Esoteric:
"Anything worth doing always starts with being scared." Art Garfunkel
Exoteric:
"Also a bunch of rot that isn't worth doing." Robynn Reilly
Copyright 12/2008
A "mostly" humorous look at real events - short stories, satire, and the vagaries of life. Join me on the couch. The doctor is wacked, but in. "A merry heart doeth good like a medicine..." Proverbs 17:22a
Sunday, December 7, 2008
Thursday, December 4, 2008
Sickness and Other Things That Make You Popular
Grab your tea or coffee and pretend you've just decided to do your good deed for the day by visiting your Great Aunt Ethel. That's the excitement level you can expect if you decide to read this post. If not, no hard feelings. I secretly admire your lack of reticence in blowing me off.
For the rest of you compassionate souls who've decided to stick around, here's the lowdown on the latest installment of, "As The Stomach Turns."
You may know I have battled "The Mysterious Malady" for about ten years. It started with my feet and legs going to sleep as I sat teaching the kids one day. Unlike the rest of me, they decided to never wake up again. Think the pins and needles after you've fallen asleep on your arm. It was maddening and it was 24/7.
For two years I sought answers and got treated for things I didn't have. One doc put me on diabetes meds because to him it was obvious I had diabetes even without a test. He almost killed me. The physicians creed seems to state: "We hold these truths to be self-evident.....if you're fat this WILL be the root cause of all your health problems." Patient: "Dr., I think I've deviated my septum, contracted strep throat, and possibly sustained potentially fatal injuries in a car accident." Doctor: "I told you to lose weight!"
So, lacking diabetes I kept seeking answers. I found a neurologist who put on me on a med that helped immensely with the leg/foot issues but didn't answer the reason why. They suspected MS and examined my cranial cavity, through an MRI, for evidence of a brain. The brain was there but lesions were not. That was a good thing. More years, more meds, fewer answers. The doctor wanted me to see an environmental specialist at UCSF or Stanford to hunt down problems with a lead exposure in my past. Someday I would if the insurance agreed. Lots of sickness plagued me in between times and I never knew why I got sick so easily or felt weird, or exhausted.
Fast forward a few years and I came home from a family vacation in Hawaii to the next phase of my adventure. Now my liver and spleen were sick, too, and bizarre things began to happen to me including intermittent tremors, weakness, stomach pain, and a near complete inability to take a variety of meds. I will spare you the details your Aunt Ethel wouldn't but, suffice it to say, there were other symptoms and you'll love me for not telling you what they were.
Now, I'm not wild about having my picture taken but there are truly places cameras just don't belong: in your body would make the top of my list. When you consider it, the medical paparazzi only have a few entrances to swarm when trying to get that perfect internal shot. And you will not have an opportunity to cover any of those entrances with a newspaper to avoid prying eyes. They never got the money shot, the smoking gun, the CSI evidence. But somewhere out there I'm sure there's a flattering picture of my colon.
At least the next phase took me to UCSF where they were promptly unable to tell me anything. Well, not that promptly actually. It took two years to discover that the damage was progressing and they had no idea why. More suspicions, more MRI's, and more needles in the muscles to measure progressive muscle loss in my feet. More glow-in-the-dark radiological tests, more dead ends, more conjecture. In the meantime I searched the internet high and low to diagnose myself. Physicians love it when you do this, especially if you offer your input. You will have "NUTCASE" stamped in red letters on the front of your chart.
Finally, with another attack of whatever this is a few months ago, I plopped myself in my primary care doctor's chair and said, "We gotta figure this out. Would you check me for this, this, and this?" He stamped "NUTCASE" on the back of my chart, too, and agreed. Son of a gun.....everything came back abnormal. Now we had a possible working diagnosis: Porphyria. Coproporphyria to be exact and also some immunity issues. Porphyria is a blood disorder that could be responsible for the majority of my issues. More tests were performed yesterday to make the final determination and I won't know the complete bottom line until the end of the month. But that's the way it's looking. I'll explain what it is in more detail in a future post when all the results are in but for now it's just good to have an idea of what it could be.
As Jamie and I sat discussing this with the hematologist yesterday he remarked, "What super smart doctor thought to look for this?" I demurred and said it was actually me who asked for the test. His tone turned decidedly away from "super smart" and he replied, "Well, you can't just figure out what you have that way." Well, there certainly hasn't been any other way, doc.
So, there you have it. I'm battling new symptoms that leave me feeling faint and shaky, and with high blood pressure. It's all making me lose weight. I've dropped 20 lbs. since August. That's the up side. And the antidote for these symptoms is immediate sugar. So, if you see me laying around in a coma, just shove a cookie in my mouth.
There really is a silver lining to just about everything.
Copyright 12/08
For the rest of you compassionate souls who've decided to stick around, here's the lowdown on the latest installment of, "As The Stomach Turns."
You may know I have battled "The Mysterious Malady" for about ten years. It started with my feet and legs going to sleep as I sat teaching the kids one day. Unlike the rest of me, they decided to never wake up again. Think the pins and needles after you've fallen asleep on your arm. It was maddening and it was 24/7.
For two years I sought answers and got treated for things I didn't have. One doc put me on diabetes meds because to him it was obvious I had diabetes even without a test. He almost killed me. The physicians creed seems to state: "We hold these truths to be self-evident.....if you're fat this WILL be the root cause of all your health problems." Patient: "Dr., I think I've deviated my septum, contracted strep throat, and possibly sustained potentially fatal injuries in a car accident." Doctor: "I told you to lose weight!"
