Wednesday, April 26, 2006

WEEK 42/ THE HOMESTRETCH

> WEEK 42/ THE HOMESTRETCH
>
>
> Da bloggety, bloggety, bloggety; sacred sound of a Harley
> Davidson idling away and waiting for the master to unleash the
> hounds. It’s the sound of raw energy bleating for the chance to run
> wide open - that’s what it is. So, you get out there with the
> “flow” and what happens? You use the compactness of your machine,
> the power of it’s torque, and the threatening nature of it’s sound
> to slide through, around, and past all forms of little monsters
> driving expensive, nimble, shiny pellets as though a checkered flag
> waited at some distant point on the horizon. You struggle to free
> yourself of the hazard by being a more aggressive rider, but
> always looking out for that MF who can’t stand being bested, or
> cramped in by the myopic slowpoke that shouldn’t be issued a driver
> license in the first place. Still, I wonder what would life be
> without my two-wheeled passion.
>
> I saw the doctor a week ago. That was at the 40th week of my
> treatment. We discussed the finish line for the meds. I am due one
> more shipment of them, which has arrived today. And with that I
> will have completed 46 weeks of Interferon/ Ribavirin medication.
> Dr Bartley, who is a very by-the-book kind of doctor (no shortcuts,
> higher dosage/accelerated treatment schedule), stated that 46
> weeks of treatment is fine and we should be alright with that. All
> my blood-work is normal without any relapses of cell volume. I can
> tell Bartley is pleased that I’ve gone the distance without
> bitching and complaining. Splice in a couple of trips to Europe, a
> killer flight to Brazil, and who knows what I’ve forgotten, and I
> stand here with the end of the road now in-sight. After the
> completion of medication I will return in 6 months for another lab
> test for a viral load. If the virus does not reappear at that time
> we can consider the treatment completed. So how do I feel? Ok, but
> still tired a lot. Weak physically, but not unhealthy. Decadent,
> but, and most importantly, happy. For all the minor irritations and
> piss-offs, I’ve got a great life and have been blessed with a
> situation beyond anything I could have hoped for. Five weeks from
> now I will be able to say “damn, I made it”. Accompanied by the
> knowledge that I am virus free and past a shadow of my former dark
> days, it’s a good feeling for the old boy, like redemption. I’ve
> never even imagined what it would feel like at the end, but it’s
> like anything else; you can’t know until you get there!
>
> The weather seems to help my mood a lot. Arrival of spring and
> warm sun on the face is a heck of a way to smile inside. Jesus, I’m
> getting sappy again. That means it’s time to take off until I get a
> better idea to talk about.
>
> My old high school buddy Jim is coming to L.A. this weekend….neat.
> I haven’t seen Jim since 1962.
>
> I’ll check back in to the blog in a week or two. And for sure
> to make a statement if I haven’t already done so, at the end of the
> big medication highway.
>
> Sayonara, M.D.

2 comments:

Anonymous said...

Wow :) I have been sitting here reading this wonderful blog (on and off) for about a week now. It has captivated me. You're an incredible person, (and incredible writer, too). I found you through a news alert link regarding Hep C, (it had your blog link in the article) and I've been reading here since. It's wonderful news that you've made it through treatment! I have Hep C, too (had acute nonA nonB in the 70's). I never knew this virus was "lurking" until around that 25th year when I began to feel awful. I was diagnosed three years ago. I didn't make it through my first attempt at treatment, but I'm in hopes to try again soon -- hopefully with the protease inhibitors or polymerase inhibitors in combination with Peg (either through a clinical trial or because they've been approved to treat Hep C.) That, though, could be several years away yet, and so -- it's possible I may have to try the "combo" again. I'm currently being followed at Duke University Liver Center.

Thank you for this blog. I hope you don't mind if I feature the news article in one of my Hep C blogs. I've read many hep c blogs, and yours is -- by far -- probably THE best I've ever come across. Frankly put -- it is the best, no doubt about it! I look forward to reading more here.

You are an inspiration! Best of luck to you.

(And a side note to Marion: If you read this, Marion, best of luck to your sister, too!)

Camila P said...

Great blog post.