Tag Archives: stress

:)

(17:08:46) px5150: you were right, it was TMJ the dr said
(17:08:51) px5150: got myself a mouth guard


17:13
(17:13:41) onlysurvivor: kewl
(17:13:57) onlysurvivor: good luck
(17:14:14) onlysurvivor: has something to do with nerves also
(17:14:27) px5150: yea, dr said stress
(17:14:33) onlysurvivor: grinding or stress in jaw
(17:14:43) px5150: stress = griding at night
(17:14:54) onlysurvivor: you might have a “stress” issue ;)
(17:14:56) px5150: it all came about when they axed my benifets
(17:15:01) px5150: I know I do
(17:15:14) px5150: this WC shit just wears me out, and puts me on edge
(17:15:19) px5150: homicidal edge
17:18
(17:20:13) onlysurvivor: know what you mean
(17:20:21) onlysurvivor: I’ve had some issues also
(17:20:39) onlysurvivor: WC just ratfucks everyone
(17:21:17) px5150: damn str8

Internet Surfing, Fibro Ranting.

Well it’s another day, of unwilling, and being bored, searching around the Internet for stuff about Fibromyalgia, and researching some information on the Doctors.

In my travels today, I found a really spectacular website, Wikipedia. On there I found a lot of good information, that is freely available to be copied and read, thanks to the lovely piece of legal artwork called the GNU Free Documentation License.

While perusing the site I found what I consider to be a pretty much dead on definition of Fibromyalgia and it’s treatments.

http://en.wikipedia.org/wiki/Fibromyalgia

http://en.wikipedia.org/wiki/Guaifenesin_Protocol

Another cool site I found is FibroHugs. I really like the article this one Doctor wrote about the treatment of Fibromyalgia. Notably this thoughts on Passive Stretching, exercise therapies that include aquatic therapy, and treatment of psychological distress.

Unfortunately, some of the research that I am doing is leading me to believe that my Fibromyalgia is genetic in some ways. Specifically the Deposition Disease Therory portions from the definition about calcium deposits in the body. But the good thing, is the same literature supports that my Fibromyalgia is secondary to my physical and psychological injuries. Which were industrial in relation.

After having had a the kidney stone a couple years ago, I think there is a possibility that I’ve always had this underlying condition, but didn’t have any symptoms till I sustained my industrial injuries, begining with being unfairly treated and stressed out at work. Also since the work injuries, dealing with my life in general has become one big stressful situation. The majority due to lawyers, adjusters, and the lack of help from the Doctors I’ve seen who don’t understand what’s wrong with me. Another cause, is illness, and if I am remembering correctly, when I first started at Eyematic, I was working long hours and got sick after about a month or so and then had to take time off work to recuperate. When I returned, the unfair stress began. Since then my nose has always been kind of stuffy, like I can usually only breathe clearly out of one nostril.

Something that kind of bothers me in the back of my mind. If my Fibromyalgia is genetic, if and when I have children will they eventually have to deal with the debilitating effects as I now live with everyday? I hope not. I hope business practices become better, and that unfair stressful situations will be a thing of the past.

Have I mentioned lately how much I like blogging? Google’s blogger makes it really easy to work on my writing, save my work and come back to it when I have more energy.

One more thing: The internet rules!

failure

In my eyes, the California Workers Compensation system, of Doctors, Lawyers, and Accountant trained Insurance Adjusters, has failed me, and they do not wish to listen or hear what I have to say, or what I have been through. I have been both physically and mentally disabled for coming on 3 years now. This accident has left me with Degenerative Disc Disease of the Lumbar Spine, my Neck, a shoulder that now makes funny noises, and a serious case of depression enhanced by stress. From what I’ve learned on my own, about how I am injured, I can understand why my body feels things it shouldn’t. Numbness, sharp burning pain, tingling, weakness. I know it will only get worse as I grow older. I have accepted that.

Up until last August, I had no idea why the pain I felt never goes away, it only gets dull at times. I also had no real idea that the purposefully given stress from my job could and would destroy my body. I’ve had numerous tests, and MRI’s done, weight bearing, standard, injected with dyes, Disc Neucleoplasty, epidurals, and more that I cannot seem to remember. Some of the procedures I have gone through I have found to be quite traumatizing, during, and after.

