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My Brush With Death…

Posted by on November 8, 2015

 

November 8, 2015. 2:20 PM.
Gulf Shores, Alabama. Bella Terra Resort.

MY BRUSH WITH DEATH. We pulled into Bella Terra Class A Resort at exactly 2:20 pm. on November 8, 2015. I parked our rig and that, literally, is the last thing I remember about the next twelve weeks. I’m told I just slumped and lost consciousness.  Florence got me to the nearest hospital by ambulance. I was placed on life support and continued that way for two entire months! All of my organs had stopped functioning. My temperature spiked to 106 degrees and I was placed on an ice mattress. A ventilator did my breathing for me during the next eight weeks. I was fed with a tube into my stomach. My heart stopped beating and I was paddled back to life three times. I was in the Intensive Care Unit for about ten weeks.  I was put on dialysis because my kidneys failed. On the first day of my stay, Florence was told I had about 12 hours to live. Bullshit! The hours passed and I was still alive. Days  passed and I was still alive. Weeks came and went. After a couple of months when I awoke and was able to understand what was going on, I decided I wasn’t going down without a fight! To hell with the doctors and their predictions of gloom!

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After about six weeks I opened my eyes and the doctors told Florence I’d probably live.

CRITICAL CARE HOSPITAL. My second stay was at a specialty critical care hospital where I remained for another seven weeks. Florence wasn’t satisfied that hospital #1 was doing all that could be done, so  I took a $20,000 specially equipped ambulance ride across town, about 30 miles, to the critical care facility. (Who needs to practice law when you can drive across town and make $10,000?) My third and final hospital stay was at a physical rehabilitation hospital, where I began to learn the basics: I couldn’t speak, walk, feed myself or even use a bathroom without help. I’m now home (see below) and in an outpatient physical therapy program  because after 3 1/2 months in a hospital bed, all my leg muscles atrophied. I’ve lost 40 pounds. I’m not tempted by food and I’ve developed an aversion to food. I go days without eating even a mouthful. I’m unable to walk on my own steam. I shake so much I can hardly write and I still need help eating. I use a rolling walker and a wheelchair. I am learning how to use a bathroom without the use of my legs. Because of my kidney failure, I must now have dialysis 3 times per week, now on an outpatient basis. Each session lasts between three and four hours, as all the blood from my body is removed, filtered and returned. It remains to be seen if my kidneys will ever recover enough that I won’t need this time consuming and unpleasant treatment. Probably not and I’ll need to continue for the rest of my life. (Update: after about three months I no longer need dialysis!) For the first time in my life, I’ve developed a heart condition which requires medication and monitoring. I’ve had a tiny little monitor surgically inserted under the skin above my heart. You can’t see it and I can’t feel it. But it works 2-7, via wi-fi of all things, to alert my cardiologist if problems occur. My lungs were seriously damaged. I often need oxygen. The lung damage is the result of severe pneumonia which caused respiratory failure. My eyesight has been affected. I’m hoping the nerve damage that’s altered my vision will repair itself if I’m just patient. I have peripheral neuropathy and my feet tingle constantly as if “asleep.” When I bear any weight on my feet, it feels as if there’s gravel underfoot. I spend hours every day with a physical therapist building strength in my legs and learning to walk again. It’s the hardest thing I’ve ever had to do. I can’t raise a fork to eat. I can’t climb the steps to our coach nor live inside it. I certainly can’t drive it. So we’ve rented an apartment for a year in Pensacola, Florida. We’ve got oodles of furniture in storage in San Diego, but we’re here and it’s there. So we’ve also rented some cheap furniture and a washer and dryer. We’ve had to rent a “regular” car, since I can’t climb into our Jeep. I’m determined not to let this get the best of me, but it’s not going to be easy. If I’m not careful, it will be easy for me to slip into a “why me?” and “poor me” place. It’s hard to resist it, but resist it I must.

COULDN’T HAVE DONE THIS WITHOUT FLORENCE. Florence was with me 24/7 in the critical care hospital …she had her own bed in my room so she could spend the night. She comes to most of my physical therapy sessions and “roots for me.” Without her help and encouragement, I couldn’t have come as far as I’ve come. I honestly don’t know what would have happened if she’d not been there every step of the way. Today I walked 150 feet with a rolling walker, three times! Florence cheered as if I’d run a 4 minute mile!

