Donations can also be made at any Wells Fargo branch:
Project Souza Family
Account number 186-527-1579
Or you can mail a check to
Souza Family
PO Box 28272
Scottsdale, AZ 85255

This blog was created by friends as a way for the Souzas to share Taylor's progress with us. Kristen and Sean have not asked for financial help, but their medical bills coupled with Kristen's loss of income is truly overwhelming. They are so appreciative of ALL of the different types of support they have received and are more grateful than you can know. Thank you!
Taylor is a beautiful, vibrant three-year-old girl who was recently diagnosed with acute myelogenous leukemia, a fast-growing cancer of the blood and bone marrow. On June 18th, Taylor began an 8-10 month hospital stay. This blog will detail her journey back to good health!


Wednesday, December 16, 2009

Well, today will go down as a good and bad day. Taylor started off feeling well and had a little energy. She enjoyed visits from Aunt Kerri, Marty, Jamie, and Kim. Then the fun started.....Taylor received her last dose of IV chemo at noon today. This very large dose of chemotherapy infused over 3 hours. She did ok the first couple of hours but started to not feel well toward the end. She got very tired and her stomach was a little upset. She then had to receive a platelet transfusion. Her platelets weren't actually critically low but because she was to receive an injection (shot) of chemotherapy at 6:00, she had to be transfused because they were low enough that she was at high risk of bleeding from the injection. As always, she was pre-medicated with Tylenol, Benadryl, and Zantac to help prevent any reaction from the platelets. Well.....within the first 15 minutes of the reaction, she started getting a very red rash and hives on her face and in her ear. The transfusion was turned off and another large dose of Benadryl was given. The rash wasn't getting much better so they decided that she would not receive any more of the transfusion. Now.....they were unsure if she should receive the chemotherapy injection because there is also a risk of reaction to the injection. They also were not sure if she had received enough platelets???? So....to make a long story short, they consulted with the doctor in charge of AML patients and were instructed to give the injection. The benefits of the injection outweigh the risk of reaction (a reaction could also be handled with medication). So......the fun began. After receiving all of the Benadryl, Taylor was sound asleep. We had to wake her and explain that she would be getting a shot in her leg. She went crazy. She was screaming and begging me to "please not let them give her the shot!!!" I was crying and I think her RN was about ready to cry. But.....they got the injection done and we are now monitoring her for signs of reaction. So far...so good!!! We will watch her closely the rest of the night.

Now for the good news....hopefully this injection will be the last dose of chemotherapy that Taylor receives. This was the last dose for this round (which is hopefully her last round). So....we wait for her counts to hit zero and then come back up. We wait to see if she gets a fever/infection and then wait to see where we are at with her treatment. It is WAY too early to speculate as to how she is actually responding. I am just focused on the next very long weeks and keeping her out of ICU. My goal is to be home by January 15th......

After all that, I am off to watch her for any reaction. More tomorrow.....

7 comments:

  1. Geez, I see what you mean by a good/bad day! Poor Tay- that little girl endures too much (as do you Kristen)...having a reaction, getting a shot..the list continues. As you said, this hopefully..fingers/toes/eyes/arms crossed will be her LAST dose of yuckie Chemo EVER!!! Hoping, wishing, praying the chemo does it's job, Tay is in Remission & stays out of the ICU!!
    Better days to come my friend! All my love always.....
    XOXO
    Jess

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  2. Kristen & Taylor,

    Thanks for allowing me into your PCH world today! I wrote a letter to Santa for Taylor and put in a good word for her and Savannah. :-)

    XOXO - Jamie

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  3. Kristen,
    I am praying that Taylor doesn't have a reaction and that this is the last dose of chemo that she has to endure. I also pray that the waiting game of her levels dropping and making sure she doesn't get sick goes smoothly! Even though it is so hard to watch her endure all of this yucky stuff, she is one lucky girl to have you by her side constantly!
    We will have our prayers in over-drive for Taylor!

    God Bless,
    Liz-Takeda, CO

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  4. Praying, praying praying for no more chemo for Tay. That will be our mantra. Hugs and love, Kelly and Carly

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  5. Sounds unreal!!! What a tough day and night. Hang in there and celebrate that this is the last dose---hopefully, forever. We continue to pray that all you you are DONE with this ordeal.

    Love you, Grandma Renee

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  6. Praying so hard that this is it! Sent a little something today to help Taylor pass the time. Thinking of you lots...-Cindy & Glen

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  7. Happy tears, sad tears...another heartfelt post. I am so happy that this is Taylor's LAST round of chemo, but I am still so saddened by how much she has had to and is STILL enduring! Please tell her that we are so proud of her and she is incredibly brave. Santa KNOWS that Taylor and Savannah are such special, loving girls, that they are surely on the GOOD LIST this year!!! :-)

    Kristen, I can't even express in words how amazing you are; so strong, so genuine, so caring! I am honored to know you and your family!

    I love you all and will send positive energy and healing thoughts all hours of the day!

    With much love,
    Laurie T

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