Advanced Prostate Cancer

Click here, sign here!

Today I am writing to ask for your help.

There is a petition that the PCa community is circualting.
On January 20, 2009, a new President of the United States will be sworn in.
On January 21, 2009, that President will receive this petition.

http://www.prostatecancerpetition.org/

Please click on the link above and, after reading it, if you feel compelled to do so, please sign it.
There are currently over 9,000 signatures and we are trying to get to 10,000 by the end of September (Prostate Cancer Awareness Month).

The Dog Days

We spent the weekend at the Lake of the Ozarks and it was HOT! The temperature was in the upper 90’s all weekend but the worse part was at night and in the evenings it was so humid sitting outside was not even an option.

Some how, we had a good time anyway. We shopped, just a little, and went out for a few good meals. The most fun was at the water park. We were there for almost five hours and wiped out when we left. The heat is supposed to break tomorrow and last through the weekend.
Mary and I are hoping to get in another long weekend before Labor Day but we’ll have to see.

While there I finally started a new book. I am reading “A Thousand Splendid Suns” by Khaled Hosseini (he wrote the Kite Runner). I’m almost finished and must say that it is quite good. A much different story than the Kite Runner. It takes place in Afghanistan and though this one did not make me cry, it is equally as engrossing. I should finish it tonight or tomorrow.

My brother is recovering at home after having his gall bladder removed last week. Apparently the stone was the size of an egg and the bladder so swollen it was pushing into his liver. It was quite painful but after a few days he’s much better.

My blood test results are due at any moment, I’ll post tomorrow

What does David actually do?

I hope this doesn’t come across as braggadocio in any way, shape or form? My intent is this; I have shared so much about me personally, but very little about work and what I actually do for a living.

I am a Product Development Manager at EMBARQ. EMBARQ is the local phone company that was spun off from Sprint in May of 2006. We are in markets across 18 States, mostly in rural or smaller communities, however we provide services Orlando, FL, Las Vegas and some medium sized communities in other states as well. We provide local, long distance, high speed internet and re-sell DISH television services.

So what do I do as a Product Development Manager? In a nut shell I am a dreamer, an innovator and an inventor. For the past eight months I have been leading this project to fruition:

It’s pretty exciting after spending months and months on a project to have it written up in the Wall Street Journal!

In addition to this project I have eight Patents on file with the US Patent Office and 16 more that are in various stages of pre-submission. Though it might sound impressive, in my opinion, until the Patent Office actually grants the Patent, it doesn’t matter a whole lot (though I do take a little pride in this).

I could go on but brevity is key! In the end I hope this provides another look into the man behind the blog.

“WBC” at an all time low….

I just received a fax with the results of Monday’s blood test and my white blood cells have run off somewhere!
WBC count: 1.7

White blood cell count (WBC)
– The number of white blood cells in a specified volume of blood. White blood cells form the mainstay of your immune system — a low number might increase your risk of infection and a high number possibly indicating that you have an infection.
According to today’s report, normal is between 4.0 and 10.5. At 1.7 all I can say is Yikes! It’s amazing that I’m not more fatigued. Overall, the key is to reach full recovery by August 11th. My red blood cell count is still in the normal range so there is some good news.
By the way, I’m sure you’ve noticed something looks different around here? Brown was so blah, this place needed a little sprucing up! I hope you like it?
Just a brief update, enough for today!

I found a cure for the lack of sleep and Dex:

Yesterday, after getting through most of the day on 3 1/2 hours of sleep I got a call from my good friend Mark. He was quick and to the point, “How are you feeing today? Great, want to go to Petty?”

So last night, along with 14,500+ other Kansas Citians, we attended the Steve Winwood and Tom Petty and the Heartbreakers show. We did not leave disappointed!
Steve Winwood’s voice is still incredible after all these years. If I closed my eyes during “Dear Mr. Fantasy“, I would have though it was off the original 1967 recording…it was awesome!

Petty and the Heartbreakers rocked for just over two hours. Here is the set list, one hit after another, after another!
You Wreck
MeListen
To Her Heart
I Won’t Back Down
Even the Losers
Free Fallin’
Mary Jane’s Last Dance
Sweet William
End of the Line
Breakdown
Saving Grace
Face in the Crowd
Honey Bee
Learning to Fly
Don’t Come Around Here No More
Refugee

Encore:
Runnin’ Down a Dream
Mystic Eyes
American Girl

All I can say is, thanks Mark for a wonderful time! Tonight, I go to bed early (after my weekly Wednesday evening ball golf game!) and try to catch up on some of that missing sleep!

I Don’t like Monday’s

…and a few others….

“Monday, Monday” -The Mamas & The Papas
“Manic Monday” -The Bangles
“Monday Morning” -Fleetwood Mac
“Come Monday” -Jimmy Buffet
“Stormy Monday” -The Allman Bros.

The Dex won the battle last night! I woke at 1:30, tossed and turned until 2:15 then got sucked into “The Wire” again until about 4:45am. Maybe 30 minute more sleep and Buck and I got up at 6:30.

I am currently attempting to function on about 3 1/2 hours of sleep. I should go home but have a number of calls to be on at work this morning.

