The events in this post took place between December 2007 & January 2008.  I’ve written a little update at the end. December 26th I went to the local clinic complaining of extreme abdominal pain. I was ushered into a doctor’s office where the nurse checked my vitals & I waited for the doctor. The doctor came in & talked to me before doing an exam. He determined that I did not have appendicitis but more probably a problematic gallbladder. I was given an injection for pain & another for nausea. Then the doctor scheduled me for a limited abdominal ultrasound for the 27th. On the 27th I had my ultrasound & was sent home. The doctor called later that day to say no gallstones had shown up on the ultrasound. I was prescribed hydrocodone for the pain (Vicodone @ 500mg/pill up to 6000mg/day). I was also prescribed hydroxyzine for nausea. The hydroxyzine also has the nifty little side effect of amplifying the effects of the hydrocodone. The next step was to schedule a nuclear imaging test for Jan 4th. I had to lie on a table for an hour without moving anything so that the tech could photograph my abdoman several hundred times. I also got a fun injection that made my gallbladder contract. This causes intense pain. Think snake bite like when you were in grade school…only to your insides and you have to lie still and not curl into a ball. On the 9th the doctor called to say that the nuclear imaging test was fine. Still no evidence of anything amiss with my gallbladder. However, I insisted on seeing the doctor on the 10th since the pain hadn’t decreased & I’m really starting to enjoy the pain medication. After talking with the doctor he determined that a CT scan on the 16th was in order. I got 2 big bottles of barium sulfate suspension to drink the morning of the test (think orange juice poured into a glass of milk…now drink & enjoy!). The 16th I had the CT scan. Pretty painless although the IV wasn’t fun. The tech there told me to expect to wait a week before getting the results. Imagine my surprise & even distress when the doctor called promptly the morning of the 17th. The news….still nothing apparently wrong with me. Still experiencing the same severe abdominal pain so now I get a reference to a surgeon. January 23rd I make the trip to the hospital to speak with the surgeon. His recommendation….endoscopy followed by a colonoscopy depending on what the endoscopy shows.
Well the story ends there. I was denied the chance at an endoscopy ‘cuz I don’t have health insurance. This whole time every test, every drop of blood, every pee cup has had to be approved by the business office. Now they tell me that unless I can come up with $650 plus by the 30th (the best date for the endoscopy) I’m out of luck. I’m not sick enough for them to make an exception. I’m too poor to afford health insurance. Even the insurance provided by my job requires so much contribution on my part I wouldn’t have any take home pay. However, I’m too “rich” to qualify for medical assistance. Of course should the worst happen & I die before my current bills are paid the hospital will be glad to harrass my husband with collections attempts while he’s busy mourning the death of his wife. So here I sit on a Thursday night unsure of what I should do next. The most likely course of action is to continue on the medication until I’m sick enough to get treatment in an ER. Of course that’s what happened to my maternal grandfather when I was in Jr. High. He nearly died until the doctors finally removed his gallbaldder. Healthcare….neither providing health nor care to millions in the US.
I wrote this note on my Facebook account over a year ago.  Since I wrote this I’ve learned to live with more pain than I thought possible.  I stopped taking the pain meds & anti-anxiety drugs so that I could lead a clear-headed life.  I was missing out on too much to keep taking enough medication to keep the pain at bay & would at this point be very addicted to them.  None of this post is intended to support the idea of socialized healthcare.  Rather it’s a look at the utter dispair I was feeling (and still do) when thinking about how sick I must become before a doctor will treat me.  What I’d really like to see happen is that healthcare professional would take charge of the “care” and provide for people based on need not wealth.  There was a time in this country when the ability to pay wasn’t what determined your treatment but rather the need.  Doctors cared for patients in their homes & took chickens, cows or what the patient could afford in lieu of payment.  Why is it that a trip to see a doctor for less than 15 minutes with no vitals taken, no blood tests etc costs at least $90?  A simple office visit to find out you have eczema & not necrotizing faciitis is ridiculously high.  I want someone to fix what we have not get rid this system for a worse one.
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