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Friday, May 20, 2011

Color Photos of America's Depression Era


Kodak's Kodachrome 35mm slide film still is, in my opinion, one of the great inventions of man. (Photo is copyright Library of Congress)

The UK's Daily Mail has published a page of stunning color images from America's depression era (just after Kodachrome was invented). Please go see these photo's.

They offer a totally different perspective than the harsh-but-compelling black and white depression photos we've seen all our lives.

Kodachrome images look so "thick" and dense with color.

Lord I miss the look of Kodachrome, but I love and have totally embraced digital photography. (I spent many hours in Photoshop Elements one weekend to come up with my own process for making digital images have the look of Kodachrome.)

Note: I hate linking stuff from online newspapers, the link may be dead fairly quick. So take a minute to go look at these images.

Wednesday, May 18, 2011

Goodbye Mr. Surgeon


Had my second and last post operation visit with the surgeon who installed my pain pump.

Said my incisions (all three!) were looking healthy and that unless they somehow get infected or I start having some of the bad side effects some pain pump recipients get, that, well, it was nice knowing me.

I see Pain Doctor next week for my first visit with him since the surgery.

Pain Doctor will use a remote control device that communicates through my skin to the pain pump to adjust the dose. (That's a photo to the right, of the same pain pump and catheter I now have, and the gizmo Pain Doctor will use to program the rate of medicine release.)

Ready to crank this puppy up a bit.

I received a medic alert type card with my pain pump info on it in the mail a couple of weeks ago, but yesterday finally read all the material that came with it.

I had carefully inspected the card to ensure all was correct, but after reading the associated letter, I needed to change the doctor's name and number on the card from the surgeon's name to Pain Doctor's name and number.

The card needs to have the doctor's info for the doctor filling and adjusting the pain pump instead of the surgeon.

I got an email today telling me my new implant ID card is on the way.

I thought it might be a good idea to get a medic alert ID bracelet or necklace and put the fact that I'm diabetic and that I now have this pain pump on the necklace or bracelet.

On several sites they mentioned that most paramedics are trained to look for a medic alert necklace or bracelet, and don't look in people's wallets.

That's good to know. I guess I'll have to buy me some BLING in the near future.

So much for my spiffy medic alert card I put in my wallet, eh?

Saturday, May 14, 2011

New Body Parts Installed or Been a Long Time Since I Posted


I can summarize my life pretty quickly since my last post in September of 2010.

Lots of back pain. Trying to work, sleep, live with lots of pain. I pretty much stunk at everything, work, relationships, life in general.

Last summer (2010) I did the trial for a "neurostimulator" or more simply, spinal cord stimulator, or what is basically a TENS unit where the electrodes that zap you are inserted in your back close to the spinal cord. This device is effective for some, but in me, they could never get the device to "buzz" in the areas where I hurt, lower back and outside left leg/butt. There are electrodes for the final two inches or so, and it's this section of the electrical cord which is implanted along the inside of the vertebrae close to the spinal cord. The Here's a brief run-down of these devices on Spine-Health.com, one of my most frequently visited sites (http://www.spine-health.com/treatment/back-surgery/spinal-cord-stimulation-chronic-pain).

So for me, the spinal cord stimulator trial was a failure, and my Pain Management Doctor and I started talking about one of the final tricks he had up his sleeve.

Intrathecal Pain Pump. Or just Pain Pump to many. Similar idea to the spinal cord stimulator, but with a pain pump, a catheter is inserted into the intrathecal space of the spine. This is the same protective sack where the spinal cord lies and in which our spinal fluid flows slowly from lower back, up to and around the brain, and back down the spine.

The idea is to deliver minute amounts of pain medication directly into the spinal fluid, allowing it to flow up and down with the spinal fluid and delivering some of the most powerful pain relief that can be given these days.

All along this path, work really sucked. I just hurt too much to be a great engineer, and I couldn't really take high enough doses of pain medicine to really cut the pain without drastically cutting my brain power, which is essential in the engineering world.

