Our Journey ~ Sharing is Caring by....... Buddy & Lee

If weird symbols are showing??       Click on the Refresh button         Updated & Revised:

April 2010 

  

Welcome  to….

 

"Our Journey”  ~ Sharing is Caring

 

The stepping-stones in our path

 The ultimate goal … to be prostate cancer free

 

by   Buddy & Lee

http://i880.photobucket.com/albums/ac6/bluebirdathealingwell/BuddyandLee.jpg

 

April 3, 2006  Radical Retropubic Prostatectomy

        

1st PSA ~ June         2006 

2nd PSA ~ February 2007

3rd PSA ~ August     2007

4th PSA ~ February  2008

5th PSA ~ August     2008

6th PSA ~ February  2009

7th PSA ~ August     2009

8th PSA ~ April 2010

 

less than 0.1  NON-DETECTABLE

 

                   

 

**  When prostate cancer is small and curable,

it is also silent—it produces no symptoms.

 

That’s why we are all so shocked at finding out that “we” have cancer.  It’s no longer an old man’s disease.  And that’s why it is very important to learn as much as we can about this disease and what our options are.

 

We’ve noticed in the forum that there are a lot of questions about what to expect?

What treatments are available?    What do I need to do to prepare?   What supplies do I need to buy?

What happens when you get there for your surgery?   What about recovery time? 

As a spouse, caregiver, partner… What do I need to expect?   What about cost?  

 

Below are areas that we’ve touched on in “Our Journey”…

 

HEALTH BEFORE SURGERY

Kegel Exercise

Items to have on hand before surgery

Preparing for Surgery Day

**Long-Term Issues: Urinary Continence and Sexual Potency

HEALTH AFTER SURGERY

PLEASE>>>>>>>>   DON’T RIDE…

PLEASE>>>>>>>>   DON’T LIFT…

BE PREPARED:  Coming home with a catheter  aka: Mr. Hang

After Catheter Removed

Issues:

(A) We felt like a BUS hit us

(B) Phone call to confirm findings

(C) We had already made our decision

(D) Preparing for surgery

(E) Bladder Spasms

(F) Constipation

 

 

KNOWLEDGE IS POWER... and POWER conquers FEAR!!!!!

 

We decided to share “Our Journey” in hopes of helping at least 1 person!

If it helps more….  If it helps you!!!!      That will truly be a blessing

At no time are we writing to tell you what you must do, or what you should do….

 

Your  Decision  is  Your  Decision!!

And it will be the right decision for you!

 

Just giving you a view of what decisions we made, what the process was for us, and the outcome as of this date. 

 

Prostate cancer... is an “US / WE” disease and must be treated as an “US / WE” Journey. 

Make this a “team” journey…. Do everything together.  You will need each other and each other’s strength!

 

“Hand-in Hand” “Heart-to Heart”… nice words borrowed from Tim G…

 

 

Read as much as you can on the forum… there are so many different scenarios.  You will gain much knowledge from all of them.  There will be so much coming at you in the next little while… I would suggest the following for any new member: 

1.      When you read a posting that you think you might want to re-visit…. Make sure you know who Started the thread… and the title of the topic/thread… so you can find it again if you want to go back to it.  There are so many postings coming in daily ~ you may not find it again….

2.      Take a pen and paper to all of your appointments… Have your loved one take notes so you can look back over the consultation when your mind is clear.  (Take a tape recorder if you need to)…  Once you hear the word “cancer” your mind will process only that word and things will become jumbled.  This is normal and you will get through it!

 

We hope our journal entries will help you.

 

Ideal scenario: Prostate cancer detected early, treated, and cured.  Prostate cancer doesn’t have to be fatal.  If it’s caught early enough, it is completely curable. 

 

Sharing   is   Caring

 

The most important thing right now is... take one~day~at~a~time.

Reserve your energy because you'll both need it.

 

One thing each of us must remember…. NO 2 SITUATIONS ARE THE SAME

 

Take a deep breath.... and know that there's a lot of us like you out there...

and we've been where you are now.

 

All different kinds of lifestyles…  different PSA scores, different treatments, different incomes, different jobs, different health issues, all different ages, and most of all… MENTAL ATTITUDES ARE DIFFERENT.

 

So ~ take a deep breath and let HealingWell forum friends help you!!!

 

Remember… YOU MAKE THE DECISIONS… YOU HAVE OPTIONS…

 

 

Sharing ~ Our Personal Threads with You!!

If you or your loved ones ~  pull “1” thing from our journey that helps you on your journey…… it will be our gift to you.

 

Direct Links to our Personal Journey…. and Our Own Personal Threads:

Very important to do the following when you click on Direct Links from within the forum…

When you Click on titles below it will take you directly to our personal Threads!

Once there… remember to click on the REFRESH button. (This is important)

 

Our Journey ~ Sharing is Caring (you are on this thread)

Give Yourself a Second Opinion... Read this book...  Dr. Walsh’s Guide to Surviving Prostate Cancer

A Special Note for Loved Ones (Wives, Partners, and Caregivers)

MURPHY Our Special Helper

Helpful Hints ~ & ~ Direct Links to Important Topic Threads ~ Hope this helps you!! :)

The hardest thing for me....

The Power of Hope

#2 WOO~HOO!! from Buddy, Lee, & Murphy :) papa & mama bluebird

3rd Woo~Hoo for Buddy, Lee & Murphy

 

**Dr. Walsh’s Guide to Surviving Prostate Cancer…(Give Yourself a Second Opinion), is truly a book of knowledge… teaching you about this disease… that affects the whole family!  Yes ~ it is a 2001 book but it will give you a “solid foundation” to start Your Journey on…  his revised edition is available.

 

It is not a book to make you scared ~ but to make you think, to make you understand, and to make you knowledgeable about this terrible cancer….. It doesn’t hold back…. 

 

But remember…being scared is part of this whole picture at the beginning anyway… so take in the information that is offered from its contents.   Just so you know… we did not read Chapter 12… but we know it’s there if we ever have to travel that path.

 

We are not promoting this treatment.... that is definitely a personal choice.  This book has information that "all of us" can use no matter what treatment you decide on. 

