine once during the night, as opposed to every 1-2 hours for the small bag. Pain after surgery will be moderate, it just felt to me like I had been kicked in the stomach. Tylenol was all that was needed after the first pain dose. Encourage him to walk and be active as much as possible. They will start semi-solid food the day after surgery, I would have waited one further day and stayed with full liquids until then (I had severe cramping). A positive attitude is what is most important. The ride has just begun and he will have to remain positive, and not look back. He will have to discuss everything with you, because there will be incontinence and ED issues. Be pro-active on the ED issues. Don't be afraid to look into injection therapy and oral ED meds early on in the post op course. Good luck.To: ProstateCancerSupport From: liz1j03@...Date: Sun, 28 Dec 2008 17:25:25 +0000Subject: RP on Monday 12/29

Good morning! My name is Liz & my husband is having RP

tomorrow, 12/29/08 for PCa. His Gleason score is 6 (3+3), age 50,

stage b1 per urologist. PSA doubled in a year to 4.47 in October

2008. Biopsy showed cancer in only one side of prostate, 12 samples

taken, think cancer was in 4-6 of them - I wrote it down somewhere

but can't find it now.

We are both scared but cannot imagine living knowing the cancer is

growing (no matter how slowly) inside him. So with the blessing of

both his GP (a close friend who lost his first wife to cancer) and

his urologist (another longtime friend), we are off to surgery

tomorrow.

I have read all I can on the internet. I want to know everything that

I can.

If anyone has tips for surviving the next few weeks including

suggestions for living with 's new friend "Mr Catheter", please

let me know!

What a way to start the New Year!! But I have to know that God is in

charge and has given us this challenge for a reason - I hope I can be

still and listen to Him as we travel this path.

Hugs - Liz

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Hi Liz:I am 53, 23 months out from LRRP. The catheter is manageable, but there may be irritation at the tip of his penis. K-Y jelly can be used to lessen the irritation. Also, there are several bags that can be used. I used a 500 cc leg bag after the surgery for during the day. At night, you can go to a surgical supply/drug store and purchase a large "drainage bag", that he can use at night. I had to drain mine once during the night, as opposed to every 1-2 hours for the small bag. Pain after surgery will be moderate, it just felt to me like I had been kicked in the stomach. Tylenol was all that was needed after the first pain dose. Encourage him to walk and be active as much as possible. They will start semi-solid food the day after surgery, I would have waited one further day and stayed with full liquids until then (I had severe cramping). A positive attitude is what is most important. The ride has just begun and he will have to remain positive, and not look back. He will have to discuss everything with you, because there will be incontinence and ED issues. Be pro-active on the ED issues. Don't be afraid to look into injection therapy and oral ED meds early on in the post op course. Good luck.To: ProstateCancerSupport From: liz1j03@...Date: Sun, 28 Dec 2008 17:25:25 +0000Subject: RP on Monday 12/29

Good morning! My name is Liz & my husband is having RP

tomorrow, 12/29/08 for PCa. His Gleason score is 6 (3+3), age 50,

stage b1 per urologist. PSA doubled in a year to 4.47 in October

2008. Biopsy showed cancer in only one side of prostate, 12 samples

taken, think cancer was in 4-6 of them - I wrote it down somewhere

but can't find it now.

We are both scared but cannot imagine living knowing the cancer is

growing (no matter how slowly) inside him. So with the blessing of

both his GP (a close friend who lost his first wife to cancer) and

his urologist (another longtime friend), we are off to surgery

tomorrow.

I have read all I can on the internet. I want to know everything that

I can.

If anyone has tips for surviving the next few weeks including

suggestions for living with 's new friend "Mr Catheter", please

let me know!

What a way to start the New Year!! But I have to know that God is in

charge and has given us this challenge for a reason - I hope I can be

still and listen to Him as we travel this path.

Hugs - Liz

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Good luck for the surgery Liz. You may

find it useful to go along to http://www.yananow.net/choices.htm#radical

and click on the links to Useful Items for Surgery at http://www.yananow.net/rprx.htm Instructions

For Care After Surgery at http://www.yananow.net/rprx.htm

and Me and My Catheter at http://www.yananow.net/Catheter.htm

All the best

Terry Herbert

I have no medical

qualifications but I was diagnosed in ā€˜96: and have learned a bit since

then.

