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The new meds seem to be good, too. The steroid appears to be helping the rash a little, even though it makes me eat everything that isn't
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It just goes to show that when you feel like something's not right, it pays to follow up on it and insist on something to help. I don't think if I would've just asked for new stuff that I would've gotten anything. I guess the squeaky wheel gets the grease in these cases.
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Anyway, enough of that.
Tomorrow I'm going out of town to present a scholarship given in memory of my dad. I'm a little nervous, and not sure what I'm gonna say, but it's such an honor to do and such a great way to remember him. Seems like 10 years ago that he passed away, and yet I guess it wasn't even 2 years yet.
I remember the first time we talked about him having cancer, and I think now how different my attitude is about living with it and how it's not the death sentence so many of us associate with it. I'm lucky that things have changed, that advancements have been made, that this was the year I had melanoma and not 2 years ago, when Interferon wasn't even around. Lucky that there's mice out there giving up recombinant DNA for suckas like me, those crafty little fools in their tiny white lab coats putting together proteins. Isn't technology wonderful? I think so, too.
Just 2 months left, and everything is going to change for me once again. It's been a crazy year, and even though it's not over yet, I'm encouraged that the end is near.
I know I'll walk away from this forever changed, but that doesn't mean it has to be a bad thing. I just know I'm excited about this new chapter in my life and looking forward to the changes.
Can't wait!
-MM
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