As we often mention, the community support we've received during the last 8 months has been a perpetual source of love and gratitude. Today, we would like to give a very special thank you to The Academy of McKay's Mill. The Class of 2018 is graduating tonight, and we really wish Caroline could be there in her little cap and gown, just like her friends, and just like her brother, when he graduated from The Academy in 2013. The Academy is where Caroline spent every working weekday since she was 16 weeks old...it was her home away from home, and she loved her teachers and friends just like they were her family. Other than telling Caroline she had cancer, telling her she couldn't go back to school and see her friends/teachers was the hardest conversation we've had with her. Although Caroline never went back to school after she was diagnosed, we've never felt like she actually "left." Our Academy family has been steadfast in their inclusion and support for Caroline - always checking on her, sending cards, videos and even homework! We were also included in the formal graduation photos, and then were surprised with a special insert for Caroline within the graduation program, which literally brought us to tears. Despite the fact that Caroline won't be able to formally graduate with her friends, having a picture of her in a little cap and gown, from a place that helped raise her, is truly priceless. Thank you, Academy of McKay's Mill - we love you all!
Hospital Update:
Right now, Caroline is having her most difficult stretch since starting the treatment protocol back in November. She has extreme mucositis through her entire GI tract (worse than during her last transplant), which is causing her to struggle with getting enough oxygen. She is now on a nasal cannula, which is giving her the oxygen assistance she needs. The other major issue she's having is blood and intestinal tissue in her stool, also as a result of her GI tract being stripped raw from the high-dose chemo. Needless to say, it is VERY painful for her; she is on continuous Dilaudid/pain medication (already more than the last transplant), as well as a patient-controlled button, which she needs to use frequently. The mucositis has also moved into her throat, which causes her so much discomfort that she doesn't want to talk; she is mostly using hand motions and a bell to get our attention. We expect her to struggle like this -- or worse -- for the next 5-7 days. She received both red blood and platelet transfusions today to help get her numbers up before we head into [what we expect to be] a very challenging weekend. Please continue to pray for her comfort and a speedy recovery.
Team Lantz
#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
Showing posts with label preschool graduation. Show all posts
Showing posts with label preschool graduation. Show all posts
Friday, July 27, 2018
Bottoming Out / Pre-School Graduation Day
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Stem Cell Transplant
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