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Anniversary Presents Part One

Well, I did say I hoped it was 8″ and vibrates…

I also got a couple of scarves from Scotland and a set of hand warmers from Scotland. Both were cashmere.

That vibrator came with free batteries. I kind of want to give the kids Benadryl or ether so we can try it out. :) It’s ultra quiet, too. I couldn’t hear it above the dish washer in the kitchen. Yes, I opened it in the kitchen. My father in law just rolled his eyes and walked away. Oh well. It wasn’t for him anyway.


Confession Time

So it’s confession time. Why not? There’s no better time than the time where I have had a personal melt-down at my oncologist’s office because his timing for my treatment sucks. What sucks more is that he refused to change my treatment date and then refused to sign off on my medical records so I could travel.

On September 28, 2010, I was diagnosed with bone spurs, bulging discs, arthritis and broken lumbars in my back. Walking is excruciating. Sitting is intolerable. Standing for more than five minutes is impossible. I spend a good amount of time in bed, a heated, waveless waterbed. That caused a blood clot to form in my lungs, and I was hospitalised for a while with that.

All last month, my friend Matt had been helping me get around. My goal was to be able to go to a close friend’s wedding in November. However, on November 6, I was scheduled for a treatment. This is where I got upset with Doc Mick. He wouldn’t sign off on anything, and he wouldn’t budge with changing the date. Either we play by his rules, or we don’t play at all.

But I played the game, hopeful that by November, I would be able to sit, stand, and walk, if even for a day. I had a reason to get well, and I had a reason to try. I was given three medications. Mixed with what I was already taking, these extra drugs made me sicker. I had 16 hour sleep stretches. I vomited daily. This caused me to lose a cap and Dr. Petit wasn’t too happy with that. Vomiting isn’t covered with my original dental warranty. The medicine made my head spin. It was like permanent LSD trips. I hallucinated. Saw writing on walls. I woke up clenching both remotes just last week. But I was hopeful. Hopeful that I would get well and things would get better. I was hopeful that I could have somewhat of a normal life.

But in the immortal words that I said at the peak of my meltdown at Doc Mick’s:

I am not going to get well.
I will never be cured.
[He] can’t cure me.
The copious amounts of medicine can’t cure me.
[The Great Being We Call God] can’t cure me.
This is all just a waste of my time and my money and I quit.

With that being said, I will not be going back to treatment in December. I will not be going back in January. It’s done. I quit. I was supposed to get better. I was supposed to go through physical therapies and be able to make a drive to Dallas. I was supposed to get better. Have I already said that? Oh.

I worked hard. I forced myself to do things even when I did not feel well or feel right. I forced myself to get up, get dressed, brush my hair, take a bath every night because I thought in the end I would feel better, accomplished. I forced myself to drive from Sand Springs to Jenks, at least once a week. I forced myself to stand for at least twenty minutes a day to build up a tolerance. I cut waaaaaay back on my pain medication because I wanted my mind to be clear. I forced myself to fall asleep early in the evening and get up before the dawn many times. I forced myself to put up with my cruel doctor, I forced myself to lay through painful MRIs, listen to his jokes about how my ass was so big, the radiation from the x-rays couldn’t penetrate it and hit the film. I forced myself to agree with him that rather than focus on cancer, I should focus on losing weight and getting weightloss surgery. All his talk of my weight made me insane.

I thought in the end it would be worth it all.

But I didn’t get that happy ending.

All that hard work didn’t pay off.

All it got me was deleted, blocked, ignored, filtered, and phased out.

It’s my fault. I don’t blame anyone who did any of that to me. I kept my physical therapy to myself. I wanted it to be this big surprise. I wanted to have this huge celebration where I was well and could move. Instead, it back-fired.

So I quit.

It’s not worth trying anymore because the harder I try, the more people push me away. I tried so hard. And that’s what I got in the end.

Back in September, Matt joked to me that I was becoming Roxanna. Maybe I am. Maybe I am as bad and rotten and evil as she is and I’m just now realising it? Maybe this is my punishment for not giving her all that she wanted or demanded, for protecting me and mine.

