Emily’s Smiles through Difficult Trials

Updates about the Emily Hollis Medulloblastoma Cancer Journey

Infection

Filed under: — sho at 9:29 pm on Monday, August 21, 2006

Good evening everyone!  Well, Emily has contracted a bacterial infection so she will not be released from the hospital to go to their “new home” until at least the end of the week.  Not sure she can have visitors and the birthday party has been postponed for the time being.  She perked up some this afternoon, Uncle Eddie Earl said, and continues to have up and down times, to be expected.  She is leary of anyone coming in the room now for fear of what they are going to do to her and perhaps, also, has her days/nights mixed up.  Hospitals are very scarey places for children and I’m sure we can all relate to that.  Please pray that the antibiotics they are giving her for the infection takes care of it and she can be released by weeks end. 

Emily – 5th Birthday Reminder

Filed under: — sho at 11:39 am on Monday, August 21, 2006
Just a quick reminder that Emily’s 5th Birthday is Wednesday, 8/23.  Anyone with cards/gifts that you want to get to her on time, may get them to me today or tomorrow (Monday/Tuesday).  Her Aunt Crystal will be taking everything up for a small family party for her on Wednesday.  We are in hopes that maybe they will be in the apt. by then, if not, they will have the party at the hospital!  Give her an exciting day!!!!     

Emily is continuing to improve ever so slightly.  She is working hard on the physical therapy and every smile or movement she makes is encouragement to the family.  We pray that the spinal tap results come in today with a good report. 

Emily Smiled!!!

Filed under: — sho at 10:15 pm on Wednesday, August 16, 2006
Emily smiled at us this evening!  Didn’t quite see the teeth, but she definitely smiled and the beautiful big blue eyes sparkled!.  Emily was propped up in bed and eating strawberries when we got there.  She nodded her head and said “Uh huh” to everything we asked her and was ready for a nap.  The Physical Therapists were very pleased with her today as she tried to do everything they asked regardless of how difficult it was. IV pain meds have been cut way back and they are focusing on oral pain meds now.  She is really wanting to get rid of the IV tubes and they were having to replace one in her sore little hand later this evening after we left.  MUCH IMPROVEMENT this afternoon after a tough couple of days!!!
The plan for now is a spinal tap on Friday and at the same time they will implant the “hickman” (not sure on spelling or correct name), tube in her chest for her treatments.  They hope she can go to her “new home” close by the hospital mid/end of next week where she will actually stay (instead of the hospital) for her 6 weeks of radiation as an outpatient, which should begin soon.  Then she will have a 6 week break (instead of 2 weeks) before starting chemotherapy.  They hope that at that point she will be able to come HOME to Hampstead and then she will be readmitted to Duke for the 4 months of chemotherapy during which time she will not be allowed to leave the hospital and visitation will, of course, be very limited.
Several good leads have come forth regarding housing for the family and they are checking into others in the next couple of days.  We sure hope they can find something very close to the hospital. 
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