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Friday, June 21, 2013

Parkinson's moving into my life


Parkinson's disease entered my life long before I was diagnoses, looking back I think it started when I was about to turn 50. At the time I was an airline pilot and an avid sailor. We had a 32 foot Ericson sailboat, I had the boat for 7 years, had spent most of my summers on it and I was very comfortable moving around under sail. It was about that time I noticed some balance problems, moving around the boat was becoming a little uncomfortable. I was more and more missing steps and tripping. Let me add here that I never drank when sailing, I would have something once the boat was tied to the earth, docked, anchored, or moored.



Other things started happening slowly but continued, depression, becoming stiffer, not moving easily. Parkinson's has many, many non-movement symptoms. When I would do anything physical I would sweat at an unbelievable amount. My blood pressure became erratic, extreme dizziness when standing. Vivid dreams, nightmares, moving and reacting to my dreams when asleep. Occasionally punching my wife in my sleep. I started having problems doing things I had been doing for years, learning a new airplane was pretty much the final straw when I almost couldn't do it. Not long before that I was diagnosed with depression, was being treated for that, but at the time airline pilots were not allowed to be depressed so I ended up having to retire early. It was shortly after that that things really started to deteriorate.



I had to work so I started driving truck over the road, had I not been depressed that would have done it.Anyway, later that year actually it was Christmas morning 2007, about 1:30 am, I got up to get something in the kitchen and collapsed. I had a syncopy event, I passed out, got up and passed out again. After a few minutes I was better but my wife made me go to the emergency room, bringing on a tremendous battery of tests. Ctscans, blood tests, stress ekgs, all ok. Not heart or stroke related. Neuro physyc tests, all good. After all that I was given an MRI, finally found something, a cervical spinal stenosis, the c4-6 vertabre were completely closed off, no spinal fluid was flowing from my spine to my brain. I was told one good fall could make me a quadraplegic. I needed and got surgery. It fixed the stenosis but none of the problems. During the testing process a strange name kept popping up, Parkinson's. Usually in the words,”that doesn't nessicarily mean you have Parkinson's”. After a while of being told that doesn't mean you have it I began to think maybe I had it. Two or three more years of tests all negative until my neuro gave me sinemet, a levadopa drug used to treat Parkinson's, it it helped, that meant I had it. It worked, I did, now after all the reasearch by us, we were pretty sure what it was, this just confirmed it.



I will continue with my story soon, living with Pd.


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