I have deleted two of my blogs. Yanked them off the web. I told Matt on the way home that he needs to find his own hosting. I was sorry. I am burning DVDs for my friend that I have failed; when they are done burning, I will mail them out, though I am sure this person doesn’t want anything more to do with me.

I understand that people will want to unfriend me over this. I am fine with that. What I have written is not out of emotion or hysteria. It’s honest. I have been calm and collected through out writing this. It will mirror on the one blog that I am keeping. I will also be keeping my journals. I don’t expect anyone to pick sides, nor do I expect anyone to be sympathetic with me. I am just putting this out there to be read and known. I wasn’t hiding or trying to be a bad friend. I was trying to help myself so I could be a better friend. That’s what I get for trying, huh?


Upcoming Appointment

I can’t post for long; As soon as my CDs finish burning (I know, I want to shut up about that too!), I’m off to my doctor appointment with Doc Mick. Part of me doesn’t want to go because I know I will just end up getting mad at him and yelling at him for causing me to miss my friend’s wedding. I want to blame someone for this horrible disease I have, and it’s not right that I have no one to point the finger at. All of my life, everything that has happened to me has been the direct result in someone doing something to me. This time, there is no one who has done this to me, and I’m at loss for what to do to settle it. My mind is racing. I have taken my medicine. I vowed not to over dose this month. The drug store sold me generic medicine and charged me for name-brand. I ended up taking it back. Matt is packing to go home. My husband’s plane lands tonight at eight.

Matt just came in and asked me if I was going to get ready for my appointment. It’s time.


Four Years

The next couple of days cannot go fast enough for me. I am at a stand still. I feel bad, as if my husband forgot about the most special time of the year. We only have two days a year that we have to remember: Our birthdays and anniversary. This year I was alone on our wedding anniversary.

I had to take something for the pain earlier. The pain was bad. It was putting poison thoughts in my head. I couldn’t let it do that. I had to stop it. After taking three different kinds of pain medicine, the poison thoughts stopped, and I was able to peacefully rest. I watched The Simpsons Halloween 21st Special through bleary eyes, but I feel fine now.

My vision has been giving me some problems lately. I see a reverse seven across my vision, in zig-zags. It lasts anywhere from 20-30 minutes, and it drives me crazy. I can’t do anything while my eyes are acting up. When it first happened, I thought my retinas had detached, but the flashes went away and I hadn’t had any head injuries.

Tomorrow I have to take the kids to school on my own. Another step towards rehabilitation. Then it’s tutoring the Grimaldo twins and my appointment with Doc Mick. All while waiting by the phone for Dennis to call me to tell me he’s home until after Thanksgiving. The holidays have more impacts on me this year. I get worn out much faster. I sleep more. We set the clocks back last night, and now we have more hours of darkness, so I just want to soak in the bath tub half the night. It’s relaxing and it calms my anxiety. By the end of next week, I will probably be on prozac again. Not something that I am really wanting. When I am on that, I have horrible heart burn and my feelings and emotions mush into nothingness. Nothingness that I try to speed through with overdosing on narcotics, which leads to overdoes of other medicines. I need to tell my doctors this, but I am afraid they would send me back to that hospital and I would never get out.

I feel that if I just had some things go my way in my home life, I would not be as anxious or afraid as I am. Everything I attempt to do, I mess it up in some way because I have next to no confidence. If they sold confidence in the form of a pill or syrup, I would ask for that rather than these narcotics or mind-numbing anti-depressants. I feel that my lack of confidence is the key to my low quality of life these days. I wish I knew what to do to make things better, but I can’t even decide where to start in this tangled mess of problems, so how can I begin to fix everything? Will they all fix themselves?

Tomorrow’s gonna be another day. Another step forward. Another brick in the wall. I may not get well tomorrow, but I will be healed more and more each day until some day I can say that I am healed. That I can look back at what happened to me and not burst into tears or sob uncontrollably. That day is not here yet. But it will be. I know it.

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