 

Read only areas that you are comfortable reading at first.  Gradually you will likely read it all…  We did not read Chapter 12 together.  After our surgery and after we had a few weeks under our belt I skimmed through the pages… and it made me really appreciate what we have just gone through….. and give thanks each day for having found this cancer early.

 

There are excellent postings in reference to this book in “Our Journey” and at the end of our posting… read them all!!!  Remember ~ we all react differently and the forum is a wonderful place to express your own feelings about certain things.  Knowledge is Power… and we gain Knowledge by reading, reading, and more reading.  There’s a Thread started by another member…titled “Dr. Patrick Walsh’s Guide to Surviving Prostate Cancer”  it has some excellent postings also…

 

There are other books that have been recommended by members.

Click on the link..>>  BOOKS... Recommended by Forum Members

 

I’m adding, “Worry???”… Wittler… asked why I hadn’t told her this before they had surgery ~ so… I thought I’d add it here because this is truly how we feel and felt.

 

   Worry??????  Why??? 

   Worry causes stress ~!@#$%^&*()_+@#$%^&*

   Stress causes all sorts of bad stuff…

   It gets you nowhere…

   It drains you of strength… and

   What’s going to happen is definitely going to happen

          whether you worry or you don’t worry

                    So ~ No More Worrying.  Okay  J

 

Knowledge is Power.... and Power takes away the fear!!!

 

 

 

HEALTH BEFORE SURGERY:

 

Start kegel exercises immediately to strengthen the external sphincter muscle.

           (no matter what treatment you decide on!!!… be prepared).

 

(A)  See Excerpt: Page 244 under

Long-Term Issues: Urinary Continence and Sexual Potency in Dr. Walsh’s book.

 

**It’s hard to believe, but urinary control does continue to improve over two years and, in an occasional patient, even longer than that.

 

**Can you do anything to speed things along, and improve your urinary control?  First, whatever you do, do not wear an incontinence device with an attached bag, a condom catheter, or clamp!  If you use any artificial device, you will hurt yourself in the long run.  You won’t be able to recover your urinary control, because you won’t develop the muscle control you need.

<end excerpt> 

 

Start walking and do stairs (machine) if possible, and walk some more…!  You know all the other stuff is automatic when it comes to treatment.  Stop smoking, Stop drinking, & Eat healthy.

 

Kegel Exercise:  See more at the end of this posting.

 

Before surgery: Our urologist said to work the muscle (kegels)… when urinating standing up.  start, stop, hold, start, stop, hold… several times during urination.  This strengthens the muscle.  Also, walking and climbing stairs are really good exercise for the little sphincter muscle. 

 

Stop kegel exercises while you are catheterized….

 

After surgery: (and once catheter is removed) we were to still continue doing kegels when urinating (standing up!!)

(Our personal Start/Stop/Hold sequence is listed below) 

 

B.  See Excerpt:  On page 247 of Dr. Walsh’s book he states:

Exercises you can do:  Every time you urinate, do it standing up.  You can’t practice the following exercises, which strengthen the external sphincter and speed up your recovery of urinary control, while you’re sitting down.  Start your stream, and once it’s in full force, stop the stream by contracting the muscles in your buttocks--- not your abdominal muscles, not the muscle “up in front” around the penis.  Tighten your buttocks: imagine you’re trying to hold a quarter between your cheeks.  Hold the urine back for 5 or 10 seconds, and repeat as many times as you can.  Note: Only perform these exercises when you’re urinating; if you keep contracting these muscles throughout the day, you’ll overdo it—the sphincter tires easily—and you’ll end up wetter than you would otherwise.

<end excerpt> 

 

Previous paragraphs in this book address… things to speed up your urinary control.  One is not using any artificial devices…… and certain high blood pressure medication relaxes this muscle so you may need to check with your doctor.

 

Special Helper needed….  @Direct Link:  Murphy ~ Our Special Helper

 

http://i880.photobucket.com/albums/ac6/bluebirdathealingwell/Murphy.jpg

 

Items to have on hand before surgery:

 

Prescriptions: Ask your doctor for “all” prescriptions ahead of time so you have them at home before you head out the door for surgery.  (Pain med, stool softener, bladder spasm, antibiotics, etc.)

 

Head Brace:  I took 2 very soft ankle socks and stuffed them with soft material. The pillows in the hospital are really not very good.  I placed them on the sides of Buddy's head so when he slept his neck was not strained, as his head would roll to the side.  This really helped!! 

 

Leg Lotion: I massaged Buddy's calves.  It really seemed to help him after the pressure cuffs were taken off.

Blanket: Used while I slept in the chair at the hospital.

 

Neck Pillow:  Used while I slept in the chair at the hospital and Buddy continues to use it today while recovering in his new lounge chair J  Helps relax his body while he reads.  It was a lifesaver coming home from the hospital too!

 

Lounge Chair:  We bought 2 and they were the best investment!!  One that allows you to lean back.  This helps keep pressure off the incision(s) and the perineum (the area between the scrotum and rectum).  Take time to practice getting up without using the abdominal muscles… this will help once you’re home…

 

Donut Pillow: Used when sitting at the computer (not in the lounge chair)… this really helps take the pressure off.  We have since…found that placing a soft pillow over the donut gives it an extra soft cushion.

 

Wedge Pillow: Used on the bed to help with sleep.  Also ~ helped in making it easier to get up out of bed. We practiced getting out of bed without using the abdominal muscles.  I stood on the side of the bed and braced myself so Buddy could use his upper arm strength to pull up holding on to my arm.  This worked beautifully!!! Both the wedge pillow and the pulling up motion.  J

 

HEALTH AFTER SURGERY:

 

PLEASE>>>>>>>>   DON’T RIDE ON LAWNMOWERS, HORSES, BIKES, during your recovery period… take the time to heal and recover completely before you try these… We personally will not be doing any of these in the future…   (SEE SPHINCTER Information at the bottom of this thread)

PLEASE>>>>>>>>   DON’T LIFT ANYTHING HEAVY ~ DON’T LIFT/PULL YOUR BODY UP for at least 8-12 weeks…

BE AWARE and LISTEN TO YOUR BODY…. If not… you will be the one to suffer.  You don’t want a HERNIA!!!!!

Practice getting out of bed, lounge chair, couch, etc… before surgery.  This will truly help once you’re home from the hospital.

