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Author Archives: kscottmullins
Mother’s Day: T+10
It’s T+10 today. The doctor told my Mom she’s finishing the “first bad third” of this transplant journey, and she’ll soon enter the “second bad third”, which is slightly less bad. The final third is recovery, but in this situation … Continue reading
Posted in May 2012, Uncategorized
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From the Trenches: Day T+2, Update from Kathy
I’ve been here eleven days. It seems like a month. I am entrenched into the routine of the ward now, and have my daily rituals, based on what times vitals are taken, blood, doctors’ rounds, etc. There is no interaction … Continue reading
Posted in May 2012, Uncategorized
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Day Zero–Let the Miracle Begin! Update by Kellie
Yesterday was Day Zero, a very special day in the world of bone marrow transplant patients. It’s considered a new birthday of sorts, and certainly a rebirth, hopefully into health. Yesterday my Mom received my bone marrow, and now those … Continue reading
Posted in May 2012, Uncategorized
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Cytoxan: Update by Kellie, May 1
Cytoxin is pretty nasty stuff. My Mom likes to look nice, and she bought a whole new wardrobe of track suits, button front tops and pajamas to wear at the hospital. You know things are bad when she abandons them … Continue reading
Posted in May 2012, Uncategorized
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Kellie’s Update, Sunday April 29
Mom was admitted to Hopkins on Thursday. It was really a comedy of errors, and the staff apologized profusely. She was scheduled to be admitted at noon, but her room wasn’t ready until nearly 5pm. She hadn’t slept any the … Continue reading
Posted in April 2012
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Kathy’s Message to Our Family, April 24, 2012
My family and I have had a wonderful weekend visiting with family who are giving us much love and support. Larry’s brother, Jerry, flew up from Atlanta to be with us a few days, and we are so grateful. The … Continue reading
Posted in April 2012
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