I've been on disability since earlier this year, and I have slowly gone through the process with my Pain Doctor to have a pain pump trial (it was deemed successful in me), visit a neurosurgeon he referred me to, get all the pre-surgery health checks done, and to have surgery to have the pain pump and catheter installed permanently.

First, the pain pump trial. in February, I went into a day-surgery center and Pain Doctor and crew sedated me a bit, and then using a fluoroscope, which is basically a live-action x-ray machine, gave me a tiny shot of morphine straight into the intrathecal space in my spine.

I've had so many shots and surgeries in my back that from the middle of my back down to almost my rear end is mostly scar tissue. But one of the beauties of the pain pump and the flow of spinal fluid up and down is that they can inject the medicine in any place along the spine and the medicine will flow with the spinal fluid, hopefully delivering sweet pain relief along the way.

I stayed at the surgery center for several hours for them to make sure that I wasn't having serious side effects from the bolus of morphine in my spine and during that time felt my pain levels really decrease. They sent me home and I was to keep a journal of sorts and to stay off oral pain meds as long as I could.

I lasted about 36 hours, but I left it too long before starting my oral medications again.

I got a good bit of pain relief for the first 24 hours and then the pain slowly started increasing again. When I took my first oral meds at the 36 hour mark I didn't know it, but the pain pendulum was swinging back to serious pain really, really fast.

It took me a couple of days to carefully dole out to myself doses of oral pain meds until the pain was back to where I could even sleep.

But the initial pain relief of the directly applied morphine was what they wanted to see, and after weeks of doctors visits and pre-surgery checks had my pain pump installed in late April at Sebastian River Medical Center in Sebastian, Florida. That's near the neurosurgeon's office and about 15-20 miles south of where we live in Palm Bay.

I had an incision along my spine for the surgeon to put the catheter tip into the intrathecal space push it up in there a couple of inches along my spinal cord.

Then they "tunneled" around my side to create a path for the flexible catheter to reach around to my front left side where another incision was made to implant the actual pain pump filled with morphine.

They also had to make a small incision on my left side to help continue the tunneling for the catheter to reach around from my back to my front.

Total, 3 incisions to heal from. Though I was able to get up easier than after my previous surgeries since they hadn't actually worked on or ground away bone, I've had a heckuva time with three incisions healing.

I'm still a week away from my first visit with Pain Doctor since my surgery, but the surgery incisions have healed enough that I can feel the pain pump having a little bit of positive effect on my pain level.

The surgeon filled the pain pump, but only set it at a super-low release rate, enough to make the pump work until Pain Doctor could see me and I had healed enough to start ramping up the the delivery rate of the pain pump.

As of today, I'm slow moving, but doing pretty well. The incisions have been slow to heal and are still pretty sore, even three weeks on.

I'm basically still in the same pain situation as before the surgery, but the fact that I can now feel the light effects of the pain pump helping gives me hope that in the coming months we can get the device adjusted to where I don't have to take much oral meds.

The initial goal is to stop taking my long acting pain meds and then only have to occasionally take a quick acting pain medicine for "breakthrough" pain as needed. Getting off the long acting stuff will be a big relief to my liver and kidneys from the years of daily oral pain medications.

The pain pump can possibly give as good relief as long acting oral pain medications, but at the rate of only 1/200 or so of what I would take orally.

In other words, you have to take a pretty big dose of oral pain medicine to help lower serious pain levels, but with the pain pump's direct delivery to the spinal fluid, many patients get the same pain relief with 1/200th of what they were taking orally.

Just tiny, tiny amounts are delivered by the pain pump in a 24 hour period but with the same effect as hefty doses of oral pain medications.

Anyway, if anyone is still out there, and you've read this far, I'll throw you a bone and stop here.