I helped :)  see information above…under wedge pillow.

 

BE PREPARED:  Coming home with a catheter  aka: Mr. Hang

The catheter was our best friend….  We let the catheter be our priority!!!  We did not go out to dinner, we did not go out to visit friends…  we took care of each other during this time and let the catheter “Mr. Hang” do his job.  Giving the body time to heal properly on the inside.

Ø       Pets…. Remember they like to jump and play so be aware that this could cause you some undue hardship if your catheter comes out inadvertently …Per: Daveed J

Ø       We kept the large bag hooked up except for 2 occasions ~ when we went for our appointments with the doctor.  The small bag will cause you problems if you let it fill up and you get backflow…  Why take that chance…

Ø       Extra big size PJ bottoms with a drawstring….  I slit the side seam from waist to mid thigh.  I re-strung the drawstring so it could be adjusted to the tightness that is comfortable for walking and sleeping.  The idea is to have the catheter tubing from the penis to the bag being a comfortable angle for walking and sleeping.  

Ø       We left the penis open (no pads or underwear worn during the time with the catheter) only the pj’s.

Ø       Expect mucus to appear on the tip of the penis…. This is normal and should not be removed.  It’s a natural body reaction with having a foreign object in the body… if cleaned off the catheter tube will be dry and will agitate the penis and infection could occur.  (Pus means possible urinary infection that is treated with an antibiotic… this is very common with a catheter.  So be aware!)

Ø       Clean the area on the leg where the mucus has dried… with light soapy water and dry.

Clean the area on the penis and tubing with water only...(soap will dry the area and make it more susceptible to chafing.  (some members use vinegar)

Ø       Container to hold catheter bag while in bed. We used a small laundry basket.  The bag hooked nicely on the inside side.  Allowing for a good downward angle for the catheter tubing from the penis to the bag.

Ø       Having a mild sleep aide during this time will allow you to get good quality sleep and this will definitely promote healing.  Wives, Partners, and Caregivers…. Sleep when he sleeps…. This will really reserve your energy!!!  We had a sleep aide before surgery to help his mind stop racing during the night.

Ø       If you are sensitive to tape ….. check on this in advance because the catheter tubing…is attached to the leg with tape….and several members have had reactions to this and you really don’t need the extra stress of this happening.

Ø       Have lots of chicken noodle soup and crackers on hand.  Jell-o too!   We did not eat any heavy meals for a week (our choice).  Hoping to help with constipation.  We also wanted the gases to get out of our system.  We did need a stool softener and we had no gas issues at all…   J This is a personal preference.  

Ø       You do not want to get constipated.... so plan ahead to have stool softeners on hand and use them!!!

Ø       With catheter in .....push lots of liquids during this time to help flush out system. 

After  Catheter Removed:

Ø       **Liquid Intake   Back off on the intake of liquids once catheter is removed 

After Catheter Removed:

Ø       Depends Adjustable Underwear (there are several brands out there… they are easy on the incision areas)

Ø       Depends Pads for Men (there are several brands out there… they have adhesive so they don’t slip)

There are many different brands… Ask your pharmacist if they have a sample for you to try!!!  Other brands listed in a Thread (see Helpful Hints thread)

 

Ø       Serenity for Men ~ is a much softer pliable pad for men. 

We definitely would have used them at the beginning knowing what we know now

 

** Until your urinary control has returned to an acceptable level, don’t force fluids. 

Reminder: Caffeine in all forms is a powerful pharmacological agent that increases the frequency and urgency with which you need to urinate.  We also stopped intake of liquid between 6-7 p.m. to help in the number of times we had to disturb our sleep.  (We still do this and will continue to do this)

~  ~  ~  ~  ~  ~  ~  ~  ~  ~  ~  ~  ~  ~  ~  ~  ~  ~  ~ 

“Our” Personal Journey February 2006 – current

papa bluebird (1953)  “Buddy” Retired  &  mama bluebird (1955) “Lee”  & Murphy (ageless :)

 

At Age 50, 2003    Complete Physical PSA 3.9

 

Age 52 on January 5th, Thursday 2006

Routine Physical PSA 5.1  

January 24th, Tuesday      

DRE indicated something going on PSA 4.6

 

Age 53 on February 2, 2006

February 7th, Tuesday, 2006

Consultation with Urologist

February 20th, Monday            

Biopsy (day before…started 5 days of antibiotics)

February 23rd, Thursday            

Phone call to confirm findings Adenocarcinoma of the prostate T2a  Gleason grade 3+3=6    5 of 7 cores right lobe, 2 of 7 cores left lobe

This is when the BUS HIT US!! (aka by members as: the Hammer, the Truck with 3 semis...)

See (A & B)  under “Issues” 

February 27th, Monday , 2006               

Consultation with Urologist to go over the Biopsy Report

We wanted surgery immediately!  Requested RRP with *wide excision…

(*We took everything out that may have cancer cells lingering…a very personal choice!!)

Waiting period after biopsy…. 6-8 weeks.  Why? The body needs time to recover

Our urologist suggested we look at all options… and suggested setting up an appointment with an oncologist, and talk with our family physician before making our decision.

See (C) under “Issues”

February 28th, Tuesday              

Family Physician to discuss Biopsy Report, Decision, & Sleep-aid to help anxiety so we can get a good night sleep preparing for surgery See (D) under “Issues”

March 28th, Tuesday      

Pre-Surgery lab work

April 3rd, Monday    

Surgery Day…RRP with wide excision ~  6 inch scar starting just below the navel downward to top of pubic bone

April 3rd -20th, Wednesday – Thursday  (17 days)

The catheter was our friend.  We let it do its job and we took the time to heal/recover by staying home during this period of time. walk/eat/sleep/walk/eat/sleep/walk/eat/sleep was our main focus.. and to this day we are so happy we took this time.  We feel strongly we benefited in the long run by doing this.  (Remember this is Our Journey… pull from it what best suits your needs)

April 5th, Wednesday, 2006                  

Headed home around 1:00 p.m. in our Jeep Wrangler.  I was concerned Buddy would have a difficult time getting in and out.  Needless concern… he did great and the neck pillow was very welcome for the 1-hour drive home.