Yesterday’s appointment was long. I guess I am just going to have to stop complaining about it and get used to it. Things were running behind again; we arrived at 8:30 and left at about 1:45. We got lunch, ran an errand and returned home just before 4:00pm.

Somehow we found the energy to got see “Momma Mia” at 5:15, it was good. Definitely a ‘chick flick’ but I really enjoyed it, even the Abba music. You know they are from Sweden, apparently they opened a museum last year in Stockholm. I guess my visit there was a year early!

My White Blood Count returned to normal levels as did most of my others. My red is right on the border line of low but nothing seemed to alarm the doc.

My PSA remained steady at 53.4, at least it has reached a plateau. We were told by Dr. Van, and had read on-line, that it can take 10-12 weeks before we see results. This was just 6 week so we are hoping the tide will begin to turn next appointment (August 11).

That’s the recap for my Monday!

Ready, set, 1, 2, 3 go!

Monday is treatment number three already. One and two have been, for the lack of a better term, a piece of cake! I have run into a number of people that, based on their reaction, are stunned I’m in the midst of chemo. Not sure what to say? We still have a long road ahead of us, but so far….so good.

The next thing I have to say might be a little controversial, but here goes anyway. I have tried to avoid topics such as this, but this one has been bothering me for quite some time. Remember, it’s my blog, I started this and continue it to share what I’m thinking, and what I am going through. Please read the following, agree, disagree…if nothing else just think about it for a minute.

On May 30, 2007, President Bush announced his proposal to double America’s initial commitment and provide an additional $30 billion to combat global HIV/AIDS over the next five years.

$30 Billion dollars! What about Americans dealing with cancer, cancer of all kinds?
In 1997 1.4M Americans were diagnosed with cancer. This was in addition to the millions who were already living with the disease, including yours truly.

The total proposed 2009 budget for the National Cancer Institute is just over $6 Billion and our government leaders send an equal amount, every year, for the next five years overseas.

That is all I have to say, I’m not going to present an argument of AIDS vs. Cancer, etc. I just wanted to present this one little position and ask you to think about it.

Check point

Nothing eventful to report today. My next treatment is in a week and I’m still feeling great, I have all my hair and am dealing with the metallic mouth.

According to this mornings blood test however, my white blood count is down to 2.9 (normal 10-12 range). This dropped from last week. During treatment 1 wbc dropped the first week and recovered in weeks 2 and 3. This time it dropped after week 1 and further after week 2. I sure hope it recovers for next week.

Overall my combined counts are fine, just a little low on the wbc and red blood cell count.
PSA will not be checked until next week.

The weekend was rather normal; disc golf three days in a row. Friday we had a department event and the managers cooked pancakes for breakfast then I taught 17 people how to play the game. I only walked along and gave guidance as we played nine holes, I think everything really enjoyed the morning.

Saturday I played with a small group but it included one of my co-workers from Friday! We were delayed by rain about half way through but finished in time to drive through a mid-summer monsoon on the way home. Sunday my brother in law Rich put a whooping on me, and even as competitive as I am, it was fun to watch!

Saturday we saw the new Indiana Jones movie, I’d give it a C+. We had most of the family over yesterday for dinner and as I mentioned above I had my monthly appointment this morning. This was for Lupron and Zometa, the chemo treatment is next week.

Back to the grind……

Ironman

I still need to see the movie “Ironman”, I hear it’s really good. Perhaps this weekend with Brad?

However, the reference and reason for my post is I now officially am experiencing my first
side-effect from chemo; metallic mouth. The best way to describe it is my tongue feels and tastes like it does after you drink something too hot. Everything tastes a little strange, though nothing has been offensive enough to stop me from eating it yet!

Now it’s off to lunch….. nothing else to report today!

…is on my side…..yes it is.

Today at Mass something reminded me of a stream of consciousness that I experienced the other night while trying to get back to sleep. At some point this blog turned into more of a diary of my life and less of what’s going on within me as I battle Advanced Prostate Cancer. I spend a lot of time writing about disc golf, music, books, movies, etc. and it has been a long time since I let you in my head.

So here we go:

I’m one week into my second treatment of chemotherapy. This one has actually been easier on me than the first. No flu like symptoms this past weekend… it was quite unremarkable (a radiology term I can’t believe I just used!). I feel better than I have in months and yet it scares me…What if my PSA number doesn’t come down? I’m not in pain, in fact it’s just the opposite, but I can’t help but wonder what is actually going on inside of me.

I guess I shouldn’t doubt or question, it’s way too early, but this is my blog and I have had that thought a few times recently. I continue to pray, a lot! I pray for guidance, a cure and peace and comfort for Mary and my family. I talk to God a lot at night. Sometimes I sneak in a request for a cure but I try not to push things, he’s a little busy and I’m just one mortal man.

Time is what I ask for the most. Time for Brad to drive and graduate and go to college. Time for Meg to get married and graduate from college herself. Time for Mary and I to grow old together……or at least just a little older. I just couldn’t get though this without one musical reference. This Stones song just came to mind; “Time, time, time is on my side…yes it is”
~~~~~~~~~~~~~~~
And so there it is….short, not necessarily sweet, but right to the point.