I’ve been through Land Therapy several times. Only to have it taken away for a month or more, from me for unknown reasons after treating for several weeks at a time. Each time the Insurance Company removed my therapy, my physical condition deteriorated more. The Orthopedic Doctor I was seeing at the time, who wanted to do nothing but get me on addictive pain killers, give me injections and fusions, decided to give up on me, and I didn’t stand for that.

I found a friendly Chiropractor, who seemed interested in helping me with my case, to find out what is wrong with me. For the next year, he referred me to other specialists, and had tests performed on my nervous system, and other important areas. None of which my previous Doctor had done. I had been interested in trying Aquatic therapy, hoping that would do the trick, of letting me excersise my body, with a minimum amount of increased pain. Still the same results. But I stuck with it, for as long as I could cope with.

Around August 2003, my Primary Treating Doctor, referred me to a Pain Management Doctor, who had an interesting idea as to why I was always in pain, even with the easiest of therapies.

He had diagnosed me with having Fibromyalgia. So I started doing research about what care I would need, what medications would be needed to help clear up this condition. After a while of researching I came to the conclusion that, Apparently in this world Fibromyalgia doesn’t exist in the eyes of most Doctors, and the Insurance Company. I knew this was going to be a battle. Since then, several of the Doctors, I’ve seen have requested in their reports, that I receive treatment for my Fibromyalgia, and Severe Depression.

Has the insurance company done anything positive to help me through this most difficult time in my life? No.

Workers Compensation doesn’t pay very well and I was getting the maximum benefit. Only $980/bi-weekly back when this started, September 2001. I lost my condo, which I earned by working my ass off. Thanks to the modern miracle of inflation or some other tool, well over a year after I sold my condo. My payments went up to roughly $1200/bi-weekly. And now as of the new year 2004, they are now $1456/bi-weekly. Still not enough to get out from underneath the debt I have had to acquire to stay alive, while trying to save my condo. I am basically bankrupt, without the filing, my debt is well over my cash. Having to move 3 times in the last 3 years hasn’t made things better. Movers cost a lot, and my friends are few and far between.

When I had to move out of my apartment, I gave my previous lawyer plenty of time to find me a new Doctors to continue my treatment. Did he help? No. He wasn’t all bad, considering the only help he really gave me was a bi-weekly appointment with a Psychologist who would listen to my problems, and help me cope with life.

When the innsurance company decided it was time for me to see their Defense Doctor, I went, knowing that my case was already prejudged, which was blatently clear after reading his Medical Report about me. Doctors need to help people, not frustrate them, and take away what life they have left.

When I had to find a new lawyer to represent me, did she take the time to understand my case, and what I have already been through. No. What has she done you ask? Well, she’s given up on my case, and now refuses to help me. Apparently she doesn’t care enough helping people. She just wants the easy cut and dry workers compensation cases. So she can get her check and run. Of course when I first met her, she seemed positive enough about things.

There is a problem in the system. I the injured worker, who did nothing wrong but do his job, have since the beginning have been treated unfairly, unjustly, and have been withheld the treatment, and therapies that I need to try and live my life. I am not able to do a lot of the things in life that I once enjoyed. I’m tired of watching my life go down the drain. I used to be someone, who had direction, an awesome job, a home to call my own. Thanks in part to the WC system, and others who care for nothing more than a piece of my settlement check, which I don’t even want. My life is in shambles, all I want is to get well.

I’m 23 years old, and the life I know is full of pain, dispair, and the evil capitalization of injured workers. The past 4 months have made me want to give up on this life, but something stronger inside me wants no one to have to go through what I have. I will make my voice be heard.

Blah

This morning when I left for my Dr appts, there was a nice lovely 3day notice on my door. Great I’m already late on my rent, and I have no money.
I called about my escrow check, but when I got home it was in the mail box.
So I thought I was out of the boiler today when I got the check, and deposited it, but I’m not, my dad calls me and says they are going to hold the check for a period of time.
So now I have until Saturday to pay my rent, or I’m fucked.
he says he’ll try to get western union to send the money, but if not he says he’ll overnight me the money, which will get here on Saturday, cutting it very close.
fuckin stress!
I hope it works out.

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>>>>>>> .r246