April 12th, Wednesday                            

Staples removed … Really amazing… they put an iodine solution on his incision and then put 14 butterfly bandages and then covered it with the iodine solution that acted like a glue.  It wore off on its own… the incision healed beautifully. 

April 20th, Thursday

Catheter removed – we had no problems with Mr. Hang. 

He was the best friend we had….  allowing “US” to sleep and heal. The information in Dr. Walsh’s book helped us tremendously in this area of concern. (Day of removal started 5 days of antibiotics)

May 15th, Monday    

Six week check-up… incision doing “great”  … walking, walking, and more walking. We are continuing to do kegels when urinating only.  You can over work the sphincter muscle if you continue doing it during the day as an exercise…   Exception… 1st pee in the morning… let it flow J 

June 1st, Thursday 

Our date to begin doing routine chores, driving, and back to the YMCA for continued wellness program. 

Mon,Wed,Fri,Sat,Sun  a 2 hour walk along the creek…and to the YMCA on Tuesday & Thursday

                  

June 29th, Wednesday, 2006  1st PSA less than 0.1,  NON-DETECTABLE….!!!!!!! J

J  8th week of recovery.  We are so happy with the results.  And we are extremely happy with our decision, our doctor, our procedure, and our recovery. We will continue to take one-day-at-a-time… and enjoy each day to the fullest.

 

July & August 2006

Buddy’s recovery has gone very well over the summer… and we decided to travel as we had previously planned to do when I retired. My sister and I drove and we kept Buddy in the backseat.  He had a nice pillow to sit on and he did great! We made sure to have a swimming pool and workout room at night and this helped with the exercise we were missing out on when driving 8-10 hour days.  Every pit stop he walked around. With over 8000 miles under our belt I can say WE DID IT!!!  And we did it well J  We will never forget “Our Journey with Prostate Cancer” but we are here to let you know!!!  You really can get back to a normal life and it just makes living each day to the fullest even more meaningful.

 

September – December 2006

Coming up on our 9th month of healing/recovery on January 4th  PSA will be in February.  We continue to take one-day-at-a-time and we are enjoying our retirement that we planned for over 22 years ago.  We are now in our Adventure stage of life… and it is more exciting because of where we were just 9 months ago with our diagnosis… 

Now it’s time to snuggle down for the winter!!!  Our PSA in February and then I hear rumblings from Buddy that another trip is in the works.  Hmmmmm time will tell.

Take care friends…

 

January –  2007  (9th Month)

Moving forward into the New Year we are heading toward our 2nd PSA on February 6th.  Our thoughts remain positive knowing that we will take each stepping-stone that is placed in our path with a positive attitude and a warm heart.  It’s gotten us this far and traveling with friends is truly a blessing.  Thank you for sharing your journeys with us!! and allowing us to be a part of your journey.

 

February – 2007 (10th month)  2nd  PSA less than 0.1, NON-DETECTABLE….!!!!!J

 

March – August 2007 (11th16th month) 3rd PSA less than 0.1, NON-DETECTABLE….!!!!! J

    
We hope our journey gives you strength…knowing  “You are not alone!” …  You have new~found friends here at HealingWell.com   Continue reaching out to all of us… as you move forward in your journey.

 

June 1st ~ a personal thread on HealingWell   Life's Journey ~ Thank you for your friendship! 

 

I will be back periodically to update “Our Journey”… we’ve traveled too many miles with Friends of HealingWell not to let you know how we are doing…

 

Living each day as it comes and living it to the fullest…  Knowing that we are never promised tomorrow so ~ taking time to smell those beautiful flowers in the garden along the path we travel.  Hugs from Lee & Buddy

 

 

We wish for you to find the strength to carry you through with

…YOUR JOURNEY…

 

Issues:                 

 

(A) We felt like a BUS hit us ~ but after processing it and talking through it ~ we felt we were going to get up from the hit and realize it was just a little mini bus that hit us!!  If we can become cancer free….. we will be thankful this bus hit us now rather than 3-5 years down the road.  As of August 2007… undetectable PSA J

 

(B) Phone call to confirm findings, scheduled Consultation for Monday.  We wanted to educate ourselves on what area of the body we were dealing with and the functions of the surrounding tissues, etc….  so he suggested reading…”Give Yourself a Second Opinion… Guide to Surviving Prostate Cancer” by Patrick C. Walsh, M.D., Professor of Urology, The Johns Hopkins Medical Institutions and Janet Farrar Worthington.

 

(C) We had already made our decision before the Consultation on Feb. 27th 

Radical Retropubic Prostatectomy…..Lift the Hood …We wanted our urologist to visually see and feel the tissue and take out all surrounding tissue that may be hiding… cancer cells. 

 

(D)  Preparations before surgery: 

 

v      Get your prescriptions filled before your surgery date so you don't have to get it on the way home..!!! 

 

(F) Constipation is something you do not want to have to deal with...

         Be prepared in advance....

A stool softener was prescribed ~ we were to start taking after we left the hospital… And start taking a mild stool softener so you don't get constipated!! You don't want to get constipated along with just having your surgery!   Even with being prepared… Buddy did have some issues with constipation.  The pharmacist.. suggested equate vegetable laxative.  We also bought equate Fiber Therapy.  We alternate between the two.  They are very mild.  (If you strain for bowel movements… you will see blood in your urine and with Mr. Hang..you will likely have urine come out around the tubing in the penis) your body is reminding you ~ Don’t strain.. and don’t sit too long on the toilet.  Get up and move around until you are ready to void…  You will also see blood in your urine if you overdo it… walking, etc…  Be aware of hemorrhoids… have something on hand to help just in case.  Preperation H Cool Gel…

 

(E) Bladder Spasms: Suppositories were given in the hospital and a prescription (Hyoscyamine) had been given to us prior to surgery which we started once we got home.  This obviously was the right formula because Buddy did not experience any spasms.

 

Preparing for Surgery Day

We stuck to clear liquids during the day before surgery and nothing after 9:00 p.m.  Our doctor specifically said they would do the enema at the hospital.  Looking back I would have been happier to have Buddy do it at home for the convenience of having the bathroom readily available!  We did one before the biopsy and it worked fine but he specifically stated he wants his done at the hospital.  Worked out fine!