My sites are at www.yananow.net and www.prostatecancerwatchfulwaiting.co.za

Dr

ā€œSnuffyā€ Myers : " As a physician, I am painfully aware that most of

the decisions we make with regard to prostate cancer are made with inadequate

data "

From: ProstateCancerSupport [mailto:ProstateCancerSupport ] On Behalf Of lg1j03

Sent: Monday, 29 December 2008

4:25 AM

To: ProstateCancerSupport

Subject:

RP on Monday 12/29

Good morning! My name is Liz & my husband is

having RP

tomorrow, 12/29/08 for PCa. His Gleason score is 6 (3+3), age 50,

stage b1 per urologist. PSA doubled in a year to 4.47 in October

2008. Biopsy showed cancer in only one side of prostate, 12 samples

taken, think cancer was in 4-6 of them - I wrote it down somewhere

but can't find it now.

We are both scared but cannot imagine living knowing the cancer is

growing (no matter how slowly) inside him. So with the blessing of

both his GP (a close friend who lost his first wife to cancer) and

his urologist (another longtime friend), we are off to surgery

tomorrow.

I have read all I can on the internet. I want to know everything that

I can.

If anyone has tips for surviving the next few weeks including

suggestions for living with 's new friend " Mr Catheter " , please

let me know!

What a way to start the New Year!! But I have to know that God is in

charge and has given us this challenge for a reason - I hope I can be

still and listen to Him as we travel this path.

Hugs - Liz

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I had robotic prostatectomy 3 months ago, I am 52, had PSA jump from 1.9 to 2.85 over a year. Second biopsy revealed prostate ca in 2/12 cores on R, 5% one core, 25% other core, gleason 3+3=6, clinical stage T1c. Like you and your husband I couldn't live knowing I had a cancer, albeit a slow one growing inside of me, my father and mother had died of cancer in their 50's and 60's, respectively. I looked into radiation and watchful waiting, did the robotic versus open surgery for quicker recovery time, I needed to get back to making money ASAP, wife doesn't work. I was in the hospital one night, very noisy, had a double room with a guy who had a thousand friends, they all showed up that night. When I woke up from surgery I had moderate pain and gas feeling. I didn't know that the way they do the robotic surgery through the belly button procedure is to pump your abdomen full of C02 gas so they can raise up the abdominal

wall and get to the prostate gland. The catheter is a big pain, I'm not going to kid you. When he comes home from hospital make sure you have plenty of tape because it unsticks from your thigh very easy and then the tube with the bag starts pulling on your penis. I had to retape every day to keep that from happening. When he sleeps at night it's better if he can sleep on one side or the other through the night to prevent pulling on the catheter. I had to turn over sometimes and had to be careful to hold on to the bag when turning. If he's sleeping in a bed it would be better to have a chair next to the bed to rest the catheter bag on to prevent the pulling. My catheter was in for 7 days. Removal was no big deal, only relief. I didn't have a bowel movement for 6 days and the gaseous feeling was uncomfortable, was taking colace, and mild pain pill for the abdominal pain and tightness, DO TAKE THE PAIN PILL. No need to

suffer for no reason. Once the catheter came out I was able to go back to work in 3 days but I had to wear diapers for the first 2 weeks. Lots of leakage, especially when standing up, or when exerting at all. I had to put a pad inside the diaper to get through the day without changing. Very discouraging at first, but I kept doing the Kegal exercises every day, 3,4 5 sets of 10 throughout the day, and then gradually the incontinence just sort of went away. At first I became dry at night, then the mornings became dry, then I was only incontinent in afternoon or when I drank alcohol or when I exercised. Now I am only incontinent when I sneeze or cough, and then even then it's very little. I no longer where any pads at all! The ED issue is another thing. I still have no signs of spontaneous erections. I take a low dose of viagra every day and penile injections 2x/wk. I tried the vacuum

device but I never seemed to get that to work right. With the injections I can have normal sex with wife 2x/wk. The penile rehabilitation goes on for 6 months, maybe by then I can have normal erections. Nonetheless I have no regrets about having the surgery, my pathological stage at surgery was T2a, it was a nerve sparing surgery, and my first post-op PSA was .01. (considered undetectable). All the best to you and your husband..............lg1j03 wrote: Good morning! My name is Liz & my husband is

