Yes, the most beautiful girl in the world is back at The Hotel – just in time for Christmas.
Sometimes you make a holiday wish and it really does comes true!
When she received a life-saving lymphocyte infusion on Nov. 19th, it was designed to do this – put her back into the hospital sometime between Day 30 and Day 60 post transfusion to experience GVHD (graft vs. host disease).
Now, we await the “natural chemotherapy” to take over and identify and attack her leukemia. The past month has been very difficult at home. She has rarely left bed over the past three weeks as this complex beast has taken over her body. As her blood counts rose and improved, her energy fell. As her bone marrow got stronger, so did the disease in attacking her.
It’s a helluva thing to witness – all of this. Jenn is very thin, very frail, and very uncomfortable. A friend asked me yesterday how she’s doing and all I’ve got for you is this: she truly hasn’t had a “good day” since August.
She spent 47 days at the hospital the first time. Then, four more after the cheesecake incident. Then, two more after the post-Thanksgiving pumpkin roll. We also did an all-nighter in the ER at Johns Hopkins (a.k.a. “hell”) on a Ravens game day morning.
Tonight, on Christmas Eve while her family gathers in New Hampshire for their traditional Polish kielbasa meal, Jenn will be spending her 112th night at Johns Hopkins in the cancer ward since March 2014.
As my mom has said: “She’s been through it…”
But it’s not over and we really don’t know where the end of this journey is leading or where the graft vs. host reaction will lead us in the coming weeks. I outlined the potential side effects here on Thanksgiving in my previous update about Jenn.
The doctors are using steroids to combat and control the GVHD. They’re also doing various things to keep her more comfortable and monitor her diabetes at the hospital. We expected a sunburn-ish rash but that hasn’t happened. Instead, it’s been high liver numbers and various cramping and all-over discomfort.
While she battles and heals, we’d love to remind you of some ways that you can help us help others in the fight.
There are two things you can do to help us during your holiday meals and visits.
Please encourage all of the healthy young people at your holiday meal to get on the bone marrow registry at deletebloodcancer.org or via www.ThereGoesMyHero.org. Tell them our story! This is how Jenn’s life was saved. We’re paying it forward by trying to get you to help us save more lives in the future.
Be a hero!
And if you’re still shopping after Christmas, please use our giveaspit.com app for your online purchases. This helps our partner at There Goes My Hero, who help local folks in the leukemia fight.
Please keep them in your thoughts as well. We lost a family friend’s daughter on Tuesday to leukemia. She was diagnosed 12 days ago and now she’s gone. It was so sudden, so incredibly sad and awful – simply beyond words.
She was 16. She was full of life. She loved sports. She was the niece of one of my incredible Dundalk High Class of 1985 classmates – a guy named Frank Vanik, who battled multiple sclerosis for three decades with such grace, dignity and “life” that it takes my breathe away.
I wanted to share this video of Michael Vick being kind to my pal Frank Vanik because it made him very happy toward the end of his journey on earth.
And we want to honor Frank’s memory – he was such an incredible pillar of strength and courage for Jenn and I and we think of him often – and his amazing, strong, beautiful family on this holiday as they’re suffering a tragedy at the hands of leukemia.
Keep them in your thoughts.
We’re sending massive holiday love to all who love us and strength to everyone who is in the fight…
8Keep the faith!
Make someone happy! Eat! Drink! Love! Live!
Merry Christmas from us over at The Hotel