So, lacking diabetes I kept seeking answers. I found a neurologist who put on me on a med that helped immensely with the leg/foot issues but didn't answer the reason why. They suspected MS and examined my cranial cavity, through an MRI, for evidence of a brain. The brain was there but lesions were not. That was a good thing. More years, more meds, fewer answers. The doctor wanted me to see an environmental specialist at UCSF or Stanford to hunt down problems with a lead exposure in my past. Someday I would if the insurance agreed. Lots of sickness plagued me in between times and I never knew why I got sick so easily or felt weird, or exhausted.
Fast forward a few years and I came home from a family vacation in Hawaii to the next phase of my adventure. Now my liver and spleen were sick, too, and bizarre things began to happen to me including intermittent tremors, weakness, stomach pain, and a near complete inability to take a variety of meds. I will spare you the details your Aunt Ethel wouldn't but, suffice it to say, there were other symptoms and you'll love me for not telling you what they were.
Now, I'm not wild about having my picture taken but there are truly places cameras just don't belong: in your body would make the top of my list. When you consider it, the medical paparazzi only have a few entrances to swarm when trying to get that perfect internal shot. And you will not have an opportunity to cover any of those entrances with a newspaper to avoid prying eyes. They never got the money shot, the smoking gun, the CSI evidence. But somewhere out there I'm sure there's a flattering picture of my colon.
At least the next phase took me to UCSF where they were promptly unable to tell me anything. Well, not that promptly actually. It took two years to discover that the damage was progressing and they had no idea why. More suspicions, more MRI's, and more needles in the muscles to measure progressive muscle loss in my feet. More glow-in-the-dark radiological tests, more dead ends, more conjecture. In the meantime I searched the internet high and low to diagnose myself. Physicians love it when you do this, especially if you offer your input. You will have "NUTCASE" stamped in red letters on the front of your chart.
Finally, with another attack of whatever this is a few months ago, I plopped myself in my primary care doctor's chair and said, "We gotta figure this out. Would you check me for this, this, and this?" He stamped "NUTCASE" on the back of my chart, too, and agreed. Son of a gun.....everything came back abnormal. Now we had a possible working diagnosis: Porphyria. Coproporphyria to be exact and also some immunity issues. Porphyria is a blood disorder that could be responsible for the majority of my issues. More tests were performed yesterday to make the final determination and I won't know the complete bottom line until the end of the month. But that's the way it's looking. I'll explain what it is in more detail in a future post when all the results are in but for now it's just good to have an idea of what it could be.
As Jamie and I sat discussing this with the hematologist yesterday he remarked, "What super smart doctor thought to look for this?" I demurred and said it was actually me who asked for the test. His tone turned decidedly away from "super smart" and he replied, "Well, you can't just figure out what you have that way." Well, there certainly hasn't been any other way, doc.
So, there you have it. I'm battling new symptoms that leave me feeling faint and shaky, and with high blood pressure. It's all making me lose weight. I've dropped 20 lbs. since August. That's the up side. And the antidote for these symptoms is immediate sugar. So, if you see me laying around in a coma, just shove a cookie in my mouth.
There really is a silver lining to just about everything.
Copyright 12/08
Wednesday, December 3, 2008
Egocentrism
I am grappling with guilt.
As I pondered my blog today it occurred to me that writing a blog might be an exercise in self aggrandizement. I mean, by its very nature aren't I saying, "Hey! Look at me and be riveted by my fascinating exploits and intrigues?" I guess if you're a biographer or journalist (and other good examples I'm too lazy to recall right now), you're writing about other people and issues. But aren't you still saying, "I can tell that story better than anyone else?" Maybe. If you are, if I am, all I have to say is, "We better be right, Bucky."
Hoping I won't let you down. Oh for Pete's sake. You KNOW I will. That'll be good for me, too. I'll get over all this naval gazing. Hey, is that lint?
Copyright 12/08
As I pondered my blog today it occurred to me that writing a blog might be an exercise in self aggrandizement. I mean, by its very nature aren't I saying, "Hey! Look at me and be riveted by my fascinating exploits and intrigues?" I guess if you're a biographer or journalist (and other good examples I'm too lazy to recall right now), you're writing about other people and issues. But aren't you still saying, "I can tell that story better than anyone else?" Maybe. If you are, if I am, all I have to say is, "We better be right, Bucky."
Hoping I won't let you down. Oh for Pete's sake. You KNOW I will. That'll be good for me, too. I'll get over all this naval gazing. Hey, is that lint?
Copyright 12/08
I'm Finally Here!
For all who have waited breathlessly for my opinions, reflections, and life-changing insights,(both of you), I have arrived.
I named my blog "Laugh Til You Die" because I can't handle life without finding something to laugh about on a nearly daily basis. While it's true there are experiences in our lives which come without any humor, most of the time we can find a chuckle even in the dark. For me, the laughing lights a light so I can navigate. If I must face all difficulties with intense sobriety and "appropriate" seriousness, I forfeit joy. And joy is God's gift to me. I hope to use it until I leave for heaven and then I hope to get new material.
Copyright 12/08
I named my blog "Laugh Til You Die" because I can't handle life without finding something to laugh about on a nearly daily basis. While it's true there are experiences in our lives which come without any humor, most of the time we can find a chuckle even in the dark. For me, the laughing lights a light so I can navigate. If I must face all difficulties with intense sobriety and "appropriate" seriousness, I forfeit joy. And joy is God's gift to me. I hope to use it until I leave for heaven and then I hope to get new material.
Copyright 12/08
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