 

Surgery Day

We arrived at 8:00 a.m.  They asked if we wanted Buddy’s name listed and we said, “No”… and the receptionist stated that if I called from home then I would not have access to him or any information about him…. SO… MAKE SURE you are listed and you have proper consent forms….. We were then taken back to the pre-surgery ward around 8:15.  Our anesthesiologist and the team of nurses came in and introduced themselves to us and said they were going to take good care of Buddy! They started an IV and got leg pressure cuffs on the lower part of his legs and an antibiotic was given also at this time.  Our surgery was at 11:30 and they came for him at 11:15.  I walked out with them as they took Buddy to surgery.  They stopped at the entrance to the OR and I leaned over and kissed him.

I then headed to the waiting room.  Just got settled in and had a call from the OR nurse letting me know that they just started the surgery.  They called again… just as they were closing up the incision and said the urologist would be down shortly to talk with me…. Buddy would then be heading to the recover room.  Another call came when he was ready to be moved to his room.

He doesn't remember anything from the time we were in the prep room.  Next thing he remembers being in the recovery room.  He doesn’t remember the breathing tube being removed and no sore throat.  Expect the sore throat and if you don’t have it!! This is a plus… : )

He had suppositories (at the hospital) to help ward off bladder spasms (medication was sent home for this).  He also had 2 drain tubes left in the abdomen.  Located on the left and right side of his incision…  Once the wound drainage decreased they were removed at the hospital.   One drain was removed on Tuesday afternoon after surgery on Monday and the second drain was removed Wednesday morning.  We left the hospital on Wednesday around 1:00 p.m.

Up walking the next morning after surgery. (Many are walking the same evening…) Buddy really felt good walking…but pushed it a little. Too many laps…Blood pressure dropped and they had to re-hook the IV that had just been taken down 1 hour before. Don't push it!  He really felt better when he got up and walked.  Do fewer laps more often than too many at one time!!  The movement really helps the system get better faster!! 

We had a 1-hour drive home and the neck pillow was priceless and I only paid $9.99 …so get one now and it’s great for your recovery period too!!  He continues to use it when he reads.  I bought 2 nice lounge chairs for OUR recovery.  He has his chair in the leaning back position to take the stress off the mid section and perineum!  We are having a Great Recovery and so will you!  

Being retired has allowed Buddy the time for recovery.  He set goals for himself and set up a daily routine of walking in the a.m., afternoon, pm… Not everyone has this time and so you must do what’s best for you. Our surgery and recovery period was well thought out…. He started back to the YMCA on June 1st to continue his Wellness program (Tuesdays & Thursdays) and on Mon,Wed,Fri,Sat,& Sun 2 mile walk on road with incline along our beautiful creek in the mountains.  He is not doing any of the seated machines… only the legs and upper body activities. (We’ve made a decision not to do the sit down machines (biking included) to save any extra stress to the sphincter muscle… it has a job to do and we want to give it the best opportunity we can to keep us from any urinary incontinence ~ in the future. 

 

Reminder:

PLEASE>>>>>>>>   DON’T RIDE ON LAWNMOWERS, HORSES, BIKES, during your recovery period… take the time to heal and recover completely before you try these… We personally will not be doing any of these in the future…   (SEE SPHINCTER Information at the bottom of this thread)

PLEASE>>>>>>>>   DON’T LIFT ANYTHING HEAVY or LIFT YOUR BODY UP for at least 8-12 weeks… BE AWARE and LISTEN TO YOUR BODY…. If not… you will be the one to suffer.  You don’t want a HERNIA!!!!!

One thing to note:  Buddy is 53 (at time of surgery), 160 lbs, 5’9” and the exercise is not the Body Building Kind!  He doesn’t smoke, he doesn’t drink, and he eats healthy …. I’m the one who eats the steaks, fries, and butter J

I was home the first 3 weeks during his recovery... so I set my body clock to his.  Slept when he slept, ate when he ate, etc... This was a lifesaver for me!

 

Radical Retropubic Prostatectomy with “wide excision”:

We requested our urologist to perform RRP with “wide excision”… We were both very adamant and put it in writing to him so there would be no questions about him leaving something behind.  Yes, this is a radical decision… but one we BOTH wanted.  Quality and Quantity was our agenda to this decision.  We wanted to do whatever we needed to do to help in the removal of all cancer cells.  Taking out the prostate with attached seminal vesicles and segments of vas deferentia, and the neurovascular bundles.

 

Our choice to have the “wide excision” is a very personal one.  We both wanted the (prostate) taken out immediately and everything that could have any hidden cancer cells in them.  Our 2 main objectives were… Cancer Free & Urinary Continence

 

** Excerpts from “Dr. Patrick Walsh’s Guide to Surviving Prostate Cancer”

 

**Long-Term Issues: Urinary Continence and Sexual Potency:

“It seems before surgery, many men focus on impotence as the major complication of radical Prostatectomy.  They are so wrong.  Recovery of urinary control is far more important and –if it happens slowly, or doesn’t happen at all – cast a far greater shadow on your life.  If something’s wrong with your ability to urinate, you’ll be reminded of it several times a day---or worse, several times an hour--- not just a few times a week or month.  And frankly, having to change your adult diaper because you just involuntarily urinated in it can dampen—literally—any romantic thoughts that you do have.

 

 

**Urinary continence: The return of urinary control:

 

I posted a sign in the bathroom…

 

**Phase One is when you can remain dry when lying down.

 

**Phase Two is when you’re dry when you’re walking around.

 

**If you can walk to the bathroom and not urinate until you get there, that’s a GREAT SIGN!!!… it means that the sphincter is intact.

 

**Phase Three, you are dry when you stand up (using muscles that put pressure on the sphincter) after sitting.

 

**Remember, the recovery of urinary control is a slow process.

 

The most important thing you can do during this time is not to get discouraged.

 

 

J Ecstatic to say “we” have accomplished all of the above….

 

**Excerpts taken from a wonderful book called “Dr. Patrick Walsh’s Guide to Surviving Prostate Cancer” by: Patrick C. Walsh, M.D. and Janet Farrar Worthington. 

 

This book gave us (and continues to give us) so much knowledge… and Knowledge is Power.  Power to help us understand what to expect which in turn helped us to reach for a very positive outcome.

