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2005 Journal Entries

June 23rd - Archie is admitted to the Hospital.
June 24th - Thanks for your e-mails and phone calls.
June 26th - Archie is improving.
June 27th - Archie is acting himself.
June 28th - Archie is doing well.
June 29th - Dr. Hayes scheduled a bone marrow aspiration.
June 30th - The bone marrow aspiration brought good news today.
 
July 1st - Archie was very much himself today.
July 11th - Archie was readmitted to the hospital tonight.
July 13th - I am exhausted.
July 14th - Archie started chemotherapy today.
July 17th - Archie started his fourth day of chemotherapy.
July 19th - Archie has been so pleasant the past few days.
July 21st - Little Man continues to be a maverick.
July 25th - Archie may get to come home tomorrow.
July 26th - We came home today. For about three hours.
July 27th - Good news today.
July 31st - Archie spiked a fever Saturday afternoon.
 
August 1st - Back to the operating room.
August 9th - Going to see Dr. Stroud today.
August 21st - The Blue Screen of Death.
August 29th - Archie is doing really well.
 
September 11th - Kit came home from the Hospital.
September 27th - Archie got home from the hospital Saturday morning.
 
January 27th, 2006 - Although each day drags by, each month passes so quickly.
April 25th, 2006 - Meyer Center for Special Children.
July 1st, 2006 - Archie isn’t a baby anymore.

 

Archie is acting himself more and more as the days move forward
by Anne Moore
06/27/2005

Just a quick update to let everyone know that Archie’s condition is improving and that he’s acting himself more and more as the days move forward. In fact on our way home from the hospital tonight John and I argued about just how well Archie is doing. ‘He’s turned the corner,” John concluded.

“No, not yet,” I countered. “But he is halfway around the bend.”

I admit that I do like these sorts of arguments much more than I like the ones in which we carry on about just how worried we should about Archie’s condition.

When we walked into the hematology/oncology unit today Dr. Hayes stopped us before we got to Archie’s room. “Alright, who’s been praying?” he hollered to us across the hallway.

Turns out that Archie’s latest blood count revealed that he has half as many white blood cells today as he did a day ago, and less than half as many blasts. His platelets are holding steady, right where they need to be, and his hematocrit and hemoglobin levels have improved, too. It is obvious that everyone is openly relieved and encouraged by this news. So relieved in fact that Dr. Hayes doesn’t feel we need to put Archie through a bone marrow aspiration after all. If his counts continue to improve this week we’ll forgo the aspiration. If they don’t, we’ll consent to an aspiration to definitely confirm or rule out leukemia.

A chest film shows that Archie’s pneumonia is no better nor no worse than it was two days ago. Just the same Archie is maintaining his sats on a half liter of oxygen, a significantly lower flow than he needed Friday afternoon. The mucus in Archie’s chest sounds as if it’s breaking up, and he doesn’t grimace every time he coughs anymore. He fights the doctors and nurses, too, just like he normally does no matter how many times I remind him that they are his friends, trying to help him feel better. But most of all I’m happy to report that Archie is eating again, polishing away bottle after bottle of Similac formula like a frat boy on a binge. I love it.

Archie still won’t hold his head up without assistance, and he’d much rather lie quietly in bed than play, but he listened intently as Dada read book after book, and even half-heartedly attempted the hand motions we taught him to “Itsy-Bitsy Spider.” Dada and I are so glad he hasn’t forgotten.

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