I'm still not out of the woods yet, but the pain pump system is successfully implanted in me. It seems to be giving a bit of help to my pain levels, and should help more and more as I resume visits with Pain Doctor who will fill the pump and adjust the release rate of it's medicines from here on out.

If you are interested, follow this link for a short video on the pain pump (http://www.spine-health.com/video/intrathecal-pump-implant-video). Just click on the "Play animation without narration" link in the frame, and then start clicking the "Next Step" button to continue the very short animated views of how the pain pump system is installed. It's only about a minute long. A picture will make all that I wrote here come clear with just a glance as to how the pieces are placed.

I seriously hope to resume blogging, I miss it very much. It's a great release valve for me.

Until next time...God bless you.

Friday, January 28, 2011

Dodge Viper SRT10 2010 better performance sport car

The Dodge Viper SRT10 ACR receives a new short-throw shifter in 2010 for enhanced driver experience and better performance. The rear wing profile and end plates are redesigned to further optimize the vehicle aerodynamics and improve rear yaw downforce. These changes combined with the new fifth gear ratio result in an increased top speed of 4 mph (to 184 mph for the ACR model).

Dodge Viper SRT10 2010 car picture
Dodge Viper SRT10 2010 car picture

Dodge Viper SRT10 2010 sport car
Dodge Viper SRT10 2010 sport car

Dodge Viper SRT10 2010 sports car
Dodge Viper SRT10 2010 sports car

Dodge Viper SRT10 2010 sporty car
Dodge Viper SRT10 2010 sporty car



Additional special edition models will be announced closer to their individual introductions. Pricing on the 2010 Dodge Viper lineup also will be announced at a later date.

Saab 9-4X 2012 New Mid-size Crossover

In true Saab tradition, the 9-4X delivers on its sporty persona. It is configured around a unique, purpose-designed crossover body structure, which has been key to delivering its exceptional handling and ride properties. Car-like driving dynamics are supported by Saab's advanced all-wheel-drive system, Saab XWD, and DriveSense adaptive chassis control.

Under the hood, nestles a choice of compact and efficient V6 engines, naturally-aspirated or turbocharged. The 265 hp, 3.0-liter motor for the entry-level model features direct fuel injection and variable valve timing; while the 300 hp, 2.8-liter exchanges direct injection for twin-scroll turbocharging and is exclusive to top-of-line Aero variants. Both engines are mated to six-speed automatic transmissions under adaptive, electronic control.

Saab 9-4X 2012 New SUV
Saab 9-4X 2012 New SUV

Saab 9-4X 2012 New Crossover
Saab 9-4X 2012 New Crossover

Saab 9-4X 2012 Crossover
Saab 9-4X 2012 Crossover


Saturday, September 25, 2010

Picture Post, Sunday September 26, 2010

My Big Sis and her Number Two Son came to Florida and visited us in June. A HUGE blessing to us.

Here are a few photos from when they were here.

We took Big Sis and Nephew Number Two to a restaurant in Sebastian, Florida, that is called Squid Lips. We'd always wanted to eat there, but finally took the chance. Wow, the food was good! How could you not want to eat at a restaurant called Squid Lips?

Here's the fambly at our table in Squid Lips. It's open to the Indian River Lagoon. It was a hot day, but surprisingly comfortable in the restaurant.

Then we went to the beach. Here's a photo of Big Sis and Nephew Number Two.

This is looking north along the beach...

...and this is looking south along the beach.

As you can tell, the water was all turquoise like it is in photos of the Bahamas, and the beach had almost no one on there, except that one couple with their blue umbrella. We were so disgusted at this turn of events that we didn't stay long, and left in a huff.

You know I'm kidding, right? These photos were taken the second week of June, and this beach was deserted. IT WAS PERFECT!

Tuesday, September 21, 2010

Count Your Blessings Every Day


Seriously.

Count them every day.

I haven't posted much here over the past two years, coinciding with an increase in pain in my lower back and left leg. I didn't want to always be talking about it, because it seemed so selfish.