 

 

Kegel Exercise ~ Our Routine/Schedule

 

Before Surgery:

Just a little back information to help understand what we are dealing with.

Getting the little guy (sphincter muscle) ready before surgery day… !!  This is why the exercises (kegels, walking, stairs) are soooooooo important to strengthen this little muscle before surgery.  So ~ when it’s time for him to kick in and start working…. He will be ready! 

The main thing our urologist told us is to “not overwork him”!!!

 

After Surgery (When catheter has been removed)

Take time to heal/recover….  Listen to your body.. it will tell you what it needs and what it doesn’t need.  Don’t push too fast because you really are going to feel good….  But you really need to take it slow!!!

 

An **excerpt from Dr. Walsh’s Guide to Surviving Prostate Cancer

 

**Men are equipped with three separate anatomical structures that control urine – a sphincter at the bladder neck, the prostate itself, and the external sphincter.  Radical Prostatectomy knocks out two of these—the sphincter at the bladder neck and, of course, the prostate—leaving only the external sphincter to do the work of three.

 

**Because of the powerful structures upstream, this (external sphincter) is never tested or even used much in most men….

 

________________________________

 

 

Right after Mr. Hang said goodbye!!! 

A small amount of leakage.  When we got home (after holding it for approximately 1 hour) ~ Buddy was thrilled to be peeing like a teenager again!!!

 

START the urine flow and once it has a good stream…

STOP  Hold (Kegel) for 10 seconds  ~  He feels the sphincter muscle tighten up

START regular flow (2-5 seconds)

STOP  Hold (Kegel) for 10 seconds

START regular flow (2-5 seconds)

STOP  Hold (Kegel) for 10 seconds

START regular flow (2-5 seconds)

STOP  Hold (Kegel) for 10 seconds

(depending on the amount of urine…you may do 5 reps)

 

(Ahhh….this is music to my (our) ears...  :)

 

During 8 week healing/recovery period Buddy added a few (in-between) kegels during the day when he was up and about in the house.  He also pushed the sphincter during his walks to hold the urine and again could feel the muscle strengthening over time.  He could also feel the muscle during the stop/start while urinating.  Definitely the time spent getting this little guy ready prior to surgery ….was a huge reason for his continence so early on.  He stopped doing the in-between kegels early on in his recover… because of being continent.  No doubt he would have continued doing more kegels if he felt it was needed.  That’s where listening to your body comes into play.  This is so important….

 

Before surgery ~ Buddy started a wellness program when he retired 4 years ago.  2.5 hours (Mon-Fri)  His routine included walking, leg lifts, stairmaster, weigh machines, hand weights, and swimming… established before being diagnosed and continued right up until surgery time…. After being diagnosed he added kegels when urinating… to start strengthening the external sphincter muscle.

 

After surgery ~ Buddy held off his regular workout routine for 8 weeks… 

He walked 3 hours daily….1 hour each… a.m. /noon /pm during this time period….. 

Week 1 through Week 3 ~ He walked the driveway which has a nice incline… gradually going further and further up the lane. 

Week 4 through Week 8 ~ He began slowly heading toward the water wheel approx 1 mile from home…which has quite a bit of incline… since we are in the mountains. 

Week 6 ~ I bought him 3 lb. hand weights to carry.  His upper body was screaming for some kind of workout J 

Week 8 through Current Date…..Back to the YMCA…  (Tuesdays & Thursdays)

How much time??? How far to walk??? ……..Listen to your body… Don’t over do it and gradually increase your time.

His new workout routine has a few personal modifications.  No sit down exercises (bicycling, machines with hard surfaces).  We are really going to take care of the little sphincter muscle that’s doing all the work in keeping his urinary control in control.  Concentrating on walking indoor track, upper body stretching, abdominal area strengthening, and the stair master machine to help strengthen the sphincter muscle.  He finishes up his workout with a gentle swim and a nice hot shower!!

 

At 16 months and currently…

Still listening to his body!!  Buddy’s 5’9” and weighs 160 and is in good health!!! J

Reminder:  We are in our 16th month of healing/recovery at the time this schedule was listed.

He started out with less time…. and at approximately 11 months reached this schedule… and continues this as of Month 16.

2.5 hour workout at the Y! 2 days / week *Tuesdays & Thursdays

 

20 minutes walking the track

20 minutes upper body stretching and arm weights

12 minutes stair machine.  He does the full step (not the little short ones)

20 minutes walking the track

20 minutes upper body stretching and arm weights

12 minutes stair machine. (full step)

06 minutes walking the track

15 minutes swimming

15 minute “nice hot shower”…. Ahhhhhhhhhhhhhh

 

Yes ~ even the doctors have different opinions and I think it’s truly up to the individual to get in tune with his “body” and the little guy (his sphincter muscle!)

 

This is such a small muscle and needs to be protected at all cost!!!

This works for us and are truly happy to share!  Happy “kegeling”… on our paths to HealingWell.

 

We've wanted to share ”Our Journey” in hopes that others can pull from it.  A good foundation is what you need to get started on your own journey.  We hope this helps you!

 

Sharing in Friendship,   Lee, Buddy, and Murphy

 

 

http://i880.photobucket.com/albums/ac6/bluebirdathealingwell/BuddyandLee.jpg

http://i880.photobucket.com/albums/ac6/bluebirdathealingwell/Murphy.jpg

post edited to add PSA results


 *bluebird  ~ Lee, Buddy, & Murphy from North Carolina

Link to our personal journey…>>>     Our Journey ~ Sharing is Caring 

April 3, 2006  Radical Retropubic Prostatectomy

4 Years ~ 8th PSA April 2010 ~  less than 0.1 NON-DETECTABLE

 

Post Edited (bluebird) : 5/14/2010 2:58:48 PM (GMT-6)

Hello Lee & Buddy,

I just wanted to say how impressed I was with your very personal account of the fight to defeat this PCa. It will be a valuable resource for those who need to know in human terms what they will be facing, and I mean for both husbands and wives. Unforturately we all had to deal with the clinical side first, and there is not much in the way of warm and fuzzy there. I wish doctors would lead new patients here first, and then they could read stories like your's. I believe a lot of the fear melts away when you know others are facing it with you.

Thanks on behalf of us all,

Glen

Amen.

