Chemo #1 and the baths every 6 hours around the clock are thankfully behind us now! Caroline is still getting Chemo #2 daily, with the last dose being tomorrow. Sunday will be a day of "rest" before her stem cell transplant on Monday.
Caroline had a feeding tube (aka: NG tube) placed today to help with getting nutrition and the medications she has been taking orally into her system. She's struggled with both eating and taking her meds the last couple of days, so having the tube will get her everything she needs, without worry. The process of getting the tube inserted can be scary, but Caroline was a trooper (as usual!) and did a great job, with minimal crying. The nurses and staff were absolutely wonderful during the procedure. We cannot express in words how grateful we are to be here with this team at Vandy!
Love,
The Lantz Family
#carolinestrong
#ftgf
November 2017: diagnosed with Stage IV, High-Risk Neuroblastoma; Nov 2017-April 2019: completed standard treatment protocol / no evidence of disease; April 2019-April 2021: enrolled in/completed DFMO clinical trial; April 2022: RELAPSE; April 2022-June 2023: completed relapse treatment protocol / no evidence of disease (again); June 2023-June 2024: enrolled in “compassionate use” high-dose DFMO clinical trial; June 2024: RELAPSE #2
Aw sweet Caroline! Tell her miss Valerie is so proud of her! I’ll be back Sunday!!
ReplyDeleteSweet baby...thinking and praying for you all always ❤️
ReplyDeletePrayers that God guides Caroline's medical team as she has her stem cell transplant on Monday! May God keep all of you comforted during her procedure and as Caroline continues her recovery! God Bless!
ReplyDeleteAwwwwww am always praying for you baby gal 🙏
ReplyDeletePraying for her. I can’t imagine how she feels. She must be so tired yet she is so strong and brave.
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