Even with back pain at a level that I've tried many strange (to me) but accepted medical procedures and untold numbers of pain shots directly into my back, and even with the stress of a demanding job, I KNOW that I am very blessed.

Lovely Wife of 26 years, two lovely daughters, family on both sides that love us and we love them.

A nice house, a job at a great company, dogs, a cat, a fish.

I keep waking up every day so far, and that in itself is the greatest blessing.

Counting my blessings, ie. thanking God every day for them in prayer, is one way that helps me keep from descending into a deep, dark pit of despair because of the grinding pain that never, ever lets up.

Counting my blessings reminds me that I have a good life and keeps both of my feet on the ground.

But today, I have to admit that things were getting to me a bit. Trying to perform my best at work. A training class and test, and the struggle of merely walking. (As I've said before, I literally have a finite number of steps I can take in a day before the pain in my left leg and back say, No More.)

My training class ended at lunchtime, so I came home to eat, and was just thankful for the nearly horizontal relief of my recliner for a few minutes with three dogs draped on me. (They're my Buds)

And on TV I saw a man who had been burned so bad when he was two in a gasoline can explosion that doctors didn't think he'd live. He has no real hands or feet, but he's grown now, a college graduate, thankful of his many gifts.

Oh, and he's an amazing drummer. He can grab one drum stick with the pincher-like claw that is his left hand, and uses a wrist sweat band with rubber bands to attach a stick to his right hand. Played an amazing drum solo.

I was sitting there, crying like I haven't in a long, long time, watching this man's joy, and you could truly see he was joyful, and begged God for forgiveness for allowing myself to have gotten down, hurting and tired by lunchtime.

The afternoon at work went OK, I made some progress on a self-guided training project at work, and I came home completely spent and really hurting, but I was not letting the pain get to me.

Then Lovely Wife gets an instant message from her first cousin's daughter, that the wife of another first cousin had died last night, Monday night.

Lovely Wife and I met while young and both living with our families in Monroe, Louisiana. A year or two after we had begun dating, her family took in one of Lovely Wife's first cousins, whose father had kicked him out.

Lovely Wife and I both were in college and working for a regional pizza chain when her cousin moved in with them in Monroe.

He later worked with me at the particular restaurant that I worked at, and eventually began dating a girl that worked there with us, a girl I had know from school in the Monroe area for five years or so.

They fell in love, and eventually moved back to J's hometown of Birmingham, Alabama.

The instant message that Lovely Wife received tonight (Tuesday) was that J's wife D had died on Monday night. She had a shortness of breath and died, they believe it was a heart attack at this point.

D was a pretty, sweet, and musically talented woman. As a teen she won two national singer/songwriter first place honors that I know of. Could sing and play guitar and sing as good as anyone I've ever heard.

I hadn't talked to D or J in years, time, distance and life in general took care of that.

But although I grieve for a lost friend who has passed, she was a year behind me in school, so that puts her at about age 45 or 46, I'm so glad that the last time I talked with her, she was beaming with happiness. She's become a Christian and tonight I praise God for touching her years ago, as no one could know she'd die so young.

My heart goes out to J, who is apparently crushed and despondent, from the sketchy news we got over the internet. I pray that he has found the comfort that becoming a Christian can provide, but last I saw him, he was not.

So I know that D is eating at the King's table in a place with no pain or sorrow.

I hope that if J hasn't found Jesus, that he might turn his heart over now.

And I've had two amazing reminders in this single day, that life is precious, it's short, and no matter what kind of pain, physical or mental, that we may be going through, every day of life is a gift, even in the middle of difficult times.

My older brother died at the age of 41, and with D's passing last night, I am reminded, yet again, that we are not guaranteed tomorrow, only the moment we're living in, so we must make the best of it, and choose to count our blessings every day and thank God for them.

We don't get a second chance at life, Every Day Is The Superbowl for all of us. We must try to make our lives count. To mean something every day.
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