It was from going back through all the threads on this site - and reading yours, Mama Bluebird, along with all the rest ofyou who have been there - that made it all seem do-able, rather than an impossible nightmare. Fears and uncertainties will always remain, but it's with the go-ahead backed by all the caring folks here. That is simply priceless and cannot be had from anyone who hasn't been through it.

Mama Bluebird,

What a helpful post! Thank you for taking the time to share your own Prosate Cancer journey, which is a fully shared experience, hand-in-hand, heart-to-heart.  My dearly beloved was indescribably loving and supportive during the long road beginning with the spike in PSA in October 2005 with negative DRE, thru the follow-up test three months later, the biopsy that found 1 core in 12 positive for CaP, and the lift-the-hood RRP surgery at the end of June to where are are now.

I agree that it is important to come to one's own decision about treating this scourge. We read extensively in all the standard Prostate Cancer books, thought/talked/prayed,consulted medical experts, and arrived at our decision in favor of surgery. It is not a decision we have ever regreted.  And as a side benefit our relationship is stronger and more loving than ever.  Through this experience we have discovered, in ways that a life-threatening illness can show, how much we mean to each other and the joy we find in our life together.  "A hard life," as Solzhenitsyn (himself a cancer survivor) writes, "improves the vision."

Six weeks post surgery, continence is nearly complete and we will begin to rebuild our sexual love life soon.  My energy level and stamina are back to where they were prior to surgery. We are fortunate in the outcome of the surgery, with the cancer totally confined to the prostate in only one area the size of a pea. 

Thanks to you and others who share their own experiences with prostate cancer on this forum.  It has helped me immensely to read and share here.

Tim 

 P.S.  I work in healthcare and the organization I work for has a research division.  They are involved in testing a prostate cancer vaccine.

 

 

 


Age 57  PSA 2.5  Gleason 5   Open Radical Retropubic Prostatectomy 6/21/06  Cancer confined to prostate

Thanks for sharing. My DaVinci surgery is scheduled for August 23, 2006 for prostate removal. I am 54 years old, and had 2 of 12 needle biopsies positive with a Gleason score of 6. An MRI of the prostate area indicated the cancer to be confined to the prostate and curable.

I proceed with the thought that the surgery is far off, but realize the date is coming up rather quickly. I have found this website
to be very helpful in understanding all that I will expect. Thanks again for sharing your experiences, for they have been very informative and helpful. God bless you.
Bluebird,
Thank you so much for sharing this with us. I will print it out for my husband.


Stay Strong!,
Wittler
 
My Husband was Diagnosed 7/13/06
*52 yrs old
*7 Gleason
*11.? PSA
*His father died of PC
*Negative Bone and CT scan

Bluebird,

Jeff's surgery is scheduled for Aug 30 and is going with radical. I'm now in the mode of reading books and making my lists. I have a hotel room near the hospital so I don't have to drive back and forth. It would be a very long drive through Wash DC. If Jeff has to stay in the hospital longer than a few days, I'll go home to see the family sometime. our children (ages 23, 19, 15) are used to us traveling and are independent, but I also don't want to shut them out at this time.

I'm very curious how you and your hubby are retired at such young ages. lucky you!! Jeff works for himself and has that taken care of. His employees are very supportive and will take care of things while he is gone. I work for the federal government and can take as much time off as I need to.

thanks again for being here.....kat
Bluebird,
I am reading your account with interest and I have learned and will take info from it for what I will need for DWT procedure.
BUT could you maybe give some advise for people that still have to work and can't stay home in their pJ for 3+ weeks. There has to be something that you think would be helpful for the non-retired ones.
SL
I have a question about when your husband was in the hospital. did he wear the hospital gown or the PJs? Jeff is also having open surgery and I'm just wondering. kat
That is a good question. My surgery with the DaVinci method is this Wednesday and I was planning on sticking with the hospital gown due to the catheter. Finding baggy pants for the return trip home,is also a little challenging.
It is definitely more practical to wear the hospital gown because of the cath./bag, and likely a drain tube. When I went home my wife had a pair of extra large sweats for me. While I was limping around the house I wore a 3x t-shirt as a night gown with a loose fitting light robe that kinda hide all the bags and tubes (I came home with a drain tube w/pouch and the cath.+ bag). The t-shirt and robe made it much more comfortable. This only lasted for about 5 days, and then normal pj's/clothes.

Good luck to you both, Jeff and Ed.

Glen
Thanks Glen.
Ed,
I bought a couple of carpenter style pants just one size larger for Paul and he loved it. The legs were plenty baggy to hide a cath and the roominess of the style gave him somethng comfortable to wear for the next 2 weeks while the bloating and discomfort resolved.
 
This surgery is so much more patient friendly these days. Not the incontinence part. That's better but still quite disconcerting for anyone.  I would have loved having such a procedure as a DaVinci available when I had a hyster in 93. I know you will do very well. Good Luck and try....try to relax a little.
Swim  

Hi bluebird,

Thanks for sharing again with us. Some of the best advice I got from you and others I wanted to add or reiterate.  Start the Kegels now.  I do not know why the docs do not suggest until afterwards, but I took the advice and started 2 months before surgery.  I think it has helped.  I just had the catheter out last Friday and only have dribbles when walking.  I went all night last night without a pad, but I was up every 2 hours to go to the bathroom.  Still, was a nice break from wearing a pad.

One of my concerns with surgery was getting nauseated.  I hate feeling sick in the stomach.  The first thing I remember when I woke up was to ask for nausea medicine.  It helps right away as they administer through your I.V.  While you are in the hospital, keep up with the pain medicine they offer.  You heal much faster if you are not in pain.  If you get behind with the medicine, it can take a while to catch back up.  It is fact being in pain slows the healing process.  My wife and I made sure I kept up with the meds every 4 hours.  The bladder spasm was what caused me the most pain, so be sure you ask for medicine for it.  They did not give me anything unitl after they started so keep this in mind.  Once the IV comes out they then offer pain killers in pill form.  Again, my past experience with them is nausea so they gave me a pills for this as well.  I took a nausea pill along with the pain killers and never had any stomach problems.  So be sure to take home with you ; pain killer pills, nausea pills, bladder spasm pills, and your anitbiotic pills.  I rarely take any medicine but be religous with them wether you think you need them or not if you want to heal quickly.  Remember, even though your not in much pain, you still have much swelling inside that benefits from the medicine.  I just took tylenol during the day and the stronger pain killer at night.