having RP tomorrow, 12/29/08 for PCa. His Gleason score is 6 (3+3), age 50, stage b1 per urologist. PSA doubled in a year to 4.47 in October 2008. Biopsy showed cancer in only one side of prostate, 12 samples taken, think cancer was in 4-6 of them - I wrote it down somewhere but can't find it now.We are both scared but cannot imagine living knowing the cancer is growing (no matter how slowly) inside him. So with the blessing of both his GP (a close friend who lost his first wife to cancer) and his urologist (another longtime friend), we are off to surgery tomorrow. I have read all I can on the internet. I want to know everything that I can.If anyone has tips for surviving the next few weeks including suggestions for living with 's new friend "Mr Catheter", please let me know! What a way to start the New Year!! But I have to know that God is in charge and has given us this challenge for

a reason - I hope I can be still and listen to Him as we travel this path.Hugs - Liz

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Hi Liz,

All of these guys who have answered have given good advice.

However, if you question 1000 men who have had robotic RP's, you

will get 1000 different stories.

Mine was about 13 months ago. I had a harder time than most with

the catheter. First of all, I could not sleep in a bed and ended up

sleeping in the recliner while it was in. I have never slept in my

recliner before or since then. My only call to the emergency

physician's number was when my bladder felt like it was overfull and

very painful which could not have been the case with the catheter.

A nurse called back and said I was having bladder spasms. She told

me to take a pain pill and be perfectly still. I did that and it

went away. That happened a few other times and was the worst pain I

had after the operation. I was in agony when I went back to the Uro

the next week and although having it taken out hurt like hell, the

relief was instant.

So keep in touch with this group and bring in if he is

inclined. Next questions might be ED issues and you should be able

to get good advice from members here.

dwayne

>

> Good morning! My name is Liz & my husband is having RP

> tomorrow, 12/29/08 for PCa. His Gleason score is 6 (3+3), age 50,

> stage b1 per urologist. PSA doubled in a year to 4.47 in October

> 2008. Biopsy showed cancer in only one side of prostate, 12

samples

> taken, think cancer was in 4-6 of them - I wrote it down somewhere

> but can't find it now.

>

> We are both scared but cannot imagine living knowing the cancer is

> growing (no matter how slowly) inside him. So with the blessing of

> both his GP (a close friend who lost his first wife to cancer) and

> his urologist (another longtime friend), we are off to surgery

> tomorrow.

>

> I have read all I can on the internet. I want to know everything

that

> I can.

>

> If anyone has tips for surviving the next few weeks including

> suggestions for living with 's new friend " Mr Catheter " ,

please

> let me know!

>

> What a way to start the New Year!! But I have to know that God is

in

> charge and has given us this challenge for a reason - I hope I can

be

> still and listen to Him as we travel this path.

>

> Hugs - Liz

>

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Hi Liz,

All of these guys who have answered have given good advice.

However, if you question 1000 men who have had robotic RP's, you

will get 1000 different stories.

Mine was about 13 months ago. I had a harder time than most with

the catheter. First of all, I could not sleep in a bed and ended up

sleeping in the recliner while it was in. I have never slept in my

recliner before or since then. My only call to the emergency

physician's number was when my bladder felt like it was overfull and

very painful which could not have been the case with the catheter.

A nurse called back and said I was having bladder spasms. She told

me to take a pain pill and be perfectly still. I did that and it

went away. That happened a few other times and was the worst pain I

had after the operation. I was in agony when I went back to the Uro

the next week and although having it taken out hurt like hell, the

relief was instant.

So keep in touch with this group and bring in if he is

inclined. Next questions might be ED issues and you should be able

to get good advice from members here.

dwayne

>

> Good morning! My name is Liz & my husband is having RP

> tomorrow, 12/29/08 for PCa. His Gleason score is 6 (3+3), age 50,

> stage b1 per urologist. PSA doubled in a year to 4.47 in October

> 2008. Biopsy showed cancer in only one side of prostate, 12

samples

> taken, think cancer was in 4-6 of them - I wrote it down somewhere

> but can't find it now.

>

> We are both scared but cannot imagine living knowing the cancer is

> growing (no matter how slowly) inside him. So with the blessing of

> both his GP (a close friend who lost his first wife to cancer) and

> his urologist (another longtime friend), we are off to surgery

> tomorrow.

