Emily’s Smiles through Difficult Trials

Updates about the Emily Hollis Medulloblastoma Cancer Journey

Possible Shunt

Filed under: — sho at 9:45 pm on Sunday, August 13, 2006

Well everyone, the last 24 hours were not kind to Emily,  BUT, as everyone
has lifted her up in prayers today, the last  hour (since about 8:30 p.m.) there
has been a big change in Emily and she is  feeling better.  Yesterday was a
good day and they pulled her around the  hall in a wagon, while she was laying
in it.  Big Brother Trey was able to  get her to smile a time or too and got
her to try and use her left arm.   However, as the evening progressed she was
in severe pain, all evening, all  night until about 2:00 this afternoon she
finally was resting peacefully.   Uncle Eddie Earl just called and said the last
hour she had acted the “best he  had seen” and she was giggling at him and had
played a little card game with  Aunt Linda.

A cat scan this a.m. showed a little fluid on the brain and another scan,  or
possibly an MRI, will be done tomorrow to see how much more fluid builds up 
overnight.  There is a possibility that a shunt will have to be permanently 
implanted.  Please continue to lift Little Emily up in prayer,  that she will
have a restful night, that Eddie & Dawn are able to rest, and  that the tests
tomorrow give us good news!

Many of you continue to ask what you can do to help.  Cards of  encouragement
and just simple “thinking of you” notes are so appreciated.   There is also
an “EMILY’S ENCOURAGERS”  fund that will be opened tomorrow and I will forward
the details  at that time. 

Radiation/Chemotherapy

Filed under: — sho at 9:30 pm on Friday, August 11, 2006

 

Please continue to pray for Emily and her family.  I’ve just talked to Eddie and they have alot of things to process this evening.  Emily will be starting radiation in approximately 1 – 2 weeks.  She will have radiation daily, Mon. – Fri., for 6 weeks.  Then she will have a 2 week break before starting chemotherapy.  Chemo will be  Mon. – Fri. for 4 weeks, then off a week.  This will continue for 4 months.  Emily will not be able to come home during any of this time.  They will be at Duke for at least 6 months. 
Emily has been getting lots of cards and is delighted to get mail.  Highlight of her day.  They will be moving to the Oncology Pediatric wing and her room # will change once again.  We should have it over the weekend.  It will be in the 5100 area. 
Please pray tonight for Eddie and Dawn as they process this information and make plans for their immediate future.

Thursday

Filed under: — sho at 9:09 pm on Thursday, August 10, 2006

Just talked to Dawn about Emily’s day.  She started out having a pretty good day, even colored a little,  but by this evening after doctors, nurses, occupational and physical therapists, she is a tired little girl and in some pain but is resting comfortably now.  Dawn said she hadn’t really eaten anything again today, tasted a little applesauce but that was it.  Still waiting on the final pathology report.  She has been moved around alot trying to strengthen her up some. Trey came home this evening with the Hollis grandparents and they are going to stay home a few days. 

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