Unfortunately, Jessie is back in the hospital. We took her into the ER on Sunday after she began to dehydrate. She has been unable to keep much liquid down since surgery on Thursday. Her last meal was on Wednesday. The poor kid has been without food for almost a week. She has kept small amounts of liquid down, but not nearly enough, so she is on IV fluids.
Dr. Donahue says that it is her body getting used to the lack of pressure on the brain. It is possible that this is the case, and we hope for a better day tomorrow. It is also possible that the new shunt is overdoing it's job and draining too much CSF (cerebral spinal fluid).
I wish that I had more information and better news.
Thanks to everyone for the prayers, cards, and gifts for Jessie.
Jessie has all that she needs. I ask that if you feel like you want to do something, please don't send gifts. Instead, please donate to one of the following organizations:
The Hemispherectomy Foundation : http://www.HemiFoundation.org
(Dedicated to children and families who have endured Hemispherectomy Brain Surgery)
or
The RE Children's Project : http://www.rechildrens.org
(Dedicated to finding a cure for Rasmussen's Encephalitis )
God Bless,
Cris
Showing posts with label Jessie Hall Hemispherectomy Foundation RE Children's Project Shunt. Show all posts
Showing posts with label Jessie Hall Hemispherectomy Foundation RE Children's Project Shunt. Show all posts
Monday, August 9, 2010
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