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JOURNALS

One girl and her mom's candid, sometimes tongue-in-cheek, day-to-day thoughts about dealing with this roller coaster ride of cancer.

TAYLOR'S JOURNAL

 

5/30/08 - Well we're still here. My friend Lauren came by yesterday and since my counts are the lowest they've been, everyone who comes to visit has to wear a mask. My mom wanted to take a picture of us, so I've included it for you to see. I think we look like bandits. What do you think? I was supposed to go and visit my friends at the Regional horse show this weekend, but with my counts being down and me being here, that's not going to happen, I guess. I have chemo again today, so my counts probably won't get better real soon and they won't let me go until they get higher. I still have a really bad headache. My mom is trying to get them to find something that will make them better but it's not working so far. I'm hoping they'll find something soon. I hope to see a few of you here if you get the chance. It can get boring in here. I hope you like the picture.

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5/28/08 - Well we're back in the hospital because I've been having a bunch of headaches. My counts have dropped way down since Saturday when they last checked them. As long as you aren't sick, you're welcome to come and visit if you want. I'll be here for at least to Friday if not longer. I shaved my head on Sunday and I've been wearing hats ever since. I got sick of hair falling out everywhere. I wore my wig to school on Tuesday where we were doing a play and I got to be in it. It went really well. I was the narrator. We were supposed to have field trips on Thursday and Friday but I won't be able to go because I'm here. My mom told me about a few neat fundraisers that are coming up, so that's cool. I've been checking my guest book and read all of your messages, so please keep sending them. I really love reading them. I'll try to keep you posted better. It's just hard to write when your head hurts. 


5/15/08 - Hi all. I hope you caught me on San Diego Living today. I don't feel good today. I've thrown up and have a major headache. We found out that that I'll have to have a transfusion tomorrow. Maybe it will make my headache better. I hope I don't end up in the hospital. Even though I don't feel good, I wanted to share some pictures from last weekend. It was really fun. I met Ruben Galvan from Fox 6 and Lauren and I got to go down on the field at Petco Park (see pic). I had a really great team of sponsors that let me go to the Relay (see pic) I also got to meet my Team In Training (a race team and I'm their Honored Teammate) on Tuesday. I'll write more when I feel better, okay?

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5/8/08 - We came out of the hospital on Saturday late and I did make part of the birthday party. The blood transfusion went well. I was back at the clinic both Monday and Tuesday (chemo was REALLY long) and then to my doctor's on Wednesday because they thought I had an infection, but I didn't. I went to school today for a little bit to do my STAR testing and I did a lot of it. Tomorrow I'm hoping to go to school too, and on Saturday I have my day of Champions followed by a Padre game which should be really fun. My hair has been falling out a lot and is really thin on top now. We got some scarves and hats for when I lose my hair because I have a feeling I am going to. Here are some pictures of my wig. Who do you think looks better in it, me or my dad? (My Grandma is in the picture with me)

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5/3/08 - We're back at our favorite place on earth, Children's Hospital (not)! I started having bad headache pain yesterday morning so my mom called and they had us come down. They thought it might be a blood clot in my brain so they did an MRI and made us stay the night. My headache is better today, but now they say I need a blood transfusion which they are going to do today. I have a birthday party I want to go to, so I hope they let me out, but we still don't know. They haven't told us what the MRI said yet. I've never had a blood transfusion, so I'm not sure what that's going to be like, but I guess I'll find out  and let you know! The pictures below show me playing Blokus with the Swensons and getting ready for my transfusion. My face is kinda fat because of the Prednisone.

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MOM'S JOURNAL

 

5/20/08 - Fundraiser - I've been involved in fundraisers before. Some for churches, some for other organizations. They're always a nice thing to do and it makes you feel good to know you're donating to a good cause. When I've worked behind the scenes, it was always great to see a good turnout and a satisfying amount of funds raised for a good cause. After last night, "fundraiser" has such a different meaning. I knew there would be people there that have been a huge support to us all along. And I knew there would be some new people there who were touched enough by Taylor's story to come out and make a contribution through their presence. But what we experienced was truly beyond words. With wait times for a table reaching 2 hours at one point and several brands of beer and food dishes selling out by the end of the night, to say that the fundraiser was a success would be a huge understatement. But the experience went far beyond that. To see our daughter flitting around the restaurant talking to such a wide variety of people as if she didn't have a care in the world would have been reward enough, but to see decade old differences melt away in an instant in the light of something so much more important, to hear stories - real, heartfelt stories - of people touched by illness, cancer, or Taylor's strength and will to survive was sobering and humbling. And to see total strangers, caught in the chaos of a restaurant under siege of those driven to support Taylor and our family, lend their hearts, prayers, and dollars, had us touched to tears so many times during the evening. The very friends who have already lent us tireless support found even more ways to express their generosity, and people we didn't even know opened doors that we didn't even know existed. We also learned that this whole event was born by one little girl's fervent wish to make a real difference and her family's desire and ability to make something happen. As good as I am with the written word, this time my words fail me and I'm left with just two small words, so inadequate yet all I have, for those that attended our fundraiser. THANK YOU.


5/15/08 - Ups and Downs - We've had a lot of these lately. Last weekend was a undeniable up. Taylor went to school both Thursday and Friday, and lasted a very long day on Saturday with her Day Of Champions at Seaport Village, a visit to our friend Aisling, and a free Padre game (they finally won!) I snapped the picture below of her with Ruben Galvan. They had a long talk about American Idol. There was a carnival and a really neat tribute to all of the kids who have passed away, those currently in treatment, and those in remission. She was the only child with her type of disease out of a very long list of kids, which made us realize how rare her cancer really is. We had a great Mother's Day together, and her chemo went well on Tuesday. Then came today. She was able to go onto the TV show as planned, and thoroughly enjoyed that even though she had a bad headache. When we got home, however, things went downhill. Her headache worsened, she got nauseous, and she spiked a temp. As I write this, we are monitoring her closely to see if the temp hits the magic 101 degrees that will send us to the hospital. So far we've been lucky, but barely. She's hovering in the 100.2 - 100.5 range. Please send prayers that it will go down soon. 

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5/1/08 - Medication - Throughout our time in the hospital, I learned to monitor Taylor's medication carefully. There were several times where meds were changed on paper but didn't get changed in practice, and some things that were ordered that simply weren't wise (such as a laxative when she was having diarrhea or a sucrose drip when her glucose levels were too high.) As time went on, I got to the point where I examined each pill in the blister wrap (I asked them to bring it to me intact so I could check) and double checked it against the information I had written down in her daily log for fear of her receiving something that was wrong. It happened enough times to warrant my concern. 

 

Recently, I refilled another medication, brought the prescription home, and began to dose out medication as I always do. But a little heavenly voice inside my head told me to double check the prescription. The name of the drug was the same, as was the dosing directions, but there was no dosage amount for the drug. At first I thought I was being silly, but I called anyway, telling myself that I checked every single pill in the hospital so why should this be any different. The pharmacy confirmed that the drug was the correct drug and the dosing directions were correct, but when she told me the mg dosage amount, it was double what Taylor was supposed to be receiving. Word to the wise - if you have a loved one getting medication, keep a log of the medications they're on and any changes made by the doctor, and check and double check each and every time you fill a prescription including dosing directions, drug name, and dosage amounts. I shudder to think at what could have been....


 

 

 

 

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