>

> I have read all I can on the internet. I want to know everything

that

> I can.

>

> If anyone has tips for surviving the next few weeks including

> suggestions for living with 's new friend " Mr Catheter " ,

please

> let me know!

>

> What a way to start the New Year!! But I have to know that God is

in

> charge and has given us this challenge for a reason - I hope I can

be

> still and listen to Him as we travel this path.

>

> Hugs - Liz

>

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Here's one of those 1000 different stories. I had robotic RP on

December 15, 2008. In the two weeks since, I have progressed very

smoothly through the stages of recovery. I tolerated the catheter quite

well. Slept through the night in my own comfortable bed with the big

bag and moved around easily during the day with the smaller, leg bag.

Bladder spasms were infrequent, and I had been given meds to take for

them when I left the hospital. BTW, I left on Wednesday morning

following Monday morning surgery.

Catheter was removed Wednesday, Dec. 24. After 24 hours of no control

of bladder, I found I was only having " squirts " on standing up from

sitting or lying position during the day and that I am completely dry at

night. I get up once or twice in the night to urinate but have no

leakage into nightime diaper. I'm still using the diaper simply because

I bought a big package. I think I coulddo well with just a pad. Still

can't control the " squirts " very well, but progress is being made.

Sitting was and is painful but getting better. Still got blue balls!

As for ED, I'm taking 25mg Viagra each day since the removal of the

catheter and " exercising " when I shower each day. Making progress

toward a usable woody. Seems that my surgeon does good work.

I was exhausted after a few hours up for the first 12 days. Took naps

and went to bed by 8-9pm. Last two days have been much more active and

less tired. I'm thankful for this good outcome.

I'm 67, in good physical shape, no other health issues or medications.

Gleason from biopsy was 3+3=6, from pathology report was 3+4=7. This is

an outcome I had known might be possible and so was not alarmed. All

was contained, no extra-capsule tumor and no involvement of lymph nodes.

> >

> > Good morning! My name is Liz & my husband is having RP

> > tomorrow, 12/29/08 for PCa. His Gleason score is 6 (3+3), age 50,

> > stage b1 per urologist. PSA doubled in a year to 4.47 in October

> > 2008. Biopsy showed cancer in only one side of prostate, 12

> samples

> > taken, think cancer was in 4-6 of them - I wrote it down somewhere

> > but can't find it now.

> >

> > We are both scared but cannot imagine living knowing the cancer is

> > growing (no matter how slowly) inside him. So with the blessing of

> > both his GP (a close friend who lost his first wife to cancer) and

> > his urologist (another longtime friend), we are off to surgery

> > tomorrow.

> >

> > I have read all I can on the internet. I want to know everything

> that

> > I can.

> >

> > If anyone has tips for surviving the next few weeks including

> > suggestions for living with 's new friend " Mr Catheter " ,

> please

> > let me know!

> >

> > What a way to start the New Year!! But I have to know that God is

> in

> > charge and has given us this challenge for a reason - I hope I can

> be

> > still and listen to Him as we travel this path.

> >

> > Hugs - Liz

> >

>

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Here's one of those 1000 different stories. I had robotic RP on

December 15, 2008. In the two weeks since, I have progressed very

smoothly through the stages of recovery. I tolerated the catheter quite

well. Slept through the night in my own comfortable bed with the big

bag and moved around easily during the day with the smaller, leg bag.

Bladder spasms were infrequent, and I had been given meds to take for

them when I left the hospital. BTW, I left on Wednesday morning

following Monday morning surgery.

Catheter was removed Wednesday, Dec. 24. After 24 hours of no control

of bladder, I found I was only having " squirts " on standing up from

sitting or lying position during the day and that I am completely dry at

night. I get up once or twice in the night to urinate but have no

leakage into nightime diaper. I'm still using the diaper simply because

I bought a big package. I think I coulddo well with just a pad. Still

can't control the " squirts " very well, but progress is being made.

Sitting was and is painful but getting better. Still got blue balls!

As for ED, I'm taking 25mg Viagra each day since the removal of the

catheter and " exercising " when I shower each day. Making progress

toward a usable woody. Seems that my surgeon does good work.

I was exhausted after a few hours up for the first 12 days. Took naps

and went to bed by 8-9pm. Last two days have been much more active and

less tired. I'm thankful for this good outcome.