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Taken from the patio of our temporary apartment home.

FEBRUARY 27, 2016: OUR LITTLE APARTMENT. Just today we “came home” to our little apartment. We’ve put our motor home in storage. I haven’t yet read even one email message from you guys since November 7, nor have I listened to any voice messages on my phone. Many, many email messages and voicemail messages are there for me to review. It’ll take a while. I trust you will now understand why I haven’t responded to you for all this time. This is the first attempt I have made to use a keyboard, and my hands shake so much that it’s almost impossible for me to type. Nerve damage. I used to type about 85 words a minute with no mistakes. This evening, it has taken me over two hours to type this post. It’s difficult for me to use utensils when I eat, although that’s not been much of a problem since I’ve developed stomach problems and an aversion to food.

MY DIAGNOSIS: Legionnaires’ disease and severe pneumonia coupled with septic shock which shut down all my organs: brain, heart, kidneys, liver, lungs…you get the drift. Sepsis is a  life-threatening complication of an infection. Sepsis occurs when chemicals released into the bloodstream to fight the infection trigger inflammatory responses throughout the body. This inflammation can trigger a cascade of changes that can damage multiple organ systems, causing them to fail. If sepsis progresses to septic shock, blood pressure drops dramatically, which usually leads to death. Recently Muhammad Ali, “the Champ” passed away. The cause of death: Septic shock. And I’m guessing he was far healthier physically than I am. Why was I spared and why did he pass?

Fine one day and on my death bed the next. When’s the last time you heard of Legionnaires disease? I think I was in about the fifth grade. It is an infection caused by a bacterium. It is often fatal. I beat the odds. I’m sure there’s a reason. Time will tell.

WHY THIS POST? I wrote this post not to whine or complain to you about how difficult my life has become. Rather, for those of you who have been “traveling with us” for the last couple of years as we explore American, you need an explanation for my absence. Also, I need for you to Heed my message to you. I’ve written about these personal matters because I want to give you some advice:

 Enjoy today, because you just never know what tomorrow will bring! Please, please heed my advice!

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I‘m not really a bird watcher, but the Cardinals in the trees by our patio are really beautiful. Watching them has kept me occupied.

OUR FUTURE PLANS. God willing, and with a lot of hard work on my part, I’ll be able to walk on a limited basis in six or seven months and be able to handle those three big steps getting inside our RV. If that’s the case and if a miracle occurs and I can stop/suspend dialysis, we’ll continue with our Adventure, albeit in a vastly different fashion taking into account my limitations. If I must continue dialysis our Adventure will abruptly end. I must be patient. I must take life one day at a time. Regardless, our Great American Adventure is and will always remain the most  enjoyable thing we’ve ever done. We have memories that will last a lifetime. Don’t hold your breath for much blog activity any time soon…I’ll post what I can, when I can. Even during this difficult time I’ll get out in my wheel chair when I can, to post the sights of Pensacola, Florida.  There’s much to  see and do in this area. For example, it’s home to the Blue Angles who practice in the sky over the shoreline frequently. Museums, such as the famed National Naval Aviation Museum, restaurants, live theater and beautiful beaches abound. I can see all of these things still, even if differently. The more I think about it, there will be lots of interesting post possibilities around here if I create them. I’m sure not going to just sit around the house feeling sorry for myself, although that would be very easy to do. And, for all of you who have called and written to me, a big “thank you.” Knowing that I have so many folks supporting me is special.

UPDATE: Since writing this post, a miracle has occurred. I’ve re-gained my health beyond the doctors’ wildest expectations. God has blessed me! And He has plans for me on this Earth. See my post dated March 18, 2016 for details and for the lessons I’ve learned as a result of having been spared!

(NOTE: I was not able to write this post until March 1, 2016. However, to keep it in chronological order with all the others, I have had to indicate a publication date of November 8, 2015.)

I’LL CONTINUE MY STORY NEXT TIME.

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