Tuesday, March 25, 2008

Yay! Hospital Food!

I went to the clinic on Friday and got to speak with the nurse practitioner who is Lita's counterpart. I believe she tried to give me good information and assistance, but I don't think I will consent to speak with her again unless Lita has been hit by that mythical bus that's just aiming to kill everyone. I felt things were going fine until she asked me if I had ever had a conversation about ceasing treatment.

Huh? Why the would I be calling asking about my symptoms and trying like heck to get back on chemo if that were the case? Why would THIS be the time to be having such a discussion? I was very upset and later, extremely angry that she would say such a thing to me. She doesn't KNOW me. Perhaps she was attempting in some clumsy way to bring up the notion of advance directives, but I've already gone through that with other people and it's not her business. I don't know to whom I can complain about this, or maybe I should just let it go.

Anyway, after an early morning MRI on Saturday, I got a call from one of the doctors I saw initially about the brain mets that I should go back to the hospital immediately. I was able to go to the floor instead of being admitted to the ER, which streamlined things somewhat, but it did mean having to be in the hospital over night for who knows how long. The plan was to radiate my thoracic spine--the MRI showed that one of the two lesions on my spine had increased in size, and the one in the T9 area is poking into my spinal column, which may account for some of my recent symptoms (but not the shingles). This is seen as an immediate problem, since delaying action can result in, oh, say, paralysis.

Sigh.

I got a private room, which was kind of nice. I also had multiple radiation/neuro people come to my room to have me squeeze their hands, follow the light with my eyes, and have invasive procedures to test the muscle tone of an area one doesn't want to have evaluated multiple times unless one has that particular fetish.

I refused the third "evaluation."

Sleeping was also a problem as they have seen fit to up my decadron to 8mg a day. I finally saw the movie Brigadoon (I have a soft spot for Gene Kelly) and a number of shows on Animal Planet about some amazing dogs that have vastly improved the lives of their owners, including one lab puppy who kept running away from home to be with a lady who eventually had her breast cancer diagnosed after the dog became upset and was poking at her breast incessantly. Dogs have been trained to detect cancer cells by smell, but this dog just did it naturally.

I did get released on Easter; I was expecting to go to my mom's for dinner, but that just wasn't going to work out. Instead, after she arrived at the hospital only to find out that I had just been discharged, we all went back to Canton and Brian's parents showed up shortly afterwards.

I've had three radiation treatments so far; they've scheduled them all at 7am, which is hilarious. This time I don't have to wear a mask; they just have me up on the table. I will have ten treatments altogether, and it will be over April 2. I don't know how long I will have to recover from the radiation before they can resume the chemo. I really hope there are no more hurdles. My other things have to heal and we are all hoping I don't get some kind of inconvenient infection.

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Saturday, December 22, 2007

Blarrrghhh! Need...Time...Machine...

Nothing else is ready, but at least there will be food when people come to visit.

Brian and I have invited some family to come and spend Christmas with us, so his parents are coming, his brother is driving up, and my mom is coming over for Christmas dinner. I need to finish making cookies (I've jettisoned the bell cookies from my menu and will probably forgo the crispy rice treats; I've made the cookie candies, but they need to be covered with fudge and I haven't made thumbprint or chocolate chip cookies yet...not like people desperately need cookies, but I LIKE them and want to do it)--I have to bake a pie, and the actual dinner will need to be prepared. I'm confident the turkey will thaw in time, although I'm pretty sure that right now it's a turkeycicle. If we have to, we can eat cereal, mixed nuts, or the chestnuts and eggnog I've asked my mom to bring over.

The problem is the other stuff. I only assembled and lit the tree today; I meant to do it earlier in the week, but I pulled a muscle in my back and have to do things in short spurts. I started physical therapy (again) this week, but it's for my hips/legs, not my back. Tension is not helping. The tree isn't even decorated with anything yet except six tassels and a tree skirt right now. I'm sure Brian would be happy to help do it, but I'm too particular. All the decoration boxes are still upstairs and need to disappear before people arrive.

Nothing is wrapped.

We also don't have quite enough seating in the living room, the guest rooms need to be cleared out (which Brian has been making a heroic effort to do), the bathrooms have to be cleaned, we desperately need to buy toilet paper and I have only a vague idea of when people are coming over.

I also volunteered to play the flute part of a flute/organ duo at my mom's church for midnight mass. Why? I haven't played at Christmas in three years because I got braces and wasn't really well enough to in any case. Why am I doing it now? I sound rusty and twisting my back into proper flute-playing position is not helping my muscular distress. I hope I don't suck in front of Brian's family.

I have a CT scan, infusion, and physical therapy the day after Christmas, but I don't have to worry about that yet. This year the holiday is going to be great. :)

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