I'm 67, in good physical shape, no other health issues or medications.

Gleason from biopsy was 3+3=6, from pathology report was 3+4=7. This is

an outcome I had known might be possible and so was not alarmed. All

was contained, no extra-capsule tumor and no involvement of lymph nodes.

> >

> > Good morning! My name is Liz & my husband is having RP

> > tomorrow, 12/29/08 for PCa. His Gleason score is 6 (3+3), age 50,

> > stage b1 per urologist. PSA doubled in a year to 4.47 in October

> > 2008. Biopsy showed cancer in only one side of prostate, 12

> samples

> > taken, think cancer was in 4-6 of them - I wrote it down somewhere

> > but can't find it now.

> >

> > We are both scared but cannot imagine living knowing the cancer is

> > growing (no matter how slowly) inside him. So with the blessing of

> > both his GP (a close friend who lost his first wife to cancer) and

> > his urologist (another longtime friend), we are off to surgery

> > tomorrow.

> >

> > I have read all I can on the internet. I want to know everything

> that

> > I can.

> >

> > If anyone has tips for surviving the next few weeks including

> > suggestions for living with 's new friend " Mr Catheter " ,

> please

> > let me know!

> >

> > What a way to start the New Year!! But I have to know that God is

> in

> > charge and has given us this challenge for a reason - I hope I can

> be

> > still and listen to Him as we travel this path.

> >

> > Hugs - Liz

> >

>

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> Be pro-active on the ED issues. Don't be afraid to look into

> injection therapy and oral ED meds early on in the post op course.

Yes, yes, yes . . .

Even supportive doctors can fall down on " penile rehabilitation " .

My post-surgical experiences included:

a) bladder spasms (they stopped as soon as the catheter was removed)

B) an almost-complete uretral stricture (I'm using a catheter once

every two days, and everything is stable after a year).

>

> Good morning! My name is Liz & my husband is having RP

> tomorrow, 12/29/08 for PCa. His Gleason score is 6 (3+3), age 50,

> stage b1 per urologist. PSA doubled in a year to 4.47 in October

> 2008. Biopsy showed cancer in only one side of prostate, 12 samples

> taken, think cancer was in 4-6 of them - I wrote it down somewhere

> but can't find it now.

>

> We are both scared but cannot imagine living knowing the cancer is

> growing (no matter how slowly) inside him. So with the blessing of

> both his GP (a close friend who lost his first wife to cancer) and

> his urologist (another longtime friend), we are off to surgery

> tomorrow.

>

> I have read all I can on the internet. I want to know everything that

> I can.

>

> If anyone has tips for surviving the next few weeks including

> suggestions for living with 's new friend " Mr Catheter " , please

> let me know!

>

> What a way to start the New Year!! But I have to know that God is in

> charge and has given us this challenge for a reason - I hope I can be

> still and listen to Him as we travel this path.

>

> Hugs - Liz

>

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Your have received excellent advice from the listserve. All will be well!

The catheter will be manageable. It's no fun, but it will be okay. Be

patient!

God Bless!

Coy

RP on Monday 12/29

> Good morning! My name is Liz & my husband is having RP

> tomorrow, 12/29/08 for PCa. His Gleason score is 6 (3+3), age 50,

> stage b1 per urologist. PSA doubled in a year to 4.47 in October

> 2008. Biopsy showed cancer in only one side of prostate, 12 samples

> taken, think cancer was in 4-6 of them - I wrote it down somewhere

> but can't find it now.

>

> We are both scared but cannot imagine living knowing the cancer is

> growing (no matter how slowly) inside him. So with the blessing of

> both his GP (a close friend who lost his first wife to cancer) and

> his urologist (another longtime friend), we are off to surgery

> tomorrow.

>

> I have read all I can on the internet. I want to know everything that

> I can.

>

> If anyone has tips for surviving the next few weeks including

> suggestions for living with 's new friend " Mr Catheter " , please

> let me know!

>

> What a way to start the New Year!! But I have to know that God is in

> charge and has given us this challenge for a reason - I hope I can be

> still and listen to Him as we travel this path.

>

> Hugs - Liz

>

>

> ------------------------------------

>

> There are just two rules for this group

> 1 No Spam

> 2 Be kind to others

>

> Please recognise that Prostate Cancerhas different guises and needs

> different levels of treatment and in some cases no treatment at all. Some

> men even with all options offered chose radical options that you would not

> choose. We only ask that people be informed before choice is made, we

> cannot and should not tell other members what to do, other than look at

> other options.