I had the catheter for 11 days.  I did not have any problems, again due to good advice from all of you.  Bring home the leg bag (great for during the day and walking) and the larger bag for overnight so as not to interrupt sleep.  I made sure to apply antibiotic ointment 3 or 4 times a day on the penis head and the tubing where it enters. I did clean the dried gunk off the tubing with warm water and a wash cloth when needed.  The velcro strap worked well for me to hold the tubing in place so as not to pull (yikes!).  I wore it well up on my thigh.  I also cut the length of the tubing to the leg bag as it was too long for my shorter legs ( I am only 5' 9'').  If you do feel cramping check to see how full your bag is and empty regularly.  On occassion, the urine would get trappe in the tubing, I simply pulled the tube apart from the rubber catheter to allow air to drain and reconnect.  The same way when changing bags. 

Walk, walk, and walk.  This has helped me heal quickly as well.  I live next to a pathway and had no reservations walking in loose shorts or my boxer shorts with the leg bag. I had my surgery two weeks ago tomorrow and started back to work part time today (4 hours each day this week).  I feel pretty good and now working on the bladder control.  That is another emotional ordeal (thanks for the warning Glen) but I should be thankful I am doing pretty well considering it has only been 3 days since the catheter.  I know I need to be patient, it is just hard.  I wanted to share as it is still fresh in my mind so it may help others as well.

Michael

Hi Michael,

Thanks for the detailed up date on your recovery. This will really help those who are about to under go the procedure. There are so many things you have mentioned that the doctors did not. Nothing like a personal account from someone thats just been there to ease the fear.

I'm glad to hear you're making such good progress in your recovery. I think you're way ahead of where I was in the 4th week. So you must be doing all the right things. Only one caution: do not attempt lifting anything that weighs more than 5-10 pounds. I don't want anyone else to go through what I did.

Keep up the good work'

Glen

Excellent points, Michael! Husb. experienced the waves of nausea, but they would pass, and we honestly didn't know you could ask for something. I wonder if it's from the anesthetic - the only time I went under, I vomited for two days after.

It is very important to monitor the bag - as you said. It can back up, stop working temporarily, vacuum action occurs, or bubbles go backward. If it backs up, you'll know for sure!

Another point is the pain meds - I see many who don't need them after the first day, but we sure did - and it was a great help! Your reiteration that it helps the healing is such a good one.

Glad to see you're up and at 'em. Hope all goes well with getting back to work.

Thanks everyone! I keep telling Jeff everything I'm learning and I'm even making notes because there is no way I'll remember it all. I think someone should publish a booklet with all of these details and every doctor and hospital should hand them out. Jeff does get nauseaous from anesthesia and pain medication, so he is telling them about that ahead of time. I checked with the hospital to see if they had wireless internet service for the patients, but they don't. I assumed they would since the staff uses it. I was hoping to get online and read a lot of these posts for motivation for Jeff and me.

Post Edited (M. Kat) : 8/22/2006 11:29:05 AM (GMT-6)

Hi!!! Forum Friends,
 
We are still on the road trip we planned years ago :)
Just finished Jasper National Park down through Banff National Park in Alberta, Canada.  Just touching base and will get caught up once we get home.  Buddy's done exceptionally well and since we're driving many hours a day (we keep Buddy in the backseat so he doesn't have to keep pressure on the sphincter muscle) ... we swim at night and this has helped!
 
Michael - It is really great to hear from you!  You old pro!!  Your account above is "priceless"... and will truly benefit so many others.  Can you believe it's already 2 weeks since surgery :)  aaaahhhhhh
 
You did really well and we are soooooo happy we posted "Our Journey".  You hit on a few things I neglected to mention.  
Bladder Spasms: Suppositiories were given in the hospital and a prescription had been given to us prior to surgery which we started once we got home.  This obviously was the right formula because Buddy did not experience any spasms.
 
I'll get caught up with your postings once we get home.  Just had an opportunity to check the forum and wanted to touch base. :)
 
GreenAcres - true true true about the pain mediation... take it even if you don't feel you need it!  A good reminder from Michael about this too and he's the new pup on the block! 
 
Ed NJ - Soon you will be the new pup.
Our positive thoughts and prayers are coming to you at this time... I know you feel them!!! 
 
Ed NJ & M.Kat - We used the hospital gown.  We kept the back opened when in the bed so he wouldn't get tangled and when he walked we used a second gown so his backside wouldn't show :) this worked nicely.  On the trip home... we had pants with a draw string so he could adjust the tightness around the incision area. 
 
Our thoughts and prayers are with all of you!!! 
 
There's several people waiting to use the hotel computer so better sign off for now.  I know I've missed a few very important dates and I want you to know my thoughts and prayers are with each and everyone of you.... each and every day... truly. 
 
In Friendship,
Lee & Buddy 
 


mama bluebird
~  ~  ~  ~  ~  ~  ~  ~  ~  ~  ~  ~  ~
Buddy 53 RRP April 3, 2006 PSA 4.6 Gleason 3+3=6 T2a Confined to Prostate
June 29th PSA Less than 0.1 Non-detectable 

BlueBird,
I just wanted to let you know how helpful your journal has been for us. We learned 4 days ago that Curtis had prostate cancer...right now I think I'm still in shock, but reading your journal has been a lifesaver to me.
Wicket
Dear Wicket..... Thank you for your posting....
 
I have wonderful happy tears streaming down my face after reading your posting...  That's why I did "Our Journey".  Know that we are all here for you!!!! and your loved one. 
 
It's a wonderful forum... so stay with us and you'll have an easier road because of it.  The fear will subside once your realize you are not alone....
 
We will keep you in our thoughts and prayers.....  And .... Keep us posted okay!!!
 
In New Friendship,
Lee & Buddy


mama bluebird
~  ~  ~  ~  ~  ~  ~  ~  ~  ~  ~  ~  ~
Buddy 53 RRP April 3, 2006 PSA 4.6 Gleason 3+3=6 T2a Confined to Prostate
June 29th PSA Less than 0.1 Non-detectable