Sunday, June 28, 2009

Going to Denver

We're frantically cleaning our house getting ready for my Danish family to visit us. They are flying in to Denver tonight and we are going up to meet them so they don't get lost/overwhelmed. It sucks for timing, I have to get my port fixed tomorrow so we won't get to hang out with them during the day tomorrow. The surgery is at 12pm but I won't get to eat all day, I hate that! I hope they can get this fixed and chemo will be much easier. Next chemo is on Wednesday. Family leaves Wednesday morning so hopefully Tuesday we can hang out. Do I actually have a job? I haven't worked in a week and hopefully I'll be in to work on Friday! I'm going to have soooo much to do.

Friday, June 26, 2009

I'm bald!

My hair was coming out in huge chunks so on Wednesday night we got out the razor and shaved it off. Matt actually was the one that did it for me. I just couldn't do it. I was going to do a mohawk just for fun but decided that it would look pretty funny to have my hair fall out of a mohawk!
Harper was so funny the next day when she saw me after school (I was asleep when she left). She kept saying, Tada! Look at Mommy's hair! Tada!!!
Met with the radiation oncologist this afternoon. He seems really smart (and McDreamy). I'll start radiation one month after I am done with chemo and will have 33 radiation treatments. That is also the number of chemo treatments that I will have had when you combine the last ones and these ones. I hate odd numbers but then if you add them together and just think of 66 treatments that is a bit better (although a whole lot). I was going to ask him if I could have 32 or 34 radiation treatments but it seems like oncologists don't like changing a whole plan just cause you don't like a certain number. So I added them to get the even number. (ok, it's not just me, I know that Matthew and Dad are reading this thinking "oh, 33, that's an odd number, too bad).

Wednesday, June 24, 2009

No work for me

My fever is gone and I called work to tell them that I was on my way in but they said No Go. I guess someone at work might have something contagious so they want me to stay home the rest of the week and get better. I guess that is good and it is great that they care but I really wanted to go to work. I'm a bit bored at home. So we're off to the library and farmer's market. And I guess I can get some knitting done. I have lots and lots of baby hats to make.
Here is the score right now: cancer 1 work 0

Tuesday, June 23, 2009

Isolation is really boring

I made it home from the hospital on Monday night which was a good suprise. I really thought I was going to be in until today. I was in isolation so everyone that came to visit me had to wear a mask and gloves and they had to keep my door closed. My friend was down the hall having a baby and I couldn't even go see her! But I am home now although I do still have a fever. I was given huge doses of very strong antibiotics so hopefully they will keep working.
I'm home from work today and trying to figure out what I need to do to stay healthy and able to go to work and do normal things. I wish the doctor's office would call me back.

Monday, June 22, 2009

Hospital Time

(Matt writing for Jessica)
Jessica came home Friday from work completely drained and with a bit of a fever. By Saturday afternoon, the fever hadn't gone away and her oncologist told her to go in to the hospital to have things checked out. Her white blood cell count came back really low and she was admitted to the hospital. They've been giving her IV antibiotics and checking her counts. We hope that she'll be able to come home on Tuesday.

Monday, June 15, 2009

Been busy...sleeping

I feel like I slept all weekend but I actually ended up doing quite a bit. On Friday I ended up leaving work early and going home and sleeping. Saturday was the annual Orchard of Hope Walk www.orchardofhope.org and walked there with the other "champions". What a nice event, some many different companies/organizations in Fremont county set up and sell things and raise money in addition to the walk. We don't have American Cancer Society in Fremont County so this kinda takes their place. They helped us out last year and we will be going back to them this year. It was nice to be able to help them out for a change. My work set up a booth and we raised a lot more money this year than last although as a whole the Orchard was down about $20,000 from last year.
Saturday afternoon we got to hang out with some friends and watch Harper swim in the kiddie pool. Then we all met up at the Holy Smoke BBQ contest and watched a Weiner Dog costume contest and race and then listened to Martini Shot. What a fun night. Harper had so much fun dancing and playing. It was great to see her see friends from school and talk to them and dance with them. And it was nice to just hang out with friends and listen to music and not think about cancer (although I had such horrible heartburn it was hard to forget I had just had chemo).
Sunday Harper and went to Pueblo and bought a few essentials and then slept the most of the day.
And today....drumroll please, I biked 4.5 miles tonight. Uphill (halfway), pulling a 35 pound kid in a bike trailer. I have had way way way too much energy today. I figured it would be a good way to get it out and get some exercise and Harper loves to ride. Matt's got a wobbly tire so he couldn't go. Now I realize 4.5 miles doesn't sound like much to the bikers who go all century and such but think that I just had chemo 5 days ago! And it was my 28th chemo threatment in the past year and a half! Now 4.5 miles seems a bit more impressive (at least to me).
Tomorrow it is an early morning to Denver for a work meeting.
Thursday giving blood for my new port to be put in on Monday. They said I would be out of work for a few days but I doubt it. Maybe Tuesday but that is it.

Thursday, June 11, 2009

So far so good

After sleeping 12 1/2 hours last night I feel pretty decent today. I'm just taking it easy and taking the meds as often as possible to prevent any puking. I'm hoping it stays like this although my immune system will be at it's low point for 7-14 days after the infusion so we'll see how next week goes.