>

> Try to delete old material that is no longer applying when clicking reply

> Try to change the title if the content requires it

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I am 9 months post RP. My opinions would be to make sure you take

the antibiotic that most docs give you to start the day of your cath

pull (which is no big deal). My opinion number 2 would be to manage

any IC problem you have so it does not effect the quality of your

life. It should only be temporary issue and it can be managed

discreetly.

>

> Good morning! My name is Liz & my husband is having RP

> tomorrow, 12/29/08 for PCa. His Gleason score is 6 (3+3), age 50,

> stage b1 per urologist. PSA doubled in a year to 4.47 in October

> 2008. Biopsy showed cancer in only one side of prostate, 12 samples

> taken, think cancer was in 4-6 of them - I wrote it down somewhere

> but can't find it now.

>

> We are both scared but cannot imagine living knowing the cancer is

> growing (no matter how slowly) inside him. So with the blessing of

> both his GP (a close friend who lost his first wife to cancer) and

> his urologist (another longtime friend), we are off to surgery

> tomorrow.

>

> I have read all I can on the internet. I want to know everything

that

> I can.

>

> If anyone has tips for surviving the next few weeks including

> suggestions for living with 's new friend " Mr Catheter " ,

please

> let me know!

>

> What a way to start the New Year!! But I have to know that God is

in

> charge and has given us this challenge for a reason - I hope I can

be

> still and listen to Him as we travel this path.

>

> Hugs - Liz

>

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;

Snip: (We are both scared but cannot imagine living knowing the

cancer is growing (no matter how slowly) inside him.)

That is exactly how my hubbie and I feel. He is having surgery

January 9th, next Friday.

We found this site that has alot of info on care of the catheter and

postate cancer.

http://www.yananow.net/choices.htm#topofpage

http://www.malecare.com/services1.htm

http://www.malecare.com/urinary-catheter_66.htm

This one is the best:

http://www.malecare.com/prostate_cancer_surgery_patient_hints.htm

Good luck and let us know how it goes.

You can also email me anytime at fun_luvin_1972@...

Marla

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I had surgery to remove my prostate 3 years 6 months ago and

everything is working fine now. It took almost 2 years to get full

use back, although I often got night time errection which were

usable. " BUT " unknown to me at the time of the surgery was that my

surgeon used surgical clips to suture my insides. They are v-shaped

clips which are used to pinch close cuts instead of using regular

string sutures. Advantages are that surgery takes much less time,

BUT, these clips are with you for ever. They do no dessolve and can

be seen in you under x-rays. You can have cat-scans & MRIs with no

problems. THE biggest problem is what happened to me. I exercise and

do sit-ups regularly. The sit-ups caused a clip to move and pierce

the tube one piss through, causing blood in my urine and pain. I had

to have the clip removed with a cystescope while under general. Hope

this helps, please feel free to cantact me for further if you wish.

Remember this above all, Knwoledge is power.

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> ...

> " BUT " unknown to me at the time of the surgery was that my

> surgeon used surgical clips to suture my insides.

> ...

> Remember this above all, Knowledge is power.

An oncologist I know once told me that some of his patients want

to know everything that will happen to them and some don't want

to know anything. Some have actually said to him: " Doc, do

whatever you have to do but don't tell me about it. I don't

want to know. " He wasn't sure which kind of patient was

happier.

Some doctors are reluctant to say much, believing that the

patient is better off not knowing, or that if the patient wants

to know, he'll ask.

If you don't want to know anything, well, I can understand that.

But if you are one of those who does want to know (and like

Pablo, I'm one of them), be sure to ask. We can't assume that

doctors will tell us everything without our asking them.

If you're getting surgery, ask the doctor just what he's going

to do. Ask about what will be cut, what will be cut out, what

will be sewn up or clipped, what will be damaged, how the

recovery and healing will go, and what the long term effects

will be. For radiation, ask what will be radiated, how much

radiation, what other parts of the body will be hit, what are

the short and long term side effects.

Do some research on your own to supplement what the doctor says,

and to enable you to ask educated questions.

For me, one of the signs of a good doctor is patience, honesty,

and clarity in answering such questions.

Alan

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