Tuesday, November 18, 2008

There's a couple thousand bucks drifting off into space...

Check out the grease gun w/ Braycote in it drift away.

Saturday, November 15, 2008

That Which Lays Heavy on My Mind

Out of the few of you who read this, most will not finish. This has the potential of being a little too long and a little too dry.  You are forewarned.

When I first started writing on this blog, it was just a place for me to write.  Nobody knew it existed, so nobody read it. Tonight, I just need a place to write.  Unfortunately, my medium is now public.  So be it.  I must not be that private person most of us think we are.  Or maybe I just don't care who knows.  Or maybe I want you to know, so I don't have to worry about what you are thinking when you take that second, or third, glance.  Yes.  I see it when you do that.

In the summer, I was diagnosed with Follicular Mucinosis.  
Say what?

Follicular mucinosis (FM) is a rare dermatosis characterized by mucin deposits in the pilosebaceous units. It is divided into a primary-benign type and a secondary type associated mostly with lymphomas. No standard effective therapy is available for the primary FM while in the secondary form treatment is aimed against the underlying disease.
So what does that mean?  

Well, there's a few things that should jump out at you, the first being it is rare.  Yipee for me.  I feel like I won the lottery.  Second, is that nasty little word lymphomas.  Although there is not a lot of data out there, I read where it turns into cancer 40% of the time.  No worries, the mortality rate is pretty damn low.  The last thing that should have jumped out at you was there is no standard effective therapy.  I've read where Corticosteroids, dapsone, mepacrimine, interferons and superficial X-ray have all been used.  Let's not forget photodynamic therapy and interferon alpha-2b at a dose of 6 million U subcutaneously three times a week, and acitretin 35 mg/day, for 6 months.

So imagine my surprise when I finally went to a dertamtologist and he told me the good news after getting the results of a biopsy.  The way he stuttered and stammered with the word lymphoma was really encouraging.  It sounded like the confidence President Bush excudes in a briefing on the economy.  

In case you have not figured it out yet, the f'ing bumps on my face are follicular mucinosis.  Just for the dummies out there thinking this was something hidden from view.  

So every morning when I look in the mirror to shave my face I here James say, "That was just your life."  Ok.  Not really, but you get the point.  No?  FFS.  Let me put it another way.  I'm reminded of my current situation all of the time.  Getting out of the shower, brushing my teeth, walking past a mirror, seeing my reflection in the mirror when I change lanes, when somebody takes that second glance, when their eyes drift to my face instead of my f'ing eyes when talking to me.  
When I go to sleep at night.  
When I give my daughter her very own Taylor Swift CD, and she says, "Thank you, Daddy", with all the sincerity only an innocent child can have.

Now do you get it?

Boo f'ing hoo!!  Not really.  I'm just framing this conversation for you.  
When I was first told, I was not that bothered by it.  As the prescriptions have not worked, and the stares have continued, I find myself thinking about it more and more.  As I research more, and see pictures of how unpleasant it could become, how unpleasant treatment could be...  it weighs on you, is all I'm saying.  Surprisingly.  It weighs on me.  When I least expect it, it weighs on me.  I am surprised at my inability to compartmentalize this in my brain.  Afterall, it is not that bad.  I mean, come on.  It could be much worse.  So I do not mean to complain.  

I thought if I wrote about it, then I could have my little moment of feeling sorry for myself.  My own little woe is me time.  And then move on.  Because it is not that bad.  All I have are bumps on my face, and a few stares.  Even a few questions now and then, a biopsy or two every 2-3 months just to make sure Mr. Lymphoma has not decided to join the party, and a band aid on the face for a week.

Tick tock.  Time to shove this into the corner of my brain.






Monday, November 03, 2008

McCain Rally

On Sunday I decided to go to a John McCain rally. Jenna tagged along on our little trip. I asked her to come for 2 reasons. The first reason was all selfish. I just wanted some company. Secondly, I wanted her to see this part of the election process. I wanted her to see a candidate ask for her vote. Now obviously she cannot vote, but you get the point. Now don't worry. I did not allow her to wave a John McCain sign or anything like that. When she gets old enough to vote, I want her to make her own WELL INFORMED decision. Since she is not old enough to make that decision, I figured it was not fair to have her showing support for a candidate.

The doors opened at 8:45 am (yeah right), so Jenna and I got there around 8 am. We stood in line outside waiting to get in. Once we got inside, we were heading towards the bleachers when I saw we could get center stage, fourth row back, if we decided to stand. This is what we did, and we proceeded to stand for a few more hours in one place. Jenna was a trooper and didn't complain. OK. She complained a little, but it did suck. Jenna had an old lady with John McCain stickers on her cheeks push in front of her. Jenna's old man had to say something to her, which gave us and the people around us something to talk about for all of 5 minutes. In the end, Jenna got a great view of her dandruff filled jacket when McCain came on stage. I was able to edge her out of the way slightly so Jenna could see. Rude bitch.

Anyways, we saw Senator Lieberman and Secretary Ridge come out and speak, and then McCain came out with his wife and a few others. Cindy spoke briefly, and then Senator McCain gave his usual speech he has been giving over the last few days. Overall, I'm glad I went. It was my first time going to something like that, and I'm glad Jenna got to tag along with me. She told me she had a great time in school today telling her friends and teachers about her experience there.

I couldn't be more disgusted with the poor quality of the pictures, especially since we were so close. i was able to salvage a few of them and make them somewhat presentable. I swear sometimes you have to be outside in bright sunlight with vivid colors for the damn camera to work right. The stage was well lit, but most of them came out blurry and dark. I should have used the small camera instead of the SLR.

Enjoy.